中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Reversal of Multidrug Resistance by Mitochondrial Targeted Self-Assembled Nanocarrier Based on Stearylamine

文献类型:期刊论文

作者Zhang, Zhiwen2; Liu, Zeying1; Ma, Li2; Jiang, Shijun1; Wang, Yixin2; Yu, Haijun2; Yin, Qi2; Cui, Jingbin1; Li, Yaping2
刊名MOLECULAR PHARMACEUTICS
出版日期2013-06
卷号10期号:6页码:2426-2434
关键词stearylamine multidrug resistance self-assembly nanocarrier teniposide mitochondria
ISSN号1543-8384
DOI10.1021/mp400039j
文献子类Article
英文摘要Multidrug resistance (MDR) remains one of the major challenges for successful chemotherapy. Herein, we tried to develope a mitochondria targeted teniposide loaded self assembled nanocarrier based on stearylamine (SA-TSN) to reverse MDR of breast cancer. SA-TSN was nanometer-sized spherical particles (31.59 +/- 3.43 nm) with a high, encapsulation efficiency (99.25 +/- 0.21%). The MDR in MCF-7/ADR cells was obviously reduced by SA-TSN, which mainly attributed to the markedly reduced expression of P-gp, increased percentages in G2 phase, selectively accumulation in mitochondria, decrease of mitochondrial membrane potential, and greatly improved apoptosis. The plasma concentration of teniposide was greatly improved by SA-TSN, and the intravenously administered SA-TSN could accumulate in the tumor site and penetrate into the inner site of tumor in MCF-7/ADR induced xenografts. In particular, the in vivo tumor inhibitory efficacy of SA-TSN in MCF-7/ADR induced models was more effective than that of teniposide loaded self-assembled nanocarrier without stearylamine (TSN) and teniposide solution (TS), which verified the effectiveness of SA-TSN in reversal of MDR. Thereby, SA-TSN has potential to circumvent the MDR for the chemotherapy of breast cancer.
WOS关键词CANCER DRUG-RESISTANCE ; POLYMERIC MICELLES ; INDUCE APOPTOSIS ; LIPOSOMES ; TENIPOSIDE ; MECHANISMS ; PACLITAXEL ; PATHWAY ; CELLS ; CHEMOTHERAPY
资助项目National Basic Research Program of China[2010CB934000] ; National Basic Research Program of China[2012CB932502] ; National Basic Research Program of China[2013CB932503] ; National Basic Research Program of China[2013CB932704] ; National Natural Science Foundation of China[30925041] ; National Natural Science Foundation of China[81270047] ; Shanghai Program[11 nm0505900]
WOS研究方向Research & Experimental Medicine ; Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000320015600033
出版者AMER CHEMICAL SOC
源URL[http://119.78.100.183/handle/2S10ELR8/277598]  
专题药物制剂研究中心
通讯作者Li, Yaping
作者单位1.E China Univ Sci & Technol, Sch Pharm, Shanghai 200237, Peoples R China
2.Chinese Acad Sci, Shanghai Inst Mat Med, Ctr Pharmaceut, Shanghai 201203, Peoples R China;
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GB/T 7714
Zhang, Zhiwen,Liu, Zeying,Ma, Li,et al. Reversal of Multidrug Resistance by Mitochondrial Targeted Self-Assembled Nanocarrier Based on Stearylamine[J]. MOLECULAR PHARMACEUTICS,2013,10(6):2426-2434.
APA Zhang, Zhiwen.,Liu, Zeying.,Ma, Li.,Jiang, Shijun.,Wang, Yixin.,...&Li, Yaping.(2013).Reversal of Multidrug Resistance by Mitochondrial Targeted Self-Assembled Nanocarrier Based on Stearylamine.MOLECULAR PHARMACEUTICS,10(6),2426-2434.
MLA Zhang, Zhiwen,et al."Reversal of Multidrug Resistance by Mitochondrial Targeted Self-Assembled Nanocarrier Based on Stearylamine".MOLECULAR PHARMACEUTICS 10.6(2013):2426-2434.

入库方式: OAI收割

来源:上海药物研究所

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