Department of Pharmaceutics and Drug Delivery, University of Mississippi, Oxford, Mississippi, 38677, USA.
Institute for Drug Delivery & Biomedical Research, Bangalore, India.
AAPS PharmSciTech. 2019 Jan 11;20(2):77. doi: 10.1208/s12249-019-1299-x.
Application of heat (hyperthermic conditions) on skin is known to enhance drug transfer and facilitate skin penetration of molecules. The aim of this work was to study the effect of hyperthermia on the drug release and skin permeation from nicotine transdermal patches. The drug release and skin permeation were characterized by in vitro release test and in vitro permeation test. The temperature was maintained at 32 °C as control (simulating normal physiological skin temperature) and 42 °C as hyperthermia condition. The in vitro release test was carried out using USP apparatus 5-Paddle over disk method for a transdermal patch. Skin permeation study was carried out across porcine skin using the flow through cells (PermeGear, Inc.) with an active diffusion area of 0.94 cm. Mechanistic studies (parameters such as partition coefficient, TEWL and electrical resistivity) were also performed to understand the mechanisms involved in determining the influence of hyperthermia on drug delivery from transdermal patches of nicotine. The rate and extent of drug release from nicotine patch was not significantly different at two temperatures (Cumulative release after 12 h was 43.99 ± 3.29% at 32 °C and 53.70 ± 5.14% at 42 °C). Whereas, in case of in vitro permeation studies, the nicotine transdermal permeation flux for patch was threefold higher at 42 °C (100.1 ± 14.83 μg/cm/h) than at 32 °C (33.3 ± 14.83 μg/cm/h). The mechanistic studies revealed that the predominant mechanism of enhancement of drug permeation by hyperthermia condition is by the way of increasing the skin permeability. There is a potential concern of dumping of higher dose of nicotine via transdermal route.
已知应用于皮肤的热量(高温条件)可以增强药物传递并促进分子穿透皮肤。本工作旨在研究高温对尼古丁透皮贴剂的药物释放和皮肤渗透的影响。药物释放和皮肤渗透通过体外释放试验和体外渗透试验进行表征。温度保持在 32°C 作为对照(模拟正常生理皮肤温度)和 42°C 作为高温条件。体外释放试验采用 USP 仪器 5 桨碟法进行透皮贴剂。皮肤渗透研究通过流动细胞(PermeGear,Inc.)进行,有效扩散面积为 0.94cm。还进行了机制研究(如分配系数、TEWL 和电阻率等参数),以了解确定高温对尼古丁透皮贴剂药物传递影响的机制。在两种温度下,尼古丁贴剂的药物释放速率和程度没有显著差异(12 小时后的累积释放率在 32°C 时为 43.99±3.29%,在 42°C 时为 53.70±5.14%)。然而,在体外渗透研究中,贴剂在 42°C 时的尼古丁透皮渗透通量是 32°C 时的三倍(100.1±14.83μg/cm/h 比 33.3±14.83μg/cm/h)。机制研究表明,高温条件下药物渗透增强的主要机制是通过增加皮肤通透性。通过透皮途径给予更高剂量尼古丁存在潜在的风险。