{ "id": "epd9bq87gh", "slug": "liquid-chromatography-tandem-mass-spectrometry", "title": "Liquid chromatography–tandem mass spectrometry", "updated": "2026-10-15", "topic_path": [ { "id": "physical", "label": "Physical world and mathematics", "api_url": "https://www.edgepedia.org/api/v1/topics/physical" }, { "id": "physical.chemistry", "label": "Chemistry", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry" }, { "id": "physical.chemistry.methods", "label": "Chemical principles and methods", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods" }, { "id": "physical.chemistry.methods.analytical-chemistry", "label": "Analytical chemistry", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods.analytical-chemistry" }, { "id": "physical.chemistry.methods.chromatography", "label": "Chromatography", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods.chromatography" }, { "id": "physical.chemistry.methods.specialized-chromatography-techniques", "label": "Specialized chromatography techniques", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods.specialized-chromatography-techniques" }, { "id": "physical.chemistry.methods.specialized-chromatography-techniques.specialized-chromatography-overview", "label": "Specialized and hyphenated chromatography (overview)", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods.specialized-chromatography-techniques.specialized-chromatography-overview" } ], "geo": [ { "id": "geo.nongeo.t1946.physical.chemistry.methods.chromatography", "label": "Non-geographic · 1946 to 2000: Chromatography", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods.chromatography", "path": [ { "id": "geo.nongeo", "label": "Non-geographic", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo" }, { "id": "geo.nongeo.t1946", "label": "Non-geographic · 1946 to 2000", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946" }, { "id": "geo.nongeo.t1946.physical", "label": "Physical world and mathematics", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical" }, { "id": "geo.nongeo.t1946.physical.chemistry", "label": "Chemistry", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry" }, { "id": "geo.nongeo.t1946.physical.chemistry.methods", "label": "Chemical principles and methods", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods" }, { "id": "geo.nongeo.t1946.physical.chemistry.methods.analytical-chemistry", "label": "Analytical chemistry", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods.analytical-chemistry" }, { "id": "geo.nongeo.t1946.physical.chemistry.methods.chromatography", "label": "Chromatography", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods.chromatography" } ] } ], "excerpt": "Liquid chromatography–tandem mass spectrometry (LC-MS/MS) couples liquid chromatographic separation with two stages of mass analysis, and is the gold standard for quantitative bioanalysis, clinical diagnostics, and environmental testing.", "snippet": "Liquid chromatography–tandem mass spectrometry (LC-MS/MS) couples liquid chromatographic separation with two stages of mass analysis, and is the gold standard for quantitative bioanalysis, clinical diagnostics, and environmental testing.", "node": "physical.chemistry.methods.specialized-chromatography-techniques.specialized-chromatography-overview", "markdown": "# Liquid chromatography–tandem mass spectrometry\n\nLiquid chromatography–tandem mass spectrometry (LC-MS/MS) couples a liquid chromatographic separation with two stages of mass analysis to identify and quantify compounds in complex mixtures. Its output is both a chromatogram and mass-resolved transition data: the chromatograph separates interferences such as isobaric compounds that the mass spectrometer alone cannot differentiate, and the tandem mass spectrometer detects the analyte through a characteristic precursor-to-product ion pair.