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Antibacterial and Anticandidal Activity of the Nanostructural Composite of a Spirothiazolidine-Derivative Assembled on Silver Nanoparticles

机译:组装在银纳米颗粒上的螺噻唑烷衍生物的纳米结构复合材料的抗菌和抗念珠菌活性

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摘要

Our aims in this work are the preparation of an ionic liquid based on heterocyclic compounds with Ag nanoparticles and the investigation of its application as an antibacterial and anticandidal agent. These goals were achieved through the fabrication of an ionic liquid based on Ag nanoparticles with 5-Amino-3-(4-fluorophenyl)-N-hexadecyl-7-(4-methylphenyl)-2-H spiro[cyclohexane1,2’-[1,3]thiazolo [4,5-b]pyridine]-6-carbonitrile (P16). The nanostructure of the prepared ionic liquid was characterized using techniques such as FTIR, 1HNMR, 13CNMR, UV, SEM, and TEM. The biological activity of the prepared compound (P16) and its nanocomposites with Ag nanoparticles was tested using five clinical bacteria (Pseudomonas aeruginosa 249; Escherichia coli 141; Enterobacter cloacae 235; Staphylococcus epidermidis BC 161, and methicillin-resistant S. aureus 217), and three Candida species (Candida utilis ATCC 9255; C. tropicalis ATCC 1362, and C. albicans ATCC 20402). The FTIR, 1HNMR, and 13CNMR results confirmed the chemical structure of the synthesized P16 compound. The nanostructure of the prepared ionic liquid was determined based on data obtained from the UV, SEM, and TEM tests. The antibacterial and anticandidal results showed that the biological activity of the compound (P16) was enhanced after the formation of nanocomposite structures with Ag nanoparticles. Moreover, the biological activity of the compound itself (P16) and that of its nanocomposite structure with Ag nanoparticles was higher than that of ampicillin and amphotericin B, which were used as control drugs in this work.
机译:我们这项工作的目标是用 Ag 纳米颗粒制备基于杂环化合物的离子液体,并研究其作为抗菌和抗念珠菌剂的应用。这些目标是通过用 5-氨基-3-(4-氟苯基)-N-十六烷基-7-(4-甲基苯基)-2-H 螺[环己烷1,2'-[1,3]噻唑并[4,5-b]吡啶]-6-碳腈 (P16) 制造基于 Ag 纳米颗粒的离子液体来实现的。使用 FTIR、1HNMR、13CNMR、UV、SEM 和 TEM 等技术对制备的离子液体的纳米结构进行了表征。使用五种临床细菌(铜绿假单胞菌 249;大肠杆菌 141;阴沟肠杆菌 235;表皮葡萄球菌 BC 161 和耐甲氧西林金黄色葡萄球菌 217)和三种念珠菌属(实用念珠菌 ATCC 9255;热带念珠菌 ATCC 1362 和白色念珠菌 ATCC 20402)。FTIR、1HNMR 和 13CNMR 结果证实了合成的 P16 化合物的化学结构。根据从 UV、SEM 和 TEM 测试获得的数据确定制备的离子液体的纳米结构。抗菌和抗念珠菌结果表明,与 Ag 纳米颗粒形成纳米复合结构后,化合物 (P16) 的生物活性增强。此外,化合物本身 (P16) 及其与 Ag 纳米颗粒的纳米复合结构的生物活性高于本工作中用作对照药物的氨苄青霉素和两性霉素 B。

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