Analysis of Testosterone Esters by Tandem Mass Spectrometry

1993 ◽  
Vol 76 (2) ◽  
pp. 306-312 ◽  
Author(s):  
Thomas Cairns ◽  
Emil G Siegmund ◽  
Bobby Rader

Abstract The electron ionization (El) and chemical ionization (CI) mass spectra of 12 representative testosterone esters were examined to explore the various analytical options available for identification and confirmation of the esters. Using El, a number of fragment ions indicated the identification of the testosterone moiety, but structural confirmation of the individual esters often required the observance of the molecular ion at very low relative abundance ratios. The acceptable analytical method involved CI/tandem mass spectrometry based on the production of the 2 generic product ions derived from the protonated molecule ion.

1994 ◽  
Vol 72 (2) ◽  
pp. 345-351 ◽  
Author(s):  
R.J. Helleur ◽  
Pierre Thibault

The operating conditions for pyrolysis–desorption ammonia chemical ionization mass spectrometry and tandem mass spectrometry have been optimized and the technique evaluated for the production and analysis of structurally-informative pyrolytic fragmentation ions corresponding to intact anhydrohexose oligosaccharides, using amylose as the model polysaccharide. Among the various parameters examined it was found that the nature of the solvent used to adhere the sample to the emitter coil and the configuration of the emitter and the rate at which it is heated all play important roles in determining the efficiency of the pyrolytic process and the production of high mass fragment ions. Adjustment of reagent gas pressure together with source temperature also influence the chemical integrity of high mass oligomeric pyrolysis products. Under optimal operating conditions using ammonia reagent gas, the analyses of cellulose, laminarin, agars, and chitin gave relatively abundant ions corresponding to ammonium (or protonated) adducts of up to anhydrohexose tetrasaccharide. More importantly, the generation of such higher mass fragment ions provided a sustained ionic current of sufficient duration to perform tandem mass spectrometric analyses.


1993 ◽  
Vol 47 (6) ◽  
pp. 844-851 ◽  
Author(s):  
S. W. Chen ◽  
G. R. Her

Desorption chemical ionization with ammonia as the reagent gas in combination with tandem mass spectrometry is described for the analysis of additives in polyethylene. The additives were extracted with toluene and then analyzed directly by desorption chemical ionization and tandem mass spectrometry. With ammonia as the reagent gas, mass spectra of additives were found to contain intense pseudomolecular ions with very little fragmentation. In addition, low-molecular-weight polyethylene molecules extracted with the additives were barely detectable, and thus there was less likelihood of interference. Collision-induced dissociation of the pseudomolecular ions provided great confidence in the assignment of additives.


2009 ◽  
Vol 13 (04n05) ◽  
pp. 524-527 ◽  
Author(s):  
M. Rosário M. Domingues ◽  
Pedro Domingues ◽  
Maria G.P.M.S. Neves ◽  
Augusto C. Tomé ◽  
José A.S. Cavaleiro

meso-tetraarylporphyrins with different substituents linked either to an aryl ring or to a β-pyrrolic position were studied by Electrospray (ESI) Tandem Mass Spectrometry (MS/MS). The electrospray mass spectra (ESI-MS) of meso-tetraarylporphyrins show the molecular ions and no significant fragmentation is noted. Structural information can be obtained by inducing fragmentation of the ions generated under ESI conditions. The product ions formed and registered in the tandem mass spectra (ESI-MS/MS) are characteristic of the chemical structure of the groups linked to the porphyrin and depend on their location. Also, the same functional group linked either to the aryl ring or to the β-pyrrolic position yields different product ions that confirm their position. Taking into consideration the Portugal-Spain special issue of the Journal of Porphyrins and Phthalocyanines, in this highlight we analyze the work done at the University of Aveiro related to the use of mass spectrometry in the structural characterization of meso-tetraarylporphyrins with carbohydrate, nitro and amino acid groups.


2018 ◽  
Author(s):  
Zhiwu An ◽  
Fuzhou Gong ◽  
Yan Fu

We have developed PTMiner, a first software tool for automated, confident filtering, localization and annotation of protein post-translational modifications identified by open (mass-tolerant) search of large tandem mass spectrometry datasets. The performance of the software was validated on carefully designed simulation data. <br>


2007 ◽  
Vol 367 (1) ◽  
pp. 40-48 ◽  
Author(s):  
Benlian Wang ◽  
Gang Sun ◽  
David R. Anderson ◽  
Minghong Jia ◽  
Stephen Previs ◽  
...  

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