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用于治疗骨髓炎的载万古霉素纳米羟基磷灰石基支架:兔体内毒理学试验及绵羊模型体内疗效试验

Vancomycin-Loaded, Nanohydroxyapatite-Based Scaffold for Osteomyelitis Treatment: In Vivo Rabbit Toxicological Tests and In Vivo Efficacy Tests in a Sheep Model.

作者信息

Alegrete Nuno, Sousa Susana R, Padrão Tatiana, Carvalho Ângela, Lucas Raquel, Canadas Raphael F, Lavrador Catarina, Alexandre Nuno, Gärtner Fátima, Monteiro Fernando J, Gutierres Manuel

机构信息

i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, R. Alfredo Allen 208, 4200-135 Porto, Portugal.

FMUP-Faculdade de Medicina, Universidade do Porto, Alameda Prof. Hernâni Monteiro, 4200-319 Porto, Portugal.

出版信息

Bioengineering (Basel). 2023 Feb 4;10(2):206. doi: 10.3390/bioengineering10020206.

Abstract

The treatment for osteomyelitis consists of surgical debridement, filling of the dead space, soft tissue coverage, and intravenous administration of antimicrobial (AM) agents for long periods. Biomaterials for local delivery of AM agents, while providing controllable antibiotic release rates and simultaneously acting as a bone scaffold, may be a valuable alternative; thus, avoiding systemic AM side effects. V-HEPHAPC is a heparinized nanohydroxyapatite (nHA)/collagen biocomposite loaded with vancomycin that has been previously studied and tested in vitro. It enables a vancomycin-releasing profile with an intense initial burst, followed by a sustained release with concentrations above the Minimum Inhibitory Concentration (MIC) for MRSA. In vitro results have also shown that cellular viability is not compromised, suggesting that V-HEPHAPC granules may be a promising alternative device for the treatment of osteomyelitis. In the present study, V-HEPHAPC (HEPHAPC with vancomycin) granules were used as a vancomycin carrier to treat MRSA osteomyelitis. First, in vivo Good Laboratory Practice (GLP) toxicological tests were performed in a rabbit model, assuring that HEPHAPC and V-HEPHAPC have no relevant side effects. Second, V-HEPHAPC proved to be an efficient drug carrier and bone substitute to control MRSA infection and simultaneously reconstruct the bone cavity in a sheep model.

摘要

骨髓炎的治疗包括手术清创、填充死腔、软组织覆盖以及长期静脉注射抗菌药物。用于局部递送抗菌药物的生物材料,在提供可控抗生素释放速率的同时还能充当骨支架,可能是一种有价值的替代方案;因此,可以避免全身使用抗菌药物的副作用。V-HEPHAPC是一种负载万古霉素的肝素化纳米羟基磷灰石(nHA)/胶原蛋白生物复合材料,此前已在体外进行过研究和测试。它能实现万古霉素的释放曲线,初期有强烈的突释,随后是持续释放,浓度高于耐甲氧西林金黄色葡萄球菌(MRSA)的最低抑菌浓度(MIC)。体外实验结果还表明,细胞活力未受影响,这表明V-HEPHAPC颗粒可能是治疗骨髓炎的一种有前景的替代装置。在本研究中,V-HEPHAPC(含万古霉素的HEPHAPC)颗粒被用作万古霉素载体来治疗MRSA骨髓炎。首先,在兔模型中进行了体内良好实验室规范(GLP)毒理学试验,确保HEPHAPC和V-HEPHAPC没有相关副作用。其次,在绵羊模型中,V-HEPHAPC被证明是一种有效的药物载体和骨替代物,可控制MRSA感染并同时重建骨腔。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8c8/9952702/ef45ae90c0fe/bioengineering-10-00206-g001.jpg

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