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庆大霉素与二氧化硅载体结合的共价方法。

A covalent method of gentamicin bonding to silica supports.

作者信息

Ginalska Grazyna, Osińska Monika, Uryniak Adam

机构信息

Department of Biochemistry, Maria Curie-Skodowska University, 20-031 Lublin, Poland.

出版信息

J Biomater Appl. 2004 Apr;18(4):279-89. doi: 10.1177/0885328204041443.

Abstract

Results of a novel method of covalent bonding of an antibiotic (gentamicin) to silica bead supports are shown. Gentamicin was immobilized to four types of matrix: silica gel and porous glass beads activated by either silanization (APTES) or by adhesively bound keratin (with immobilization yield ranging from 36.5 to 91%). Gentamicin was immobilized to the supports after opening its carbohydrate ring in the molecule. This method of gentamicin activation before the immobilization process did not inhibit its antibiotic activity. The four gentamicin-containing immobilized preparations were stable, meaning that they did not release the antibiotic into the solution during the 30 days of incubation, not even during shaking experiments.

摘要

展示了一种将抗生素(庆大霉素)与硅胶珠载体进行共价键合的新方法的结果。庆大霉素被固定在四种类型的基质上:通过硅烷化(APTES)或通过粘附结合的角蛋白活化的硅胶和多孔玻璃珠(固定化产率在36.5%至91%之间)。庆大霉素在分子中的碳水化合物环打开后被固定在载体上。在固定化过程之前这种庆大霉素活化方法不会抑制其抗生素活性。四种含庆大霉素的固定化制剂是稳定的,这意味着在孵育的30天内它们不会将抗生素释放到溶液中,即使在振荡实验期间也不会。

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