WO1997019083A9 - Procede pour extraire et purifier de la morphine a partir d'opium - Google Patents
Procede pour extraire et purifier de la morphine a partir d'opiumInfo
- Publication number
- WO1997019083A9 WO1997019083A9 PCT/US1996/018793 US9618793W WO9719083A9 WO 1997019083 A9 WO1997019083 A9 WO 1997019083A9 US 9618793 W US9618793 W US 9618793W WO 9719083 A9 WO9719083 A9 WO 9719083A9
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- basic
- solution
- methanol
- extracting
- morphine
- Prior art date
Links
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 title claims abstract description 103
- 229960005181 morphine Drugs 0.000 title claims abstract description 50
- 238000000034 method Methods 0.000 title claims abstract description 41
- 239000008896 Opium Substances 0.000 title claims abstract description 33
- 229960001027 opium Drugs 0.000 title claims abstract description 33
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims abstract description 36
- 239000007864 aqueous solution Substances 0.000 claims abstract description 36
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 34
- 238000000605 extraction Methods 0.000 claims abstract description 27
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000000706 filtrate Substances 0.000 claims abstract description 22
- 239000000243 solution Substances 0.000 claims abstract description 22
- 150000003839 salts Chemical class 0.000 claims abstract description 10
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 8
- 239000000839 emulsion Substances 0.000 claims abstract description 8
- 239000007787 solid Substances 0.000 claims abstract description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 69
- 239000002904 solvent Substances 0.000 claims description 16
- 238000001914 filtration Methods 0.000 claims description 14
- 238000010992 reflux Methods 0.000 claims description 9
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 8
- 239000003637 basic solution Substances 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 6
- 239000001632 sodium acetate Substances 0.000 claims description 6
- 235000017281 sodium acetate Nutrition 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- 239000003960 organic solvent Substances 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 4
- 229910001854 alkali hydroxide Inorganic materials 0.000 claims description 4
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 4
- AMXOYNBUYSYVKV-UHFFFAOYSA-M lithium bromide Chemical compound [Li+].[Br-] AMXOYNBUYSYVKV-UHFFFAOYSA-M 0.000 claims description 4
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 claims description 4
- 239000013618 particulate matter Substances 0.000 claims description 4
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 claims description 4
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 claims description 4
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 3
- 239000011236 particulate material Substances 0.000 claims description 3
- 239000011780 sodium chloride Substances 0.000 claims description 3
- 239000008096 xylene Substances 0.000 claims description 3
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 claims description 2
- 235000011056 potassium acetate Nutrition 0.000 claims description 2
- 239000001103 potassium chloride Substances 0.000 claims description 2
- 235000011164 potassium chloride Nutrition 0.000 claims description 2
- 239000011343 solid material Substances 0.000 claims description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims 2
- 238000003808 methanol extraction Methods 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 230000001476 alcoholic effect Effects 0.000 abstract description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- 229930013930 alkaloid Natural products 0.000 description 21
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- 239000000284 extract Substances 0.000 description 11
- 239000002244 precipitate Substances 0.000 description 9
- 238000011084 recovery Methods 0.000 description 8
- 239000006286 aqueous extract Substances 0.000 description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 238000000746 purification Methods 0.000 description 6
- -1 methanol at pH 9 Chemical compound 0.000 description 5
- OROGSEYTTFOCAN-DNJOTXNNSA-N codeine Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC OROGSEYTTFOCAN-DNJOTXNNSA-N 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 239000000401 methanolic extract Substances 0.000 description 3
- 229930013053 morphinan alkaloid Natural products 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229940035676 analgesics Drugs 0.000 description 2
- 239000000730 antalgic agent Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 229960004126 codeine Drugs 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000012458 free base Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- OROGSEYTTFOCAN-UHFFFAOYSA-N hydrocodone Natural products C1C(N(CCC234)C)C2C=CC(O)C3OC2=C4C1=CC=C2OC OROGSEYTTFOCAN-UHFFFAOYSA-N 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 150000007529 inorganic bases Chemical class 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- 239000003434 antitussive agent Substances 0.000 description 1
- 229940124584 antitussives Drugs 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000002152 aqueous-organic solution Substances 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 229940127240 opiate Drugs 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Definitions
- This invention relates to an improved process for the extraction and purification of morphine from opium.
