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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Controlled drug release capability of paclitaxel-loaded poly(butylcyanoacrylate)-pluronic P123/F68 polymeric micells

Zhang Yang-de1, Xu Hong-juan1, Liang Jian2, Wang Ji-wei1, Pan Yi-feng1, Deng Xin2   

  1. 1 National Hepatobiliary and Enteric Surgery Research Center, Ministry of Health, Central South University, Changsha  410008, Hunan Province, China
    2 Ruikang Hospital, Guangxi University of Chinese Medicine, Nanning  530011, Guangxi Zhuang Autonomous Region, China
  • Received:2013-01-19 Revised:2013-03-15 Online:2013-04-16 Published:2013-04-16
  • 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*

Abstract:

BACKGROUND: Paclitaxel-loaded poly(butylcyanoacrylate)-pluronic P123 polymeric micells can effectively prolong drug circulation time, and change the paclitaxel targets. However, the stability in solution and drug loading capacity of this kind of paclitaxel polymer micelles need to be improved.
OBJECTIVE: To investigate the pharmaceutical characteristics and antitumor ability of paclitaxel-loaded poly(butylcyanoacrylate)-pluronic P123/F68 polymeric micells.
METHODS: We prepared the paclitaxel-loaded poly(butylcyanoacrylate)-pluronic P123/F68 polymeric micells using the method of film dispersion and studied their characteristics, such as morphology, size, zeta potential, encapsulation efficiency, drug loading, the critical micelle concentration, drug release, micelle stability and cytotoxity in vitro.
RESULTS AND CONCLUSION: The morphology of the prepared micells was spherical with the mean size of 100 nm and the zeta potential of -10 mV. The mean encapsulation efficiency and drug loading were (93.3±2.15)% and (1.82±0.04)%, respectively. The critical micelle concentration was 0.067 g/L. The in vitro release and stability experiments showed that the micells exhibited controlled release ability and good stability. The paclitaxel-loaded poly(butylcyanoacrylate)-pluronic P123/F68 polymeric micells were apparently more potent in killing MCF-7 cells than the free drug. Therefore, paclitaxel-loaded poly(butylcyanoacrylate)-pluronic P123/F68 polymeric micells with good controlled release ability and stability may serve as nanoscopic and long-circulating carriers for poorly water-soluble anticancer drugs.

Key words: biomaterials, biomaterials and controlled drug release, paclitaxel, stablized micelles, long cycle, poly(butylcyanoacrylate), cytotoxicity, tumor, characterization, biocompatibility, International S&T Cooperation Program of China

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