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Dgu 20a3 a5

Manufactured by Shimadzu

The DGU-20A3/A5 is a degasser unit designed for use in high-performance liquid chromatography (HPLC) systems. Its core function is to remove dissolved gases from the mobile phase, preventing bubble formation and improving the stability and reliability of HPLC analysis.

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2 protocols using dgu 20a3 a5

1

HPLC Analysis of Anthocyanins

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HPLC analysis was conducted according to the method described by Darniadi et al. (2019) . A UFLCXR system (Shimadzu) comprising of a binary pump, a photodiode array with multiple wavelengths (SPD-20A), a Solvent Delivery Module (LC-20AD) coupled with an online unit degasser (DGU-20A3/A5) and a thermostat auto sampler/injector unit (SIL-20A). The photodiode array detector was set to measure at a wavelength of 520 nm.
Identification of anthocyanins in the reconstituted powders was achieved by comparing the retention time with external standards of phenolic compounds run under similar conditions, UV-visible spectrum and spiking of the sample with the corresponding standard phenolic compound. A standard curve was developed using cyanidin-3-glucoside (Cyn3Gl) to express total monomeric anthocyanin (TMA) as mg/g Cyn3Gl solids, while quantification of individual anthocyanins was done by external standards:
cyanidin-3-glucoside (Cyn3Gl), delphinidin-3-glucoside (Del3Gl) and malvidin-3-glucoside (Mal3Gl).
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2

Phenolic Compounds in Roselle Wine

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The identification and quantification of phenolic compounds in roselle wine was carried out as described in Ifie et al. (2016) . A UFLCXR system (Shimadzu) consisting of a binary pump, coupled with an online unit degasser (DGU-20A3/A5), a solvent delivery module (LC-20AD), a thermostat autosampler/injector unit (SIL-20A) and a photodiode array with multiple wavelength (SPD-20A) was used for the analysis. The mobile phase was 0.1 % (v/v) trifluoroacetic acid (mobile phase A) and trifluoroacetic acid/acetonitrile/water (50:49.9:0.1) (mobile phase B). The flow rate was set to 1 mL/min and the injection volume was 10 L.
Chromatographic separation was performed on a Gemini C18 5 m, 250 mm ×4.6 mm column (Phenomenex, Macclesfield, UK) and the oven temperature was maintained at 35 °C.
The photodiode array detector was set to measure at wavelengths of 265, 320, 360 and 520 nm. The gradient program was started at 8 % B and increased linearly until 18 % solvent B was achieved at 3.50 min, solvent B was increased to 32 % at 18 min, 60 % at 28 min, and then 100 % at 32 min. Finally, 100 % B was kept constant for 4 min, followed by 3.5 min isocratic re-equilibration for initial conditions.
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