Jain Anekant, Jain Sanjay K
Pharmaceutics Research Projects Laboratory, Department of Pharmaceutical Sciences, Dr. Hari Singh Gour Vishwavidyalaya, Sagar 470003, MP, India.
Eur J Pharm Sci. 2008 Dec 18;35(5):404-16. doi: 10.1016/j.ejps.2008.08.008. Epub 2008 Sep 7.
Hyaluronic acid (HA) coupled chitosan nanoparticles (HACTNP) bearing 5-flurouracil (5FU) were prepared, by ionotropic gelation method, for the effective delivery of drug to the colon tumors. HACTNP appeared to be spherical in shape and mean size was found to be around 150+/-3.4nm with low polydispersity index. The in vitro drug release was investigated using USP dissolution test (paddle type) apparatus in different simulated GIT fluids. The biocompatibility of NPs formulations were evaluated for in vitro cytotoxicity by MTT assay using HT-29 cell lines and cell uptake was assessed by fluorescent microscopy. Cellular uptake of HACTNP was determined by incorporating calcein as a fluorescent marker. The cellular uptake of fluorescent HACTNP was clearly evidenced by fluorescence microscopy. HACTNP nanoparticles showed significant higher uptake by cancer cells as compared to uncoupled nanoparticles and the uptake of HA coupled CTNPs by HT-29 colon cancer cells were observed to be 7.9 times more as compared to uncoupled CTNPs at the end of 4h. The cytotoxicity of 5FU incorporated in HACTNP was higher compared to the conventional 5FU solution, even at the lower concentrations. 5FU in HACTNP was about 2.60-folds more effective than free 5FU on HT-29 cells.
采用离子凝胶法制备了负载5-氟尿嘧啶(5FU)的透明质酸(HA)偶联壳聚糖纳米粒(HACTNP),用于将药物有效递送至结肠肿瘤。HACTNP呈球形,平均粒径约为150±3.4nm,多分散指数较低。使用USP溶出度试验(桨式)装置在不同模拟胃肠道液中研究了体外药物释放。通过使用HT-29细胞系的MTT法评估NP制剂的体外细胞毒性,并通过荧光显微镜评估细胞摄取。通过掺入钙黄绿素作为荧光标记物来测定HACTNP的细胞摄取。荧光显微镜清楚地证明了荧光HACTNP的细胞摄取。与未偶联的纳米粒相比,HACTNP纳米粒在癌细胞中的摄取明显更高,并且在4小时结束时,观察到HT-29结肠癌细胞对HA偶联CTNP的摄取是未偶联CTNP的7.9倍。与传统的5FU溶液相比,即使在较低浓度下,HACTNP中掺入的5FU的细胞毒性也更高。HACTNP中的5FU对HT-29细胞的有效性比游离5FU高约2.60倍。