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Quantitative Investigation of Terbinafine Hydrochloride Absorption into a Living Skin Equivalent Model by MALDI-MSI

  • Cristina Russo
    Cristina Russo
    Centre for Mass Spectrometry Imaging, Biomolecular Research Centre, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, U.K.
  • Neil Brickelbank
    Neil Brickelbank
    Centre for Mass Spectrometry Imaging, Biomolecular Research Centre, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, U.K.
  • Catherine Duckett
    Catherine Duckett
    Centre for Mass Spectrometry Imaging, Biomolecular Research Centre, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, U.K.
  • Steve Mellor
    Steve Mellor
    Croda International Plc, Cowick Hall, Snaith, Goole, East Yorkshire DN14 9AA, U.K.
    More by Steve Mellor
  • Stephen Rumbelow
    Stephen Rumbelow
    Croda Inc., 315 Cherry Lane New Castle, Delaware 19720, United States
  • , and 
  • Malcolm R. Clench*
    Malcolm R. Clench
    Centre for Mass Spectrometry Imaging, Biomolecular Research Centre, Sheffield Hallam University, Howard Street, Sheffield S1 1WB, U.K.
    *E-mail: [email protected]
Cite this: Anal. Chem. 2018, 90, 16, 10031–10038
Publication Date (Web):July 19, 2018
https://doi.org/10.1021/acs.analchem.8b02648
Copyright © 2018 American Chemical Society
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Abstract

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The combination of microspotting of analytical and internal standards, matrix sublimation, and recently developed software for quantitative mass spectrometry imaging has been used to develop a high-resolution method for the determination of terbinafine hydrochloride in the epidermal region of a full thickness living skin equivalent model. A quantitative assessment of the effect of the addition of the penetration enhancer (dimethyl isosorbide (DMI)) to the delivery vehicle has also been performed, and data have been compared to those obtained from LC–MS/MS measurements of homogenates of isolated epidermal tissue. At 10% DMI, the levels of signal detected for the drug in the epidermis were 0.20 ± 0.072 mg/g tissue for QMSI and 0.28 ± 0.040 mg/g tissue for LC–MS/MS at 50% DMI 0.69 ± 0.23 mg/g tissue for QMSI and 0.66 ± 0.057 mg/g tissue for LC–MS/MS. Comparison of means and standard deviations indicates no significant difference between the values obtained by the two methods.

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The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.analchem.8b02648.

  • Data from measurement of spot size reproducbility experiments (PDF)

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Cited By


This article is cited by 4 publications.

  1. Hélène Cazier, Carole Malgorn, Nathalie Fresneau, Dominique Georgin, Antoine Sallustrau, Céline Chollet, Jean-Claude Tabet, Stéphane Campidelli, Mathieu Pinault, Martine Mayne, Frédéric Taran, Vincent Dive, Christophe Junot, François Fenaille, Benoit Colsch. Development of a Mass Spectrometry Imaging Method for Detecting and Mapping Graphene Oxide Nanoparticles in Rodent Tissues. Journal of the American Society for Mass Spectrometry 2020, 31 (5) , 1025-1036. https://doi.org/10.1021/jasms.9b00070
  2. Guillaume Hochart, David Bonnel, Jonathan Stauber, Georgios N. Stamatas. Biomarker Mapping on Skin Tape Strips Using MALDI Mass Spectrometry Imaging. Journal of the American Society for Mass Spectrometry 2019, 30 (10) , 2082-2091. https://doi.org/10.1021/jasms.8b06223
  3. Maria Jove, Jade Spencer, Malcolm Clench, Paul M. Loadman, Chris Twelves. Precision pharmacology: Mass spectrometry imaging and pharmacokinetic drug resistance. Critical Reviews in Oncology/Hematology 2019, 141 , 153-162. https://doi.org/10.1016/j.critrevonc.2019.06.008
  4. Melanie Köllmer, Parinaz Mossahebi, Elena Sacharow, Sascha Gorissen, Nicole Gräfe, Dirk-Heinrich Evers, Michael E. Herbig. Investigation of the Compatibility of the Skin PAMPA Model with Topical Formulation and Acceptor Media Additives Using Different Assay Setups. AAPS PharmSciTech 2019, 20 (2) https://doi.org/10.1208/s12249-019-1305-3

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