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WO1998007817A1 - Compositions detergentes possedant une activite lipolytique regulee par anticorps - Google Patents

Compositions detergentes possedant une activite lipolytique regulee par anticorps Download PDF

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Publication number
WO1998007817A1
WO1998007817A1 PCT/US1996/013323 US9613323W WO9807817A1 WO 1998007817 A1 WO1998007817 A1 WO 1998007817A1 US 9613323 W US9613323 W US 9613323W WO 9807817 A1 WO9807817 A1 WO 9807817A1
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WO
WIPO (PCT)
Prior art keywords
alkyl
detergent
lipolytic enzyme
antibody
enzyme
Prior art date
Application number
PCT/US1996/013323
Other languages
English (en)
Inventor
Ivan Maurice Alfons Jan Herbots
Andre Cesar Baeck
Tim Maria Joris Van Hauwermeiren
Jean Wevers
Original Assignee
The Procter & Gamble Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to PCT/US1996/013323 priority Critical patent/WO1998007817A1/fr
Priority to AU67772/96A priority patent/AU6777296A/en
Priority to EP97939411A priority patent/EP0922089A1/fr
Priority to AU41506/97A priority patent/AU4150697A/en
Priority to CA002263435A priority patent/CA2263435A1/fr
Priority to BR9713172-5A priority patent/BR9713172A/pt
Priority to CN97198838.2A priority patent/CN1233279A/zh
Priority to PCT/US1997/014287 priority patent/WO1998006810A1/fr
Priority to JP10510013A priority patent/JP2000500817A/ja
Priority to ARP970103728A priority patent/AR009257A1/es
Publication of WO1998007817A1 publication Critical patent/WO1998007817A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/38—Products with no well-defined composition, e.g. natural products
    • C11D3/386—Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38627—Preparations containing enzymes, e.g. protease or amylase containing lipase
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/38—Products with no well-defined composition, e.g. natural products
    • C11D3/384—Animal products
    • C11D3/3845—Antibodies

