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首页> 外文期刊>RSC Advances >Reduction-responsive core-crosslinked micelles based on a glycol chitosan-lipoic acid conjugate for triggered release of doxorubicin
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Reduction-responsive core-crosslinked micelles based on a glycol chitosan-lipoic acid conjugate for triggered release of doxorubicin

机译:基于乙二醇壳聚糖-硫辛酸缀合物的还原反应性核交联胶束,可触发阿霉素的释放

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摘要

Reduction-responsive core-crosslinked micelles were developed based on a glycol chitosan-lipoic acid (GC-LA) conjugate and used for triggered release of doxorubicin (DOX). The substitution degree of GC-LA was 8.3 lipoic acid groups per 100 sugar units of glycol chitosan. GC-LA could form nanoscaled micelles in aqueous solution, wherein the critical micelle concentration (CMC) of 0.081 mg mL(-1) was determined. Furthermore GC-LA micelles can be crosslinked by a catalytic amount of dithiothreitol. The mean diameter of DOX-loaded core-crosslinked GC-LA (DOX-GC-LA/cc) micelles increased from 305 to 408 nm as the DOX-loading content increased from 6.03% to 10.74%. DOX-loaded crosslinked micelles demonstrated obvious reduction-triggered destabilization. DOX release from non-crosslinked GC-LA micelles was 87.6% for up to 96 h, whereas 25.3% of DOX release from DOX-GC-LA/cc micelles was observed in phosphate buffered saline (PBS, pH 7.4). Notably, in the presence of a 20 mM GSH-containing environment, accelerated DOX release from DOX-GC-LA/cc micelles was found. The blank micelles had low cytotoxicity in vitro, and DOX-GC-LA/cc micelles demonstrated intracellular redox-responsive characteristics in A549 cancer cells. These results suggested that GC-LA core-crosslinked micelles could be promising carriers for anticancer drug delivery.
机译:基于乙二醇壳聚糖-硫辛酸(GC-LA)共轭物开发了具有还原反应能力的核心交联胶束,并用于触发释放阿霉素(DOX)。每100糖单位的乙二醇壳聚糖,GC-LA的取代度为8.3个硫辛酸基团。 GC-LA可以在水溶液中形成纳米级胶束,其中临界胶束浓度(CMC)为0.081 mg mL(-1)。此外,GC-LA胶束可通过催化量的二硫苏糖醇交联。随着DOX负载量从6.03%增加到10.74%,负载DOX的芯交联GC-LA(DOX-GC-LA / cc)胶束的平均直径从305 nm增大到408 nm。载有DOX的交联胶束表现出明显的还原触发的去稳定作用。在长达96小时的时间内,未交联的GC-LA胶束释放的DOX为87.6%,而在磷酸盐缓冲液(PBS,pH 7.4)中观察到DOX-GC-LA / cc胶束释放的DOX为25.3%。值得注意的是,在含有20 mM GSH的环境中,发现DOX-GC-LA / cc胶束促进了DOX的释放。空白的胶束在体外具有较低的细胞毒性,而DOX-GC-LA / cc胶束在A549癌细胞中表现出细胞内氧化还原反应特性。这些结果表明,GC-LA核交联的胶束可能是抗癌药物传递的有希望的载体。

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