CA2340546A1 - Soft capsules comprising polymers of vinyl esters and polyethers, the use and production thereof - Google Patents
Soft capsules comprising polymers of vinyl esters and polyethers, the use and production thereof Download PDFInfo
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- CA2340546A1 CA2340546A1 CA002340546A CA2340546A CA2340546A1 CA 2340546 A1 CA2340546 A1 CA 2340546A1 CA 002340546 A CA002340546 A CA 002340546A CA 2340546 A CA2340546 A CA 2340546A CA 2340546 A1 CA2340546 A1 CA 2340546A1
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- Prior art keywords
- soft capsule
- appropriate
- polymers
- polyether
- alkyl
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4816—Wall or shell material
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/06—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polyethers, polyoxymethylenes or polyacetals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/08—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2351/00—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
- C08J2351/08—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
- Manufacturing Of Micro-Capsules (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Formation And Processing Of Food Products (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
- Graft Or Block Polymers (AREA)
Abstract
The present invention relates to soft capsules comprising (a) polymers prepared by polymerization of vinyl esters in the presence of polyethers (b) where appropriate structure-improving auxiliaries and (c) where appropriate other conventional constituents, the use and production thereof.
Claims (26)
1. A soft capsule comprising (a) polymers prepared by polymerization of vinyl esters in the presence of polyethers (b) where appropriate structure-improving auxiliaries and (c) where appropriate other conventional constituents.
2. A soft capsule as claimed in claim 1, wherein the polymers (a) are obtainable by free-radical polymerization of a) at least one vinyl ester of C1-C24-carboxylic acids in the presence of b) polyether-containing compounds and a) where appropriate one or more copolymerizable monomers and subsequent at least partial hydrolysis of the ester functions in the original monomers a).
3. A soft capsule as claimed in either of claims 1 or 2, wherein the polymers (a) are obtainable by free-radical polymerization of a) at least one vinyl ester of C1-C24-carboxylic acids in the presence of b) polyether-containing compounds of the general formula I
in which the variables have, independently of one another, the following meaning;
R1 hydrogen. C1-C24-alkyl. R6-C (=O) -, R6-NH-C (=O) -, polyalcohol residue;
R5 hydrogen, C1-C24-alkyl, R6-C (=O) -, R6-NH-C (=O) -;
R2 to R4 -(CH2)2-, -(CH2)3-, -(CH2)4-, -CH2-CH(R6)-, -CH2-CHOR7-CH2-;
R6 C1-C24-alkyl;
R7 hydrogen, C1-C24-alkyl, R6-C (=O)-, R6-NH-C(=O)-;
A -C(=O)-O, -C(=O) -B-C(=O)-O, -C(=O)-NH-B-NH-C(=O)-O, B -(CH2)t-, arylene, optionally substituted;
n 1 to 1000;
s 0 to 1000;
t 1 to 12;
u 1 to 5000;
v 0 to 5000;
w 0 to 5000;
x 0 to 5000;
y 0 to 5000;
z 0 to 5000;
and c) where appropriate one or more other copolymerizable monomers and subsequent at least partial hydrolysis of the ester functions in the original monomers a).
in which the variables have, independently of one another, the following meaning;
R1 hydrogen. C1-C24-alkyl. R6-C (=O) -, R6-NH-C (=O) -, polyalcohol residue;
R5 hydrogen, C1-C24-alkyl, R6-C (=O) -, R6-NH-C (=O) -;
R2 to R4 -(CH2)2-, -(CH2)3-, -(CH2)4-, -CH2-CH(R6)-, -CH2-CHOR7-CH2-;
R6 C1-C24-alkyl;
R7 hydrogen, C1-C24-alkyl, R6-C (=O)-, R6-NH-C(=O)-;
A -C(=O)-O, -C(=O) -B-C(=O)-O, -C(=O)-NH-B-NH-C(=O)-O, B -(CH2)t-, arylene, optionally substituted;
n 1 to 1000;
s 0 to 1000;
t 1 to 12;
u 1 to 5000;
v 0 to 5000;
w 0 to 5000;
x 0 to 5000;
y 0 to 5000;
z 0 to 5000;
and c) where appropriate one or more other copolymerizable monomers and subsequent at least partial hydrolysis of the ester functions in the original monomers a).
