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Acquity tqd triple quadrupole system

Manufactured by Waters Corporation
Sourced in United States

The Acquity TQD Triple Quadrupole system is a highly sensitive and selective mass spectrometry instrument designed for analytical applications. It consists of two quadrupole mass filters and a collision cell, allowing for the detection and quantification of target analytes with high precision and accuracy.

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5 protocols using acquity tqd triple quadrupole system

1

Metabolite Profiling in Maternal Serum

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Conventional clinical metabolite and targeted metabolomics assays were conducted as previously described using maternal serum obtained fasting and 1 h after a glucose load [17 (link),18 (link)]. Briefly, 15 amino acids, 45 acylcarnitines and 5 conventional clinical and targeted metabolites were analyzed. Levels of conventional clinical metabolites, including lactate, triglycerides, 3-hydroxybutyrate, glycerol, and nonesterified fatty acids (NEFA), were measured on a Unicel DxC 600 clinical analyzer (Beckman Coulter, Brea, CA, USA). Targeted metabolomics assays for acylcarnitines and amino acids were conducted by tandem mass spectrometry (MS) with addition of known quantities of stable isotope-labeled internal standards on an Acquity TQD Triple Quadrupole system (Waters Corporation, Milford, MA, USA).
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2

Comprehensive Metabolite Profiling Protocol

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Sixty-two conventional and targeted metabolites were assayed as previously described [12 (link)]. Briefly, conventional metabolite levels (lactate, triacylglycerols, 3-hydroxybutyrate, glycerol, NEFA) were measured on a Unicel DxC 600 clinical analyser (Beckman Coulter, Brea, CA, USA). Targeted metabolomics assays for acylcarnitines and amino acids were performed by tandem MS with addition of known quantities of stable isotope-labelled internal standards on an Acquity TQD Triple Quadrupole system (Waters Corporation, Milford, MA, USA).
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3

Quantitative Metabolite Profiling Protocol

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Sixty-two conventional clinical and targeted metabolites were quantitatively assayed, as previously described [15 (link)]. Briefly, levels of conventional clinical metabolites (lactate, triglycerides, 3-hydroxybutyrate, glycerol, and NEFA) were measured using a Unicel DxC 600 clinical analyzer (Beckman Coulter, Brea, CA, USA). Targeted metabolomic assays for acylcarnitines and amino acids were performed via tandem mass spectrometry (MS), for which known quantities of stable isotope-labelled internal standards were added using an Acquity TQD Triple Quadrupole system (Waters Corporation, Milford, MA, USA).
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4

Quantifying Metabolites and Amino Acids

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Conventional metabolites were measured on a Beckman-Coulter DxC600 autoanalyzer using reagents from Beckman (Brea, CA; lactate) and Wako USA (Richmond, VA; beta-hydroxybutyrate). For free glycerol, reagents by Roche (Indianapolis, IN) for glycerol-blanked triglycerides were modified. To 84 mL of the Roche R1 reagent, 6.0 mg 4-aminoantipyrine dye (Sigma, St. Louis, MO) was added. This assay was run by combining 250 μL reagent with 20 μL sample volume, calibrated against a glycerol standard (2.29 mM) with detection at 520 nm after 5 min. Targeted assays of amino acids using stable-isotope-labeled internal standards were performed on an Acquity TQD Triple Quadrupole system (Waters Corporation, Milford, MA). Absolute metabolite concentrations were calculated based on the linear relationship between concentration and peak area, and calibrated against internal standards with known concentrations, as previously described [34 (link), 35 (link)]. Conventional metabolite and targeted amino acid data are used here to evaluate whether each normalization method can improve correlation of non-targeted GC/MS data with targeted measurements that are quantified using internal standards and not subject to batch effects.
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5

Conventional and Targeted Metabolomics Assays

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Conventional clinical metabolite and targeted metabolomics assays were conducted as previously described (18 (link)). In brief, conventional metabolites (lactate, triglycerides, β-hydroxybutyrate, glycerol, and nonesterified fatty acids [NEFA]) were measured on a Beckman-Coulter Unicell DxC 600 clinical analyzer. Targeted metabolomics assays for acylcarnitines and amino acids used tandem mass spectrometry with addition of known quantities of stable isotope-labeled internal standards on an Acquity TQD Triple Quadrupole system (Waters Corporation, Milford, MA). Sixty-two conventional and targeted metabolites were analyzed.
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