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Comparison of Two Immunoassay Screening Methods and a LC-MS/MS in Detecting Traditional and Designer Benzodiazepines in Urine

Sensitive and specific immunoassay screening methods for the detection of benzodiazepines in urine represent an important prerequisite for routine analysis in clinical and forensic toxicology. Moreover, emerging designer benzodiazepines force labs to keep their methodologies updated, in order to eva...

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Autores principales: Rossi, Brian, Freni, Francesca, Vignali, Claudia, Stramesi, Cristiana, Collo, Giancarlo, Carelli, Claudia, Moretti, Matteo, Galatone, Dario, Morini, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746686/
https://www.ncbi.nlm.nih.gov/pubmed/35011344
http://dx.doi.org/10.3390/molecules27010112
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author Rossi, Brian
Freni, Francesca
Vignali, Claudia
Stramesi, Cristiana
Collo, Giancarlo
Carelli, Claudia
Moretti, Matteo
Galatone, Dario
Morini, Luca
author_facet Rossi, Brian
Freni, Francesca
Vignali, Claudia
Stramesi, Cristiana
Collo, Giancarlo
Carelli, Claudia
Moretti, Matteo
Galatone, Dario
Morini, Luca
author_sort Rossi, Brian
collection PubMed
description Sensitive and specific immunoassay screening methods for the detection of benzodiazepines in urine represent an important prerequisite for routine analysis in clinical and forensic toxicology. Moreover, emerging designer benzodiazepines force labs to keep their methodologies updated, in order to evaluate the reliability of the immunochemical techniques. This study aimed at evaluating the sensitivity and specificity of two different immunoassay methods for the detection of benzodiazepines in urine, through a comparison with the results obtained by a newly developed liquid chromatographic tandem mass spectrometric (LC-MS/MS) procedure. A cohort of authentic urine samples (N = 501) were processed, before and after a hydrolysis procedure, through two immunoassays and an LC-MS/MS method. The LC-MS/MS target procedure was optimized for monitoring 25 different molecules, among traditional and designer benzodiazepines, including some metabolites. At least one of the monitored substances was detected in 100 out of the 501 samples. A good specificity was observed for the two immunoassays (>0.99), independently of the cut-offs and the sample hydrolysis. The new kit demonstrated a fairly higher sensitivity, always higher than 0.90; in particular, a high cross-reactivity of the new immunoassay was observed for samples that tested positive for lorazepam and 7-aminoclonazepam. The two immunoassays appeared adequate to monitor not only traditional benzodiazepines but also new designer ones.
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spelling pubmed-87466862022-01-11 Comparison of Two Immunoassay Screening Methods and a LC-MS/MS in Detecting Traditional and Designer Benzodiazepines in Urine Rossi, Brian Freni, Francesca Vignali, Claudia Stramesi, Cristiana Collo, Giancarlo Carelli, Claudia Moretti, Matteo Galatone, Dario Morini, Luca Molecules Article Sensitive and specific immunoassay screening methods for the detection of benzodiazepines in urine represent an important prerequisite for routine analysis in clinical and forensic toxicology. Moreover, emerging designer benzodiazepines force labs to keep their methodologies updated, in order to evaluate the reliability of the immunochemical techniques. This study aimed at evaluating the sensitivity and specificity of two different immunoassay methods for the detection of benzodiazepines in urine, through a comparison with the results obtained by a newly developed liquid chromatographic tandem mass spectrometric (LC-MS/MS) procedure. A cohort of authentic urine samples (N = 501) were processed, before and after a hydrolysis procedure, through two immunoassays and an LC-MS/MS method. The LC-MS/MS target procedure was optimized for monitoring 25 different molecules, among traditional and designer benzodiazepines, including some metabolites. At least one of the monitored substances was detected in 100 out of the 501 samples. A good specificity was observed for the two immunoassays (>0.99), independently of the cut-offs and the sample hydrolysis. The new kit demonstrated a fairly higher sensitivity, always higher than 0.90; in particular, a high cross-reactivity of the new immunoassay was observed for samples that tested positive for lorazepam and 7-aminoclonazepam. The two immunoassays appeared adequate to monitor not only traditional benzodiazepines but also new designer ones. MDPI 2021-12-24 /pmc/articles/PMC8746686/ /pubmed/35011344 http://dx.doi.org/10.3390/molecules27010112 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rossi, Brian
Freni, Francesca
Vignali, Claudia
Stramesi, Cristiana
Collo, Giancarlo
Carelli, Claudia
Moretti, Matteo
Galatone, Dario
Morini, Luca
Comparison of Two Immunoassay Screening Methods and a LC-MS/MS in Detecting Traditional and Designer Benzodiazepines in Urine
title Comparison of Two Immunoassay Screening Methods and a LC-MS/MS in Detecting Traditional and Designer Benzodiazepines in Urine
title_full Comparison of Two Immunoassay Screening Methods and a LC-MS/MS in Detecting Traditional and Designer Benzodiazepines in Urine
title_fullStr Comparison of Two Immunoassay Screening Methods and a LC-MS/MS in Detecting Traditional and Designer Benzodiazepines in Urine
title_full_unstemmed Comparison of Two Immunoassay Screening Methods and a LC-MS/MS in Detecting Traditional and Designer Benzodiazepines in Urine
title_short Comparison of Two Immunoassay Screening Methods and a LC-MS/MS in Detecting Traditional and Designer Benzodiazepines in Urine
title_sort comparison of two immunoassay screening methods and a lc-ms/ms in detecting traditional and designer benzodiazepines in urine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746686/
https://www.ncbi.nlm.nih.gov/pubmed/35011344
http://dx.doi.org/10.3390/molecules27010112
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