Issue 5, 2012

On-demand serum-degradable amylopectin-based in situ gellable hydrogel

Abstract

This paper describes the hydrogels which are quickly degradable, even on-demand, by exposure to serum, as well as in situ gellable under mild conditions for cells. In addition, potential applications of these hydrogels to tissue engineering and regenerative medicine are also described. The hydrogels were produced from aqueous solution of amylopectin derivatives bearing phenolic hydroxyl moieties (AP-Ph) via horseradish peroxidase-catalysed reaction. The degradation rate in the presence of serum was enhanced with increasing the content of fetal bovine serum (FBS) and decreasing the content of Ph moieties in AP-Ph. A 1 mm thick hydrogel enclosing mouse embryonic fibroblastSTO cells prepared under conditions giving gelation in about 30 s disappeared within 3 h of incubation in FBS. The cells released from the hydrogel attached onto a culture dish and showed similar morphology to those seeded without being enclosed in the hydrogels. Furthermore, confluent human epithelial cells cultured on the AP-Ph-based hydrogel in serum-free medium can be harvested within 10 min by soaking in FBS while without separating into individual cells. These results indicate that the in situ gellable serum-degradable AP-Ph hydrogels may be a promising new tool for tissue engineering.

Graphical abstract: On-demand serum-degradable amylopectin-based in situ gellable hydrogel

Article information

Article type
Paper
Submitted
08 Sep 2011
Accepted
14 Nov 2011
First published
06 Dec 2011

J. Mater. Chem., 2012,22, 1944-1949

On-demand serum-degradable amylopectin-based in situ gellable hydrogel

S. Sakai, Y. Liu, T. Matsuyama, K. Kawakami and M. Taya, J. Mater. Chem., 2012, 22, 1944 DOI: 10.1039/C1JM14460J

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements