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    • 2. 发明申请
    • Temperature and Ph Sensitive Block Copolymer and Polymeric Hydrogels Using the Same
    • 温度和Ph敏感嵌段共聚物和聚合物水凝胶使用它
    • US20080293827A1
    • 2008-11-27
    • US11815960
    • 2006-03-31
    • Doo Sung LeeMin Sang KimJe Sun YouHuynh Dai PhuBong Sup KimMinh Khanh Nguyen
    • Doo Sung LeeMin Sang KimJe Sun YouHuynh Dai PhuBong Sup KimMinh Khanh Nguyen
    • A61K47/32C08L71/00C08G65/08
    • C08G65/33306C08G65/331C08G65/3322C08G65/3324C08G73/028C08G81/00C08L53/00C08L67/00C08L71/02C08L2203/02C08L2205/05C08L2666/02C08L2666/18
    • 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)至少一种选自聚(β-氨基酯)和聚(酰氨基胺)的低聚物(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。
    • 6. 发明授权
    • pH sensitive block copolymer and polymeric micelle using the same
    • pH敏感嵌段共聚物和使用其的聚合物胶束
    • US08318204B2
    • 2012-11-27
    • US11573858
    • 2005-12-27
    • Doo Sung LeeMin Sang Kim
    • Doo Sung LeeMin Sang Kim
    • A61K9/14A61K47/00
    • C08F299/024
    • Disclosed is a pH-sensitive block copolymer obtained by copolymerization of: (a) a polyethylene glycol compound (A); and (b) at least one poly(amino acid) compound selected from the group consisting of a poly(β-amino ester) and poly(amido amine) or a copolymer thereof (B). A method for preparing the same block copolymer, and a polymer micelle type drug composition comprising the pH-sensitive block copolymer and a physiologically active substance that can be encapsulated with the block copolymer are also disclosed. The pH-sensitive block copolymer is obtained by polymerization of a hydrophilic polyethylene glycol compound with a pH-sensitive biodegradable poly(amino acid) compound. Therefore, the pH-sensitive block copolymer can form a micelle structure due to its amphiphilicity and ionization characteristics depending on pH variations, and thus can be used as drug carrier for target-directed drug delivery depending on pH variations in the body.
    • 公开了通过以下方法获得的pH敏感性嵌段共聚物:(a)聚乙二醇化合物(A); 和(b)至少一种选自聚(亚氨基酯)和聚(酰氨基胺)或其共聚物(B)的聚(氨基酸)化合物。 还公开了制备相同嵌段共聚物的方法,以及包含该pH敏感性嵌段共聚物的聚合物胶束型药物组合物和可以用嵌段共聚物包封的生理活性物质。 通过亲水性聚乙二醇化合物与pH敏感的可生物降解的聚(氨基酸)化合物的聚合获得pH敏感性嵌段共聚物。 因此,pH敏感性嵌段共聚物由于其两亲性和离子化特性而根据pH变化而形成胶束结构,因此可以根据体内的pH变化用作靶向药物递送的药物载体。