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Schimek, D; Raml, R; Francesconi, KA; Bodenlenz, M; Sinner, F.
Quantification of acyclovir in dermal interstitial fluid and human serum by ultra-high-performance liquid-high-resolution tandem mass spectrometry for topical bioequivalence evaluation.
Biomed Chromatogr. 2018; 32(6):e4194-e4194 Doi: 10.1002/bmc.4194
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Co-Autor*innen der Med Uni Graz
Sinner Frank Michael
Weiss Manfred
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Abstract:
Time-concentration curves for the topical anti-viral drug acyclovir can provide valuable information for drug development. Open flow microperfusion is used for continuous sampling of dermal interstitial fluid but it requires validated methods for subsequent sample analysis. Therefore, we developed a sensitive, selective and high-throughput ultra-high-performance liquid chromatography-high-resolution tandem mass spectrometry method to determine acyclovir in human dermal interstitial fluid and serum. We validated the method over a concentration range of 0.1-25 ng/mL for a sample volume of just 20 μL and employed cation-exchange solid-phase extraction in a fully automated sample treatment procedure. Short- and long-term sample stability data and the analysis of 5000 samples from a clinical trial demonstrate the successful application of our method. Copyright © 2018 John Wiley & Sons, Ltd.
Find related publications in this database (using NLM MeSH Indexing)
Acyclovir - analysis
Acyclovir - blood
Acyclovir - pharmacokinetics
Chromatography, High Pressure Liquid - methods
Dermis - chemistry
Dermis - cytology
Dermis - metabolism
Extracellular Fluid - chemistry
Extracellular Fluid - metabolism
Humans -
Limit of Detection -
Linear Models -
Reproducibility of Results -
Solid Phase Extraction -
Tandem Mass Spectrometry - methods
Therapeutic Equivalency -

Find related publications in this database (Keywords)
dermal interstitial fluid
dermal open flow microperfusion
serum
solid-phase extraction
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