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Protein-loaded PLGA-PEO blend nanoparticles: encapsulation, release and degradation characteristics

机译:载有蛋白质的PLGA-PEO共混纳米颗粒:包封,释放和降解特性

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The aim of this work was to study the variables that affect the encapsulation and release of proteins from nanoparticles based on poly(lactic-co-glycolic acid; PLGA)-polox-amer and PLGA-poloxamine blend matrices, using bovine serum albumin (BSA) and immuno-γ-globulin (IgG) as model proteins. The nanoparticles were prepared by a solvent diffusion technique, and the studied variables were (1) PLGA molecular weight, (2) type of PEO-block copolymers, (3) protein loading, (4) pH and, (5) volume of the protein solution. Our results showed that the proteins can be efficiently incorporated into and released from the blend matrices. The type of the PEO derivative and the pH of the internal aqueous phase were the most important factors influencing protein encapsulation and release kinetics. Moreover, comparative degradation study of PLGA, PLGA-poloxamer and PLGA-poloxamine nanoparticles confirmed that the degradation and release characteristics of polyester particles can be improved by the incorporation of polyoxyethylene derivatives with different hydrophilia-lipophiha balance.
机译:这项工作的目的是使用牛血清白蛋白(BSA)研究影响基于聚乳酸-乙醇酸; PLGA)-polox-amer和PLGA-poloxamine混合基质的纳米颗粒中蛋白质的包封和释放的变量。 )和免疫-γ-球蛋白(IgG)作为模型蛋白。通过溶剂扩散技术制备纳米颗粒,研究变量为(1)PLGA分子量,(2)PEO-嵌段共聚物的类型,(3)蛋白质负载量,(4)pH和(5)体积蛋白质溶液。我们的结果表明,蛋白质可以有效地掺入混合基质并从混合基质中释放出来。 PEO衍生物的类型和内部水相的pH是影响蛋白质包封和释放动力学的最重要因素。此外,通过对PLGA,PLGA-泊洛沙姆和PLGA-泊洛沙明纳米粒子的比较降解研究,证实通过掺入具有不同亲水性-脂类平衡的聚氧乙烯衍生物可以改善聚酯粒子的降解和释放特性。

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