Monitoring the hormones in equine matrix is crucial to understanding the health status of horses , and also to monitoring the abuse of these substances before a race or a horse transaction. Few analytical procedures exist and those that do are “self made methods”, generally based on immunoassay analysis, often impossible to replicate in other laboratories or too complex for the staff. On that, it is necessary to develop new sensitive analytical methods, that can be diffused to external vets and giving correct and comparable results. Furthermore, the few analytical procedures involving an HPLC-MS-MS system reported in literature allow for simultaneous quantification of no more than three or four hormones [1][2]. The proposed method makes it possible to detect and quantify seventeen hormones and metabolites in a single assay, in just eleven minutes. Quantifiable hormones with the proposed method are: Pregnenolon, 17-OH-Pregnenolon, Progesteron, 17-OH-Progesteron, Androsteron, Androstenedion, DHEA, DHEAS, Testosteron, Cortisol, Corticosteron, Aldosteron, 11-Deossicortisol, 11-Deossicorticosteron, Diidrotestosteron, Estron, Estradiol. Three deuterated hormones (Cortisol-D4, Aldosteron-D7, Testosteron-D3) have been used as internal standards in order to set a more accurate and precise procedure. The method was developed using the Agilent UHPLC chromatographic system (1290) using a Zorbax RRHD C18 – 1,8 μm column and a 6420Agilent Mass Spectrometer . The procedure is fast and intuitive; the sample preparation is very easy, with the serum deproteinized in vials using a deproteinizing solution, centifuged and injected into the system. The mobile phases are made of water and acetonitrile, both containing formic acid. Overall, the method is very simple and robust and it brings about a remarkable saving of time and money with respect to previously reported methods; in fact, using the UHPLC–Tandem Mass spectrometer enables simultaneous quantification of seventeen Steroidal Hormones.

DEVELOPMENT OF A LC-MS-MS METHOD FOR THE SIMULTANEOUS DETERMINATION OF STEROIDAL HORMONES IN EQUINE SERUM.

GENANGELI, MICHELE;CAPRIOLI, GIOVANNI;CORTESE, Manuela;PETRELLI, Riccardo;SAGRATINI, Gianni;VITTORI, Sauro
2015-01-01

Abstract

Monitoring the hormones in equine matrix is crucial to understanding the health status of horses , and also to monitoring the abuse of these substances before a race or a horse transaction. Few analytical procedures exist and those that do are “self made methods”, generally based on immunoassay analysis, often impossible to replicate in other laboratories or too complex for the staff. On that, it is necessary to develop new sensitive analytical methods, that can be diffused to external vets and giving correct and comparable results. Furthermore, the few analytical procedures involving an HPLC-MS-MS system reported in literature allow for simultaneous quantification of no more than three or four hormones [1][2]. The proposed method makes it possible to detect and quantify seventeen hormones and metabolites in a single assay, in just eleven minutes. Quantifiable hormones with the proposed method are: Pregnenolon, 17-OH-Pregnenolon, Progesteron, 17-OH-Progesteron, Androsteron, Androstenedion, DHEA, DHEAS, Testosteron, Cortisol, Corticosteron, Aldosteron, 11-Deossicortisol, 11-Deossicorticosteron, Diidrotestosteron, Estron, Estradiol. Three deuterated hormones (Cortisol-D4, Aldosteron-D7, Testosteron-D3) have been used as internal standards in order to set a more accurate and precise procedure. The method was developed using the Agilent UHPLC chromatographic system (1290) using a Zorbax RRHD C18 – 1,8 μm column and a 6420Agilent Mass Spectrometer . The procedure is fast and intuitive; the sample preparation is very easy, with the serum deproteinized in vials using a deproteinizing solution, centifuged and injected into the system. The mobile phases are made of water and acetonitrile, both containing formic acid. Overall, the method is very simple and robust and it brings about a remarkable saving of time and money with respect to previously reported methods; in fact, using the UHPLC–Tandem Mass spectrometer enables simultaneous quantification of seventeen Steroidal Hormones.
2015
0000000000
273
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11581/392792
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