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首页> 外文期刊>International Journal of Polymeric Materials >Simple Fabrication of Glutathione-Responsive PEGylated Micellar Nanocarriers for Dual Drugs Delivery
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Simple Fabrication of Glutathione-Responsive PEGylated Micellar Nanocarriers for Dual Drugs Delivery

机译:谷胱甘肽响应的PEG化胶束纳米载体的简单制备双药物输送。

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摘要

The authors report a feasible simple method to fabricate two kinds of micellar nanocarriers (MPEG-SS-CPT/DOX) with polyethylene glycol (PEG) based on the self-assembly of glutathione (GSH)-responsive amphiphilic PEGylated polymers (MPEG-SS-CPT) in free doxorubicin (DOX) solution, which could carry two anticancer drugs of camptothecin (CPT) and DOX toward cancer cells together. In in vitro release studies, the micelles of MPEG-SS-CPT/DOX could undergo the triggered disassembly to release CPT and DOX under GSH stimulus much faster than without GSH. Furthermore, the MPEG-SS-CPT nanocarriers could release CPT with no change of its original structure after degradation. From the experiments of loading and release of drugs, the cell viability assay, cellular uptake, and flow cytometry studies, it was found that the fibrous micelles modified by PEG with a molecular weight of 350 had greater potential in the field of drug delivery than the other with a molecular weight of 1900.
机译:作者报告了一种基于谷胱甘肽(GSH)响应的两亲性聚乙二醇化聚合物(MPEG-SS-)的自组装,用聚乙二醇(PEG)制备两种胶束纳米载体(MPEG-SS-CPT / DOX)的可行简单方法。游离阿霉素(DOX)溶液中的CPT),可以将喜树碱(CPT)和DOX的两种抗癌药物一起携带给癌细胞。在体外释放研究中,在GSH刺激下,MPEG-SS-CPT / DOX的胶束可以触发分解,释放CPT和DOX的速度比没有GSH时要快得多。此外,MPEG-SS-CPT纳米载体在降解后可以释放CPT,而其原始结构没有变化。从药物装载和释放的实验,细胞活力测定,细胞摄取和流式细胞术研究中发现,分子量为350的PEG修饰的PEG修饰的纤维微胶粒在药物递送领域的潜力更大。其他的分子量为1900。

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