Enhanced Detection of Sialylated and Sulfated Glycans with Negative Ion Mode Nanoliquid Chromatography/Mass Spectrometry at High pH

2010 ◽  
Vol 82 (4) ◽  
pp. 1470-1477 ◽  
Author(s):  
Kristina A. Thomsson ◽  
Malin Bäckström ◽  
Jessica M. Holmén Larsson ◽  
Gunnar C. Hansson ◽  
Hasse Karlsson
2018 ◽  
Author(s):  
Gilian T. Thomas ◽  
Landon MacGillivray ◽  
Natalie L. Dean ◽  
Rhonda L. Stoddard ◽  
Lars Yunker ◽  
...  

<p>Reactions carried out in the presence of rubber septa run the risk of additives being leached out by the solvent. Normally, such species are present at low enough levels that they do not interfere with the reaction significantly. However, when studying reactions using sensitive methods such as mass spectrometry, the appearance of even trace amounts of material can confuse dynamic analyses of reactions. A wide variety of additives are present in rubber along with the polymer: antioxidants, dyes, detergent, and vulcanization agents, and these are all especially problematic in negative ion mode. A redesigned Schlenk flask for pressurized sample infusion (PSI) is presented as a means of practically eliminating the presence of contaminants during reaction analyses.</p>


1985 ◽  
Vol 68 (3) ◽  
pp. 427-430
Author(s):  
Peter P Schmid ◽  
Markus D Muller

Abstract A method is described for detection of chlorinated paraffins (CPs) in biological and environmental samples. Sample preparation includes sulfuric acid treatment followed by adsorption chromatography on ilumina, which yields the CPs in one fraction that is almost free of interfering material. Using gas chromatography/mass spectrometry j with negative-ion chemical ionization, the limit of detection is 5 ng (corresponding to the lower ppb range). CP levels of 30 ppm, 200 ppb, ' and 5 ppb were found in sewage sludge, human fat, and sediment, respectively.


2019 ◽  
Vol 25 (1) ◽  
pp. 157-163 ◽  
Author(s):  
Morgan Stickney ◽  
Qiangwei Xia ◽  
I Jonathan Amster

Capillary zone electrophoresis (CZE) paired with mass spectrometry (MS) is a powerful analytical technique for examining mixtures of ionic analytes such as glycosaminoglycans. This study examines the mechanics of the electrospray process for a sheath flow CZE-MS interface under reverse polarity negative ionization conditions. Liquid flow in a sheath flow nano-electrospray CZE-MS interface is driven by two mechanisms, electroosmotic flow and electrospray nebulization. The contribution of these two processes to the overall flow of solution to the electrospray tip is influenced by the surface coatings of the sheath flow emitter tip and by the solvent composition. We have investigated the application of this interface to the reverse polarity separation of glycosaminoglycans and find that the role of electroosmotic flow is far less than has been reported previously, and the electrospray process itself is the largest contributor to the flow of the sheath liquid.


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