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首页> 外文期刊>Journal of Controlled Release: Official Journal of the Controlled Release Society >Encapsulation of plasmid DNA in biodegradable poly(D, L-lactic-co-glycolic acid) microspheres as a novel approach for immunogene delivery.
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Encapsulation of plasmid DNA in biodegradable poly(D, L-lactic-co-glycolic acid) microspheres as a novel approach for immunogene delivery.

机译:质粒DNA在可生物降解的聚(D,L-乳酸-乙醇酸)微球体中的封装作为一种免疫基因传递的新方法。

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摘要

A plasmid DNA encoding bacterial beta-galactosidase gene was encapsulated in poly(d,l-lactic-co-glycolic acid) (PLGA) microspheres. Plasmid DNA extracted from PLGA microspheres retained both structural and functional integrity as evidenced by its restriction endonuclease digestion pattern and its ability to transfect COS-1 cells in vitro. PLGA microspheres protected plasmid DNA from digestion by deoxyribonuclease I (DNase I) in vitro. The encapsulation efficiency of plasmid DNA and its release rate depended on the molecular mass of PLGA. Lastly, J-774A macrophages phagocytosed PLGA microspheres loaded with plasmid DNA. Co-encapsulated monophosphoryl lipid A increased the rate of phagocytosis. These results suggest that biodegradable PLGA microspheres can deliver intact and functional plasmid DNA at controlled rates. Thus, PLGA microspheres may be used to jointly deliver genes and other biologically active molecules, e.g., immunomodulators, to antigen presenting cells.
机译:将编码细菌β-半乳糖苷酶基因的质粒DNA封装在聚(d,1-乳酸-乙醇酸共聚物)(PLGA)微球中。从PLGA微球中提取的质粒DNA保留了结构和功能的完整性,这由其限制性核酸内切酶消化模式及其在体外转染COS-1细胞的能力证明。 PLGA微球可保护质粒DNA免受体外脱氧核糖核酸酶I(DNase I)的消化。质粒DNA的包封效率及其释放速率取决于PLGA的分子量。最后,J-774A巨噬细胞吞噬了载有质粒DNA的PLGA微球。共包封的单磷酰脂质A增加了吞噬作用的速率。这些结果表明,可生物降解的PLGA微球可以控制的速率递送完整和功能性的质粒DNA。因此,PLGA微球可用于将基因和其他生物活性分子例如免疫调节剂共同递送至抗原呈递细胞。

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