Key result
Novel UPLC-MS/MS assay rapidly and accurately quantifies four DOACs simultaneously in plasma and urine.
Why the study?
DOACs are increasingly used for thromboembolic disorders, and monitoring their concentrations may be valuable in specific scenarios to prevent adverse events.
Effect estimate: R2 ≥ 0.99
A rapid, one-step dilution UPLC-MS/MS method allows for the reliable simultaneous measurement of four DOACs in plasma and urine, facilitating therapeutic monitoring in complex clinical scenarios.
The new direct oral anticoagulants (DOACs) are increasingly used to treat and prevent thromboembolic disorders, and monitoring concentrations may be valuable in some special scenarios to prevent clinical adverse events. This study aimed to develop generic methods for the rapid and simultaneous analysis of four DOACs in human plasma and urine. Protein precipitation and one-step dilution were used to prepare the plasma and urine; the extracts were injected to ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) for analysis. Chromatographic separation was performed on an Acquity™ UPLC BEH C18 column (2.1 × 50 mm, 1.7 μm) with gradient elution of 7 min. A triple quadrupole tandem mass spectrometer with an electrospray ionization source was employed to analyze DOACs in a positive ion mode. The methods showed great linearity in the plasma (1~500 ng/mL) and urine (10~10,000 ng/mL) for all analytes (R2 ≥ 0.99). The intra- and inter-day precision and accuracy were within acceptance criteria. The matrix effect and extraction recovery were 86.5~97.5% and 93.5~104.7% in the plasma, while 97.0~101.9% and 85.1~99.5% in the urine. The stability of samples during the routine preparation and storage were within the acceptance criteria of less than ±15%. The methods developed were accurate, reliable, and simple for the rapid and simultaneous measurement of four DOACs in human plasma and urine, and successfully applied to patients and subjects with DOACs therapy for anticoagulant activity assessment.
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Ren et al. (2023) studied Patients on DOAC therapy requiring drug monitoring (n=32). UPLC-MS/MS assay for simultaneous DOAC analysis was evaluated on Analytical method validity (linearity, matrix effect, extraction recovery) (R2 ≥ 0.99). The developed UPLC-MS/MS method demonstrated high linearity (R2 ≥ 0.99) and extraction recovery (93.5-104.7% in plasma) for the rapid, simultaneous measurement of four direct oral anticoagulants in human plasma and urine.
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