Cargando…

An ultrasensitive UHPLC-ESI-MS/MS method augmented with a controlled microwave derivatization reaction for quantitation of vitamin D3 and its major metabolites in COVID-19 patients

It is established that vitamin D deficiency is correlated with the disease severity in COVID-19 patients. However, the reliable and sensitive quantitation of vitamin D3 (D3) and its metabolites remains a difficult challenge. Herein, a novel ultrasensitive and reliable UHPLC-ESI-MS/MS method was deve...

Descripción completa

Detalles Bibliográficos
Autores principales: Ahmed, Sameh A., Khojah, Hani M.J., Al-Thagfan, Sultan S., Alahmadi, Yaser M., Mohammed, Yasser A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023092/
https://www.ncbi.nlm.nih.gov/pubmed/35487016
http://dx.doi.org/10.1016/j.talanta.2022.123497
_version_ 1784690259193233408
author Ahmed, Sameh A.
Khojah, Hani M.J.
Al-Thagfan, Sultan S.
Alahmadi, Yaser M.
Mohammed, Yasser A.
author_facet Ahmed, Sameh A.
Khojah, Hani M.J.
Al-Thagfan, Sultan S.
Alahmadi, Yaser M.
Mohammed, Yasser A.
author_sort Ahmed, Sameh A.
collection PubMed
description It is established that vitamin D deficiency is correlated with the disease severity in COVID-19 patients. However, the reliable and sensitive quantitation of vitamin D3 (D3) and its metabolites remains a difficult challenge. Herein, a novel ultrasensitive and reliable UHPLC-ESI-MS/MS method was developed and validated for the quantitation of D3 and its major metabolites in COVID-19 patients. The mass spectral sensitivity was augmented via controlled microwave-assisted derivatization reaction (CMDR) with 2-nitrosopyridine (Pyr-NO) at 65 °C for 2 min. CMDR hyphenation with UHPLC-MS/MS improves detection sensitivity while shortening separation and derivatization reaction times. The precursor to product ion transitions for D3, 25-hydroxy D3 (25(OH)D3), 1,25-dihydroxy D3 (1,25-(OH)2D3) and calcipotriol (CPT) as an internal standard were m/z 493.4 → 231.3, m/z 509.4 → 231.3, m/z 525.4 → 247.3, and m/z 521.4 → 247.3; respectively. The separation of the formed derivatives was conducted using a gradient elution mode with mobile phase A: formic acid (0.1%) in water and mobile phase B: formic acid (0.1%) in acetonitrile. The elution started with 40% (v/v) of B for 0.3 min then increased linearly to 90% (v/v) at 2 min on an Agilent EclipsePlus C18 (50 × 2.1 mm, 1.8 μm) column at a flow rate of 0.3 mL min(−1). The method was validated using FDA standards for bioanalytical method validation over a concentration range of 0.02–50 ng mL(−1) with correlation coefficient ≥0.9987 and the lower limit of quantitation (LLOQ) were 0.02–0.05 ng mL(−1) in human plasma. The developed method has demonstrated excellent comparability to a well-established chemiluminescent immunoassay (CLIA) method for the analysis of D3 metabolites in human samples. The developed UHPLC-ESI-MS/MS method was implemented for routine and reliable quantitation of D3 and its major metabolites in COVID-19 patients.
format Online
Article
Text
id pubmed-9023092
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier B.V.
record_format MEDLINE/PubMed
spelling pubmed-90230922022-04-22 An ultrasensitive UHPLC-ESI-MS/MS method augmented with a controlled microwave derivatization reaction for quantitation of vitamin D3 and its major metabolites in COVID-19 patients Ahmed, Sameh A. Khojah, Hani M.J. Al-Thagfan, Sultan S. Alahmadi, Yaser M. Mohammed, Yasser A. Talanta Article It is established that vitamin D deficiency is correlated with the disease severity in COVID-19 patients. However, the reliable and sensitive quantitation of vitamin D3 (D3) and its metabolites remains a difficult challenge. Herein, a novel ultrasensitive and reliable UHPLC-ESI-MS/MS method was developed and validated for the quantitation of D3 and its major metabolites in COVID-19 patients. The mass spectral sensitivity was augmented via controlled microwave-assisted derivatization reaction (CMDR) with 2-nitrosopyridine (Pyr-NO) at 65 °C for 2 min. CMDR hyphenation with UHPLC-MS/MS improves detection sensitivity while shortening separation and derivatization reaction times. The precursor to product ion transitions for D3, 25-hydroxy D3 (25(OH)D3), 1,25-dihydroxy D3 (1,25-(OH)2D3) and calcipotriol (CPT) as an internal standard were m/z 493.4 → 231.3, m/z 509.4 → 231.3, m/z 525.4 → 247.3, and m/z 521.4 → 247.3; respectively. The separation of the formed