Definitions

  • the present invention relates to detergent compositions including laundry, dishwashing and hard surface cleaning compositions comprising a lipolytic enzyme and a lipolytic enzyme-directed antibody in order to prevent timing malodour formation related to the hydrolytic activity of lipolytic enzyme while maintaining excellent wash performance.
  • the humoral immune system An important part of the system which protects vertebrates against infections by bacteria and viruses is the humoral immune system. Specialised cells present in bone marrow, lymphoid tissues and blood, produce immunoglobulins (antibody) which appear in response to the introduction of micro- or macromolecule foreign to that body and bind the body-foreign structure initiating its destruction. Such a body- foreign molecule is called an antigen.
  • the antibody is directed against the antigenic determinant or hapten of the antigen e.g. an amino acid sequence, parts of oligosaccharides, polysaccharides, lipopolysaccharides, glycoproteins, lipoproteins lipoteichoinic acids.
  • Antibody molecules have binding sites that are very specific for and complementary to the structural features of the antigen that induced their formation.
  • EP 479 600, EP 453 097 and EP 450 800 relate to the use of antibodies or fragments thereof for the delivery of active ingredients to a target site.
  • EP 481 701 discloses treatment compositions for topical application containing microcapsules which enclose a beneficial agent at a target location, the microcapsules having an antibody or antibody fragment specific to the target location or a lectin.
  • WO92/04380 describes reshaped human antibody or reshaped human antibody fragments having specificity for human polymorphic epithelial ucin to be used in the treatment or diagnosis of cancer.
  • Epstein-Barr virus specific polypeptides for the production of antibodies and the diagnostic and treatment of said disease is disclosed in WO94/06470.
  • compositions comprising antibodies as anti-carie or periodontal diseases treatment have been extensively described in WO95/01155, WO95/00110, O95/10612, EP 140 498, GB 2 151 923, GB 2 176 400, GB 2 167 299, DE 4324859, US 5 401 723 and EP 280 576.
  • EP 673 683 and EP 542 309 disclose hair cosmetic compositions containing an antibody to hair or hair extract, obtained from egg yolk or poultry immunised with the hair or hair extract and a polymer emulsion to provide reduced hair damage, softness, moistened feel and smoothness, said composition being adsorbed only onto a specified part of the hair.
  • compositions containing antagonists ⁇ tyrphostins or antibodies) against epidermal and transforming growth factors, suitable for use in treatment of acne are described in W095/24896.
  • EP 400 569 discloses a method for preparing vaccine composition for dental caries in nasal drops comprising an antigen produced by integrating a protein antigen-expressing gene into the chromosomal gene of a streptococcus mutants GS-5 strain.
  • 094/25591 discloses the production of antibodies or functionalised fragments thereof derived from heavy chain immunoglobulins of camelidae .
  • Detergent compositions include nowadays a complex combination of active ingredients which fulfill certain specific needs : a surfactant system, enzymes providing cleaning and fabric care benefits, bleaching agents, a builder system, suds suppressors, soil-suspending agents, soil-release agents, optical brighteners, softening agents, dispersants, dye transfer inhibition compounds, abrasives, bactericides, perfumes, and their overall performance has indeed improved over the years .
  • current laundry detergent formulations generally include detergent enzymes and more specifically lipolytic enzymes.
  • lipolytic activity can be fully controlled during the cleaning process so that the potential negative effects, i.e. malodor formation due to the overexposure of the substrate to the active lipolytic enzyme can now be avoided.
  • the above need has been met by specific detergent compositions including laundry, dishwashing and hard surface cleaning, comprising a lipolytic enzyme and an antibody directed to the lipolytic enzyme.
  • the present invention relates to detergent compositions including laundry, dishwashing and hard surface cleaning compositions comprising a lipolytic enzyme and a lipolytic enzyme-directed antibody in order to prevent timing malodour formation related to the hydrolytic activity of lipolytic enzyme while maintaining excellent wash performance.
  • An essential element of the detergent compositions of the present invention is an antibody.
  • the immunoglobulins are classified into 5 classes, respectively : IgM, IgG, IgA, IgD and IgE.
  • Preferred types of immunoglobulins are IgG and IgA.
  • Secretory slgA which are found into human excreted body fluids such as milk, saliva, respiratory and intestinal fluids are especially designed to survive in said secretions, they have enhanced binding characteristics and are resistant to proteolytic hydrolysis .
  • the antibody which may be monoclonal or polyclonal or an antibody fragment, may be generated by techniques conventional in the art, for example by using recombinant DNA techniques allowing to produce antibodies variants with new properties : reduced immunogenecity, enhanced affinity, altered size, ... Specific binding subunits or antibody fragments may also be used. These may be similarly generated by conventional techniques such as enzymatic digestion by papain or pepsin, or using recombinant DNA techniques. Antibody fragments may also be generated by conventional recombinant DNA techniques.
  • Heavy and light chains are indeed composed of constant and variable domains.
  • the constant domains are very important for a number of functions, but for many applications in industrial processes and products their variable domains are sufficient. Consequently many methods have been described to produce antibody fragments.
  • Antibody fragments which are used may be a Fab, a Fv, a scFv or any other fragment having similar binding properties.
  • Preferred routes to antibodies fragments are through recombinant DNA technology, so that the fragment is expressed by a genetically transformed organism.
  • Antibodies and antibody fragments produced by recombinant DNA technology do not need to be identical to fragment of antibodies produced in vertebrates, having nevertheless the same binding properties evaluated by their Km, Ki and Kcat .
  • they may include sequences of amino acids and/or glycosylations which differ from those found in antibodies produced in other ways, especially sequences at the end of fragments.
  • antibody fragments produced through recombinant DNA technology may include extra amino acid sequences at their termini which have no counterpart in antibodies produced in other ways .
  • a binding agent for use in this invention is a natural or synthetic polymer which mimics the specific binding activity of a natural antibody's complementary region (s).
  • a polymer is for example a polypeptide or a polymer imprinting (Angew. Chem. Int. Ed. Engl. 1995, 34, 1812-1832).
  • the usual method for the production of antibodies may be adopted in immunising mammals or poultry with the corresponding antigens.
  • mammals to be immunised mouses, rabbits, goats, sheep, horses, cows, etc. may be used.
  • the antibody immunoglobulin fraction
  • the antibody may be separated from the antiserum, the milk or the eggs according to the ordinary antibody purification method including salting-out method, Poison extraction, gel-filtration chromatography, ion-exchange chromatography, affinity chromatography and the like, the salting-out method using ammonium sulfate to produce the precipitates, followed by dialysing the precipitates against physiological saline to obtain the purified precipitates as the antibody.
  • Plants are also capable of synthesising and assembling every kind of antibody molecule and allow a large scale of production of antibodies as described in Tibtech. Dec 1995, Vol 13, pp 522-527; Plant Mol. Biol., 26, pp 1701-1710, 1994 and Biotechnol . proj . 1991 , 7, pp 455-461 and in US patent 5, 202,422.
  • Antibodies can also be produced into microorganisms such as E. coli or S. cerevisiae via biofermentation process as illustrated in the EP patent 667 394.
  • the drawbacks due to prolonged activity of the enzyme can be avoided by an effective control of the enzymatic activity trough the introduction of the specifically corresponding antibody.
  • Such antibodies can be either polyclonal - directed to the whole enzyme structure - or monoclonal - directed to specific epitopes of the enzyme activity controlling regions of the enzyme structure .
  • Antibodies raised against specific enzyme can effectively deactivate the enzyme by the antibody-antigen binding in or very near the active site. The formation of such complex leads to the enzyme deactivation and could be explained by the distortion of the 3 -dimensional structure and/or steric hindrance at the substrate cleft.
  • the deactivation of the enzyme can also be achieved by the precipitation of the complex antibody-antigen from the washing solution. Due to very high specificity and efficiency of the antibody- antigen interaction, no other detergent active is thereby affected .
  • the lipolytic enzyme-directed antibodies are preferably comprised in the detergent compositions of the present invention at a level of from 10E-6% to 10E+1% by weight of total composition.
  • antibodies raised against a specific lipolytic enzyme have the capability of binding other lipolytic enzymes of high structural similarity, providing cross-reactivity.
  • the antibodies raised against the lipolytic enzyme are released in the wash solution after a lag-period allowing to deliver excellent benefits to be achieved by the end of the wash process .
  • the antibodies are preferably incorporated into a release agent in order to control their release timing and rate in the wash solution.
  • the physical form of the antibody-containing release agent is adapted to the physical form of the corresponding detergent or additive.
  • the antibodies and release agents can be contained in a granulate.
  • Said antibody granulate can suitably contain various granulation aids, binders, fillers, plasticizers, lubricants, cores and the like.
  • granulation aids include cellulose (e.g. cellulosic fibers or in microcrystalline form) , cellulose derivatives (CMC, MC, HPC, HPMC) , gelatin, starch, dextrins, sugars, polyvinylpyrrolidone, PVA, PEG, salts (e.g. sodium sulfate, calcium sulfate) , titanium dioxide, talc, clays (kaolin or bentonite) and nonionic surfactants.
  • Other materials of relevance for incorporation in the granulate are described in EP 304 331.
  • the release agent may be, for example, a coating.
  • Said coating protects said granulates in the wash environment for a certain period of time.
  • the coating will normally be applied to said granulates in an amount in the range of 1% to 50% by weight (calculated on the basis of the weight of the uncoated, dry granulate) , preferably in the range of 5 % to 40 % by weight.
  • the amount of coating to be applied to said granulates will depend to a considerable extent on the nature and composition of the desired coating, and to the kind of protection said coating should offer to said granulates.
  • the thickness of said coating or a multi-layered coating applied onto any of the above granulates may determine the period in which the content of said granulates is released.
  • a possible multi-layered coating may be a coating in which, for example, a fast release coating is applied over a slow release coating.
  • co-granulates can be constructed containing in the outer layer the detergent enzyme and a fast releasing agent and in the inner core, the antibody and a slow releasing agent .
  • Suitable release coatings are coatings which give rise to release of the contents of antibody-containing granulates under the conditions prevailing during the use thereof.
  • a preparation of the invention is to be introduced into a washing liquor containing a washing detergent (normally comprising, e.g. one or more types of surfactants)
  • the coating should be one which ensures the release of the contents of said granulates from the release agent when it is introduced into the washing medium.
  • Preferred release coating are coatings which are substantially insoluble in water.
  • Release coatings which are appropriate in washing media may suitably comprise substances selected from the following: cellulose and cellulase derivatives, PVA, PVP, tallow; hydrogenated tallow; partially hydrolyzed tallow; fatty acids and fatty alcohols of natural and synthetic origin; long-chain fatty acid mono-, di- and triesters of glycerol (e.g. glycerol monostearate) ; ethoxylated fatty alcohols; latexes; hydrocarbons of melting point in the range of 50-80°C; and waxes.
  • Melt -coating agents are a preferred class of fast or slow release coating agents which can be used without dilution with water. Reference may be made to Controlled Release Systems : Fabrication Technology, Vol. I, CRC Press, 1988, for further information on slow release coating .
  • Coatings may suitably further comprise substances such as clays (e.g. kaolin), titanium dioxide, pigments, salts (such as calcium carbonate) and the like.
  • clays e.g. kaolin
  • titanium dioxide titanium dioxide
  • pigments such as calcium carbonate
  • salts such as calcium carbonate
  • the antibody in liquid detergent compositions, can be incorporated as a dispersion of particles containing in addition to the antibody, a release agent.
  • the antibody can be present in a liquid or solid form.
  • Suitable particles consist of a porous hydrophobic material (e.g. silica with an average pore diametre of 500 Angstrom or higher) containing into the pores a solution of antibodies and a surfactant as described in EP 583 512 of Surutzidis A. et al.
  • the release agent might be a coating which protects said particles in the wash cycle for a certain period of time.
  • the coating is preferably a hydrophobic coating material such as a hydrophibic liquid polymer.
  • Said polymer can be an organo polysiloxane oil, alternatively a high olecula weight hydrocarbon or water insoluble but water permeable polymeric material such as carboxymethylcellulose , PVA, PVP.
  • the polymer properties are selected to achieve a suitable release profile of the antibody in the wash solution .
