专利号:US-9650407-B2 优先权日:2011-11-02 标 题 :Reprogramming of cellular adhesion 发明人:GARTNER ZEV JORDAN; SELDEN NICHOLAS SCOTT; TODHUNTER MICHAEL E; LIANG SAMANTHA ISABEL; WEBER ROBERT JOSEPH; JEE NOEL YOUNGHO; LIU JENNIFER S 权利人:UNIV CALIFORNIA 摘要:Disclosed are membrane-anchored polynucleotides, and compositions comprising the membrane-anchored polynucleotides. Also disclosed are the processes for the synthesis of these compounds, compositions comprising such compounds, and the use of such compounds and compositions in research and therapeutic applications.
专利号:SU-1120654-A1 优先权日:1983-01-27 标题 :Salts of mesidides of alpha-piperidincarboxylic acids possessing locallyanesthetic, antiarythmic and antifibrillatory activity and mesidides of alpha-puperidincarboxylic acids as intermediate products for synthesis of salts of mesidides of piperidincarboxylic acids
专利号:US-7993390-B2 优先权日:2002-02-08 标 题:Implantable or insertable medical device resistant to microbial growth and biofilm formation 发明人:MILLER KATHLEEN M; BUCAY-COUTO WEENNA; LI JIANMIN 权利人:BOSTON SCIENT SCIMED INC 摘要:Disclosed are implantable or insertable medical devices that provide resistance to microbial growth on and in the environment of the device and resistance to microbial adhesion and biofilm formation on the device. In particular, the invention discloses implantable or insertable medical devices that comprise at least one biocompatible matrix polymer region, an antimicrobial agent for providing resistance to microbial growth and/or a microbial adhesion/biofilm synthesis inhibitor for inhibiting the attachment of microbes and the synthesis and accumulation of biofilm on the surface of the medical device. Also disclosed are methods of manufacturing such devices under conditions that substantially prevent preferential partitioning of any of said bioactive agents to a surface of the biocompatible matrix polymer and substantially prevent chemical modification of said bioactive agents.
专利号:US-2012232031-A1 优先权日:2009-10-19 标 题:Injectable formulations for intra-articular or peri-articular administration 发明人:HUTCHINSON JOHN HOWARD; PRASIT PETPIBOON PEPPI; DEARMOND ISABELLE MARGUERITE 权利人:HUTCHINSON JOHN HOWARD; PRASIT PETPIBOON PEPPI; DEARMOND ISABELLE MARGUERITE; PANMIRA PHARMACEUTICALS LLC 摘要:Described herein are injectable formulations for intra-articular or peri-articular administration, wherein the formulation is administered to treat joint pain. An injectable formulation for intra-articular or peri-articular administration disclosed herein comprises a therapeutically-effective amount of a leukotriene synthesis inhibitor compound formulated for intra-articular or peri-articular administration.
1: Hart R, Wendsche P, Kočiš J, Komzák M, Okál F, Krejzla J. [Injection of anaesthetic-corticosteroid to relieve sacroiliac joint pain after lumbar stabilisation]. Acta Chir Orthop Traumatol Cech. 2011;78(4):339-42. Czech. doi: 10.1007/s00405-010-1435-4. Epub 2011 Feb 17. Russian. doi: 10.1007/s00246-008-9294-0. Epub 2008 Aug 15. Erratum in: Pediatr Cardiol. 2009 Nov;30(8):1197. Slovak. 9: Balashov VP, Blinov DS, Kazachenko VN, Astashev ME, Agenosova OG. Membrane mechanisms of antiarrhythmic effect of quaternidine. Bull Exp Biol Med. 2005 Jun;139(6):688-91. Slovak. Russian. Russian. Russian. Czech. Russian. Russian. Russian. Russian.
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