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Synthesis and characterization of poly-alpha,beta-[N-(2-hydroxyethyl)-L-aspartamide]-g-poly(glycolide)amphiphilic graft copolymers as potential drug carriers

机译:聚-α,β-[N-(2-羟乙基)-L-天冬酰胺] -g-聚乙交酯两亲性接枝共聚物的合成和表征

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摘要

A series of biodegradable amphiphilic graft polymers were successfully synthesized by grafting poly(glycolide)(PGA)sequences onto a water-soluble poly-alpha,beta-[N-(2-hy-droxyethyl)-L-aspartamide](PHEA)backbone.These novel graft polymers were synthesized by the ring-opening polymerization initiated by the macroinitiator PHEA bearing hydrox-yl groups without adding any catalyst.The graft polymers were characterized by Fourier transform infrared spec-troscopy(FTIR),~1H nuclear magnetic resonance spectroscopy(~1H NMR),combined size-exclusion chromatog-raphy(SEC)and multiangle laser light scattering(MALLS)analysis,and differential scanning calorimetry(DSC).By controlling the feed ratio of the macroinitiator to the monomer,graft polymers with different branch lengths can be obtained.The degradation behaviors of the copolymers were studied.Based on the amphi-philicity of the graft copolymers,nanoparticle drug delivery systems were prepared by the direct dissolution method and the dialysis method,and the in vitro drug release behavior was investigated.Transmission electron microscopy(TEM)images demonstrated that these nanoparticles were regularly spherical in shape.The particle size and distribution of the nanoparticles were measured.
机译:通过将聚乙交酯(PGA)序列接枝到水溶性聚α,β-[N-(2-羟乙基)-L-天冬酰胺](PHEA)骨架上,成功合成了一系列可生物降解的两亲性接枝聚合物这些新型接枝聚合物是通过在不添加任何催化剂的情况下由带有羟基的大分子引发剂PHEA引发的开环聚合反应而合成的。通过傅里叶变换红外光谱(FTIR),〜1H核磁共振光谱对接枝聚合物进行了表征。 (〜1H NMR),尺寸排阻色谱(SEC)和多角度激光散射(MALLS)分析以及差示扫描量热(DSC)相结合。通过控制大分子引发剂与单体的进料比,接枝不同的聚合物研究了共聚物的降解行为。基于接枝共聚物的两亲性,通过直接溶解法和渗析法制备了纳米颗粒药物递送系统。透射电子显微镜(TEM)图像显示这些纳米粒子呈规则球形,并测量了纳米粒子的粒径和分布。

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