Chinese Journal of Tissue Engineering Research ›› 2013, Vol. 17 ›› Issue (16): 2935-2942.doi: 10.3969/j.issn.2095-4344.2013.16.012
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Zhang Yang-de1, Xu Hong-juan1, Liang Jian2, Wang Ji-wei1, Pan Yi-feng1, Deng Xin2
Received:2013-01-19
Revised:2013-03-15
Online:2013-04-16
Published:2013-05-24
Contact:
Liang Jian, Doctor, Professor, Ruikang Hospital, Guangxi University of Chinese Medicine, Nanning 530011, Guangxi Zhuang Autonomous Region, China
About author:Zhang Yang-de☆, Doctor, Professor, National Hepatobiliary and Enteric Surgery Research Center, Ministry of Health, Central South University, Changsha 410008, Hunan Province, China
530222867@qq.com
Supported by:the International S&T Cooperation Program of China, No. 2011DFA32620*
CLC Number:
Zhang Yang-de, Xu Hong-juan, Liang Jian, Wang Ji-wei, Pan Yi-feng, Deng Xin. Controlled drug release capability of paclitaxel-loaded poly(butylcyanoacrylate)-pluronic P123/F68 polymeric micells[J]. Chinese Journal of Tissue Engineering Research, 2013, 17(16): 2935-2942.
2.6 载药胶束的细胞毒性 体外抗癌活性的研究是确定抗肿瘤药物药效的方法之一。抗肿瘤药物的抗癌活性可用半数抑制浓度(IC50)进行定量表示,IC50是指在用药后存活的细胞数量减少一半所需的药物浓度[5] 。采用MTT方法,探测紫杉醇-聚氰基丙烯酸正丁酯- P123/F68对MCF-7的IC50,并与紫杉醇原料药和Taxol注射液进行比较,见图5。 由图5可见,当药物与细胞作用24 h时,紫杉醇原料药、Taxol注射液、载药胶束的IC50分别是13.47,7.59,2.38 mg/L;而当作用时间为48 h时,三者的IC50分别变为10.64,6.25,2.03 mg/L。因此,在两个时间点,与游离药物和注射液相比,载药胶束均显示较强的杀死肿瘤细胞的能力。同时,普朗尼克P123和F68在一定的作用时间和浓度下,对肿瘤细胞同样具有一定的杀伤效应,这与文献记载是一致的,但是聚氰基丙烯酸正丁酯对肿瘤的抑制效应较弱,具有良好的生物相容性。"
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