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1260 hip degasser

Manufactured by Agilent Technologies

The Agilent 1260 HiP Degasser is a laboratory equipment designed to remove dissolved gases from liquids prior to liquid chromatography analysis. It operates by applying a vacuum to the liquid samples, effectively removing any dissolved air or other gases. This process helps to improve the stability and consistency of the liquid samples, ensuring accurate and reliable analytical results.

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2 protocols using 1260 hip degasser

1

Phenolic Compounds Extraction and Quantification in Semolina and Spaghetti

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The phenolic compounds were extracted from semolina, olive paste flour (OPF), spaghetti CTRL and spaghetti enriched with 10% OPF in two separated fractions: soluble free and bound, following the method reported by Mattilla [20 (link)] without acid hydrolysis. The difference between total and free polyphenols represented the bound phenolic compounds. HPLC-DAD analysis was performed using the Agilent 1260 infinity system, equipped with a 1260 binary pump, 1260 HiP Degasser, 1260 TCC Thermostat, 1260 Diode Array Detector and Agilent Open Lab Chem Station Rev C.01.05 (35) software. The UV–visible absorption chromatogram was detected at 280 nm, 325 nm and 360 nm. The separation was performed by gradient elution on a 4.6 × 250 mm reversed phase Luna C-18 (5 μm) column (Phenomenex Torrance, California, USA). The elution was performed using methanol (eluent A) and water/acetic acid 95:5 (eluent B). The gradient profile was: 85–60% B (0–25 min), 60% B (25–30 min), 60–37% B (30–45 min), 37% B (45–47 min), 37–0% B (47–52 min). The flow rate was 1 mL/min and the injection volume was 25 μL. Phenolics were identified and quantified by the retention time, spectra and response factors of the pure standards.
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2

Multiangle Light Scattering Analysis

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Multiangle Light Scattering (MALS). Samples were dissolved in the mobile phase (0.15 M NaNO3 with 10 mM EDTA) and filtered (0.45 μm) prior to injection. An Agilent Technologies 1260 IsoPump with a 1260 HiP degasser was used to maintain a flow of 0.5 ml/min during analyses. 50 -100 μl were injected from an Agiel Technologies Vialsampler. TKS Gel columns 4000 and 2500 PWXL were connected in series.
DAWN Heleos-II and ViscoStar II detectors from Wyatt Technology were connected in series with a Shodex refractive index detector (RI-5011). Astra 7.3.0 software was used for data collection and processing.
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