SK10772001A3 - Materiál na zošitie rán na báze metylidénmalonátu - Google Patents

Materiál na zošitie rán na báze metylidénmalonátu Download PDF

Info

Publication number: SK10772001A3
Authority: SK; Slovakia
Prior art keywords: weight; methylidene malonate; molecular weight; formula; methylidene
Prior art date: 1999-02-09

Application number

SK1077-2001A

Other languages

English (en)

Slovak (sk)

Inventor

Nicole Bru-Magniez

Pascal Breton

Claude Roques-Carmes

Isabelle Beliard

Original Assignee

Virsol

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.)

1999-02-09

Filing date

2000-02-09

Publication date

2001-12-03

2000-02-09 Application filed by Virsol filed Critical Virsol

2001-12-03 Publication of SK10772001A3 publication Critical patent/SK10772001A3/sk

Links

XJDDLMJULQGRLU-UHFFFAOYSA-N 1,3-dioxane-4,6-dione Chemical compound O=C1CC(=O)OCO1 XJDDLMJULQGRLU-UHFFFAOYSA-N 0.000 title claims abstract description 64
239000003356 suture material Substances 0.000 title claims abstract description 22
206010052428 Wound Diseases 0.000 title abstract description 57
208000027418 Wounds and injury Diseases 0.000 title abstract description 57
239000000203 mixture Substances 0.000 claims abstract description 89
229920000642 polymer Polymers 0.000 claims abstract description 23
239000000227 bioadhesive Substances 0.000 claims abstract description 6
239000000463 material Substances 0.000 claims description 16
239000000178 monomer Substances 0.000 claims description 15
229920001577 copolymer Polymers 0.000 claims description 10
230000009477 glass transition Effects 0.000 claims description 8
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
-1 polyoxyalkylenes Polymers 0.000 claims description 4
150000004676 glycans Chemical class 0.000 claims description 3
229920000058 polyacrylate Polymers 0.000 claims description 3
229920001282 polysaccharide Polymers 0.000 claims description 3
239000005017 polysaccharide Substances 0.000 claims description 3
229920001308 poly(aminoacid) Polymers 0.000 claims description 2
229920002635 polyurethane Polymers 0.000 claims description 2
239000004814 polyurethane Substances 0.000 claims description 2
229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
235000019422 polyvinyl alcohol Nutrition 0.000 claims description 2
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229920002721 polycyanoacrylate Polymers 0.000 claims 1
239000000853 adhesive Substances 0.000 description 19
230000001070 adhesive effect Effects 0.000 description 19
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 16
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
241000700199 Cavia porcellus Species 0.000 description 12
238000000034 method Methods 0.000 description 12
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AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 4
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CPKVUHPKYQGHMW-UHFFFAOYSA-N 1-ethenylpyrrolidin-2-one;molecular iodine Chemical compound II.C=CN1CCCC1=O CPKVUHPKYQGHMW-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
241001465754 Metazoa Species 0.000 description 3
239000002390 adhesive tape Substances 0.000 description 3
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KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
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QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
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RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
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239000007924 injection Substances 0.000 description 2
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
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CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
238000007619 statistical method Methods 0.000 description 2
238000004659 sterilization and disinfection Methods 0.000 description 2
UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
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230000000472 traumatic effect Effects 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
IIEDMRRXMKUOQQ-UHFFFAOYSA-N 2-(cyanomethylidene)butanoic acid Chemical compound CCC(C(O)=O)=CC#N IIEDMRRXMKUOQQ-UHFFFAOYSA-N 0.000 description 1
CQVWXNBVRLKXPE-UHFFFAOYSA-N 2-octyl cyanoacrylate Chemical compound CCCCCCC(C)OC(=O)C(=C)C#N CQVWXNBVRLKXPE-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
241001521809 Acoma Species 0.000 description 1
206010002091 Anaesthesia Diseases 0.000 description 1
102000004506 Blood Proteins Human genes 0.000 description 1
108010017384 Blood Proteins Proteins 0.000 description 1
102000016359 Fibronectins Human genes 0.000 description 1
108010067306 Fibronectins Proteins 0.000 description 1
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
239000013032 Hydrocarbon resin Substances 0.000 description 1
206010061218 Inflammation Diseases 0.000 description 1
NNJVILVZKWQKPM-UHFFFAOYSA-N Lidocaine Chemical compound CCN(CC)CC(=O)NC1=C(C)C=CC=C1C NNJVILVZKWQKPM-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 description 1
MWCLLHOVUTZFKS-UHFFFAOYSA-N Methyl cyanoacrylate Chemical compound COC(=O)C(=C)C#N MWCLLHOVUTZFKS-UHFFFAOYSA-N 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
241000283973 Oryctolagus cuniculus Species 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
208000007536 Thrombosis Diseases 0.000 description 1
241000700605 Viruses Species 0.000 description 1
239000013543 active substance Substances 0.000 description 1
238000004026 adhesive bonding Methods 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
230000002009 allergenic effect Effects 0.000 description 1
230000037005 anaesthesia Effects 0.000 description 1
229940035676 analgesics Drugs 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000000730 antalgic agent Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
230000001580 bacterial effect Effects 0.000 description 1
230000003385 bacteriostatic effect Effects 0.000 description 1
102000023732 binding proteins Human genes 0.000 description 1
108091008324 binding proteins Proteins 0.000 description 1
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239000013533 biodegradable additive Substances 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
238000001574 biopsy Methods 0.000 description 1
230000037396 body weight Effects 0.000 description 1
KRIJKJDTULGZJO-UHFFFAOYSA-N butan-2-yl 2-cyanoprop-2-enoate Chemical compound CCC(C)OC(=O)C(=C)C#N KRIJKJDTULGZJO-UHFFFAOYSA-N 0.000 description 1
230000010261 cell growth Effects 0.000 description 1
238000012412 chemical coupling Methods 0.000 description 1
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239000006260 foam Substances 0.000 description 1
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235000019256 formaldehyde Nutrition 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
238000005227 gel permeation chromatography Methods 0.000 description 1
238000002695 general anesthesia Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000003292 glue Substances 0.000 description 1
BCQZXOMGPXTTIC-UHFFFAOYSA-N halothane Chemical compound FC(F)(F)C(Cl)Br BCQZXOMGPXTTIC-UHFFFAOYSA-N 0.000 description 1
229960003132 halothane Drugs 0.000 description 1
238000011597 hartley guinea pig Methods 0.000 description 1
230000035876 healing Effects 0.000 description 1
230000036074 healthy skin Effects 0.000 description 1
230000023597 hemostasis Effects 0.000 description 1
239000008240 homogeneous mixture Substances 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
229920006270 hydrocarbon resin Polymers 0.000 description 1
230000002757 inflammatory effect Effects 0.000 description 1
230000004054 inflammatory process Effects 0.000 description 1
239000003999 initiator Substances 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical class OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
DKYWVDODHFEZIM-UHFFFAOYSA-N ketoprofen Chemical compound OC(=O)C(C)C1=CC=CC(C(=O)C=2C=CC=CC=2)=C1 DKYWVDODHFEZIM-UHFFFAOYSA-N 0.000 description 1
229960000991 ketoprofen Drugs 0.000 description 1
229960004194 lidocaine Drugs 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000002690 local anesthesia Methods 0.000 description 1
239000003589 local anesthetic agent Substances 0.000 description 1
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238000003760 magnetic stirring Methods 0.000 description 1
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210000003205 muscle Anatomy 0.000 description 1
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QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
125000006353 oxyethylene group Chemical group 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
230000003071 parasitic effect Effects 0.000 description 1
238000010827 pathological analysis Methods 0.000 description 1
230000007170 pathology Effects 0.000 description 1
DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 description 1
229960002695 phenobarbital Drugs 0.000 description 1
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239000002243 precursor Substances 0.000 description 1
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239000011734 sodium Substances 0.000 description 1
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239000008117 stearic acid Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
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239000000126 substance Substances 0.000 description 1
150000003505 terpenes Chemical class 0.000 description 1
235000007586 terpenes Nutrition 0.000 description 1
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239000006200 vaporizer Substances 0.000 description 1
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Classifications

