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Establishment of HPLC fingerprint and determination of multi-componentsof Qingre Lidan Tablet
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DOI   10.11656/j.issn.1672-1519.2023.11.18
Key Words   Qingre Lidan Tablet;HPLC;fingerprint;content determination
Author NameAffiliationE-mail
QIAO Xiaoli Tianjin Nankai Hospital, Tianjin 300100, China  
CAO Ningning Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300250, China  
WANG Qingguo School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China  
LIU Xiaojun Tianjin Nankai Hospital, Tianjin 300100, China  
ZHANG Haifang Graduate School, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China 343697126@qq.com 
XIAO Xuefeng School of Chinese Materia Medica, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China kai1219@163.com 
Abstract
    [Objective] To establish ahigh performance liquid chromatography(HPLC) fingerprint and a determination method of 14 components in Qingre Lidan Tablets, so as toevaluate the quality of Qingre Lidan Tablets. [Methods] Eclipse XDB-C18(5 μm, 4.6 mm×250 mm) was used for gradient elution with 0.1% phosphoric acid in water and acetonitrileas mobile phase. The column temperature was 35℃, the flow rate was 1.0 mL/min, and the detection wavelength was 294 nm. HPLC fingerprints of 15 batches of Qingre Lidan Tablets were established, and similarity analysis was conducted by using similarity evaluation software of Chinese medicine chromatographic fingerprint(2012), afterwords, calibrated the common peak and identified it, and on this basis, determined the content of the identified components. [Results] The similarity of different batches of Qingre Lidan Tablets was above 0.983. There were 62 common peaks in the fingerprints of 15 batches of samples, among which 14 components were identified, including Chlorogenic acid, Hyperoside, Quercetin, Kaempferol, Rutinum, Rosmarinic acid, Baicalin, Aloeemodin, Rhein, Emodin, Chrysophanic acid, Physcion, Magnolol, and Honokiol. The average content of them was (0.31±0.04)(0.04±0.01)(0.25±0.02)(0.20±0.06)(0.10±0.02)(0.23±0.05)(0.17±0.01)(0.19±0.02)(0.18±0.03)(0.56±0.08)(0.14±0.02)(1.98±0.17)(1.03±0.12)(0.65±0.04) mg/tablet, respectively. [Conclusion] The established HPLC fingerprint combined with multi-component content determination method for Qingre Lidan Tablets is sensitive and stable, and can be used for quality evaluation of Qingre Lidan Tablets.

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