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防晒霜体外光谱学:在 UVA 防护评估中的应用及与体内持久性色素沉着的相关性。

Sunscreen in vitro spectroscopy: application to UVA protection assessment and correlation with in vivo persistent pigment darkening.

机构信息

Lancaster - Coty, International Research & Development Centre, Athos Palace MC 98000, Monaco.

出版信息

Int J Cosmet Sci. 2002 Apr;24(2):63-70. doi: 10.1046/j.1467-2494.2002.00130.x.

Abstract

In the present study, we have described an in vitro spectroscopic method to evaluate the sunscreen products for UVA sun protection factor. The roughened PMMA plates have been used as a transparent substrate on to which the test product is spread. The UVA protection factors have been deduced from the UV-transmittance data measured in the UVA area. In order to be as close as possible to the in vivo protection factors, issued from the PPD end-point, the treated polymethylmethacrylate (PMMA) plates are submitted to different UV-irradiation doses, before the measurement. The correlation in vitro/in vivo is poor when the sunscreens are not irradiated. A UV dose of about 2 minimal pigmenting dose (MPD) is enough to achieve a good correlation between in vitro and in vivo data issued from the 13 tested sunscreens. These results are consistent with the fact that the photostability of sunscreens is challenged during an in vivo PPD test.

摘要

在本研究中,我们描述了一种用于评估防晒产品 UVA 防晒因子的体外分光光度法。将粗糙化的 PMMA 板用作透明基底,将测试产品涂覆在其上。通过测量 UVA 区域的紫外线透过率来推导 UVA 保护因子。为了尽可能接近由 PPD 终点得出的体内保护因子,在测量之前,将处理过的聚甲基丙烯酸甲酯(PMMA)板暴露于不同的紫外线剂量下。当防晒霜未受到照射时,体外/体内相关性较差。大约 2 个最小色素沉着剂量(MPD)的紫外线剂量足以实现 13 种测试防晒霜的体外和体内数据之间的良好相关性。这些结果与防晒霜的光稳定性在体内 PPD 测试中受到挑战的事实一致。

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