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基于碳纳米管给药系统的 SMMC-7721 肝癌的体内外靶向治疗。

Targeted therapy of SMMC-7721 liver cancer in vitro and in vivo with carbon nanotubes based drug delivery system.

机构信息

Department of Gastroenterology, Zhongshan Hospital, Fudan University, Shanghai 200032, PR China.

出版信息

J Colloid Interface Sci. 2012 Jan 1;365(1):143-9. doi: 10.1016/j.jcis.2011.09.013. Epub 2011 Sep 12.

Abstract

A new type of drug delivery system (DDS) involved chitosan (CHI) modified single walled carbon nanotubes (SWNTs) for controllable loading/release of anti-cancer doxorubicin (DOX) was constructed. CHI was non-covalently wrapped around SWNTs, imparting water-solubility and biocompatibility to the nanotubes. Folic acid (FA) was also bounded to the outer CHI layer to realize selective killing of tumor cells. The targeting DDS could effectively kill the HCC SMMC-7721 cell lines and depress the growth of liver cancer in nude mice, showing superior pharmaceutical efficiency to free DOX. The results of the blood routine and serum biochemical parameters, combined with the histological examinations of vital organs, demonstrating that the targeting DDS had negligible in vivo toxicity. Thus, this DDS is promising for high treatment efficacy and low side effects for future cancer therapy.

摘要

构建了一种新型的药物传递系统(DDS),涉及壳聚糖(CHI)修饰的单壁碳纳米管(SWNTs),用于可控加载/释放抗癌阿霉素(DOX)。CHI 非共价包裹在 SWNTs 上,赋予纳米管水溶性和生物相容性。叶酸(FA)也结合到外 CHI 层上,以实现对肿瘤细胞的选择性杀伤。靶向 DDS 可以有效杀死 HCC SMMC-7721 细胞系,并抑制裸鼠肝癌的生长,显示出比游离 DOX 更高的药物疗效。血液常规和血清生化参数的结果,结合重要器官的组织学检查,表明靶向 DDS 在体内具有可忽略的毒性。因此,这种 DDS 有望在未来的癌症治疗中具有高治疗效果和低副作用。

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