Issue 32, 2015

Complementary hydrogen bonding interaction triggered co-assembly of an amphiphilic peptide and an anti-tumor drug

Abstract

We report a new tumor-targeting amphiphilic peptide that can form complementary hydrogen bonds with anti-tumor drug methotrexate (MTX), leading to reversible self-assembled morphology transition from loose micelles to densely packed nanorods or nanofibers. The MTX loaded nanorods can target tumor cells and show more than 2-fold higher cytotoxicity (IC50 = 0.38 mg L−1) than that towards normal cells (IC50 = 0.89 mg L−1).

Graphical abstract: Complementary hydrogen bonding interaction triggered co-assembly of an amphiphilic peptide and an anti-tumor drug

Supplementary files

Article information

Article type
Communication
Submitted
18 Jan 2015
Accepted
11 Mar 2015
First published
11 Mar 2015

Chem. Commun., 2015,51, 6936-6939

Author version available

Complementary hydrogen bonding interaction triggered co-assembly of an amphiphilic peptide and an anti-tumor drug

H. Cheng, Y. Cheng, S. Bhasin, J. Zhu, X. Xu, R. Zhuo and X. Zhang, Chem. Commun., 2015, 51, 6936 DOI: 10.1039/C5CC00501A

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