Chromatography
Compound Based Scanning Software Simplifies Multi- Residue Analysis with GC-MS/MS
Jan 05 2012
Designed as ‘the gas chromatographers’ GC-MS system, Bruker’s new SCION TQ™ GC-MS/MS promotes ease of use and increased workflow in busy analytical laboratories.
The advantages offered by hardware innovations – reducing the instrument footprint by half but at the same time improving performance over traditional gas chromatography systems – are supplemented by the utility and ease of use of the unique SCION Compound Based Scanning (CBS) software.
Bruker’s software for the SCION TQ includes a number of important tools and features to make method set up, data analysis and comparisons of similar spectra much easier.
With gas chromatographers in mind, the SCION software package includes: a CBS Multiple Reaction Monitoring (MRM) compound library for easy set up of methods; additional spectral libraries; plug in to multiple user-customisable spectral libraries with automatic search functions; and Bruker’s mass spectrometry (MS) workstation software.
Kefei Wang, Global GCMS Product Manager at Bruker CAM, said: “The software makes complicated analysis easy, particularly for those with little prior mass spectrometry knowledge. MRM set up requires no expert knowledge - the
compound name may be simply dragged from the pre-installed compound library and the software auto-fills the full details of the method and manages the full duty cycle of the triple quad.“
Jim Koers, Bruker CAM Software Manager, added: “To put this into context, manual TQ method development for a 200 compound method would require around 12,000 keystrokes and take several days. With CBS, we can achieve
a fully optimised method in a matter of hours, and with less than 200 keystrokes.”
The SCION TQ system comes complete with the Bruker compound library, which details some 2,500 MRM transitions. Results are presented in a standard pro-forma accepted across the industry and may be cross-referenced against
known spectral libraries to aid interpretation and final delivery.
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