Yang Soo In, Liu Shuanghui, Brooks Geoffrey J, Lanctot Yves, Gruber James V
Botaneco Inc, Calgary, AB, Canada.
Botaneco Inc, Lambertville, NJ, USA.
J Cosmet Dermatol. 2018 Jun;17(3):518-522. doi: 10.1111/jocd.12390. Epub 2017 Aug 23.
Current in vitro SPF screening method for plant oil body (oleosome)-based SPF products possesses significant inconsistency and low reliability in the SPF rating.
The primary objective of this study was to evaluate the reliability and reproducibility of spectrophotometrically determined sun protection factor (SPF) from oleosome-based SPF products. The secondary objective was the data comparison of the spectrophotometric measurements against in vivo SPF testing to establish a reliable in vitro test method as a screening assay.
Octyl methoxycinnamate (UVB filter) and avobenzone (UVA filter) were loaded into safflower oil bodies and formulated into oil-in-water emulsion-based finished products. To evaluate the reliability between in vivo and spectrophotometric test methods, samples were dispatched to a clinical laboratory, and the reported SPF values were compared with spectrophotometric test results.
The observed SPF from the in vivo and spectrophotometric test results demonstrated a high correlation for SPF 30 products. Proportional correlation between the two evaluation methods was observed for SPF 15 and 50 products with slightly lesser accuracy with a smaller number of population tested in the clinical studies.
A reliable spectrophotometric screening method for oil body-based SPF formulas has been developed using two broadly used organic UV sunscreen actives as a case study. The results demonstrated a high level of reproducibility and reliability compared to the US FDA-guided in vivo SPF testing method.
目前用于基于植物油体(油体)的防晒系数(SPF)产品的体外SPF筛选方法在SPF评级方面存在显著的不一致性和低可靠性。
本研究的主要目的是评估基于油体的SPF产品通过分光光度法测定的防晒系数(SPF)的可靠性和可重复性。次要目的是将分光光度测量数据与体内SPF测试数据进行比较,以建立一种可靠的体外测试方法作为筛选试验。
将甲氧基肉桂酸辛酯(UVB滤光剂)和阿伏苯宗(UVA滤光剂)负载到红花油体中,并配制成水包油乳液型成品。为了评估体内和分光光度测试方法之间的可靠性,将样品送到临床实验室,并将报告的SPF值与分光光度测试结果进行比较。
体内和分光光度测试结果观察到的SPF对SPF 30产品显示出高度相关性。对于SPF 15和50产品,两种评估方法之间观察到比例相关性,但在临床研究中测试的人群数量较少,准确性略低。
以两种广泛使用的有机紫外线防晒活性成分作为案例研究,开发了一种用于基于油体的SPF配方的可靠分光光度筛选方法。结果表明,与美国食品药品监督管理局(FDA)指导的体内SPF测试方法相比,该方法具有高度的可重复性和可靠性。