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Viva c18 column

Manufactured by Restek
Sourced in United States

The Viva C18 column is a high-performance liquid chromatography (HPLC) column designed for the separation and analysis of a wide range of analytes. It features a silica-based stationary phase with C18 bonded ligands, providing excellent retention and selectivity for a variety of compounds.

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2 protocols using viva c18 column

1

HPLC Analysis of Chemical Compounds

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Chromatography was conducted on an Agilent 1260 Infinity II system with a diode array detector (Agilent Technologies, Santa Clara, CA, USA). A Restek Viva C18 column (200 mm × 4.6 mm; 5 um pore size) (Restek, Bellefonte, PA, USA) was used and the diode array detector was set to a wavelength of 214 nm. The mobile phase consisted of two solvents. Solvent A was 0.1% trifluoroacetic acid (TFA) (Sigma Aldrich, St. Louis, MO, USA) in nanopure water and Solvent B was 0.09% TFA in 90% acetonitrile (Fisher Scientific, Waltham, MA, USA) in nanopure water. The gradient began at 42.5% B and increased to 45.0% B at 5 min, then increased to 50% B from 5 to 8 min. From 8 to 9 min solvent B remained at 50%. From 9 to 12 min solvent B increased to 70%. From 12 to 13 min solvent B increased to 100%, and was held at 100% until 14 min. The solvents were returned to starting conditions from 14 min to 16 min. The column was equilibrated at starting condition for an additional 3 min, providing a method with a total runtime of 19 min.
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2

Determination of Lutein in Egg Yolks

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For the analysis of lutein in egg yolks, 12 eggs, or six per group, were used. The yolk samples were prepared according to the Leeson and Caston's method (2004). Lutein in egg yolks was determined using the Shimadzu HPLC system by weighing 0.5 g of egg yolk in a test tube, overflowing it with 5 ml of acetone and vigorously stirring on a vortex mixer for 30 seconds. The samples were left to stand in the dark for one hour. Subsequent to a rest and filtration through a 0.45 μm membrane filter CHROMAFIL ® Xtra CA-45/25 (MACHEREY-NAGEL GmbH&Co. KG, Düren, Germany), 1 ml of acetone extract was transferred to the HPLC vials and gently evaporated by heating. The residue in the vial was dissolved by the addition of 1 ml of hexane / ethyl acetate solution (65:35, v/v) and mixed on the vortex. The sample thus prepared was analyzed on a Viva C18 column (5 μm, 250x4.6 mm; RESTEK Corporation, Bellefonte, PA, USA). The mobile phase consisted of a mixture of methanol and tetrahydrofuran (THF) 9:1 (v/v). The flow rate was 1 ml/min, the analysis time was 20 minutes, and the measurement wavelength was 450 nm. The injection volume was 20 μl. The standard lutein curve was prepared using the lutein standard purchased from ChromaDex (Irvine, CA, USA).
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