Injectable in situ forming drug delivery system for cancer chemotherapy using a novel tissue adhesive: Characterization and in vitro evaluation

被引:44
作者
Kakinoki, Sachiro
Taguchi, Tetsushi
Saito, Hirofumi
Tanaka, Junzo
Tateishi, Tetsuya
机构
[1] Natl Inst Mat Sci, Ctr Biomat, Tsukuba, Ibaraki 3050044, Japan
[2] Furuuchi Chem Corp, Tokyo, Japan
关键词
tissue adhesive; hydrogel; drug delivery; human serum albumin; tartaric acid; injectable; in situ forming; N-hydroxysuccinimide; doxorubicin;
D O I
10.1016/j.ejpb.2006.11.022
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Injectable polymers that are biocompatible and biodegradable are important biomaterials for drug delivery system (DDS) and tissue engineering. We have already developed novel tissue adhesives consisting of biomacromolecules and organic acid derivatives with active ester groups. The resulting tissue adhesive forms in situ as a gel and has high bonding strength for living tissue as well as it has good biocompatibility and biodegradability. Here, we report on the physicochemical properties and in vitro evaluation of this novel tissue adhesive consisting of human serum albumin (HSA) and tartaric acid derivative (TAD) containing doxorubicin hydrochloride (DOX). The results of the measurement of physicochemical characteristics indicate that the gelation time and gel strength of HSA-TAD gels can be controlled according to the material composition. The bonding strength of HSA-TAD adhesives was found to be sufficient to adhere at focus and to correspond with the cross-linking density of HSA-TAD gels. Furthermore, the release of DOX from HSA-TAD gels was sustained for approximately 100 It in an in vitro evaluation. The novel tissue adhesive, therefore, is expected to be applicable for use as an injectable in situ forming DDS. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:383 / 390
页数:8
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