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纳米偶联万古霉素体外抗耐药金黄色葡萄球菌的活性。

In vitro antimicrobial activity of nanoconjugated vancomycin against drug resistant Staphylococcus aureus.

机构信息

Immunology and Microbiology Laboratory, Department of Human Physiology with Community Health, Vidyasagar University, Midnapore 721102, West Bengal, India.

出版信息

Int J Pharm. 2012 Oct 15;436(1-2):659-76. doi: 10.1016/j.ijpharm.2012.07.033. Epub 2012 Jul 25.


DOI:10.1016/j.ijpharm.2012.07.033
PMID:22841851
Abstract

The mounting problem of antibiotic resistance of Staphylococcus aureus has prompted renewed efforts toward the discovery of novel antimicrobial agents. The present study was aimed to evaluate the in vitro antimicrobial activity of nanoconjugated vancomycin against vancomycin sensitive and resistant S. aureus strains. Folic acid tagged chitosan nanoparticles are used as Trojan horse to deliver vancomycin into bacterial cells. In vitro antimicrobial activity of nanoconjugated vancomycin against VSSA and VRSA strains was determined by minimum inhibitory concentration, minimum bactericidal concentration, tolerance and disc agar diffusion test. Cell viability and biofilm formation was assessed as indicators of pathogenicity. To establish the possible antimicrobial mechanism of nanoconjugated vancomycin, the cell wall thickness was studied by TEM study. The result of the present study reveals that nano-sized vehicles enhance the transport of vancomycin across epithelial surfaces, and exhibits its efficient drug-action which has been understood from studies of MIC, MBC, DAD of chitosan derivative nanoparticle loaded with vancomycin. Tolerance values distinctly showed that vancomycin loaded into nano-conjugate is very effective and has strong bactericidal effect on VRSA. These findings strongly enhanced our understanding of the molecular mechanism of nanoconjugated vancomycin and provide additional rationale for application of antimicrobial therapeutic approaches for treatment of staphylococcal pathogenesis.

摘要

金黄色葡萄球菌的抗生素耐药问题日益严重,促使人们重新努力寻找新的抗菌药物。本研究旨在评估纳米偶联万古霉素对万古霉素敏感和耐药金黄色葡萄球菌菌株的体外抗菌活性。叶酸标记壳聚糖纳米粒被用作特洛伊木马将万古霉素递送入细菌细胞。通过最小抑菌浓度、最小杀菌浓度、耐受性和圆盘琼脂扩散试验测定纳米偶联万古霉素对 VSSA 和 VRSA 菌株的体外抗菌活性。细胞活力和生物膜形成被评估为致病性的指标。为了确定纳米偶联万古霉素的可能抗菌机制,通过 TEM 研究研究了细胞壁厚度。本研究结果表明,纳米载体增强了万古霉素穿过上皮表面的转运,并表现出其高效的药物作用,这从对壳聚糖衍生物纳米粒载万古霉素的 MIC、MBC、DAD 的研究中得到了理解。耐受性值明显表明,负载到纳米偶联物中的万古霉素非常有效,对 VRSA 具有很强的杀菌作用。这些发现极大地增强了我们对纳米偶联万古霉素的分子机制的理解,并为应用抗菌治疗方法治疗葡萄球菌病提供了更多的依据。

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In vitro antimicrobial activity of nanoconjugated vancomycin against drug resistant Staphylococcus aureus.

Int J Pharm. 2012-7-25

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