- the object of this invention is to provide a more economical method of preparing morphine that utilizes less environmentally toxic solvents.
- Morphine is useful as an analgesic drug. It is also used as the starting material for the preparation of codeine, which is another analgesic and antitussive drug. Morphine occurs naturally in opium to the extent of 9 to 17% by weight, depending upon the opium source.
- the present invention relates to a process for extracting morphine from opium.
- the process of the invention answers the deficiencies of prior art processes.
- opium is extracted with a basic alcoholic solution.
- the basic alcoholic solution is filtered and the alcohol removed from the filtrate to leave a residue.
- the residue is then extracted with a basic aqueous solution having a pH of at least 11.
- the basic aqueous solution may be filtered to remove any solid matter remaining after the aqueous extraction step, and may then be stirred with a sufficient amount of a salt to avoid emulsion formation.
- the basic aqueous solution is then extracted with a substantially water- immiscible solvent such as benzene or toluene.
- adjusting the pH of the basic aqueous solution to pH 8.5 to 9.5 allows the morphine to precipitate and be recovered.
- Figure 1 depicts a preferred process according to the invention for extracting and purifying morphine from opium. Description of the Invention
- morphine is extracted from opium by stirring and/or heating, or preferably refluxing, opium in a basic solution of an alcohol, preferably methanol at about pH 9.
- the pH may be adjusted by the addition of an inorganic base (alkali hydroxide, or carbonate), ammonia, and the like.
- inorganic bases include, but are not limited to, sodium hydroxide and potassium hydroxide.
- the resulting residue, which contains the alkaloids, is mixed or extracted with an basic aqueous solution having a pH of at least 11, preferably an aqueous solution of an alkali hydroxide.
- This converts the morphine free base present into its anionic (morphinate) form which is soluble in basic solutions at pH values of 1 1 or above.
- Other opium alkaloids are relatively insoluble and, in general, at least partially precipitate out of the basic aqueous solution.
- the remaining alkaloids are separated from the morphine-containing basic aqueous solution by extraction with a substantially water- immiscible solvent, such as toluene or benzene.
- the morphine free base is precipitated out of the resulting aqueous solution by adjusting the pH of the aqueous filtrate to pH 8.5 to 9.5.
- the pH to precipitate the morphine ranges from about
- the extraction of morphine from opium may be accomplished by stirring and/or heating, preferably refluxing, opium with a basic solution of an alcohol capable dissolving morphine in its neutral, cationic, and/or anionic form.
- the alcohol is a C,-C 6 alcohol.
- Particularly preferred alcohols include methanol, ethanol, and isopropanol. Mixtures of alcohols may also be used.
- Methanol the preferred solvent for the invention, is a excellent solvent for extracting alkaloids from opium. Almost all of the alkaloids, especially morphine, are highly soluble in methanol.
- the alkaloids are soluble in methanol in their neutral, cationic, or anionic forms.
- an alkali, alkaline earth, or other suitable base to adjust the pH of the alcohol, to about 9, makes the extraction process more efficient. This results in more alkaloids and less impurities being extracted into the alcohol.
- Refluxing opium in a basic solution of the alcohol, preferably methanol at about pH 9, for approximately one to two hours extracts more than 90% of the morphine present.
- 5 g of opium, cut into small pieces may be extracted by reflux with 0.2 to 0.6 g, preferably 0.4 g, of sodium hydroxide in 25 ml of methanol for 1 to 2 hrs.
- An additional extraction of the opium with a basic alcohol, such as methanol at pH 9, can recover essentially all of the alkaloids from opium.
