Codelivery of Sorafenib and Curcumin by Directed Self-Assembled Nanoparticles Enhances Therapeutic Effect on Hepatocellular Carcinoma
Cao, Haiqiang1,2; Wang, Yixin1,2,3; He, Xinyu1,2; Zhang, Zhiwen1,2; Yin, Qi1,2; Chen, Yi1,2; Yu, Haijun1,2; Huang, Yongzhuo1,2; Chen, Lingli1,2; Xu, Minghua1,2
刊名MOLECULAR PHARMACEUTICS
2015-03
卷号12期号:3页码:922-931
关键词sorafenib curcumin nanoparticles codelivery hepatocellular carcinoma
ISSN号1543-8384
DOI10.1021/mp500755j
文献子类Article
英文摘要Hepatocellular carcinoma (HCC) is one of the most common causes of cancer-related mortality worldwide. Herein, we first reported the codelivery of sorafenib and curcumin by directed self-assembled nanoparticles (SCN) to enhance the therapeutic effect on HCC. SCN was formed by employing the hydrophobic interactions among the lipophilic structure in sorafenib, curcumin, and similar hydrophobic segments of polyethylene glycol derivative of vitamin E succinate (PEG-VES), which comprised uniform spherical particles with particle size of 84.97 +/- 6.03 nm. SCN presented superior effects over sorafenib, curcumin, and their physical mixture (Sora + Cur) on enhancing in vitro cytotoxicity and cell apoptosis in BEL-7402 cells and Hep G2 cells, and antiangiogenesis activities in tube formation and microvessel formation from aortic rings. Moreover, the tissue concentration of sorafenib and curcumin in gastrointestinal tract and major organs were significantly improved after their coassembly into SCN. In particular, in BEL-7402 cells induced tumor xenograft, SCN treatment displayed the obviously enhanced inhibitory effect on tumor progression over free drug monotherapy or their physical mixture, with significantly increased antiproliferation and antiangiogenesis capability. Thereby, the codelivered nanoassemblies of sorafenib and curcumin provided a promising strategy to enhance the combinational therapy of HCC.
资助项目National Basic Research Program of China[2015CB932103] ; National Basic Research Program of China[2012CB932502] ; National Natural Science Foundation of China[81270047] ; National Natural Science Foundation of China[81373359]
WOS关键词BREAST-CANCER ; MULTIDRUG-RESISTANCE ; ORAL DELIVERY ; TUMOR-GROWTH ; CO-DELIVERY ; COMBINATION ; DOXORUBICIN ; METASTASIS ; INHIBITION ; PACLITAXEL
WOS研究方向Research & Experimental Medicine ; Pharmacology & Pharmacy
语种英语
出版者AMER CHEMICAL SOC
WOS记录号WOS:000350390900025
内容类型期刊论文
源URL[http://119.78.100.183/handle/2S10ELR8/276624]  
专题药物制剂研究中心
中科院受体结构与功能重点实验室
新药研究国家重点实验室
通讯作者Zhang, Zhiwen
作者单位1.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China;
2.Chinese Acad Sci, Shanghai Inst Mat Med, Ctr Pharmaceut, Shanghai 201203, Peoples R China;
3.Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Peoples R China
推荐引用方式
GB/T 7714
Cao, Haiqiang,Wang, Yixin,He, Xinyu,et al. Codelivery of Sorafenib and Curcumin by Directed Self-Assembled Nanoparticles Enhances Therapeutic Effect on Hepatocellular Carcinoma[J]. MOLECULAR PHARMACEUTICS,2015,12(3):922-931.
APA Cao, Haiqiang.,Wang, Yixin.,He, Xinyu.,Zhang, Zhiwen.,Yin, Qi.,...&Li, Yaping.(2015).Codelivery of Sorafenib and Curcumin by Directed Self-Assembled Nanoparticles Enhances Therapeutic Effect on Hepatocellular Carcinoma.MOLECULAR PHARMACEUTICS,12(3),922-931.
MLA Cao, Haiqiang,et al."Codelivery of Sorafenib and Curcumin by Directed Self-Assembled Nanoparticles Enhances Therapeutic Effect on Hepatocellular Carcinoma".MOLECULAR PHARMACEUTICS 12.3(2015):922-931.
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