Simultaneous Determination of Cyclosporine A, Tacrolimus, Sirolimus, and Everolimus in Whole-Blood Samples by LC-MS/MS

Author:

Karapirli Mustafa1ORCID,Kizilgun Murat2,Yesilyurt Ozgur3,Gul Husamettin3,Kunak Zeki Ilker4,Akgul Emin Ozgur56,Macit Enis3,Cayci Tuncer5,Gulcan Kurt Yasemin5,Aydin Ibrahim5,Yaren Hakan4,Seyrek Melik3,Cakir Erdinc5,Yaman Halil5

Affiliation:

1. Council of Forensic Medicine, Ankara Branch, Kecioren, 06018 Ankara, Turkey

2. Department of Biochemistry, Diskapi Children' Health and Diseases, Hematology, Oncology Training and Research Hospital, Ministry of Health, 06590 Ankara, Turkey

3. Department of Pharmacology, Gulhane Military Medical Academy, 06018 Ankara, Turkey

4. Department of Medical Chemical/Biological/Radiological/Nuclear Defense, Gulhane Military Medical Academy, Etlik, 06018 Ankara, Turkey

5. Department of Clinical Biochemistry, Gulhane Military Medical Academy, 06018 Ankara, Turkey

6. Department of Clinical Chemistry, Gulhane Military Medical Academy, Etlik, 06018 Ankara, Turkey

Abstract

Objectives. Cyclosporine A (CyA), tacrolimus (TRL), sirolimus (SIR), and everolimus (RAD) are immunosuppressive drugs frequently used in organ transplantation. Our aim was to confirm a robust sensitive and selective liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for determination of CyA, TRL, SIR, and RAD in whole-blood samples.Materials and Methods. We used an integrated online solid-phase extraction-LC-MS/MS system and atmospheric pressure ionization tandem mass spectrometry (API-MS/MS) in the multiple reaction monitoring (MRM) detection mode. CyA, TRL, SIR, and RAD were simultaneously analyzed in whole blood treated with precipitation reagent taken from transplant patients.Results. System performance parameters were suitable for using this method as a high-throughput technique in clinical practice. The high concentration of one analyte in the sample did not affect the concentration of other analytes. Total analytical time was 2.5 min, and retention times of all analytes were shorter than 2 minutes.Conclusion. This LC-MS/MS method can be preferable for therapeutic drug monitoring of these immunosuppressive drugs (CyA, TRL, SRL, and RAD) in whole blood. Sample preparation was too short and simple in this method, and it permits robust, rapid, sensitive, selective, and simultaneous determination of these drugs.

Publisher

Hindawi Limited

Subject

General Environmental Science,General Biochemistry, Genetics and Molecular Biology,General Medicine

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