4. A soft capsule as claimed in any of claims 1 to 3, wherein the polymers (a) are obtainable by free-radical polymerization of a) at least one vinyl ester of C1-C24-carboxylic acids is the presence of b) polyether-containing compounds of the general formula I
with a number average molecular weight of from 300 to 100000, in which the variables have, independently of one another, the following meaning:
R1 hydrogen. C1-C12-alkyl, R6-C(=O)-, R6-NH-C(=O)-, polyalcohol residues;
R5 hydrogen, C1-C12-alkyl, R6-C (=O)-, R6-NH-C(=O)-:
R2 to R4 -(CH2)2-, (CH2)3-, -(CH2)4-, -CH2-CH(R6)-, R6 C-C12-alkyl;
R7 hydrogen, C1-C12-alkyl, R6-C(=O)-, R6-NH-C(=O)-:
n 1 to 8;
s 0;
u 2 to 2000;
v 0 to 2000;
w 0 to 2000;
and c) where appropriate one or more other copolymerizable monomers and subsequent at least partial hydrolysis of the ester functions is the original monomers a).
with a number average molecular weight of from 300 to 100000, in which the variables have, independently of one another, the following meaning:
R1 hydrogen. C1-C12-alkyl, R6-C(=O)-, R6-NH-C(=O)-, polyalcohol residues;
R5 hydrogen, C1-C12-alkyl, R6-C (=O)-, R6-NH-C(=O)-:
R2 to R4 -(CH2)2-, (CH2)3-, -(CH2)4-, -CH2-CH(R6)-, R6 C-C12-alkyl;
R7 hydrogen, C1-C12-alkyl, R6-C(=O)-, R6-NH-C(=O)-:
n 1 to 8;
s 0;
u 2 to 2000;
v 0 to 2000;
w 0 to 2000;
and c) where appropriate one or more other copolymerizable monomers and subsequent at least partial hydrolysis of the ester functions is the original monomers a).
5. A soft capsule as claimed in any of claims 1 to 4, wherein the polymers (a) are obtainable by free-radical polymerization of a) at least, one vinyl ester of C1-C24-carboxylic acids in the presence of b) polyether-containing compounds of the general formula I
with a number average molecular weight of from 500 to 50000, in which the variables have, independently of one another, the following meaning:
R1 hydrogen. C1-C6-alkyl, R6-C (=O)-, R6-NH-C(=O)-;
R5 hydrogen, C1-c6-alkyl, R6-C(=O)-, R6-NH-C(=O)-;
R2 to R4 -(CH2)2-, -(CH2)3-, -(CH2)4-, -CH2-CH(R6)-, -CH2-CHOR7-CH2-;
R6 C1-C6-alkyl;
R7 hydrogen. C1-C6-alkyl, R6-C(=O)-, R6-NH-C(=O)-;
n 1;
s 0;
u 5 to 1000;
v 0 to 1000;
w 0 to 1000 and c) where appropriate one or more other copolymerizable monomers and subsequent at least partial hydrolysis of the ester functions in the original monomers a).
with a number average molecular weight of from 500 to 50000, in which the variables have, independently of one another, the following meaning:
R1 hydrogen. C1-C6-alkyl, R6-C (=O)-, R6-NH-C(=O)-;
R5 hydrogen, C1-c6-alkyl, R6-C(=O)-, R6-NH-C(=O)-;
R2 to R4 -(CH2)2-, -(CH2)3-, -(CH2)4-, -CH2-CH(R6)-, -CH2-CHOR7-CH2-;
R6 C1-C6-alkyl;
R7 hydrogen. C1-C6-alkyl, R6-C(=O)-, R6-NH-C(=O)-;
n 1;
s 0;
u 5 to 1000;
v 0 to 1000;
w 0 to 1000 and c) where appropriate one or more other copolymerizable monomers and subsequent at least partial hydrolysis of the ester functions in the original monomers a).