  • Suitable specific lipolytic enzymes for use herein include those of bacterial and fungal origin . Origin can further be mesophilic or extremophilic (psychrophilic, psychrotrophic, thermophilic, barophilic, alkalophilic, acidophilic, halophilic, etc.). Purified or non-purified forms of these enzymes may be used. Also included by definition, are mutants of native enzymes. Mutants can be obtained e.g. by protein and/or genetic engineering, chemical and/or physical modifications of native enzymes. Common practice as well is the expression of the enzyme via host organisms in which the genetic material responsible for the production of the enzyme has been cloned.
  • lipolytic enzyme is intended to indicate an enzyme exhibiting a lipid degrading capability, such as a capability of degrading a triglyceride, a phospholipid, a wax-ester or cutin.
  • the lipolytic enzyme may, e.g., be a lipase, a phospholipase, an esterase or a cutinase.
  • An essential element of the present invention is carboxylic ester hydrolase EC 3.1.1 and especially a lipase EC 1.1.1.3.
  • Said lipolytic enzyme is incorporated at a level of from 0.0001 to 2%, preferably from 0.0002% to 1%, more preferably from 0.0005% to 0.1% pure enzyme by weight of total composition.
  • Suitable lipolytic enzyme enzymes for detergent usage include those produced by microorganisms of the Pseudomonas group, such as Pseudomonas stutzeri ATCC 19.154, as disclosed in British Patent 1,372,034.
  • Suitable lipases include those which show a positive immunological cross- reaction with the antibody of the lipase, produced by the microorganism Pseudomonas fluorescen t IAM 1057. This lipase is available from Amano Pharmaceutical Co. Ltd., Nagoya, Japan, under the trade name Lipase P "Amano, " hereinafter referred to as "Amano-P" .
  • lipases include Amano-CES, lipases ex Chro ⁇ iobacter viscosum, e.g. Chromobacter viscosum var . lipolyticum NRRLB 3673 from Toyo Jozo Co., Tagata, Japan; Chromobacter viscosum lipases from U.S. Biochemical Corp., U.S.A. and Disoynth Co., The Netherlands, and lipases ex Pseudomonas gladioli .
  • lipases such as Ml Lipase R and ipomax R (Gist-Brocades) and Lipolase R and Lipolase Ultra R (Novo) which have found to be very effective when used in combination with the compositions of the present invention.
  • cutinases [EC 3.1.1.50] which can be considered as a special kind of lipase, namely lipases which do not require interfacial activation.
  • Suitable cutinases are described in WO 94/14963 and WO 94/14964. Addition of cutinases to detergent compositions have been described in e.g. WO-A-88/09367 (Genencor) .
  • cutinases are normally incorporated in the detergent composition at levels from 0.0001% to 2% of active enzyme by weight of the detergent composition.
  • detergent compositions of the invention may also contain additional detergent components.
  • additional detergent components The precise nature of these additional components, and levels of incorporation thereof will depend on the physical form of the composition, and the nature of the cleaning operation for which it is to be used.
  • the detergent compositions according to the invention can be liquid, paste, gels, bars, tablets, powder or granular forms.
  • Granular compositions can also be in "compact " form, the liquid compositions can also be in a "concentrated” form.
  • compositions of the invention may for example, be formulated as hard surface cleaner, hand and machine dishwashing compositions, hand and machine laundry detergent compositions including laundry additive compositions and compositions suitable for use in the soaking and/or pretreatment of stained fabrics, rinse added fabric softener compositions.
  • compositions of the invention When formulated as compositions for use in manual dishwashing methods the compositions of the invention preferably contain a surfactant and preferably other detergent compounds selected from organic polymeric compounds, suds enhancing agents, group II metal ions, solvents, hydrotropes and additional enzymes.
  • a surfactant preferably other detergent compounds selected from organic polymeric compounds, suds enhancing agents, group II metal ions, solvents, hydrotropes and additional enzymes.
  • the compositions of the invention When formulated as compositions suitable for use in a laundry machine washing method, the compositions of the invention preferably contain both a surfactant and a builder compound and additionally one or more detergent components preferably selected from organic polymeric compounds, bleaching agents, additional enzymes, suds suppressors, dispersants, lime-soap dispersants, soil suspension and anti-redeposition agents and corrosion inhibitors. Laundry compositions can also contain softening agents, as additional detergent components.
  • the compositions of the invention can also be used as detergent additive products comprising a lipolytic enzyme- directed antibody and will be added to conventional detergent lipolytic enzyme-containing compositions.
  • the detergent additives can also comprise a lipolytic enzyme and a lipolytic enzyme-directed antibody. Such additive products are intended to supplement or boost the performance of conventional detergent compositions preferably comprise up to 50% antibodies by weight of total composition.
  • the density of the granular laundry detergent compositions herein ranges from 400 to 1200 g/litre, preferably 600 to 950 g/litre of composition measured at 20 °C.
  • inorganic filler salts are conventional ingredients of detergent compositions in powder form; in conventional detergent compositions, the filler salts are present in substantial amounts, typically 17-35% by weight of the total composition.
  • the filler salt is present in amounts not exceeding 15% of the total composition, preferably not exceeding 10%, most preferably not exceeding 5% by weight of the composition.
  • the inorganic filler salts are selected from the alkali and alkaline-earth-metal salts of sulphates and chlorides.
  • a preferred filler salt is sodium sulphate.
  • Liquid detergent compositions according to the present invention can also be in a "concentrated form", in such case, the liquid detergent compositions according the present invention will contain a lower amount of water, compared to conventional liquid detergents.
  • the water content of the concentrated liquid detergent is preferably less than 50%, more preferably less than 40%, most preferably less than 30% by weight of the detergent composition.
  • the detergent compositions according to the present invention comprise a surfactant system wherein the surfactant can be selected from nonionic and/or anionic and/or cationic and/or a pholytic and/or zwitterionic and/or semi-polar surfactants.
  • the surfactant is typically present at a level of from 0.1% to 60% by weight. More preferred levels of incorporation are 1% to 35% by weight, most preferably from 1% to 30% by weight of detergent compositions in accord with the invention.
  • the surfactant is preferably formulated to be compatible with enzyme components present in the composition.
  • the surfactant is most preferably formulated such that it promotes, or at least does not degrade, the stability of any enzyme in these compositions .
  • Preferred surfactant systems to be used according to the present invention comprise as a surfactant one or more of the nonionic and/or anionic surfactants described herein.
  • Polyethylene, polypropylene, and polybutylene oxide condensates of alkyl phenols are suitable for use as the nonionic surfactant of the surfactant systems of the present invention, with the polyethylene oxide condensates being preferred.
  • These compounds include the condensation products of alkyl phenols having an alkyl group containing from about 6 to about 14 carbon atoms, preferably from about 8 to about 14 carbon atoms, in either a straight - chain or branched-chain configuration with the alkylene oxide.
  • the ethylene oxide is present in an amount equal to from about 2 to about 25 moles, more preferably from about 3 to about 15 moles, of ethylene oxide per mole of alkyl phenol .
  • nonionic surfactants of this type include IgepalTM CO-630, marketed by the GAF Corporation; and TritonTM X-45, X-114, X-100 and X-102, all marketed by the Rohm & Haas Company. These surfactants are commonly referred to as alkylphenol alkoxylates (e.g., alkyl phenol ethoxylates) .
  • the condensation products of primary and secondary aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide are suitable for use as the nonionic surfactant of the nonionic surfactant systems of the present invention.
  • the alkyl chain of the aliphatic alcohol can either be straight or branched, primary or secondary, and generally contains from about 8 to about 22 carbon atoms.
  • About 2 to about 7 moles of ethylene oxide and most preferably from 2 to 5 moles of ethylene oxide per mole of alcohol are present in said condensation products.
  • nonionic surfactants of this type include TergitolTM 15-S-9 (the condensation product of ⁇ i-C ⁇ linear alcohol with 9 moles ethylene oxide) , TergitolTM 24- L-6 NMW (the condensation product of i2 _c l4 primary alcohol with 6 moles ethylene oxide with a narrow molecular weight distribution) , both marketed by Union Carbide Corporation; NeodolTM 45-9 (the condensation product of C 14 -C15 linear alcohol with 9 moles of ethylene oxide), NeodolTM 23-3 (the condensation product of C ⁇ -C ⁇ linear alcohol with 3.0 moles of ethylene oxide), NeodolTM 45-7 (the condensation product of C 4-C 15 linear alcohol with 7 moles of ethylene oxide), NeodolTM 45-5 (the condensation product of C 1 4-C15 linear alcohol with 5 moles of ethylene oxide) marketed by Shell Chemical Company, KyroTM EOB (the condensation product of C13-C15 alcohol with 9 moles ethylene oxide) , marketed by The Proc
  • nonionic surfactant of the surfactant systems of the present invention are the alkylpolysaccharides disclosed in U.S. Patent 4,565,647, Llenado, issued January 21, 1986, having a hydrophobic group containing from about 6 to about 30 carbon atoms, preferably from about 10 to about 16 carbon atoms and a polysaccharide, e.g. a polyglycoside, hydrophilic group containing from about 1.3 to about 10, preferably from about 1.3 to about 3, most preferably from about 1.3 to about 2.7 saccharide units.
  • a hydrophobic group containing from about 6 to about 30 carbon atoms, preferably from about 10 to about 16 carbon atoms and a polysaccharide, e.g. a polyglycoside, hydrophilic group containing from about 1.3 to about 10, preferably from about 1.3 to about 3, most preferably from about 1.3 to about 2.7 saccharide units.
  • Any reducing saccharide containing 5 or 6 carbon atoms can be used, e.g., glucose, galactose and galactosyl moieties can be substituted for the glucosyl moieties (optionally the hydrophobic group is attached at the 2-, 3-, 4-, etc. positions thus giving a glucose or galactose as opposed to a glucoside or galactoside) .
  • the intersaccharide bonds can be, e.g., between the one position of the additional saccharide units and the 2-, 3-, 4-, and/or 6- positions on the preceding saccharide units.
  • the preferred alkylpolyglycosides have the formula
  • R 2 0 (C n H 2n 0) t (glycosyl) x
  • R 2 is selected from the group consisting of alkyl, alkylphenyl, hydroxyalkyl, hydroxyalkylphenyl , and mixtures thereof in which the alkyl groups contain from about 10 to about 18, preferably from about 12 to about 14, carbon atoms; n is 2 or 3, preferably 2; t is from 0 to about 10, preferably 0; and x is from about 1.3 to about 10, preferably from about 1.3 to about 3, most preferably from about 1.3 to about 2.7.
  • the glycosyl is preferably derived from glucose.
  • the alcohol or alkylpolyethoxy alcohol is formed first and then reacted with glucose, or a source of glucose, to form the glucoside (attachment at the 1-position) .
  • the additional glycosyl units can then be attached between their 1-position and the preceding glycosyl units 2-, 3-, 4- and/or 6-position, preferably predominately the 2-position.
  • the condensation products of ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol are also suitable for use as the additional nonionic surfactant systems of the present invention.
  • the hydrophobic portion of these compounds will preferably have a molecular weight of from about 1500 to about 1800 and will exhibit water insolubility.
  • the addition of polyoxyethylene moieties to this hydrophobic portion tends to increase the water solubility of the molecule as a whole, and the liquid character of the product is retained up to the point where the polyoxyethylene content is about 50% of the total weight of the condensation product, which corresponds to condensation with up to about 40 moles of ethylene oxide.
  • Examples of compounds of this type include certain of the commercially- available PlurafacTM LF404 and PluronicTM surfactants, marketed by BASF.
  • nonionic surfactant of the nonionic surfactant system of the present invention are the condensation products of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylenediamine .
  • the hydrophobic moiety of these products consists of the reaction product of ethylenediamine and excess propylene oxide, and generally has a molecular weight of from about 2500 to about 3000.
  • This hydrophobic moiety is condensed with ethylene oxide to the extent that the condensation product contains from about 40% to about 80% by weight of polyoxyethylene and has a molecular weight of from about 5,000 to about 11,000.
  • this type of nonionic surfactant include certain of the commercially available TetronicTM compounds, marketed by BASF.
  • Preferred for use as the nonionic surfactant of the surfactant systems of the present invention are polyethylene oxide condensates of alkyl phenols, condensation products of primary and secondary aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide, alkylpolysaccharides , and mixtures thereof. Most preferred are Cg - C- ⁇ . alkyl phenol ethoxylates having from 3 to 15 ethoxy groups and Cg-C ⁇ e alcohol ethoxylates (preferably C ⁇ g av 9 • ) having from 2 to 10 ethoxy groups, and mixtures thereof.
  • Highly preferred nonionic surfactants are polyhydroxy fatty acid amide surfactants of the formula.
  • R 1 is H, or R 1 is C ⁇ _4 hydrocarbyl , 2-hydroxy ethyl, 2-hydroxy propyl or a mixture thereof
  • R 2 is C5_3i hydrocarbyl
  • Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative thereof.
  • R 1 is methyl
