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两亲嵌段共聚物聚乙二醇-聚谷氨酸苄酯纳米粒药物载体的合成研究 被引量:1

Synthesis and Characterization of PEG-PBLG Block Copolymer Nanoparticles as Drug Carriers
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摘要 用磺酸酯法制备单端氨基聚乙二醇引发剂,引发谷氨酸苄酯羧酸酐开环聚合,生成可生物降解的两亲嵌段共聚物聚乙二醇﹣聚谷氨酸苄酯(PEG-PBLG),用IR,NMR和GPC表征了共聚物。用超微透析法制备PEG-PBLG聚合物纳米粒,荧光芘探针法测定纳米粒的临界聚集浓度(cac)。紫外分光光度计考察纳米粒对疏水性药物的增溶作用,PEG-PBLG可作为亚微粒药物输送系统的载体。 The biodegradable block copolymer poly (ethylene glycol)-poly(γ-benzyle-L-glutamate) (PEG-PBLG) was synthesized by polymerization of γ-benzyle-L-glutamate-N-carboxyanhydride initiated with MePEG; Their structure and molecular weight were characterized by IR, NMR and GPC. The PEG-PBLG nanoparticles were prepared by diafiltration method. Solubilization was investigated by UV spectrophotometer; the critical aggregation concentration (cac) obtained by fluorescence spectroscopy.
出处 《广州化学》 CAS 2005年第4期9-16,共8页 Guangzhou Chemistry
关键词 聚乙二醇-聚谷氨酸苄酯 纳米粒 临界聚集浓度 poly(ethylene glycol)-poly(γ-benzyle-L-glutamate), nanoparticles, critical aggregation concentration
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二级参考文献1

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