- 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
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L24/00—Surgical adhesives or cements; Adhesives for colostomy devices
- A61L24/04—Surgical adhesives or cements; Adhesives for colostomy devices containing macromolecular materials
- A61L24/06—Surgical adhesives or cements; Adhesives for colostomy devices containing macromolecular materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
- 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
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/10—Esters
- C08F222/1006—Esters of polyhydric alcohols or polyhydric phenols
- 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
- C08F291/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Surgery (AREA)
Epidemiology (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Materials For Medical Uses (AREA)
Compositions Of Macromolecular Compounds (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

SK1077-2001A 1999-02-09 2000-02-09 Materiál na zošitie rán na báze metylidénmalonátu SK10772001A3 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
FR9901485A FR2789314B1 (fr)	1999-02-09	1999-02-09	Materiau de suture de plaies a base de methylidene malonate
PCT/FR2000/000305 WO2000047242A1 (fr)	1999-02-09	2000-02-09	Materiau de suture de plaies a base de methylidene malonate

Publications (1)

Publication Number	Publication Date
SK10772001A3 true SK10772001A3 (sk)	2001-12-03

Family

ID=9541764

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1077-2001A SK10772001A3 (sk)	1999-02-09	2000-02-09	Materiál na zošitie rán na báze metylidénmalonátu

Country Status (22)

