Issue 8, 2016

Construction of coumarin-based cross-linked micelles with pH responsive hydrazone bond and tumor targeting moiety

Abstract

It is still a major challenge for targeted cancer chemotherapy to design a stable biocompatible micellar drug delivery system. To address this dilemma, novel responsive cross-linked micelles (x-micelles) based on polyurethane with photo-responsive coumarin derivatives and pH-responsive hydrazone groups were synthesized. The polymers could be self-assembled into micelles using a typical and facile way. The x-micelles were stable at physiological conditions after UV light induced cross-linking, and can be disassociated under acidic condition. The drug loading content (DLC) and the encapsulation efficiency (EE) of the obtained x-micelles (15.2% and 60.8% respectively) were higher than those of micelles (9.8% and 39.2% respectively), and the DOX release rate of x-micelles was also improved. For targeted therapy, folic acid (FA) was then conjugated to x-micelles, resulting in x-micelles–FA. Cellular viability experiments show that both x-micelles and micelles had a low cytotoxicity and good biocompatibility of up to 1000 μg mL−1, and DOX-loaded x-micelles–FA and x-micelles exhibited half-maximal inhibitory concentration (IC50) values of 1.17 and 2.40 μg mL−1, respectively, to HeLa cells, but have lower cytotoxicity to L929 cells. The pH-responsive x-micelles–FA exhibited superior extracellular stability but activated intracellular drug release. We have demonstrated that the polyurethane with UV- and pH-responsive properties as a novel platform for tumor-targeting drug delivery.

Graphical abstract: Construction of coumarin-based cross-linked micelles with pH responsive hydrazone bond and tumor targeting moiety

Supplementary files

Article information

Article type
Paper
Submitted
24 Dec 2015
Accepted
27 Jan 2016
First published
28 Jan 2016

J. Mater. Chem. B, 2016,4, 1480-1488

Construction of coumarin-based cross-linked micelles with pH responsive hydrazone bond and tumor targeting moiety

Y. Long, W. Gu, C. Pang, J. Ma and H. Gao, J. Mater. Chem. B, 2016, 4, 1480 DOI: 10.1039/C5TB02729B

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