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Anticancer drug nanomicelles formed by self-assembling amphiphilic dendrimer to combat cancer drug resistance

机译:通过自组装两亲树状大分子形成的抗癌药物纳米胶束来对抗癌症耐药性

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摘要

Drug resistance and toxicity constitute challenging hurdles for cancer therapy. The application of nanotechnology for anticancer drug delivery is expected to address these issues and bring new hope for cancer treatment. In this context, we established an original nanomicellar drug delivery system based on an amphiphilic dendrimer (AmDM), which could generate supramolecular micelles to effectively encapsulate the anticancer drug doxorubicin (DOX) with high drug-loading capacity (>40%), thanks to the unique dendritic structure creating large void space for drug accommodation. The resulting AmDM/DOX nanomicelles were able to enhance drug potency and combat doxorubicin resistance in breast cancer models by significantly enhancing cellular uptake while considerably decreasing efflux of the drug. In addition, the AmDM/DOX nanoparticles abolished significantly the toxicity related to the free drug. Collectively, our studies demonstrate that the drug delivery system based on nanomicelles formed with the self-assembling amphiphilic dendrimer constitutes a promising and effective drug carrier in cancer therapy.
机译:耐药性和毒性构成了癌症治疗的挑战性障碍。纳米技术在抗癌药物递送中的应用有望解决这些问题,并为癌症治疗带来新的希望。在此背景下,我们建立了基于两亲树状聚合物(AmDM)的原始纳米胶束药物递送系统,该系统可以产生超分子胶束,从而有效地封装具有高载药量(> 40%)的抗癌药物阿霉素(DOX)。独特的树突结构为药物容纳创造了巨大的空隙空间。所得的AmDM / DOX纳米胶束能够通过显着提高细胞摄取同时显着降低药物的外排量,从而增强乳腺癌模型中的药物效力并对抗阿霉素抗性。此外,AmDM / DOX纳米颗粒大大消除了与游离药物有关的毒性。总的来说,我们的研究表明,基于与自组装两亲树状聚合物形成的纳米胶束的药物递送系统构成了癌症治疗中一种有希望且有效的药物载体。

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