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Diclofenac in vitro microdialysis study comparing different experimental set‐ups to improve quantitative recovery

Several studies investigated diclofenac tissue concentrations using microdialysis (MD). However, thorough evaluations of the optimal MD set‐up for diclofenac are unavailable. Thus, this in vitro MD study aimed to compare different set‐ups to improve quantitative recovery of diclofenac. In forward an...

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Autores principales: Jorda, Anselm, Armogida, Marianna, Lackner, Edith, Saikumar, Sivasankari, Sucharski, Filip, Weber, Maria, Zeitlinger, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305941/
https://www.ncbi.nlm.nih.gov/pubmed/35048557
http://dx.doi.org/10.1111/bcpt.13709
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author Jorda, Anselm
Armogida, Marianna
Lackner, Edith
Saikumar, Sivasankari
Sucharski, Filip
Weber, Maria
Zeitlinger, Markus
author_facet Jorda, Anselm
Armogida, Marianna
Lackner, Edith
Saikumar, Sivasankari
Sucharski, Filip
Weber, Maria
Zeitlinger, Markus
author_sort Jorda, Anselm
collection PubMed
description Several studies investigated diclofenac tissue concentrations using microdialysis (MD). However, thorough evaluations of the optimal MD set‐up for diclofenac are unavailable. Thus, this in vitro MD study aimed to compare different set‐ups to improve quantitative recovery of diclofenac. In forward and reverse in vitro MD experiments with diclofenac at two concentrations (1 and 100 ng/ml), the perfusion solutions physiological saline 0.9% (PS) and human albumin 1% (HSA) were compared using tissue probes (10‐mm membrane) and customized intravenous (iv) probes (30‐mm membrane). Using PS, the mean relative recovery of diclofenac at 1 ng/ml was 1.6% ± 0.04% and 3.12% ± 0.00% with the tissue probe and the iv probe, respectively. The respective mean relative recovery for diclofenac at 100 ng/ml was 0.02% ± 0.01% and 0.21% ± 0.11%. Using HSA, the mean relative recovery was 314% ± 25% (tissue probe) and 1064% ± 97% (iv probe) for diclofenac at 1 ng/ml and 444% ± 91% and 1415% ± 217% for diclofenac at 100 ng/ml. In reverse dialysis using PS, the mean relative loss of diclofenac was 99.2% ± 0.5% (tissue probe) and 95.8% ± 1.7% (iv probe). Using HSA, the mean relative loss was −4.4% ± 7.2% and 0.2% ± 7.5%, respectively. PS and HSA were not suitable perfusion solutions for quantification of absolute diclofenac concentrations. Despite methodological challenges, HSA may be used for comparative experiments or bioequivalence studies.
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spelling pubmed-93059412022-07-28 Diclofenac in vitro microdialysis study comparing different experimental set‐ups to improve quantitative recovery Jorda, Anselm Armogida, Marianna Lackner, Edith Saikumar, Sivasankari Sucharski, Filip Weber, Maria Zeitlinger, Markus Basic Clin Pharmacol Toxicol Basic Pharmacology Several studies investigated diclofenac tissue concentrations using microdialysis (MD). However, thorough evaluations of the optimal MD set‐up for diclofenac are unavailable. Thus, this in vitro MD study aimed to compare different set‐ups to improve quantitative recovery of diclofenac. In forward and reverse in vitro MD experiments with diclofenac at two concentrations (1 and 100 ng/ml), the perfusion solutions physiological saline 0.9% (PS) and human albumin 1% (HSA) were compared using tissue probes (10‐mm membrane) and customized intravenous (iv) probes (30‐mm membrane). Using PS, the mean relative recovery of diclofenac at 1 ng/ml was 1.6% ± 0.04% and 3.12% ± 0.00% with the tissue probe and the iv probe, respectively. The respective mean relative recovery for diclofenac at 100 ng/ml was 0.02% ± 0.01% and 0.21% ± 0.11%. Using HSA, the mean relative recovery was 314% ± 25% (tissue probe) and 1064% ± 97% (iv probe) for diclofenac at 1 ng/ml and 444% ± 91% and 1415% ± 217% for diclofenac at 100 ng/ml. In reverse dialysis using PS, the mean relative loss of diclofenac was 99.2% ± 0.5% (tissue probe) and 95.8% ± 1.7% (iv probe). Using HSA, the mean relative loss was −4.4% ± 7.2% and 0.2% ± 7.5%, respectively. PS and HSA were not suitable perfusion solutions for quantification of absolute diclofenac concentrations. Despite methodological challenges, HSA may be used for comparative experiments or bioequivalence studies. John Wiley and Sons Inc. 2022-02-02 2022-04 /pmc/articles/PMC9305941/ /pubmed/35048557 http://dx.doi.org/10.1111/bcpt.13709 Text en © 2022 The Authors. Basic & Clinical Pharmacology & Toxicology published by John Wiley & Sons Ltd on behalf of Nordic Association for the Publication of BCPT (former Nordic Pharmacological Society). https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Basic Pharmacology
Jorda, Anselm
Armogida, Marianna
Lackner, Edith
Saikumar, Sivasankari
Sucharski, Filip
Weber, Maria
Zeitlinger, Markus
Diclofenac in vitro microdialysis study comparing different experimental set‐ups to improve quantitative recovery
title Diclofenac in vitro microdialysis study comparing different experimental set‐ups to improve quantitative recovery
title_full Diclofenac in vitro microdialysis study comparing different experimental set‐ups to improve quantitative recovery
title_fullStr Diclofenac in vitro microdialysis study comparing different experimental set‐ups to improve quantitative recovery
title_full_unstemmed Diclofenac in vitro microdialysis study comparing different experimental set‐ups to improve quantitative recovery
title_short Diclofenac in vitro microdialysis study comparing different experimental set‐ups to improve quantitative recovery
title_sort diclofenac in vitro microdialysis study comparing different experimental set‐ups to improve quantitative recovery
topic Basic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305941/
https://www.ncbi.nlm.nih.gov/pubmed/35048557
http://dx.doi.org/10.1111/bcpt.13709
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