WO2009077970A1 - Procédé d'obtention d'extraits aqueux contenant des caroténoïdes et extraits obtenus - Google Patents
Procédé d'obtention d'extraits aqueux contenant des caroténoïdes et extraits obtenus Download PDFInfo
- Publication number
- WO2009077970A1 WO2009077970A1 PCT/IB2008/055306 IB2008055306W WO2009077970A1 WO 2009077970 A1 WO2009077970 A1 WO 2009077970A1 IB 2008055306 W IB2008055306 W IB 2008055306W WO 2009077970 A1 WO2009077970 A1 WO 2009077970A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- products
- process according
- extract
- skins
- lycopene
- Prior art date
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Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/179—Colouring agents, e.g. pigmenting or dyeing agents
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L5/00—Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
- A23L5/40—Colouring or decolouring of foods
- A23L5/42—Addition of dyes or pigments, e.g. in combination with optical brighteners
- A23L5/43—Addition of dyes or pigments, e.g. in combination with optical brighteners using naturally occurring organic dyes or pigments, their artificial duplicates or their derivatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/81—Solanaceae (Potato family), e.g. tobacco, nightshade, tomato, belladonna, capsicum or jimsonweed
Definitions
- the present invention relates to a process to obtain aqueous extracts containing carotenoids and to the obtained extracts.
- the agri-food sector is one of the productive fields that produces the largest amount of special wastes, for the most part non hazardous.
- European level farming by-products have a significant potential for the development of bio-energetic industry and are estimated being as much as 250 million ton/year.
- the management and the disposal of these by-products is a complex issue that has to be faced at social, economical and environmental level, aiming to rationally and sustainably use these resources .
- Tomato ⁇ Lycopersicum esculentum a Solanaceae plant of the dicotyledonous family, is one of the most relevant production of the Italian agri-food sector.
- ISTAT a total production of more than 59 million of quintal
- a 30% is for fresh consumption while the other 70% is for food processing industry.
- the main products obtained by tomato processing are peeled tomatoes, concentrated tomato paste, tomato puree and several variety of tomato sauces.
- the by-product is essentially constituted by the fibrous parts of the fruit, seeds and skins.
- the traditional use of byproducts obtained by tomato industrial transformations is the animal feeding in the zootechnic sector; in some cases these are used for thermo-valorisation purposes.
- Lycopene a terpene of the carotenoid family, is the main antioxidant molecule contained in tomato and its content is estimated in 50-600 ⁇ g/g in each tomato skin.
- Lycopene is the main carotenoid in human body; this is essentially due to the high amount of tomatoes consumed with the diet.
- lycopene The antioxidant properties of lycopene allow to use this molecule not only in the pharmaceutical sector, but also as food supplement in new food products (nutraceuticals) or in the cosmetic sector to neutralize free radicals responsible of skin aging.
- the oxidative reactions of human metabolism are responsible of the production of free radicals that have to be balanced with several molecules defined as antioxidants. This increasing interest in using lycopene attracted the attention on new methods of production and extraction of this molecule.
- lycopene production has a low cost but the final product is contaminated by residues of toxic-hazardous organic solvents.
- the second process in addition to the issue related to the solvents used for the extraction, there is also the need of long and expensive purification costs in order to separate other molecules (carotenoids, xantophyllins) , extracted in a non selective way that lead to a low purity grade product.
- the vegetal material used for the extraction of lycopene become a special waste that needs to be properly disposed and will not be reused in any way, with a considerable increase of the overall process costs.
- Supercritical CO 2 replaces traditional solvents on an industrial scale.
- the process that use this solvent has some advantages i.e. good extraction performances by CO 2 in the supercritical phase of non-polar compounds, non toxicity of this substance, straightforward availability, non hazardousness, short time of extraction. There are anyway some non negligible drawbacks such as reaching and keeping the supercritical phase of CO 2 . Considering the high pressure needed there are also relevant problem related to the high industrial costs and safety of the process.
- the central point of this invention is the use of surfactants that allows to pseudo-solubilise lycopene in water phase and to extract with relevant yields. This direct use on vegetal matrixes is not described in the state of the art.
- a process to obtain an aqueous extract containing carotenoids, in particular lycopene comprising the following steps: a) mixing of plant material and, or fibrous plant byproducts containing carotenoids with an amount of water from 1 to 10 times the weight of said materials and, or by-products until a mixture is obtained; b) adding said mexture of an enzymatic catalytic system characterized by the fact that after or during step b) a surfactant is added in order to obtain an aqueous extract containing carotenoids.
