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Chromafil xtra ca 45 25

Manufactured by Macherey-Nagel
Sourced in Germany

Chromafil® Xtra CA-45/25 is a syringe filter product designed for filtration purposes. It features a cellulose acetate membrane with a pore size of 0.45 μm and an effective filtration area of 25 mm².

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3 protocols using chromafil xtra ca 45 25

1

Solubility of Resveratrol in Solvents

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The solubility of RSV was determined in (1) pure solvents, namely, distilled water (W), phosphate buffer of pH = 6.8 (PBS, Ph. Eur. 4th ed.), propylene glycol (PG), and Labrasol (L) and (2) a mixture of solvents, i.e., PG and water (1:1). These solvents were chosen taking into account their suitability to prepare wound dressings, i.e., low toxicity and low risk of irritation. An excess amount of RSV was added to a conical flask containing 20 mL of the solvent. The samples, protected from light, were shaken at 37°C for 24 h using a laboratory shaker (Memmert WNB 22, Schwabach, Germany) to reach the saturation. After 24 h, the samples were withdrawn and they were centrifuged (MPW 221, Poland) at 3600 rpm for 30 min. Then, they were filtered through syringe membrane filters of 0.45 μm (Chromafil® Xtra CA-45/25, Macherey-Nagel, Düren, Germany). After dilution, the concentration of RSV was measured spectrophotometrically (Shimadzu UV-1800, Shimadzu USA Manufacturing Inc., Canby, OR, USA) at 306 nm. Mean values (n=3) ± standard deviations (SD) were calculated.
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2

Organic Synthesis Reaction Protocol

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The equipment and materials included are a scale (model AY220; Shimadzu), reaction flasks with a 100-mL mouth, oil bath (silicone+glassware), magnetic bar, a laminar flow hood (TROX-100), Heating and stirring plate (model C-MAG HS4; IKA), 50-mL volumetric flasks, 10-mL volumetric flask, 5-mL weighing beakers, spatulas (nonmetallic), a 0.45-μm filter (Chromafil Xtra CA-45/25; Macherey-Nagel), nitrile gloves, 1-mL micropipette, safety glasses, Pasteur pipettes, plastic syringes, Nalgene 10-mL, and 50-mL Teflon tubes.
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3

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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