ImaBiotech SAS, Parc Eurasanté, 885 Avenue Eugène Avinée, 59120, Loos, France.
LEO Pharma A/S, Industriparken 55, 2750, Ballerup, Denmark.
Anal Bioanal Chem. 2018 Apr;410(11):2815-2828. doi: 10.1007/s00216-018-0964-3. Epub 2018 Mar 15.
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.
在开发治疗银屑病和特应性皮炎等皮肤病的局部产品的过程中,生成皮肤分布曲线并可靠地确定目标区域的药物分子浓度是至关重要的。成像技术,如质谱成像(MSI),具有足够的空间分辨率,可以生成药物分子在皮肤切片上的有意义的分布曲线。在这项研究中,我们使用基质辅助激光解吸/电离质谱成像(MALDI-MSI),根据人皮肤外植体横截面中四种不同分子的组织消光系数(TEC)测定,生成定量的皮肤分布曲线。这四种药物分子:罗氟司特、托法替尼、芦可替尼和 LEO 29102 具有不同的物理化学性质。此外,托法替尼以两种不同的制剂给药。该研究表明,通过 MALDI-MSI,我们能够观察到两种制剂和四种药物分子的渗透曲线的差异,从而证明其作为开发局部药物产品的筛选工具的适用性。此外,该研究表明,MALDI-MSI 技术的灵敏度似乎与药物分子与周围组织结合的能力成反比,这可以通过它们的 Log D 值来估计。