Derivation and performance of an entirely autologous injectable hydrogel delivery system for cell-based therapies

被引:20
作者
Bryan, Nicholas [1 ]
Rhodes, Nicholas P. [1 ]
Hunt, John A. [1 ]
机构
[1] Univ Liverpool, Sch Clin Sci, UKCTE, Div Clin Engn, Liverpool L69 3GA, Merseyside, England
关键词
stem cells; Injectable gel; Hydrogel; Fibrin; Animal model; DIFFERENTIATION; PROLIFERATION; HYPOXIA; ENHANCEMENT; ACID;
D O I
10.1016/j.biomaterials.2008.09.003
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
A host-derived hydrogel has been designed and validated as an entirely autologous, injectable delivery system for cells with potential for cell-based therapies and tissue engineering applications. Each individual has components in their blood from which can be formed a mechanically stable hydrogel having the capacity to maintain cellular phenotype and support cellular proliferation of multiple cell types through several Culture passages ex vivo. The hydrogel can be triggered to gel at the time of implantation into the patient through an injection system that facilitates a liquid injection of components of the donor plasma and cells into the site of interest. This results in stable ectopic tissue formation at the site of implantation. Our Studies have demonstrated excellent integration of the neotissue with host tissues with maintenance of the phenotype of implanted cells whilst observing minimal host innate immune cell recruitment. These findings could provide the fundamental basis for new hydrogel-based biomaterial therapies, overcoming the histocompatibility factors associated with implantable biomaterials whilst providing a stable three dimensional medium for cellular growth both in vivo and ex vivo. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:180 / 188
页数:9
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