ZHAN Lili. Study on Fingerprint and Multi-components Determination of Niuhuang Qinggan Capsules by HPLC[J]. Chinese Journal of Modern Applied Pharmacy, 2020, 37(1): 45-49. DOI: 10.13748/j.cnki.issn1007-7693.2020.01.009
    Citation: ZHAN Lili. Study on Fingerprint and Multi-components Determination of Niuhuang Qinggan Capsules by HPLC[J]. Chinese Journal of Modern Applied Pharmacy, 2020, 37(1): 45-49. DOI: 10.13748/j.cnki.issn1007-7693.2020.01.009

    Study on Fingerprint and Multi-components Determination of Niuhuang Qinggan Capsules by HPLC

    • OBJECTIVE To establish the HPLC fingerprint and determine the contents of seven compounds in Niuhuang Qinggan capsules simultaneously. METHODS The separation was carried out on an Agilent SB-C18 column(250 mm×4.6 mm, 5 μm). The mobile phase was acetonitrile(A)-0.1% acetic acid solution(B) with gradient elution, the detection wavelength was 210 nm, and column temperature was 30℃. "Similarity evaluation system for chromatographic fingerprint of TCM (2004A)" was used to conduct, and the seven markers were quantified. RESULTS The common mode of the fingerprint showed 22 common peaks, 7 of which were identified by comparison with the reference substances. They were chlorogenic acid, caffeic acid, luteolin-7-o-glucoside, baicalin, baicalein, wogonoside and wogonin. The similar degrees of 12 batches of samples were > 0.90, and the average recoveries varied from 99.1%-104.8% with RSDs of 1.30%-1.88%. CONCLUSION The established method can be used for the quality control of Niuhuang Qinggan capsules.
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