用白桦和白桦生物活性酚类化合物提取物合成纳米银及其抗菌活性评价

M. Kausar, B. Manjunatha, C. Purvika, Mizba Farkana
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摘要

本文研究了白桉和头桉生物活性酚类提取物的抑菌活性。以水:乙醇(1:3,v/v)为溶剂,采用氢乙醇萃取法提取酚类化合物。对乙醇提取物进行定性和红外光谱分析,以确定酚类物质的存在。采用酸水解法制备银纳米粒子,并对其进行紫外可见分光光度、SEM、TEM和XRD分析,以确定所标记的生物活性化合物为agno3。其纳米粒径分布范围在50 ~ 94 nm之间,在40 ~ 67 nm之间。采用粗酚提取物和合成纳米颗粒对大肠杆菌(ATCC®8739™)、铜绿假单胞菌(ATCC®25619™)、金黄色葡萄球菌(ATCC®6538™)、枯草芽孢杆菌(ATCC®11774™)和肺炎克雷伯菌(ATCC®13882™)5种病原菌进行抑菌活性测试。从本研究结果来看,头莲粗提物对试验病原菌的抑菌效果较好,其中铜绿假单胞菌抑菌效果最好,其次为枯草芽孢杆菌和金黄色葡萄球菌,平均抑菌范围分别为23、14和12 mm;粗提物对铜绿假单胞菌的抑制作用最强,其次是金黄色葡萄球菌和大肠杆菌,平均抑制范围分别为12、11和10 mm;枯草芽孢杆菌和肺炎克雷伯菌的平均抑制范围分别为8和7 mm。统计学分析采用单因素方差分析(One - way ANOVA)计算,p < 0.05有统计学意义。
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Synthesis of Silver Nanoparticle Using Bioactive Phenolic Compound Extracts of Leucas aspera and Leucas cephalotes and Evaluation of its Antibacterial Activity
The present study was carried out to investigate the antibacterial activity of the bioactive phenolic extract from Leucas aspera and Leucas cephalotes. The phenolic compounds were extracted using water: ethanol (1:3, v/v) by hydroethanolic extraction method. The hydroethanolic extracts were subjected to qualitative and FTIR analysis as a confirmatory step for the presence of phenolics. Synthesis of silver nanoparticle from both plants was carried out by acid hydrolysis method and subjected to UV-visible spectrophotometry, SEM, TEM and XRD analysis, for confirmation of tagged bioactive compound to AgNO3. The nanoparticle size distribution ranged between 50-94 nm in L. aspera and 40-67 nm in L. cephalotes. The antibacterial study was carried out using both crude phenolic extract and synthesized nanoparticles and tested against 5 pathogens namely Escherichia coli (ATCC® 8739™), Pseudomonas aeruginosa (ATCC® 25619™), Staphylococcus aureus (ATCC® 6538™), Bacillus subtilis (ATCC® 11774™) and Klebsiella pneumonia (ATCC® 13882™) for their antibacterial activity. From present study, the crude extract of L. cephalotes showed good antibacterial effect against test pathogen species wherein highest inhibition was observed in, P. aeruginosa, followed by B. subtilis and S. aureus with an average zone of inhibition of 23, 14 and 12 mm, E. coli and K. pneumonia measured 9 and 7 mm. The crude extract of L. aspera showed the highest inhibition in P. aeruginosa followed by S. aureus and E. coli with an average zone of inhibition of 12,11 and 10 mm B. subtilis and K. pneumonia measured 8 and 7 mm. Statistical analysis was calculated using One way ANOVA and was found to be statistically significant with p < 0.05.
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