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Preparation and characterization of N-succinyl-N '-octyl chitosan micelles as doxorubicin carriers for effective anti-tumor activity

机译:N-琥珀酰-N'-辛基壳聚糖胶束的制备和表征作为阿霉素载体,具有有效的抗肿瘤活性

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摘要

N-Succinyl-N'-octyl chitosan (SOC) was prepared and characterized by elemental analysis, FTIR, H-1 NMR, WAXD and TG. An anticancer drug, doxorubicin (DOX), was incorporated into polymeric micelles forming by SOC in aqueous solutions. Critical micelle concentrations (CMC) of SOC were determined by fluorescence spectroscopy. The DOX-loaded SOC micelles were characterized by measurement of size and drug loading. The loading content of DOX increased with increasing drug-to-carrier ratio, and the more amount of the octyl chain, the higher the drug loading content. The average size, which was affected by the amount of octyl chain and drug loading content, was in the range of 100-200 nm. The polymeric micelles containing doxorubicin in the core region exhibited a sustained release and more cytotoxic activity against HepG2, A549, BGC and K562 than doxorubicin alone, this can be attributed to an endocytosis mechanism rather than passive diffusion. (C) 2006 Elsevier B.V. All rights reserved.
机译:制备了N-琥珀酰-N'-辛基壳聚糖(SOC),并通过元素分析,FTIR,H-1 NMR,WAXD和TG对其进行了表征。将一种抗癌药阿霉素(DOX)掺入水溶液中通过SOC形成的聚合物胶束中。 SOC的临界胶束浓度(CMC)通过荧光光谱法测定。通过测量尺寸和载药量表征了载有DOX的SOC胶束。 DOX的负载量随药物/载体比的增加而增加,并且辛基链的数量越多,药物的负载量就越高。受辛基链数量和载药量影响的平均大小在100-200 nm范围内。与单独的阿霉素相比,在核心区域含有阿霉素的聚合物胶束表现出持续释放和对HepG2,A549,BGC和K562的更多细胞毒活性,这可以归因于内吞作用机制而不是被动扩散。 (C)2006 Elsevier B.V.保留所有权利。

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