6. A soft capsule as claimed in any of claims 1 to 5, wherein the polymers (a) are obtainable by free-radical polymerization of a) at least one vinyl ester of C1-C24-carboxylic acids in the presence of b) polyether-containing compounds and c) where appropriate one or more other copolymerizable monomers and subsequent at least partial hydrolysis of the ester functions in the original monomers a), wherein the polyether-containing compounds b) have been prepared by polymerization of ethylenically unsaturated alkylene oxide-containing monomers and, where appropriate, other copolymerizable monomers.
7. A soft capsule as claimed in Claim 6, wherein the polyether-containing compounds b) have been prepared by polymerization of polyalkylene oxide vinyl ethers and, where appropriate, other copolymerizable monomers.
8. A soft capsule as claimed in claim 6, wherein the polyether-containing compounds b) have been prepared by polymerization of polyalkylene oxide (meth)acrylates and, where appropriate, other copolymerizable monomers.
9. A soft capsule as claimed in any of claims 1 to 8, wherein the other copolymerizable monomer c) is selected from the group of:
acrylic acid, methacrylic acid, maleic acid, fumaric acid, crotonic acid, maleic anhydride and its monoesters, methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, n-butyl acrylate, n-butyl methacrylate, t-butyl acrylate, t-butyl methacrylate, isobutyl acrylate, isobutyl methacrylate, 2-ethylhexyl acrylate, stearyl acrylate, stearyl methacrylate, N-t-butylacrylamide, N-octylacrylamide, 2-hydroxyethyl acrylate, hydroxypropyl acrylates, 2-hydroxyethyl methacrylate, hydroxypropyl methacrylates, alkylene glycol (meth)acrylates, styrene, unsaturated sulfonic acids such as, for example, acrylamidopropanesulfonic acid, vinylpyrrolidone, vinylcaprolactam, vinyl ethers (for example: methyl, ethyl, butyl or dodecyl vinyl ether), vinylformamide, vinylmethylacetamide, vinylamine, 1-vinylimidazole, 1-vinyl-2-methylimidazole, N,N-dimethylaminomethyl methacrylate and N-(3-(dimethylamino)propyl)methacrylamide;
3-methyl-1-vinylimidazolium chloride, 3-methyl-1-vinylimidazolium methyl sulfate, N,N-dimethylaminoethyl methacrylate, N-[3-(dimethylamino)-propyl]methacrylamide quaternized with methyl chloride, methyl sulfate or diethyl sulfate.
acrylic acid, methacrylic acid, maleic acid, fumaric acid, crotonic acid, maleic anhydride and its monoesters, methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, n-butyl acrylate, n-butyl methacrylate, t-butyl acrylate, t-butyl methacrylate, isobutyl acrylate, isobutyl methacrylate, 2-ethylhexyl acrylate, stearyl acrylate, stearyl methacrylate, N-t-butylacrylamide, N-octylacrylamide, 2-hydroxyethyl acrylate, hydroxypropyl acrylates, 2-hydroxyethyl methacrylate, hydroxypropyl methacrylates, alkylene glycol (meth)acrylates, styrene, unsaturated sulfonic acids such as, for example, acrylamidopropanesulfonic acid, vinylpyrrolidone, vinylcaprolactam, vinyl ethers (for example: methyl, ethyl, butyl or dodecyl vinyl ether), vinylformamide, vinylmethylacetamide, vinylamine, 1-vinylimidazole, 1-vinyl-2-methylimidazole, N,N-dimethylaminomethyl methacrylate and N-(3-(dimethylamino)propyl)methacrylamide;
3-methyl-1-vinylimidazolium chloride, 3-methyl-1-vinylimidazolium methyl sulfate, N,N-dimethylaminoethyl methacrylate, N-[3-(dimethylamino)-propyl]methacrylamide quaternized with methyl chloride, methyl sulfate or diethyl sulfate.
10. A soft capsule as claimed in any of claims 1 to 9, wherein the ratios of amounts are a) 10 to 98% by weight b) 2 to 90% by weight c) 0 to 50% by weight.