- examples of carotenoids are lycopene and, or ⁇ -carotene and as plant materials and, or fibrous by-products are advantageously used whole tomatoes and, or carrots and, or fibrous by-products of the agri-food transformation industries.
- fibrous by-products tomato skins, solid cellulosic residues derived from peeled tomatoes and puree productions can be cited. It is possible to use both fresh and cryoconserved skins, generally at temperature of - 2O 0 C, defrosted and processed within 24 hours from de-icing.
- thermal water that is to say spring water characterised by chemico-physical properties and peculiar inorganic salts due to the specific geochemical properties of the lands surrounding the spring.
- the enzymatic biocatalytic system, used in the step b) of the present invention at T 20 - 50 0 C and pH 3 - 6 comprises enzymes chosen from the class formed by cellulases, pectinases, xylanases, amylases, proteases, cutinases and arylesterases .
- step b) In order to accelerate the reaction before than step b) it is possible to perform a thermal and, or mechanical treatment of the mixture referred to in step a) .
- mechanical treatment homogenisation and whipping can be cited.
- the surfactants used, acting in aqueous solution are .part of the class of food-grade, natural and, or synthetic surfactants.
- As favourites surfactants can be cited surfactants belonging to the classe formed by polysorbates, lecitins, saponins, alkyl-glucosides, sodium dodecyl sulphate, cetylstearilic alcohols, betaines, imidazolines, sarcosinates, sulphosuccinates, quaternium and polyquaternium.
- food grade surfactants are used, among these can be cited Tween
- the aqueous extract undergoes a filtration process to separate particles larger than 100 ⁇ m, as the smaller particles of plant material and, or by-products still contain significant amounts of lycopene; the main uses of lycopene allow to use this extract.
- the extract obtained by the process according to the present invention undergoes a pasteurisation process, advantageously at T 90 0 C for 20-200 minutes, and hot- packed and, or added with stabilizers chosen among those generally used in the relevant technological sector.
- the use of enzymatic catalytic systems gives several advantages.
- the enzymatic products, as well as the surfactants, are water soluble so the entire process can be performed in water phase.
- an extraction performed using non-hazardous enzymes and surfactants can be carried out by non specifically trained operators, i.e. in a farm, as no toxic-hazardous substance is used.
- the enzymes contribute to make the recovery of chemicals more efficient as, hydrolyzing in a selective way plant material, the enzymes promote the release and the pseudo-solubilisation of these chemicals.
- the process of the invention moreover, the overall cost of the lycopene extraction process is reduced if compared to similar processes. Furthermore in this way, the solid by-products of this process after contact only with water, enzymes (considered safe as already used for food applications) and surfactants (food grade or natural) are not considered as special wastes. This allows both a disposal in landfill and their reuse of the production of bio-polymers or dried products used in agriculture as fertilizer or for animal consumption or as bio-fuels, allowing to recover part of the energy used during the productive processes.
- the agri-food by-products are generally used in fertiliser production, for animal consumption, to produce biogas, in the biological depuration and thermo-valorisation processes. Just a small fraction of these by-products nowadays is valorised by the recovery of phyto-molecules through extraction processes.
- the extracts obtainable through the process of the invention can be used in nutraceutical, pharmaceutical and cosmetic sector.
- the extracts of the invention can be used to produce creams, ointments, lotions, emulsions, gels, operculum, medical devices, drops, eventually added to other pharmaceutical principles .
- Example 1 Production of an extract containing lycopene for food applications.
- aqueous extract containing pseudo-solubilised lycopene from tomato skins for food applications the transformation of the raw material . within 12 hours from the production is preferred.
- the skins are re-suspended in tap water or deionised water in a proportion equal to 2 folds the weight of skins to be treated.
- the water re-suspended skins are treated at a temperature of 75°C for 90 minutes.
- the pre-treated skins are cooled down to 3O 0 C and undergo a biocatalytic process for 4 hours at a constant temperature of 30 0 C with food grade enzymatic products having cellulasic and pectinasic activities and at least one of the following other activities: xylanasic, amylasic, proteasic, cutinasic and aryl-esterasic.
- the hydrolysed skins are added with a food grade surfactant (i.e. Tween 20/60/80) in concentration of 5% of the skin weight at a temperature of 30 0 C for 4 hour.
