Sensitivity and acquisition speed with triple quadrupole technology
Technical notes | 2021 | Thermo Fisher ScientificInstrumentation
Ultra-high performance liquid chromatography coupled with triple quadrupole mass spectrometry (LC-MS/MS) has become a cornerstone technique for trace-level quantitation across diverse fields, including pharmaceuticals, environmental monitoring and food safety. Its combination of sensitivity, selectivity and throughput supports rigorous analysis of complex matrices.
This white paper examines the critical performance metrics of triple quadrupole LC-MS/MS systems, focusing on sensitivity definitions, acquisition speed and their impact on multi-analyte quantitation. It reviews how selected reaction monitoring (SRM) parameters influence limits of detection and quantitation, and compares SRM acquisition rate with traditional scan rate.
Achieving optimal balance among sensitivity, selectivity and throughput requires careful tuning of SRM parameters, dwell times and cycle times. Advances in ion optics, mass analyzer design and data processing are extending the capabilities of triple quadrupole LC-MS/MS systems, fostering their continued role as workhorses in high-throughput quantitation.
LC/MS, LC/MS/MS, LC/QQQ
IndustriesManufacturerThermo Fisher Scientific
Summary
Significance of the Topic
Ultra-high performance liquid chromatography coupled with triple quadrupole mass spectrometry (LC-MS/MS) has become a cornerstone technique for trace-level quantitation across diverse fields, including pharmaceuticals, environmental monitoring and food safety. Its combination of sensitivity, selectivity and throughput supports rigorous analysis of complex matrices.
Objectives and Overview of the Study
This white paper examines the critical performance metrics of triple quadrupole LC-MS/MS systems, focusing on sensitivity definitions, acquisition speed and their impact on multi-analyte quantitation. It reviews how selected reaction monitoring (SRM) parameters influence limits of detection and quantitation, and compares SRM acquisition rate with traditional scan rate.
Methods and Instrumentation
- Chromatography: Ultra-high performance liquid chromatography (UHPLC) for narrow peak separations.
- Mass spectrometry: Thermo Scientific TSQ Plus triple quadrupole system operating in SRM mode, capable of up to 600 SRMs per second with 5 ms polarity switching and dwell times from 500 µs to 10 ms.
- Advanced techniques: High resolution accurate mass (HRAM) detectors, highly selective reaction monitoring (H-SRM) and field asymmetric ion mobility spectrometry (FAIMS) for enhanced selectivity and noise reduction.
Main Results and Discussion
- Sensitivity assessment using signal-to-noise ratio proves variable due to noise calculation methods and region selection, with root-mean-square algorithms yielding up to 40% higher S/N than peak-to-peak.
- Dwell time extension from 500 µs to 10 ms improves precision and accuracy by averaging noise and stabilizing ion transmission, without loss of peak intensity.
- Limits of detection (LoD), instrument detection limits (IDL) and limits of quantitation (LoQ) are defined and contrasted, highlighting the importance of precision and accuracy benchmarks (less than 20% CV and bias) in regulatory contexts.
- SRM acquisition rate, distinct from scan rate, is crucial for multi-analyte assays. Fast interscan delays and scheduled SRM windows enable hundreds of transitions per run and maintain quantitative performance for narrow chromatographic peaks.
Benefits and Practical Applications of the Method
- Enables robust quantitation of numerous analytes in a single run with injection-to-injection times under two minutes.
- Complies with stringent regulatory guidances (FDA, EPA, EURL) for precision and accuracy at low concentration levels.
- Applicable to pharmaceuticals, environmental contaminants, food safety and forensic toxicology, offering reliable multi-residue screening.
Future Trends and Applications
- Continued integration of orthogonal separation (FAIMS) and high-resolution detectors to drive background noise to undetectable levels.
- Enhanced data acquisition algorithms for standardized noise estimation and automated quality assessment.
- Further acceleration of SRM rates and dynamic scheduling to accommodate growing analyte panels without sacrificing sensitivity.
Conclusion
Achieving optimal balance among sensitivity, selectivity and throughput requires careful tuning of SRM parameters, dwell times and cycle times. Advances in ion optics, mass analyzer design and data processing are extending the capabilities of triple quadrupole LC-MS/MS systems, fostering their continued role as workhorses in high-throughput quantitation.
References
- Foundation review: Principles and applications of LC-MS in new drug discovery W A Korfmacher 2005
- Principles and Applications of Liquid Chromatography-Mass Spectrometry in Clinical Biochemistry J J Pitt 2009
- Guidance Document on the Estimation of LOD and LOQ for Measurements in the Field of Contaminants in Feed and Food
- Environmental Protection Agency 40 CFR Part 136 Appendix B
- FDA Bioanalytical Method Validation Guidance for Industry
- EMA Guideline on Bioanalytical Method Validation
- EURL SANTE Guidelines
- LC-MS/MS in the Clinical Laboratory – Where to From Here?
- Fast Analysis of Multi-Class Pesticides Panel in Wine Using Single Run LC-Triple Quadrupole Mass Spectrometry
- Tomorrow's Quantitation With LC-MS/MS: Fast Screening And Quantitation Of Drugs Of Abuse In Urine For Forensic Toxicology
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