Determination of pharmaceutical compounds in skin by imaging matrix‐assisted laser desorption/ionisation mass spectrometry
- 15 November 2004
- journal article
- research article
- Published by Wiley in Rapid Communications in Mass Spectrometry
- Vol. 18 (24) , 3051-3060
- https://doi.org/10.1002/rcm.1725
Abstract
Matrix-assisted laser desorption/ionisation (MALDI) quadrupole time-of-flight mass spectrometry (Q-TOFMS) has been used to detect and image the distribution of a xenobiotic substance in skin. Porcine epidermal tissue was treated with ‘Nizoral’, a medicated shampoo containing ketoconazole ((±)-1-acetyl-4-[p-[[(2R,4S)-2-(2,4-dichlorophenyl)-2-(imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazine) as active ingredient. Following incubation for 1 h at 37°C all excess formulation was washed from the surface. A cross-section of the drug-treated tissue was then blotted onto a cellulose membrane, precoated in matrix (α-cyano-4-hydroxycinnamic acid (CHCA)), by airspray deposition. In separate experiments the tissue surface was treated with Nizoral within a triangular former, and subsequently blotted onto a matrix-coated membrane. Sample membranes were then mounted into the recess of specialised MALDI targets with adhesive tape. All samples were analysed by MALDI-TOFMS using an Applied Biosystem ‘Q-star Pulsar i’ hybrid Q-TOF mass spectrometer fitted with an orthagonal MALDI ion source and imaging software. Detection of the protonated molecule was readily achievable by this technique. Treatment of the tissue within a template gave rise to images depicting the expected distribution of the drug, demonstrating that this technique is capable of producing spatially useful data. Ion images demonstrating the permeation of the applied compound into the skin were achieved by imaging a cross-sectional imprint of treated tissue. A calibration graph for the determination of ketoconazole was prepared using the sodium adduct of the matrix ion as an internal standard. This enabled construction of a quantitative profile of drug in skin. Conventional haematoxylin and eosin staining and microscopy methods were employed to obtain a histological image of the porcine epidermal tissue. Superimposing the mass spectrometric and histological images appeared to indicate drug permeation into the dermal tissue layer. Copyright © 2004 John Wiley & Sons, Ltd.Keywords
This publication has 24 references indexed in Scilit:
- Direct analysis of drug candidates in tissue by matrix‐assisted laser desorption/ionization mass spectrometryJournal of Mass Spectrometry, 2003
- Direct tissue analysis using matrix‐assisted laser desorption/ionization mass spectrometry: practical aspects of sample preparationJournal of Mass Spectrometry, 2003
- Imaging of thin-layer chromatograms using matrix-assisted laser desorption/ionization mass spectrometryAnalytical Chemistry, 1995
- Surfaces for interfacing protein gel electrophoresis directly with mass spectrometryMass Spectrometry Reviews, 1995
- Polyethylene Membrane as a Sample Support for Direct Matrix-Assisted Laser Desorption/Ionization Mass Spectrometric Analysis of High Mass ProteinsAnalytical Chemistry, 1995
- Reproducibility and quantitation of matrix-assisted laser desorption ionization mass spectrometry: Effects of nitrocellulose on peptide ion yieldsJournal of Mass Spectrometry, 1993
- In vivo Evaluation of the Penetration of Topically Applied Drugs into Human Skin by Spectroscopic MethodsSkin Pharmacology and Physiology, 1993
- Topical Delivery Enhancement with Multilamellar Liposomes into Pilosebaceous Units: I. In Vitro Evaluation Using Fluorescent Techniques with the Hamster Ear ModelJournal of Investigative Dermatology, 1992
- Localization of lipophilic molecules penetrating rat skin in vivo by quantitative autoradiographyInternational Journal of Pharmaceutics, 1991
- Epidermal Lipids, Membranes, and Keratinization.International Journal of Dermatology, 1981