首页> 外文期刊>Analytical and bioanalytical chemistry >MALDI imaging facilitates new topical drug development process by determining quantitative skin distribution profiles
【24h】

MALDI imaging facilitates new topical drug development process by determining quantitative skin distribution profiles

机译:马尔迪成像通过确定定量皮肤分布型材来促进新的局部药物开发过程

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Generation of skin distribution profiles and reliable determination of drug molecule concentration in the target region are crucial during the development process of topical products for treatment of skin diseases like psoriasis and atopic dermatitis. Imaging techniques like mass spectrometric imaging (MSI) offer sufficient spatial resolution to generate meaningful distribution profiles of a drug molecule across a skin section. In this study, we use matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) to generate quantitative skin distribution profiles based on tissue extinction coefficient (TEC) determinations of four different molecules in cross sections of human skin explants after topical administration. The four drug molecules: roflumilast, tofacitinib, ruxolitinib, and LEO 29102 have different physicochemical properties. In addition, tofacitinib was administrated in two different formulations. The study reveals that with MALDI-MSI, we were able to observe differences in penetration profiles for both the four drug molecules and the two formulations and thereby demonstrate its applicability as a screening tool when developing a topical drug product. Furthermore, the study reveals that the sensitivity of the MALDI-MSI techniques appears to be inversely correlated to the drug molecules’ ability to bind to the surrounding tissues, which can be estimated by their Log D values. Graphical abstract.
机译:皮肤分布型材的产生和可靠测定目标区域中的药物分子浓度在局部产品的开发过程中是至关重要的,用于治疗牛皮癣和特应性皮炎等皮肤疾病。像质谱成像(MSI)等成像技术提供足够的空间分辨率,以在皮肤部分产生药物分子的有意义的分布型材。在该研究中,我们使用基于组织消光系数(TEC)在局部给药后的人体皮肤外,基于组织消光系数(TEC)的组织消光系数(TEC)测定来产生定量皮肤分布型材的定量皮肤分布谱。四种药物分子:Roflumilast,Tofacitinib,Raxolitinib和Leo 29102具有不同的物理化学性质。此外,TOFACITINIB在两种不同的配方中施用。该研究表明,通过MALDI-MSI,我们能够观察四种药物分子和两种制剂的渗透型材的差异,从而在开发局部药品时,证明其作为筛选工具的适用性。此外,该研究表明,MALDI-MSI技术的敏感性似乎与药物分子与周围组织结合的能力相反,这可以通过它们的LOG D值估计。图形概要。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号