TY - JOUR
T1 - The analysis of antipsychotic drugs in human matrices using LC-MS(/MS)
AU - Saar, Eva
AU - Beyer, Jochen
AU - Gerostamoulos, Dimitri
AU - Drummer, Olaf Heino
PY - 2012
Y1 - 2012
N2 - Antipsychotic drugs (APs) are prescribed for a wide range of psychotic illnesses. Withmore than 35 APs currently available worldwide,
this drug class has rapidly gained importance in both clinical and forensic settings. On account of their chemical properties,
many APs are present in human specimens at very low concentrations, which complicate their detection using standard gas chromatography?
mass spectrometry (GC-MS) procedures that often cannot provide the required sensitivity. Recent advances in liquid
chromatography-(tandem) mass spectrometry LC-MS(/MS) technology have enabled accurate detection and quantification of
these compounds in various human specimens, indicated by the increasing number of published methods. Method validation
has been a particular focus of analytical chemistry in recent times. Recommendations set by several guidance documents are
now widely accepted by the toxicology community, as reflected by the guidelines drafted by leading toxicological societies. This
review provides a critical review of single-stage and tandem LC-MS procedures for the detection and quantification of APs, with a
particular emphasis on appropriate method validation.
The quality of published methods is inconsistent throughout the literature. While the majority of authors incorporate some
validation experiments in their respective method development, a large number of published methods lack essential components
of method validation, which are considered mandatory according to the guidelines.
If adapting a method for the detection of APs for use in a laboratory, analysts should ensure successful validation experiments
for appropriateness and completeness have been conducted, and perform additional experiments when indicated.
Copyright ? 2012 John Wiley Sons, Ltd.
AB - Antipsychotic drugs (APs) are prescribed for a wide range of psychotic illnesses. Withmore than 35 APs currently available worldwide,
this drug class has rapidly gained importance in both clinical and forensic settings. On account of their chemical properties,
many APs are present in human specimens at very low concentrations, which complicate their detection using standard gas chromatography?
mass spectrometry (GC-MS) procedures that often cannot provide the required sensitivity. Recent advances in liquid
chromatography-(tandem) mass spectrometry LC-MS(/MS) technology have enabled accurate detection and quantification of
these compounds in various human specimens, indicated by the increasing number of published methods. Method validation
has been a particular focus of analytical chemistry in recent times. Recommendations set by several guidance documents are
now widely accepted by the toxicology community, as reflected by the guidelines drafted by leading toxicological societies. This
review provides a critical review of single-stage and tandem LC-MS procedures for the detection and quantification of APs, with a
particular emphasis on appropriate method validation.
The quality of published methods is inconsistent throughout the literature. While the majority of authors incorporate some
validation experiments in their respective method development, a large number of published methods lack essential components
of method validation, which are considered mandatory according to the guidelines.
If adapting a method for the detection of APs for use in a laboratory, analysts should ensure successful validation experiments
for appropriateness and completeness have been conducted, and perform additional experiments when indicated.
Copyright ? 2012 John Wiley Sons, Ltd.
UR - http://onlinelibrary.wiley.com.ezproxy.lib.monash.edu.au/doi/10.1002/dta.1337/pdf
U2 - 10.1002/dta.1337
DO - 10.1002/dta.1337
M3 - Article
SN - 1942-7603
VL - 4
SP - 376
EP - 394
JO - Drug Testing and Analysis
JF - Drug Testing and Analysis
IS - 6
ER -