王金成, 薛白, 葛葵葵, 汪益涵, 李国栋, 黄青山. 搭载溶葡萄球菌酶羟基磷灰石/壳聚糖复合材料的可控释放J. 药学学报, 2014,49(9): 1331-1339.
引用本文: 王金成, 薛白, 葛葵葵, 汪益涵, 李国栋, 黄青山. 搭载溶葡萄球菌酶羟基磷灰石/壳聚糖复合材料的可控释放J. 药学学报, 2014,49(9): 1331-1339.
WANG Jin-cheng, XUE Bai, GE Kui-kui, WANG Yi-han, LI Guo-dong, HUANG Qing-shan. Controlled release by novel lysostaphin-loaded hydroxyapatite/chitosan compositesJ. Acta Pharmaceutica Sinica, 2014,49(9): 1331-1339.
Citation: WANG Jin-cheng, XUE Bai, GE Kui-kui, WANG Yi-han, LI Guo-dong, HUANG Qing-shan. Controlled release by novel lysostaphin-loaded hydroxyapatite/chitosan compositesJ. Acta Pharmaceutica Sinica, 2014,49(9): 1331-1339.

搭载溶葡萄球菌酶羟基磷灰石/壳聚糖复合材料的可控释放

Controlled release by novel lysostaphin-loaded hydroxyapatite/chitosan composites

  • 摘要: 溶葡萄球菌酶是一种高效杀灭耐甲氧西林金黄色葡萄球菌的生物酶类,为了实现溶葡萄球菌酶有效的可控释放,需要一种具有优异释放性能与良好生物相容性的载药材料。本文选用羟基磷灰石/壳聚糖复合材料作为溶葡萄球菌酶的载药材料,并制备了不同羟基磷灰石与壳聚糖比例 (80/20,70/30,60/40,40/60) 的样品。通过扫描电镜 (SEM)、X射线衍射 (XRD) 和红外光谱 (FTIR) 等检测方法分析材料的结构,将含酶的复合材料于Tris-HCl (0.05 mol·L-1) 中测定释放行为,同时利用MC3T3-E1细胞培养评价复合材料的生物相容性。结构显示,4种比例的材料主要成分相同,电镜观察显示其中两种材料聚合性良好; 体外释放结果显示,羟基磷灰石/壳聚糖比例为60/40时表现出释放率最高,达到 (87.4 ± 2.8)%,持续时间约为120 h; 生物相容性实验显示,MC3T3-E1细胞在材料表面生长增殖良好,4天后达到密集生长状态; 材料浸出液未表现出明显的细胞毒性,4天后浸出液有促使细胞生长的作用。这些结果均表明溶葡萄球菌酶可以实现在羟基磷灰石/壳聚糖复合材料中的可控释放,且这种复合材料具有良好的生物相容性,显示出该复合材料在骨感染中的应用潜力。

     

    Abstract: Lysostaphin is highly effective on eliminating methicillin resistant Staphylococcus aureus (MRSA). In order to achieve controlled release of lysostaphin, a biocompatible drug carrier is needed. Hydroxyapatite/chitosan (HA/CS) composites were chosen to carry lysostaphin and sample composites with different weight ratios of HA to CS, including 80/20, 70/30, 60/40, and 40/60, were prepared. Multiple analyses were performed to determine the structural and physicochemical properties of the composites, including scanning electron microscopy, X-ray diffraction and Fourier transform infrared spectroscopy. We immersed HA/CS composites loaded with 1wt% lysostaphin to test in vitro release activity and cultured MC3T3-E1 cells to carry out biocompatibility test. The result of the release behavior of the composites revealed that the controlled release of lysostaphin from 60/40 HA/CS composites was the highest release rate of (87.4 ± 2.8)%, which lasted for 120 hours. In biocompatibility testing, MC3T3-E1 cells were able to proliferate on the surface of these composites, and the extract liquid from the composites could increase the growth of the cells. These results demonstrate the controlled release of lysostaphin from HA/CS composites and their biocompatibility, suggesting the potential application of these composites to bone injury and infection applications.

     

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