- the second extract can either be combined with the first extract or can be used to extract another batch of opium. Separation of the alcohol extract from the undissolved residue by filtration or other similar means is generally easy and fast. Unlike an aqueous extraction process, the assistance of filter aid at this step is generally unnecessary.
- the removal of alcohol by distillation, under reduced pressure, at elevated temperatures, or by other known techniques is much easier and more rapid than the concentration of aqueous extracts or organic solutions (e.g. toluene) usually required in prior art methods.
- a small amount of filter aid may be added to the alcohol extract before distillation to prevent the alcohol extract from foaming and bumping.
- the recovered alcohol particularly methanol, can be recycled and used for another extraction without further purification.
- morphine is usually kept as an acid salt due to concerns regarding the stability of morphine in basic solutions.
- HPLC High Performance Liquid Chromatography
- the residue remaining after removing the alcohol is then extracted with a basic aqueous solution having a pH of at least 11.
- the basic aqueous solution is a solution of an alkali hydroxide such as sodium hydroxide or potassium hydroxide. Solutions of other bases may also be used. Maintaining the pH of the aqueous extract at this pH and preferably within a relatively narrow preferred range allows high quality morphine to be obtained with good recovery. At lower pH values, greater amounts of morphine may be lost in the initial precipitate. At higher pH values, less impurities may be extracted into toluene. Maintaining the pH in the range of 11.5 to 11.9 is, therefore, preferred.
- the basic aqueous solution may optionally be filtered to remove any solid material remaining after the aqueous extraction step. Filtering the basic aqueous solution at this point removes insoluble non-morphine alkaloids. Any precipitate may be washed with an additional quantity of the basic aqueous solution to ensure increased recovery of the morphine.
- the basic aqueous solution or filtrate if filtered, is then extracted with a substantially water-immiscible organic solvent to remove the remaining alkaloids from the basic aqueous filtrate.
- Suitable solvents include, but are not limited to, benzene, toluene, xylene, diethyl ether, and chloroform. Separation of the resulting aqueous and organic phases may be accomplished by techniques known in the art.
- non-morphine alkaloids are supposed to precipitate out of concentrated aqueous solutions at pH values around 11-12.
- the presence of concentrated morphinate ions may increase the solubility of the other alkaloids.
- substantial amounts of non-morphine alkaloids may remain in solution.
- Direct extraction of the basic aqueous solution or filtrate, if filtered, with a substantially water-immiscible solvent can remove those alkaloids, but may result in formation of an emulsion.
- the aqueous solution/filtrate may, before extraction with the substantially water-immiscible solvent, first be treated with a sufficient amount of an alkali metal salt or alkaline earth metal salt, for example 0.5 to 5 grams salt for each 5 grams of opium.
- Preferred salts are, for example, lithium chloride, lithium bromide, lithium acetate, sodium chloride, sodium bromide, sodium acetate, potassium chloride, potassium bromide, or potassium acetate.
- a preferred amount of the salt is 0.5 to 2 grams per 5 grams of opium.
- Sodium chloride and sodium acetate are preferred salts with sodium acetate being particularly preferred.
- the extract may then preferably filtered again to get rid of any gummy or other precipitate prior to extracting with a substantially water-immiscible solvent, such as benzene or toluene.
- the sequence of the morphine purification procedure may, however, affect the recovery of morphine. For example, if, to avoid emulsion formation upon extraction, a salt is added to the basic aqueous solution before it is filtered after the aqueous extraction step, as much as about 20% of the morphine may precipitate out along with the other alkaloids. Accordingly, the recovery of morphine will be substantially lower.
- a substantially water- immiscible solvent such as toluene or benzene
- a small amount, generally about 8%, of the morphine may be extracted into the solvent. This may be recovered by back extraction with additional basic solution, for instance, a sodium hydroxide solution. Any loss of morphine in the aqueous mother liquor, about 2%, may be recovered by additional extraction with the solvent.
- the use of toluene is preferred, particularly over benzene, in the process of the invention.
- Any alkaloids precipitated on a filter aid or paper in the process may be recovered by extraction with an alcohol, preferably methanol.
