Determination of Oral Dosage and Pharmacokinetic Analysis of Flecainide in Horses
To determine oral dosage and to evaluate the pharmacokinetics in horses of orally administered flecainide, an antiarrhythmic drug, the correlations between its plasma concentration and PR, QRS and QT intervals in equine electrocardiograms (ECG) were investigated. Six healthy horses were administered...
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Published in | Journal of Veterinary Medical Science Vol. 63; no. 5; pp. 511 - 514 |
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Language | English |
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Japan
JAPANESE SOCIETY OF VETERINARY SCIENCE
01.05.2001
Japan Science and Technology Agency |
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Abstract | To determine oral dosage and to evaluate the pharmacokinetics in horses of orally administered flecainide, an antiarrhythmic drug, the correlations between its plasma concentration and PR, QRS and QT intervals in equine electrocardiograms (ECG) were investigated. Six healthy horses were administered a randomly ordered dose of 4 or 6 mg/kg of flecainide acetate. The ECG was monitored (heart rate (HR), PR, QRS, and QT intervals) and blood was taken at timed intervals to measure the plasma flecainide concentrations pre- and post-administration. The maximum plasma concentration reached 1014 ± 285 (SD) ng/ml in 45 ± 13 min and 1301 ± 400 ng/m l in 60 ± 37 min for doses of 4 and 6 mg/kg flecainide, respectively. From the pharmacokinetic analysis, clearance rates were 14.6 ± 6.4 and 11.7 ± 5.2 ml/kg/min and terminal elimination half-lives were 228 ± 53 and 304 ± 87 min. The QRS and QT intervals increased significantly for both doses following administration, though HR and PR intervals did not change. Plasma flecainide concentrations were significantly correlated with QRS (r=0.935, P<0.001) and QT intervals (r=0.753, P<0.001). In conclusion, plasma concentrations of flecainide for treating equine atrial fibrillation were obtained by oral administration of 4 and 6 mg/kg, and the drug was rapidly eliminated from plasma in horses. |
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AbstractList | To determine oral dosage and to evaluate the pharmacokinetics in horses of orally administered flecainide, an antiarrhythmic drug, the correlations between its plasma concentration and PR, QRS and QT intervals in equine electrocardiograms (ECG) were investigated. Six healthy horses were administered a randomly ordered dose of 4 or 6 mg/kg of flecainide acetate. The ECG was monitored (heart rate (HR), PR, QRS, and QT intervals) and blood was taken at timed intervals to measure the plasma flecainide concentrations pre- and post-administration. The maximum plasma concentration reached 1014 ± 285 (SD) ng/ml in 45 ± 13 min and 1301 ± 400 ng/m l in 60 ± 37 min for doses of 4 and 6 mg/kg flecainide, respectively. From the pharmacokinetic analysis, clearance rates were 14.6 ± 6.4 and 11.7 ± 5.2 ml/kg/min and terminal elimination half-lives were 228 ± 53 and 304 ± 87 min. The QRS and QT intervals increased significantly for both doses following administration, though HR and PR intervals did not change. Plasma flecainide concentrations were significantly correlated with QRS (r=0.935, P<0.001) and QT intervals (r=0.753, P<0.001). In conclusion, plasma concentrations of flecainide for treating equine atrial fibrillation were obtained by oral administration of 4 and 6 mg/kg, and the drug was rapidly eliminated from plasma in horses. To determine oral dosage and to evaluate the pharmacokinetics in horses of orally administered flecainide, an antiarrhythmic drug, the correlations between its plasma concentration and PR, QRS and QT intervals in equine electrocardiograms (ECG) were investigated. Six healthy horses were administered a randomly ordered dose of 4 or 6 mg/kg of flecainide acetate. The ECG was monitored (heart rate (HR), PR, QRS, and QT