Esterase-activated release of naproxen from supramolecular nanofibres

被引:39
作者
Conda-Sheridan, Martin [1 ]
Lee, Sungsoo S. [2 ]
Preslar, Adam T. [3 ]
Stupp, Samuel I. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Northwestern Univ, Simpson Querrey Inst BioNanotechnol, Chicago, IL 60611 USA
[2] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[4] Northwestern Univ, Dept Med, Chicago, IL 60611 USA
[5] Northwestern Univ, Dept Biomed Engn, Evanston, IL 60208 USA
基金
美国国家卫生研究院;
关键词
PEPTIDE-AMPHIPHILE NANOFIBERS; DRUG-RELEASE; CYCLOOXYGENASE INHIBITION; IN-VITRO; IBUPROFEN; MICELLES; DELIVERY; CANCER; NANOSTRUCTURES; SURVIVAL;
D O I
10.1039/c4cc06340f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanofibre forming peptide amphiphiles were conjugated to naproxen through an esterase-sensitive linker. The amount of naproxen released, in the presence of enzymes, was influenced by the linker conjugating the drug to the supramolecular assembly. In vitro studies showed the anti-inflammatory activity of the released drug was maintained.
引用
收藏
页码:13757 / 13760
页数:4
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