Campus Units

Chemistry

Document Type

Article

Publication Version

Published Version

Publication Date

8-2013

Journal or Book Title

Journal of the American Chemical Society

Volume

135

Issue

34

First Page

12552

Last Page

12555

DOI

10.1021/ja406089c

Abstract

A tripropargylammonium surfactant with a methacrylate-terminated hydrophobic tail was combined with a bile salt derivative, divinyl benzene (DVB), and a photo-cross-linker above its critical micelle concentration (CMC). Surface-cross-linking with a diazide, surface-functionalization with an azido sugar derivative, and free-radical-core-cross-linking under UV irradiation yielded molecularly imprinted nanoparticles (MINPs) with template-specific binding pockets. The MINPs resemble protein receptors in size, complete water-solubility, and tailored binding sites in their hydrophobic cores. Strong and selective binding of bile salt derivatives was obtained, depending on the cross-linking density of the system.

Comments

Reprinted (adapted) with permission from Journal of the American Chemical Society 135 (2013): 12552, doi:10.1021/ja406089c. Copyright 2013 American Chemical Society.

Copyright Owner

American Chemical Society

Language

en

File Format

application/pdf

Included in

Chemistry Commons

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