Liquid chromatography-mass spectrometry. Coupling of a liquid chromatograph to a mass spectrometer

1973 ◽  
Vol 45 (8) ◽  
pp. 1553-1556 ◽  
Author(s):  
R. E. Lovins ◽  
S. R. Ellis ◽  
G. D. Tolbert ◽  
C. R. McKinney
The Analyst ◽  
2019 ◽  
Vol 144 (9) ◽  
pp. 2867-2871 ◽  
Author(s):  
Päivi Pöhö ◽  
Anu Vaikkinen ◽  
Markus Haapala ◽  
Petri Kylli ◽  
Risto Kostiainen

The first report on capillary photoionization interfacing a liquid chromatograph and mass spectrometer.


2016 ◽  
Vol 60 (1) ◽  
pp. 35-41 ◽  
Author(s):  
Ewelina Patyra ◽  
Krzysztof Kwiatek

Abstract Introduction: The article presents a rapid and simple analytical procedure for determination of four tetracyclines (oxytetracycline, tetracycline, chlortetracycline, and doxycycline) in animal medicated feedingstuffs. Material and Methods: Two-gramme samples were extracted by a Na2EDTA-McIlvaine buffer (pH 4)/methanol mixtures (40/60, v/v). The determination was achieved by liquid chromatography using a Zorbax Eclipse XDB C18 analytical column with mass spectrometer detection (LC-MS). Results: Recoveries of the antibiotics from spiked feed samples ranged from 78.2% to 113.5%. The LOD and LOQ for tetracyclines in feeds ranged from 2.8 to 4.2 and from 4.3 to 5.7 mg/kg, respectively. Conclusion: The method was successfully validated and proved to be efficient, precise, and useful for quantification of tetracyclines in medicated feedingstuffs.


2000 ◽  
Vol 83 (3) ◽  
pp. 742-747 ◽  
Author(s):  
Hans G J Mol ◽  
Ruud C J Van Dam ◽  
Rob J Vreeken ◽  
Odile M Steijger

Abstract A straightforward and reliable method was developed for the determination of chlormequat in pears by liquid chromatography/mass spectrometry (LC/MS). Water and methanol were compared as extraction solvents. Because no significant differences in extraction efficiency or repeatability were found, water was chosen as the extraction solvent. The extracts were analyzed without cleanup by either an ion-trap liquid chromatograph/mass spectrometer in the single MS mode or a triple-quadrupole instrument in the MS/MS mode, using electrospray ionization. Both instruments were equally suitable for quantitation and confirmation of identity. Recoveries were 76–103%, and reproducibility was ≤12%. The lowest detection limit (0.007 mg/kg) was obtained with the triple-quadrupole instrument in the MS/MS mode.


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