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/) This combination of chromatographic and mass-resolved specificity, with attogram-level detection on modern triple quadrupoles, has made the technique the \"gold standard\" for quantitative analysis in bioanalysis, clinical diagnostics, and environmental testing.[2](https://pmc.ncbi.nlm.nih.gov/articles/PMC9115313/)\n\n| Key fact | Value | Source |\n|---|---|---|\n| Output | Chromatographic peaks recorded as precursor-to-product ion transitions | [1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/) |\n| Example transitions | Testosterone: 289.1/97.1 and 289.1/109.1 m/z | [1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/) |\n| Routine clinical run time | 2 to 5 min per test | [1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/) |\n| LLOQ achieved (SCIEX Triple Quad 6500) | 700 attograms on-column (alprazolam, protein-precipitated plasma, 7.6% CV) | [3](https://sciex.com/content/dam/pdf/technotes/6500-System-for-High-Sensitivity-Analysis.pdf) |\n| Linear dynamic range | 5.4 orders of magnitude (SCIEX Triple Quad 6500 with IonDrive detector) | [3](https://sciex.com/content/dam/pdf/technotes/6500-System-for-High-Sensitivity-Analysis.pdf) |\n| Carryover acceptance (ICH M10) | ≤20% of LLOQ analyte response, ≤5% of internal standard response | [4](https://www.casrai.org/guides/triple-quadrupole-lc-ms-ms-configuration-quantitation-setup) |\n| Dwell-time rule | At least 15–20 data points across each chromatographic peak | [1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/) |\n\n## How it works\n\nA triple quadrupole places three quadrupoles in series. Q1 is a mass filter that transmits only the precursor ion of interest; q2 is an RF-only collision cell that applies collision-induced dissociation (CID) with an inert collision gas; Q3 is a second mass filter tuned to pass one specific product ion.[4](https://www.casrai.org/guides/triple-quadrupole-lc-ms-ms-configuration-quantitation-setup) The precursor/product pair is called a transition; for testosterone the monitored transitions are 289.1/97.1 and 289.1/109.1 m/z.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/) Monitoring one or a few transitions continuously while the analyte elutes is multiple reaction monitoring (MRM, also called selected reaction monitoring, SRM). Low-energy CID in an RF-only multipole remains the basis of modern tandem mass spectrometers, whether triple quadrupole, time-of-flight, or Fourier-transform designs.[2](https://pmc.ncbi.nlm.nih.gov/articles/PMC9115313/)\n\nIonization is usually at atmospheric pressure. [Electrospray ionization](https://www.edgepedia.org/electrospray-ionization) (ESI) suits polar compounds and dominates clinical work; atmospheric pressure chemical ionization (APCI) suits non-polar compounds such as steroids and cannabinoids. The distinction matters for robustness: in ESI, charged droplets produced at the capillary tip shrink by solvent evaporation and Coulomb fission and ultimately yield gas-phase ions by mechanisms that depend on the analyte and conditions, whereas in APCI the vaporized analyte is ionized through gas-phase reagent-ion chemistry, which is the main reason APCI is sometimes less prone to matrix effects.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/) • [5](https://www.mdpi.com/1420-3049/25/13/3047)\n\n## How it is done\n\n**Sample preparation** ranges from dilution or protein precipitation to solid-phase extraction, liquid-liquid extraction, or supported-liquid extraction; an internal standard is added to all calibrators, QC materials, and patient samples as the first preparation step.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/)\n\n**Transition development** typically yields two transitions per analyte after validation, a quantifier and a qualifier; product ions from water loss (−18 m/z) or below 100 m/z may be nonspecific and should be evaluated against interferences and qualifier-ion criteria, being used when validation demonstrates adequate selectivity.