Analysis of Peptides in Plasma by High Performance Liquid Chromatography Coupled with Electrospray Ionization Mass Spectrometry

2011 ◽  
Vol 340 ◽  
pp. 273-279
Author(s):  
Hai Yan Fang ◽  
Yin Liu ◽  
Shu Fang Wang

In this study, a high performance liquid chromatography coupled with electrospray ionization mass spectrometry (HPLC-ESI-MS) method for the determination of eight endogenous peptides, which included angiotensin-II, neurotensin, 5-met-enkephalin, 5-leu-enkephalin, somatostatin, bradykinin, dynorphin A and oxidized glutathione, was developed. MS parameters were optimized in order to obtain the best signal intensity. The optimum MS parameters were: fragmentor: 100 V; nebulizer gas (N2) pressure: 40 psi; drying gas (N2) flow rate: 10 L/min; drying gas temperature: 350 °C; capillary voltage: 2000 V. Validation of the method showed positive results. The correlation coefficients (R2) between the peak areas and the corresponding concentrations of peptides were greater than 0.9903. The limits of detection (LODs) (S/N = 3) of the eight peptides were 3.88 ng/mL ~ 17.5 ng/mL. The developed method had been successfully applied to analyzing the human plasma fortified with the eight peptides, which indicated the potential of the methodology for the analysis of biological sample.

2014 ◽  
Vol 28 (8) ◽  
pp. 1064-1069 ◽  
Author(s):  
Marcella Herbstrith de Oliveira ◽  
Graciela Carlos ◽  
Ana Maria Bergold ◽  
Flavio Pechansky ◽  
Renata Pereira Limberger ◽  
...  

1999 ◽  
Vol 82 (4) ◽  
pp. 956-962 ◽  
Author(s):  
Alexander J Krynitsky ◽  
Steven J Stout ◽  
Huns Nejad ◽  
Thomas C Cavalier

Abstract A new multiresidue method was developed to determine 6 imidazolinone herbicides in 5 different soil types, using high-performance liquid chromatography/electrospray ionization mass spectrometry (HPLC/ESMS). Good recoveries and sensitivity were obtained for the compounds investigated at the 2.0 ppb limit of quantitation. A 50 g portion of soil was extracted with 0.5N NaOH. A portion of the extract was acidified to precipitate humic acids, and the supernatant was loaded onto a preconditioned tC-18 solid-phase extraction (SPE) cartridge and eluted with ethyl acetate. Further cleanup was achieved by using a tandem strong-anion-ex- change SPE/strong-cation-exchange (SCX) SPE. Analytes were eluted from the SCX SPE with saturated KCI in methanol. After cleanup, the sample was desalted with an RP-102 SPE cartridge. Quantitation was achieved by monitoring the [M + H]+ ions for each compound, with a time-scheduled selective-ion-monitoring program (positive mode). The extraction and cleanup procedure produced a purified extract for MS confirmation using 3 ions with “in-source” collision-induced dissociation.


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