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公开(公告)号:WO2016081820A1
公开(公告)日:2016-05-26
申请号:PCT/US2015/061808
申请日:2015-11-20
IPC分类号: A61L26/00
CPC分类号: A61K47/36 , A61K38/08 , A61L26/0023 , A61L26/0061 , A61L26/0066 , A61L26/008 , A61L26/009 , A61L2400/06 , C08L5/04
摘要: Described herein are compositions of alginate formulations and their use for treating incisional wounds, such as intra-incisional application.
摘要翻译: 本文描述了藻酸盐制剂的组合物及其用于治疗切口伤口的用途,例如切入内应用。
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公开(公告)号:WO2016013700A1
公开(公告)日:2016-01-28
申请号:PCT/KR2014/006767
申请日:2014-07-24
申请人: (주)메디톡스
CPC分类号: A61K31/77 , A61K31/74 , A61K47/02 , A61K47/36 , A61L26/0004 , A61L26/0019 , A61L26/0023 , A61L26/009 , A61L31/041 , A61L31/14 , A61L2300/424 , A61L2300/604 , A61L2300/802 , A61L2400/06 , A61L2400/16 , C08L71/02 , C08L5/08
摘要: 폴리에틸렌옥시드(polyethylene oxide, PEO) 함유 공중합체, 카르복시폴리사카라이드, 및 1가 양이온을 포함하는 것인 열감응성(temperature sensitive) 유착 방지용 조성물, 이의 제조 방법을 제공한다.
摘要翻译: 提供了一种温敏粘合防止组合物及其制备方法,该组合物包含含聚环氧乙烷(PEO)的共聚物,羧基多糖和一价阳离子。
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公开(公告)号:WO2015123734A1
公开(公告)日:2015-08-27
申请号:PCT/AU2015/050069
申请日:2015-02-23
发明人: LITTLE, David Graham , CHENG, Tegan Laura , SCHINDELER, Aaron , DEHGHANI, Fariba , VALTCHEV, Peter
CPC分类号: C07H13/04 , A61K9/146 , A61L26/0023 , A61L26/0066 , A61L26/009 , A61L27/34 , A61L27/54 , A61L27/58 , A61L2300/414 , A61L2400/06 , A61L2430/02 , C07H13/06 , C08B37/0006 , C08B37/006 , C08L5/00
摘要: Abstract The invention relates to polymeric high viscosity liquid carrier materials (HVLCMs), in particular esterified polysaccharides, compositions comprising these HVLCMs, coatings for implants which are based on these HVLCMs, methods of their production and their use in delivering substances, including drugs and bioactive agents, systemically to a body as a sustained release device, or locally, as employed in bone tissue engineering and other applications.
摘要翻译: 摘要本发明涉及聚合物高粘度液体载体材料(HVLCM),特别是酯化多糖,包含这些HVLCM的组合物,基于这些HVLCM的植入物涂层,其生产方法及其在递送物质中的用途,包括药物和生物活性 代谢物,全身地作为持续释放装置的身体,或局部施用于骨组织工程和其它应用中。
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公开(公告)号:WO2015088275A1
公开(公告)日:2015-06-18
申请号:PCT/KR2014/012265
申请日:2014-12-12
CPC分类号: A61L24/08 , A61L24/0031 , A61L24/0042 , A61L26/0023 , A61L26/008 , A61L26/009 , A61L27/20 , A61L27/52 , A61L27/58 , A61L31/042 , A61L31/145 , A61L31/148
摘要: 본 발명은 산화 글리코사미노글리칸과 폴리아민을 포함하는 생분해성 의료용 접착제 또는 실란트 조성물을 제공한다. 본 발명의 조성물은 생분해성, 도포성, 겔화 시간, 지혈능, 접착력 및 수분 흡수력 등에서 개선된 효과를 나타내어, 생체 조직의 접착, 충전, 도포, 유착 방지, 창상 피복, 누출방지 및 지혈 등 의료용 접착제 또는 실란트가 사용 가능한 다양한 의료 용도로 활용될 수 있다.
