Literature DB >> 21882113

Sample collection, biobanking, and analysis.

Maurice J Ahsman1, Dick Tibboel, Ron A A Mathot, Saskia N de Wildt.   

Abstract

Pediatric pharmacokinetic studies require sampling of biofluids from neonates and children. Limitations on sampling frequency and sample volume complicate the design of these studies. In addition, strict guidelines, designed to guarantee patient safety, are in place. This chapter describes the practical implications of sample collection and their storage, with special focus on the selection of the appropriate type of biofluid and withdrawal technique. In addition, we describe appropriate measures for storage of these specimens, for example, in the context of biobanking, and the requirements on drug assay methods that they pose. Pharmacokinetic studies in children are possible, but they require careful selection of an appropriate sampling method, specimen volume, and assay method. The checklist provided could help prospective researchers with the design of an appropriate study protocol and infrastructure.

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Year:  2011        PMID: 21882113     DOI: 10.1007/978-3-642-20195-0_10

Source DB:  PubMed          Journal:  Handb Exp Pharmacol        ISSN: 0171-2004


  2 in total

Review 1.  Ethics of drug research in the pediatric intensive care unit.

Authors:  Niina Kleiber; Krista Tromp; Miriam G Mooij; Suzanne van de Vathorst; Dick Tibboel; Saskia N de Wildt
Journal:  Paediatr Drugs       Date:  2015-02       Impact factor: 3.022

2.  How to build an integrated biobank: the Washington University Translational Cardiovascular Biobank & Repository experience.

Authors:  Kathryn A Yamada; Akshar Y Patel; Gregory A Ewald; Donna S Whitehead; Michael K Pasque; Scott C Silvestry; Deborah L Janks; Douglas L Mann; Jeanne M Nerbonne
Journal:  Clin Transl Sci       Date:  2013-04-18       Impact factor: 4.689

  2 in total

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