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Intellistart

Manufactured by Waters Corporation
Sourced in United States

The IntelliStart is a lab equipment product from Waters Corporation. It is designed to automate and streamline various laboratory processes, providing consistent and reliable results. The core function of the IntelliStart is to enable efficient and accurate sample preparation and analysis.

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3 protocols using intellistart

1

Optimized Dopamine Metabolites Analysis

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Detection was performed on a Waters® Xevo TQ MS Triple Quadrupole equipped with ESI source and coupled online with an Aquity UHPLC (Waters, Milford, MA, USA). The MS operated in positive ionization mode, setting the capillary at 270 °C, the source at 300 °C and source voltage at 3 kV. Detection of IS, DOPAC, DOPAC-d5 and HVA were performed in negative ion mode in the same run by setting polarity switching. Ultra-high purity argon was used as collision gas. MS and MS/MS conditions were optimised via software (Intellistart, Waters, Milford, MA, USA) by infusing analytical standards.
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2

Quantitative Analysis of Bisphenol A Analogues

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The separation and quantitation of bisphenol A analogues were performed on a Waters Acquity Ultra Performance Liquid Chromatography (UPLC) system (Milford, MA, USA) coupled to a Waters Xevo TQD triple quadrupole mass spectrometer (Milford, MA, USA). Ten μL of sample extract was injected in full loop and the separation was performed at 30 °C on an Acquity UPLC BEH C18 column (1.7 μm, 2.1 mm × 50 mm, Waters) with a Van Guard BEH C18 pre-column (1.7 μm, 2.1 × 5 mm, Waters). The mobile phase consisted of (A): 5% methanol in water and (B): 2 mM NH4OH in methanol. The gradient program was as follows: initial gradient 100% (A) hold for 1min, to 55% (B) in 1 min, to 100% (B) in 10 min, back to 100% (A) in 0.5 min, and hold for 3.5 min at 100% (A). Flow rate was set at 0.2 mL/min. The MS/MS was operated in multiple reaction monitoring (MRM) using electrospray ionization in negative ion mode (ESI-). The MRM transitions and MS parameters were obtained and optimized using Waters IntelliStart (Waters, MA, USA). MRM transitions and optimized MS parameters are summarized in Table 1. Source temperature, desolvation temperature, and gas flow were set at 150 °C, 350 °C and 600 L/h, respectively. Capillary voltage was set at 2.5 kV and extractor voltage at 10 V.
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3

UPLC-MS/MS Quantification Protocol

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Samples were analyzed at the University of Connecticut Center for Environmental Sciences and Engineering (Storrs, CT) using a Waters Acquity ultraperformance liquid chromatograph (UPLC) coupled with an Acquity TQD tandem mass spectrometer (Waters Co., Milford, MA) as described previously (22 (link)). A total of 450 μL of test or quality control samples were spiked with 25 μL internal standard solution and 25 μL of methanol. An Acquity UPLC BEH C18 (1.7 μm, 2.1 × 50 mm) column, maintained at 25°C and with a sample injection volume of 10 μL on a 20-μL loop, was utilized for analyte separation. Analyte signal optimization was performed using the Waters IntelliStart, whereas analyte detection, quantification, and statistical analysis were performed using the Waters QuanLynx within MassLynx software v.4.2 in electrospray ionization (ESI) plus tandem MS (MS/MS) mode.
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