  • R 2 is a straight Cn-15 alkyl or C ⁇ g,. ⁇ alkyl or alkenyl chain such as coconut alkyl or mixtures thereof
  • Z is derived from a reducing sugar such as glucose, fructose, maltose, lactose, in a reductive amination reaction.
  • Suitable anionic surfactants to be used are linear alkyl benzene sulfonate, alkyl ester sulfonate surfactants including linear esters of Cg-C2o carboxylic acids (i.e., fatty acids) which are sulfonated with gaseous S0 3 according to "The Journal of the American Oil Chemists Society", 52 (1975), pp. 323-329.
  • Suitable starting materials would include natural fatty substances as derived from tallow, palm oil, etc.
  • alkyl ester sulfonate surfactant especially for laundry applications, comprise alkyl ester sulfonate surfactants of the structural formula :
  • R 3 is a Cg-C2o hydrocarbyl, preferably an alkyl, or combination thereof
  • R 4 is a C ⁇ -Cg hydrocarbyl, preferably an alkyl, or combination thereof
  • M is a cation which forms a water soluble salt with the alkyl ester sulfonate.
  • Suitable salt-forming cations include metals such as sodium, potassium, and lithium, and substituted or unsubstituted ammonium cations, such as monoethanolamine, diethanolamine, and triethanolamine .
  • R 3 is c 10 ⁇ c 16 alkyl
  • R 4 is methyl, ethyl or isopropyl.
  • methyl ester sulfonates wherein R 3 is C ⁇ o _c l6 alkyl.
  • alkyl sulfate surfactants which are water soluble salts or acids of the formula ROSO3M wherein R preferably is a ⁇ 0 ⁇ 2 hydrocarbyl, preferably an alkyl or hydroxyalkyl having a c 10 ⁇ c 20 alkyl component, more preferably a alkyl or hydroxyalkyl , and M is H or a cation, e.g., an alkali metal cation (e.g. sodium, potassium, lithium), or ammonium or substituted ammonium (e.g.
  • R preferably is a ⁇ 0 ⁇ 2 hydrocarbyl, preferably an alkyl or hydroxyalkyl having a c 10 ⁇ c 20 alkyl component, more preferably a alkyl or hydroxyalkyl
  • M is H or a cation, e.g., an alkali metal cation (e.g. sodium, potassium, lithium), or ammonium or substituted ammonium (e.g.
  • alkyl chains of Ci2 ⁇ i6 are preferred for lower wash temperatures (e.g. below about 50°C) and C 1 g_ 1 ⁇ alkyl chains are preferred for higher wash temperatures (e.g. above about 50 °C) .
  • anionic surfactants useful for detersive purposes can also be included in the detergent compositions of the present invention. These can include salts (including, for example, sodium, potassium, ammonium, and substituted ammonium salts such as mono-, di- and triethanolamine salts) of soap, C g-C22 primary of secondary alkanesulfonates, C g-C24 olefinsulfonates, sulfonated polycarboxylic acids prepared by sulfonation of the pyrolyzed product of alkaline earth metal citrates, e.g., as described in British patent specification No.
  • salts including, for example, sodium, potassium, ammonium, and substituted ammonium salts such as mono-, di- and triethanolamine salts
  • C g-C22 primary of secondary alkanesulfonates C g-C24 olefinsulfonates
  • sulfonated polycarboxylic acids prepared by sulfonation of the pyroly
  • alkylpolyglycolethersulfates (containing up to 10 moles of ethylene oxide) ; alkyl glycerol sulfonates, fatty acyl glycerol sulfonates, fatty oleyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, paraffin sulfonates, alkyl phosphates, isethionates such as the acyl isethionates, N-acyl taurates, alkyl succinamates and sulfosuccinates, monoesters of sulfosuccinates (especially saturated and unsaturated C ⁇ -C ⁇ monoesters) and diesters of sulfosuccinates (especially saturated and unsaturated c 6 _c 12 diesters) , acyl sarcosinates, sulfates of alkylpolysaccharides such
  • laundry detergent compositions of the present invention typically comprise from about 1% to about 40%, preferably from about 3% to about 20% by weight of such anionic surfactants .
  • alkyl alkoxylated sulfate surfactants hereof are water soluble salts or acids of the formula R0(A) m S03M wherein R is an unsubstituted CIQ _C 24 alkyl or hydroxyalkyl group having a c 10 _c 24 alkyl component, preferably a C 1 2-C2o alkyl or hydroxyalkyl, more preferably i2 _c i8 alkyl or hydroxyalkyl, A is an ethoxy or propoxy unit, m is greater than zero, typically between about 0.5 and about 6, more preferably between about 0.5 and about 3, and M is H or a cation which can be, for example, a metal cation (e.g., sodium, potassium, lithium, calcium, magnesium, etc.), ammonium or substituted-ammonium cation.
  • R is an unsubstituted CIQ _C 24 alkyl or hydroxyalkyl group having a c 10 _c 24 al
  • Alkyl ethoxylated sulfates as well as alkyl propoxylated sulfates are contemplated herein.
  • Specific examples of substituted ammonium cations include methyl-, dimethyl, trimethyl- ammonium cations and quaternary ammonium cations such as tetramethyl-ammonium and dimethyl piperdinium cations and those derived from alkylamines such as ethylamine, diethylamine, triethylamine, mixtures thereof, and the like.
  • Exemplary surfactants are c i2 ⁇ c 18 alkyl polyethoxylate (1.0) sulfate (C 12 -C 18 E (1.0) ) , C 12 -C 18 alkyl polyethoxylate (2.25) sulfate (C 12 -C 18 E (2.25) M) , C 12 - C 18 alkyl polyethoxylate (3.0) sulfate (C 12 -C 18 E (3.0) M) , and C 1 -C ⁇ 8 alkyl polyethoxylate (4.0) sulfate (C 1 - C ⁇ 8 E(4.0)M), wherein M is conveniently selected from sodium and potassium.
  • the detergent compositions of the present invention may also contain cationic, ampholytic, zwitterionic , and semi- polar surfactants, as well as the nonionic and/or anionic surfactants other than those already described herein.
  • Cationic detersive surfactants suitable for use in the detergent compositions of the present invention are those having one long-chain hydrocarbyl group.
  • cationic surfactants include the ammonium surfactants such as alkyltrimethylammonium halogenides, and those surfactants having the formula :
  • R 2 is an alkyl or alkyl benzyl group having from about 8 to about 18 carbon atoms in the alkyl chain
  • each R 3 is selected from the group consisting of -CH2CH2-, CH 2 CH(CH 3 )-, -CH 2 CH(CH 2 OH) -, -CH 2 CH 2 CH 2 -, and mixtures thereof
  • each R 4 is selected from the group consisting of c l" c 4 alkyl, C ⁇ -C4 hydroxyalkyl, benzyl ring structures formed by joining the two R 4 groups, -CH2CHOH- CHOHCOR 6 CHOHCH 2 OH wherein R 6 is any hexose or hexose polymer having a molecular weight less than about 1000, and hydrogen when y is not 0
  • R 5 is the same as R 4 or is an alkyl chain wherein the total number of carbon atoms of R 2 plus R 5 is not more than about 18
  • each y is from 0 to about
  • Quaternary ammonium surfactant suitable for the present invention has the formula (I) :
  • Rl is a short chainlength alkyl (C6-C10) or alkylamidoalkyl of the formula (II) :
  • y is 2-4, preferably 3. whereby R2 is H or a C1-C3 alkyl, whereby x is 0-4, preferably 0-2, most preferably 0, whereby R3 , R4 and R5 are either the same or different and can be either a short chain alkyl (C1-C3) or alkoxylated alkyl of the formula III,
  • X" is a counterion, preferably a halide, e.g. chloride or methylsulfate .
  • R6 is C1-C4 and z is 1 or 2.
  • Highly preferred cationic surfactants are the water- soluble quaternary ammonium compounds useful in the present composition having the formula :
  • the preferred alkyl chain length for R- is C12-C15 particularly where the alkyl group is a mixture of chain lengths derived from coconut or palm kernel fat or is derived synthetically by olefin build up or OXO alcohols synthesis.
  • Preferred groups for R2 3 and R4 are methyl and hydroxyethyl groups and the anion X may be selected from halide, methosulphate, acetate and phosphate ions.
  • suitable quaternary ammonium compounds of formulae (i) for use herein are : coconut trimethyl ammonium chloride or bromide; coconut methyl dihydroxyethyl ammonium chloride or bromide ; decyl triethyl ammonium chloride; decyl dimethyl hydroxyethyl ammonium chloride or bromide ;
  • the detergent compositions of the present invention typically comprise from 0.2% to about 25%, preferably from about 1% to about 8% by weight of such cationic surfactants.
  • Ampholytic surfactants are also suitable for use in the detergent compositions of the present invention. These surfactants can be broadly described as aliphatic derivatives of secondary or tertiary amines, or aliphatic derivatives of heterocyclic secondary and tertiary amines in which the aliphatic radical can be straight- or branched-chain.
  • One of the aliphatic substituents contains at least about 8 carbon atoms, typically from about 8 to about 18 carbon atoms, and at least one contains an anionic water-solubilizing group, e.g. carboxy, sulfonate, sulfate. See U.S. Patent No. 3,929,678 to Laughlin et al . , issued December 30, 1975 at column 19, lines 18-35, for examples of ampholytic surfactants.
  • the detergent compositions of the present invention typically comprise from 0.2% to about 15%, preferably from about 1% to about 10% by weight of such ampholytic surfactants.
  • Zwitterionic surfactants are also suitable for use in detergent compositions. These surfactants can be broadly described as derivatives of secondary and tertiary amines, derivatives of heterocyclic secondary and tertiary amines, or derivatives of quaternary ammonium, quaternary phosphonium or tertiary sulfonium compounds. See U.S. Patent No. 3,929,678 to Laughlin et al . , issued December 30, 1975 at column 19, line 38 through column 22, line 48, for examples of zwitterionic surfactants.
  • the detergent compositions of the present invention typically comprise from 0.2% to about 15%, preferably from about 1% to about 10% by weight of such zwitterionic surfactants.
  • Semi-polar nonionic surfactants are a special category of nonionic surfactants which include water-soluble amine oxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from about 1 to about 3 carbon atoms; water- soluble phosphine oxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from about 1 to about 3 carbon atoms; and water-soluble sulfoxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and a moiety selected from the group consisting of alkyl and hydroxyalkyl moieties of from about 1 to about 3 carbon
  • Semi -polar nonionic detergent surfactants include the amine oxide surfactants having the formula
  • R 3 (OR 4 )xN(R 5 ) 2 wherein R 3 is an alkyl, hydroxyalkyl, or alkyl phenyl group or mixtures therof containing from about 8 to about 22 carbon atoms; R 4 is an alkylene or hydroxyalkylene group containing from about 2 to about 3 carbon atoms or mixtures thereof; x is from 0 to about 3; and each R 5 is an alkyl or hydroxyalkyl group containing from about 1 to about 3 carbon atoms or a polyethylene oxide group containing from about 1 to about 3 ethylene oxide groups.
  • the R 5 groups can be attached to each other, e.g., through an oxygen or nitrogen atom, to form a ring structure.
  • amine oxide surfactants in particular include CI Q - C 18 alkyl dimethyl amine oxides and C 8 -C!2 alkoxy ethyl dihydroxy ethyl amine oxides .
  • the detergent compositions of the present invention typically comprise from 0.2% to about 15%, preferably from about 1% to about 10% by weight of such semi-polar nonionic surfactants.
  • the detergent composition of the present invention may further comprise a cosurfactant selected from the group of primary or tertiary amines.
  • Suitable primary amines for use herein include amines according to the formula R NH2 wherein R]_ is a g-C ⁇ preferably C -C ⁇ o alkyl chain or R 4 X(CH2 )n , X is -0-,- C(0)NH- or -NH- ( R 4 is a Cg-C]_2 alkyl chain n is between 1 to 5, preferably 3.
  • Ri alkyl chains may be straight or branched and may be interrupted with up to 12, preferably less than 5 ethylene oxide moieties.
  • Preferred amines according to the formula herein above are n-alkyl amines.
  • Suitable amines for use herein may be selected from 1-hexylamine, 1-octylamine, 1-decylamine and laurylamine .
  • Other preferred primary amines include C8-C10 oxypropyla ine, octyloxypropylamine, 2-ethylhexyl- oxypropylamine , lauryl amido propyla ine and amido propylamine .
  • Suitable tertiary amines for use herein include tertiary amines having the formula R ⁇ R2 R 3 N wherein Rl and R2 are C ⁇ C 8 alkylchains or
  • R3 is either a Cg-C ⁇ , preferably Cg-C 10 alkyl chain, or R3 is R 4 X(CH 2)n , whereby X is -O- , -C(0)NH- or -NH- f R 4 is a c 4" c 12 n I s between 1 to 5, preferably 2-3. R 5 is H or C]_- C2 alkyl and x is between 1 to 6 .
  • R3 and R4 may be linear or branched ; R3 alkyl chains may be interrupted with up to 12, preferably less than 5, ethylene oxide moieties.
  • R ⁇ _ is Cg-C ⁇ 2 alkyl; n is 2-4, preferably n is 3; R2 and R3 is C1-C4
  • Most preferred amines of the present invention include 1-octylamine, 1-hexylamine, 1-decylamine, 1- dodecylamine, C8-10oxypropylamine, N coco l-3diaminopropane , coconutalkyldimethylamine, lauryldimethylamine, lauryl bis (hydroxyethyl) amine, coco bis (hydroxyehtyl) amine, lauryl amine 2 moles propoxylated, octyl amine 2 moles propoxylated, lauryl amidopropyldimethylamine, C8-10 amidopropyldimethylamine and CIO amidopropyldimethylamine.
  • the most preferred amines for use in the compositions herein are 1-hexylamine, 1-octylamine, 1-decylamine, 1- dodecylamine .
  • Especially desirable are n- dodecyldimethylamine and bishydroxyethylcoconutalkylamine and oleylamine 7 times ethoxylated, lauryl amido propylamine and cocoamido propylamine .
  • the detergent compositions can further comprise one or more enzymes which provide detergent performance and/or fabric care benefits.
  • Said enzymes include enzymes selected from hemicellulases, peroxidases, proteases, gluco-amylases, amylases, xylanases, pectinases, keratanases, reductases, oxidases, phenoloxidases, lipoxygenases, ligninases, pullulanases , tannases, pentosanases, malanases, ⁇ - glucanases, arabinosidases, hyaluronidase, chondroitinase , laccase or mixtures thereof .
  • a preferred combination is a detergent composition having cocktail of conventional applicable enzymes like protease, amylase, lipase, cutinase and/or cellulase in conjunction with one or more plant cell wall degrading enzymes .
  • the cellulases usable in the present invention include both bacterial or fungal cellulase. Preferably, they will have a pH optimum of between 5 and 9.5. Suitable cellulases are disclosed in U.S. Patent 4,435,307, Barbesgoard et al, which discloses fungal cellulase produced from Humicola insolens . Suitable cellulases are also disclosed in GB-A- 2.075.028; GB-A-2.095.275 and DE-OS-2.247.832.
