标题:Docetaxel-Loaded Pluronic P123 Polymeric Micelles: in Vitro and in Vivo Evaluation
作者:Liu, Zhihong; Liu, Donghua; Wang, Lili; Zhang, Juan; Zhang, Na
作者机构:[Liu, Zhihong; Liu, Donghua; Wang, Lili; Zhang, Juan; Zhang, Na] Shandong Univ, Sch Pharmaceut Sci, Jinan 250012, Shandong, Peoples R China.
通讯作者:Zhang, N
通讯作者地址:[Zhang, N]Shandong Univ, Sch Pharmaceut Sci, 44 Wenhua Xi Rd, Jinan 250012, Shandong, Peoples R China.
来源:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
出版年:2011
卷:12
期:3
页码:1684-1696
DOI:10.3390/ijms12031684
关键词:docetaxel; Pluronic P123; micelles; cytotoxicity; anticancer efficacy
摘要:In this work, novel docetaxel (DTX)-loaded Tween 80-free Pluronic P123 ( P123) micelles with improved therapeutic effect were developed. The freeze-dried DTX-loaded P123 micelles (DTX-micelles) were analyzed by HPLC, TEM and DLS to determine the DTX loading, micelle morphology, size, respectively. The in vitro cytotoxic activity of DTX-micelles in HepG2, A549 and malignant melanoma B16 cells were evaluated by MTT assay. The corresponding in vivo antitumor efficacy was assessed in Kunming mice bearing B16 tumor after intravenous administration. The DTX-loading and efficiency into the micelles were 2.12 +/- 0.09% and 86.34 +/- 3.32%, respectively. The DTX-micelles were spherical with a mean particle size of 50.7 nm and size distribution from 22 to 84 nm, which suggested that they should be able to selectively accumulate in solid tumors by means of EPR effect, with a zeta potential of -12.45 +/- 3.24 mV. The in vitro release behavior of DTX from DTX-micelles followed the Weibull equation. Compared with Duopafei (R), DTX-micelles showed higher cytotoxicity against HepG2 (P < 0.01), A549 (P < 0.05) and B16 ( P < 0.01) cells. In addition, DTX-micelles exhibited remarkable antitumor activity and reduced toxicity on B16 tumor in vivo. The tumor inhibition rates (TIR) of DTX-micelles was 91.6% versus 76.3% of Duopafei (R) (P < 0.01). These results suggested that P123 micelles might be considered as an effective DTX delivery system.
收录类别:SCOPUS;SCIE
WOS核心被引频次:61
Scopus被引频次:63
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-79953319256&doi=10.3390%2fijms12031684&partnerID=40&md5=ef2bf8950fae644cf6ac04d65ea35c10
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