JP2007500679A - 自動混合可能なパテ型材 - Google Patents
自動混合可能なパテ型材 Download PDFInfo
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- JP2007500679A JP2007500679A JP2006521545A JP2006521545A JP2007500679A JP 2007500679 A JP2007500679 A JP 2007500679A JP 2006521545 A JP2006521545 A JP 2006521545A JP 2006521545 A JP2006521545 A JP 2006521545A JP 2007500679 A JP2007500679 A JP 2007500679A
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- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 1
- 238000013038 hand mixing Methods 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- 125000006038 hexenyl group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000006459 hydrosilylation reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- QXLPXWSKPNOQLE-UHFFFAOYSA-N methylpentynol Chemical compound CCC(C)(O)C#C QXLPXWSKPNOQLE-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- MCCIMQKMMBVWHO-UHFFFAOYSA-N octadecanoic acid;titanium Chemical compound [Ti].CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O MCCIMQKMMBVWHO-UHFFFAOYSA-N 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 150000002941 palladium compounds Chemical class 0.000 description 1
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 238000004987 plasma desorption mass spectroscopy Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 150000003057 platinum Chemical class 0.000 description 1
- 150000003058 platinum compounds Chemical class 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 125000006684 polyhaloalkyl group Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- PXDRFTPXHTVDFR-UHFFFAOYSA-N propane;titanium(4+) Chemical compound [Ti+4].C[CH-]C.C[CH-]C.C[CH-]C.C[CH-]C PXDRFTPXHTVDFR-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 238000000926 separation method Methods 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
- 238000010561 standard procedure Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- IUTCEZPPWBHGIX-UHFFFAOYSA-N tin(2+) Chemical compound [Sn+2] IUTCEZPPWBHGIX-UHFFFAOYSA-N 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- NJMOHBDCGXJLNJ-UHFFFAOYSA-N trimellitic anhydride chloride Chemical compound ClC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 NJMOHBDCGXJLNJ-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 150000003755 zirconium compounds Chemical class 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/90—Compositions for taking dental impressions
Landscapes
- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dental Preparations (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Sealing Material Composition (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP03017488A EP1502572B1 (en) | 2003-08-01 | 2003-08-01 | Automixable putty impression material |
| PCT/EP2004/008592 WO2005013925A1 (en) | 2003-08-01 | 2004-07-30 | Automixable putty impression material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007500679A true JP2007500679A (ja) | 2007-01-18 |
| JP2007500679A5 JP2007500679A5 (https=) | 2007-04-19 |
Family
ID=33522340
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006521545A Withdrawn JP2007500679A (ja) | 2003-08-01 | 2004-07-30 | 自動混合可能なパテ型材 |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US7572842B2 (https=) |
| EP (1) | EP1502572B1 (https=) |
| JP (1) | JP2007500679A (https=) |
| AT (1) | ATE548017T1 (https=) |
| WO (1) | WO2005013925A1 (https=) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1502572B1 (en) | 2003-08-01 | 2012-03-07 | 3M Deutschland GmbH | Automixable putty impression material |
| DE102006001126A1 (de) * | 2006-01-09 | 2007-07-12 | Kettenbach Gmbh & Co. Kg | Dentalabformmassen, daraus hergestellte gehärtete Produkte und Verwendung von Tensiden zur Herstellung von Dentalabformmassen |