derivatives was conducted using a gradient elution mode with mobile phase A: formic acid (0.1%) in water and mobile phase B: formic acid (0.1%) in acetonitrile. The elution started with 40% (v/v) of B for 0.3 min then increased linearly to 90% (v/v) at 2 min on an Agilent EclipsePlus C18 (50 × 2.1 mm, 1.8 μm) column at a flow rate of 0.3 mL min(−1). The method was validated using FDA standards for bioanalytical method validation over a concentration range of 0.02–50 ng mL(−1) with correlation coefficient ≥0.9987 and the lower limit of quantitation (LLOQ) were 0.02–0.05 ng mL(−1) in human plasma. The developed method has demonstrated excellent comparability to a well-established chemiluminescent immunoassay (CLIA) method for the analysis of D3 metabolites in human samples. The developed UHPLC-ESI-MS/MS method was implemented for routine and reliable quantitation of D3 and its major metabolites in COVID-19 patients. Elsevier B.V. 2022-08-15 2022-04-22 /pmc/articles/PMC9023092/ /pubmed/35487016 http://dx.doi.org/10.1016/j.talanta.2022.123497 Text en © 2022 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Ahmed, Sameh A.
Khojah, Hani M.J.
Al-Thagfan, Sultan S.
Alahmadi, Yaser M.
Mohammed, Yasser A.
An ultrasensitive UHPLC-ESI-MS/MS method augmented with a controlled microwave derivatization reaction for quantitation of vitamin D3 and its major metabolites in COVID-19 patients
title An ultrasensitive UHPLC-ESI-MS/MS method augmented with a controlled microwave derivatization reaction for quantitation of vitamin D3 and its major metabolites in COVID-19 patients
title_full An ultrasensitive UHPLC-ESI-MS/MS method augmented with a controlled microwave derivatization reaction for quantitation of vitamin D3 and its major metabolites in COVID-19 patients
title_fullStr An ultrasensitive UHPLC-ESI-MS/MS method augmented with a controlled microwave derivatization reaction for quantitation of vitamin D3 and its major metabolites in COVID-19 patients
title_full_unstemmed An ultrasensitive UHPLC-ESI-MS/MS method augmented with a controlled microwave derivatization reaction for quantitation of vitamin D3 and its major metabolites in COVID-19 patients
title_short An ultrasensitive UHPLC-ESI-MS/MS method augmented with a controlled microwave derivatization reaction for quantitation of vitamin D3 and its major metabolites in COVID-19 patients
title_sort ultrasensitive uhplc-esi-ms/ms method augmented with a controlled microwave derivatization reaction for quantitation of vitamin d3 and its major metabolites in covid-19 patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023092/
https://www.ncbi.nlm.nih.gov/pubmed/35487016
http://dx.doi.org/10.1016/j.talanta.2022.123497
work_keys_str_mv AT ahmedsameha anultrasensitiveuhplcesimsmsmethodaugmentedwithacontrolledmicrowavederivatizationreactionforquantitationofvitamind3anditsmajormetabolitesincovid19patients
AT khojahhanimj anultrasensitiveuhplcesimsmsmethodaugmentedwithacontrolledmicrowavederivatizationreactionforquantitationofvitamind3anditsmajormetabolitesincovid19patients
AT althagfansultans anultrasensitiveuhplcesimsmsmethodaugmentedwithacontrolledmicrowavederivatizationreactionforquantitationofvitamind3anditsmajormetabolitesincovid19patients
AT alahmadiyaserm anultrasensitiveuhplcesimsmsmethodaugmentedwithacontrolledmicrowavederivatizationreactionforquantitationofvitamind3anditsmajormetabolitesincovid19patients
AT mohammedyassera anultrasensitiveuhplcesimsmsmethodaugmentedwithacontrolledmicrowavederivatizationreactionforquantitationofvitamind3anditsmajormetabolitesincovid19patients
AT ahmedsameha ultrasensitiveuhplcesimsmsmethodaugmentedwithacontrolledmicrowavederivatizationreactionforquantitationofvitamind3anditsmajormetabolitesincovid19patients
AT khojahhanimj ultrasensitiveuhplcesimsmsmethodaugmentedwithacontrolledmicrowavederivatizationreactionforquantitationofvitamind3anditsmajormetabolitesincovid19patients
AT althagfansultans ultrasensitiveuhplcesimsmsmethodaugmentedwithacontrolledmicrowavederivatizationreactionforquantitationofvitamind3anditsmajormetabolitesincovid19patients
AT alahmadiyaserm ultrasensitiveuhplcesimsmsmethodaugmentedwithacontrolledmicrowavederivatizationreactionforquantitationofvitamind3anditsmajormetabolitesincovid19patients
AT mohammedyassera ultrasensitiveuhplcesimsmsmethodaugmentedwithacontrolledmicrowavederivatizationreactionforquantitationofvitamind3anditsmajormetabolitesincovid19patients