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Binary solvent delivery system

Manufactured by Waters Corporation
Sourced in United States

The Binary Solvent Delivery System is a core component of liquid chromatography instrumentation. It is designed to precisely deliver two separate solvents or mobile phases to the system, enabling solvent mixing and gradient elution capabilities for a wide range of analytical applications.

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3 protocols using binary solvent delivery system

1

FFA Analysis in Serum Samples

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All of serum samples were stored at −80 °C until use. Sample preparation were performed according to a modified protocol based on Püttmann et al.33 (link). Forty FFAs were analyzed using an ACQUITY ultra-performance liquid chromatography (UPLC) system (Waters Corporation, Milford, USA) equipped with a binary solvent delivery system and an auto-sampler (Waters Corporation, Milford, USA), coupled to a tandem quadrupole-time-of-flight (Q-TOF) mass spectrometry (Waters Corporation, Milford, USA)16 (link). For details, see the Supplementary information. A mixture of all the reference standards at an appropriate concentration was prepared and run after every ten serum samples for quality control. Twenty-four FFAs ratios were calculated by the absolute concentrations of product- to-precursor.
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2

UPLC-Q-Tof Mass Spectrometry Protocol

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A UPLC system equipped with a binary solvent delivery system was sourced from Waters Corp. (Milford, MA, USA), coupled with an auto-sampler and a UV detector as previously reported [22 (link)]. The quadrupole time-of-flight mass spectrometer (Q-Tof Premier™, Waters Corp., Milford, MA, USA) was used. The lock mass used was a reference solution of leucine-enkephalin ([M − H] − m/z 554.2615) in the form of a spray.
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3

Quantification of Triptan Drugs in Milk

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Milk samples, spiked standards and QC samples were extracted as follows: 50 µL sample, 25 µL internal standard solution, 25 µL 0.1 mol/L Na 2 CO 3 (pH 11) and 1 mL n-chlorobutane:acetonitrile (4:1) were mixed and centrifuged. The organic phase was pipetted off, transferred to new tubes and evaporated to dryness under a stream of nitrogen at 40°C, and the remaining extracts were reconstituted in 100 µL water:methanol (95:5) with 0.1% formic acid. 2.4.3 | Liquid chromatography-tandem mass spectrometry Samples were analysed by LC-MS/MS using a Waters Acquity UPLC system with an autosampler and a binary solvent delivery system (Waters) interfaced to Waters Xevo TQ-S benchtop tandem quadrupole mass spectrometer (Waters). Separation was performed on a 2.1 × 100 mm Waters Acquity HSS T3 column maintained at 50°C.
Lower limit of quantification (LLOQ) was found to be 0.25 nM for almotriptan and naratriptan, 0.5 nM for sumatriptan, zolmitriptan and rizatriptan, and 1 nM for eletriptan, N-desmethyleletriptan and N-desmethylzolmitriptan. For a more detailed description of the LC-MS/MS method, preparation of calibrators and controls, and precision and accuracy, see Appendix S1.
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