| ATE509613T1 (de) | 2006-11-16 | 2011-06-15 | Muehlbauer Ernst Gmbh & Co Kg | Silikonabformmasse mit zweistufigem aushärtungsmechanismus |
| DE102007003604A1 (de) * | 2007-01-18 | 2008-07-24 | Heraeus Kulzer Gmbh | Zweikomponenten-Abformmassen |
| DE102007015842A1 (de) | 2007-03-30 | 2008-10-02 | Heraeus Kulzer Gmbh | Maschinenanmischbares A-Siliconputty und dessen Verwendung |
| DE202008012785U1 (de) | 2008-09-25 | 2008-12-11 | Heraeus Kulzer Gmbh | Maschinenanmischbares A-Siliconputty und dessen Verwendung |
| WO2010126606A2 (en) * | 2009-05-01 | 2010-11-04 | Nanosys, Inc. | Functionalized matrixes for dispersion of nanostructures |
| EP2255748A1 (en) | 2009-05-29 | 2010-12-01 | 3M Innovative Properties Company | Dental retraction composition, method of production and use thereof |
| WO2011034705A1 (en) * | 2009-09-15 | 2011-03-24 | 3M Innovative Properties Company | Methods and compositions for dental impressions |
| KR101289201B1 (ko) * | 2010-03-29 | 2013-07-29 | 주식회사 삼양사 | 에스테르 결합을 갖는 히드록시 말단 실록산, 폴리실록산-폴리카보네이트 공중합체 및 그 제조 방법 |
| WO2013025494A1 (en) | 2011-08-12 | 2013-02-21 | 3M Innovative Properties Company | Curable composition with shortened setting time, process of production and use thereof |
| WO2014104719A1 (ko) * | 2012-12-26 | 2014-07-03 | 제일모직 주식회사 | 광학기기용 경화형 폴리실록산 조성물, 봉지재 및 광학기기 |
| US10682290B2 (en) | 2015-05-29 | 2020-06-16 | 3M Innovative Properties Company | Kit of parts for conducting a dental impression and retraction process |
| US11766386B2 (en) | 2016-11-07 | 2023-09-26 | 3M Innovative Properties Company | Medical composition containing guanidinyl-containing polymer(s) and carrageenane(s) |
| US11123267B2 (en) | 2016-11-07 | 2021-09-21 | 3M Innovative Properties Company | Dental retraction composition with guanidinyl-containing polymer |
| US11684553B2 (en) | 2017-01-18 | 2023-06-27 | 3M Innovative Properties Company | Curable composition for dental retraction |
| RU2683930C2 (ru) * | 2017-09-04 | 2019-04-02 | Общество с ограниченной ответственностью "Научно-производственная компания "Силикон" (ООО НПК "СИЛИКОН") | Композиция для изготовления стоматологических оттисков |
| US11891484B2 (en) | 2019-09-17 | 2024-02-06 | Crayola Llc | Putty and putty base compounds and methods of making thereof |
| WO2021205371A1 (en) * | 2020-04-08 | 2021-10-14 | Self-Ie Enterprise Private Limited | Dental impression kit and method |
| WO2022123395A1 (en) | 2020-12-11 | 2022-06-16 | 3M Innovative Properties Company | Dental retraction composition |
| DE102022211217A1 (de) * | 2022-10-21 | 2024-05-02 | Siemens Healthineers Ag | Verfahren zur Herstellung einer Lokalspule für eine MRT-Messung |
Family Cites Families (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US515096A (en) * | 1894-02-20 | Max scheuer | ||
| US3082527A (en) * | 1955-08-05 | 1963-03-26 | Wacker Chemie Gmbh | Process for making dental impression masses |
| US3814730A (en) | 1970-08-06 | 1974-06-04 | Gen Electric | Platinum complexes of unsaturated siloxanes and platinum containing organopolysiloxanes |
| US3715334A (en) | 1970-11-27 | 1973-02-06 | Gen Electric | Platinum-vinylsiloxanes |
| US3758418A (en) | 1971-03-22 | 1973-09-11 | Shell Oil Co | Process for preparing a supported catalyst |
| US3950300A (en) * | 1972-10-11 | 1976-04-13 | Wacker-Chemie Gmbh | Dental impression materials |
| US4035453A (en) * | 1974-05-28 | 1977-07-12 | Wacker-Chemie Gmbh | Dental impression materials |
| US3933880A (en) | 1974-12-02 | 1976-01-20 | Dow Corning Corporation | Method of preparing a platinum catalyst inhibitor |
