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Small volume rapid equilibrium dialysis (RED) measures effects of interstitial parameters on the protein-bound fraction of topical drugs

The importance of plasma protein binding in the early stages of drug development is well recognized. Free and bound drug fractions in plasma are routinely determined with well-established methods. However, for physiological fluids with a small accessible volume and low protein concentrations, such a...

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Published in:Journal of pharmaceutical and biomedical analysis 2023-09, Vol.234, p.115571-115571, Article 115571
Main Authors: Wiltschko, Laura, Roblegg, Eva, Raml, Reingard, Birngruber, Thomas
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Roblegg, Eva
Raml, Reingard
Birngruber, Thomas
description The importance of plasma protein binding in the early stages of drug development is well recognized. Free and bound drug fractions in plasma are routinely determined with well-established methods. However, for physiological fluids with a small accessible volume and low protein concentrations, such as dermal interstitial fluid (dISF) validated methods are currently missing. Due to the low protein concentration and highly dynamic processes in the dermis, protein binding data obtained from plasma samples may underestimate in-vivo efficacy. This study aimed to validate a small volume rapid equilibrium dialysis (RED) for low protein samples, as a tool to examine drug-protein binding directly in the biological fluid at the site of action. The sample volume required for RED was successfully downscaled to 50 µl and plasma protein binding values of the four model drugs were consistent with previous studies with an average recovery of 88 ± 8% which makes all tested drugs suitable for small volume RED. Inter- and intra-batch variability showed sufficient reproducibility across RED plates. Small volume RED was successfully applied to assess the effects of interstitial parameters, including the evaluation of the major binding protein and the effects of binding protein concentration, drug concentration, and pH on the protein-bound drug fraction using 2% HSA and/or diluted human plasma as a surrogate for dISF. [Display omitted] •Small volume RED was fully validated in a quality controlled approach.•RED was successfully used to test protein binding in low volume, low protein samples.•pH, protein and drug concentration affected protein binding of drugs.•The efficacy of topical drugs is influenced by these parameters.•RED allows to test protein binding of topical drugs directly in interstitial fluid.
doi_str_mv 10.1016/j.jpba.2023.115571
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Free and bound drug fractions in plasma are routinely determined with well-established methods. However, for physiological fluids with a small accessible volume and low protein concentrations, such as dermal interstitial fluid (dISF) validated methods are currently missing. Due to the low protein concentration and highly dynamic processes in the dermis, protein binding data obtained from plasma samples may underestimate in-vivo efficacy. This study aimed to validate a small volume rapid equilibrium dialysis (RED) for low protein samples, as a tool to examine drug-protein binding directly in the biological fluid at the site of action. The sample volume required for RED was successfully downscaled to 50 µl and plasma protein binding values of the four model drugs were consistent with previous studies with an average recovery of 88 ± 8% which makes all tested drugs suitable for small volume RED. Inter- and intra-batch variability showed sufficient reproducibility across RED plates. Small volume RED was successfully applied to assess the effects of interstitial parameters, including the evaluation of the major binding protein and the effects of binding protein concentration, drug concentration, and pH on the protein-bound drug fraction using 2% HSA and/or diluted human plasma as a surrogate for dISF. [Display omitted] •Small volume RED was fully validated in a quality controlled approach.•RED was successfully used to test protein binding in low volume, low protein samples.•pH, protein and drug concentration affected protein binding of drugs.•The efficacy of topical drugs is influenced by these parameters.•RED allows to test protein binding of topical drugs directly in interstitial fluid.</description><identifier>ISSN: 0731-7085</identifier><identifier>EISSN: 1873-264X</identifier><identifier>DOI: 10.1016/j.jpba.2023.115571</identifier><identifier>PMID: 37527618</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Albumin ; Alpha 1-acid glycoprotein ; HPLC-MS ; Interstitial fluid ; Protein binding ; Rapid equilibrium dialysis</subject><ispartof>Journal of pharmaceutical and biomedical analysis, 2023-09, Vol.234, p.115571-115571, Article 115571</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2023 The Authors. 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Small volume RED was successfully applied to assess the effects of interstitial parameters, including the evaluation of the major binding protein and the effects of binding protein concentration, drug concentration, and pH on the protein-bound drug fraction using 2% HSA and/or diluted human plasma as a surrogate for dISF. 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subjects Albumin
Alpha 1-acid glycoprotein
HPLC-MS
Interstitial fluid
Protein binding
Rapid equilibrium dialysis
title Small volume rapid equilibrium dialysis (RED) measures effects of interstitial parameters on the protein-bound fraction of topical drugs
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