11. A soft capsule as claimed in any of claims 1 to 10, wherein the ratios of amounts are a) 50 to 97% by weight b) 3 to 50% by weight c) 0 to 20% by weight.
12. A soft capsule as claimed in any of claims 1 to 11, wherein the ratios of amounts are a) 65 to 97% by weight b) 3 to 35% by weight c) 0 to 20% by weight.
13. A soft capsule as claimed in any of claims 1 to 12, wherein the resulting polymers are subsequently crosslinked by a polymer-analogous reaction.
14. A soft capsule as claimed in any of claims 1 to 13, wherein dialdehydes, diketones, dicarboxylic acids, boric acid, boric acid salts, and salts o~ multiply charged cations are employed for the subsequent crosslinking.
15. A soft capsule as claimed in any of claims 1 to 14, wherein the structure-improving auxiliaries (b) employed are compounds from the following classes:
a) Polymers with a molecular weight of more than 50000 b) substances leading to crosslinking of the polymer chains of the polymers, c) and, where appropriate, substances which lead to crosslinking of the polymer chains of the structure-improving auxiliaries.
a) Polymers with a molecular weight of more than 50000 b) substances leading to crosslinking of the polymer chains of the polymers, c) and, where appropriate, substances which lead to crosslinking of the polymer chains of the structure-improving auxiliaries.
16. A soft Capsule as claimed in any of claims 1 to 15, wherein the structure-improving auxiliaries employed are polymers from the following classes of substances:
Polyamino acids such as gelatin, zein, soybean protein and derivatives thereof, polysaccharides such as starch, degraded starch, maltodextrins, carboxymethylstarch, cellulose, hydroxypropylmethylcellulose, hydroxypropylcellulose, hydroxyethylcellulose, methylcellulose, carboxymethylcellulose, ethylcellulose. cellulose acetate, cellulose acetate phthalate, hydroxypropyloellulose acetate phthalate, hydroxypropylcellulose acetate succinate, hemicellulose, galactomannans, pectins, alginates, carrageenans, xanthan, gellan, dextran, curdlan, pullulan, gum Arabic, chitin, and derivatives thereof, synthetic polymers such as polyacrylic acid, polymethacrylic acid, copolymers of acrylic esters and methacrylio eaters, polyvinyl alcohols, polyvinyl acetate, polyethylene glycols, polyoxyethylene/polyoxypropylene block copolymers.
polyvinylpyrrolidones and derivatives thereof.
Polyamino acids such as gelatin, zein, soybean protein and derivatives thereof, polysaccharides such as starch, degraded starch, maltodextrins, carboxymethylstarch, cellulose, hydroxypropylmethylcellulose, hydroxypropylcellulose, hydroxyethylcellulose, methylcellulose, carboxymethylcellulose, ethylcellulose. cellulose acetate, cellulose acetate phthalate, hydroxypropyloellulose acetate phthalate, hydroxypropylcellulose acetate succinate, hemicellulose, galactomannans, pectins, alginates, carrageenans, xanthan, gellan, dextran, curdlan, pullulan, gum Arabic, chitin, and derivatives thereof, synthetic polymers such as polyacrylic acid, polymethacrylic acid, copolymers of acrylic esters and methacrylio eaters, polyvinyl alcohols, polyvinyl acetate, polyethylene glycols, polyoxyethylene/polyoxypropylene block copolymers.
polyvinylpyrrolidones and derivatives thereof.
17. A soft capsule as claimed in any of claims 1 to 16, wherein other conventional constituents of the shell which are present are fillers, release agents, flow aids, dyes, pigments, opacifiers, flavorings, sweeteners, plasticizers, preservatives and/or active ingredients.
18. A soft capsule as claimed in any of claims 1 to 17, wherein the shell consists of from 10 to 100% by weight of polymers of vinyl esters on polyether, where appropriate from 0 to 80%
of structure-improving auxiliaries and, where appropriate, from 0 to 30% of other conventional constituents.
of structure-improving auxiliaries and, where appropriate, from 0 to 30% of other conventional constituents.
