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Ods 2 c18 analytical column

Manufactured by Waters Corporation
Sourced in United States

The ODS-2 C18 analytical column is a high-performance liquid chromatography (HPLC) column designed for the separation and analysis of a wide range of organic compounds. The column features a stable, non-polar C18 stationary phase that provides efficient and reproducible separations. The column dimensions and particle size can vary depending on the specific application requirements.

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3 protocols using ods 2 c18 analytical column

1

Extraction and Characterization of HJD Herbal Compound

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HL, HB, HQ and ZZ were purchased from Nanning Wanyaotang Pharmaceutical Co., Ltd. (Nanning, China) and authenticated by Professor Songji Wei (College of Pharmacy, Guangxi University of Chinese Medicine, China). The voucher specimens, deposited at the Guangxi University of Chinese Medicine, were HL-2017-0401, HQ-2017-0402, HB-2017-0403, and ZZ-2017-0104 for HL, HQ, HB, and ZZ, respectively.
Briefly, 300 g of HL, 200 g of HB, 200 g of HQ, and 300 g of ZZ were extracted twice, for 2 h each time, by refluxing in water according to the weight ratio of 15:1 of water to herbal. Then, the aqueous solution was combined, then filtered and concentrated in a rotary evaporator to a fluid extract with a relative density of about 1.05–1.20 (measured at 50–60 ℃), and then was stored in a refrigerator at 4 ℃. The content of berberine hydrochloride, a kind of active compound, in HJD extract was 20.39 mg/g, which was analyzed by high-performance liquid chromatography (Alliance 2695, Waters, USA) on a Inertsil ODS-2 C18 analytical column (4.6 mm × 250 mm, 5 μm) with elution by acetonitrile-0.05 moL/L phosphoric acid aqueous solution (50:50), a flow rate at 1.0 mL/min and the detection wavelength of 345 nm. The column temperature was 30 ℃, and the injection volume was 10 μL.
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2

Extraction and Analysis of Plant Pigments

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Chlorophylls and carotenoids were isolated from rosette leaves according to Pogson et al. (1996) (link). One hundred milligram of leaves was ground in liquid nitrogen into fine powder and mixed thoroughly with 250 μl 80% acetone containing 10 μg deuteroporphyrin IX dimethyl ester (Sigma–Aldrich, St. Louis, MO, United States) as an internal standard. The extract was then mixed with 250 μl ethyl acetate, followed by 200 μl of water. After a centrifugation at 4°C, 15,000 g for 10 min, the upper organic phase was collected and dried under a stream of nitrogen. The pigment was re-dissolved in Solvent A (acetonitrile:water:trimethylamine = 9:1:0.01) for high-performance liquid chromatography (HPLC) analysis. All steps were carried out under dim light.
Total pigment samples were analyzed by HPLC (Waters 2695 separation module) with a Waters ODS2 C18 analytical column (5 μm, 4.6 mm × 250 mm) and 2998 photodiode array detector (Waters, Milford, MA, United States) according to Wang et al. (2016) (link).
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3

Huanglian Decoction Preparation and Analysis

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The formula of Huanglian decoction used in this study is different from the previously reported formula. This formulation consisted of 50 g of Coptidis Rhizoma, Zingiberis Rhizoma (25 g), Folium Artemisiae Argyi (25 g), and Mume Fructus (10 g). All the above-mentioned herbs were acquired from the Chinese TongRenTang pharmacy. Briefly, all herbs were mixed and soaked for 30 min, then boiled in a casserole (1000 mL of distilled water) for 2 h. Subsequently, the supernatant was centrifuged at 8000 rpm (4293 × g) for 30 min, at which point the whole procedure was repeated twice and the supernatants were mixed together and then evaporated to dryness. Finally, the precipitate was redissolved in distilled water to a concentration of 10 mg/mL and filtered using a 0.22 μm pore-size filter and stored at 4 °C. The active compound of Huanglian Decoction (berberine hydrochloride) was approximately 0.26 mg/mL, which was analyzed by high-performance liquid chromatography (Alliance 2695, Waters, Milford, MA, United States) on an Inertsil ODS-2 C18 analytical column (4.6 mm × 250 mm, 5 μm) with a detection wavelength of 345 nm. It was eluted with acetonitrile-0.05 moL/L phosphoric acid aqueous solution (50:50), the flow rate was 1.0 mL/min, and the column temperature was 30 °C.
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