Direct (non-chromatographic) quantification of drugs and their metabolites from human plasma utilizing chemical ionization mass spectrometry and stable isotope labeling: quinidine and lidocaine.

Preliminary results are reported for the quantitative determination of the antiarrhythmic agents quinidine and lidocaine in human plasma by combined isobutane chemical ionization mass spectrometry and stable isotope labeling. The concentration of monoethylglycinexylidide, a known metabolite of lidocaine, was also determined using this method. In the procedure used, stable isotope analogs of the materials to be determined were added to serial plasma samples. The plasma was then made basic and extracted with benzene. The residue after evaporation of the solvent was placed directly into the mass spectrometer via the direct insertion probe and the spectrum determined. In this manner the above named compounds could readily be quantitated without recourse to either derivitization or further purification.

[1]  Kelly Rw Method for the measurement of prostaglandin F2alpha in biological fluids by gas chromatography-mass spectrometry. , 1973 .

[2]  L. Bertilsson,et al.  Quantitative determination of carbamazepine in plasma by mass fragmentography , 1973, Clinical pharmacology and therapeutics.

[3]  M. Horning,et al.  Use of stable isotopes in measuring low concentrations of drugs and drug metabolites by GC-MS-COM procedures. , 1973, Clinical chemistry.

[4]  D J Jenden,et al.  Deuterium substituted amphetamine as an internal standard in a gas chromatographic-mass spectrometric (GC-MS) assay for amphetamine. , 1973, Analytical chemistry.

[5]  D. Jenden,et al.  Applications of integrated gas chromatography-mass spectrometry in pharmacology and toxicology. , 1973, Annual review of pharmacology.

[6]  A. Atkinson,et al.  Simultaneous measurement of plasma concentratons of lidocaine and its deethylated metabolite by mass fragmentography , 1972 .

[7]  D. Knapp,et al.  Use of stable isotopes in pharmacology‐clinical pharmacology , 1972, Clinical pharmacology and therapeutics.

[8]  G. Milne,et al.  Identification of dangerous drugs by isobutane chemical ionization mass spectrometry. , 1971, Analytical Chemistry.

[9]  L. Keefer,et al.  Alkylation of nucleic acids of rat liver and lung by deuterated N-nitrosodiethylamine in vivo. , 1971, Journal of the National Cancer Institute.

[10]  C. Hammar,et al.  Novel peak matching technique by means of a new and combined multiple ion detector-peak matcher device. Elemental analyses of compounds in submicrogram quantities without prior isolation , 1971 .

[11]  L. Mcdonald,et al.  Sustained-release quinidine (Kinidin Durules) in maintaining sinus rhythm after electroversion of atrial dysrhythmias. , 1971, British heart journal.

[12]  D. Scott,et al.  Pharmacokinetics of lidocaine in man , 1971, Clinical pharmacology and therapeutics.

[13]  G. Milne,et al.  Chemical ionization mass spectrometry of complex molecules. II. Alkaloids. , 1970, Journal of the American Chemical Society.

[14]  R. Ryhage,et al.  Mass fragmentography. Identification of chlorpromazine and its metabolites in human blood by a new method. , 1968, Analytical biochemistry.

[15]  B. Isaksson,et al.  QUANTITATIVE DETERMINATION OF QUINIDINE IN PLASMA. , 1963, Scandinavian journal of clinical and laboratory investigation.