Laboratory of Microbiology Research, Universidade Franciscana, Andradas, 1614, Santa Maria, 97010-032, Brazil.
Post-Graduate Program in Nanosciences, Universidade Franciscana, Andradas, 1614, Santa Maria, 97010-032, Brazil.
Naunyn Schmiedebergs Arch Pharmacol. 2019 Sep;392(9):1131-1140. doi: 10.1007/s00210-019-01663-w. Epub 2019 May 11.
The glycerol monolaurate (GML) is a surfactant used in the food industry and has potent antimicrobial activity against many microorganisms; however, the use of GML is not expanded due its high melting point and poor solubility in water. The aim of the study was to produce, characterize, and evaluate in vitro the cytotoxicity of GML and GML nanocapsules. The GML nanocapsules were produced and characterized by a mean diameter, zeta potential, and polydispersity index. The cytotoxicity was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), lactate dehydrogenase (LDH) release, thiobarbituric acid reactive substances (TBARS), and hemolytic activity. The genotoxicity was verified by comet assay. The physicochemical parameters showed a mean diameter of 192.5 ± 2.8 nm, a polydispersity index of 0.061 ± 0.018, and a zeta potential about - 21.9 ± 1 mV. The viability test demonstrated the protector effect of GML nanocapsule compared with the GML on peripheral blood mononuclear cells (PBMC) and VERO cells (isolated from kidney epithelial cells extracted from an African green monkey). A reduction in lipid peroxidation and lactate dehydrogenase release in GML nanocapsule-exposed cells compared with GML treated cells was observed. The damage on erythrocytes was addressed in treatment with GML, while the treatment with GML nanocapsules did not cause an effect. Moreover, the comet assay showed that the GML-caused genotoxicity and GML nanocapsules do not demonstrate damage. The study showed the reduction of toxicity of GML nanocapsules by many methods used in antimicrobial therapy.
甘油单月桂酸酯(GML)是一种在食品工业中使用的表面活性剂,对许多微生物具有强大的抗菌活性;然而,由于其熔点高和在水中的溶解度差,GML 的使用并未得到扩展。本研究的目的是生产、表征和体外评价 GML 和 GML 纳米胶囊的细胞毒性。通过平均直径、Zeta 电位和多分散指数对 GML 纳米胶囊进行了生产和表征。通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)、乳酸脱氢酶(LDH)释放、硫代巴比妥酸反应物质(TBARS)和溶血活性评估细胞毒性。通过彗星试验验证遗传毒性。物理化学参数显示平均直径为 192.5 ± 2.8nm,多分散指数为 0.061 ± 0.018,Zeta 电位约为-21.9 ± 1mV。活力试验表明 GML 纳米胶囊对外周血单个核细胞(PBMC)和 VERO 细胞(从非洲绿猴提取的肾上皮细胞中分离)具有保护作用,与 GML 相比。与 GML 处理的细胞相比,暴露于 GML 纳米胶囊的细胞中的脂质过氧化和乳酸脱氢酶释放减少。在 GML 处理的细胞中观察到红细胞损伤,而 GML 纳米胶囊处理的细胞中没有引起这种损伤。此外,彗星试验表明 GML 引起的遗传毒性和 GML 纳米胶囊不会造成损伤。该研究表明,GML 纳米胶囊通过多种抗菌治疗方法降低了 GML 的毒性。