Country	Link
US (1)	US6610078B1 (da)
EP (1)	EP1150723B1 (da)
JP (1)	JP4863550B2 (da)
KR (1)	KR20010104341A (da)
CN (2)	CN1559622A (da)
AR (1)	AR022549A1 (da)
AT (1)	ATE223739T1 (da)
AU (1)	AU767823B2 (da)
BR (1)	BR0008091A (da)
CA (1)	CA2361628A1 (da)
CZ (1)	CZ20012896A3 (da)
DE (1)	DE60000437D1 (da)
DK (1)	DK1150723T3 (da)
ES (1)	ES2183782T3 (da)
FR (1)	FR2789314B1 (da)
HU (1)	HUP0200330A2 (da)
PL (1)	PL350244A1 (da)
PT (1)	PT1150723E (da)
RU (1)	RU2241494C2 (da)
SK (1)	SK10772001A3 (da)
TW (1)	TW492883B (da)
WO (1)	WO2000047242A1 (da)

Families Citing this family (62)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US8795332B2 (en)	2002-09-30	2014-08-05	Ethicon, Inc.	Barbed sutures
US6241747B1 (en)	1993-05-03	2001-06-05	Quill Medical, Inc.	Barbed Bodily tissue connector
US5931855A (en)	1997-05-21	1999-08-03	Frank Hoffman	Surgical methods using one-way suture
FR2774096B1 (fr) *	1998-01-29	2000-04-07	Virsol	Nouveaux copolymeres tensioactifs a base de methylidene malonate
FR2812551B1 (fr) *	2000-08-07	2003-03-28	Virsol	Forme pharmaceutique comprenant un materiau support a base de methylidene malonate et un facteur de regulation cellulaire
US7056331B2 (en)	2001-06-29	2006-06-06	Quill Medical, Inc.	Suture method
US6848152B2 (en)	2001-08-31	2005-02-01	Quill Medical, Inc.	Method of forming barbs on a suture and apparatus for performing same
US6773450B2 (en)	2002-08-09	2004-08-10	Quill Medical, Inc.	Suture anchor and method
US20040088003A1 (en)	2002-09-30	2004-05-06	Leung Jeffrey C.	Barbed suture in combination with surgical needle
US8100940B2 (en)	2002-09-30	2012-01-24	Quill Medical, Inc.	Barb configurations for barbed sutures
US7624487B2 (en)	2003-05-13	2009-12-01	Quill Medical, Inc.	Apparatus and method for forming barbs on a suture
WO2005112787A2 (en)	2004-05-14	2005-12-01	Quill Medical, Inc.	Suture methods and devices
RU2284824C1 (ru) *	2005-03-18	2006-10-10	Общество с ограниченной ответственностью "Сирена"	Клей хирургический антисептический "аргакол"
JP2007100108A (ja) *	2007-01-22	2007-04-19	Dainippon Ink & Chem Inc	硬化性樹脂組成物
US8915943B2 (en)	2007-04-13	2014-12-23	Ethicon, Inc.	Self-retaining systems for surgical procedures
EP2550978B1 (en)	2007-09-27	2014-04-30	Ethicon, LLC	A system for cutting a retainer in a suture
EP2222233B1 (en)	2007-12-19	2020-03-25	Ethicon, LLC	Self-retaining sutures with heat-contact mediated retainers
US8916077B1 (en)	2007-12-19	2014-12-23	Ethicon, Inc.	Self-retaining sutures with retainers formed from molten material
US8118834B1 (en)	2007-12-20	2012-02-21	Angiotech Pharmaceuticals, Inc.	Composite self-retaining sutures and method
US8875607B2 (en)	2008-01-30	2014-11-04	Ethicon, Inc.	Apparatus and method for forming self-retaining sutures
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1999
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- 2000-02-09 CZ CZ20012896A patent/CZ20012896A3/cs unknown
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AU2554300A (en)	2000-08-29
EP1150723B1 (fr)	2002-09-11
US6610078B1 (en)	2003-08-26
ATE223739T1 (de)	2002-09-15
ES2183782T3 (es)	2003-04-01
HUP0200330A2 (en)	2002-06-29
CN1339974A (zh)	2002-03-13
JP2002536124A (ja)	2002-10-29
CA2361628A1 (en)	2000-08-17
PT1150723E (pt)	2003-01-31
WO2000047242A1 (fr)	2000-08-17
DK1150723T3 (da)	2003-01-20
AR022549A1 (es)	2002-09-04
BR0008091A (pt)	2001-11-13
FR2789314A1 (fr)	2000-08-11
FR2789314B1 (fr)	2001-04-27
JP4863550B2 (ja)	2012-01-25
AU767823B2 (en)	2003-11-27
TW492883B (en)	2002-07-01
CZ20012896A3 (cs)	2002-01-16
RU2241494C2 (ru)	2004-12-10
DE60000437D1 (de)	2002-10-17
EP1150723A1 (fr)	2001-11-07
CN1559622A (zh)	2005-01-05
KR20010104341A (ko)	2001-11-24
PL350244A1 (en)	2002-12-02

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