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Quadrupole time of flight instrument

Manufactured by Bruker
Sourced in United States

The Quadrupole Time of Flight (QTOF) instrument is an analytical tool that combines a quadrupole mass analyzer with a time-of-flight (TOF) mass analyzer. This configuration allows for high-resolution mass analysis and accurate mass measurement of a wide range of molecular species. The QTOF instrument is designed to deliver precise and sensitive detection, making it a versatile tool for applications such as proteomics, metabolomics, and small molecule analysis.

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3 protocols using quadrupole time of flight instrument

1

Mass Spectrometry Analysis of Cyclopamine

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Cyclopamine isolated from each alkaloid mixture was analyzed by mass spectrometry using an ultra-high resolution Quadrupole Time of Flight (QTOF) instrument (Bruker maXis). The electrospray ionization (ESI) source was operated under the following conditions: positive ion mode; nebulizer pressure: 0.8 Bar; flow rate of drying gas (N2): 4 L/min; drying gas temperature: 200 °C; voltage between HV capillary and HV end-plate offset: 3000 V to −500 V; mass range was set from 80 to 1000 m/z; and the quadrupole ion energy was 4.0 eV. Samples were analyzed by direct infusion with a syringe pump at a flow rate of 240 μL/hr. Sodium formate was used to calibrate the system in the mass range. Spectra were collected for intact parent ions followed by isolation and fragmentation using collision induced decay MS/MS over a range of collision energies (0-40 eV). Fragmentation patterns were compared to cyclopamine and veratramine standards. Data were analyzed using the Compass Data Analysis software package (Bruker Corporation, Billerica, Massachusetts).
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2

Identification of Steroidal Alkaloids in Veratrum californicum

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To identify the steroidal alkaloids in V. californicum aerial and root/rhizome extracts, samples were analyzed by HPLC-MS, where the mass spectrometer was an ultra-high resolution Quadrupole Time of Flight (QTOF) instrument (Bruker maXis, Billerica, MA, USA). The electrospray ionization (ESI) source was operated under the following conditions: positive ion mode, 1.2 bar nebulizer pressure, 8 L/min flow of N2 drying gas heated to a temperature of 200°C, 3000 V to −500 V voltage between HV capillary and HV end-plate offset, mass range set from 80 to 800 m/z, and the quadrupole ion energy at 4.0 eV. Sodium formate was used to calibrate the system in this mass range. HPLC separation was achieved using a XTerra MS C18 column, 3.5 μm, 2.1 × 150 mm (Waters, Milford, MA, USA). The flow rate was 250 μL/min. The mobile phases were 5% acetonitrile and 0.1% formic acid in water (Buffer A) and acetonitrile and 0.1% formic acid (Buffer B). The linear gradient method was used to separate analytes starting at 5% Buffer B and increasing to 60% Buffer B over 25 min. A 1 μL sample injection volume was used. Data were analyzed with the Compass Data Analysis software package (Bruker Corporation).
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3

Steroidal Alkaloid Identification in V. californicum

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In order to identify the steroidal alkaloids in V. californicum leaf, stem and root/rhizome extracts, samples were analyzed by HPLC-MS, where the mass spectrometer was an ultra-high resolution Quadrupole Time of Flight (QTOF) instrument (Bruker maXis, Billerica, MA, USA). The electrospray ionization (ESI) source was operated under the following conditions: positive ion mode, 1.2 bar nebulizer pressure, 8 L/min flow of N2 drying gas heated to a temperature of 200 °C, 3000 V to −500 V voltage between HV capillary and HV end-plate offset, mass range set from 80 to 800 m/z, and the quadrupole ion energy at 4.0 eV. Sodium formate was used to calibrate the system in this mass range of 80 to 800 m/z. HPLC separation was achieved using a XTerra MS C18 column, 3.5 μm, 2.1 × 150 mm (Waters, Milford, MA, USA). The flow rate was 250 μL/min. The mobile phases were 5% acetonitrile and 0.1% formic acid in water (Buffer A) and acetonitrile and 0.1% formic acid (Buffer B). The linear gradient method was used to separate analytes starting at 5% Buffer B and increasing to 60% Buffer B over 25 min. A 1 μL sample injection was used. Data were analyzed with the Compass Data Analysis software package (Bruker Corporation).
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