19. A soft capsule as claimed in any of claims 1 to 18, obtainable by processes such as the rotary die process, Accogel process, Norton process, drop or blow process or the Colton-Upjohn process.
20. A soft capsule as claimed is nay of claims 1 to 19, which comprises one or more active pharmaceutical ingredients, vitamins, carotenoids, minerals, trace elements, food supplements, cosmetic active ingredients, crop protection agents, bath additives, perfume, flavoring, cleaner or detergent.
21. A soft capsule as claimed in any or claims 1 to 20, wherein the shell comprises from 20 to 80% of a polymer resistant to gastric fluid.
22. A soft capsule as claimed in any of claims 1 to 21, wherein resistance to gastric fluid is achieved by applying after production a coating resistant to gastric fluid by conventional pharmaceutical coating processes.
23. The use of the soft capsules as claimed in any of claims 1 to 22 for pharmaceutical applications.
24. The use of the soft capsules as claimed is any of claims 1 to 22 for cosmetic applications, applications in crop protection, for cleaners or food supplements.
25. The use of polymers obtainable by free-radical polymerization of a) at least one vinyl ester of C1-C24-carboxylic acids in the presence of b) polyether-containing compounds and c) where appropriate one or more copolymerizable monomers and subsequent at least partial hydrolysis of the ester functions in the original monomers a) to produce soft capsules as claimed in any of claims 1 to 22.
26. The use of polymers obtainable by free-radical polymerization of at least one vinyl ester of C1-C24-carboxylic acids in the presence of b) polyether-containing compounds and c) where appropriate one ox more copolymerizable monomers and subsequent at least partial hydrolysis of the ester functions in the original monomers a) wherein the polyether-containing compounds b) have been prepared by polymerization of ethylenically unsaturated alkylene oxide-containing monomers and, where appropriate, other copolymerizable monomers, for producing soft capsules as claimed in any of claims 1 to 22.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10012063.6 | 2000-03-14 | ||
| DE10012063A DE10012063A1 (en) | 2000-03-14 | 2000-03-14 | Soft plasticizer-free capsules for use in pharmaceuticals, cosmetics, detergents or plant protectants are made from a polymers obtained by polymerizing a vinyl ester in presence of a polyether substrate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2340546A1 true CA2340546A1 (en) | 2001-09-14 |
| CA2340546C CA2340546C (en) | 2010-05-18 |
Family
ID=7634468
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2340546A Expired - Fee Related CA2340546C (en) | 2000-03-14 | 2001-03-13 | Soft capsules comprising polymers of vinyl esters and polyethers, the use and production thereof |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6770293B2 (en) |
| EP (1) | EP1136070B1 (en) |
| JP (1) | JP5095890B2 (en) |
| KR (1) | KR20010092341A (en) |
| CN (1) | CN1212832C (en) |
| AT (1) | ATE321539T1 (en) |
| BR (1) | BRPI0102338B1 (en) |
| CA (1) | CA2340546C (en) |
| DE (2) | DE10012063A1 (en) |
| ES (1) | ES2261287T3 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114392698A (en) * | 2022-01-19 | 2022-04-26 | 南昌大学 | High-stability photo-thermal hydrogel sponge and preparation method and application thereof |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0005016D0 (en) * | 2000-03-01 | 2000-04-26 | Jumik Technologies Limited | PVA-Containing compositions |
