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5500 q trap hybrid triple quadrupole linear ion trap mass spectrometer

Manufactured by Thermo Fisher Scientific
Sourced in United States

The 5500 Q-TRAP hybrid/triple quadrupole linear ion trap mass spectrometer is an analytical instrument designed to perform high-performance mass spectrometry. It combines the features of a triple quadrupole and a linear ion trap, enabling comprehensive qualitative and quantitative analysis of a wide range of analytes.

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3 protocols using 5500 q trap hybrid triple quadrupole linear ion trap mass spectrometer

1

Quantification of Analytes by LC-MS/MS

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Samples were analyzed using a 5500 Q-TRAP hybrid/triple quadrupole linear ion trap mass spectrometer (Applied Biosystems, Carlsbad, CA) with electrospray ionization (ESI) in negative mode. The mass spectrometer was interfaced to a Shimadzu (Columbia, MD) SIL-20AC XR auto-sampler followed by 2 LC-20AD XR LC pumps. The scheduled MRM transitions were monitored within a 1.5 min time-window (supplemental Table 1). Optimal instrument parameters were determined by direct infusion of each analyte. The gradient mobile phase was delivered at a flow rate of 0.5 ml/min, and consisted of two solvents, 0.05% acetic acid in water and acetonitrile. The analytes were resolved on a Betabasic-C18 (100 × 2 mm, 3 μm) column at 40 °C using the Shimadzu column oven. Data was acquired using Analyst 1.5.1 and analyzed using Multiquant 3.0.1(AB Sciex, Ontario, Canada).
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2

Plasma Analysis of Antioxidants in Animal Blood

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In Group II animals (6 with US treatment and 5 with no US treatment), 1.6 mL of whole blood was collected in ethylenediaminetetraacetic acid (EDTA)-treated tubes from a cardiac puncture. Cells were removed by centrifugation and anti-oxidant comprising 0.2 mg/mL butylated hydroxytoluene (Sigma B-1378), 2 mg/mL triphenylphosphine (Fluka 93090) and 2 mg/mL indomethacin in methanol:ethanol (1:1) was added to the resulting plasma. Samples were analyzed by liquid chromatography tandem mass spectrometry using a 5500 Q-TRAP hybrid/triple quadrupole linear ion trap mass spectrometer (Applied Biosystems, Foster City, CA, USA) as described previously21 (link),22 (link).
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3

Analytical Methods for Organic Contaminants

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Target organic contaminants were analyzed with a 5500 QTRAP hybrid triple quadrupolelinear ion trap mass spectrometer with a turbo Ion Spray source (Applied Biosystems), coupled to a Waters Acquity Ultra-Performance TM liquid chromatograph (Milford) . The details of the target analytical method are given in Text S3 and Table S1. Free chlorine and ozone were measured in the presence and absence of 20 mM NaCl, respectively, immediately after sampling and using a diethyl-p-phenylene diamine (DPD) colorimetric method, i.e., Chlorine/Ozone/Chlorine dioxide cuvette tests LCK 310 (Hach Lange Spain Sl). The detection limit for the measurement of free chlorine (HOCl/OCl -) using the DPD method was 0.05 mg L -1 . Chloride, chlorate and perchlorate were measured by high-pressure ion chromatography (HPIC) using a Dionex ICS-5000 HPIC system. The quantification limits for the measurements of Cl -, ClO3 -and ClO4 -were 0.025 mg L -1 , 0.015 mg L -1 and 0.004 mg L -1 , respectively.
Hydrogen peroxide (H2O2) was measured by a spectrophotometric method using 0.01 M copper (II) sulphate solution and 0.1% w/v 2,9 dimethyl -1,10 -phenanthroline (DMP) solution, based on the formation of Cu(DMP) + 2 cation, which shows an absorption maximum at 454 nm (Baga et al. 1988) (link).
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