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    • 2. 发明申请
    • TEMPERATURE AND PH SENSITIVE BLOCK COPOLYMER AND POLYMERIC HYDROGLES USING THE SAME
    • 使用温度和敏感性嵌段共聚物和聚合氢化物
    • WO2006109945A1
    • 2006-10-19
    • PCT/KR2006/001185
    • 2006-03-31
    • SUNGKYUNKWAN UNIVERSITY FOUNDATION FOR CORPORATE COLLABORATIONLEE, Doo-SungKIM, Min-SangYOU, Je-SunPHU, Huynh DaiKIM, Bong-SupNGUYEN, Minh Khanh
    • LEE, Doo-SungKIM, Min-SangYOU, Je-SunPHU, Huynh DaiKIM, Bong-SupNGUYEN, Minh Khanh
    • C08G65/48
    • C08G81/00C08L7/02C08L67/00C08L71/02C08L77/00C08L2205/05C08L2666/18C08L2666/20
    • Disclosed is a block copolymer formed by coupling the following components with each other: (a) a copolymer (A) of a polyethylene glycol (PEG) type compound with a biodegradable polymer; and (b) at least one oligomer (B) selected from the group consisting of poly (β-amino ester) and poly(amido amine). A method for preparing the same block copolymer, and a polymeric hydrogel type drug composition comprising the temperature and pH-sensitive block copolymer and a physiologically active substance that can be encapsulated with the block copolymer are also disclosed. The multiblock copolymer is obtained by copolymerization of a pH-sensitive poly (β-amino ester) and/or poly(amido amine) type oligomer, a hydrophilic and temperature-sensitive polyethylene glycol type compound and a hydrophobic and biodegradable polymer. Therefore, the block copolymer can form a polymeric hydrogel structure due to its amphiphilicity resulting from the combination of a hydrophilic group and a hydrophobic group in the copolymer and ionization characteristics depending on pH variations, and thus can be used as a drug carrier for target-directed drug delivery depending on pH variations in the body.
    • 公开了通过将以下组分彼此偶联而形成的嵌段共聚物:(a)聚乙二醇(PEG)型化合物与可生物降解聚合物的共聚物(A) 和(b)选自聚(β-氨基酯)和聚(酰氨基胺)中的至少一种低聚物(B)。 还公开了制备相同嵌段共聚物的方法和包含温度和pH敏感性嵌段共聚物的聚合物水凝胶型药物组合物和可以用嵌段共聚物包封的生理活性物质。 多嵌段共聚物通过pH敏感的聚(β-氨基酯)和/或聚(酰氨基胺)型低聚物,亲水和温度敏感的聚乙二醇型化合物和疏水和可生物降解的聚合物的共聚获得。 因此,嵌段共聚物由于其在共聚物中的亲水基团和疏水基团的组合引起的两亲性而形成聚合物水凝胶结构,并且根据pH变化而具有电离特性,因此可以用作靶向的药物载体, 定向药物递送取决于体内的pH变化。