Cytotoxicity evaluation of gelatin sponges prepared with different cross-linking agents

被引:120
|
作者
Ulubayram, K
Aksu, E
Gurhan, SID
Serbetci, K
Hasirci, N [1 ]
机构
[1] Middle E Tech Univ, Dept Chem, TR-06531 Ankara, Turkey
[2] Hacettepe Univ, Fac Pharm, Dept Basic Pharmaceut Sci, TR-06100 Ankara, Turkey
[3] Ege Univ, Fac Engn, Dept Bioengn, TR-35000 Izmir, Turkey
[4] Baskent Univ, Dept Biomed Engn, TR-06530 Ankara, Turkey
关键词
gelatin sponged cytotoxicity; cross-linking agents; glutaraldehyde; carbodiimide fructose; solubility; degradation;
D O I
10.1163/156856202320892966
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Gelatin is a natural polymer used in pharmaceutical and medical applications, especially in the production of biocompatible and biodegradable wound dressings and drug delivery systems. Gelatin granules hydrate, swell and solubilize in water, and rapidly degrade in vivo. The durability of these materials could, however, be prolonged by cross-linking by aldehydes, carbodiimides, and aldose sugars, but the biocompatibility of collagenous biomaterials is profoundly influenced by the nature and extent of cross-linking. In this study, gelatin sponges were prepared by using various crosslinkers such as glutaraldehyde (GA), 1-ethl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (EDAC), and D-fructose. The effects of the type and the amount of cross-linker on thermal and mechanical properties. stability, and cytotoxicity were investigated. The mechanical analysis data showed that an increase in the amount of GA in the sponge structures caused a slight increase in the modulus of elasticity but had almost no effect on the tensile strength. Increase in the EDAC concentration produced a maximum in the modulus of elasticity and tensile strength values. The stability of the sponges and the time required for complete degradation in aqueous media increased in parallel with the cross-linker content. In vitro studies carried out with fibroblast cells demonstrated a higher cell viability for the samples cross-linked with low concentrations of GA than for those crosslinked with EDAC.
引用
收藏
页码:1203 / 1219
页数:17
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