- the filter aid can be used again without further purification.
- the other opiate alkaloids that were extracted into the substantially water-immiscible solvent may be combined with the alkaloids which precipitated from the aqueous extract at pH 11.5 to 11.9 and further purified by other known methods.
- the pH of the basic aqueous solution/filtrate is adjusted to about 8.5 to 9.5 to precipitate the morphine.
- the pH is adjusted to 9 to 9.3 and more preferably to 9.1.
- the pH may be adjusted using an acid such as, for example, sulfuric acid, hydrochloric acid or acetic acid.
- an acid such as, for example, sulfuric acid, hydrochloric acid or acetic acid.
- a 50% acetic acid in water solution is used.
- the precipitated morphine may then be recovered using techniques known in the art such as filtration or decantation.
- the recovered morphine is preferably washed with water before drying.
- Figure 1 depicts a preferred process of the invention. The whole process, from extraction of opium to precipitation of purified morphine, can generally be completed in one day. This is much more efficient than other existing commercial purification methods.
- the combined aqueous filtrate was stirred with 0.5 g of sodium acetate for 10 minutes and filtered again.
- the filtrate was then extracted twice with 5 ml of toluene and the pH of the aqueous filtrate was then adjusted to pH 9.1, with 50% acetic acid in water.
- the mixture was allowed to remain for a period of 6-10 hrs at room temperature for complete precipitation and was then filtered.
- This precipitate was washed with water and dried at room temperature.
- This final precipitate contained 400-426 mg of morphine, which represented a recovery of 86-88% based upon the amount of morphine in the initial methanol extract.
- the purity of morphine following this procedure was 84% to 86% by weight.
Abstract
Cette invention se rapporte à un procédé pour extraire de la morphine contenue dans de l'opium. Dans ce procédé, l'opium est extrait au moyen d'une solution alcoolique basique. Cette solution alcoolique basique est filtrée et l'alcool est retiré du filtrat pour laisser un résidu. Le résidu est ensuite extrait au moyen d'une solution aqueuse basique ayant un pH d'au moins 11. Cette solution aqueuse basique peut être filtrée pour que soit éliminée toute matière solide restant après l'étape d'extraction aqueuse, et ladite solution aqueuse basique peut ensuite être agitée avec un sel en quantité suffisante pour éviter la formation d'émulsion. La solution aqueuse basique ou le filtrat aqueux basique est ensuite extrait avec du benzène ou du toluène. L'ajustement du pH du filtrat aqueux basique dans des limites comprises entre 8,5 à 9,5 permet ensuite à la morphine de précipiter et d'etre recupérée.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU10815/97A AU1081597A (en) | 1995-11-21 | 1996-11-21 | Process for extracting and purifying morphine from opium |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US741895P | 1995-11-21 | 1995-11-21 | |
US60/007,418 | 1995-11-21 | ||
US08/753,061 | 1996-11-19 | ||
US08/753,061 US6054584A (en) | 1996-11-19 | 1996-11-19 | Process for extracting and purifying morphine from opium |
Publications (2)
Publication Number | Publication Date |
---|---|
WO1997019083A1 WO1997019083A1 (fr) | 1997-05-29 |
WO1997019083A9 true WO1997019083A9 (fr) | 1997-10-16 |
Family
ID=26676955
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1996/018793 WO1997019083A1 (fr) | 1995-11-21 | 1996-11-21 | Procede pour extraire et purifier de la morphine a partir d'opium |
Country Status (1)
Country | Link |
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WO (1) | WO1997019083A1 (fr) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN102749402A (zh) * | 2012-08-07 | 2012-10-24 | 公安部禁毒情报技术中心 | 吗啡盐酸盐标准物质的制备方法 |
CN110713494A (zh) * | 2019-09-20 | 2020-01-21 | 甘肃省药物碱厂 | 一种从高纯度吗啡中除去杂质的处理方法 |
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1996
- 1996-11-21 WO PCT/US1996/018793 patent/WO1997019083A1/fr active Application Filing
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