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Abi 5500 qtrap

Manufactured by AB Sciex
Sourced in Canada

The ABI-5500 Qtrap is a triple quadrupole mass spectrometer designed for quantitative and qualitative analysis. It features a linear ion trap and a quadrupole mass analyzer, enabling high-performance, sensitive, and selective detection of target compounds.

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2 protocols using abi 5500 qtrap

1

Quantitative LC-MS/MS Analysis of SERMs

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The LC‒MS/MS analysis was performed on ABI-5500 Qtrap (Sciex, Ontario, Canada) mass spectrometer with electrospray ionization source, interfaced with a Shimadzu high performance liquid chromatography (HPLC) system. LC system parameters were set with separation performed on a Waters Xbridge C18 column (Milford, MA, USA) (50 mm × 2.1 mm ID, 3.5 μm), mobile phase composed by A (100% H2O with 0.1% formic acid) and B (100% acetonitrile with 0.1% formic acid), and the flow rate set at 0.4 mL/min. The mass spectrometer was operated in a positive mode with multiple reaction monitoring (MRM) for analysis. The MRM transitions (Q1/Q3) were monitored with 372.2/71.5 for tamoxifen, 406.2/72 for toremifene, 388.2/71.8 for afimoxifene, 388.2/71.8 for droloxifene, 414.2/98.2 for lasofoxifene, 426.2/98 for nafoxidine or 474.2/269.2 for raloxifene. The acquisition and processing of data were conducted by Analyst Software version 1.6 from Applied Biosystems (MDS SCIEX; Carlsbad, CA, USA). The analytical assay was validated according to U.S. Food and Drug Administration (FDA) guidance for linearity (2–5000 ng/mL), matrix effect, recovery, low detection limit, quality control (QC) in different biological matrix, including plasma, blood, tumor, and each different organ homogenates.
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2

Comprehensive LC-MS/MS Analysis of Paclitaxel and Doxorubicin

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The total drug is measured in our study including released and unreleased drug, as well as protein bound drug in plasma to illustrate the questions below, unlike other studies provided the detail analysis of three different types of drugs [51 (link),52 ], The LC-MS/MS analysis of paclitaxel was performed using docetaxel as internal standard (IS). LC-MS/MS analysis of doxorubicin was performed using daunarubicin as internal standard (IS). The analytical assay was validated according FDA guidance for linearity (2–5000 ng/mL), matrix effect, recovery, low detection limit, Quality control (QC) in different biological matrix, including plasma, blood, tumor, and each different organ homogenates. LC-MS/MS was performed using ABI-5500 Qtrap (Sciex, Ontario, Canada) mass spectrometer with electrospray ionization source was interfaced with Shimadzu high performance liquid chromatography (HPLC) system with Xbridge C18 column (50 × 2.1 mm ID, 3.5 μm). The mass spectrometer was operated in a positive mode with multiple reaction monitoring (MRM) for analysis. The MRM transitions were monitored at m/z 854.4 to 286.1 for paclitaxel and m/z 808.0 to 226.0 for internal standard. The MRM transitions were monitored at m/z 544.1 to 397.2 for doxorubicin and m/z 528.5 to 321 for internal standard.
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