Institut Dr. Schrader Hautphysiologie, Holzminden, Germany. Mathias.Rohr @ Schrader-Institute.de
Skin Pharmacol Physiol. 2010;23(4):201-12. doi: 10.1159/000292777. Epub 2010 Mar 9.
In the past, several attempts have been made to develop in vitro methods for determining protection against UV radiation. To date however, there is no broadly accepted method. Various known and unknown parameters influence the transmission measurements of scattering films, such as the multifaceted compositions of sunscreens, the technical limitations of measurement devices as well as the difficulty to apply very thin films of sunscreen in a reproducible manner throughout different laboratories. In vitro data were measured in this multicenter study to compare possible methodologies and strategies for an in vitro approach to the sun protection factor (SPF). This publication will not present a final in vitro SPF test method, but it will point out which technical side effects may influence such a method. Influential factors such as the quality of spectrophotometer used, the amount of product applied, pretreatment of samples, time and temperature of equilibration, size of the measured surface, the application process or the calculation on the basis of standardized data are presented and discussed. Finally, a reduction of the standard deviations within single laboratories could be realized for in vitro SPF testing, but no improvement of the interlaboratory comparison was obtained. The development of a valid and reliable SPF in vitro test still remains a challenge, and further work is necessary to develop a satisfactory method.
过去,人们曾多次尝试开发用于测定紫外线防护的体外方法。然而,到目前为止,还没有被广泛接受的方法。各种已知和未知的参数会影响散射膜的透射测量,例如防晒霜的多方面成分、测量设备的技术限制以及在不同实验室中以可重复的方式应用非常薄的防晒霜的困难。本多中心研究中测量了体外数据,以比较用于防晒因子(SPF)的体外方法的可能方法和策略。本出版物不会提出最终的体外 SPF 测试方法,但它将指出哪些技术副作用可能会影响这种方法。本研究介绍并讨论了有影响的因素,例如所用分光光度计的质量、使用的产品量、样品预处理、平衡的时间和温度、测量表面的大小、应用过程或基于标准化数据的计算。最终,可以实现体外 SPF 测试中单个实验室的标准偏差降低,但未能提高实验室间的可比性。开发有效的和可靠的体外 SPF 测试仍然是一个挑战,需要进一步的工作来开发令人满意的方法。