  • cellulases examples include cellulases produced by a strain of Humicola insolens (Humicola grisea var. thermoidea) , particularly the Humicola strain DSM 1800.
  • Other suitable cellulases are cellulases originated from Humicola insolens having a molecular weight of about 50KDa, an isoelectric point of 5.5 and containing 415 amino acids and a ⁇ 43kD endoglucanase derived from Humicola insolens, DSM 1800, exhibiting cellulase activity; a preferred endoglucanase component has the amino acid sequence disclosed in PCT Patent Application No. WO 91/17243.
  • suitable cellulases are the EGIII cellulases from Trichoderma longibrachiatum described in WO94/21801, Genencor, published September 29, 1994. Especially suitable cellulases are the cellulases having color care benefits. Examples of such cellulases are cellulases described in European patent application No. 91202879.2, filed November 6, 1991 (Novo) .
  • Peroxidase enzymes are used in combination with oxygen sources, e.g. percarbonate, perborate, persulfate, hydrogen peroxide, etc. They are used for "solution bleaching", i.e. to prevent transfer of dyes or pigments removed from substrates during wash operations to other substrates in the wash solution. Peroxidase enzymes are known in the art, and include, for example, horseradish peroxidase, ligninase, and haloperoxidase such as chloro- and bromo- peroxidase .
  • Peroxidase-containing detergent compositions are disclosed, for example, in PCT International Application WO 89/099813 and in European Patent application EP No. 91202882.6, filed on November 6, 1991.
  • Suitable oxidases is the laccase enzyme, using oxugen, hydrogen peroxide as primary substrates.
  • Said cellulases and/or peroxidases are normally incorporated in the detergent composition at levels from 0.0001% to 2% of active enzyme by weight of the detergent composition .
  • Suitable proteases are the subtilisins which are obtained from particular strains of B . subtilis and B . lichenifoirmis (subtilisin BPN and BPN' ) .
  • One suitable protease is obtained from a strain of Bacillus, having maximum activity throughout the pH range of 8-12, developed and sold as ESPERASE ® by Novo Industries A/S of Denmark, hereinafter "Novo" .
  • the preparation of this enzyme and analogous enzymes is described in GB 1,243,784 to Novo.
  • proteases include ALCALASE ® , DURAZYM ® and SAVINASE ® from Novo and MAXATASE ® / MAXACAL®, PROPERASE ® and MAXAPEM® (protein engineered Maxacal) from Gist- Brocades.
  • proteases also encompass modified bacterial serine proteases, such as those described in European Patent Application Serial Number 87 303761.8, filed April 28, 1987 (particularly pages 17, 24 and 98), and which is called herein "Protease B", and in European Patent Application 199,404, Venegas, published October 29, 1986, which refers to a modified bacterial serine protealytic enzyme which is called "Protease A" herein.
  • Protease C is a variant of an alkaline serine protease from Bacillus in which lysine replaced arginine at position 27, tyrosine replaced valine at position 104, serine replaced asparagine at position 123, and alanine replaced threonine at position 274.
  • Protease C is described in EP 90915958:4, corresponding to WO 91/06637, Published May 16, 1991. Genetically modified variants, particularly of Protease C, are also included herein. See also a high pH protease from Bacillus sp. NCIMB 40338 described in WO 93/18140 A to Novo.
  • Enzymatic detergents comprising protease, one or more other enzymes, and a reversible protease inhibitor are described in WO 92/03529 A to Novo.
  • a protease having decreased adsorption and increased hydrolysis is available as described in WO 95/07791 to Procter & Gamble.
  • a recombinant trypsin- like protease for detergents suitable herein is described in WO 94/25583 to Novo.
  • protease referred to as "Protease D” is a carbonyl hydrolase variant having an amino acid sequence not found in nature, which is derived from a precursor carbonyl hydrolase by substituting a different amino acid for a plurality of amino acid residues at a position in said carbonyl hydrolase equivalent to position +76, preferably also in combination with one or more amino acid residue positions equivalent to those selected from the group consisting of +99, +101, +103, +104, +107, +123, +27, +105, +109, +126, +128, +135, +156, +166, +195, +197, +204, +206, +210, +216, +217, +218, +222, +260, +265, and/or +274 according to the numbering of Bacillus amyloliquefaciens subtilisin, as described in WO95/10591 and in the patent application of C.
  • proteases described in patent applications EP 251 446 and WO91/06637 and protease BLAP ® described in WO91/02792.
  • the proteolytic enzymes are incorporated in the detergent compositions of the present invention a level of from 0.0001% to 2%, preferably from 0.001% to 0.2%, more preferably from 0.005% to 0.1% pure enzyme by weight of the composition.
  • Amylases ( ⁇ and/or ⁇ ) can be included for removal of carbohydrate-based stains.
  • WO94/02597 Novo Nordisk A/S published February 03, 1994, describes detergent compositions which incorporate mutant amylases. See also W094/18314, Genencor, published August 18, 1994 and WO95/10603, Novo Nordisk A/S, published April 20, 1995 .
  • Other amylases known for use in detergent compositions include both ⁇ - and ⁇ -amylases.
  • ⁇ -Amylases are known in the art and include those disclosed in US Pat. no.
  • amylases include Purafact Ox Am R described in WO 94/18314, pulished August 18, 1994; WO96/05295, Genencor, published February 22, 1996 and amylase variants having additional modification in the immediate parent available from Novo Nordisk A/S, disclosed in WO 95/10603, published April 95.
  • ⁇ -amylases examples are Termamyl ® , Ban ® , Fungamyl ® and Duramyl ® , all available from Novo Nordisk A/S Denmark.
  • W095/26397 describes other suitable amylases : ⁇ -amylases characterised by having a specific activity at least 25% higher than the specific activity of Termamyl ® at a temperature range of 25°C to 55°C and at a pH value in the range of 8 to 10, measured by the Phadebas ® cc-amylase activity assay.
  • Other amylolytic enzymes with improved properties with respect to the activity level and the combination of thermostability and a higher activity level are described in W095/35382.
  • the above-mentioned enzymes may be of any suitable origin, such as vegetable, animal, bacterial, fungal and yeast origin. Origin can further be mesophilic or extremophilic (psychrophilic, psychrotrophic, thermophilic, barophilic, alkalophilic, acidophilic, halophilic, etc.). Purified or non-purified forms of these enzymes may be used. Also included by definition, are mutants of native enzymes. Mutants can be obtained e.g. by protein and/or genetic engineering, chemical and/or physical modifications of native enzymes. Common practice as well is the expression of the enzyme via host organism in which the genetic material responsible for the production of the enzyme has been cloned.
  • Said enzymes are normally incorporated in the detergent composition at levels from 0.0001% to 2% of active enzyme by weight of the detergent composition.
  • the enzymes can be added as separate single ingredients (prills, granulates, stabilized liquids, etc... containing one enzyme ) or as mixtures of two or more enzymes ( e.g. cogranulates ) .
  • enzyme oxidation scavengers which are described in Copending European Patent application 92870018.6 filed on January 31, 1992.
  • enzyme oxidation scavengers are ethoxylated tetraethylene polyamines .
  • a range of enzyme materials and means for their incorporation into synthetic detergent compositions is also disclosed in WO 9307263 A and WO 9307260 A to Genencor International, WO 8908694 A to Novo, and U.S. 3,553,139, January 5, 1971 to McCarty et al .
  • Enzymes are further disclosed in U.S. 4,101,457, Place et al, July 18, 1978, and in U.S. 4,507,219, Hughes, March 26, 1985.
  • Enzyme materials useful for liquid detergent formulations, and their incorporation into such formulations are disclosed in U.S. 4,261,868, Hora et al , April 14, 1981. Enzymes for use in detergents can be stabilised by various techniques.
  • Enzyme stabilisation techniques are disclosed and exemplified in U.S. 3,600,319, August 17, 1971, Gedge et al, EP 199,405 and EP 200,586, October 29, 1986, Venegas . Enzyme stabilisation systems are also described, for example, in U.S. 3,519,570. A useful Bacillus, sp . AC13 giving proteases, xylanases and cellulases, is described in WO 9401532 A to Novo.
  • the detergent compositions of the present invention can further include bleaching agents such as hydrogen peroxide, PB1, PB4 and percarbonate with a particle size of 400-800 microns.
  • bleaching agent components can include one or more oxygen bleaching agents and, depending upon the bleaching agent chosen, one or more bleach activators. When present oxygen bleaching compounds will typically be present at levels of from about 1% to about 25%..
  • the bleaching agent component for use herein can be any of the bleaching agents useful for detergent compositions including oxygen bleaches as well as others known in the art .
  • the bleaching agent suitable for the present invention can be an activated or non-activated bleaching agent .
  • One category of oxygen bleaching agent that can be used encompasses percarboxylic acid bleaching agents and salts thereof. Suitable examples of this class of agents include magnesium monoperoxyphthalate hexahydrate, the magnesium salt of meta-chloro perbenzoic acid, 4 -nonylamino-4 - oxoperoxybutyric acid and diperoxydodecanedioic acid.
  • Such bleaching agents are disclosed in U.S. Patent 4,483,781, U.S.
  • Highly preferred bleaching agents also include 6-nonylamino-6- oxoperoxycaproic acid as described in U.S. Patent 4,634,551.
  • bleaching agents that can be used encompasses the halogen bleaching agents.
  • hypohalite bleaching agents include trichloro isocyanuric acid and the sodium and potassium dichloroisocyanurates and N-chloro and N-bromo alkane sulphonamides .
  • Such materials are normally added at 0.5-10% by weight of the finished product, preferably 1-5% by weight .
  • the hydrogen peroxide releasing agents can be used in combination with bleach activators such as tetraacetylethylenediamine (TAED) , nonanoyloxybenzene- sulfonate (NOBS, described in US 4,412,934), 3,5,- trimethylhexanoloxybenzenesulfonate (ISONOBS, described in EP 120,591) or pentaacetylglucose (PAG) or Phenolsulfonate ester of N-nonanoyl-6-aminocaproic acid (NACA-OBS, described in WO94/28106) , which are perhydrolyzed to form a peracid as the active bleaching species, leading to improved bleaching effect.
  • bleach activators such as tetraacetylethylenediamine (TAED) , nonanoyloxybenzene- sulfonate (NOBS, described in US 4,412,934), 3,5,- trimethylhexanol
  • bleaching agents including peroxyacids and bleaching systems comprising bleach activators and peroxygen bleaching compounds for use in detergent compositions according to the invention are described in our co-pending applications USSN 08/136,626, PCT/US95/07823, W095/27772, W095/27773, W095/27774 and W095/27775.
  • the hydrogen peroxide may also be present by adding an enzymatic system (i.e. an enzyme and a substrate therefore) which is capable of generating hydrogen peroxide at the beginning or during the washing and/or rinsing process.
  • an enzymatic system i.e. an enzyme and a substrate therefore
  • Such enzymatic systems are disclosed in EP Patent Application 91202655.6 filed October 9, 1991.
  • Metal-containing catalysts for use in bleach compositions include cobalt-containing catalysts such as Pentaamine acetate cobalt (III) salts and manganese- containing catalysts such as those described in EPA 549 271; EPA 549 272; EPA 458 397; US 5,246,621; EPA 458 398; US 5,194,416 and US 5,114,611.
  • Bleaching composition comprising a peroxy compound, a manganese-containing bleach catalyst and a chelating agent is described in the patent application No 94870206.3.
  • Bleaching agents other than oxygen bleaching agents are also known in the art and can be utilized herein.
  • One type of non-oxygen bleaching agent of particular interest includes photoactivated bleaching agents such as the sulfonated zinc and/or aluminum phthalocyanines . These materials can be deposited upon the substrate during the washing process. Upon irradiation with light, in the presence of oxygen, such as by hanging clothes out to dry in the daylight, the sulfonated zinc phthalocyanine is activated and, consequently, the substrate is bleached.
  • Preferred zinc phthalocyanine and a photoactivated bleaching process are described in U.S. Patent 4,033,718.
  • detergent compositions will contain about 0.025% to about 1.25%, by weight, of sulfonated zinc phthalocyanine . Builder system
  • compositions according to the present invention may further comprise a builder system.
  • a builder system Any conventional builder system is suitable for use herein including aluminosilicate materials, silicates, polycarboxylates, alkyl- or alkenyl-succinic acid and fatty acids, materials such as ethylenediamine tetraacetate, diethylene triamine pentamethyleneacetate, metal ion sequestrants such as aminopolyphosphonates, particularly ethylenediamine tetramethylene phosphonic acid and diethylene triamine pentamethylenephosphonic acid.
  • Phosphate builders can also be used herein.
  • Suitable builders can be an inorganic ion exchange material, commonly an inorganic hydrated aluminosilicate material, more particularly a hydrated synthetic zeolite such as hydrated zeolite A, X, B, HS or MAP.
  • SKS-6 is a crystalline layered silicate consisting of sodium silicate (Na2Si2 ⁇ 5> .
  • Suitable polycarboxylates containing one carboxy group include lactic acid, glycolic acid and ether derivatives thereof as disclosed in Belgian Patent Nos. 831,368, 821,369 and 821,370.
  • Polycarboxylates containing two carboxy groups include the water-soluble salts of succinic acid, malonic acid, (ethylenedioxy) diacetic acid, maleic acid, diglycollic acid, tartaric acid, tartronic acid and fumaric acid, as well as the ether carboxylates described in German Offenlegenschrift 2,446,686, and 2,446,687 and U.S. Patent No. 3,935,257 and the sulfinyl carboxylates described in Belgian Patent No. 840,623.
  • Polycarboxylates containing three carboxy groups include, in particular, water-soluble citrates, aconitrates and citraconates as well as succinate derivatives such as the carboxymethyloxysuccinates described in British Patent No. 1,379,241, lactoxysuccinates described in Netherlands Application 7205873, and the oxypolycarboxylate materials such as 2-oxa-l, 1, 3 -propane tricarboxylates described in British Patent No. 1,387,447.
