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引用本文:������,��ΰ,���Ӹ�,��Ψ˶,�����.�ذ����������Ҷ���������-������˫Ƕ�ι��������׽������Ʊ������������⿹�������Ե��о�[J].中国药学杂志,2015,50(19):1688-1695.
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Preparation,Pharmaceutical Characterization and in Vitro Anti-tumor Effects of Aziditaxel-loaded mPEG-PLA Micelles
CHEN Li-qing,HUANG Wei,GAO Zhong-gao,FANG Wei-shuo,JIN Ming-ji.Preparation,Pharmaceutical Characterization and in Vitro Anti-tumor Effects of Aziditaxel-loaded mPEG-PLA Micelles[J].Chinese Pharmaceutical Journal,2015,50(19):1688-1695.
Authors:CHEN Li-qing  HUANG Wei  GAO Zhong-gao  FANG Wei-shuo  JIN Ming-ji
Institution:a. State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China;
b.Department of Pharmaceutics, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China;
c.Department of Natural Medicinal Chemistry, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
Abstract:??OBJECTIVE To prepare aziditaxel-loaded mPEG-PLA polymeric micelles, investigate its pharmaceutical characteristics and study its anti-tumor effects in vitro. METHODS Aziditaxel-loaded polymeric micelles were prepared by thin-film dispersion method. The morphology of aziditaxel-loaded micelles was observed under transmission electron microscope. The particle size distribution and Zeta potential of aziditaxel-loaded micelles were determined by dynamic light scattering method using a Malvern Zetasizer Nano ZS90 analyzer. The technical reproducibility and reconstitution stability of aziditaxel-loaded micelles were also checked. The drug loading and encapsulation efficiency were measured by HPLC. Dialysis method was used to investigate the in vitro release of aziditaxel-loaded micelles, and the release manner was fitted using the mathematic models. The in vitro anti-tumor activities were evaluated by proliferation inhibition and cycle block experiment. RESULTS Aziditaxel-loaded polymeric micelles were prepared successfully. Aziditaxel-loaded polymeric micelles showed spherical shape with a mean particle size of 24.50 nm, polydispersity index of 0.117 and Zeta potential of -10.06 mV. The mean drug loading and entrapment efficiency were (16.00??0.15)% and (95.80??0.10)%, respectively. The preparation reproducibility was fine, and the reconstitution solution of lyophilized preparation of aziditaxel-loaded polymeric micelles maintained stable within 6 h. The release behavior of aziditaxel-loaded micelles conformed to the ambiexponent model. Drug-loaded micelles could obviously inhibit the proliferation of MCF-7 breast cancer cell lines in vitro, and induce significant G2/M cycle arrest and apoptosis on MCF-7 cancer cells. CONCLUSION Aziditaxel-loaded mPEG-PLA polymeric micelles are successfully prepared. The preparation method is simple, and the pharmaceutical properties of the products conform to the requirements of the subsequent study. The prepared aziditaxel-loaded polymeric micelles exhibit good application prospect with favourable in vitro anti-tumor activities.
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