Amrita Centre for Nanosciences and Molecular Medicine, Amrita Institute of Medical Sciences and Research Centre, Amrita Vishwa Vidyapeetham University, Kochi, India.
J Colloid Interface Sci. 2011 Aug 1;360(1):39-51. doi: 10.1016/j.jcis.2011.04.006. Epub 2011 Apr 14.
This study aims at the formulation of curcumin with biodegradable thermoresponsive chitosan-g-poly (N-vinylcaprolactam) nanoparticles (TRC-NPs) for cancer drug delivery. The spherical curcumin-loaded nanoparticles of size 220 nm were characterized, and the biological properties were studied using flow cytometry and cytotoxicity by MTT assay. The in vitro drug release was higher at above LCST compared to that at below LCST. TRC-NPs in the concentration range of 100-1000 μg/mL were non-toxic to an array of cell lines. The cellular localization of the curcumin-loaded TRC-NPs was confirmed from green fluorescence inside the cells. The time-dependent curcumin uptake by the cells was quantified by UV spectrophotometer. Curcumin-loaded TRC-NPs showed specific toxicity to cancer cells at above their LCST. Flow cytometric analysis showed increased apoptosis on PC3 compared to L929 by curcumin-loaded TRC-NPs. These results indicate that novel curcumin-loaded TRC-NPs could be a promising candidate for cancer drug delivery.
本研究旨在制备载姜黄素的可生物降解温敏性壳聚糖-g-聚(N-乙烯基己内酰胺)纳米粒子(TRC-NPs)用于癌症药物传递。对粒径为 220nm 的球形载姜黄素纳米粒子进行了表征,并通过流式细胞术和 MTT 法细胞毒性试验研究了其生物学特性。与低于 LCST 相比,高于 LCST 时,TRC-NPs 的体外药物释放更高。浓度范围在 100-1000μg/mL 的 TRC-NPs 对一系列细胞系均无毒性。从细胞内的绿色荧光证实了载姜黄素的 TRC-NPs 的细胞内定位。通过紫外分光光度计定量了时间依赖性细胞摄取姜黄素的情况。在高于其 LCST 时,载姜黄素的 TRC-NPs 对癌细胞表现出特异性毒性。流式细胞术分析表明,与 L929 相比,载姜黄素的 TRC-NPs 使 PC3 细胞的凋亡增加。这些结果表明,新型载姜黄素的 TRC-NPs 可能是癌症药物传递的有前途的候选物。