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Nano-Sized Albumin-Copolymer Micelles for Efficient Doxorubicin Delivery

机译:纳米级白蛋白共聚物胶束,高效递送阿霉素

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We present the discovery of a nano-sized protein-derived micellar drug delivery system based on the polycationic albumin precursor protein cBSA-147. The anticancer drug doxorubicin (DOX) was efficiently encapsulated into nanosized micelles based on hydrophobic interactions with the polypeptide scaffold. These micelles revealed attractive stabilities in various physiological buffers and a wide pH range as well as very efficient uptake into A549 cells after 1?h incubation time only. In vitro cytotoxicity was five-times increased compared to free DOX also indicating efficient intracellular drug release. In addition, multiple functional groups are available for further chemical modifications. Based on the hydrophobic loading mechanism, various classical anti-cancer drugs, in principle, could be delivered even synergistically in a single micelle. Considering these aspects, this denatured albumin-based drug delivery system represents a highly attractive platform for nanomedicine approaches towards cancer therapy.
机译:我们介绍了基于聚阳离子白蛋白前体蛋白cBSA-147的纳米级蛋白质衍生的胶束药物递送系统的发现。基于与多肽支架的疏水相互作用,将抗癌药阿霉素(DOX)有效地封装到了纳米胶束中。这些胶束在各种生理缓冲液和宽pH范围内显示出有吸引力的稳定性,并且仅在1小时的孵育时间后即可非常有效地吸收到A549细胞中。与游离DOX相比,体外细胞毒性增加了五倍,也表明有效的细胞内药物释放。另外,多个官能团可用于进一步的化学修饰。基于疏水性加载机制,原则上甚至可以在单个胶束中协同递送各种经典的抗癌药物。考虑到这些方面,该基于变性白蛋白的药物递送系统代表了用于癌症治疗的纳米医学方法的极具吸引力的平台。

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