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Cyto/Genotoxicity Study of Polyoxyethylene (20) Sorbitan Monolaurate (Tween 20)

机译:聚氧乙烯(20)山梨糖醇单月桂酸酯(吐温20)的细胞/遗传毒性研究

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摘要

Polyoxyethylene (20) sorbitan monolaurate (tween 20) is a non-ionic surfactant that is widely used as an emulsifier and stabilizer in pharmaceutical formulations, food and cosmetic industries. Although a number of studies have showed its non-toxic impacts on target cells, still, it is essential to investigate its effect on target cells. Therefore, in the present study, the anti-cell proliferation and cyto/genotoxicity effects of tween 20 are reported to address the possible mechanism for induction of apoptosis. At 40%–50% confluency, A549 cells and human umbilical vein endothelial cells were exposed to tween 20 at a recommended concentration for 24 h. After 24 h, to detect apoptosis and DNA damage, the treated cells were subjected to 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, fluorescein isothiocyanate (FITC)-labeled annexin V flow cytometry, DAPI staining, comet, and DNA ladder assays. Tween 20 decreased the growth of treated cells dose and time dependently, and single-strand DNA cleavage has been confirmed by comet assay. In addition, morphological alteration of DAPI-stained cells showed clear fragmentation in the chromatin and DNA rings within the nucleus of tween 20-treated cells. In addition, flow cytometry and DNA fragmentation assays confirmed DAPI staining assay results and indicated the occurrence of a programmed cell death (apoptosis) in the treated cells. These results demonstrate that, despite consideration of tween 20 as a safe non-ionic surfactant, it can induce apoptosis in target cells.
机译:聚氧乙烯(20)脱水山梨糖醇单月桂酸酯(介于20之间)是一种非离子型表面活性剂,在药物制剂,食品和化妆品工业中广泛用作乳化剂和稳定剂。尽管许多研究表明其对靶细胞无毒影响,但是,研究其对靶细胞的作用仍然至关重要。因此,在本研究中,据报道吐温20的抗细胞增殖和细胞/遗传毒性作用解决了诱导凋亡的可能机制。在融合度为40%至50%的情况下,将A549细胞和人脐静脉内皮细胞以推荐浓度暴露于吐温20中24 h。 24小时后,为了检测细胞凋亡和DNA损伤,对处理过的细胞进行3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)分析,异硫氰酸荧光素(FITC)标记的膜联蛋白V流式细胞仪,DAPI染色,彗星和DNA阶梯检测。 Tween 20依赖于剂量和时间降低了处理细胞的生长,并且通过彗星分析已证实单链DNA裂解。此外,DAPI染色的细胞的形态学改变显示,吐温20处理的细胞核内的染色质和DNA环明显断裂。另外,流式细胞术和DNA片段化测定证实了DAPI染色测定结果,并表明在处理过的细胞中程序性细胞死亡(凋亡)的发生。这些结果表明,尽管将吐温20作为安全的非离子表面活性剂,但它可以诱导靶细胞凋亡。

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