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载盐酸林可霉素的磷酸钙生物材料的体外特性研究及其在骨缺损植入中的应用。

In vitro characterization of calcium phosphate biomaterial loaded with linezolid for osseous bone defect implantation.

机构信息

INSERM, U 791, Laboratoire d'Ingénierie Ostéo-Articulaire et Dentaire, LIOAD, Faculté de Chirurgie Dentaire, 1 Place A. Ricordeau, Nantes, F-44042, France.

出版信息

J Biomater Appl. 2012 Mar;26(7):811-28. doi: 10.1177/0885328210381535. Epub 2010 Sep 28.

Abstract

Osteomyelitis is a severe bone infection frequently caused by Staphylococcus aureus, which shows significant resistance to methicillin. One therapeutic treatment would be to insert a bone substitute loaded to an antibiotic, which would enable the bone to be filled while the illness is being treated. Linezolid is an oxazolidinone antibiotic with a large spectrum of action. It is effective against most Gram-positive bacteria and displays a specific mode of action. The aim of this work was to study the association of linezolid with a calcium phosphate-deficient apatite matrix. Granules containing 10% and 50% linezolid were prepared by wet granulation and characterized. Porosity analyses performed by mercury porosimetry and scanning electron microscopy revealed that grain porosity with 50% linezolid was higher than that of the grains containing 10% linezolid. NMR analyses showed no change in structure of linezolid when linked to calcium-deficient apatite. These results were confirmed by studying the antibacterial activity of linezolid, which remained proportional to the quantity of loaded linezolid, proving that the antibiotic released was active. The in vitro release time varied from 9 days for granules containing 10% linezolid to 26 days for granules containing 50% linezolid.

摘要

骨髓炎是一种严重的骨感染,通常由金黄色葡萄球菌引起,金黄色葡萄球菌对甲氧西林表现出显著的耐药性。一种治疗方法是将抗生素负载到骨替代物中插入,在治疗疾病的同时填充骨骼。利奈唑胺是一种具有广谱作用的恶唑烷酮类抗生素。它对大多数革兰氏阳性菌有效,并具有特定的作用模式。本工作旨在研究利奈唑胺与磷酸钙缺乏的磷灰石基质的结合。通过湿法制粒制备了含有 10%和 50%利奈唑胺的颗粒,并对其进行了表征。通过压汞法和扫描电子显微镜进行的孔隙率分析表明,含有 50%利奈唑胺的颗粒的颗粒孔隙率高于含有 10%利奈唑胺的颗粒。NMR 分析表明,当与缺钙磷灰石结合时,利奈唑胺的结构没有变化。通过研究利奈唑胺的抗菌活性证实了这一结果,其活性与负载的利奈唑胺的量成正比,证明释放的抗生素是有效的。体外释放时间从含有 10%利奈唑胺的颗粒的 9 天到含有 50%利奈唑胺的颗粒的 26 天不等。

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