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阴离子表面活性剂引起的刺激的体外预测试验比较。

Comparison of in vitro predictive tests for irritation induced by anionic surfactants.

作者信息

Goffin V, Paye M, Piérard G E

机构信息

Department of Dermatopathology, University of Liège, Belgium.

出版信息

Contact Dermatitis. 1995 Jul;33(1):38-41. doi: 10.1111/j.1600-0536.1995.tb00445.x.

Abstract

Skin compatibility of anionic surfactants may often but not always be predicted by in vitro tests. For instance, the correlation between in vivo and in vitro data is classically hampered in the presence of magnesium. This ion is known to interfere with in vitro skin irritation predictive tests based on protein denaturation. This study was conducted to compare a recently introduced assay, corneosurfametry, with other in vitro tests including the pH-rise of bovine serum albumin, collagen swelling, and zein solubilization tests. Corneosurfametry entails collection of cyanoacrylate skin surface strippings and short contact time with surfactants, followed by staining samples with toluidine blue and basic fuchsin dyes. Measurements are made by reflectance colorimetry. Data show that irritation potentials predicted by corneosurfametry agree with those obtained by established in vivo and in vitro irritation tests. Moreover, corneosurfametry data are not artificially lowered by addition of magnesium in surfactant solutions. In conclusion, corneosurfametry should be viewed as one of the realistic predictive tests for surfactant irritancy.

摘要

阴离子表面活性剂的皮肤相容性通常但并非总是可以通过体外试验来预测。例如,在存在镁的情况下,体内和体外数据之间的相关性通常会受到阻碍。已知这种离子会干扰基于蛋白质变性的体外皮肤刺激性预测试验。本研究旨在将最近引入的一种检测方法——角质层表面活性剂测定法,与其他体外试验进行比较,这些试验包括牛血清白蛋白的pH值升高、胶原蛋白肿胀和玉米醇溶蛋白溶解试验。角质层表面活性剂测定法需要收集用氰基丙烯酸酯剥离的皮肤表面样品,并使其与表面活性剂短时间接触,然后用甲苯胺蓝和碱性品红染料对样品进行染色。通过反射比色法进行测量。数据表明,角质层表面活性剂测定法预测的刺激潜能与通过既定的体内和体外刺激试验获得的结果一致。此外,在表面活性剂溶液中添加镁不会人为降低角质层表面活性剂测定法的数据。总之,角质层表面活性剂测定法应被视为表面活性剂刺激性的一种切实可行的预测试验。

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