Fentanyl and fentalogs’ intake as drugs of abuse is experiencing a great increase in recent years. For this reason, there are more and more cases in which it is important to recognize and quantify these molecules and related metabolites in biological matrices. Oral fluid (OF) is often used to find out if a subject has recently used a psychoactive substance and if, therefore, the person is still under the effect of psychotropics. Given its difficulty in handling, good sample preparation and the development of instrumental methods for analysis are essential. In this work, an analytical method is proposed for the simultaneous determination of 25 analytes, including fentanyl, several derivatives and metabolites. OF was collected by means of passive drool; sample pretreatment was developed in order to be fast, simple and possibly semi-automated by exploiting microextraction on packed sorbent (MEPS). The analysis was performed by means of LC–HRMS/MS obtaining good identification and quantification of all the analytes in less than 10 min. The proposed method was fully validated according to the Scientific Working Group for Forensic Toxicology (SWGTOX) international guidelines. Good results were obtained in terms of recoveries, matrix effect and sensitivity, showing that this method could represent a useful tool in forensic toxicology. The presented method was successfully applied to the analysis of proficiency test samples.

Simultaneous quantification of 25 fentanyl derivatives and metabolites in oral fluid by means of microextraction on packed sorbent and lc–hrms/ms analysis / Vincenti, F.; Montesano, C.; Pirau, S.; Gregori, A.; Di Rosa, F.; Curini, R.; Sergi, M.. - In: MOLECULES. - ISSN 1420-3049. - 26:19(2021), pp. 1-13. [10.3390/molecules26195870]

Simultaneous quantification of 25 fentanyl derivatives and metabolites in oral fluid by means of microextraction on packed sorbent and lc–hrms/ms analysis

Vincenti F.;Montesano C.;Curini R.;Sergi M.
2021

Abstract

Fentanyl and fentalogs’ intake as drugs of abuse is experiencing a great increase in recent years. For this reason, there are more and more cases in which it is important to recognize and quantify these molecules and related metabolites in biological matrices. Oral fluid (OF) is often used to find out if a subject has recently used a psychoactive substance and if, therefore, the person is still under the effect of psychotropics. Given its difficulty in handling, good sample preparation and the development of instrumental methods for analysis are essential. In this work, an analytical method is proposed for the simultaneous determination of 25 analytes, including fentanyl, several derivatives and metabolites. OF was collected by means of passive drool; sample pretreatment was developed in order to be fast, simple and possibly semi-automated by exploiting microextraction on packed sorbent (MEPS). The analysis was performed by means of LC–HRMS/MS obtaining good identification and quantification of all the analytes in less than 10 min. The proposed method was fully validated according to the Scientific Working Group for Forensic Toxicology (SWGTOX) international guidelines. Good results were obtained in terms of recoveries, matrix effect and sensitivity, showing that this method could represent a useful tool in forensic toxicology. The presented method was successfully applied to the analysis of proficiency test samples.
2021
fentanyl; LC–HRMS/MS; microextraction on packed sorbent; oral fluid; adult; chromatography, liquid; female; fentanyl; healthy volunteers; humans; limit of detection; male; mass spectrometry; middle aged; narcotics; saliva; solid phase microextraction; young adult
01 Pubblicazione su rivista::01a Articolo in rivista
Simultaneous quantification of 25 fentanyl derivatives and metabolites in oral fluid by means of microextraction on packed sorbent and lc–hrms/ms analysis / Vincenti, F.; Montesano, C.; Pirau, S.; Gregori, A.; Di Rosa, F.; Curini, R.; Sergi, M.. - In: MOLECULES. - ISSN 1420-3049. - 26:19(2021), pp. 1-13. [10.3390/molecules26195870]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1623714
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