JP2003517066A - ラジカル的に硬化可能なウレタンプレポリマー類及びそれらの使用 - Google Patents
ラジカル的に硬化可能なウレタンプレポリマー類及びそれらの使用Info
- Publication number
- JP2003517066A JP2003517066A JP2001544823A JP2001544823A JP2003517066A JP 2003517066 A JP2003517066 A JP 2003517066A JP 2001544823 A JP2001544823 A JP 2001544823A JP 2001544823 A JP2001544823 A JP 2001544823A JP 2003517066 A JP2003517066 A JP 2003517066A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- materials
- meth
- acrylate
- group
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
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- 238000006243 chemical reaction Methods 0.000 claims abstract description 7
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- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 3
- 150000007656 barbituric acids Chemical class 0.000 description 3
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- 239000002904 solvent Substances 0.000 description 3
- QGLRLXLDMZCFBP-UHFFFAOYSA-N 1,6-diisocyanato-2,4,4-trimethylhexane Chemical compound O=C=NCC(C)CC(C)(C)CCN=C=O QGLRLXLDMZCFBP-UHFFFAOYSA-N 0.000 description 2
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 2
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- 239000005058 Isophorone diisocyanate Substances 0.000 description 2
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- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
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- 229940106691 bisphenol a Drugs 0.000 description 2
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- 238000001035 drying Methods 0.000 description 2
- 229940093476 ethylene glycol Drugs 0.000 description 2
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- 150000002430 hydrocarbons Chemical group 0.000 description 2
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- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
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- AGKBXKFWMQLFGZ-UHFFFAOYSA-N (4-methylbenzoyl) 4-methylbenzenecarboperoxoate Chemical compound C1=CC(C)=CC=C1C(=O)OOC(=O)C1=CC=C(C)C=C1 AGKBXKFWMQLFGZ-UHFFFAOYSA-N 0.000 description 1
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- YXTRBIFAXXDANU-UHFFFAOYSA-N 3-[2-[[6-[2-(2-carboxyprop-1-enoxy)ethoxycarbonylamino]-3,5,5-trimethylhexyl]carbamoyloxy]ethoxy]-2-methylprop-2-enoic acid Chemical compound OC(=O)C(C)=COCCOC(=O)NCCC(C)CC(C)(C)CNC(=O)OCCOC=C(C)C(O)=O YXTRBIFAXXDANU-UHFFFAOYSA-N 0.000 description 1
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 1
- ABRWESLGGMHKEA-UHFFFAOYSA-N n-tert-butylaniline Chemical class CC(C)(C)NC1=CC=CC=C1 ABRWESLGGMHKEA-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- UJYOGEVPKUSMAO-UHFFFAOYSA-N phenyl-[2-(2,4,6-trimethylbenzoyl)phenyl]phosphinic acid Chemical compound CC1=CC(C)=CC(C)=C1C(=O)C1=CC=CC=C1P(O)(=O)C1=CC=CC=C1 UJYOGEVPKUSMAO-UHFFFAOYSA-N 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 239000006223 plastic coating Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001692 polycarbonate urethane Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002577 pseudohalo group Chemical group 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002522 swelling effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical group NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229940105963 yttrium fluoride Drugs 0.000 description 1
- RBORBHYCVONNJH-UHFFFAOYSA-K yttrium(iii) fluoride Chemical compound F[Y](F)F RBORBHYCVONNJH-UHFFFAOYSA-K 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/73—Polyisocyanates or polyisothiocyanates acyclic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
- A61K6/891—Compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- A61K6/893—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
