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首页> 外文期刊>Nano science & nano technology: an Indian journal >Can penicillin-bound nanoparticles restore the activity of ????-lactam antibiotics against methicillin-resistant staphylococcus aureus?
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Can penicillin-bound nanoparticles restore the activity of ????-lactam antibiotics against methicillin-resistant staphylococcus aureus?

机译:结合青霉素的纳米颗粒能否恢复β-内酰胺抗生素对耐甲氧西林的金黄色葡萄球菌的活性?

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摘要

Loss of effectiveness of commonly used antibiotics such as penicillin and other â-lactam drugs against MRSA lead to calling for immediate need for improvement in drug design, discovery, and delivery. The application of nanotechnology to drug delivery system is widely expected to change the landscape of pharmaceutical and biotechnology industries for foreseeable future, where nanoparticles represent a very promising chitosan approach to this aim. The aim of this work was to assess whether penicillin-bound chitosan nanoparticles will display antibacterial activity against MRSA and to determine the bioactivity of penicillin-bound nanoparticles. Chitosan nanoparticles were prepared by iontogelation method and penicllin were loaded during processing of nanoparticles by incorporation method. Prepared nanoparticles were characterized using transmission electron microscope, particle size analyzer and drug encapsulation efficiency. Staphylococcus aureus isolates were subjected to oxacillin and cefoxitin disc diffusion method, and PCR for detection of mecA gene or identification ofMRSA andMSSA isolates. FiftyMRSA and 30 MSSA were selected and further tested. Determination of penicillin and penicillin-bound chitosan nanoparticles MIC by broth microdilution method was performed. All MRSA isolates were resistant to penicillin using both methods. As for the MSSA isolates, using penicillin- bound chitosan nanoparticles, none displayed resistance at a dilution of eÂ?? 512 µg/ml (0.0%), ten (33%) revealed an MIC of eÂ?? 16 µg/ml, whereas 7 revealed an MIC of 16 µg/ml. It was observed that 3 isolates (10%) of MSSA turned sensitive to penicillin when performing the MIC broth microdilution test, using penicillin-bound chitosan nanoparticles. Though 27 MSSA isolate remained resistant; yet the MIC of penicillinbound chitosan nanoparticles was significantly reduced. In conclusion, penicillin-bound chitosan nanoparticles was effective only with MSSA producing penicillinase in reducing MIC of penicillin or even making MSSA sensitive to penicillin. But with MRSA, penicillin-bound chitosan nanoparticles gave no effect.
机译:常用的抗生素(例如青霉素和其他β-内酰胺类药物)对MRSA的有效性下降导致迫切需要改进药物设计,发现和交付。纳米技术在药物输送系统中的应用在可预见的将来有望改变制药和生物技术行业的格局,纳米颗粒代表了实现这一目标的非常有希望的壳聚糖方法。这项工作的目的是评估与青霉素结合的壳聚糖纳米颗粒是否会表现出对MRSA的抗菌活性,并确定与青霉素结合的纳米颗粒的生物活性。通过离子凝胶法制备了壳聚糖纳米颗粒,并通过掺入法在纳米颗粒加工过程中加载了青霉素。使用透射电子显微镜,粒度分析仪和药物包封效率对制备的纳米颗粒进行表征。对金黄色葡萄球菌分离株进行奥沙西林和头孢西丁圆盘扩散法检测,并进行PCR检测mecA基因或鉴定MRSA和MSSA分离株。选择了FiftyMRSA和30个MSSA并进行了进一步测试。肉汤微稀释法测定青霉素和与青霉素结合的壳聚糖纳米粒MIC。使用这两种方法,所有MRSA分离株均对青霉素具有抗性。至于MSSA分离株,使用青霉素结合的壳聚糖纳米颗粒,没有显示出在稀释后的抗性? 512 µg / ml(0.0%),十(33%)的MIC为eÂ?? 16 µg / ml,而7显示MIC为16 µg / ml。观察到,当使用结合青霉素的壳聚糖纳米粒子进行MIC肉汤微稀释测试时,有3个MSSA分离株(10%)对青霉素敏感。尽管有27种MSSA分离株仍具有抗性;然而,青霉素结合的壳聚糖纳米颗粒的MIC显着降低。总之,与青霉素结合的壳聚糖纳米颗粒仅对产生青霉素酶的MSSA有效降低青霉素的MIC甚至使MSSA对青霉素敏感。但是,对于MRSA,与青霉素结合的壳聚糖纳米颗粒没有作用。

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