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

被引:31
作者
Balmayor, E. R. [1 ,2 ]
Baran, E. T. [1 ,2 ]
Azevedo, H. S. [1 ,2 ]
Reis, R. L. [1 ,2 ]
机构
[1] Univ Minho, Res Grp Biomat Biodegradables & Biomimet 3Bs, Dept Polymer Engn, Headquarters European Inst Excellence Tissue Engn, P-4806909 Taipas, Guimaraes, Portugal
[2] IBB Inst Biotechnol & Bioengn, PT Associated Lab, Guimaraes, Portugal
关键词
Starch-conjugated chitosan; Gentamicin; Microparticles; Sustained release; Staphylococcus aureus; NUCLEAR-MAGNETIC-RESONANCE; ORAL DELIVERY; CHITOSAN; MICROCAPSULES; DEACETYLATION; ANTIBIOTICS; FABRICATION; ASSIGNMENT; CAPSULES; DRUGS;
D O I
10.1016/j.carbpol.2011.06.078
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
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 80-150 mu m. Gentamicin was entrapped into the starch-conjugated chitosan microparticles and its release profile was studied in vitro. Increasing concentrations of gentamicin (from 50 to 150 mg/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 17 mm (70-100% of relative activity). (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:32 / 39
页数:8
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