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/) Dwell times are fixed to give at least 15–20 points per peak.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/) Because cycle time equals the number of transitions times (dwell time plus pause time, with pause typically about 5 ms), scheduled MRM monitors each transition only inside a retention-time window; ion counting is Poissonian, so halving the dwell time degrades the signal-to-noise ratio by roughly \\( \\sqrt{2} \\).[6](https://www.casrai.org/guides/mrm-transitions-dwell-cycle-time-optimization)\n\n**Calibration and validation** follow regulatory templates. FDA bioanalytical guidance requires calibrators and QCs in the same biological matrix, blank matrix from at least six sources to show selectivity, LLOQ accuracy within ±20% of nominal with response at least five times the response in the blank sample, and at least three independent accuracy-and-precision runs.[7](https://www.fda.gov/media/70858/download) ICH M10 requires at least six non-zero calibration standards including the LLOQ and ULOQ, accuracy within ±15% (±20% at the LLOQ) met by at least 75% of standards, and carryover after the ULOQ standard not exceeding 20% of the LLOQ analyte response and 5% of the internal standard response.[4](https://www.casrai.org/guides/triple-quadrupole-lc-ms-ms-configuration-quantitation-setup)\n\n## Origin\n\nThe tandem quadrupole emerged from photodissociation physics. Marvin L. Vestal and Jean H. Futrell described a triple quadrupole used for photodissociation of CH₃Cl⁺ and CH₃Br⁺ in 1974[8](https://doi.org/10.1016/0009-2614%2874%2980104-1), and D. C. McGilvery and J. D. Morrison at La Trobe built a triple quadrupole for laser-induced photodissociation of mass-selected ions, published in 1978.[9](https://doi.org/10.1016/0020-7381%2878%2980071-0) R. A. Yost and C. G. Enke reported the analytical use of the tandem quadrupole with low-energy CID in the [Journal of the American Chemical Society](https://www.edgepedia.org/journal-of-the-american-chemical-society) in 1978[10](https://doi.org/10.1021/ja00475a072); experts at the 1977 ASMS meeting doubted that fragmenting ions at roughly 10 eV in an RF-only center quadrupole would work.[2](https://pmc.ncbi.nlm.nih.gov/articles/PMC9115313/)\n\nIn 1980 Donald F. Hunt, Jeffrey Shabanowitz, and Anne B. Giordani built a triple stage quadrupole (TSQ) from Finnigan parts for collision-activated decompositions in mixture analysis, later marketed by Finnigan.[11](https://doi.org/10.1021/ac50053a004) • [12](https://asms.org/docs/default-source/history-posters/tech_triple-quadrupole-and-beginnings-of-analytical-ms-ms_01_alt.pdf?sfvrsn=e13476c3_0) The TAGA 6000 was a commercial triple quadrupole MS/MS instrument.[12](https://asms.org/docs/default-source/history-posters/tech_triple-quadrupole-and-beginnings-of-analytical-ms-ms_01_alt.pdf?sfvrsn=e13476c3_0) An early LC-tandem-MS application, determination of sulfa drugs in biological fluids by Jack D. Henion, Bruce A. Thomson, and Peter H. Dawson, followed in 1982.[13](https://doi.org/10.1021/ac00240a023) J. V. Iribarne and B. A. Thomson described the ion evaporation model for charged droplets in 1976[14](https://doi.org/10.1063/1.432536), and the ion spray interface for combined liquid chromatography/atmospheric pressure ionization mass spectrometry, pneumatically assisted electrospray, was reported by Andries P. Bruins, Thomas R. Covey, and Jack D. Henion in 1987.[15](https://doi.org/10.1021/ac00149a003)\n\n## Variants\n\nMass analysers can be combined as identical pairs (triple quadrupole, TOF/TOF) or hybrids (Q-TOF, Q-Trap).[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/) For targeted small-molecule quantification, QqQ-based LC-SRM remains the preferred option with the highest dynamic range and sensitivity, while Orbitrap-based high-resolution MS (HRMS) is the most widely used platform for full-scan integrated qualitative and quantitative analysis.