- C08G18/622—Polymers of esters of alpha-beta ethylenically unsaturated carboxylic acids
- C08G18/6245—Polymers having terminal groups containing active hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Epidemiology (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Dental Preparations (AREA)
- Polyurethanes Or Polyureas (AREA)
- Materials For Medical Uses (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19961342A DE19961342B4 (de) | 1999-12-17 | 1999-12-17 | Radikalisch härtbare Urethanpräpolymere und deren Verwendung |
| DE19961342.7 | 1999-12-17 | ||
| PCT/EP2000/012775 WO2001044338A1 (de) | 1999-12-17 | 2000-12-15 | Radikalisch härtbare urethanpräpolymere und deren verwendung in dentalmassen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003517066A true JP2003517066A (ja) | 2003-05-20 |
| JP2003517066A5 JP2003517066A5 (enExample) | 2008-03-06 |
Family
ID=7933341
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001544823A Withdrawn JP2003517066A (ja) | 1999-12-17 | 2000-12-15 | ラジカル的に硬化可能なウレタンプレポリマー類及びそれらの使用 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7141616B2 (enExample) |
| EP (1) | EP1242493B1 (enExample) |
| JP (1) | JP2003517066A (enExample) |
| AT (1) | ATE251650T1 (enExample) |
| AU (1) | AU769994B2 (enExample) |
| DE (2) | DE19961342B4 (enExample) |
| WO (1) | WO2001044338A1 (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001234117A (ja) * | 2000-02-21 | 2001-08-28 | Arakawa Chem Ind Co Ltd | コーティング剤組成物 |
| JP2008285489A (ja) * | 2007-05-18 | 2008-11-27 | Ormco Corp | 矯正用接着剤 |
| WO2009001826A1 (ja) * | 2007-06-27 | 2008-12-31 | Nippon Polyurethane Industry Co., Ltd. | 有機ポリイソシアネート組成物、並びにそれを用いた塗料組成物及び接着剤組成物 |
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| DE60305025T2 (de) | 2003-07-14 | 2006-10-12 | 3M Espe Ag | Klebstoffzusammensetzung mit verringerter Polarität nach der Polymerisation |
| KR20060122919A (ko) * | 2004-01-14 | 2006-11-30 | 사이텍 설패이스 스페셜티즈, 에스.에이. | 접착제 |
| EP1639987B1 (en) * | 2004-09-24 | 2009-08-12 | 3M Espe AG | Dental adhesive composition |
| DE102005018451B4 (de) * | 2005-04-20 | 2008-07-24 | Heraeus Kulzer Gmbh | Verwendung von dendritischen Verbindungen in Dentalmaterialien |
| DE102005025915A1 (de) * | 2005-06-06 | 2006-12-07 | Wacker Chemie Ag | Vernetzbare Zusammensetzungen auf der Basis von Organosiliciumverbindungen |
| EP1922053B1 (en) * | 2005-08-10 | 2014-11-19 | DENTSPLY International Inc. | Methods for preparing chair-side dental crowns |
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| EP2009039A1 (en) | 2007-06-27 | 2008-12-31 | Universiteit Gent | Functionalised polyurethanes |
| EP2008636A1 (en) * | 2007-06-29 | 2008-12-31 | 3M Innovative Properties Company | Dental composition containing a polyfunctional (meth)acrylate comprising urethane, urea or amide groups, method of production and use thereof |
| EP2042486A1 (en) * | 2007-09-26 | 2009-04-01 | 3M Innovative Properties Company | Methacrylate Based Monomers containing a Urethane Linkage, Process for Production and Use thereof |
| DE102009058638A1 (de) | 2009-12-16 | 2011-06-22 | Ernst Mühlbauer GmbH & Co. KG, 25870 | Mehrkomponentensystem zur Herstellung eines Dentalmaterials |
| EP2401998A1 (en) | 2010-07-02 | 2012-01-04 | 3M Innovative Properties Company | Dental composition, kit of parts and use thereof |
| US8292625B2 (en) | 2010-07-23 | 2012-10-23 | Pulpdent Corporation | Radically curable urethane dimethacrylates and compositions thereof for tougher dental prosthetics |
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| DE102011077248B3 (de) | 2011-06-09 | 2012-09-27 | Hilti Aktiengesellschaft | Verwendung eines Inhibitors, Harzmischung, Reaktionsharzmörtel, Zweikomponenten - Mörtelsystem und dessen Verwendung sowie Patrone, Kartusche oder Folienbeutel enthaltend ein Zweikomponenten - Mörtelsystem |
