Literature DB >> 24852096

Injectable multifunctional microgel encapsulating outgrowth endothelial cells and growth factors for enhanced neovascularization.

Pyung-Hwan Kim1, Hyun-Gu Yim2, Young-Jin Choi1, Byung-Jae Kang1, Joohyun Kim1, Sang-Mo Kwon3, Byung-Soo Kim2, Nathaniel S Hwang2, Je-Yoel Cho4.   

Abstract

Recent cell-based therapy approaches have employed both nanotechnologies and other biomedical technologies to enhance their therapeutic potential. A combined strategy using therapeutic stem/progenitor cells and angiogenic proteins is attractive for the treatment of vascular disease. In this study, we developed an injectable multifunctional micro-sized gel system (microgel), composed of arginine-glycine-aspartic acid (RGD)-conjugated alginate, for the delivery of both cells and growth factors in vivo. The microgels encapsulated with outgrowth endothelial cells (OECs) and growth factors (vascular endothelial growth factor, VEGF, and hepatocyte growth factor, HGF) were formed via electrospraying. Cells encapsulated within the microgel exhibited a time-dependent proliferation with enhanced cell viability, and the size-controlled microgels resulted in sustained release of growth factors for enhanced new vessel formation by tube formation and rat aorta sprouting in vitro. Increased angiogenesis was also estimated in mice treated with RGD-microgel containing OECs and growth factors. Furthermore, injection of the multifunctional microgel into a hindlimb ischemia model improved blood flow perfusion and increased the capillary density by histological analysis. Compared with hydrogel system, injectable microgel system was shown to be superior with no toxicity. Overall, our injectable multifunctional microgel system can be attributed to deliver potential therapeutic agents/cells for the treatment of vascular diseases.
Copyright © 2014. Published by Elsevier B.V.

Entities:  

Keywords:  Cell therapy; Electrospraying; Neovascularization; Outgrowth endothelial cells; RGD-conjugated microgel

Mesh:

Substances:

Year:  2014        PMID: 24852096     DOI: 10.1016/j.jconrel.2014.05.010

Source DB:  PubMed          Journal:  J Control Release        ISSN: 0168-3659            Impact factor:   9.776


  28 in total

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