Ultra-low bleed and exceptional inertness assure complete separation of sulfur compounds (hydrogen sulfide, carbonyl sulfide, dimethyl sulfide, mercaptans) on our new column, with excellent peak shapes and reliable quantification at ppbv levels. A Sulfinert treated sampling/transfer system assures no adsorption losses of these very reactive compounds.
Carrier gas changes for SimDist methods, such as ASTM Method D7213, can be easily implemented in your daily process. Using MXT-1HT SimDist columns and EZGC method translation software, helium-based SimDist methods can be easily translated to alternative carrier gases while maintaining ASTM Method D7213 requirements.
An Rxi-5ms column and a wool-packed inlet liner provide the stability and inertness needed for these basic, active analytes. Chromatography from a six-replicate system suitability analysis was well within normal acceptance criteria. USP tailing factors were approximately 1.00 for all analytes; retention times and area responses were very stable.
Dietary supplements, which are consumed worldwide, are made from various botanical ingredients. To be safe from pesticides exposure, residual pesticides must be monitored by chromatographic instrumentation. Issues arise, however, due to the fact these botanical samples are dried and cause large interferences in the chromatography. This study shows that the modified QuEChERS method combined with GC-MS/MS achieves consistent pesticides monitoring in botanical ingredients.
Two options for the analysis of PGIs in API have been developed by Merck and Restek to meet different laboratory needs. The first option is a fast method for the analysis of sulfonate esters on the Rxi-5Sil MS column. The second option is a comprehensive method for the analysis of both sulfonate esters and alkyl halides on the Rtx-200 column. Both methods require very little sample preparation, which helps increase laboratory productivity.
Dr. Radomír Čabala, Head of the Toxicology Department at the General University Hospital in Prague, presents work on the potential utility of GC-TOFMS analysis of cellular fatty acid methyl esters (FAMEs) in identifying clinically relevant bacteria.
Numerous articles have been published on faster methods for gas chromatography (GC), yet uncertainty remains on how best to speed up separations. Here, Dr. Hans-Gerd Janssen clarifies the confusion surrounding fast GC and recommends a strategic approach based on 3 steps: 1) minimizing resolution to a value just sufficient, 2) maximizing the selectivity of the chromatographic system, and 3) implementing a method that reduces analysis time while holding resolution constant.
Even validated methods run on certified equipment are unlikely to be foolproof. Real quality assurance needs to be based on direct verification using internal standards and control samples. By Dr. Konrad Grob, Kantonales Laboratory, Zurich
Protein precipitation is frequently used to minimize matrix impact when analyzing biological samples. However, the effects of highly organic protein precipitation sample extracts on LC peak shape can negatively impact accurate quantification. Dilution or further sample preparation steps are often used to minimize these effects; however, here we show that direct injection of sample extracts is a viable option that can be used to prevent peak distortion, while avoiding the time and variability associated with additional sample preparation.
Methods for LC-MS peptide analysis often use acidified mobile phases, which can alter retention and selectivity. Here, we demonstrate the effects of modifying acid type, acid concentration, temperature, and gradient slope using several test probes. A Raptor ARC-18 column was employed for this work because it is sterically protected making it extremely stable and resistant to acid damage at low pHs, which is an important characteristic when developing LC-MS methods for peptide analysis.