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| DE3316592A1 (de) | 1983-05-06 | 1984-11-08 | Basf Ag, 6700 Ludwigshafen | Verwendung zur herstellung von (meth) acrylsaeureestern und deren verwendung |
| DE3443221A1 (de) | 1984-11-27 | 1986-06-05 | ESPE Fabrik pharmazeutischer Präparate GmbH, 8031 Seefeld | Bisacylphosphinoxide, ihre herstellung und verwendung |
| DE3681757D1 (de) * | 1985-05-24 | 1991-11-07 | Teroson Gmbh | Verfahren zur herstellung von niedermolekularen hydroxyfunktionellen (meth)acrylatpolymeren, deren verwendung zur herstellung von isocyanat-endgruppen enthaltenden prepolymeren sowie daraus hergestellte dicht- und klebstoffe. |
| CA1289394C (en) | 1986-08-25 | 1991-09-24 | Duncan E. Waller | Method for making a dental impression |
| DE3704098A1 (de) | 1987-02-11 | 1988-08-25 | Basf Ag | Strahlungshaertbare acrylate |
| AU631586B2 (en) | 1988-12-19 | 1992-12-03 | 3M Espe Ag | Dental compounds which contain bifunctional acrylic-acid esters or methacrylic-acid esters |
| DD293487A5 (de) * | 1989-03-09 | 1991-09-05 | Friedrich-Schiller-Universitaet,De | Dentalkomposite |
| DE4010176A1 (de) * | 1990-03-30 | 1991-10-02 | Basf Lacke & Farben | Verfahren zur herstellung einer mehrschichtigen lackierung und waessriger lack |
| DE4018183A1 (de) | 1990-06-07 | 1991-12-12 | Bayer Ag | Lichthaertende abformmaterialien |
| DE4040290C2 (de) | 1990-12-17 | 1996-05-15 | Synthopol Chemie Dr Koch | Verfahren zur Herstellung von strahlungshärtbaren Polyesteracrylat-Bindemitteln |
| DE4314111A1 (de) * | 1993-04-29 | 1994-11-03 | Goldschmidt Ag Th | alpha,omega-Polymethacrylatdiole, Verfahren zu ihrer Herstellung und deren Verwendung zur Herstellung von Polymeren, insbesondere Polyurethanen und Polyestern |
| DE4445266A1 (de) | 1994-12-19 | 1996-06-20 | Thera Ges Fuer Patente | Fluoridabgebende Composite-Massen |
| DE19618446A1 (de) * | 1996-05-08 | 1997-11-13 | Basf Lacke & Farben | Aus mindestens 3 Komponenten bestehendes Beschichtungsmittel |
| DE19813353A1 (de) | 1998-03-26 | 1999-09-30 | Bayer Ag | Verfahren zur Herstellung von Telechelen, so hergestellte Telechele und ihre Verwendung |
| DE19928238A1 (de) | 1999-06-21 | 2000-12-28 | Espe Dental Ag | Polymerisierbare Dentalmasse |
-
1999
- 1999-12-17 DE DE19961342A patent/DE19961342B4/de not_active Expired - Fee Related
-
2000
- 2000-12-15 US US10/149,607 patent/US7141616B2/en not_active Expired - Lifetime
- 2000-12-15 EP EP00985164A patent/EP1242493B1/de not_active Expired - Lifetime
- 2000-12-15 WO PCT/EP2000/012775 patent/WO2001044338A1/de not_active Ceased
- 2000-12-15 AT AT00985164T patent/ATE251650T1/de not_active IP Right Cessation
- 2000-12-15 JP JP2001544823A patent/JP2003517066A/ja not_active Withdrawn
- 2000-12-15 DE DE50004033T patent/DE50004033D1/de not_active Expired - Lifetime
- 2000-12-15 AU AU21664/01A patent/AU769994B2/en not_active Ceased
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001234117A (ja) * | 2000-02-21 | 2001-08-28 | Arakawa Chem Ind Co Ltd | コーティング剤組成物 |
| JP2008285489A (ja) * | 2007-05-18 | 2008-11-27 | Ormco Corp | 矯正用接着剤 |
| WO2009001826A1 (ja) * | 2007-06-27 | 2008-12-31 | Nippon Polyurethane Industry Co., Ltd. | 有機ポリイソシアネート組成物、並びにそれを用いた塗料組成物及び接着剤組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1242493B1 (de) | 2003-10-08 |
| DE50004033D1 (de) | 2003-11-13 |
| AU2166401A (en) | 2001-06-25 |
| AU769994B2 (en) | 2004-02-12 |
| US20030008967A1 (en) | 2003-01-09 |
| WO2001044338A1 (de) | 2001-06-21 |
| ATE251650T1 (de) | 2003-10-15 |
| DE19961342A1 (de) | 2001-07-12 |
| DE19961342B4 (de) | 2004-02-19 |
| US7141616B2 (en) | 2006-11-28 |
| EP1242493A1 (de) | 2002-09-25 |
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