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Agilent 6410 q tof ms ms

Manufactured by Agilent Technologies
Sourced in United States

The Agilent 6410 Q‐TOF MS/MS is a high-performance liquid chromatography-tandem mass spectrometry (LC-MS/MS) system. It is designed to provide accurate and sensitive detection and identification of a wide range of analytes in complex samples.

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3 protocols using agilent 6410 q tof ms ms

1

Targeted LC-MS Metabolite Analysis

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Liquid chromatography‐MS analysis was carried out with a ultra high performance liquid chromatography system (Infinity 1290; Agilent Technologies) connected to a Q‐TOF/MS instrument (Agilent 6410 Q‐TOF MS/MS; Agilent Technologies). Elution with solvent A (0.1% formic acid) and solvent B (acetonitrile) in a linear gradient manner was undertaken at a flow rate of 0.4 mL/min as follows: 5% B (0‐2 minutes), 50% B (2‐10 minutes), 100% B (10‐18 minutes), 100% B (18‐18.5 minutes), 5% B (18.5‐19 minutes), and 5% B (19‐20 minutes). The injection volume was 5 μL, the flow rate was 300 μL/min, and the temperature was 40°C. Electrospray ionization in positive ionization mode was carried out with the following parameters: the capillary voltage and cone voltage were set at 4.5 and 35 kV, respectively, the drying gas temperature was set at 400°C, and the mass range was scanned as m/z 50‐1000. The LC‐MS data were collected and analyzed using MassHunter B.03.01 (Agilent Technologies).
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2

Mass Spectrometry-Based Metabolomic Analysis

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Agilent 1290 Infinity LC and Agilent 6410 Q‐TOF MS/MS were provided by Agilent Technologies (Santa Clara, CA, USA). SpeedVac SPD121P used for centrifuges was provided by Thermo Fisher Scientific (Waltham, MA, USA). GTR16‐2 was provided by BJSDBL (Beijing, China), and XW‐80A was provided by Shanxi (Shanghai, China). IKA T10basic‐S25 was provided by IKA (Staufen, Germany), and double distilled water was provided by Millipore (Milan, Italy). Formic acid (#399388), acetonitrile (#34851), 2‐propanol ethyl carbinol (#1570428), methanol (#34860), saturated fatty acid methyl esters (#ME10‐1KT), xylene substitute (#A5597), ethanol (#443611), hematoxylin (#H9627), hydrochloric acid (32 wt. % in H2O, #W530574), ammonia (28% NH3 in H2O, #338818), and eosin (#E4009) were purchased from Sigma‐Aldrich (Milwaukee, WI, USA).
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3

Metabolite Identification by LC-MS/MS

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LC‐MS analysis was conducted by an UHPLC system (Infinity 1290; Agilent Technologies). The system was connected to a Q‐TOF/MS instrument (Agilent 6410 Q‐TOF MS/MS, Agilent Technologies). LC‐MS data were collected and analysed by MassHunter B.03.01 (Agilent Technologies). The injection of each sample was performed twice, 2 μL for negative ionization mode analysis and positive ionization mode analysis, respectively. The column compartment temperature was 40°C, the setup of flow rate was 0.4 mL/min, the total separation time of two ionization modes was 20 minutes and the autosampler temperature was kept at 4°C. The mobile phase comprised Solvents A (5 mmol/L 0.1% formic acid) and Solvents B (acetonitrile with 0.2% acetic acid). By spiking the pooled serum samples containing mixtures of five standard metabolites, the identities of metabolites were proved.
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