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Capcellpak mgii c18

Manufactured by Shiseido
Sourced in Japan

CapcellPAK MGII C18 is a type of lab equipment used for liquid chromatography. It is a reversed-phase column containing octadecylsilane (C18) bonded silica particles as the stationary phase. The column is designed for the separation and analysis of a wide range of compounds.

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2 protocols using capcellpak mgii c18

1

HPLC Fingerprinting of Guettarda speciosa

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The methanol extract of the stem and leaves of Guettarda speciosa Linn. (MGS; voucher #: FBM224–095) was obtained from the International Biological Material Research Center at the Korea Research Institute of Bioscience and Biotechnology, Daejeon, Korea. Fingerprinting MGS was conducted with Agilent 1200 series high-performance liquid chromatographic (HPLC) system. MGS (15 μl in methanol) was injected onto a column (CapcellPAK MGII C18, Shiseido, Japan, 4.6 × 150 mm ID, 3 μm). The column temperature was 35 °C, and the flow rate was 0.5 mL/min. Samples were eluted in a gradient of 0.1% formic acid and incremental acetonitrile in water. Standards and samples were detected at wavelengths of 254 ~ 320 nm. Index chemicals, including 3-O-caffeoylquinic acid, quercetin 3-O-galactoside, quercetin 3-O-glucoside, 3,4-di-O-caffeoylquinic acid, apigenin 7-O-glucuronide, and quercetin rutinoside, were purchased from Sigma-Aldrich (St. Louis, MO, USA). Chemstation software (Agilent Corporation, Germany) was used for data acquisition. The chemical constituents of MGS were identified by comparing their retention times to those of standard chemicals under identical analysis conditions and the UV spectra.
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2

HPLC Separation of Target Analyte

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A Capcell Pak MGII-C18 (2 mm × 100 mm, 3 m) (Shiseido, Tokyo, Japan) was used as the chromatographic column. Mobile phase A used pure water and mobile phase B used methanol, both containing 0.5% acetic acid. The gradient elution procedure was as follows: 0 min → mobile phase B 10%, 0.5 min → mobile phase B 30%, 1.0 min → mobile phase B 90%, 2 min → mobile phase B 90%, 2.3 min → mobile phase B 93%, 2.5 min → mobile phase B 10%, and 0.5 min → mobile phase B 30%. Other conditions included column temperature of 25 °C; injection volume of 1 µL, flow rate of 0.3 mL/min and running time of 4 min. Under the above conditions, the baseline separation was realized between the targeting analyte and the internal standard.
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