聚乳酸-羟基乙酸(PLGA)纳米颗粒增强纳米药物对万古霉素耐药粪肠球菌作用的步骤和附着条件研究

Bahare Rafian, A. Eghdami, G. Moradi
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摘要

背景:传染病仍然是世界各地最大的健康挑战之一,其次是抗生素耐药性和过度使用抗生素引起的问题。一般来说,粪肠球菌是院内感染的主要原因,也是外科溃疡感染的最常见原因。本研究考察了万古霉素纳米药物如何附着在聚乳酸-羟基乙酸(PLGA)纳米颗粒上。确定万古霉素纳米药物对降低粪便肠球菌(临床医院分离株)万古霉素耐药性的作用,并确定纳米药物的细胞毒性作用。材料与方法:本方法首先将万古霉素抗生素与PLGA纳米颗粒通过乳剂等化学过程进行附着,并将所得抗生素在耐万古霉素粪肠杆菌上进行检测。结果:本研究结果表明纳米药物与抗生素的附着是一种有效的方法,通过x射线衍射确定了纳米药物的附着是精确的。在抗生素谱法中,纳米药物对万古霉素抗生素的最小抑菌浓度(MIC)和最小杀菌浓度(MBC)均有所增加。结论:自制纳米抗菌药物的治疗效果优于耐药抗菌药物。
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Examination of the Steps and Attachment Circumstances of the Poly Lactic-co-glycolic Acid (PLGA) Nano-particle to Increase the Effect of Nanomedicine on Vancomycin-Resistant Enterococcus Faecalis
Background: Infectious diseases continue to be one of the biggest health challenges around the world, followed by problems caused by antibiotic resistance and excessive use of antibiotics. In general, Enterococcus faecalis is the main cause of nosocomial infections and is the most common cause of surgical ulcer infections. This study examines how a vancomycin nanomedicine attaches to poly lactic-co-glycolic acid (PLGA) nanoparticle. Determining the role of vancomycin nanomedicine on reducing the drug resistance of vancomycin in E. faecalis (clinical hospital isolates) and determining the cytotoxicity effects of nanomedicine. M aterials and Methods: In this method, first, attachment made through chemical processes such as emulsion between vancomycin antibiotic and a PLGA nanoparticle, and resultant antibiotic tested on vancomycin resistant E. faecalis . R es ults: The results of this study indicate that the method of nanomedicine attachment to antibiotics was an effective method and it was determined by X-ray Diffraction that the attachment was precisely performed. In the antibiogram method, the minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) of the nanomedicine increased in respect to vancomycin antibiotic. Conclusion: The results showed that produced Nano-antibiotics had a better effect than resistant antibiotics.
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