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Using Counter Equilibrium Dialysis (CED) to Increase Confidence in the Measurement of Free Fraction for Challenging Compounds.
Huang, Julie; Yan, Zhengyin; Cai, Jingwei.
Afiliación
  • Huang J; Department of Drug Metabolism and Pharmacokinetics, Genentech, Inc.,South San Francisco, CA 94080, USA.
  • Yan Z; Department of Drug Metabolism and Pharmacokinetics, Genentech, Inc.,South San Francisco, CA 94080, USA.
  • Cai J; Department of Drug Metabolism and Pharmacokinetics, Genentech, Inc.,South San Francisco, CA 94080, USA. Electronic address: cai.jingwei@gene.com.
J Pharm Sci ; 112(9): 2561-2569, 2023 09.
Article en En | MEDLINE | ID: mdl-37187260
ABSTRACT
The confidence in fraction unbound (ƒu) using equilibrium dialysis (ED) is often questioned (e.g., highly bound, labile compounds) due to uncertainty in whether true equilibrium is achieved. Different methods have been developed to increase confidence in ƒu measurements, such as the presaturation, dilution, and bi-directional ED methods. However, confidence in ƒu measurement can still suffer due to non-specific binding and inter-run variations introduced during equilibrium and analysis. To address this concern, we introduce an orthogonal approach called counter equilibrium dialysis (CED) in which non-labeled and isotope-labeled compounds are dosed counter-directionally in rapid equilibrium dialysis (RED). ƒu values of both non-labeled and labeled compounds are measured simultaneously in the same run. These tactics not only minimize non-specific binding and inter-run variability but also enable the confirmation of true equilibrium. If equilibrium is reached in both dialysis directions, the ƒu for the non-labeled compound and the labeled compound will converge. The refined methodology was extensively tested with various compounds of diverse physicochemical properties and plasma binding characteristics. Our results demonstrated that, by using the CED method, ƒu values for a wide range of compounds could be accurately determined with significantly improved confidence, including the challenging highly bound and labile compounds.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Sanguíneas / Diálisis Renal Idioma: En Revista: J Pharm Sci Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Sanguíneas / Diálisis Renal Idioma: En Revista: J Pharm Sci Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos
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