| DE10015468A1 (en) | 2000-03-29 | 2001-10-11 | Basf Ag | Hard capsules containing polymers and vinyl esters and polyethers, their use and production |
| DE10128531A1 (en) * | 2001-06-13 | 2002-12-19 | Basf Ag | Water soluble water dispersible film forming graft polymerisate consisting of vinyl esters of 1-24C carboxylic acids in presence of polyethers useful as coating agents, matrix builders, and agrochemical packaging materials |
| EP1451231B1 (en) * | 2001-11-24 | 2008-12-31 | Basf Se | Aqueous dispersions of water-soluble polymers of N-vinyl carboxylic acid amides, method for the production thereof and their use |
| JP4139383B2 (en) * | 2002-05-03 | 2008-08-27 | ビーエーエスエフ ソシエタス・ヨーロピア | Cosmetics comprising at least one water-soluble copolymer containing (meth) acrylamide units |
| UY28056A1 (en) * | 2002-10-31 | 2003-12-31 | Alza Corp | DOSAGE FORMS THAT PROVIDE THE ASCENDING RELEASE OF A LIQUID FORMULATION. |
| DE10261197A1 (en) * | 2002-12-20 | 2004-07-08 | Basf Ag | Aqueous polymer dispersion |
| US8541051B2 (en) | 2003-08-14 | 2013-09-24 | Halliburton Energy Services, Inc. | On-the fly coating of acid-releasing degradable material onto a particulate |
| US7829507B2 (en) | 2003-09-17 | 2010-11-09 | Halliburton Energy Services Inc. | Subterranean treatment fluids comprising a degradable bridging agent and methods of treating subterranean formations |
| US7674753B2 (en) | 2003-09-17 | 2010-03-09 | Halliburton Energy Services, Inc. | Treatment fluids and methods of forming degradable filter cakes comprising aliphatic polyester and their use in subterranean formations |
| US7833944B2 (en) | 2003-09-17 | 2010-11-16 | Halliburton Energy Services, Inc. | Methods and compositions using crosslinked aliphatic polyesters in well bore applications |
| US20070141137A1 (en) * | 2004-03-04 | 2007-06-21 | Naoki Nagahara | Stable capsule preparation |
| DE102004031835A1 (en) * | 2004-06-30 | 2006-01-19 | Basf Ag | Fast-dispersible, finely divided, non-segregating powdery film coating composition based on polyvinyl alcohol-polyether graft copolymers characterized by particular physical stability and low roughness |
| US20060093560A1 (en) * | 2004-10-29 | 2006-05-04 | Jen-Chi Chen | Immediate release film coating |
| US7648946B2 (en) | 2004-11-17 | 2010-01-19 | Halliburton Energy Services, Inc. | Methods of degrading filter cakes in subterranean formations |
| US20080009423A1 (en) | 2005-01-31 | 2008-01-10 | Halliburton Energy Services, Inc. | Self-degrading fibers and associated methods of use and manufacture |
| US8598092B2 (en) | 2005-02-02 | 2013-12-03 | Halliburton Energy Services, Inc. | Methods of preparing degradable materials and methods of use in subterranean formations |
| US7662753B2 (en) | 2005-05-12 | 2010-02-16 | Halliburton Energy Services, Inc. | Degradable surfactants and methods for use |
| DE102005043172A1 (en) * | 2005-09-09 | 2007-03-15 | Basf Ag | Process for the preparation of soft capsule shells based on polyvinyl alcohol-polyethylene glycol graft copolymers |
| US7713916B2 (en) | 2005-09-22 | 2010-05-11 | Halliburton Energy Services, Inc. | Orthoester-based surfactants and associated methods |
| DE102005053066A1 (en) | 2005-11-04 | 2007-05-10 | Basf Ag | Use of copolymers as solubilizers for sparingly water-soluble compounds |
| WO2007065846A2 (en) * | 2005-12-09 | 2007-06-14 | Basf Se | Use of polyvinyl lactam-polyoxyalkylene block copolymers as solubilisers for poorly water-soluble compounds |
| US8329621B2 (en) * | 2006-07-25 | 2012-12-11 | Halliburton Energy Services, Inc. | Degradable particulates and associated methods |
