Hamadeh Abdullah, Troutman John, Edginton Andrea N
School of Pharmacy, University of Waterloo, Kitchener, ON N2G 1C5, Canada.
The Procter & Gamble Company, Global Product Stewardship, Mason, OH 45040, USA.
Pharmaceutics. 2021 May 28;13(6):807. doi: 10.3390/pharmaceutics13060807.
Systemic disposition of dermally applied chemicals is often formulation-dependent. Rapid evaporation of the vehicle can result in crystallization of active compounds, limiting their degree of skin penetration. In addition, the choice of vehicle can affect the permeant's degree of penetration into the stratum corneum. The aim of this study is to build a predictive, mechanistic, dermal absorption model that accounts for vehicle-specific effects on the kinetics of permeant transport into skin. An existing skin penetration model is extended to explicitly include the effect of vehicle volatility over time. Using in vitro measurements of skin penetration by chemicals applied in both a saline and an ethanol solvent, the model is optimized to learn two vehicle-specific quantities: the solvent evaporation rate and the extent of permeant deposition into the upper stratum corneum immediately following application. The dermal disposition estimates of the trained model are subsequently compared against those of the original model using further in vitro measurements. The trained model showed a 1.5-fold improvement and a 19-fold improvement in overall goodness of fit among compounds tested in saline and ethanol solvents, respectively. The proposed model structure can thus form a basis for in vitro to in vivo extrapolations of dermal disposition for skin formulations containing volatile components.
经皮肤施用的化学物质的全身分布通常取决于配方。载体的快速蒸发会导致活性化合物结晶,限制其皮肤渗透程度。此外,载体的选择会影响渗透剂对角质层的渗透程度。本研究的目的是建立一个预测性的、基于机制的皮肤吸收模型,该模型考虑载体对渗透剂向皮肤转运动力学的特定影响。现有的皮肤渗透模型被扩展以明确包括载体随时间的挥发性影响。利用在盐水和乙醇溶剂中施用化学物质后皮肤渗透的体外测量结果,对模型进行优化以了解两个特定于载体的量:溶剂蒸发速率和施用后立即向上层角质层中渗透剂沉积的程度。随后使用进一步的体外测量结果将训练模型的皮肤分布估计值与原始模型的估计值进行比较。在盐水和乙醇溶剂中测试的化合物中,训练模型的整体拟合优度分别提高了1.5倍和19倍。因此,所提出的模型结构可为含有挥发性成分的皮肤制剂的皮肤分布从体外到体内的外推提供基础。