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通过体外细胞毒性和光毒性模型评估原发性眼和皮肤刺激物:基于精氨酸的新型表面活性剂诱导刺激的体外研究方法。

Assessment of primary eye and skin irritants by in vitro cytotoxicity and phototoxicity models: an in vitro approach of new arginine-based surfactant-induced irritation.

作者信息

Benavides T, Mitjans M, Martínez V, Clapés P, Infante M R, Clothier R H, Vinardell M P

机构信息

Department Fisiologia-Divisió IV, Facultat de Farmàcia, Av. Joan XXIII s/N, 08028 Barcelona, Spain.

出版信息

Toxicology. 2004 May 3;197(3):229-37. doi: 10.1016/j.tox.2004.01.011.

DOI:10.1016/j.tox.2004.01.011
PMID:15033545
Abstract

Extensive efforts have been made, recently, to find surfactants with lower irritation potential than those presently commercially available, for use in pharmaceutical and cosmetic preparations. Cytotoxic and phototoxic effects of a novel family of dicationic arginine-diglyceride surfactant compounds, 1,2-diacyl,3-O-(l-arginyl)-rac-glycerol with alkyl chain lengths in the range from 8 to 14 carbon atoms, were compared to three commercial surfactants. The end-points used to assess toxicity were the red blood cell lysis assay and uptake of the vital dye neutral red 24h after dosing (NRU), respectively. Two immortalized cell lines, murine fibroblast cell line, 3T3, and one human keratinocyte cell line, HaCaT, were used as in vitro models to predict the potential phototoxicity which could result in irritation, determined by resazurin reduction to resorufin and neutral red uptake (NRU). All tested surfactants had cytotoxicity effects as demonstrated by and decrease of NR uptake, which showed a clear concentration-response relationship. Concentrations resulting in 50% inhibition of NR uptake (IC(50)) range from 1 microM(-1) (hexadecyl trimethyl ammonium bromide) to 565 microM(-1) (12,12-l-arginine). Erythrocyte haemolysis also showed a clear concentration-response relationship, the 50% of haemolysis ranged from 37 microM(-1) (10,10-l-arginine) to 151 microM(-1) (sodium lauryl sulphate). Phototoxicity was performed with 12,12-l-acetyl-arginine, the most stable chemical structure. The validated 3T3 NRU photoxicity assay was used and revealed a phototoxic potential.

摘要

最近,人们付出了巨大努力来寻找刺激性比目前市售产品更低的表面活性剂,用于制药和化妆品制剂。将一类新型的双阳离子精氨酸 - 甘油二酯表面活性剂化合物,即烷基链长度在8至14个碳原子范围内的1,2 - 二酰基 - 3 - O -(l - 精氨酰基)- rac - 甘油的细胞毒性和光毒性效应,与三种商业表面活性剂进行了比较。用于评估毒性的终点分别是红细胞裂解试验和给药后24小时活性染料中性红摄取(NRU)。两种永生化细胞系,小鼠成纤维细胞系3T3和一种人角质形成细胞系HaCaT,被用作体外模型来预测可能导致刺激的潜在光毒性,通过刃天青还原为试卤灵和中性红摄取(NRU)来确定。所有测试的表面活性剂都具有细胞毒性作用,表现为NR摄取减少,呈现出明显的浓度 - 反应关系。导致NR摄取50%抑制(IC(50))的浓度范围从1 microM(-1)(十六烷基三甲基溴化铵)到565 microM(-1)(12,12 - l - 精氨酸)。红细胞溶血也呈现出明显的浓度 - 反应关系,50%溶血的浓度范围从37 microM(-1)(10,10 - l - 精氨酸)到151 microM(-1)(十二烷基硫酸钠)。使用最稳定的化学结构12,12 - l - 乙酰基 - 精氨酸进行光毒性试验。采用经过验证的3T3 NRU光毒性试验,结果显示其具有光毒性潜力。

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