Quantification of acyclovir in dermal interstitial fluid and human serum by ultra-high-performance liquid-high-resolution tandem mass spectrometry for topical bioequivalence evaluation

Author:

Schimek Denise12,Raml Reingard1,Francesconi Kevin A.2,Bodenlenz Manfred1,Sinner Frank13ORCID

Affiliation:

1. Joanneum Research Forschungsgesellschaft mbH; HEALTH Institute for Biomedicine and Health Sciences; Graz Austria

2. Institute of Chemistry; NAWI Graz, University of Graz; Austria

3. Division of Endocrinology and Diabetology, Department of Internal Medicine; Medical University of Graz; Austria

Funder

U.S. Food and Drug Administration

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

Reference24 articles.

1. Key aspects of analytical method validation and linearity evaluation;Araujo;Journal of Chromatography B, Analytical Technologies in the Biomedical and Life Sciences,2009

2. Determination of acyclovir in human serum by high-performance liquid chromatography using liquid-liquid extraction and its application in pharmacokinetic studies;Bahrami;Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences,2005

3. Clinical applicability of dOFM devices for dermal sampling;Bodenlenz;Skin Research and Technology,2013

4. Open Flow Microperfusion as a Dermal Pharmacokinetic Approach to Evaluate Topical Bioequivalence;Bodenlenz;Clinical Pharmacokinetics,2017

5. Survey of international regulatory bioequivalence recommendations for approval of generic topical dermatological drug products;Braddy;The AAPS Journal,2015

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