Tissue reactions of in situ formed dextran hydrogels crosslinked by stereocomplex formation after subcutaneous implantation in rats

被引:53
作者
Bos, GW
Hennink, WE
Brouwer, LA
den Otter, W
Veldhuis, TFJ
van Nostrum, CF
van Luyn, MJA
机构
[1] Univ Groningen, Fac Med Sci, Dept Pathol Lab Med, NL-9713 GZ Groningen, Netherlands
[2] Univ Utrecht, Dept Pharmaceut, Utrecht Inst Pharmaceut Sci, UIPS, NL-3508 TB Utrecht, Netherlands
[3] Univ Utrecht, Fac Vet Med, Dept Cell Biol & Histol, NL-3508 TD Utrecht, Netherlands
关键词
hydrogel; in situ gelation; tissue reactions; biocompatibility; drug delivery; stereocomplex; dextran;
D O I
10.1016/j.biomaterials.2004.10.008
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In this study, the in vivo biocompatibility of physically crosslinked dextran hydrogels was investigated. These hydrogels were obtained by mixing aqueous solutions of dextran grafted with L-lactic acid oligomers and dextran grafted with D-lactic acid oligomers. Gelation occurs due to stereocomplex formation of the lactic acid oligomers of opposite chirality. Since gelation takes some time, in situ gel formation is possible with this system. A number of sterilization methods was evaluated for their effect on the chemical and physical properties of the hydrogel. It was shown that of the investigated options (filtration, gamma irradiation, dry-heat and autoclaving) dry-heat sterilization was the preferred method to prepare sterile gels suitable for in vivo evaluations. Two types of stereocomplex gels were prepared and implanted subcutaneously in rats. The tissue reaction was evaluated over a period of 30 days. A mild ongoing foreign body reaction was observed characterized by infiltration of macrophages. Giant cells were only scarcely formed and the low numbers of lymphocytes showed that priming of the immune system is hardly involved. Importantly, the gels fully degraded in vivo within 15 days, which is in good agreement with the in vitro degradation behaviour of these gels. In conclusion, stereocomplexed dextran-oligolactic gels showed good biocompatibility which makes them suitable candidates for the design of controlled release devices for pharmaceutically active proteins. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3901 / 3909
页数:9
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