Good Practices in Forensic Toxicology

Title:Good Practices in Forensic Toxicology

Volume: 23 Issue: 36

Author(s): Olaf H. Drummer*

Affiliation:

• Department of Forensic Medicine, Monash University, Melbourne,Australia

Keywords: Specimen, collection protocols, assay validation, quality systems, pharmacokinetics, redistribution, contextual information.

Abstract: This manuscript provides an overview for analysts, medical and scientific investigators, and laboratory administrators, the range of factors that should be considered to implement best practice forensic toxicology. These include laboratory influence over the collection of specimens, their proper transport and chain-of-custody before arrival in the laboratory. In addition, the laboratory needs to ensure properly trained staff use suitably validated and documented analytical procedures that meet the intended purpose and type of case in an accredited or suitably quality oriented management system. To assist the investigating officers laboratory results require an interpretation over their possible significance when sufficient details are available over the circumstances of the case. This requires a thorough understanding of the various factors that influence concentrations of substances and ultimately their likely physiological effect. These include consideration of the route of ingestion, influence over chronicity of usage on tissue concentrations and tolerance, possible combined drug effects or likely adverse reactions and consideration of relevant genetic factors that may have influenced pharmacokinetic or pharmacodynamic response.

Cite this article as:

Drummer H. Olaf *, Good Practices in Forensic Toxicology, Current Pharmaceutical Design 2017; 23 (36) . https://dx.doi.org/10.2174/1381612823666170704123836