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用于庆大霉素持续释放以治疗骨感染的可注射生物可降解淀粉/壳聚糖递送系统。

Injectable biodegradable starch/chitosan delivery system for the sustained release of gentamicin to treat bone infections.

作者信息

Balmayor E R, Baran E T, Azevedo H S, Reis R L

机构信息

3B's Research Group - Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4806-909 Taipas, Guimarães, Portugal(1); IBB - Institute for Biotechnology and Bioengineering, PT Associated Laboratory, Guimarães, Portugal(2).

3B's Research Group - Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4806-909 Taipas, Guimarães, Portugal(1); IBB - Institute for Biotechnology and Bioengineering, PT Associated Laboratory, Guimarães, Portugal(2).

出版信息

Carbohydr Polym. 2012 Jan 4;87(1):32-39. doi: 10.1016/j.carbpol.2011.06.078. Epub 2011 Jul 7.

DOI:10.1016/j.carbpol.2011.06.078
PMID:34662968
Abstract

Starch-conjugated chitosan microparticles were produced aimed to be used as a carrier for the long term sustained/controlled release of antibiotic drugs to control bone infection. The microparticles were prepared by a reductive alkylation crosslinking method. The obtained microparticles showed a spherical shape, with a slightly rough and porous surface, and a size range of 80-150μm. Gentamicin was entrapped into the starch-conjugated chitosan microparticles and its release profile was studied in vitro. Increasing concentrations of gentamicin (from 50 to 150mg/mL) led to a decrease in the encapsulation efficiency (from 67 to 55%), while drug loading increased from 4 to 27%. A sustained release of gentamicin was observed over a period of 30 days. The release kinetics could be controlled using an ionic crosslinker agent. In addition, a bacterial inhibition test on Staphylococcus aureus shows a diameter of the sample inhibition zone ranging from 12 to 17mm (70-100% of relative activity).

摘要

制备淀粉共轭壳聚糖微粒的目的是将其用作载体,用于抗生素药物的长期持续/控释,以控制骨感染。通过还原烷基化交联法制备微粒。所得微粒呈球形,表面略粗糙且多孔,尺寸范围为80 - 150μm。将庆大霉素包封于淀粉共轭壳聚糖微粒中,并对其体外释放曲线进行了研究。庆大霉素浓度增加(从50mg/mL至150mg/mL)导致包封效率降低(从67%降至55%),而载药量从4%增加至27%。在30天的时间内观察到庆大霉素的持续释放。使用离子交联剂可控制释放动力学。此外,对金黄色葡萄球菌的抑菌试验表明,样品抑菌圈直径范围为12至17mm(相对活性为70 - 100%)。

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