Kasting Gerald B, Miller Matthew A, Bhatt Varsha D
James L. Winkle College of Pharmacy, University of Cincinnati Academic Health Center, Cincinnati, Ohio 45267-0004, USA.
J Occup Environ Hyg. 2008 Oct;5(10):633-44. doi: 10.1080/15459620802304245.
The disposition of N,N-diethyl-3-methylbenzamide (DEET) applied to split-thickness human cadaver skin was measured in modified Franz cells maintained at 32 degrees C and fitted with a vapor trap. Ethanolic solutions of DEET (1% w/w) spiked with (14)C radiolabel were applied to skin at a dose of 10 microL per cell, corresponding to a DEET dose of 127 microg/cm(2). Room air was drawn over the skin at velocities ranging from 10-100 mL/min. Evaporation of radiolabel from the skin surface and absorption into the receptor solution were monitored for 24 hr post-dose. The percentage of radioactivity collected in the vapor trap after 24 hr increased with airflow, ranging from 16 +/- 4% at 10 mL/min to 59 +/- 7% at 70 mL/min. The percentage of radioactivity absorbed through the skin after 24 hours decreased with increasing airflow, ranging from 69 +/- 7% at 10 mL/min to 20 +/- 1% at 80 mL/min. Tissue retention after 24 hr was 6-14% of the radioactive dose with no clear correlation to airflow. This data as well as DEET absorption data from two previous in vitro studies in which dose and location (fume hood or bench top) was varied were analyzed in terms of a recently developed diffusion/evaporation model for skin implemented on an Excel spreadsheet. A priori model calculations based on independently estimated transport parameters (Model 1) were compared with calculations based on fitted parameters (Models 2 and 3). The analysis of the combined dataset (n = 272 observations) showed that the Model 1 estimates matched the cumulative disposition profiles to within a root mean square error of 12.4% of the applied dose (r(2) = 0.65), whereas the Model 2 and Model 3 fits matched to within 9.4% (r(2) = 0.80) and 6.5% (r(2) = 0.91), respectively. The Model 3 fits were obtained using a concentration-dependent diffusivity of DEET in the stratum corneum, the value of which increased 3.4-fold between low concentrations and saturation. This result was consistent with the mild skin penetration enhancement effect for DEET reported elsewhere. [Supplementary materials are available for this article. Go to the publisher's online edition of Journal of Occupational and Environmental Hygiene for the following free supplemental resource: a word document containing tables and figures including more information on the spreadsheet skin absorption model.]
在保持于32摄氏度并配备有蒸汽阱的改良Franz扩散池内,测定了涂抹于人类断层尸体皮肤的N,N - 二乙基 - 3 - 甲基苯甲酰胺(避蚊胺,DEET)的分布情况。将添加了¹⁴C放射性标记物的避蚊胺乙醇溶液(1% w/w)以每个扩散池10微升的剂量涂抹于皮肤上,这相当于避蚊胺剂量为127微克/平方厘米。以10 - 100毫升/分钟的流速使室内空气流经皮肤。给药后24小时监测放射性标记物从皮肤表面的蒸发以及其向受体溶液中的吸收情况。24小时后收集在蒸汽阱中的放射性百分比随气流增加而升高,范围从10毫升/分钟时的16±4%到70毫升/分钟时的59±7%。24小时后经皮肤吸收的放射性百分比随气流增加而降低,范围从10毫升/分钟时的69±7%到80毫升/分钟时的20±1%。24小时后组织滞留量为放射性剂量的6 - 14%,与气流无明显相关性。这些数据以及之前两项体外研究中避蚊胺吸收数据(其中剂量和位置(通风橱或实验台)有所变化)依据一个最近开发的、在Excel电子表格上实现的皮肤扩散/蒸发模型进行了分析。将基于独立估计的转运参数的先验模型计算(模型1)与基于拟合参数的计算(模型2和模型3)进行了比较。对合并数据集(n = 272个观测值)的分析表明,模型1的估计值与累积分布曲线的匹配程度在应用剂量的均方根误差12.4%以内(r² = 0.65),而模型2和模型3的拟合分别在9.4%(r² = 0.80)和6.5%(r² = 0.91)以内。模型3的拟合是使用避蚊胺在角质层中浓度依赖性扩散系数获得的,其值在低浓度和饱和浓度之间增加了3.4倍。这一结果与其他地方报道的避蚊胺对皮肤渗透的轻微增强作用一致。[本文提供补充材料。前往《职业与环境卫生杂志》出版商的在线版本获取以下免费补充资源:一个包含表格和图表的Word文档,其中包括关于电子表格皮肤吸收模型的更多信息。]