Evaluation of the Inhibitory Activity of Syzygium aromaticum Extract -Chitosan Nanoparticles Against Biofilm Formation of Klebsiella pneumonia

Hussein Ali shaghati, Emad Hamdi Jassim, Labib A. Kadhim AL-Zubaidi
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Abstract

The increasing resistance of Klebsiella pneumoniae to antibiotics has led to difficulties in treating infections due to its virulence factors. As one of its major pathogenic factors, this opportunistic pathogen may develop a thick biofilm coating, allowing the bacteria to attach to living or nonliving surfaces and promote drug resistance. Searching for therapeutic alternatives from a plant source that was safe and effective in treating this multi-drug-resistant bacteria was necessary. In this concept, Syzygium aromaticum extract (SAE) is used to combat K. pneumonia. The extract was confirmed by GC-MS and loaded onto chitosan nanoparticles (SACSNPs). The SACSNPs were prepared by the ionic gelation method with tripolyphosphate (TPP). And then characterized using UVvis, FTIR, AFM, SEM, and XRD techniques. The K. pneumonia isolates were obtained and identified using the VITEK-2 system. The MIC of SAE and SACSNPs were confirmed using a 96-well resazurin-aided microdilution method, which was 6.25 μg/ml for SACSNPs and 75.5 μg/ml for SAE. The inhibitory activity using sub-MIC of analytical substances was determined by measuring the optical density using a microplate reader with a 96-well plate and 0.1% crystal violet dye. The results show that the S. aromaticum extract loaded with chitosan nanoparticles has higher inhibitory activity against the biofilm formation of K. pneumonia than the S. aromaticum extract. Keywords: Chitosan nanoparticles, S. aromaticum, K. pneumonia, Biofilm, GCMS, resazurin, XRD.
丁香提取物-壳聚糖纳米颗粒对肺炎克雷伯菌生物膜形成的抑制作用评价
肺炎克雷伯菌对抗生素的耐药性日益增加,由于其毒力因素,给治疗感染带来了困难。作为其主要致病因素之一,这种机会性病原体可能会形成一层厚厚的生物膜涂层,使细菌能够附着在生物或非生物表面并促进耐药性。从植物源中寻找安全有效的治疗方法来治疗这种多重耐药细菌是必要的。在这个概念中,Syzygium aromaticum提取物(SAE)被用来对抗克雷伯氏肺炎。采用气相色谱-质谱法对提取液进行确证,并将其负载于壳聚糖纳米颗粒(sacsnp)上。用三聚磷酸盐(TPP)离子凝胶法制备了sacsnp。然后用UVvis, FTIR, AFM, SEM和XRD等技术对其进行了表征。肺炎克雷伯菌分离株采用VITEK-2系统进行鉴定。采用96孔reazurin辅助微量稀释法确定SAE和sacsnp的MIC, sacsnp为6.25 μg/ml, SAE为75.5 μg/ml。利用亚mic测定分析物质的抑制活性,采用96孔板和0.1%结晶紫染料的微孔板读卡器测定光密度。结果表明,载壳聚糖颗粒的香薷提取物对肺炎链球菌生物膜形成的抑制活性高于香薷提取物。关键词:壳聚糖纳米颗粒,芳香梭菌,肺炎梭菌,生物膜,GCMS,复蓝脲,XRD
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