[16](https://link.springer.com/article/10.1186/s43094-026-01011-9)\n\nProteomics uses untargeted acquisition on high-resolution instruments. In data-independent acquisition (DIA) the instrument fragments all precursors in wide windows.[17](https://www.nature.com/articles/nbt.2841) John D. Venable and colleagues reported an automated windowed DIA approach for quantitative analysis of complex peptide mixtures in 2004.[18](https://doi.org/10.1038/nmeth705) Ludovic C. Gillet and colleagues introduced [SWATH-MS](https://www.edgepedia.org/swath-ms), targeted data extraction of DIA spectra for consistent proteome analysis, in 2012[19](https://doi.org/10.1074/mcp.o111.016717); Hannes L. Röst and colleagues enabled automated, targeted analysis of DIA data with OpenSWATH in 2014[17](https://www.nature.com/articles/nbt.2841); and Florian Meier and colleagues combined parallel accumulation–serial fragmentation with DIA on trapped-ion-mobility instruments in 2020 (diaPASEF).[20](https://doi.org/10.1038/s41592-020-00998-0)\n\n## Applications\n\n**Clinical diagnostics and toxicology** use LC-MS/MS for routine tests with 2 to 5 min analyses. Urine immunoassay screens detect drug classes rather than specific drugs with poor specificity and sensitivity, so definitive testing by LC-MS/MS or GC-MS is recommended as follow-up; LC-MS/MS also overcomes immunoassay cross-reactivity and measures multiple analytes in one method.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/) **Pharmacokinetics and bioanalysis** operate under ICH M10 validation.[4](https://www.casrai.org/guides/triple-quadrupole-lc-ms-ms-configuration-quantitation-setup) **Proteomics and metabolomics** use DIA and HRMS workflows.[21](https://onlinelibrary.wiley.com/doi/10.1002/prca201400117) **Environmental water analysis** quantifies antibiotics and other residues at sub-µg/L levels.[22](https://strathprints.strath.ac.uk/93596/1/Ansari-etal-Analyst-2025-Comparative-performance-evaluation-of-triple-quadrupole-tandem-mass-spectrometry-and-orbitrap-high-resolution-mass-spectrometry.pdf) Across drug development, LC-MS/MS surpasses HPLC and immunoassays in sensitivity, specificity, and multi-analyte capability, and offers better throughput than GC-MS while accommodating higher molecular weight or highly polar molecules.[16](https://link.springer.com/article/10.1186/s43094-026-01011-9) Consolidated clinical platforms have been attempted: the Thermo Fisher Cascadion SM Clinical Analyzer, the first all-in-one certified clinical mass analyser with regulatory clearance, combined LC and MS/MS in one automated instrument, with 25-hydroxy vitamin D as its only commercial application; Thermo Fisher has since discontinued the analyzer, moving away from the fully automated, sample-to-answer model in favor of more flexible instrumentation, and it is no longer orderable.[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/)\n\n## Limitations and alternatives\n\n**Matrix effects** are among the key limitations of LC-MS/MS[16](https://link.springer.com/article/10.1186/s43094-026-01011-9); Paul J. Taylor called them the Achilles heel of quantitative LC-[ESI-MS/MS](https://www.edgepedia.org/esi-ms-ms).[23](https://doi.org/10.1016/j.clinbiochem.2004.11.007) Co-eluting matrix components suppress or enhance ionization; a mechanistic investigation of ionization suppression in ESI by Richard King and colleagues appeared in 2000.[24](https://doi.org/10.1016/s1044-0305%2800%2900163-x) Three assessment techniques are standard: post-column infusion, the post-extraction spike method introduced by B. K. Matuszewski, M. L. Constanzer, and C. M. Chavez-Eng in 2003[25](https://doi.org/10.1021/ac020361s), and slope ratio analysis.