| DE3406233A1 (de) | 1984-02-21 | 1985-08-22 | Bayer Ag, 5090 Leverkusen | Modifizierte fuellstoffe fuer silikonpasten, deren verwendung und diese fuellstoffe enthaltende dentalabformmassen |
| DE3409139A1 (de) * | 1984-03-13 | 1985-09-19 | Wacker-Chemie GmbH, 8000 München | Platin, organopolysiloxan und fuellstoff enthaltende pasten |
| DE3416694A1 (de) * | 1984-05-05 | 1985-11-07 | Bayer Ag, 5090 Leverkusen | Verwendung von paraffin- oder mikrowachsen fuer silikonpasten, deren konfektionierung und verwendung |
| DE3532687A1 (de) | 1985-09-13 | 1987-03-26 | Bayer Ag | Silicon-abformmassen |
| US4657959A (en) | 1985-11-15 | 1987-04-14 | Minnesota Mining And Manufacturing Company | Hydrophilic silicones |
| ATE66807T1 (de) | 1986-02-06 | 1991-09-15 | Dentsply Gmbh | Zahnabdruckmaterial. |
| US4782101A (en) | 1986-11-19 | 1988-11-01 | Manufacturers Hanover Trust Company | Prevention of outgassing in polyvinylsiloxane elastomers by the use of finely divided platinum black |
| JPS63215770A (ja) * | 1987-03-04 | 1988-09-08 | Shin Etsu Chem Co Ltd | 室温硬化性オルガノポリシロキサン組成物 |
| US5220033A (en) * | 1990-06-13 | 1993-06-15 | Shin-Etsu Chemical Co., Ltd. | Siloxane compounds and their preparation |
| JP3108427B2 (ja) * | 1990-07-30 | 2000-11-13 | 東レ・ダウコーニング・シリコーン株式会社 | カルビノール基含有オルガノポリシロキサンの製造方法 |
| DE4031759A1 (de) | 1990-10-06 | 1992-04-09 | Bayer Ag | Hydrophilierte abformmassen |
| DE9017323U1 (de) | 1990-12-21 | 1992-04-16 | Thera Patent GmbH & Co KG Gesellschaft für industrielle Schutzrechte, 8031 Seefeld | Dynamischer Mischer |
| DE9017322U1 (de) | 1990-12-21 | 1992-04-16 | THERA Patent GmbH & Co. KG Gesellschaft für industrielle Schutzrechte, 82229 Seefeld | Gerät zum Mischen und Ausbringen von Mehrkomponenten-Massen |
| US5159096A (en) | 1991-09-30 | 1992-10-27 | Union Carbide Chemicals & Plastics Technology Corporation | Process for the preparation of siloxane-oxyalkylene copolymers |
| US5371162A (en) * | 1992-07-09 | 1994-12-06 | Minnesota Mining And Manufacturing Company | Storage-stable silicone composition |
| US5249864A (en) * | 1992-10-23 | 1993-10-05 | Gas Research Institute | System for characterizing temperature of fluids |
| DE4306997A1 (de) | 1993-03-05 | 1994-09-08 | Thera Ges Fuer Patente | Hydrophilierte Polyether |
| EP0615787B1 (de) | 1993-03-17 | 1998-12-16 | Wilhelm A. Keller | Handbetätigtes Austraggerät für eine Doppelaustragkartusche |
| US5290901A (en) * | 1993-06-14 | 1994-03-01 | Dow Corning Corporation | Method for preparation of carbinol-functional siloxanes |
| US5364921A (en) | 1993-08-17 | 1994-11-15 | Dow Corning Corporation | Silicone rubber with self-adhesion to glass and metal |
| DE4427528C2 (de) | 1994-08-04 | 1999-05-20 | Ge Bayer Silicones Gmbh & Co | Siliconmassen mit Titanaten, Zirkonaten und Hafnaten |
| DE4433139A1 (de) | 1994-09-16 | 1996-03-21 | Thera Ges Fuer Patente | Hydrophilierte Zahnabdruckmassen |
| WO1996026246A1 (de) * | 1995-02-21 | 1996-08-29 | Ernst Mühlbauer KG | Abformmasse auf silikonbasis mit wachszusatz |
| ES2164750T3 (es) | 1995-03-07 | 2002-03-01 | Wilhelm A Keller | Dispositivo de fijacion por bayoneta para sujetar un accesorio a un cartucho de componentes multiples o dispositivo distribuidor. |
| US6552104B1 (en) * | 1995-04-13 | 2003-04-22 | Dentsply Research & Development Corp. | Method of making hydrophilic non-sweating polymerizable dental impression material |
| WO1997003110A1 (de) | 1995-07-13 | 1997-01-30 | Wacker-Chemie Gmbh | (meth)acryloxygruppen aufweisende organosiliciumverbindungen, deren herstellung und verwendung |
| US5595826A (en) * | 1995-10-11 | 1997-01-21 | Dow Corning Corporation | Curable organopolysiloxane compositions with improved adhesion |
