Measurement of Warfarin in the Oral Fluid of Patients Undergoing Anticoagulant Oral Therapy
Articolo
Data di Pubblicazione:
2011
Abstract:
Background: Patients on warfarin therapy undergo invasive and expensive checks for the coagulability of their blood. No
information on coagulation levels is currently available between two controls.
Methodology: A method was developed to determine warfarin in oral fluid by HPLC and fluorimetric detection. The
chromatographic separation was performed at room temperature on a C-18 reversed-phase column, 65% PBS and 35%
methanol mobile phase, flow rate 0.7 mL/min, injection volume 25 mL, excitation wavelength 310 nm, emission wavelength
400 nm.
Findings: The method was free from interference and matrix effect, linear in the range 0.2-100 ng/mL, with a detection
limit of 0.2 ng/mL. Its coefficient of variation was ,3% for intra-day measurements and ,5% for inter-day measurements.
The average concentration of warfarin in the oral fluid of 50 patients was 2.561.6 ng/mL (range 0.8-7.6 ng/mL). Dosage
was not correlated to INR (r =20.03, p = 0.85) but positively correlated to warfarin concentration in the oral fluid (r = 0.39,
p = 0.006). The correlation between warfarin concentration and pH in the oral fluid (r = 0.37, p = 0.009) confirmed the
importance of pH in regulating the drug transfer from blood. A correlation between warfarin concentration in the oral fluid
and INR was only found in samples with pH values $7.2 (r = 0.84, p = 0.004).
Conclusions: Warfarin diffuses from blood to oral fluid. The method allows to measure its concentration in this matrix and
to analyze correlations with INR and other parameters.
information on coagulation levels is currently available between two controls.
Methodology: A method was developed to determine warfarin in oral fluid by HPLC and fluorimetric detection. The
chromatographic separation was performed at room temperature on a C-18 reversed-phase column, 65% PBS and 35%
methanol mobile phase, flow rate 0.7 mL/min, injection volume 25 mL, excitation wavelength 310 nm, emission wavelength
400 nm.
Findings: The method was free from interference and matrix effect, linear in the range 0.2-100 ng/mL, with a detection
limit of 0.2 ng/mL. Its coefficient of variation was ,3% for intra-day measurements and ,5% for inter-day measurements.
The average concentration of warfarin in the oral fluid of 50 patients was 2.561.6 ng/mL (range 0.8-7.6 ng/mL). Dosage
was not correlated to INR (r =20.03, p = 0.85) but positively correlated to warfarin concentration in the oral fluid (r = 0.39,
p = 0.006). The correlation between warfarin concentration and pH in the oral fluid (r = 0.37, p = 0.009) confirmed the
importance of pH in regulating the drug transfer from blood. A correlation between warfarin concentration in the oral fluid
and INR was only found in samples with pH values $7.2 (r = 0.84, p = 0.004).
Conclusions: Warfarin diffuses from blood to oral fluid. The method allows to measure its concentration in this matrix and
to analyze correlations with INR and other parameters.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
saliva; warfarin; INR
Elenco autori:
Onor, Massimo; Trivella, MARIA GIOVANNA
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