中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Co-delivery of 10-Hydroxycamptothecin with Doxorubicin Conjugated Prodrugs for Enhanced Anticancer Efficacy

文献类型:期刊论文

作者Zhang Y ; Xiao CS ; Li MQ ; Chen J ; Ding JX ; He CL ; Zhuang XL ; Chen XS
刊名macromolecular bioscience
出版日期2013
卷号13期号:5页码:584-594
关键词IN-VITRO EVALUATION DRUG-DELIVERY BLOCK-COPOLYMER POLY(ETHYLENE OXIDE) ANTITUMOR EFFICACY NANOPARTICLES CAMPTOTHECIN MICELLES THERAPY CELLS
ISSN号1616-5187
通讯作者chen xs
中文摘要well-defined amphiphilic linear-dendritic prodrugs (mpeg-b-pamam-dox) are synthesized by conjugating doxorubicin (dox), to mpeg-b-pamam through the acid-labile hydrazone bond. the amphiphilic prodrugs form self-assembled nanoparticles in deionized water and encapsulate the hydrophobic anticancer drug 10-hydroxycamptothecin (hcpt) with a high drug loading efficiency. studies on drug release and cellular uptake of the co-delivery system reveal that both drugs are released in a ph-dependent manner and effectively taken up by mcf-7 cells. in vitro methyl thiazolyl tetrazolium (mtt) assays and drug-induced apoptosis tests demonstrate the hcpt-loaded nanoparticles suppress cancer cell growth more efficiently than the mpeg-b-pamam-dox prodrugs, free hcpt, and physical mixtures of mpeg-b-pamam-dox and hcpt at equivalent dox or hcpt doses.
收录类别SCI收录期刊论文
语种英语
WOS记录号WOS:000319331100008
公开日期2014-04-15
源URL[http://ir.ciac.jl.cn/handle/322003/49879]  
专题长春应用化学研究所_长春应用化学研究所知识产出_期刊论文
推荐引用方式
GB/T 7714
Zhang Y,Xiao CS,Li MQ,et al. Co-delivery of 10-Hydroxycamptothecin with Doxorubicin Conjugated Prodrugs for Enhanced Anticancer Efficacy[J]. macromolecular bioscience,2013,13(5):584-594.
APA Zhang Y.,Xiao CS.,Li MQ.,Chen J.,Ding JX.,...&Chen XS.(2013).Co-delivery of 10-Hydroxycamptothecin with Doxorubicin Conjugated Prodrugs for Enhanced Anticancer Efficacy.macromolecular bioscience,13(5),584-594.
MLA Zhang Y,et al."Co-delivery of 10-Hydroxycamptothecin with Doxorubicin Conjugated Prodrugs for Enhanced Anticancer Efficacy".macromolecular bioscience 13.5(2013):584-594.

入库方式: OAI收割

来源:长春应用化学研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。