新型抗生素洗脱生物包膜预防CIED感染的临床前评价。

Frontiers in drug delivery Pub Date : 2024-09-10 eCollection Date: 2024-01-01 DOI:10.3389/fddev.2024.1441956
Zerelda Esquer Garrigos, John N Catanzaro, Daniel Deegan, Ji Zhang, M Rizwan Sohail
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引用次数: 0

摘要

感染风险仍然是心血管植入式电子设备的一个重要问题,需要开发新的策略。本研究探讨了一种新型抗生素洗脱生物包膜的功效,该生物包膜旨在通过局部抗生素递送来降低感染风险,同时保留生物基质的再生特性。抗生素,利福平和米诺环素,通过聚合物光盘释放,确保延长药物释放。利用已建立的新西兰大白兔感染模型,该研究评估了对革兰氏阳性菌株的性能,包括与CIED感染相关的常见病原体,如金黄色葡萄球菌和表皮葡萄球菌,以及革兰氏阴性菌株。结果显示出很强的抗菌活性,可以完全根除细菌菌落,并且所有菌株的定植量都减少了6倍以上。药代动力学分析显示,植入部位的局部抗生素浓度可维持长达14天,而全身暴露最少,证明了局部给药的优势。与对照组相比,抗生素生物包膜组的健康状况明显改善,没有感染迹象或体温异常。尸检后的肉眼检查证实,在接受抗生素生物包膜的动物植入部位没有感染。在再生基质中结合局部抗生素递送使抗生素生物包膜成为预防cied相关感染的有希望的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Preclinical evaluation of a novel antibiotic-eluting BioEnvelope for CIED infection prevention.

Preclinical evaluation of a novel antibiotic-eluting BioEnvelope for CIED infection prevention.

Preclinical evaluation of a novel antibiotic-eluting BioEnvelope for CIED infection prevention.

Preclinical evaluation of a novel antibiotic-eluting BioEnvelope for CIED infection prevention.

The risk of infection remains a significant concern with cardiovascular implantable electronic devices, necessitating the development of new strategies. This study explores the efficacy of a novel antibiotic-eluting biologic envelope designed to mitigate infection risk through localized antibiotic delivery while preserving the regenerative properties of biological matrix. Antibiotics, rifampin and minocycline, are released through polymer discs, ensuring extended drug release. Utilizing an established model of infection in a New Zealand White rabbit, the study assessed performance against Gram-positive bacterial strains, including common pathogens such as Staphylococcus aureus and S. epidermidis associated with CIED infections, and Gram-negative bacterial strains. Results demonstrated strong antibacterial activity, achieving complete eradication of bacterial colonies and greater than 6-log reductions in colonization for all strains. Pharmacokinetic analysis revealed sustained local antibiotic concentrations at the implantation site for up to 14 days, with minimal systemic exposure, demonstrating the advantages of localized drug delivery. Health outcomes in the antibiotic bioenvelope group were significantly improved, with no signs of infection or abnormal body temperatures, in contrast to the control group. Macroscopic examinations post-necropsy confirmed the absence of infection at the implantation sites of animals receiving the antibiotic bioenvelope. The combination of localized antibiotic delivery in a regenerative matrix positions the antibiotic bioenvelope as a promising solution for preventing CIED-related infections.

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