摘要翻译: 本发明提供一种可生物降解的医用粘合剂或含有氧化的糖胺聚糖和多胺的密封剂组合物。 本发明的组合物在生物降解,涂布性,凝胶化时间,止血能力,粘合力,吸湿能力等方面表现出改善的效果,因此可以应用于可以使用医用粘合剂或密封剂的各种医疗用途 ,如生物组织粘附,填充,涂层,防粘附,伤口涂层,防漏和止血。
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公开(公告)号:WO2014162906A1
公开(公告)日:2014-10-09
申请号:PCT/JP2014/057927
申请日:2014-03-21
申请人: 株式会社糖鎖工学研究所
CPC分类号: A61L26/008 , A61K47/42 , A61K47/61 , A61L15/32 , A61L26/0028 , A61L26/0047 , A61L26/009 , A61L33/12 , A61L2300/418 , A61L2300/604 , A61L2400/04
摘要: 【課題】本発明は、広範囲なpHにおいて透明で均質なヒドロゲルを形成し得る糖鎖-ポリペプチド複合体を提供することを課題とした。 【解決手段】本発明は、糖鎖-ポリペプチド複合体であって、前記ポリペプチドが、極性アミノ酸残基と非極性アミノ酸残基が交互に配置された、8~34個のアミノ酸残基からなるアミノ酸配列を含むポリペプチドであり、前記ポリペプチドに1または複数の糖鎖が結合していることを特徴とする、糖鎖-ポリペプチド複合体を提供する。
摘要翻译: 本发明解决了提供(糖链) - 多肽复合物的问题,其可以在宽的pH范围内形成为透明均匀的水凝胶。 [解决方案]本发明提供(糖链) - 多肽复合物,所述复合物的特征在于,所述多肽包含由8至34个氨基酸残基组成的氨基酸序列,其中极性氨基酸残基和非多氨基酸残基 极性氨基酸残基交替排列,并且一个或多个糖链与多肽结合。
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公开(公告)号:WO2014116717A1
公开(公告)日:2014-07-31
申请号:PCT/US2014/012571
申请日:2014-01-22
CPC分类号: A61L26/0019 , A61L24/0015 , A61L24/0031 , A61L24/0036 , A61L24/0042 , A61L24/043 , A61L24/06 , A61L24/10 , A61L26/0066 , A61L26/008 , A61L26/0085 , A61L26/009 , A61L2300/216 , A61L2300/604 , C09B11/24 , C09B57/02
摘要: The invention provides sealants wherein biodegradable hydrogels that do not otherwise comprise protein-reactive groups for binding to membranes or tissue are provided said groups optionally through a linker. The linker may be biodegradable and may be biodegradable by an elimination reaction. The invention also provides multilayer gels for drug delivery wherein a porous gel in contact with a tissue or organ to which the drug is to be delivered is protected by a microporous layer from the surrounding bodily fluid.
摘要翻译: 本发明提供了密封剂,其中任选地通过连接体为所述基团提供其中不另外包含用于结合膜或组织的蛋白质反应性基团的可生物降解的水凝胶。 接头可以是可生物降解的并且可以通过消除反应生物降解。 本发明还提供用于药物递送的多层凝胶,其中与药物将被递送的组织或器官接触的多孔凝胶被来自周围体液的微孔层保护。
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公开(公告)号:WO2013140190A1
公开(公告)日:2013-09-26
申请号:PCT/GB2013/050775
申请日:2013-03-25
发明人: GLADMAN, June , HARDY, Craig , HOGGARTH, Andrew
CPC分类号: C08B37/003 , A61L26/0023 , A61L26/0066 , A61L26/008 , A61L26/009 , A61L2300/232 , A61L2300/404 , A61L2300/418 , A61L2400/04 , C08L5/08
摘要: The present invention relates to a process for producing a low endotoxin alkali chitosan, and also to a process for producing low endotoxin neutral chitosan, chitosan salt and chitosan derivatives, and to the products of such processes. The process comprises contacting chitosan with an alkali solution to form a mixture and leaving the mixture for at least about 12 hours. The low endotoxin alkali chitosan may be used in the manufacture of other useful chitosan based products.
摘要翻译: 本发明涉及一种生产低内毒素碱性壳聚糖的方法,还涉及一种生产低内毒素中性壳聚糖,壳聚糖盐和壳聚糖衍生物的方法及其制备方法。 该方法包括使壳聚糖与碱溶液接触以形成混合物并将混合物离开至少约12小时。 低内毒素碱性壳聚糖可用于制造其他有用的基于壳聚糖的产品。
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公开(公告)号:WO2013003045A3
公开(公告)日:2013-04-25
申请号:PCT/US2012042346
申请日:2012-06-14
申请人: ETHICON INC , WANG YI-LAN , ZHANG GUANGHUI
发明人: WANG YI-LAN , ZHANG GUANGHUI
IPC分类号: A61L15/32
CPC分类号: A61L26/0052 , A61K38/39 , A61L24/0015 , A61L24/108 , A61L26/009 , A61L2300/25 , A61L2300/252 , A61L2300/418 , A61L2400/04
摘要: The present invention is directed to a hemostatic or tissue sealing material having (a) a peptide having a sequence SEQ ID NO: 1 or an amino acid analog sequence thereof, and (b) a scaffold for said peptide or amino acid analogue sequence. The scaffold is preferably hemostatic, such as a natural or genetically engineered absorbable polymer, a synthetic absorbable polymer, or combinations thereof. The natural or genetically engineered absorbable polymers can be selected from the group consisting of a protein, a polysaccharide, or combinations thereof.
