中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enzyme-responsive multistage vector for drug delivery to tumor tissue

文献类型:期刊论文

作者Mi, Yu4; Wolfram, Joy3,4; Mu, Chaofeng4; Liu, Xuewu4; Blanco, Elvin4; Shen, Haifa2,4; Ferrari, Mauro1,4
刊名PHARMACOLOGICAL RESEARCH
出版日期2016-11-01
卷号113页码:92-99
ISSN号1043-6618
关键词Enzyme-responsive release Lung metastasis MMP2 Multistage vector Porous silicon
DOI10.1016/j.phrs.2016.08.024
通讯作者Ferrari, Mauro(mferrari@houstonmethodist.org)
英文摘要Various nanodelivery systems have been designed to release therapeutic agents upon contact with specific enzymes. However, enzyme-triggered release typically takes place in the tissue interstitium, thereby resulting in the extracellular delivery of drugs. Here, we have designed an enzyme-stimulated multistage vector (ESMSV), which enables stimulus-triggered release of drug-encapsulated nanoparticles from a microparticle. Specifically, polymeric nanoparticles with a surface matrix metalloproteinase-2 (MMP2) peptide substrate were conjugated to the surface of porous silicon microparticles. In the presence of MMP2, the polymeric nanoparticles were released into the tumor interstitium. This platform can be used to attain triggered drug release, while simultaneously facilitating the cellular internalization of drugs. The results indicate that nanoparticle release was MMP2-specific and resulted in improved intracellular uptake of hydrophobic agents in the presence of MMP2. Furthermore, in a mouse model of melanoma lung metastasis, systemic delivery of ESMSVs caused a substantial increase in intracellular accumulation of agents in cancer cells in comparison to delivery with non-stimulus-responsive particles. (C) 2016 Elsevier Ltd. All rights reserved.
WOS关键词POLYMERIC NANOPARTICLES ; CELLULAR UPTAKE ; MATRIX METALLOPROTEINASES ; BIOLOGICAL BARRIERS ; SIRNA DELIVERY ; GENE DELIVERY ; BREAST-CANCER ; PARTICLE-SIZE ; THERAPEUTICS ; NANOMEDICINE
资助项目Houston Methodist Research Institute ; Ernest Cockrell Jr. Distinguished Endowed Chair ; US Department of Defense[W81XWH-09-1-0212] ; National Institute of Health[U54CA143837] ; National Institute of Health[U54CA151668] ; Department of Defense[W81XWH-12-1-0414] ; State of Texas CPRIT[RP121071]
WOS研究方向Pharmacology & Pharmacy
语种英语
出版者ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
WOS记录号WOS:000389086800009
资助机构Houston Methodist Research Institute ; Ernest Cockrell Jr. Distinguished Endowed Chair ; US Department of Defense ; National Institute of Health ; Department of Defense ; State of Texas CPRIT
源URL[http://ir.ihep.ac.cn/handle/311005/281942]  
专题中国科学院高能物理研究所
通讯作者Ferrari, Mauro
作者单位1.Weill Cornell Med, Dept Med, 1300 York Ave, New York, NY 10065 USA
2.Weill Cornell Med, Dept Cell & Dev Biol, 1300 York Ave, New York, NY 10065 USA
3.Univ Chinese Acad Sci, Natl Ctr Nanosci & Technol China, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
4.Houston Methodist Res Inst, Dept Nanomed, 6670 Benner Ave, Houston, TX 77030 USA
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GB/T 7714
Mi, Yu,Wolfram, Joy,Mu, Chaofeng,et al. Enzyme-responsive multistage vector for drug delivery to tumor tissue[J]. PHARMACOLOGICAL RESEARCH,2016,113:92-99.
APA Mi, Yu.,Wolfram, Joy.,Mu, Chaofeng.,Liu, Xuewu.,Blanco, Elvin.,...&Ferrari, Mauro.(2016).Enzyme-responsive multistage vector for drug delivery to tumor tissue.PHARMACOLOGICAL RESEARCH,113,92-99.
MLA Mi, Yu,et al."Enzyme-responsive multistage vector for drug delivery to tumor tissue".PHARMACOLOGICAL RESEARCH 113(2016):92-99.

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来源:高能物理研究所

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