Quantification of dabigatran and indirect quantification of dabigatran acylglucuronides in human plasma by LC–MS/MS

Author:

Saffian Shamin Mohd12,Zhang Mei34,Leong Chin Paul Ken3,Jensen Berit Packert4

Affiliation:

1. School of Pharmacy, University of Otago, PO Box 56, Dunedin 9054, New Zealand

2. Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, 50300 Kuala Lumpur, Malaysia

3. Clinical Pharmacology, Department of Medicine, University of Otago, Christchurch, 2 Riccarton Avenue, PO Box 4345, Christchurch 8140, New Zealand

4. Toxicology, Specialist Cluster, Canterbury Health Laboratories, PO Box 151, Christchurch 8140, New Zealand

Abstract

Background: An assay for the quantification of dabigatran and its active metabolites, dabigatran acylglucuronides, has not previously been described in detail. Results: For the quantification of total dabigatran concentration (free dabigatran and acylglucuronides), samples were subjected to alkaline hydrolysis. For the quantification of free dabigatran, samples were acidified with ammonium formate. Following acetonitrile protein precipitation, the samples were analyzed by LC–MS/MS using gradient elution to ensure separation of dabigatran from dabigatran acylglucuronides. Mean recoveries ≥98% were achieved. The assay was validated over the range 2.5–1000 ng/ml dabigatran, imprecision was <9% CV (<15% at LLOQ) and accuracy was 101–114%. Conclusion: An assay for dabigatran with indirect quantification of dabigatran acylglucuronides in plasma was developed, validated and applied.

Publisher

Future Science Ltd

Subject

Medical Laboratory Technology,Clinical Biochemistry,General Pharmacology, Toxicology and Pharmaceutics,General Medicine,Analytical Chemistry

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