Targeted therapy for cancer using pH-responsive nanocarrier systems

被引:148
|
作者
Manchun, Somkamon [1 ,2 ]
Dass, Crispin R. [3 ]
Sriamornsak, Pornsak [1 ,2 ]
机构
[1] Silpakorn Univ, Fac Pharm, Dept Pharmaceut Technol, Nakhon Pathom 73000, Thailand
[2] Silpakorn Univ, Fac Pharm, Pharmaceut Biopolymer Grp PBiG, Nakhon Pathom 73000, Thailand
[3] Victoria Univ, Sch Biomed & Hlth Sci, St Albans 3021, Australia
关键词
Cancer; Chemotherapy; Drug delivery; Nanocarrier; pH-responsive; IN-VITRO EFFICACY; DRUG-DELIVERY; POLYMERIC MICELLES; PAMAM DENDRIMER; TUMOR PH; DOXORUBICIN; NANOPARTICLES; CHITOSAN; RELEASE; NANOTECHNOLOGY;
D O I
10.1016/j.lfs.2012.01.008
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Most of the conventional chemotherapeutic agents used against cancer have poor efficacy. An approach to improve the efficacy of cancer chemotherapy is the development of carrier systems that can be triggered to release the anticancer drug in response to extracellular or intracellular chemical stimuli. To this end, pH-responsive nanocarriers have been developed to target drugs either to the slightly acidic extracellular fluids of tumor tissue or, after endocytosis, to the endosomes or lysosomes within cancer cells. These systems can release the drug by specific processes after accumulation in tumor tissues via the enhanced permeability and retention (EPR) effect or they can release the drugs in endosomes or lysosomes by pH-controlled hydrolysis after they are taken up by the cell via the endocytic pathway. This strategy facilitates the specific delivery of the drug while reducing systemic side-effects with high potential for improving the efficacy of cancer chemotherapy. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:381 / 387
页数:7
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