  • Polycarboxylates containing four carboxy groups include oxydisuccinates disclosed in British Patent No. 1,261,829, 1, 1, 2, 2-ethane tetracarboxylates, 1,1,3,3- propane tetracarboxylates and 1 , 1, 2 , 3 -propane tetracarboxylates.
  • Polycarboxylates containing sulfo substituents include the sulfosuccinate derivatives disclosed in British Patent Nos. 1,398,421 and 1,398,422 and in U.S. Patent No. 3,936,448, and the sulfonated pyrolysed citrates described in British Patent No. 1,082,179, while polycarboxylates containing phosphone substituents are disclosed in British Patent No. 1,439,000.
  • Alicyclic and heterocyclic polycarboxylates include cyclopentane-cis , cis , cis-tetracarboxylates , cyclopentadienide pentacarboxylates, 2, 3 , 4 , 5-tetrahydro- furan - cis, cis, cis-tetracarboxylates, 2 , 5-tetrahydro- furan -cis - dicarboxylates, 2 , 2 , 5 , 5-tetrahydrofuran tetracarboxylates, 1 , 2 , 3 , 4 , 5 , 6-hexane -hexacar-boxylates and and carboxymethyl derivatives of polyhydric alcohols such as sorbitol, mannitol and xylitol.
  • Aromatic polycarboxylates include mellitic acid, pyromellitic acid and the phthalic acid derivatives disclosed in British Patent No
  • the preferred polycarboxylates are hydroxycarboxylates containing up to three carboxy groups per molecule, more particularly citrates.
  • Preferred builder systems for use in the present compositions include a mixture of a water- insoluble aluminosilicate builder such as zeolite A or of a layered silicate (SKS-6), and a water-soluble carboxylate chelating agent such as citric acid, preferred builder systems for use in liquid detergent compositions of the present invention are soaps and polycarboxylates.
  • a water- insoluble aluminosilicate builder such as zeolite A or of a layered silicate (SKS-6)
  • a water-soluble carboxylate chelating agent such as citric acid
  • preferred builder systems for use in liquid detergent compositions of the present invention are soaps and polycarboxylates.
  • a suitable chelant for inclusion in the detergent compositions in accordance with the invention is ethylenediamine-N, ' -disuccinic acid (EDDS) or the alkali metal, alkaline earth metal, ammonium, or substituted ammonium salts thereof, or mixtures thereof.
  • Preferred EDDS compounds are the free acid form and the sodium or magnesium salt thereof. Examples of such preferred sodium salts of EDDS include Na 2 EDDS and Na 4 EDDS. Examples of such preferred magnesium salts of EDDS include MgEDDS and Mg2EDDS .
  • the magnesium salts are the most preferred for inclusion in compositions in accordance with the invention.
  • Preferred builder systems include a mixture of a water- insoluble aluminosilicate builder such as zeolite A, and a watersoluble carboxylate chelating agent such as citric acid.
  • Suitable water-soluble organic salts are the homo- or co-polymeric acids or their salts, in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms .
  • Polymers of this type are disclosed in GB-A-1, 596 , 756.
  • Examples of such salts are polyacrylates of MW 2000-5000 and their copolymers with maleic anhydride, such copolymers having a molecular weight of from 20,000 to 70,000, especially about 40,000.
  • Detergency builder salts are normally included in amounts of from 5% to 80% by weight of the composition preferably from 10% to 70% and most usually from 30% to 60% by weight .
  • a suds suppressor exemplified by silicones, and silica-silicone mixtures.
  • Silicones can be generally represented by alkylated polysiloxane materials while silica is normally used in finely divided forms exemplified by silica aerogels and xerogels and hydrophobic silicas of various types. These materials can be incorporated as particulates in which the suds suppressor is advantageously releasably incorporated in a water-soluble or water-dispersible, substantially non- surface-active detergent impermeable carrier.
  • the suds suppressor can be dissolved or dispersed in a liquid carrier and applied by spraying on to one or more of the other components .
  • a preferred silicone suds controlling agent is disclosed in Bartollota et al . U.S. Patent 3 933 672.
  • Other particularly useful suds suppressors are the self- emulsifying silicone suds suppressors, described in German Patent Application DTOS 2 646 126 published April 28, 1977.
  • An example of such a compound is DC-544, commercially available from Dow Corning, which is a siloxane-glycol copolymer.
  • Especially preferred suds controlling agent are the suds suppressor system comprising a mixture of silicone oils and 2-alkyl-alcanols .
  • Suitable 2-alkyl-alkanols are 2- butyl-octanol which are commercially available under the trade name Isofol 12 R.
  • Such suds suppressor system are described in Copending European Patent application N 92870174.7 filed 10 November, 1992.
  • Especially preferred silicone suds controlling agents are described in Copending European Patent application N°92201649.8.
  • Said compositions can comprise a silicone/silica mixture in combination with fumed nonporous silica such as Aerosil R .
  • the suds suppressors described above are normally employed at levels of from 0.001% to 2% by weight of the composition, preferably from 0.01% to 1% by weight.
  • detergent compositions may be employed, such as soil-suspending agents, soil-release agents, optical brighteners, abrasives, bactericides, tarnish inhibitors, coloring agents, and/or encapsulated or non-encapsulated perfumes.
  • encapsulating materials are water soluble capsules which consist of a matrix of polysaccharide and polyhydroxy compounds such as described in GB 1,464, 616.
  • Suitable water soluble encapsulating materials comprise dextrins derived from ungelatinized starch acid- esters of substituted dicarboxylic acids such as described in US 3,455,838. These acid-ester dextrins are, preferably, prepared from such starches as waxy maize, waxy sorghum, sago, tapioca and potato. Suitable examples of said encapsulating materials include N-Lok manufactured by National Starch. The N-Lok encapsulating material consists of a modified maize starch and glucose. The starch is modified by adding monofunctional substituted groups such as octenyl succinic acid anhydride.
  • Antiredeposition and soil suspension agents suitable herein include cellulose derivatives such as methylcellulose, carboxymethylcellulose and hydroxyethylcellulose, and homo- or co-polymeric polycarboxylic acids or their salts.
  • Polymers of this type include the polyacrylates and maleic anhydride-acrylic acid copolymers previously mentioned as builders, as well as copolymers of maleic anhydride with ethylene, methylvinyl ether or methacrylic acid, the maleic anhydride constituting at least 20 mole percent of the copolymer . These materials are normally used at levels of from 0.5% to 10% by weight, more preferably from 0.75% to 8%, most preferably from 1% to 6% by weight of the composition.
  • Preferred optical brighteners are anionic in character, examples of which are disodium 4,4' -bis- (2- diethanolamino-4 -anilino -s- triazin-6-ylamino) stilbene- 2:2' disulphonate, disodium 4, - 4 ' -bis- (2-morpholino-4- anilino-s-triazin-6-ylamino-stilbene-2 : 2 ' - disulphonate, disodium 4,4' - bis- (2 , 4-dianilino-s-triazin-6- ylamino) stilbene-2 : 2 ' - disulphonate, monosodium 4',4'' bis- (2 , 4-dianilino-s-tri-azin-6 ylamino) stilbene-2- sulphonate, disodium 4,4' -bis- (2 -anilino-4 - (N-methyl-N-2- hydroxyethylamino) -s-triazin-
  • polyethylene glycols particularly those of molecular weight 1000-10000, more particularly 2000 to 8000 and most preferably about 4000. These are used at levels of from 0.20% to 5% more preferably from 0.25% to 2.5% by weight. These polymers and the previously mentioned homo- or co-polymeric polycarboxylate salts are valuable for improving whiteness maintenance, fabric ash deposition, and cleaning performance on clay, proteinaceous and oxidizable soils in the presence of transition metal impurities.
  • Soil release agents useful in compositions of the present invention are conventionally copolymers or terpolymers of terephthalic acid with ethylene glycol and/or propylene glycol units in various arrangements. Examples of such polymers are disclosed in the commonly assigned US Patent Nos. 4116885 and 4711730 and European Published Patent Application No. 0 272 033. A particular preferred polymer in accordance with EP-A-0 272 033 has the formula
  • PEG is - (OC 2 H ) O-
  • PO is (OC 3 H 6 0)
  • T is (pcOCgH 4 CO) .
  • modified polyesters as random copolymers of dimethyl terephthalate, dimethyl sulfoisophthalate, ethylene glycol and 1-2 propane diol , the end groups consisting primarily of sulphobenzoate and secondarily of mono esters of ethylene glycol and/or propane-diol .
  • the target is to obtain a polymer capped at both end by sulphobenzoate groups, "primarily", in the present context most of said copolymers herein will be end- capped by sulphobenzoate groups.
  • some copolymers will be less than fully capped, and therefore their end groups may consist of monoester of ethylene glycol and/or propane 1-2 diol, thereof consist “secondarily” of such species .
  • the selected polyesters herein contain about 46% by weight of dimethyl terephthalic acid, about 16% by weight of propane -1.2 diol, about 10% by weight ethylene glycol about 13% by weight of dimethyl sulfobenzoic acid and about 15% by weight of sulfoisophthalic acid, and have a molecular weight of about 3.000.
  • the polyesters and their method of preparation are described in detail in EPA 311 342.
  • chlorine scavenger such as perborate, ammonium sulfate, sodium sulphite or polyethyleneimine at a level above 0.1% by weight of total composition, in the formulas will provide improved through the wash stability of the detergent enzymes.
  • Compositions comprising chlorine scavenger are described in the European patent application 92870018.6 filed January 31, 1992.
  • Alkoxylated polycarboxylates such as those prepared from polyacrylates are useful herein to provide additional grease removal performance. Such materials are described in WO 91/08281 and PCT 90/01815 at p. 4 et seq., incorporated herein by reference. Chemically, these materials comprise polyacrylates having one ethoxy side- chain per every 7-8 acrylate units.
  • the side-chains are of the formula - (CH CH 2 0) m (CH 2 ) n CH 3 wherein m is 2-3 and n is 6-12.
  • the side-chains are ester-linked to the polyacrylate "backbone” to provide a "comb" polymer type structure.
  • the molecular weight can vary, but is typically in the range of about 2000 to about 50,000.
  • Such alkoxylated polycarboxylates can comprise from about 0.05% to about 10%, by weight, of the compositions herein.
  • Fabric softening agents can also be incorporated into laundry detergent compositions in accordance with the present invention. These agents may be inorganic or organic in type. Inorganic softening agents are exemplified by the smectite clays disclosed in GB-A-1 400 898 and in USP 5,019,292. Organic fabric softening agents include the water insoluble tertiary amines as disclosed in GB-A1 514 276 and EP-BO Oil 340 and their combination with mono C12- C14 quaternary ammonium salts are disclosed in EP-B-0 026 527 and EP-B-0 026 528 and di-long-chain amides as disclosed in EP-B-0 242 919. Other useful organic ingredients of fabric softening systems include high molecular weight polyethylene oxide materials as disclosed in EP-A-0 299 575 and 0 313 146.
  • Levels of smectite clay are normally in the range from 2% to 20%, more preferably from 5% to 15% by weight, with the material being added as a dry mixed component to the remainder of the formulation.
  • Organic fabric softening agents such as the water- insoluble tertiary amines or dilong chain amide materials are incorporated at levels of from 0.5% to 5% by weight, normally from 1% to 3% by weight whilst the high molecular weight polyethylene oxide materials and the water soluble cationic materials are added at levels of from 0.1% to 2%, normally from 0.15% to 1.5% by weight.
  • These materials are normally added to the spray dried portion of the composition, although in some instances it may be more convenient to add them as a dry mixed particulate, or spray them as molten liquid on to other solid components of the composition.
  • the detergent composition of the present invention can also contain dispersants : Suitable water-soluble organic salts are the homo- or co-polymeric acids or their salts, in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms .
  • Polymers of this type are disclosed in GB-A-1 , 596 , 756. Examples of such salts are polyacrylates of MW 2000-5000 and their copolymers with maleic anhydride, such copolymers having a molecular weight of from 1,000 to 100,000.
  • copolymer of acrylate and methylacrylate such as the 480N having a molecular weight of 4000, at a level from 0.5-20% by weight of composition can be added in the detergent compositions of the present invention.
  • compositions of the invention may contain a lime soap peptiser compound, which has a lime soap dispersing power (LSDP) , as defined hereinafter of no more than 8, preferably no more than 7, most preferably no more than 6.
  • LSDP lime soap dispersing power
  • the lime soap peptiser compound is preferably present at a level from 0% to 20% by weight.
  • LSDP lime soap dispersant power
  • Surfactants having good lime soap peptiser capability will include certain amine oxides, betaines, sulfobetaines, alkyl ethoxysulfates and ethoxylated alcohols.
  • Polymeric lime soap peptisers suitable for use herein are described in the article by M.K. Nagarajan, W.F. Masler, to be found in Cosmetics and Toiletries, volume 104, pages 71-73, (1989).
  • Hydrophobic bleaches such as 4 - [N-octanoyl-6- aminohexanoyl] benzene sulfonate, 4 - [N-nonanoyl-6- aminohexanoyl] benzene sulfonate, 4- [N-decanoyl- ⁇ - aminohexanoyl] benzene sulfonate and mixtures thereof; and nonanoyloxy benzene sulfonate together with hydrophilic / hydrophobic bleach formulations can also be used as lime soap peptisers compounds.
  • the detergent compositions of the present invention can also include compounds for inhibiting dye transfer from one fabric to another of solubilized and suspended dyes encountered during fabric laundering operations involving colored fabrics.
