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聚氧乙烯(20)山梨醇单月桂酸酯(吐温 20)的细胞/遗传毒性研究。

Cyto/Genotoxicity study of polyoxyethylene (20) sorbitan monolaurate (tween 20).

机构信息

Research Center for Pharmaceutical Nanotechnology, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

DNA Cell Biol. 2013 Sep;32(9):498-503. doi: 10.1089/dna.2013.2059. Epub 2013 Jul 11.

Abstract

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.

摘要

聚氧乙烯(20)山梨醇单月桂酸酯(吐温 20)是一种广泛用作药物制剂、食品和化妆品工业中的乳化剂和稳定剂的非离子表面活性剂。尽管许多研究表明它对靶细胞无毒影响,但仍有必要研究它对靶细胞的影响。因此,在本研究中,报告了吐温 20 的抗细胞增殖和细胞/遗传毒性作用,以探讨诱导细胞凋亡的可能机制。在 40%-50%汇合度时,将 A549 细胞和人脐静脉内皮细胞暴露于吐温 20 中,推荐浓度为 24 小时。24 小时后,为了检测细胞凋亡和 DNA 损伤,将处理后的细胞进行 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)测定、异硫氰酸荧光素(FITC)标记的 Annexin V 流式细胞术、DAPI 染色、彗星和 DNA 梯状电泳。吐温 20 降低了处理细胞的生长,呈剂量和时间依赖性,彗星试验证实了单链 DNA 的断裂。此外,DAPI 染色细胞的形态改变显示,在吐温 20 处理的细胞中,染色质明显碎裂,核内出现 DNA 环。此外,流式细胞术和 DNA 片段化测定证实了 DAPI 染色试验的结果,并表明处理细胞中发生了程序性细胞死亡(凋亡)。这些结果表明,尽管考虑到吐温 20 是一种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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