Research & Development Division, Mikasa Seiyaku Co. Ltd, Nerima-ku, Tokyo, Japan.
Pharm Dev Technol. 2010 Dec;15(6):658-65. doi: 10.3109/10837450.2010.516437. Epub 2010 Oct 1.
The dispositions and pharmacokinetic parameters of non-steroidal anti-inflammatory drugs (NSAIDs) after patch applications have typically been evaluated on a whole-skin basis, and the detailed permeation profiles remain unclear. The aim of this study was to establish a new method for clearly analyzing the flow of drugs in the skin layers and evaluating the drug levels in the target area of the skin tissue.
The skin tissue areas where flurbiprofen and ketoprofen patches were applied were cut into 20 μm-thick lateral slices from the surface to the deepest layer and the drug concentrations in the slices were measured.
The results revealed the presence of depth-dependent concentration gradients from the surface to the deep layer and that the drug concentration in the deepest layer was less than one tenth of the surface concentration for both flurbiprofen and ketoprofen. In addition, flurbiprofen yielded higher and more rapid concentrations in the deepest skin layer adjacent to the intramuscular tissue.
The present data suggest that our technique involving lateral slicing of skin tissues and measurement of drug concentrations allows visual understanding of drug dispositions in the skin layers and makes it possible to evaluate the drug levels in the target area of the skin tissue.
贴剂应用后,非甾体抗炎药(NSAIDs)的处置和药代动力学参数通常基于整个皮肤进行评估,其详细的渗透情况仍不清楚。本研究旨在建立一种新方法,以清楚地分析药物在皮肤层中的流动,并评估皮肤组织靶区的药物水平。
将氟比洛芬和酮洛芬贴剂应用的皮肤组织区域从表面到最深处切成 20μm 厚的侧切片,并测量切片中的药物浓度。
结果表明,从表面到深层存在浓度梯度,氟比洛芬和酮洛芬在最深层的药物浓度均不到表面浓度的十分之一。此外,氟比洛芬在与肌肉组织相邻的最深皮肤层中产生更高和更快的浓度。
本研究数据表明,我们的皮肤组织横向切片和药物浓度测量技术可以直观地了解药物在皮肤层中的分布情况,并能够评估皮肤组织靶区的药物水平。