摘要翻译: 本发明涉及一种止血或组织密封材料,其具有(a)具有序列SEQ ID NO:1或其氨基酸类似物序列的肽,和(b)所述肽或氨基酸类似物序列的支架。 支架优选为止血剂,例如天然或遗传工程可吸收聚合物,合成可吸收聚合物或其组合。 天然或遗传工程可吸收聚合物可以选自蛋白质,多糖或其组合。
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公开(公告)号:WO2010042952A1
公开(公告)日:2010-04-15
申请号:PCT/US2009/060544
申请日:2009-10-13
IPC分类号: A61F2/00
CPC分类号: A61L31/041 , A61L17/12 , A61L24/0042 , A61L24/043 , A61L26/0052 , A61L26/009 , A61L27/26 , A61L27/58 , A61L28/0026 , A61L28/0057 , A61L29/049 , A61L29/148 , A61L31/148 , C08L67/04 , C08L2205/02 , C08L2666/18
摘要: The bioabsorbable polymers and compositions of the present invention may be formed into medical devices such as stents that can be crimped onto a catheter system for delivery into a blood vessel. The properties of the bioabsorbable polymers allow for both crimping and expansion of the stent. The crystal properties of the bioabsorbable polymers may change during crimping and/or expansion allowing for improved mechanical properties such as tensile strength and slower degradation kinetics. Typically, bioabsorbable polymers comprise aliphatic polyesters based on lactide backbone such as poly L-lactide, poly D-lactide, poly D,L-lactide, mesolactide, glycolides, lactones, as homopolymers or copolymers, as well as formed in copolymer moieties with co-monomers such as, trimethylene carbonate (TMC) or ε-caprolactone (ECL).
摘要翻译: 本发明的生物可吸收聚合物和组合物可以形成医疗装置,例如可以卷曲到导管系统上用于输送到血管中的支架。 生物可吸收聚合物的性质允许支架的卷曲和膨胀。 生物可吸收聚合物的结晶特性可以在卷曲和/或膨胀期间改变,从而允许改进的机械性能如拉伸强度和较慢的降解动力学。 通常,生物可吸收聚合物包括基于丙交酯骨架的脂肪族聚酯,例如聚L-丙交酯,聚D-丙交酯,聚D,L-丙交酯,乳酰胺,乙交酯,内酯作为均聚物或共聚物,以及在共聚物部分中与共聚物形成 单体如三亚甲基碳酸酯(TMC)或ε-己内酯(ECL)。
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公开(公告)号:WO2009020612A1
公开(公告)日:2009-02-12
申请号:PCT/US2008/009431
申请日:2008-08-06
申请人: STB LIFESAVING TECHNOLOGIES, INC. , MACPHEE, Martin , KANELLOS, Jerry , WILMER, Belinda , BEALL, Dawson
IPC分类号: A61F15/00
CPC分类号: A61L15/64 , A61B17/00491 , A61B17/0057 , A61B2017/0065 , A61F2013/00472 , A61K38/363 , A61K38/4833 , A61L15/28 , A61L15/32 , A61L15/44 , A61L26/0042 , A61L26/009 , A61L2300/23 , A61L2300/252 , A61L2300/254 , A61L2400/04 , C12Y304/21005
摘要: Disclosed are solid and frozen haemostatic materials and dressings consisting essentially of a fibrinogen component and a fibrinogen activator. Also disclosed are methods of treating internal wounded tissue in a mammal by applying one or more of these haemostatic materials and dressings.
摘要翻译: 披露了基本上由纤维蛋白原组分和纤维蛋白原激活剂组成的固体和冷冻止血材料和敷料。 还公开了通过应用这些止血材料和敷料中的一种或多种来治疗哺乳动物的内部受伤组织的方法。
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