Pharmacokinetics, Efficacy, and Safety Evaluation of Docetaxel/Hydroxypropyl-Sulfobutyl-β-Cyclodextrin Inclusion Complex

被引:22
作者
Huang, Xing-Xing [1 ,2 ]
Zhou, Cheng-Liang [1 ]
Wang, Hui [2 ]
Chen, Cheng [1 ]
Yu, Shu-Qin [1 ,2 ]
Xu, Qian [3 ]
Zhu, Yin-Yan [2 ]
Ren, Yong [1 ]
机构
[1] Nanjing Normal Univ, Coll Life Sci, Jiangsu Key Lab Supramol Med Mat & Applicat, Nanjing 210046, Peoples R China
[2] Nanjing Normal Univ, Jiangsu Key Lab Biofunct Mat, Nanjing 210046, Peoples R China
[3] Southeast Univ, Sch Publ Hlth, Nanjing 210009, Peoples R China
关键词
antitumor efficacy; biodistribution; DTX/HP-SBE-beta-CD; pharmacokinetics; safety evaluation; BREAST-CANCER; INDUCED HEMOLYSIS; PHASE-II; DOCETAXEL; DELIVERY; TAXOTERE; NANOPARTICLES; CHEMOTHERAPY; ASSOCIATION; CHEMISTRY;
D O I
10.1208/s12249-011-9631-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hydroxypropyl-sulfobutyl-beta-cyclodextrin (HP-SBE-beta-CD) inclusion complex was developed and used as a drug delivery system for DTX (DTX/HP-SBE-beta-CD). The objective of the present study was to evaluate and compare the biological properties of DTX/HP-SBE-I'-CD with TaxotereA (R). The pharmacokinetics, biodistribution, antitumor efficacy in vivo and in vitro, and safety evaluation of DTX/HP-SBE-beta-CD were studied. The most significant finding was that it was possible to prepare a Polysorbate-80-free inclusion complex for DTX. Studies based on pharmacokinetics, biodistribution, and antitumor efficacy indicated that DTX/HP-SBE-beta-CD had similar pharmacokinetic properties and antitumor efficacy both in vitro and in vivo as TaxotereA (R). Fortunately, this new drug delivery system attenuated the side effects when used in vivo. As a consequence, DTX/HP-SBE-beta-CD may be a promising alternative to TaxotereA (R) for cancer chemotherapy treatment with reduced side effects. The therapeutic potential against a variety of human tumors and low toxicity demonstrated in a stringent study clearly warrant clinical investigation of DTX/HP-SBE-beta-CD for possible use against human tumors.
引用
收藏
页码:665 / 672
页数:8
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