[5](https://www.mdpi.com/1420-3049/25/13/3047) Mitigation uses isotope-labeled internal standards, chromatographic clean-up, source adjustment, or surrogate matrices[5](https://www.mdpi.com/1420-3049/25/13/3047); using as high a dilution as sensitivity allows also helps[1](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/), and increasing chromatographic resolution is described as the most reliable fix.[26](https://synapse.koreamed.org/articles/1147601)\n\n**Dynamic range** is bounded in practice: a reliable working range beyond a 2,000-fold difference between lower and upper limits of measurement is quite rare for LC-MS/MS, because of ionization and detection nonlinearity and carryover.[26](https://synapse.koreamed.org/articles/1147601)\n\n**Against alternatives**: for nine antibiotics in creek water, a QqQ gave LODs of 0.05–0.11 µg/L and LOQs of 0.16–0.34 µg/L, while Orbitrap HRMS achieved LODs of 0.01–0.06 µg/L and LOQs of 0.03–0.20 µg/L; MRM gave marginally better precision (intra-day RSD 2.1–3.5% versus 3.6–6.4%).[22](https://strathprints.strath.ac.uk/93596/1/Ansari-etal-Analyst-2025-Comparative-performance-evaluation-of-triple-quadrupole-tandem-mass-spectrometry-and-orbitrap-high-resolution-mass-spectrometry.pdf) Compared with GC-MS, LC-MS/MS offers better throughput and handles polar and higher molecular weight analytes; compared with immunoassays and HPLC-UV it offers higher sensitivity, specificity, and multi-analyte capability.[16](https://link.springer.com/article/10.1186/s43094-026-01011-9)\n\n## References\n\n1. [Liquid chromatography–tandem mass spectrometry for clinical diagnostics (Nature Reviews Methods Primers)](https://pmc.ncbi.nlm.nih.gov/articles/PMC9735147/)\n2. [The triple quadrupole: Innovation, serendipity and persistence (Yost, JASMS 2022)](https://pmc.ncbi.nlm.nih.gov/articles/PMC9115313/)\n3. [SCIEX Triple Quad 6500 and QTRAP 6500 Systems for Targeted Quantitation (technical note)](https://sciex.com/content/dam/pdf/technotes/6500-System-for-High-Sensitivity-Analysis.pdf)\n4. [Triple Quadrupole LC-MS/MS: Configuration and Quantitation Setup (CASRAI technical guide)](https://www.casrai.org/guides/triple-quadrupole-lc-ms-ms-configuration-quantitation-setup)\n5. [Compensate for or Minimize Matrix Effects? Strategies for Overcoming Matrix Effects in LC-MS (Molecules, 2020 tutorial review)](https://www.mdpi.com/1420-3049/25/13/3047)\n6. [Multiple Reaction Monitoring: Building and Optimizing MRM Transitions (CASRAI technical guide)](https://www.casrai.org/guides/mrm-transitions-dwell-cycle-time-optimization)\n7. [FDA Guidance for Industry: Bioanalytical Method Validation](https://www.fda.gov/media/70858/download)\n8. [Photodissociation of CH3Cl+ and CH3Br+ in a tandem quadrupole mass spectrometer (Chemical Physics Letters, 1974)](https://doi.org/10.1016/0009-2614%2874%2980104-1)\n9. [A mass spectrometer for the study of laser-induced photodissociation of ions (International Journal of Mass Spectrometry and Ion Physics, 1978)](https://doi.org/10.1016/0020-7381%2878%2980071-0)\n10. [R. A. Yost, C. G. Enke (1978). Selected ion fragmentation with a tandem quadrupole mass spectrometer. Journal of the American Chemical Society.](https://doi.org/10.1021/ja00475a072)\n11. [Donald F. Hunt, Jeffrey. Shabanowitz, Anne B. Giordani (1980). Collision activated decompositions in mixture analysis with a triple quadrupole mass spectrometer. Analytical Chemistry.](https://doi.org/10.1021/ac50053a004)\n12. [The Triple Quadrupole and the Beginnings of Analytical MS/MS (ASMS history poster, Grayson, Enke, Yost)](https://asms.org/docs/default-source/history-posters/tech_triple-quadrupole-and-beginnings-of-analytical-ms-ms_01_alt.pdf?sfvrsn=e13476c3_0)\n13. [Jack D. Henion, Bruce A. Thomson, Peter H. Dawson (1982). Determination of sulfa drugs in biological fluids by liquid chromatography/mass spectrometry/mass spectrometry. Analytical Chemistry.](https://doi.org/10.1021/ac00240a023)\n14. [J. V. Iribarne, B. A. Thomson (1976). On the evaporation of small ions from charged droplets. The Journal of Chemical Physics.](https://doi.org/10.1063/1.432536)\n15. [Andries P. Bruins, Thomas R. Covey, Jack D. Henion (1987). Ion spray interface for combined liquid chromatography/atmospheric pressure ionization mass spectrometry. Analytical Chemistry.](https://doi.org/10.1021/ac00149a003)\n16. [Recent applications of liquid chromatography tandem mass spectrometry at various stages of drug development (Future J. Pharm. Sci., Springer)](https://link.springer.com/article/10.1186/s43094-026-01011-9)\n17. [OpenSWATH enables automated, targeted analysis of data-independent acquisition MS data (Nature Biotechnology, 2014)](https://www.nature.com/articles/nbt.2841)\n18. [John D Venable and colleagues (2004). Automated approach for quantitative analysis of complex peptide mixtures from tandem mass spectra. Nature Methods.](https://doi.org/10.1038/nmeth705)\n19. [Ludovic C. Gillet and colleagues (2012). Targeted Data Extraction of the MS/MS Spectra Generated by Data-independent Acquisition: A New Concept for Consistent and Accurate Proteome Analysis. Molecular & Cellular Proteomics.](https://doi.org/10.1074/mcp.o111.016717)\n20. [Florian Meier and colleagues (2020). diaPASEF: parallel accumulation–serial fragmentation combined with data-independent acquisition. Nature Methods.](https://doi.org/10.1038/s41592-020-00998-0)\n21. [Using data-independent, high-resolution mass spectrometry in protein biomarker research (Proteomics Clinical Applications)](https://onlinelibrary.wiley.com/doi/10.1002/prca201400117)\n22. [Comparative performance evaluation of triple quadrupole tandem MS and Orbitrap HRMS for antibiotics in creek water (Analyst, 2025)](https://strathprints.strath.ac.uk/93596/1/Ansari-etal-Analyst-2025-Comparative-performance-evaluation-of-triple-quadrupole-tandem-mass-spectrometry-and-orbitrap-high-resolution-mass-spectrometry.pdf)\n23. [Paul J. Taylor (2005). Matrix effects: the Achilles heel of quantitative high-performance liquid chromatography–electrospray–tandem mass spectrometry. Clinical Biochemistry.](https://doi.org/10.1016/j.clinbiochem.2004.11.007)\n24. [Mechanistic investigation of ionization suppression in electrospray ionization (Journal of the American Society for Mass Spectrometry, 2000)](https://doi.org/10.1016/s1044-0305%2800%2900163-x)\n25. [B. K. Matuszewski, M. L. Constanzer, C. M. Chavez-Eng (2003). Strategies for the Assessment of Matrix Effect in Quantitative Bioanalytical Methods Based on HPLC−MS/MS. Analytical Chemistry.](https://doi.org/10.1021/ac020361s)\n26. [LC-MS/MS method development review (KoreaMed Synapse)](https://synapse.koreamed.org/articles/1147601)\n\n---\n*Topic: Encyclopedia › Physical world and mathematics › Chemistry › Chemical principles and methods › Analytical chemistry › Chromatography › Specialized chromatography techniques › Specialized and hyphenated chromatography (overview)*\n\n*Initially written Sep 29, 2026 · Edited: Oct 15, 2026*\n\n*Copyright 2026 EdgeChat AI, a subsidiary of Biostate AI.*\n\nLicense: Edgepedia Community License 1.0, https://www.edgepedia.org/edgepedia/license\n", "same_as": [], "url": "https://www.edgepedia.org/liquid-chromatography-tandem-mass-spectrometry", "markdown_url": "https://www.edgepedia.org/liquid-chromatography-tandem-mass-spectrometry.md", "license": { "name": "Edgepedia Community License 1.0", "url": "https://www.edgepedia.org/edgepedia/license", "summary": "Free with credit, commercial use included. AI training is open to everyone. 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Edgepedia Community License 1.0.", "speakable": "Liquid chromatography–tandem mass spectrometry couples liquid chromatographic separation with two stages of mass analysis, and is the gold standard for quantitative bioanalysis, clinical diagnostics, and environmental testing." }