首页> 美国卫生研究院文献>The Scientific World Journal >Glycyrrhetinic Acid-Poly(ethylene glycol)-glycyrrhetinic Acid Tri-Block Conjugates Based Self-Assembled Micelles for Hepatic Targeted Delivery of Poorly Water Soluble Drug
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Glycyrrhetinic Acid-Poly(ethylene glycol)-glycyrrhetinic Acid Tri-Block Conjugates Based Self-Assembled Micelles for Hepatic Targeted Delivery of Poorly Water Soluble Drug

机译:甘草次酸-聚(乙二醇)-甘草次酸三嵌段共轭胶束的自组装胶束用于肝靶向输送水溶性差的药物

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摘要

The triblock 18β-glycyrrhetinic acid-poly(ethylene glycol)-18β-glycyrrhetinic acid conjugates (GA-PEG-GA) based self-assembled micelles were synthesized and characterized by FTIR, NMR, transmission electron microscopy, and particle size analysis. The GA-PEG-GA conjugates having the critical micelle concentration of 6 × 10−5 M were used to form nanosized micelles, with mean diameters of 159.21 ± 2.2 nm, and then paclitaxel (PTX) was incorporated into GA-PEG-GA micelles by self-assembly method. The physicochemical properties of the PTX loaded GA-PEG-GA micelles were evaluated including in vitro cellular uptake, cytotoxicity, drug release profile, and in vivo tissue distribution. The results demonstrate that the GA-PEG-GA micelles had low cytotoxicity and good ability of selectively delivering drug to hepatic cells in vitro and in vivo by the targeting moiety glycyrrhetinic acid. In conclusion, the GA-PEG-GA conjugates have potential medical applications for targeted delivery of poor soluble drug delivery.
机译:合成了基于三嵌段的18β-甘草次酸-聚(乙二醇)-18β-甘草次酸共轭物(GA-PEG-GA)自组装胶束,并通过FTIR,NMR,透射电子显微镜和粒度分析对其进行了表征。使用临界胶束浓度为6×10 -5 M的GA-PEG-GA共轭物形成平均粒径为159.21±2.2 nm的纳米胶束,然后加入紫杉醇(PTX)通过自组装方法将其制成GA-PEG-GA胶束。评估了载有PTX的GA-PEG-GA胶束的理化特性,包括体外细胞摄取,细胞毒性,药物释放曲线和体内组织分布。结果表明,GA-PEG-GA胶束具有较低的细胞毒性,并具有通过靶向部分甘草次酸选择性地将药物体外和体内递送至肝细胞的良好能力。总之,GA-PEG-GA共轭物具有潜在的医学应用,可用于靶向递送不良可溶性药物。

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