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Ug120 column

Manufactured by Shiseido
Sourced in United States

The UG120 column is a laboratory equipment designed for liquid chromatography. It is used to separate and purify chemical compounds or biological samples based on their size or molecular weight. The column features a porous matrix that allows for efficient separation and high-resolution analysis. The specific details and intended uses of this product are not available.

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2 protocols using ug120 column

1

Quantification of Bioactive Compounds in PV Extract

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Oleanolic acid (OA) (99% purity) and rosmarinic acid (RA) (98% purity) were purchased from Sigma-Aldrich, and ursolic acid (UA) (92.84% purity) was purchased from the Resource Bank of Korean Medicine, National Institute for Korean Medicine Development. The compounds were dissolved in methanol at a concentration of 10 mM for use as controls, according to the methods described in previous studies (Qiang et al., 2011 (link); Chen et al., 2012 (link)). The PV extract was dissolved to 3.12 mg/ml, sonicated using ultrasound for 20 min, and filtered through a 0.45 μm syringe filter (Millipore Sigma, Burlington, MA, United States). HPLC analysis was conducted on an Agilent 1200 series system (Agilent Technologies, Santa Clara, CA, United States) equipped with a Shiseido UG120 column (5 μm, 6.4 × 250 mm) maintained at 25°C. The mobile phase was methanol (90%): 0.5% ammonium acetate (10%) for OA, UA, and methanol (52%), and 0.01% phosphoric acid (48%) for RA. Samples (20 μl) were analyzed at a flow rate of 0.6 ml/min using an ultraviolet detector at 210 nm for OA and UA, and at 310 nm for RA.
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2

Extraction and Identification of S. baicalensis

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S. baicalensis roots were obtained from Jung-do Herb, Co., Ltd. (Seoul, Korea). 50 g of dried S. baicalensis was extracted with 1 L boiling distilled water for 1 h 30 min. The extracts were filtered, concentrated and lyophilized. The dry weight of the S. baicalensis was 16.4 g (yield: 32.77% (w/w)). The voucher specimens were deposited at our laboratory. SB was identified by three standards, baicalin, baicalein and wogonin, using an Agilent Series 1100 HPLC system (Palo Alto, CA, USA) with a binary pump, an auto-sampler, a column oven, and a diode array detector (DAD). The Shiseido UG 120 column (250 × 4.6 mm, 5 μm) was tested with a guard column. The analysis was carried out at a flow rate of 1.0 mL/min with the detection wavelength at 280 nm. The HPLC peaks on SB were synchronized with baicalin, baicalein and wogonin (Fig. 1).
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