| US7686080B2 (en) | 2006-11-09 | 2010-03-30 | Halliburton Energy Services, Inc. | Acid-generating fluid loss control additives and associated methods |
| US8220548B2 (en) | 2007-01-12 | 2012-07-17 | Halliburton Energy Services Inc. | Surfactant wash treatment fluids and associated methods |
| EP2173781A1 (en) * | 2007-07-26 | 2010-04-14 | Basf Se | Process for preparing copolymers obtained by graft polymerization in solution and based on polyethers in solid form |
| EP2057986A1 (en) * | 2007-11-09 | 2009-05-13 | Basf Se | Soft capsules based on natural polysaccharides containing polyvinyl alcohol - polyethylenglycol - plug copolymers |
| US20090214641A1 (en) * | 2008-02-26 | 2009-08-27 | Joar Opheim | Sweetened Capsules for Administration |
| US8006760B2 (en) | 2008-04-10 | 2011-08-30 | Halliburton Energy Services, Inc. | Clean fluid systems for partial monolayer fracturing |
| US7906464B2 (en) | 2008-05-13 | 2011-03-15 | Halliburton Energy Services, Inc. | Compositions and methods for the removal of oil-based filtercakes |
| CA2730760A1 (en) * | 2008-07-16 | 2010-01-21 | Surmodics Pharmaceuticals, Inc. | Process for preparing microparticles containing bioactive peptides |
| US7833943B2 (en) | 2008-09-26 | 2010-11-16 | Halliburton Energy Services Inc. | Microemulsifiers and methods of making and using same |
| CH700543A2 (en) | 2009-03-03 | 2010-09-15 | Innogel Ag | Film based on starch. |
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| US9993793B2 (en) | 2010-04-28 | 2018-06-12 | The Procter & Gamble Company | Delivery particles |
| US9186642B2 (en) | 2010-04-28 | 2015-11-17 | The Procter & Gamble Company | Delivery particle |
| JP6283607B2 (en) | 2011-04-07 | 2018-02-21 | ザ プロクター アンド ギャンブル カンパニー | Personal cleansing composition with increased deposition of polyacrylate microcapsules |
| US8980292B2 (en) | 2011-04-07 | 2015-03-17 | The Procter & Gamble Company | Conditioner compositions with increased deposition of polyacrylate microcapsules |
| CN103458858B (en) | 2011-04-07 | 2016-04-27 | 宝洁公司 | There is the shampoo Compositions of the deposition of the polyacrylate microcapsule of enhancing |
| KR102044734B1 (en) | 2012-04-20 | 2019-11-15 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | Encapsulated formulation |
| CN103739852B (en) * | 2013-12-30 | 2016-04-20 | 中国科学院长春应用化学研究所 | MPEG grafting α-zein polymkeric substance and preparation method thereof |
| US10188133B2 (en) | 2015-04-23 | 2019-01-29 | Basf Se | Gel capsule containing sterol and solubilising agent |
| WO2017094856A1 (en) * | 2015-12-02 | 2017-06-08 | 株式会社日本触媒 | Water-soluble film and manufacturing method therefor |
| CN106243408B (en) * | 2016-08-26 | 2018-04-24 | 湖南尔康制药股份有限公司 | A kind of starch capsule for improving mechanical performance |
| CN111304027A (en) * | 2020-03-31 | 2020-06-19 | 苏州十一方生物科技有限公司 | Preparation method and device of alkaline detergent |
| CN114159402A (en) * | 2021-12-21 | 2022-03-11 | 湖州展望天明药业有限公司 | Opaque plant capsule and preparation method thereof |
| CN114865097B (en) * | 2022-05-25 | 2023-07-25 | 华中科技大学 | Polymer electrolyte based on boric acid transesterification reaction, preparation method and application thereof |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1077430B (en) | 1958-04-15 | 1960-03-10 | Hoechst Ag | Process for the production of graft polymers of polyvinyl esters |
| FR1222944A (en) * | 1958-04-15 | 1960-06-14 | Hoechst Ag | Graft polymers and their preparation process |
