alexa Rapid Equilibrium Dialysis (RED): an In-vitro High-Throughput Screening Technique for Plasma Protein Binding using Human and Rat Plasma | OMICS International | Abstract
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Journal of Bioequivalence & Bioavailability
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Research Article

Rapid Equilibrium Dialysis (RED): an In-vitro High-Throughput Screening Technique for Plasma Protein Binding using Human and Rat Plasma

Jitendra Kumar Singh1*, Anant Solanki1, Reema C Maniyar1, Debarupa Banerjee1 and Vikas S Shirsath2

1In vitro Pharmacology Lab, Oxygen Healthcare Research Pvt Ltd, Plot-35, Pancharatna Industrial Estate, Sarkhej Bawla Highway, Changodar, Ahmedabad, Gujarat-382213, India

2Medicinal Chemistry Lab, Oxygen Healthcare Research Pvt Ltd, Plot-35, Pancharatna Industrial Estate, Sarkhej Bawla Highway, Changodar, Ahmedabad, Gujarat-382213, India

*Corresponding Author:
Jitendra Kumar Singh
In vitro Pharmacology Lab, India
Tel: +91-2717656415
Fax: +91-2717250262
E-mail: [email protected]

Received Date: April 21, 2012; Accepted Date: May 10, 2012; Published Date: May 12, 2012

Citation: Jitendra Kumar S, Anant S, Reema CM, Debarupa B, Vikas SS (2012) Rapid Equilibrium Dialysis (RED): an In-vitro High-Throughput Screening Technique for Plasma Protein Binding using Human and Rat Plasma. J Bioequiv Availab S14:005. doi: 10.4172/jbb.S14-005

Copyright: © 2012 Jitendra Kumar S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Determining the extent to which a molecule binds to plasma proteins is a critical phase of drug development because the amount of plasma-bound drug influences compound dosing, efficacy, clearance rate and potential for drug interactions. Determination of the free (%Fu) and bound (%Bound) fractions of a test article in plasma is therefore a critical parameter, which is routinely determined in the process of drug discovery and development. This determination is enabled by equilibrium dialysis, an accepted and standard method for reliable estimation of the non-bound drug fraction in plasma. Although it is the preferred method, equilibrium dialysis has historically been labor-intensive, time-consuming, cost-prohibitive and difficult to automate. A Rapid Equilibrium Dialysis (RED) drug-protein binding assay using LC-MS/MS was developed using a novel technique that resulted in significantly improved assay precision and offers a speed advantage. A panel of compounds covering a range of expected protein binding was tested in plasma of human and rat species. A sensitive and selective method using quadruple tandem mass spectrophotometer interfaced with electro spray ionization was developed for the quantification of unbound drug in pretreated plasma. The mobile phases used were 0.1% Formic acid in Acetonitrile: 0.1% Formic acid in Water with gradient HPLC method. The unbound fraction of drugs was detected by mass spectrometer operated in ESI mode. In addition, data for a set of ten compounds was compared with literature values. With the described method, it is possible to screen a relatively large number of compounds for PPB in a drug discovery environment.

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