Ingredient Analysis

Simultaneous determination of 13 components in Yankening tablets by UPLC

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  • 1. Liaoning Institute of Traditional Chinese MedicineThe Second Hospital Affiliated to Liaoning University of Traditional Chinese Medicine, Shenyang 110034, China;
    2. Dalian Inspection and Certification Technical Service Center, Dalian 116021, China

Received date: 2023-10-01

  Online published: 2024-08-05

Abstract

Objective: To establish an UPLC quantitative analysis method for the simultaneous determination of 13 components in Yankening tablets, including phellodendrine, coptisine, baicalin, palmatine, berberine, wogonoside, baicalein, aloe-emodin, rhein, wogonin, emodin, chrysophanol, physcion. Methods: Agilent Eclipse Plus C18(100 mm×2.1 mm, 1.8 μm) column was used with acetonitrile-0.1% phosphoric acid as mobile phase, and gradient elution at a flow rate of 0.3 mL·min-1. The detection wavelengths were 210 nm and 254 nm. The column temperature was 40 ℃. Results: Phellodendrine hydrochloride, coptisine hydrochloride, palmatine hydrochloride, berberine hydrochloride, baicalin, wogonoside, baicalein, aloe-emodin, rhein, wogonin, emodin, chrysophanol, physcion showed good linear relationships within their concentration range of 0.97-48.63 μg·mL-1, 0.95-47.52 μg·mL-1, 0.86-43.15 μg·mL-1, 0.86-43.19 μg·mL-1, 0.89-44.37 μg·mL-1, 1.00-49.84 μg·mL-1, 1.02-51.01 μg·mL-1, 0.97-48.31 μg·mL-1, 0.99-49.50 μg·mL-1, 1.04-51.80 μg·mL-1, 1.00-50.04 μg·mL-1, 1.00-49.80 μg·mL-1, 1.01-50.64 μg·mL-1. The average recoveries(n=6) were 95.2%, 96.7%, 95.9%, 98.3%, 94.1%,97.6%, 99.2%, 96.6%, 95.5%, 97.2%, 97.0%, 97.8%, 98.7%, RSD values were all less than 2.0%. The contents of the 13 chemical components in 3 batches of samples were 1.367-1.488 mg·g-1(calculated as phellodendrine hydrochloride), 0.378-0.412 mg·g-1(calculated as coptisine hydrochloride), 4.611-5.505 mg·g-1, 0.324-0.407 mg·g-1(calculated as palmatine hydrochloride), 3.665-3.878 mg·g-1(calculated as berberine hydrochloride), 1.107-1.682 mg·g-1, 0.392-0.941 mg·g-1, 0.076-0.105 mg·g-1, 0.097-0.116 mg·g-1, 1.059-1.213 mg·g-1, 0.149-0.167 mg·g-1, 0.213-0.239 mg·g-1, 0.047-0.059 mg·g-1. Conclusion: The method is accurate, high analysis efficiency, good repeatability, it can be used to control the quality of Yankening tablets.

Cite this article

DONG Xiao-qian, YAN Chang-yu, MA Jin . Simultaneous determination of 13 components in Yankening tablets by UPLC[J]. Chinese Journal of Pharmaceutical Analysis, 2024 , 44(7) : 1195 -1201 . DOI: 10.16155/j.0254-1793.2023-0639

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