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Api 5000 triple quadrupole lc ms ms mass spectrometer

Manufactured by AB Sciex

The API 5000 Triple Quadrupole LC/MS/MS Mass Spectrometer is a high-performance analytical instrument designed for quantitative and qualitative analysis of small molecules. It utilizes triple quadrupole technology to provide accurate and sensitive mass spectrometry measurements.

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2 protocols using api 5000 triple quadrupole lc ms ms mass spectrometer

1

Plasma Free Amino Acid Analysis

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Blood for amino acid analysis was drawn from a fresh catheter in the forearm in non-fasting adults immediately following study enrolment and usually before a first dose of antimalarials was provided. Blood samples was collected in lithium-heparin tubes that were immediately centrifuged and flash-frozen in liquid-nitrogen. Samples were shipped on dry ice and stored at −80 °C. In brief, amino acids were extracted by solid-phase extraction using sorbent tips (Phenomenex EZ:faast™), as described previously38 (link). Plasma free amino acids (PFAA) were separated on an AAA-MS™ column (250 × 3.0 mm, Phenomenex, Torrance, California) placed in a Thermo LC system. Mass spectrometry with multiple reaction monitoring was done in positive ion mode with electrospray ionization on an ABSciex API 5000 Triple Quadrupole LC/MS/MS Mass Spectrometer. Inter-assay variation scores were determined for three amino acid standards and the individual amino acids. Concentrations were based on interpolation on a linear standard curve. We excluded amino acids if they could be measured in less than 50 cases. The final amino acid data set is publicly available on GitHub, found at: https://github.com/Stije/PFAA.
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2

HPLC-MS/MS for m/z 73.1 Screening

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HPLC-MS/MS precursor ion screening for m/z 73.1 was performed using an Agilent 1260 HPLC instrument (Agilent Technologies) coupled to an API5000 Triple Quadrupole LC/MS/MS mass spectrometer (AB Sciex, Darmstadt) equipped with an electrospray ionization (ESI) unit operated in negative mode. A CID energy of −34 was applied. Chromatographic separations were achieved using an Agilent ZORBAX Eclipse XDB-C18 column (50 × 4.6 mm, 1.8 µm particle diameter) (Agilent Technologies) with a flow rate of 1.1 mL/min and gradient elution starting at 5% acetonitrile in 0.05% aqueous formic acid followed by a linear increase to 95% acetonitrile with 0.05% formic acid within 10 min. Data were analyzed with the Analyst 1.6 software (AB Sciex).
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