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公开(公告)号:US20150231273A1
公开(公告)日:2015-08-20
申请号:US14434731
申请日:2013-03-26
发明人: Zhaohui Tang , Haiyang Yu , Wantong Song , Mingqiang Li , Xiuli Zuang , Xuesi Chen
CPC分类号: C08G81/00 , A61K33/24 , A61K47/60 , A61K47/64 , A61K47/645 , C08G69/10 , C08G69/40 , C08L77/04
摘要: A CDDP complex is formed by complexation of CDDP and a polymer having a structure of Formula (I). The CDDP complex has good biocompatibility and is degradable. A side chain of the polymer is grafted with polyethylene glycol, which gives the CDDP complex good dissolvability. When dissolved in an aqueous medium, the CDDP is protected by a hydrophilic polyethylene glycol chain segment and a hydrophobic amino acid chain segment, which can effectively avoid a sudden release of the CDDP due to the influence of the blood circulation system after intravenous injection, thus improving the stability of the CDDP complex. A carboxyl group contained in the CDDP complex has pH value sensitivity and tends to be deprotonated in a low pH environment, which is advantageous for promoting the release of a drug, and improving the efficiency of the drug.
摘要翻译: 通过CDDP与具有式(I)结构的聚合物的络合形成CDDP复合物。 CDDP复合物具有良好的生物相容性,是可降解的。 聚合物的侧链用聚乙二醇接枝,这使得CDDP复合物具有良好的溶解性。 当溶解在水性介质中时,CDDP被亲水性聚乙二醇链段和疏水性氨基酸链段保护,这可以有效地避免由于静脉注射后血液循环系统的影响,CDDP突然释放,因此 提高CDDP复合物的稳定性。 CDDP复合物中所含的羧基具有pH值敏感性,并且在低pH环境中倾向于去质子化,这有利于促进药物的释放并提高药物的效率。
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公开(公告)号:US09629923B2
公开(公告)日:2017-04-25
申请号:US14434731
申请日:2013-03-26
发明人: Zhaohui Tang , Haiyang Yu , Wantong Song , Mingqiang Li , Xiuli Zuang , Xuesi Chen
CPC分类号: C08G81/00 , A61K33/24 , A61K47/60 , A61K47/64 , A61K47/645 , C08G69/10 , C08G69/40 , C08L77/04
摘要: A CDDP complex is formed by complexation of CDDP and a polymer having a structure of Formula (I). The CDDP complex has good biocompatibility and is degradable. A side chain of the polymer is grafted with polyethylene glycol, which gives the CDDP complex good dissolvability. When dissolved in an aqueous medium, the CDDP is protected by a hydrophilic polyethylene glycol chain segment and a hydrophobic amino acid chain segment, which can effectively avoid a sudden release of the CDDP due to the influence of the blood circulation system after intravenous injection, thus improving the stability of the CDDP complex. A carboxyl group contained in the CDDP complex has pH value sensitivity and tends to be deprotonated in a low pH environment, which is advantageous for promoting the release of a drug, and improving the efficiency of the drug.
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