Using oxidant susceptibility of thiol stabilized nanoparticles to develop an inflammation triggered drug release system
Author:
Affiliation:
1. State Key Laboratory of Inorganic Synthesis and Preparative Chemistry
2. College of Chemistry
3. Jilin University
4. Changchun
5. China
6. College of Life Science
7. China Japan Union Hospital
Abstract
Ultrasmall thiol passivated ZnS NPs are prepared using a newly developed synthetic protocol. Exposure to hydroxyl radicals results in oxidation of the thiol groups, thus destabilizing the ZnS nanolids to open drug encompassing pores for attaining an inflammation responsive drug delivery system.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Materials Science,Biomedical Engineering,General Chemistry,General Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/2015/TB/C4TB01709A
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