Nanoparticle approaches to combating drug resistance

被引:26
|
作者
Moon, Jae Hyon [1 ,2 ]
Moxley, James W., Jr. [1 ,2 ]
Zhang, Pengcheng [1 ,2 ]
Cui, Honggang [1 ,2 ,3 ,4 ,5 ]
机构
[1] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Inst NanoBioTechnol, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Dept Oncol, Sch Med, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Sch Med, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Ctr Nanomed, Baltimore, MD 21231 USA
基金
美国国家科学基金会;
关键词
INHIBITING P-GLYCOPROTEIN; MULTIDRUG-RESISTANCE; CANCER; DOXORUBICIN; DELIVERY; NANOMEDICINE; REVERSAL; EFFICACY;
D O I
10.4155/fmc.15.82
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Multidrug resistance (MDR) among cancer cells is a serious impediment to the success of conventional chemotherapy. The emergence of nanomedicine demonstrates great promise in overcoming MDR through multiple mechanisms. Nanoparticles have been shown to overcome the MDR at the tissue level through increased intratumoral accumulation resulting from enhanced permeation and retention, neovascular cell targeting, and externally triggered local drug release. Nanoparticles have also demonstrated the ability to overcome the MDR at the cellular/subcellular level by enhancing intracellular drug accumulation, improving drug-target accessibility, or even interfering with existing MDR mechanisms.
引用
收藏
页码:1503 / 1510
页数:8
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