Sweat Cortisol and Cortisone Determination in Healthy Adults: UHPLC-MS/MS Assay Validation and Clinical Application

A simple and effective ultra-high-performance liquid chromatography assay linked to tandem mass spectrometry (UHPLC-MS/MS) for measuring cortisol and cortisone levels in human sweat has been developed and validated. A noninvasive world standard sweat collecting equipment was utilized to collect samp...

Full description

Saved in:
Bibliographic Details
Main Authors: Syed N. Alvi, Kafa Abuhdeeb, Muhammad M. Hammami
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Advances in Pharmacological and Pharmaceutical Sciences
Online Access:http://dx.doi.org/10.1155/2022/3133640
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832551043899064320
author Syed N. Alvi
Kafa Abuhdeeb
Muhammad M. Hammami
author_facet Syed N. Alvi
Kafa Abuhdeeb
Muhammad M. Hammami
author_sort Syed N. Alvi
collection DOAJ
description A simple and effective ultra-high-performance liquid chromatography assay linked to tandem mass spectrometry (UHPLC-MS/MS) for measuring cortisol and cortisone levels in human sweat has been developed and validated. A noninvasive world standard sweat collecting equipment was utilized to collect samples. The samples were analyzed using an Atlantis dC18 (2.1 × 100 mm, 3 μm) column with a 2 mM ammonium acetate and acetonitrile (1 : 1, v : v) mobile phase. In an isocratic condition, the mobile phase was delivered at a flow rate of 0.3 ml/minute. A positive electrospray ionization interface with multiple-reaction monitoring mode was used to provide simultaneous quantification of cortisol, cortisone, and internal standard at transitions of 363.11 to 121.00, 361.18 to 163.11, and 367.19 to 121.24, respectively. The method was validated for cortisol and cortisone determination over a concentration range of 0.5–50 ng/mL The detection limits for cortisol and cortisone in human sweat were 0.3 and 0.2 ng/ml, respectively. The interday coefficients of variation of cortisol and cortisone were ≤8.5% and ≤10.01%, whereas bias was in the range from −7.9% to 2.1% and from −4.3% to 3.0%, respectively. The assay was successfully applied to evaluate the cortisol-to-cortisone ratio in sweat samples collected from healthy adult volunteers.
format Article
id doaj-art-4a0e73a7d230436a9318529f1b3d8366
institution Kabale University
issn 2633-4690
language English
publishDate 2022-01-01
publisher Wiley
record_format Article
series Advances in Pharmacological and Pharmaceutical Sciences
spelling doaj-art-4a0e73a7d230436a9318529f1b3d83662025-02-03T06:05:01ZengWileyAdvances in Pharmacological and Pharmaceutical Sciences2633-46902022-01-01202210.1155/2022/3133640Sweat Cortisol and Cortisone Determination in Healthy Adults: UHPLC-MS/MS Assay Validation and Clinical ApplicationSyed N. Alvi0Kafa Abuhdeeb1Muhammad M. Hammami2Clinical Studies and Empirical Ethics DepartmentClinical Studies and Empirical Ethics DepartmentClinical Studies and Empirical Ethics DepartmentA simple and effective ultra-high-performance liquid chromatography assay linked to tandem mass spectrometry (UHPLC-MS/MS) for measuring cortisol and cortisone levels in human sweat has been developed and validated. A noninvasive world standard sweat collecting equipment was utilized to collect samples. The samples were analyzed using an Atlantis dC18 (2.1 × 100 mm, 3 μm) column with a 2 mM ammonium acetate and acetonitrile (1 : 1, v : v) mobile phase. In an isocratic condition, the mobile phase was delivered at a flow rate of 0.3 ml/minute. A positive electrospray ionization interface with multiple-reaction monitoring mode was used to provide simultaneous quantification of cortisol, cortisone, and internal standard at transitions of 363.11 to 121.00, 361.18 to 163.11, and 367.19 to 121.24, respectively. The method was validated for cortisol and cortisone determination over a concentration range of 0.5–50 ng/mL The detection limits for cortisol and cortisone in human sweat were 0.3 and 0.2 ng/ml, respectively. The interday coefficients of variation of cortisol and cortisone were ≤8.5% and ≤10.01%, whereas bias was in the range from −7.9% to 2.1% and from −4.3% to 3.0%, respectively. The assay was successfully applied to evaluate the cortisol-to-cortisone ratio in sweat samples collected from healthy adult volunteers.http://dx.doi.org/10.1155/2022/3133640
spellingShingle Syed N. Alvi
Kafa Abuhdeeb
Muhammad M. Hammami
Sweat Cortisol and Cortisone Determination in Healthy Adults: UHPLC-MS/MS Assay Validation and Clinical Application
Advances in Pharmacological and Pharmaceutical Sciences
title Sweat Cortisol and Cortisone Determination in Healthy Adults: UHPLC-MS/MS Assay Validation and Clinical Application
title_full Sweat Cortisol and Cortisone Determination in Healthy Adults: UHPLC-MS/MS Assay Validation and Clinical Application
title_fullStr Sweat Cortisol and Cortisone Determination in Healthy Adults: UHPLC-MS/MS Assay Validation and Clinical Application
title_full_unstemmed Sweat Cortisol and Cortisone Determination in Healthy Adults: UHPLC-MS/MS Assay Validation and Clinical Application
title_short Sweat Cortisol and Cortisone Determination in Healthy Adults: UHPLC-MS/MS Assay Validation and Clinical Application
title_sort sweat cortisol and cortisone determination in healthy adults uhplc ms ms assay validation and clinical application
url http://dx.doi.org/10.1155/2022/3133640
work_keys_str_mv AT syednalvi sweatcortisolandcortisonedeterminationinhealthyadultsuhplcmsmsassayvalidationandclinicalapplication
AT kafaabuhdeeb sweatcortisolandcortisonedeterminationinhealthyadultsuhplcmsmsassayvalidationandclinicalapplication
AT muhammadmhammami sweatcortisolandcortisonedeterminationinhealthyadultsuhplcmsmsassayvalidationandclinicalapplication