Update of the EBF recommendation for the use of DBS in regulated bioanalysis integrating the conclusions from the EBF DBS-microsampling consortium

Author:

Timmerman Philip1,White Steve2,Cobb Zoe3,de Vries Ronald4,Thomas Elizabeth5,van Baar Ben6

Affiliation:

1. Janssen R&D NV, Turnhoutseweg, 30 B-2340 Beerse, Belgium.

2. GlaxoSmithKline, Ware, UK

3. Quotient Bio Analytical Sciences (part of the LGC group), Cambridgeshire, UK

4. Janssen R&D NV, Turnhoutseweg, 30 B-2340 Beerse, Belgium

5. ICON plc, Manchester, UK (at time of writing this article)

6. QPS Netherlands bv Groningen, The Netherlands

Abstract

The European Bioanalysis Forum dried blood spots/microsampling consortium is reporting back from the experiments they performed on further documenting the potential hurdles of the DBS technology. Their experiments focused on the impact of hematocrit changes, IS addition, spot homogeneity, aging of spots and stability of fresh blood and cards. Results from these experiments demonstrate that the issues of DBS in regulated bioanalysis are real and that the technology will need additional improvements to be ready for use as a general tool for regulated bioanalysis. In addition, results on fresh blood and card stability were shared at international meetings and will be reported at a later date.

Publisher

Future Science Ltd

Subject

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

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