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Advanced nanoscale carrier-based approaches to overcome biopharmaceutical issues associated with anticancer drug 'Etoposide'

机译:基于先进的纳米级载体的方法来克服与抗癌药物“依托税物”相关的生物制药问题

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摘要

Etoposide (ETS), topoisomerase-II inhibitor, is a first-line anticancer therapeutics used in diverse cancer types. However, the therapeutic potential of this molecule has mainly impeded due to its detrimental toxicity profile, unfavorable rejection by the cancer cells due to P-glycoprotein (P-gp) efflux activity, and rapid hepatic clearance through extensive metabolism by Cytochrome-P450. To increase the therapeutic potency without significant adverse effects, the implication of novel ETS-nanoformulation strategies have recommended mainly. Nanomedicine based nanoformulation approaches based on nanoparticles (NPs), dendrimers, carbon-nanotubes (CNTs), liposomes, polymeric micelles, emulsions, dendrimers, solid -lipid NPs, etc offers immense potential opportunities to improve the therapeutic potential of pharmaceutically problematic drugs. This review provides an up-to-date argument on the work done in the field of nanomedicine to resolve pharmacokinetic and pharmacodynamic issues associated with ETS. The review also expounds the progress in regards to the regulatory, patenting and clinical trials related to the innovative formulation aspects of ETS.
机译:胸腺苷(ETS),Topoisomerase-II抑制剂是一种用于各种癌症类型的一线抗癌治疗剂。然而,该分子的治疗潜力主要因其有害的毒性剖面而受到癌症细胞的不利抑制,由于P-糖蛋白(P-GP)流出活性,并通过细胞色素-P450通过广泛的代谢快速肝脏清除。为了增加治疗效力而无明显不良反应,主要推荐了新的ETS-NANOFORMULICE策略的含义。基于纳米颗粒(NPS),树枝状大分子,碳 - 纳米管(CNT),脂质体,聚合物胶束,乳液,树枝状大分子,固体 - 胃NPS等的纳米型纳米型纳米型纳米造型方法提供了巨大的潜在机会,以改善药学问题药物的治疗潜力。本综述提供了关于在纳米医生领域所做的工作的最新论点,以解决与ETS相关的药代动力学和药物动力学问题。审查还阐述了与ETS创新配方方面相关的监管,专利和临床试验的进展。

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