Therapeutic monoclonal antibody concentration monitoring: free or total?

Author:

Kuang Bing1,King Lindsay2,Wang Huifen Faye3

Affiliation:

1. Pharmacokinetics, Dynamics and Metabolism, Biotherapeutics Research and Development, Pfizer Inc. San Diego, CA 92121, USA.

2. Pharmacokinetics, Dynamics and Metabolism, Biotherapeutics Research and Development, Pfizer Inc. Groton, CT 06340, USA

3. Clinical Pharmacology, Emerging Markets Business Unit, Pfizer Inc. New London, CT 06320, USA

Abstract

Most therapeutic monoclonal antibodies are designed to bind a specific antigen to elicit pharmacological effects. Accurate quantification of a therapeutic monoclonal antibody in biological matrices is essential for assessing its pharmacokinetics and selecting an effective dosing regimen. Therapeutic antibodies may exist in free, partially bound and fully bound forms in the bloodstream. The choice of which form(s) to measure and how to measure them is gaining much attention with the increase in the number of soluble therapeutic targets. This article will review the bioanalytical methods used in supporting the clinical development of the US FDA-approved therapeutic monoclonal antibodies and also discuss how different factors, such as assay format, target and antibody concentrations, and sample dilutions, can have an impact on the measurement of each form of antibody. Appreciation of which form of drug is being measured and what factors may impact measurement under different conditions are important for interpretation of the pharmacokinetics of therapeutic antibodies.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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