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Synthesis, characterization and improved anti bacterial activity of chitosan nanoparticles incorporated ofloxacin drug nanoconjugate

机译:氧氟沙星药物纳米结合物壳聚糖纳米粒的合成,表征及改善的抗菌活性

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The objective of the present study was to investigate enhanced anti bacterial activity of chitosan nanoparticles incorporated ofloxacin nanoconjugate against clinical isolate of human pathogenic bacteria Pseudomonas aeruginosa. Nano drug conjugate was prepared by ionotrophic gelation of chitosan with sodium tri poly phosphate and ofloxacin as the model drug. Synthesized nanoconjugate was characterized by scanning electron microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDX) and Fourier transform infrared spectroscopy (FT-IR) and the anti bacterial activity was studied against Pseudomonas aeruginosa adopting well diffusion assay with different concentration. Scanning electron microscopy of drug nanoconjugate revealed spherical particles with the size range of 60-100nm, Further confirmation with FTIR showed distinct absorbed peaks. EDX revealed all the elements in the nanoconjugate. The tested pathogenic bacteria susceptible to all the concentration with the increased zone of inhibition. This result suggests that the synergistic activity of nanoparticles with antibiotics which will lead to new generation of antimicrobial agents with highest efficacy to prevent pathogenic infection.
机译:本研究的目的是研究掺入氧氟沙星纳米缀合物的壳聚糖纳米粒对人类病原菌铜绿假单胞菌的临床分离物的增强的抗菌活性。以三聚磷酸钠和氧氟沙星为模型药物,通过壳聚糖的离子营养凝胶化制备了纳米药物偶联物。通过扫描电子显微镜(SEM),能谱X射线能谱(EDX)和傅里叶变换红外光谱(FT-IR)对合成的纳米共轭物进行了表征,并采用不同浓度的良好扩散试验研究了铜绿假单胞菌的抗菌活性。药物纳米共轭物的扫描电子显微镜显示大小范围为60-100nm的球形颗粒,FTIR进一步证实显示出明显的吸收峰。 EDX揭示了纳米共轭物中的所有元素。被测致病菌对所有浓度的细菌敏感,抑制区增加。该结果表明纳米颗粒与抗生素的协同活性将导致新一代具有最高预防病原性感染功效的抗微生物剂。

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