scholarly journals Evaluation of the capabilities of atmospheric pressure chemical ionization source coupled to tandem mass spectrometry for the determination of dioxin-like polychlorobiphenyls in complex-matrix food samples

2016 ◽  
Vol 937 ◽  
pp. 96-105 ◽  
Author(s):  
T. Portolés ◽  
C. Sales ◽  
M. Abalos ◽  
J. Sauló ◽  
E. Abad
2011 ◽  
Vol 2011 ◽  
pp. 1-7 ◽  
Author(s):  
Xingchen Zhou ◽  
Zeneng Cheng ◽  
Liling Ran ◽  
Xin Guo ◽  
Zhi Liu ◽  
...  

A sensitive, specific, and rapid high-performance liquid chromatography-atmospheric pressure chemical ionization source-tandem mass spectrometry (HPLC-APCI-MS/MS) method for the determination of glucosamine in human plasma was developed and validated. Plasma samples were processed by protein precipitation with dehydrated ethanol, and the chromatographic separation was performed on an Agilent XDB-C18 column with a mobile phase of methanol—0.2% formic acid solution (70 : 30, v/v). Mass spectrometric quantification was carried out in the multiple reaction monitoring (MRM) mode, monitoring ion transitions of m/z 180.1 to m/z 162.1 with collision energy (CE) of 2 eV for glucosamine and m/z 181.1 to m/z 163.1 with CE of 2 eV for the internal standard (IS) in positive ion mode. The linear calibration curves covered a concentration range of 53.27–3409 ng/mL with a lower limit of quantification (LLOQ) of 53.27 ng/mL. The extraction recovery of glucosamine was greater than 101.7%. The intra- and interday precisions for glucosamine were less than 10%, and the accuracies were between 93.7% and 102.6%, determined from quality control (QC) samples of three representative concentrations. The method has been successfully applied to determining the plasma concentration of glucosamine in a clinical pharmacokinetic study involving 20 healthy Chinese male volunteers.


2008 ◽  
Vol 80 (8) ◽  
pp. 2646-2653 ◽  
Author(s):  
Francisco J. Andrade ◽  
Jacob T. Shelley ◽  
William C. Wetzel ◽  
Michael R. Webb ◽  
Gerardo Gamez ◽  
...  

2004 ◽  
Vol 76 (22) ◽  
pp. 6659-6664 ◽  
Author(s):  
Pekka Östman ◽  
Seppo J. Marttila ◽  
Tapio Kotiaho ◽  
Sami Franssila ◽  
Risto Kostiainen

2010 ◽  
Vol 93 (4) ◽  
pp. 1293-1301 ◽  
Author(s):  
Joann Grant ◽  
Carol A Rodgers ◽  
Clark D Chickering ◽  
Sidney J Hill ◽  
James J Stry

Abstract An analytical method is presented for the determination of chlorantraniliprole residues in crops. Chlorantraniliprole residues were extracted from crop matrixes with acetonitrile after a water soak. The extracts were passed through a strong anion-exchange (SAX) SPE cartridge stacked on top of a reversed-phase (RP) polymer cartridge. After both cartridges were rinsed and vacuum-dried, the SAX cartridge was removed, and chlorantraniliprole was eluted from the RP polymer cartridge with acetonitrile. The acetonitrile eluate was evaporated to dryness, reconstituted, and analyzed using an LC/MS/MS instrument equipped with an atmospheric pressure chemical ionization source. The method was successfully validated at 0.010, 0.10, and 10 mg/kg for the following crop matrixes: potatoes, sugar beets (tops), lettuce, broccoli, soybeans, soybean forage, tomatoes, cucumbers, oranges, apples, pears, peaches, almonds (nutmeat), rice grain, wheat grain, wheat hay, corn stover, alfalfa forage, cottonseed, grapes, and corn grain. The average recoveries from all crop samples fortified at the method LOQ ranged from 91 to 108, with an overall average recovery of 97. The average recoveries from all crop samples fortified at 10 times the method LOQ ranged from 89 to 115, with an overall average recovery of 101. For all of the fortified control samples analyzed in this study, the overall average recovery was 99.


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