intervals) and blood was taken at timed intervals to measure the plasma flecainide concentrations pre- and post-administration. The maximum plasma concentration reached 1014+/-285 (SD) ng/m/ in 45+/-13 min and 1301+/-400 ng/ m/l in 60+/-37 min for doses of 4 and 6 mg/kg flecainide, respectively. From the pharmacokinetic analysis, clearance rates were 14.6+/-6.4 and 11.7+/-5.2 ml/kg/min and terminal elimination half-lives were 228+/-53 and 304+/-87 min. The QRS and QT intervals increased significantly for both doses following administration, though HR and PR intervals did not change. Plasma flecainide concentrations were significantly correlated with QRS (r=0.935, P<0.001) and QT intervals (r=0.753, P<0.001). In conclusion, plasma concentrations of flecainide for treating equine atrial fibrillation were obtained by oral administration of 4 and 6 mg/kg, and the drug was rapidly eliminated from plasma in horses. To determine oral dosage and to evaluate the pharmacokinetics in horses of orally administered flecainide, an antiarrhythmic drug, the correlations between its plasma concentration and PR, QRS and QT intervals in equine electrocardiograms (ECG) were investigated. Six healthy horses were administered a randomly ordered dose of 4 or 6 mg/kg of flecainide acetate. The ECG was monitored (heart rate (HR), PR, QRS, and QT intervals) and blood was taken at timed intervals to measure the plasma flecainide concentrations pre- and post-administration. The maximum plasma concentration reached 1014+/-285 (SD) ng/m/ in 45+/-13 min and 1301+/-400 ng/ m/l in 60+/-37 min for doses of 4 and 6 mg/kg flecainide, respectively. From the pharmacokinetic analysis, clearance rates were 14.6+/-6.4 and 11.7+/-5.2 ml/kg/min and terminal elimination half-lives were 228+/-53 and 304+/-87 min. The QRS and QT intervals increased significantly for both doses following administration, though HR and PR intervals did not change. Plasma flecainide concentrations were significantly correlated with QRS (r=0.935, P<0.001) and QT intervals (r=0.753, P<0.001). In conclusion, plasma concentrations of flecainide for treating equine atrial fibrillation were obtained by oral administration of 4 and 6 mg/kg, and the drug was rapidly eliminated from plasma in horses. |
Author | AIDA, Hiroko NUKADA, Toshio OHMURA, Hajime TAKAHASHI, Toshiyuki HIRAGA, Atsushi |
Author_xml | – sequence: 1 fullname: OHMURA, Hajime organization: Equine Science Division, Hidaka Yearling Training Farm of Japan Racing Association (JRA) – sequence: 2 fullname: HIRAGA, Atsushi organization: Equine Science Division, Hidaka Yearling Training Farm of Japan Racing Association (JRA) – sequence: 3 fullname: AIDA, Hiroko organization: Equine Science Division, Hidaka Yearling Training Farm of Japan Racing Association (JRA) – sequence: 4 fullname: TAKAHASHI, Toshiyuki organization: Equine Research Institute of JRA – sequence: 5 fullname: NUKADA, Toshio organization: Joban Branch Equine Research Institute of JRA |
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Cites_doi | 10.1016/0735-1097(90)90326-K 10.1016/0002-9149(84)90501-0 10.1016/0002-9149(84)90497-1 10.1016/0002-9149(89)90253-1 10.1016/0031-6989(86)90115-3 10.1292/jvms.62.711 10.1016/0002-9149(81)90331-3 10.1136/hrt.48.2.140 10.3999/jscpt.27.713 10.1016/0002-9149(92)91079-J 10.1093/eurheartj/14.8.1127 |
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SubjectTerms | Administration, Oral Animals Anti-Arrhythmia Agents - administration & dosage Anti-Arrhythmia Agents - blood Anti-Arrhythmia Agents - pharmacokinetics Area Under Curve Electrocardiography - veterinary equine Female flecainide Flecainide - administration & dosage Flecainide - blood Flecainide - pharmacokinetics Half-Life Heart Rate - drug effects Horses - metabolism Male oral administration pharmacokinetics Random Allocation |
Title | Determination of Oral Dosage and Pharmacokinetic Analysis of Flecainide in Horses |
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