Literature DB >> 3577433

Positive and negative ion mass spectrometry of tricyclic antidepressants.

O Suzuki, H Hattori, M Asano, H Brandenberger.   

Abstract

Positive electron impact (EI), positive chemical ionization (CI), and negative CI mass spectra of eight tricyclic antidepressants are presented. In the positive EI mode, peak(s) at m/z 193 and/or 195, which corresponded to the tricyclic nucleus, appeared for five compounds; a peak at m/z 58 was common to compounds having a gamma-dimethylaminopropyl group as their side chain. Molecular ions appeared for all compounds though they were very small in some compounds in the positive EI mode. In the positive CI mode, [M + H]+ quasi-molecular peaks appeared together with [M + C2H5]+ peaks in five compounds; the ion at m/z 196, which corresponded to the tricyclic nucleus also appeared in five compounds. In the negative CI mode with 1 Torr chamber pressure, [M - 1]- quasi-molecular ions were observed for all compounds except for lofepramine; [M + 43]- anions, which probably corresponded to [M + C3H4]-, appeared in five compounds; strong [M + Cl]- ions appeared in carpipramine and clocapramine. The anions due to the tricyclic nucleus also appeared in this mode. In the negative CI mode at low pressure (0.01 Torr), the spectra were generally similar to those in the 1 Torr negative CI mode. However, the cluster anions never appeared at the low pressure. Some data on extraction for some antidepressants from human urine and plasma, and their separation by gas chromatography, are also presented.

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Year:  1986        PMID: 3577433     DOI: 10.1007/bf00200603

Source DB:  PubMed          Journal:  Z Rechtsmed        ISSN: 0044-3433


  8 in total

1.  Simultaneous measurement of imipramine and desipramine by selected ion recording with deuterated internal standards.

Authors:  M Claeys; G Muscettola; S P Markey
Journal:  Biomed Mass Spectrom       Date:  1976-06

2.  A comprehensive GC-MS reference data system for toxicological and biomedical purposes.

Authors:  B S Finkle; R L Foltz; D M Taylor
Journal:  J Chromatogr Sci       Date:  1974-05       Impact factor: 1.618

3.  Quantitative analysis for tricyclic antidepressant drugs in plasma or serum by gas chromatography-chemical-ionization mass spectrometry.

Authors:  D M Chinn; T A Jennison; D J Crouch; M A Peat; G W Thatcher
Journal:  Clin Chem       Date:  1980-07       Impact factor: 8.327

4.  A sensitive method for the simultaneous determination in biological fluids of imipramine and desipramine or clomipramine and N-desmethylclomipramine by gas chromatography mass spectrometry.

Authors:  D Alkalay; J Volk; S Carlsen
Journal:  Biomed Mass Spectrom       Date:  1979-05

5.  Mass fragmentographic determination of lofepramine and its metabolites in human plasma and urine using deuterated internal standards.

Authors:  K Matsubayashi; H Hakusui; M Sano
Journal:  J Chromatogr       Date:  1977-11-01

6.  Negative ion mass spectrometry of phenothiazines.

Authors:  R Ryhage; H Brandenberger
Journal:  Biomed Mass Spectrom       Date:  1978-11

7.  Reversed-phase liquid chromatography and gas chromatography/mass fragmentography compared for determination of tricyclic antidepressant drugs.

Authors:  D A Breutzmann; L D Bowers
Journal:  Clin Chem       Date:  1981-11       Impact factor: 8.327

8.  Analysis of tricyclic antidepressants in human plasma by GLC--chemical-ionization mass spectrometry with selected ion monitoring.

Authors:  R G Jenkins; R O Friedel
Journal:  J Pharm Sci       Date:  1978-01       Impact factor: 3.534

  8 in total

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