Schons Aline B, Appelt Patrícia, Correa Jamille S, Cunha Mário A A, Rodrigues Mauricio G, Anaissi Fauze J
Department of Chemistry, Universidade Estadual do Centro-Oeste, Guarapuava 85040-167, Brazil.
Department of Chemistry, Universidade Tecnológica Federal do Paraná, Pato Branco 85503-390, Brazil.
Antibiotics (Basel). 2023 Mar 4;12(3):514. doi: 10.3390/antibiotics12030514.
The growing concern about the emergence of increasingly antibiotic-r4esistant bacteria imposes the need to search and develop drugs to combat these microorganisms. This, combined with the search for low-cost synthesis methods, was the motivation for the elaboration of this work. Abietic acid present in the resin of was used to generate a sodium salt by salification. The synthesis route was low-cost, consisting of only two reaction steps at mild temperatures without toxic organic solvents, and eco-friendly and easy to conduct on an industrial scale. Sodium abietate (Na-C20H29O2) was characterized by mass spectrometry, infrared spectroscopy, elemental analysis, X-ray diffraction, scanning electron microscopy, and energy-dispersive spectroscopy. To perform the antimicrobial tests, the determination of minimum inhibitory concentration and the disk diffusion assay was performed. The results obtained showed that the salt Na abietate performed an antimicrobial action against the bacterial strains , , , and Typhimurium and the yeast . The disk diffusion test showed a high inhibition potential against compared to the standard antimicrobial tetracycline, as an inhibition index of 1.17 was found. For the other bacterial strains, the inhibition values were above 40%. The MIC test showed promising results in the inhibition of , , and , indicating bacteriostatic activity against the first microorganism and bactericidal and fungicidal activities against the others. Therefore, the results showed the action of Na abietate as a possible effective antimicrobial drug, highlighting its sustainability within a circular economy.
对日益增多的抗生素耐药细菌出现的日益关注,使得有必要寻找和开发对抗这些微生物的药物。这一点,再加上对低成本合成方法的探索,是开展这项工作的动机。从[具体来源]树脂中提取的枞酸通过成盐反应生成钠盐。该合成路线成本低,仅由两个在温和温度下进行的反应步骤组成,无需使用有毒有机溶剂,且环保且易于在工业规模上进行。通过质谱、红外光谱、元素分析、X射线衍射、扫描电子显微镜和能量色散光谱对枞酸钠(Na - C₂₀H₂₉O₂)进行了表征。为进行抗菌测试,开展了最低抑菌浓度测定和纸片扩散法试验。所得结果表明,枞酸钠盐对[具体细菌菌株]、鼠伤寒沙门氏菌和酵母[具体酵母菌株]表现出抗菌作用。纸片扩散试验表明,与标准抗菌药物四环素相比,其对[具体细菌菌株]具有较高的抑制潜力,因为发现其抑制指数为1.17。对于其他细菌菌株,抑制值均高于40%。最低抑菌浓度测试在抑制[具体细菌菌株]、[具体细菌菌株]和[具体细菌菌株]方面显示出有前景的结果,表明对第一种微生物具有抑菌活性,对其他微生物具有杀菌和杀真菌活性。因此,结果表明枞酸钠作为一种可能有效的抗菌药物具有作用,突出了其在循环经济中的可持续性。