Yu Xiaoling, Pan Qingqing, Zheng Zongfu, Chen Yongzhong, Chen Yuyuan, Weng Shaohuang, Huang Liying
Department of Pharmaceutical Analysis, School of Pharmacy, The Higher Educational Key Laboratory for Nano Biomedical Technology of Fujian Province, Fujian Medical University Fuzhou 350122 P. R. China
Department of Pharmaceutical, Mengchao Hepatobiliary Hospital of Fujian Medical University Fuzhou 350025 China.
RSC Adv. 2018 Nov 7;8(65):37424-37432. doi: 10.1039/c8ra06659k. eCollection 2018 Nov 1.
Adequate delivery of antibiotics to infected sites is crucial for the effective treatment of bacterial infections. A controlled and sustained release system based on porous and pH-responsive poly(lactic--glycolic acid) (PLGA)-vancomycin (Van) microspheres was developed. In this system, drug release is triggered by the weakly acidic environment, like local inflamed tissues. The microspheres, developed through the W/O/W double-emulsion evaporation method, comprised a PLGA-based shell and a core containing Van and the bubble-generating agent of NaHCO. The optimized preparation conditions for PLGA-NaHCO-Van microspheres were investigated and characterized. The PLGA-NaHCO-Van microspheres exhibited porous microstructures with regular shape and uniform size and the characteristic of controlled drug release, which could be attributed to the incorporation of NaHCO. The results of the Kirby-Bauer assay confirmed that released Van retained effective antibacterial activity towards standard and methicillin-resistant (MRSA) infected clinical samples, suggesting their further promising application in local anti-infection.
将抗生素充分输送到感染部位对于有效治疗细菌感染至关重要。基于多孔且对pH敏感的聚乳酸-乙醇酸共聚物(PLGA)-万古霉素(Van)微球开发了一种控释和缓释系统。在该系统中,药物释放由弱酸性环境触发,如局部发炎组织。通过W/O/W双乳液蒸发法制备的微球由PLGA基壳和含有Van及气泡产生剂NaHCO₃的核心组成。研究并表征了PLGA-NaHCO₃-Van微球的优化制备条件。PLGA-NaHCO₃-Van微球呈现出形状规则、尺寸均匀的多孔微结构以及药物控释特性,这可归因于NaHCO₃的加入。 Kirby-Bauer试验结果证实,释放出的Van对标准菌株和耐甲氧西林金黄色葡萄球菌(MRSA)感染的临床样本仍保留有效的抗菌活性,表明它们在局部抗感染方面具有进一步的应用前景。