Department of Chemistry, Faculty of Applied Sciences, University of Sri Jayewardenepura, Gangodawila, Nugegoda, Sri Lanka.
Center for Advanced Materials Research, Faculty of Applied Sciences, University of Sri Jayewardenepura, Gangodawila, Nugegoda, Sri Lanka.
Microbiologyopen. 2019 May;8(5):e00723. doi: 10.1002/mbo3.723. Epub 2018 Sep 17.
The study aimed to determine the antibacterial/antibiofilm effect and mechanism of interaction of curcuminoids-intercalated Mg/Al layered double hydroxide (curcuminoids-LDH) against three different bacteria. Antimicrobial effect of curcuminoids-LDH nanohybrid was investigated against P. aeruginosa, S. aureus, and E. faecalis (for both standard strains and clinical isolates), using agar well diffusion method. Minimum inhibitory concentrations (MIC) of planktonic bacteria were determined using the broth microdilution method. MIC of biofilms (MBIC ) and killing time for 48 hr matured biofilms were determined by MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. Scanning electron microscopy (SEM) was used to determine pre- and postexposure architecture of biofilms. The mechanism of the antibiofilm activity of curcuminoids-LDH was determined using UV-visible spectroscopy. All tested bacteria had given a zone of inhibition in the presence of curcuminoids-LDH. The MIC values were 0.200 g/ml for P. aeruginosa, 0.025 g/ml for S. aureus, and 0.100 g/ml for E. faecalis. The 48 hr matured biofilms were reduced by curcuminoids-LDH with an MBIC of 0.100 g/ml. The minimum time to achieve MBIC was 3 hr, and the reduction was constant until 48 hr. SEM images showed a significant reduction of biofilm cell density and exopolymer matrics for all biofilms in the presence of curcuminoids-LDH. UV-visible studies revealed the antibiofilm activity of curcuminoids-LDH as due to the auto-oxidation of curcuminoids. The oxidation products are more limited in both product concentration per unit time and the variety of products, compared to pure curcuminoids, resulting in sharper UV-visible peaks than in the case of the latter. Curcuminoids-LDH has a potential antibacterial activity against P. aeruginosa, S. aureus, and E. faecalis. An antibiofilm activity has been achieved within 3 hr of the treatment. Curcuminoids released from the LDH showed the antibacterial activity due to oxidation products interfering with bacterial cell functions, and also encapsulation in the LDH causes curcuminoids to exhibit the activity in a persistent manner compared to pure curcuminoids.
这项研究旨在确定姜黄素插层镁/铝层状双氢氧化物(姜黄素-LDH)对三种不同细菌的抗菌/抗生物膜作用及其相互作用机制。采用琼脂孔扩散法研究了姜黄素-LDH 纳米杂化物对铜绿假单胞菌、金黄色葡萄球菌和粪肠球菌(包括标准株和临床分离株)的抗菌作用。使用肉汤微量稀释法测定浮游菌的最小抑菌浓度(MIC)。通过 MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴化物)测定法确定 48 小时成熟生物膜的最小生物膜抑制浓度(MBIC)和 48 小时成熟生物膜的杀灭时间。扫描电子显微镜(SEM)用于确定生物膜暴露前后的结构。通过紫外可见光谱法确定姜黄素-LDH 抗生物膜活性的机制。所有测试的细菌在存在姜黄素-LDH 的情况下都有抑制区。铜绿假单胞菌的 MIC 值为 0.200 g/ml,金黄色葡萄球菌为 0.025 g/ml,粪肠球菌为 0.100 g/ml。姜黄素-LDH 将 48 小时成熟的生物膜减少到 MBIC 为 0.100 g/ml。达到 MBIC 的最短时间为 3 小时,并且直到 48 小时为止,减少量保持恒定。SEM 图像显示,在存在姜黄素-LDH 的情况下,所有生物膜的生物膜细胞密度和胞外聚合物基质都有显著减少。紫外可见研究表明,姜黄素-LDH 的抗生物膜活性是由于姜黄素的自动氧化。与纯姜黄素相比,氧化产物在单位时间内的产物浓度和产物种类都受到限制,导致紫外可见峰比后者更尖锐。姜黄素-LDH 对铜绿假单胞菌、金黄色葡萄球菌和粪肠球菌具有潜在的抗菌活性。在治疗 3 小时内就实现了抗生物膜活性。从 LDH 中释放的姜黄素由于氧化产物干扰细菌细胞功能而表现出抗菌活性,并且与纯姜黄素相比,包封在 LDH 中使姜黄素以持续的方式表现出活性。