| BE579240A (en) | 1958-05-31 | |||
| DE2363853A1 (en) | 1973-12-21 | 1975-07-03 | Hoechst Ag | SELF-SUPPORTING PACKAGES OR CAPSULES FOR WRAPPING MEDICINES |
| GB9013307D0 (en) | 1990-06-14 | 1990-08-08 | Allied Colloids Ltd | Polymeric films for forming capsule shells |
| US5342626A (en) | 1993-04-27 | 1994-08-30 | Merck & Co., Inc. | Composition and process for gelatin-free soft capsules |
| DE4403866A1 (en) | 1994-02-08 | 1995-08-10 | Basf Ag | Amphiphilic polyesters, process for their preparation and their use in detergents |
| JPH08311290A (en) * | 1995-05-23 | 1996-11-26 | Showa Denko Kk | Composition for liquid-absorbing material, molding of liquid-absorbing material, and production thereof |
| GB9606371D0 (en) | 1996-03-26 | 1996-06-05 | Brown Malcolm D | An encapsulation process |
| DE19645024A1 (en) * | 1996-10-31 | 1998-05-07 | Basf Ag | Bleaching aid containing microcapsules |
| FR2757173A1 (en) | 1996-12-17 | 1998-06-19 | Warner Lambert Co | POLYMERIC COMPOSITIONS OF NON-ANIMAL ORIGIN FOR FILM FORMATION |
| FR2767070B1 (en) | 1997-08-08 | 1999-09-17 | Laurence Paris | AQUEOUS VISCOUS COMPOSITION, LIMPID OR NOT, FOR THE MANUFACTURE OF SOFT CAPSULES AND HARD CAPSULES, AND METHOD FOR MANUFACTURING FILMS FOR SUCH CAPSULES |
| BR9907699A (en) | 1998-02-06 | 2002-01-15 | Union Carbide Chem Plastic | Polymeric compositions of alkylene oxide |
| EP1124541B1 (en) * | 1998-09-30 | 2003-11-26 | Basf Aktiengesellschaft | Application of water-soluble or water-dispersible graft polymerizates which contain poly-ether and which are used as a coating agent, a binding agent and/or as a film-forming auxiliary agent in pharmaceutical forms of administration |
-
2000
- 2000-03-14 DE DE10012063A patent/DE10012063A1/en not_active Withdrawn
-
2001
- 2001-03-12 DE DE50109347T patent/DE50109347D1/en not_active Expired - Lifetime
- 2001-03-12 AT AT01106041T patent/ATE321539T1/en not_active IP Right Cessation
- 2001-03-12 ES ES01106041T patent/ES2261287T3/en not_active Expired - Lifetime
- 2001-03-12 EP EP01106041A patent/EP1136070B1/en not_active Expired - Lifetime
- 2001-03-13 CA CA2340546A patent/CA2340546C/en not_active Expired - Fee Related
- 2001-03-14 KR KR1020010013238A patent/KR20010092341A/en not_active Application Discontinuation
- 2001-03-14 BR BRPI0102338A patent/BRPI0102338B1/en not_active IP Right Cessation
- 2001-03-14 US US09/805,239 patent/US6770293B2/en not_active Expired - Lifetime
- 2001-03-14 JP JP2001072868A patent/JP5095890B2/en not_active Expired - Fee Related
- 2001-03-14 CN CNB01121435XA patent/CN1212832C/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114392698A (en) * | 2022-01-19 | 2022-04-26 | 南昌大学 | High-stability photo-thermal hydrogel sponge and preparation method and application thereof |
| CN114392698B (en) * | 2022-01-19 | 2023-08-18 | 南昌大学 | High-stability photo-thermal water gel sponge and preparation method and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1136070B1 (en) | 2006-03-29 |
| BRPI0102338B1 (en) | 2016-08-23 |
| DE50109347D1 (en) | 2006-05-18 |
| ATE321539T1 (en) | 2006-04-15 |
| EP1136070A1 (en) | 2001-09-26 |
| JP5095890B2 (en) | 2012-12-12 |
| CA2340546C (en) | 2010-05-18 |
| US20020119169A1 (en) | 2002-08-29 |
| JP2001329029A (en) | 2001-11-27 |
| BR0102338A (en) | 2001-10-16 |
| KR20010092341A (en) | 2001-10-24 |
| CN1212832C (en) | 2005-08-03 |
| ES2261287T3 (en) | 2006-11-16 |
| CN1326732A (en) | 2001-12-19 |
| US6770293B2 (en) | 2004-08-03 |
| DE10012063A1 (en) | 2001-09-20 |
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