  • the detergent compositions according to the present invention also comprise from 0.001% to 10 %, preferably from 0.01% to 2%, more preferably from 0.05% to 1% by weight of polymeric dye transfer inhibiting agents.
  • Said polymeric dye transfer inhibiting agents are normally incorporated into detergent compositions in order to inhibit the transfer of dyes from colored fabrics onto fabrics washed therewith. These polymers have the ability to complex or adsorb the fugitive dyes washed out of dyed fabrics before the dyes have the opportunity to become attached to other articles in the wash.
  • polymeric dye transfer inhibiting agents are polyamine N-oxide polymers, copolymers of N- vinylpyrrolidone and N-vinylimidazole, polyvinylpyrrolidone polymers, polyvinyloxazolidones and polyvinylimidazoles or mixtures thereof .
  • polyamine N-oxide polymers suitable for use contain units having the following structure formula : P
  • R wherein P is a polymerisable unit, whereto the R-N-0 group can be attached to or wherein the R-N-0 group forms part of the polymerisable unit or a combination of both.
  • II II II A is NC, CO, C, -0-,-S-, -N- ; x is 0 or 1;
  • R are aliphatic, ethoxylated aliphatics, aromatic, heterocyclic or alicyclic groups or any combination thereof whereto the nitrogen of the N-0 group can be attached or wherein the nitrogen of the N-0 group is part of these groups.
  • the N-0 group can be represented by the following general structures :
  • Rl , R2 , and R3 are aliphatic groups, aromatic, heterocyclic or alicyclic groups or combinations thereof, x or/and y or/and z is 0 or 1 and wherein the nitrogen of the N-O group can be attached or wherein the nitrogen of the N-O group forms part of these groups .
  • the N-O group can be part of the polymerisable unit (P) or can be attached to the polymeric backbone or a combination of both.
  • Suitable polyamine N-oxides wherein the N-O group forms part of the polymerisable unit comprise polyamine N-oxides wherein R is selected from aliphatic, aromatic, alicyclic or heterocyclic groups.
  • polyamine N-oxides comprises the group of polyamine N-oxides wherein the nitrogen of the N-O group forms part of the R-group.
  • Preferred polyamine N-oxides are those wherein R is a heterocyclic group such as pyrridine, pyrrole, imidazole, pyrrolidine, piperidine, quinoline, acridine and derivatives thereof.
  • polyamine N-oxides comprises the group of polyamine N-oxides wherein the nitrogen of the N-O group is attached to the R-group.
  • suitable polyamine N-oxides are the polyamine oxides whereto the N-O group is attached to the polymerisable unit.
  • Preferred class of these polyamine N-oxides are the polyamine N-oxides having the general formula (I) wherein R is an aromatic, heterocyclic or alicyclic groups wherein the nitrogen of the N-O functional group is part of said R group .
  • polyamine N-oxides are the polyamine oxides having the general formula (I) wherein R are aromatic, heterocyclic or alicyclic groups wherein the nitrogen of the N-O functional group is attached to said R groups .
  • polyamine oxides wherein R groups can be aromatic such as phenyl.
  • Any polymer backbone can be used as long as the amine oxide polymer formed is water-soluble and has dye transfer inhibiting properties.
  • suitable polymeric backbones are polyvinyls, polyalkylenes , polyesters, polyethers, polyamide, polyimides, polyacrylates and mixtures thereof .
  • the amine N-oxide polymers of the present invention typically have a ratio of amine to the amine N-oxide of 10:1 to 1:1000000.
  • the amount of amine oxide groups present in the polyamine oxide polymer can be varied by appropriate copolymerization or by appropriate degree of N- oxidation.
  • the ratio of amine to amine N-oxide is from 2:3 to 1:1000000. More preferably from 1:4 to 1:1000000, most preferably from 1:7 to 1:1000000.
  • the polymers of the present invention actually encompass random or block copolymers where one monomer type is an amine N- oxide and the other monomer type is either an amine N-oxide or not.
  • the amine oxide unit of the polyamine N-oxides has a PKa ⁇ 10, preferably PKa ⁇ 7, more preferred PKa ⁇ 6.
  • the polyamine oxides can be obtained in almost any degree of polymerisation. The degree of polymerisation is not critical provided the material has the desired water- solubility and dye-suspending power.
  • the average molecular weight is within the range of 500 to 1000,000; preferably from 1,000 to 50,000, more preferably from 2,000 to 30,000, most preferably from 3,000 to 20,000.
  • N-vinylimidazole N-vinylpyrrolidone polymers used in the present invention have an average molecular weight range from 5,000-1,000,000, preferably from 5,000-200,000.
  • Highly preferred polymers for use in detergent compositions according to the present invention comprise a polymer selected from N-vinylimidazole N-vinylpyrrolidone copolymers wherein said polymer has an average molecular weight range from 5,000 to 50,000 more preferably from 8,000 to 30,000, most preferably from 10,000 to 20,000.
  • the average molecular weight range was determined by light scattering as described in Barth H.G. and Mays J.W. Chemical Analysis Vol 113, "Modern Methods of Polymer Characterization" .
  • N-vinylimidazole N-vinylpyrrolidone copolymers have an average molecular weight range from 5,000 to 50,000; more preferably from 8,000 to 30,000; most preferably from 10,000 to 20,000.
  • the N-vinylimidazole N-vinylpyrrolidone copolymers characterized by having said average molecular weight range provide excellent dye transfer inhibiting properties while not adversely affecting the cleaning performance of detergent compositions formulated therewith.
  • the N-vinylimidazole N-vinylpyrrolidone copolymer of the present invention has a molar ratio of N-vinylimidazole to N-vinylpyrrolidone from 1 to 0.2, more preferably from 0.8 to 0.3, most preferably from 0.6 to 0.4 .
  • the detergent compositions of the present invention may also utilize polyvinylpyrrolidone ("PVP") having an average molecular weight of from about 2,500 to about 400,000, preferably from about 5,000 to about 200,000, more preferably from about 5,000 to about 50,000, and most preferably from about 5,000 to about 15,000.
  • PVP polyvinylpyrrolidone
  • Suitable polyvinylpyrrolidones are commercially vailable from ISP Corporation, New York, NY and Montreal, Canada under the product names PVP K-15 (viscosity molecular weight of 10,000), PVP K-30 (average molecular weight of 40,000), PVP K-60 (average molecular weight of 160,000), and PVP K-90 (average molecular weight of 360,000) .
  • polyvinylpyrrolidones which are commercially available from BASF Cooperation include Sokalan HP 165 and Sokalan HP 12; polyvinylpyrrolidones known to persons skilled in the detergent field (see for example EP-A-262,897 and EP-A- 256,696) .
  • the detergent compositions of the present invention may also utilize polyvinyloxazolidone as a polymeric dye transfer inhibiting agent.
  • Said polyvinyloxazolidones have an average molecular weight of from about 2,500 to about 400,000, preferably from about 5,000 to about 200,000, more preferably from about 5,000 to about 50,000, and most preferably from about 5,000 to about 15,000.
  • Polyvinylimidazole The detergent compositions of the present invention may also utilize polyvinylimidazole as polymeric dye transfer inhibiting agent. Said polyvinylimidazoles have an average about 2,500 to about 400,000, preferably from about 5,000 to about 200,000, more preferably from about 5,000 to about 50,000, and most preferably from about 5,000 to about 15,000.
  • Cross-linked polymers are polymers whose backbone are interconnected to a certain degree; these links can be of chemical or physical nature, possibly with active groups n the backbone or on branches; cross- linked polymers have been described in the Journal of Polymer Science, volume 22, pages 1035-1039.
  • the cross-linked polymers are made in such a way that they form a three-dimensional rigid structure, which can entrap dyes in the pores formed by the three-dimensional structure.
  • the cross -linked polymers entrap the dyes by swelling.
  • compositions of the invention may be used in essentially any washing or cleaning methods, including soaking methods, pretreatment methods and methods with rinsing steps for which a separate rinse aid composition may be added.
  • the process described herein comprises contacting fabrics with a laundering solution in the usual manner and exemplified hereunder.
  • the process of the invention is conveniently carried out in the course of the cleaning process.
  • the method of cleaning is preferably carried out at 5 °C to 95 °C, especially between 10°C and 60°C.
  • the pH of the treatment solution is preferably from 7 to 11.
  • a preferred machine dishwashing method comprises treating soiled articles with an aqueous solution of the machine diswashing or rinsing composition.
  • a conventional effective amount of the machine dishwashing composition means from 8-60 g of product dissolved or dispersed in a wash volume from 3-10 litres.
  • soiled dishes are contacted with an effective amount of the diswashing composition, typically from 0.5-20g (per 25 dishes being treated) .
  • Preferred manual dishwashing methods include the application of a concentrated solution to the surfaces of the dishes or the soaking in large volume of dilute solution of the detergent composition.
  • compositions of the invention may also be formulated as hard surface cleaner compositions.
  • the level of the enzymes are expressed in pure enzyme by weight of total composition and the abbreviated component identifications have the following meanings : LAS Sodium linear C ⁇ alkyl benzene sulphonate
  • Nonionic c 13" c 15 mixed ethoxylated/propoxylated fatty alcohol with an average degree of ethoxylation of 3.8 and an average degree of propoxylation of 4.5 sold under the tradename Plurafac LF404 by BASF Gmbh.
  • Neodol 45-13 C14-C15 linear primary alcohol ethoxylate sold by Shell Chemical CO.
  • Carbonate Anhydrous sodium carbonate with a particle size between 200 ⁇ m and 900 ⁇ m.
  • Bicarbonate Anhydrous sodium bicarbonate with a particle size between 400 ⁇ m and 1200 ⁇ m.
  • PA30 Polyacrylic acid of average molecular weight of approximately 8,000.
  • PAAC Pentaamine acetate cobalt (III) salt.
  • Paraffin Paraffin oil sold under the tradename
  • Antibody Anti-Lipolase antibody LAJR 009-012, available from Novo Nordisk A/S.
  • Lipolytic Lipolytic enzymes sold under the enzyme tradename Lipolase, Lipolase Ultra by
  • Protease Proteolytic enzyme sold under the tradename Savinase, Alcalase, Durazym by Novo Nordisk A/S, Maxacal, Maxapem sold by Gist-Brocades and proteases described in patents WO91/06637 and/or WO95/10591 and/or EP 251 446.
  • Amylase Amylolytic enzyme sold under the tradename Purafact Ox Am R described in WO 94/18314, O96/05295 sold by Genencor; Termamyl ® , Funga yl ® and Duramyl ® , all available from Novo Nordisk A/S and those described in W095/26397.
  • Cellulase Cellulytic enzyme sold under the tradename Carezyme, Celluzyme and/or Endolase by Novo Nordisk A/S.
  • CMC Sodium carboxymethyl cellulose.
  • HEDP 1, 1-hydroxyethane diphosphonic acid.
  • DETPMP Diethylene triamine penta (methylene phosphonic acid) , marketed by Monsanto under the Trade name Dequest 2060.
  • Brightener 1 Disodium 4,4 '-bis (2- sulphostyryl) biphenyl .
  • Silicone Polydimethylsiloxane foam controller antifoam with siloxane-oxyalkylene copolymer as dispersing agent with a ratio of said foam controller to said dispersing agent of 10:1 to 100:1.
  • SRP 1 Sulfobenzoyl end capped esters with oxyethylene oxy and terephtaloyl backbone .
  • Bismuth nitrate Bismuth nitrate salt
  • Encapsulated Insoluble fragrance delivery technology perfume utilising zeolite 13x, perfume and a particles dextrose/glycerin agglomerating binder.
  • Hydroxide pH Measured as a 1% solution in distilled water at 20°C.
  • Chickens were injected in the breast muscle with 1 ml of a 1 mg/ml Lipolase ® emulsion.
  • the lipolytic emulsion was prepared with a Freunds completed adjuvants (Freund and McDermott, 1942; Freund 1956) by intensively mixing an equal amount of the Lipolase ® solution (2 mg/ml) and Freunds complete adjuvant.
  • the immunisation scheme was completed with injections using a Freunds uncomplete adjuvant and after a 4 weeks period, the eggs were collected during one week.
  • the extraction of the antibodies from the eggs yolks was done according to the Poison extraction method as described in Immunological Investigation 19, 1990, pp 253-258.
  • a Phosphate Buffer (0.05M KH2P04, pH 6.8) contained the antibody (0.18 mg/ml).
  • the interaction lipolytic enzyme (Final concentration of 0.08%) / antibody was achieved Tris buffers and commercially available detergent solutions comprising Ariel liquid (0.8% in city water, pH 8.5) and Ariel Color Futur(0.8% in city water, pH 9.5) during 5 minutes at 0°C.
  • the lipolytic residual activity was measured according the method based on the butyric acid 4 nitrophenol ester hydrolysis. Within 5 minutes the enzymatic activity of the lipase was successfully blocked as shown in the table below.
  • laundry detergent compositions were prepared in accord with the invention:
  • Brightener 1 0.08 0.19 0.19 Brightener 2 0.04 0.04 Encapsulated perfume 0.3 0.3 0.3 particles Silicone antifoam 0.5 2.4 2.4 Minors/misc to 100%
  • Antibody lOE-1 0.002 10E-3 Dry mixed sodium 3.0 3.0 5.0 sulfate
  • Brightener 1 0.2 0.2 0.2 -
  • Zeolite A 15.0 15.0 15.0
  • Brightener 1 3.05 - 0.04 0.04 0.04 Brightener 2 0.1 0.3 0.05 0.13 0.13 Water and Minors up to 100%
  • liquid detergent formulations according to the present invention were prepared:
  • Granular fabric cleaning compositions which provide "softening through the wash” capability were prepared in accord with the present invention :
  • Syndet bar fabric cleaning compositions were prepared in accord with the present invention :
  • detergent composition tablets of 25g weight were prepared in accord with the present invention by compression of a granular dishwashing detergent composition at a pressure of 13KN/cm 2 using a standard 12 head rotary press:
  • liquid dishwashing detergent compositions were prepared in accord with the present invention I to II, of density 1.40Kg/L :
  • liquid hard surface cleaning compositions were prepared in accord with the present invention :
  • Antibody 0. 007 0.05 0.1 0.3 0.6 0.5
  • Detergent additives were prepared in accord with the present invention :