- a food grade surfactant i.e. Tween 20/60/80
- the raw extract undergoes to several filtration treatments (using bag, cardboard and cartridge technologies) .
- the filtrate extract is added with suitable preservatives (potassium sorbate 0.3- 2 % and/or citric acid 0.1-5% w/v and/or lactic acid 0.1- 6%) and pasteurised at 9O 0 C for 30 minutes and hot-packed in suitable containers (bag-in-boxes, tanks and cisterns among others) .
- aqueous extract containing pseudo-solubilised lycopene from tomato skins for cosmetic applications, fresh tomato skins or stored at - 20 0 C and treated within 24 hours from the de-icing can be used.
- the skins are re-suspended in tap water or deionised water in a proportion equal to 5 folds the weight of skins to be treated.
- the water re-suspended skins undergo whipping processes and are treated at a temperature of 90 0 C for 10 minutes.
- the pre-treated skins are cooled down to room temperature and undergo a biocatalytic process for 12 hours at room temperature with enzymatic products having cellulasic and pectinasic activities and at least one of the following other activities: xylanasic, amylasic, proteasic, cutinasic and aryl-esterasic.
- the hydrolysed skins are added with a cosmetic grade surfactant, i.e. sodium dodecyl sulfate in concentration of 1% of the skin weight at room temperature for 8 hour.
- a cosmetic grade surfactant i.e. sodium dodecyl sulfate in concentration of 1% of the skin weight at room temperature for 8 hour.
- the raw extract undergoes several filtration treatments (using bag, cardboard and cartridge technologies) .
- the filtrate extract is added with suitable stabilizers (m- parabenzoate 0.01-1 % w/v and/or citric acid 0.1-5% w/v and/or EDTA 0.1-3% w/v and/or phenoxyethanol 2-5 % w/v) and packed in suitable containers (bag-in-boxes, tanks and cisterns among others) .
- aqueous extract containing pseudo-solubilised lycopene from tomato skins for cosmetic applications fresh tomato skins or stored at -20 0 C and treated within 24 hours from the de-icing can be used.
- the skins are re-suspended in tap water or deionised water in a proportion equal to 3 times the weight of skins to be treated.
- the water re-suspended skins are treated at a temperature of 90 0 C for 20 minutes.
- the skins are added with a natural surfactant, such as natural saponins, natural alkyl glucosides or grounded Sapindus mukorossi nut in concentration of 3% of the skin weight at a temperature of 60 0 C for 6 hour.
- the raw extract undergoes several filtration treatments (using bag, cardboard, cartridge and microfiltration technologies) .
- the filtrate extract is added with suitable preservatives (bitter orange extract 0.01-1 % w/v and/or citric acid 0.1-5% w/v lactic acid 0.1-6%w/v) and packed in suitable containers (bag-in-boxes, tanks and cisterns among others) .
- aqueous extract containing pseudo-solubilised ⁇ -carotene from carrots for food applications the transformation of fresh raw material is preferred.
- the skins are re-suspended in tap water or deionised water in a proportion equal to 3 folds the weight of skins to be treated.
- the water re-suspended carrots are treated at a temperature of 85°C for 90 minutes.
- the pre-treated skins are cooled down to 30 0 C and undergo a biocatalytic process for 4 hours at a constant temperature of 30 °C with food grade enzymatic products having cellulasic and amylasic activities and at least one of the following other activities: xylanasic, pectinasic, proteasic, cutinasic and aryl-esterasic.
- the hydrolysed carrots are added with a food grade surfactant (i.e. tween 20/60/80) in concentration of 3% of the skin weight at a temperature of 30 °C for 4 hour.
- a food grade surfactant i.e. tween 20/60/80
- the raw extract undergoes several filtration treatment (using bag, cardboard and cartridge technologies) .
- the filtrate extract is added with suitable preservatives (potassium sorbate 0.3-2 % and/or citric acid 0.1-5% w/v and/or lactic acid 0.1-6%) and pasteurised at 90 0 C for 30 minutes and hot-packed in suitable containers (bag-in- boxes, tanks and cisterns among others) .
