Make the Leap from GC to LC-MS/MS

Jun 27, 2019 | Blogs, Technology | 0 comments

Choosing the best technique for your analysis can be tough. Should you go with gas chromatography/mass spectrometry (GC-MS) or liquid chromatography/tandem mass spectrometry (LC-MS/MS)? That’s the key question. That’s why we’re here to help.

The Limitations of GC-MS
GC-MS is an established technique to analyze volatile organic compounds (VOCs) and trihalomethanes (THMs). Simply put, it’s a technique that’s best used for thermally stable molecules. Traditionally, GC-MS is the preferred technique for the analysis of less polar and more volatile compounds such as organochlorine pesticides, dioxins, and polychlorinated biphenyl.

While the technique can offer good separation, the high temperatures used for vaporization during GC analysis can alter or degrade half of the analytes in a sample1. This is the primary concern for life science researchers who deal with relatively labile biological molecules that break down easily at high temperatures. GC-MS also becomes a challenge because it can involve labor-intensive sample preparation and long chromatographic run times.

The LC-MS/MS Advantage
LC-MS/MS combines the separation power of liquid chromatography with the identification and quantification power of tandem mass spectrometry.

The strength of this technique is in the ability of LC to separate a wide range of compounds before the tandem MS quantifies them with a high degree of sensitivity and selectivity based on the unique mass/charge (m/z) transitions of each compound of interest.

LC-MS/MS systems offer these basic benefits:

  • Faster, simpler sample preparation
  • Direct injection of aqueous samples
  • Less need for derivatization
  • Shorter chromatographic run times
  • Increased selectivity and sensitivity with multiple reaction monitoring (MRM)
  • Screening for a wider range of compounds in a single analysis

Many scientists who need increased levels of sensitivity, reproducibility, and robustness over GC-MS are either considering or have already made the leap to LC-MS/MS. When will you?

Let SCIEX Help You Make the Leap from GC-MS to LC-MS/MS

If your budget is holding you back, we have news for you. The SCIEX Triple Quad™ 3500 System provides all the advantages of modern LC-MS/MS technology. It’s the ideal choice for labs operating on a tight budget, and its simplicity of operation has the potential to expand your operation beyond the restrictions of gas chromatography.

Simply put, the Triple Quad 3500 LC-MS/MS System explained in fewer than 140 characters: Legendary power, speed, and accuracy are more affordable than ever.

Download your copy of the compendium to see what the SCIEX Triple Quad 3500 LC-MS/MS system can do for your laboratory.

Reference:

  1. Fang, Mingliang, et al. “Thermal degradation of small molecules: a global metabolomic investigation.”  Analytical Chemistry 87.21 (2015): 10935-10941.

Why SCIEX partners with experts around the world

Innovation in mass spectrometry does not happen in isolation. Some of the most impactful scientific advances emerge from highly specialized research communities – proteomics experts developing new peptide identification workflows, metabolomics researchers curating spectral databases, toxicologists building compound libraries, and biopharma scientists creating novel characterization methods.

Managing ADC characterization: The challenge of turning complexity into confidence

Unlike traditional monoclonal antibodies, ADCs combine an antibody backbone with linker chemistry and a cytotoxic payload. This multi-component architecture introduces overlapping layers of heterogeneity, including drug-to-antibody ratio (DAR) distributions, charge variants, post-translational modifications, and structural changes at both the intact and subunit levels. Across ADC development, these characteristics are considered critical quality attributes that must be characterized, understood, and monitored.

3 reasons ZT Scan DIA is changing the game in metabolomics

For years, metabolomics researchers have faced a frustrating reality: modern high-resolution mass spectrometers can detect tens of thousands of molecular features, yet only a fraction can be confidently identified. The challenge is no longer finding molecules. It is generating the high-quality MS/MS data needed to confidently assign structures and extract meaningful biological insights.

Posted by

0 Comments

Submit a Comment

Pin It on Pinterest

Share This

Share this post with your network