Population pharmacokinetics of exogenous biotin and the relationship between biotin serum levels and in vitro immunoassay interference

Author:

Grimsey Paul1,Frey Nicolas2,Bendig Garnet3,Zitzler Juergen3,Lorenz Oliver3,Kasapic Dusanka4,Zaugg Christian E4

Affiliation:

1. Roche Pharmaceuticals, Roche Innovation Center Welwyn, Welywn Garden City, UK

2. Roche Pharmaceuticals, Basel, Switzerland

3. Roche Diagnostics GmbH, Penzberg, Germany

4. Roche Diagnostics International Ltd, Forrenstrasse 2, CH-6343 Rotkreuz, Switzerland

Abstract

Aim: Biotin in human serum is a potential interfering factor for streptavidin-biotin-based assays. We aimed to evaluate the effective half-life of biotin and biotin metabolites, and establish a pharmacokinetic (PK) model to simulate the time taken for the biotin concentration to fall below a series of thresholds. Materials & methods: PK properties of biotin (5, 10 and 20 mg daily) were evaluated in healthy participants. Biotin serum concentrations were simulated for high-dose regimens (1 mg daily to 300 mg q.i.d.) using a population PK model. Results: Washout periods required for biotin concentrations to reach thresholds ranging from 10 to 100 ng/ml were successfully simulated. Conclusion: Our simulations provide valuable guidance on biotin washout periods necessary to avoid false assay results.

Publisher

Future Science Ltd

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