Adina Institute of Pharmaceutical Sciences, Sagar, 470002, M.P., India.
Department of Pharmaceutics, Institute of Pharmaceutical Research, GLA University, Mathura, 281406, U.P., India.
Int J Biol Macromol. 2019 Feb 15;123:691-703. doi: 10.1016/j.ijbiomac.2018.11.116. Epub 2018 Nov 13.
Purpose of the present research was to evaluate in vitro and in vivo potential of gemcitabine (GEM) loaded hyaluronic acid (HA) conjugated PEGylated multi-walled carbon nanotubes (GEM/HA-PEG-MWCNTs) for effective colon cancer targeting. HA was conjugated onto the surface of aminated or PEGylated MWCNTs which were evaluated for size, surface morphology, entrapment efficiency (~90%), in vitro drug release, in vitro cytotoxicity and in vivo performance in Sprague Dawley rats. In vitro release showed that the release rate of GEM in acidic conditions (pH 5.3) was faster than physiological conditions (PBS, pH 7.4) followed by a sustained release pattern. The developed GEM/HA-PEG-MWCNTs indicated significantly less hemolytic toxicity (7.73 ± 0.4%) paralleled to free GEM (18.71 ± 0.44%) and showed higher cytotoxicity against HT-29 colon cancer cell line. The antitumor study assured that GEM/HA-PEG-MWCNTs significantly reduced tumor volume as compared to free GEM and increased survival rate without noticeable loss in body weight. In vivo studies showed an improvement in pharmacokinetics in terms of remarkable escalation in mean residence time, half-life, AUC, AUMC, median survival time in tumor bearing rats treated with GEM/HA-MWCNTs and GEM/HA-PEG-MWCNTs as compared to free GEM (p ˂ 0.001). These outcomes proved engineered MWCNTs as a safe and effective nanomedicine in colon cancer targeting.
本研究旨在评估载吉西他滨(GEM)的透明质酸(HA)修饰的聚乙二醇化多壁碳纳米管(GEM/HA-PEG-MWCNTs)在体外和体内的有效结肠癌靶向潜力。HA 被修饰到氨基化或聚乙二醇化 MWCNTs 的表面,对其进行了大小、表面形态、包封效率(~90%)、体外药物释放、体外细胞毒性以及 Sprague Dawley 大鼠体内性能的评估。体外释放结果表明,在酸性条件(pH 5.3)下 GEM 的释放速率快于生理条件(PBS,pH 7.4),随后呈持续释放模式。所开发的 GEM/HA-PEG-MWCNTs 显示出明显较低的溶血毒性(7.73 ± 0.4%),与游离 GEM(18.71 ± 0.44%)相似,并且对 HT-29 结肠癌细胞系表现出更高的细胞毒性。抗肿瘤研究证实,与游离 GEM 相比,GEM/HA-PEG-MWCNTs 可显著降低肿瘤体积,并提高存活率,而体重无明显减轻。体内研究表明,在药代动力学方面有了改善,表现在载药 MWCNTs 处理的荷瘤大鼠的平均驻留时间、半衰期、AUC、AUMC、中位生存时间显著延长,与游离 GEM 相比(p ˂ 0.001)。这些结果证明了工程 MWCNTs 是一种安全有效的结肠癌靶向纳米医学。