螯合复合胶束递送细胞保护剂氨磷汀及其在辐射防护中的应用

Chau-Hui Wang, Chia-Yi Cheng, Chia-Hung Chen, W. Liao, Johnson Lin
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引用次数: 4

摘要

为了克服传统给药系统的缺点,提出了一种新型纳米药物载体。阿米索汀是一种亲水性和半衰期极短的细胞保护剂,它是基于螯合络合物胶束(CCM)负载的,以提供对辐射的保护。在不使用任何有机溶剂的情况下,简单地将氯化亚铁、聚乙二醇-嵌段聚谷氨酸(PEG-b-PGA)和氨fostine在水溶液中混合制备氨fostine负载CCM (CCM- ami)。所得CCM-Ami单分散,平均粒径为25 nm,与氨磷汀相比,表现出缓释行为。此外,与相应剂量的氨磷汀治疗相比,CCM-Ami预处理提高了C57BL/6小鼠的存活率和中位生存期。这些结果指出了CCM作为一种新型药物载体的潜在用途。可作为配体的药物分子可考虑通过该平台技术进行递送。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chelating Complex Micelles for Delivering Cytoprotectant Amifostine and its Application in Radiation Protection
A new nano-size drug carrier was proposed to overcome the shortcomings of conventional drug delivery systems. Amifsotine, a hydrophilic and extremely short half-life cytoprotective agent, was loaded based on chelating complex micelles (CCM) in order to provide the protection from radiation exposure. The preparation of amifostine-loaded CCM (CCM-Ami) was simply mixing ferrous chloride, poly(ethylene glycol)-block-poly (glutamic acid) (PEG-b-PGA) and amifostine in an aqueous solution without using any organic solvent. The resulting CCM-Ami monodispersed with a mean particle size 25 nm and showed a slow release behavior as compared to amifostine. Furthermore, CCM-Ami pretreatment improved survival rates and median survival in C57BL/6 mice than did treatment with a corresponding dose of amifostine. These results point to a potential use of CCM as a novel drug carrier. Drug molecules that may act as ligands can be considered delivering by this platform technology.
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