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Abstract

La présente invention se rapporte à des compositions détergentes destinées notamment à la lessive, à la vaisselle et au nettoyage des surfaces dures, qui contiennent un enzyme lipolytique et un anticorps dirigé contre ledit enzyme lipolytique afin d'empêcher la formation éventuelle de mauvaises odeurs liées à l'activité hydrolytique de l'enzyme lipolytique tout en assurant d'excellents résultats de lavage.
PCT/US1996/013323 1996-08-16 1996-08-16 Compositions detergentes possedant une activite lipolytique regulee par anticorps WO1998007817A1 (fr)

Priority Applications (10)

Application Number Priority Date Filing Date Title
PCT/US1996/013323 WO1998007817A1 (fr) 1996-08-16 1996-08-16 Compositions detergentes possedant une activite lipolytique regulee par anticorps
AU67772/96A AU6777296A (en) 1996-08-16 1996-08-16 Detergent compositions comprising antibody controlled lipolytic activity
EP97939411A EP0922089A1 (fr) 1996-08-16 1997-08-13 Compositions detergentes a activite lipolytique regulee par des anticorps
AU41506/97A AU4150697A (en) 1996-08-16 1997-08-13 Detergent compositions comprising antibody controlled lipolytic activity
CA002263435A CA2263435A1 (fr) 1996-08-16 1997-08-13 Compositions detergentes a activite lipolytique regulee par des anticorps
BR9713172-5A BR9713172A (pt) 1996-08-16 1997-08-13 Composições detergentes compreendendo atividade lipolìtica controlada por anticorpo
CN97198838.2A CN1233279A (zh) 1996-08-16 1997-08-13 具有抗体控制的脂解活性的洗涤剂组合物
PCT/US1997/014287 WO1998006810A1 (fr) 1996-08-16 1997-08-13 Compositions detergentes a activite lipolytique regulee par des anticorps
JP10510013A JP2000500817A (ja) 1996-08-16 1997-08-13 抗体で制御される脂肪分解活性を有する洗剤組成物
ARP970103728A AR009257A1 (es) 1996-08-16 1997-08-15 Composiciones detergentes con actividad de anticuerpos lipoliticos controlada

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US8999911B2 (en) 2011-11-04 2015-04-07 Bissell Homecare, Inc. Enzyme cleaning composition and method of use
WO2022074056A2 (fr) 2020-10-07 2022-04-14 Basf Se Cellule de bacillus présentant des activités annexes réduites de lipase et/ou d'estérase

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US6809070B2 (en) 2001-09-28 2004-10-26 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Toilet bar having a latent acidifier
US6660699B2 (en) 2001-09-28 2003-12-09 Unilever Home & Personal Care Usa Toilet bar having a latent acidifier
WO2004074419A2 (fr) 2003-02-18 2004-09-02 Novozymes A/S Compositions detergentes
US7662761B2 (en) 2005-05-31 2010-02-16 Conopco, Inc. Soap bars comprising insoluble multivalent ion soap complexes
JP6238451B2 (ja) * 2014-04-16 2017-11-29 ライオン株式会社 繊維製品用液体洗浄剤
WO2016184944A1 (fr) * 2015-05-19 2016-11-24 Novozymes A/S Réduction des odeurs
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WO1994014964A1 (fr) * 1992-12-23 1994-07-07 Unilever N.V. Cutinases modifiees, adn, vecteur et hote
EP0709452A1 (fr) * 1994-10-27 1996-05-01 The Procter & Gamble Company Compositions de nettoyage contenant des xylanases

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EP0298654A2 (fr) * 1987-07-07 1989-01-11 Hybrisens Ltd. Utilisation des interactions entre anticorps et antigènes pour protéger ou moduler l'activité biologique
WO1991006574A1 (fr) * 1989-11-02 1991-05-16 Novo Nordisk A/S Procede de preparation d'acides peroxycarboxyliques
GB2247025A (en) * 1990-08-13 1992-02-19 Unilever Plc Enzymatic dishwashing and rinsing composition
WO1993004158A1 (fr) * 1991-08-21 1993-03-04 The Procter & Gamble Company Compositions pour detergents contenant de la lipase et du terpene
WO1994014964A1 (fr) * 1992-12-23 1994-07-07 Unilever N.V. Cutinases modifiees, adn, vecteur et hote
EP0709452A1 (fr) * 1994-10-27 1996-05-01 The Procter & Gamble Company Compositions de nettoyage contenant des xylanases

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US8999911B2 (en) 2011-11-04 2015-04-07 Bissell Homecare, Inc. Enzyme cleaning composition and method of use
WO2022074056A2 (fr) 2020-10-07 2022-04-14 Basf Se Cellule de bacillus présentant des activités annexes réduites de lipase et/ou d'estérase

Also Published As

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EP0922089A1 (fr) 1999-06-16
AU6777296A (en) 1998-03-06
AR009257A1 (es) 2000-04-12
AU4150697A (en) 1998-03-06
WO1998006810A1 (fr) 1998-02-19
CN1233279A (zh) 1999-10-27
JP2000500817A (ja) 2000-01-25
BR9713172A (pt) 2000-02-08
CA2263435A1 (fr) 1998-02-19

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