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Nutrition Science (AREA)
- Botany (AREA)
- Mycology (AREA)
- Alternative & Traditional Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Husbandry (AREA)
- Biotechnology (AREA)
- Medical Informatics (AREA)
- Medicinal Chemistry (AREA)
- Microbiology (AREA)
- Zoology (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Cosmetics (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
La présente invention porte sur un procédé d'obtention d'extraits aqueux contenant des caroténoïdes et sur les extraits obtenus.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ITRM2007A000651 | 2007-12-17 | ||
IT000651A ITRM20070651A1 (it) | 2007-12-17 | 2007-12-17 | Procedimento per ottenere estratti acquosi a base di carotenoidi e estratti ottenuti. |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2009077970A1 true WO2009077970A1 (fr) | 2009-06-25 |
Family
ID=40315830
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2008/055306 WO2009077970A1 (fr) | 2007-12-17 | 2008-12-15 | Procédé d'obtention d'extraits aqueux contenant des caroténoïdes et extraits obtenus |
Country Status (2)
Country | Link |
---|---|
IT (1) | ITRM20070651A1 (fr) |
WO (1) | WO2009077970A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016146837A1 (fr) * | 2015-03-18 | 2016-09-22 | Pierre Fabre Dermo-Cosmetique | Procede de preparation d'un extrait de matrice vegetale avec un compose amphiphile non ionique comme adjuvant d'extraction en milieu aqueux |
US9788561B2 (en) | 2012-12-20 | 2017-10-17 | Conopco, Inc. | Tomato fibre composition and method for the preparation thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4316917A (en) * | 1980-04-21 | 1982-02-23 | Hoffman-La Roche Inc. | Stable carotenoid solutions |
WO1991018058A1 (fr) * | 1990-05-16 | 1991-11-28 | Kalamazoo Holdings, Inc. | Compositions de pigment carotenoide a couleur stabilisee et denrees alimentaires ainsi colorees |
WO2006036125A1 (fr) * | 2004-09-28 | 2006-04-06 | Gao Shen Sdn Bhd | Procede pour la production d'extrait de lycopene |
-
2007
- 2007-12-17 IT IT000651A patent/ITRM20070651A1/it unknown
-
2008
- 2008-12-15 WO PCT/IB2008/055306 patent/WO2009077970A1/fr active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4316917A (en) * | 1980-04-21 | 1982-02-23 | Hoffman-La Roche Inc. | Stable carotenoid solutions |
WO1991018058A1 (fr) * | 1990-05-16 | 1991-11-28 | Kalamazoo Holdings, Inc. | Compositions de pigment carotenoide a couleur stabilisee et denrees alimentaires ainsi colorees |
WO2006036125A1 (fr) * | 2004-09-28 | 2006-04-06 | Gao Shen Sdn Bhd | Procede pour la production d'extrait de lycopene |
Non-Patent Citations (1)
Title |
---|
"Biological enzyme extraction process of high-purity lycopene from tomato jam", DERWENT,, 1 January 1900 (1900-01-01), XP002337768 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9788561B2 (en) | 2012-12-20 | 2017-10-17 | Conopco, Inc. | Tomato fibre composition and method for the preparation thereof |
WO2016146837A1 (fr) * | 2015-03-18 | 2016-09-22 | Pierre Fabre Dermo-Cosmetique | Procede de preparation d'un extrait de matrice vegetale avec un compose amphiphile non ionique comme adjuvant d'extraction en milieu aqueux |
FR3033702A1 (fr) * | 2015-03-18 | 2016-09-23 | Pierre Fabre Dermo-Cosmetique | Procede de preparation d'un extrait de plante avec un compose amphiphile non ionique comme adjuvant d'extraction en milieu aqueux |
CN107404926A (zh) * | 2015-03-18 | 2017-11-28 | 皮埃尔·法布尔皮肤化妆品公司 | 用于在水介质中用非离子两亲性化合物作为提取佐剂制备植物来源的基质的提取物的方法 |
US10299502B2 (en) | 2015-03-18 | 2019-05-28 | Pierre Fabre Dermo-Cosmetique | Method for producing an extract of a matrix of vegetable origin with a non-ionic amphiphilic compound as extraction adjuvant in an aqueous medium |
CN107404926B (zh) * | 2015-03-18 | 2021-03-16 | 皮埃尔·法布尔皮肤化妆品公司 | 用于在水介质中用非离子两亲性化合物作为提取佐剂制备植物来源的基质的提取物的方法 |
Also Published As
Publication number | Publication date |
---|---|
ITRM20070651A1 (it) | 2009-06-18 |
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