| US5684060A (en) | 1996-04-09 | 1997-11-04 | Minnesota Mining And Manufacturing Company | Compositions containing inorganic, organic and organometallic palladium hydrogen scavengers |
| US5814679A (en) * | 1996-10-18 | 1998-09-29 | General Electric Company | Premium release photo-curable silicone compositions |
| US5683527A (en) * | 1996-12-30 | 1997-11-04 | Dow Corning Corporation | Foamable organosiloxane compositions curable to silicone foams having improved adhesion |
| DE19711314A1 (de) * | 1997-03-18 | 1998-09-24 | Wacker Chemie Gmbh | Lagerstabile, permanent wasserbenetzbare Vulkanisate ergebende Polysiloxanmasse |
| DE29705741U1 (de) | 1997-04-01 | 1998-08-06 | Muehlbauer Ernst Kg | Dynamischer Mischer für zahnärztliche Abdruckmassen |
| DE29706235U1 (de) | 1997-04-08 | 1998-08-27 | Ernst Mühlbauer KG, 22547 Hamburg | Anordnung zum Ausgeben einer gemischten dentaltechnischen Mehrkomponentenmasse |
| DE19730515A1 (de) * | 1997-07-16 | 1999-01-21 | Espe Dental Ag | Abformmaterial auf Silikonbasis |
| DE19736665A1 (de) * | 1997-08-22 | 1999-02-25 | Espe Dental Ag | Härtbare Masse mit Silan-Dendrimeren |
| FR2781808B1 (fr) * | 1998-07-31 | 2000-10-20 | Rhodia Chimie Sa | Systeme elastomere silicone ayant des proprietes biocides utilisable notamment pour la prise d'empreintes par exemple dentaires |
| DE19852056A1 (de) * | 1998-11-11 | 2000-05-18 | Duerr Dental Gmbh Co Kg | Dentaler Abformlöffel sowie Abformmaterial zur Verwendung mit einem solchen |
| DE19860364C2 (de) * | 1998-12-24 | 2001-12-13 | 3M Espe Ag | Polymerisierbare Dentalmassen auf der Basis von zur Aushärtung befähigten Siloxanverbindungen, deren Verwendung und Herstellung |
| DE10026432A1 (de) * | 2000-05-29 | 2002-02-14 | 3M Espe Ag | Präpolymere (Meth)acrylate mit polycyclischen oder aromatischen Segmenten |
| DE10103446C5 (de) * | 2001-01-25 | 2007-06-28 | Kettenbach Gmbh & Co. Kg | Zweistufig härtbare mischergängige Materialien |
| US7005460B2 (en) | 2001-01-25 | 2006-02-28 | Kettenbach Gmbh & Co. Kg | Two-step curable mixer-suitable materials |
| DE10116223A1 (de) * | 2001-03-30 | 2002-10-10 | 3M Espe Ag | Automatisch mischbare Abformassen mit Putty-Konsistenz |
| ATE381917T1 (de) | 2001-05-17 | 2008-01-15 | Kettenbach Gmbh & Co Kg | Chemisch aushärtendes dental-bleachingmaterial |
| US6482888B1 (en) * | 2001-06-06 | 2002-11-19 | Dow Corning Corporation | Silicone composition and cured silicone product |
| US6512037B1 (en) * | 2001-06-06 | 2003-01-28 | Dow Corning Corporation | Silicone composition and cured silicone product |
| EP1523455A1 (en) * | 2002-07-23 | 2005-04-20 | Shell Internationale Research Maatschappij B.V. | Hydrophobic surface treatment composition and method of making and using same |
| EP1502572B1 (en) * | 2003-08-01 | 2012-03-07 | 3M Deutschland GmbH | Automixable putty impression material |
-
2003
- 2003-08-01 EP EP03017488A patent/EP1502572B1/en not_active Expired - Lifetime
- 2003-08-01 AT AT03017488T patent/ATE548017T1/de active
-
2004
- 2004-07-30 JP JP2006521545A patent/JP2007500679A/ja not_active Withdrawn
- 2004-07-30 US US10/566,926 patent/US7572842B2/en not_active Expired - Fee Related
- 2004-07-30 WO PCT/EP2004/008592 patent/WO2005013925A1/en not_active Ceased
-
2009
- 2009-07-13 US US12/501,655 patent/US7732508B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20090275722A1 (en) | 2009-11-05 |
| EP1502572A1 (en) | 2005-02-02 |
| ATE548017T1 (de) | 2012-03-15 |
| EP1502572B1 (en) | 2012-03-07 |
| US20060293469A1 (en) | 2006-12-28 |
| US7572842B2 (en) | 2009-08-11 |
| WO2005013925A1 (en) | 2005-02-17 |
| US7732508B2 (en) | 2010-06-08 |
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