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Compositions comprising microparticles of a Copolymer of lactic acid and Glycolic Acid (PLGA) with an active substance in the form of a Salt insoluble peptide

机译:包含乳酸和乙醇酸(PLGA)共聚物微粒与盐不溶性肽形式的活性物质的组合物

摘要

A pharmaceutical composition made of microparticles for the slow release of an active substance, at least during a period covering the 6th month after the injection of the composition, the composition comprises a group of microparticles made of a PLGA type copolymer, which incorporates an active substance in the form of a water insoluble peptide sa the copolymer further comprises at least 75% lactic acid and an inherent viscosity between 0.1 and 0.9 dl / g, measured in chloroform at 25 ° C, and at a polymer concentration of 0.5 g / dL; The microparticles also have a defined size distribution as follows: - D (v,D (V, 0.5) is 30 to 70 microns and D (V, 0.9) is 50 to 110 microns. 1. - the drug composition of the microparticle, whose active substance is released slowly for at least six months after injection, including a group of microparticles made of PLGA type copolymers containing active substance In the form of water-insoluble peptides; the copolymer also contains at least 75% lactic acid and an intrinsic viscosity of 0.1 to 0.9 DL / g,seg n se mide en cloroformo a 25 C y una concentraci n de pol mero de 0 5 g 2FdL dichas micropart culas adem s tienen una distribuci n de grano que se define de la siguiente manera - D (v 0 1) est entre 10 y
机译:由微粒制成的用于缓慢释放活性物质的药物组合物,至少在注射组合物后的第6个月期间,该组合物包含一组由PLGA型共聚物制成的微粒,其中掺入了活性物质以水不溶性肽盐的形式;所述共聚物还包含至少75%的乳酸和在25℃下在氯仿中且在0.5g / dL的聚合物浓度下测得的比浓对数粘度在0.1至0.9dl / g之间;微粒还具有如下定义的尺寸分布:-D(v,D(V,0.5)为30至70微米,D(V,0.9)为50至110微米。1.-微粒的药物组合物,其活性物质在注射后至少六个月缓慢释放,包括一组由PLGA型共聚物制成的微粒,该微粒含有水不溶性肽形式的活性物质;该共聚物还包含至少75%的乳酸和特性粘度浓度为0.1至0.9 DL / g,中等浓度的氯仿25 y浓度为0 5 g 2FdL dichas微粒的数量,其分布范围为siguiente的定义-D( v 0 1)est entre 10年

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