European Bioanalysis Forum: recommendation for dealing with internal standard variability-Reference-Cited by-同舟云学术

European Bioanalysis Forum: recommendation for dealing with internal standard variability

Published:2014-10 Issue:20 Volume:6 Page:2767-2774
ISSN:1757-6180
Container-title:Bioanalysis
language:en
Short-container-title:Bioanalysis

Author:

White Stephen¹,Adcock Neil²,Elbast Walid³,Hiller Jim⁴,Knutsson Magnus⁵,Lausecker Berthold⁶,Long Jeff⁷,McDougall Stuart⁸,Salavert Fabrice⁹,Sangster Timothy¹⁰,Verhaeghe Tom¹¹,Amsterdam Peter van¹²

Affiliation:

1. Bioanalytical Science & Toxicokinetics, Drug Metabolism & Pharmacokinetics, GlaxoSmithKline R&D, Ware, UK

2. LGC, UK

3. Novartis, Switzerland

4. HOLOGIC Ltd., UK

5. Ferring, Denmark

6. CRS, Germany

7. Formerly of Shire, UK

8. Covance, UK

9. Actelion, Switzerland

10. Charles River Laboratories, UK

11. Janssen R&D, Belgium

12. Abbott Healthcare Products, The Netherlands

Abstract

Adequate monitoring of internal standard (IS) response across an analytical run and identification of anomalies is now a common expectation. However, the means to conduct this assessment in an appropriate manner is unclear and differs widely between laboratories. A European Bioanalysis Forum (EBF) topic team was formed to survey current practices within European Bioanalysis Forum member companies and to recommend a best practice approach for dealing with IS response variability.

Publisher

Future Science Ltd

Subject

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

Link

http://www.future-science.com/doi/pdf/10.4155/bio.14.221

Reference9 articles.

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5. About sound science, stable isotope dilution, blasphemy and heresy

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