Stereoselective determination of flecainide in human plasma by high-performance liquid chromatography with fluorescence detection.
暂无分享,去创建一个
D. Roden | J. Turgeon | C. Prakash | H. Kroemer | I. Blair
[1] C. Prakash,et al. Simultaneous determination of propranolol enantiomers in plasma by high-performance liquid chromatography with fluorescence detection. , 1989, Journal of pharmaceutical sciences.
[2] D. Roden,et al. Stereoselective disposition and pharmacologic activity of propafenone enantiomers. , 1989, Circulation.
[3] C. Prakash,et al. Resolution of enantiomers of the antiarrhythmic drug encainide and its major metabolites by chiral derivatization and high-performance liquid chromatography. , 1989, Journal of chromatography.
[4] M. Eichelbaum,et al. Is there a genetic factor in flecainide toxicity? , 1988, BMJ.
[5] H. Duff,et al. Determinants of stereospecific binding of type I antiarrhythmic drugs to cardiac sodium channels. , 1988, Molecular pharmacology.
[6] B. Sweetman,et al. 3-Nitrobenzyl alcohol has wide applicability as a matrix for FAB-MS. , 1988, Biomedical & environmental mass spectrometry.
[7] N. Grgurinovich. A simple high-performance liquid chromatographic method for the routine measurement of flecainide in plasma. , 1988, Journal of analytical toxicology.
[8] D. Roden,et al. Drug therapy. Flecainide. , 1986, The New England journal of medicine.
[9] R. Maes,et al. Measurement of flecainide plasma concentrations by high performance liquid chromatography with fluorescence detection. , 1986, Journal of analytical toxicology.
[10] B. Testa. The chromatographic analysis of enantiomers in drug metabolism studies. , 1986, Xenobiotica; the fate of foreign compounds in biological systems.
[11] J. R. Schmid,et al. Resolution of flecainide acetate, N-(2-piperidylmethyl)-2,5-bis(2,2,2-trifluoroethoxy)benzam ide acetate, and antiarrhythmic properties of the enantiomers. , 1986, Journal of medicinal chemistry.
[12] G. D. Johnston,et al. A comparison of the cardiovascular effects of (+)-sotalol and (+/-)-sotalol following intravenous administration in normal volunteers. , 1985, British journal of clinical pharmacology.
[13] J. Knoll. Estimation of the limit of detection in chromatography , 1985 .
[14] H. Boudoulas,et al. Stereoselective pharmacokinetics of disopyramide enantiomers in man. , 1985, Drug metabolism and disposition: the biological fate of chemicals.
[15] M. Eichelbaum,et al. Effects of d,l‐verapamil on atrioventricular conduction in relation to its stereoselective first‐pass metabolism , 1985, Clinical pharmacology and therapeutics.
[16] M. Eichelbaum,et al. Stereoselective first-pass metabolism of highly cleared drugs: studies of the bioavailability of L- and D-verapamil examined with a stable isotope technique. , 1984, British journal of clinical pharmacology.
[17] B. Lucchesi,et al. Antiarrhythmic and antifibrillatory actions of the levo- and dextrorotatory isomers of sotalol. , 1984, Journal of cardiovascular pharmacology.
[18] J. Johnson,et al. Quantitation of flecainide acetate, a new antiarrhythmic agent, in biological fluids by gas chromatography with electron-capture detection. , 1984, Journal of pharmaceutical sciences.
[19] G. Shenfield,et al. A Rapid Liquid Chromatographic Method for Determination of Flecainide in Human Blood Plasma Using Ultraviolet Detection , 1984 .
[20] J. Anderson. Experience with electrophysiologically guided therapy of ventricular tachycardia with flecainide: summary of long-term follow-up. , 1984, The American journal of cardiology.
[21] D. Roden,et al. Flecainide dose-response relations in stable ventricular arrhythmias. , 1984, The American journal of cardiology.
[22] G. Gentzkow,et al. Extracardiac adverse effects of flecainide. , 1984, The American journal of cardiology.
[23] D. Holt,et al. High-performance liquid chromatographic method for the measurement of mexiletine and flecainide in blood plasma or serum. , 1984, Journal of chromatography.
[24] A. Miller,et al. Application of a bonded-phase extraction column for rapid sample preparation of flecainide from human plasma for high-performance liquid chromatographic analysis--fluorescence or ultraviolet detection. , 1984, Therapeutic drug monitoring.
[25] A. Miller,et al. High-performance liquid chromatographic method for the quantitation of flecainide, a new antiarrhythmic, in human plasma and urine. , 1983, Journal of chromatography.
[26] W. L. Nelson,et al. The Cardiac Effects of d‐ and 1‐Disopyramide in Normal Subjects: A Noninvasive Study , 1982, Circulation.
[27] R. Asinger,et al. Suppression of Ventricular Ectopic Depolarizations by Flecainide Acetate, A New Antiarrhythmic Agent , 1982, Circulation.
[28] D. Roden,et al. Suppression of resistant ventricular arrhythmias by twice daily dosing with flecainide. , 1981, The American journal of cardiology.
[29] B. Pitt,et al. Oral flecainide acetate for the treatment of ventricular arrhythmias. , 1981, The New England journal of medicine.
[30] J. C. Bailey,et al. Electrophysiological Effects of the Optical Isomers of Disopyramide and Quinidine in the Dog , 1981, Circulation research.
[31] J. Westley,et al. The use of /-/-menthyl chloroformate in the optical analysis of asymmetric amino and hydroxyl compounds by gas chromatography. , 1968 .