用户名: 密码: 验证码:
An ionically crosslinked hydrogel containing vancomycin coating on a porous scaffold for drug delivery and cell culture
详细信息    查看全文
文摘
Alginate hydrogels were prepared with varying degrees of covalent cross-linking and different pore characteristics. Dehydrated scaffolds were compressed into smaller, temporary forms, introduced into the dorsal subcutaneous space of CD-1 mice by minimally invasive delivery through a 10 gauge angiocatheter and rehydrated in situ with a saline solution delivered through the same catheter. Ionically cross-linked calcium alginate gel served as a control. Specimens were harvested at 2, 6, 12 and 24 weeks to evaluate implant shape retention and volume, cell infiltration and calcification, and the presence of an inflammatory response.

Results:

A total of 90 scaffolds were implanted and 95 % were recovered at the site of injection. All of these scaffolds successfully rehydrated and 80 % recovered and maintained their original 3-dimensional shape for 6 months. Scaffold volume and tissue infiltration varied depending on the degree of alginate cross-linking. Highly cross-linked materials (20 % and 35 % ) demonstrated the best volume maintenance with the latter facilitating the most tissue infiltration. The inflammatory response was minimal except with the 80 % cross-linked material. Calcification was not observed in covalently cross-linked scaffolds. In contrast, 98 % of calcium alginate implants were calcified.

Conclusions:

Shape retaining porous hydrogels meet many of the requirements necessary for a successful injectable bulking agent and offer advantages over currently used agents.


Purchase PDF (1360 K)
View More Related Articles
View Record in Scopus
doi:10.1016/j.ijpharm.2007.11.023
Copyright © 2007 Elsevier B.V. All rights reserved.

An ionically crosslinked hydrogel containing vancomycin coating on a porous scaffold for drug delivery and cell culture

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700