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SUN Xiaomeng, BI Xueyan, QU Fanna, ZHANG Qingbo, YANG Huibing, ZHANG Xue, ZHOU Nan. Studies on fingerprint of Shenkang injection[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(6): 543-547,576. doi: 10.3969/j.issn.1006-0111.2019.06.014
Citation: SUN Xiaomeng, BI Xueyan, QU Fanna, ZHANG Qingbo, YANG Huibing, ZHANG Xue, ZHOU Nan. Studies on fingerprint of Shenkang injection[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(6): 543-547,576. doi: 10.3969/j.issn.1006-0111.2019.06.014

Studies on fingerprint of Shenkang injection

doi: 10.3969/j.issn.1006-0111.2019.06.014
  • Received Date: 2018-11-14
  • Rev Recd Date: 2019-11-05
  • Objective To establish an ultra-high performance liquid chromatography (UPLC) fingerprint of Shenkang injection and identify the common peaks of Shenkang injection fingerprint. Methods The UPLC method was established by employing ACQUITY UPLC® CSH-C18 column(2.1 mm×100 mm,1.7 μm) with methanol(A) -0.1% formic acid(B) aqueous solution as mobile phase in gradient elution.The detection wavelength was 280 nm.The flow rate was 0.4ml/min.The injection volume was 2 μl and the column temperature was 30℃.Time of flight mass spectrometer was used with negative ion mode scanning. Results The UPLC chromatographic fingerprint of Shenkang injection was established.26 common peaks of shenkang injection were identified by UPLC/ESI-Q-TOF MS.The similarity of 20 batches of shenkang injection was over 0.90,which was evaluated by similarity evaluation system for chromatographic fingerprint of TCM(Version 2012.130723). Conclusion This method is highly sensitive,stable and reliable,and can be used for the quality control of shenkang injection.
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    [7] 刘芳,郭丝影,柴士伟,等.肾康注射液中化学成分的UPLC-Q-TOF-MS分析[J].现代药物与临床,2017,32(6):975-977.
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Studies on fingerprint of Shenkang injection

doi: 10.3969/j.issn.1006-0111.2019.06.014

Abstract: Objective To establish an ultra-high performance liquid chromatography (UPLC) fingerprint of Shenkang injection and identify the common peaks of Shenkang injection fingerprint. Methods The UPLC method was established by employing ACQUITY UPLC® CSH-C18 column(2.1 mm×100 mm,1.7 μm) with methanol(A) -0.1% formic acid(B) aqueous solution as mobile phase in gradient elution.The detection wavelength was 280 nm.The flow rate was 0.4ml/min.The injection volume was 2 μl and the column temperature was 30℃.Time of flight mass spectrometer was used with negative ion mode scanning. Results The UPLC chromatographic fingerprint of Shenkang injection was established.26 common peaks of shenkang injection were identified by UPLC/ESI-Q-TOF MS.The similarity of 20 batches of shenkang injection was over 0.90,which was evaluated by similarity evaluation system for chromatographic fingerprint of TCM(Version 2012.130723). Conclusion This method is highly sensitive,stable and reliable,and can be used for the quality control of shenkang injection.

SUN Xiaomeng, BI Xueyan, QU Fanna, ZHANG Qingbo, YANG Huibing, ZHANG Xue, ZHOU Nan. Studies on fingerprint of Shenkang injection[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(6): 543-547,576. doi: 10.3969/j.issn.1006-0111.2019.06.014
Citation: SUN Xiaomeng, BI Xueyan, QU Fanna, ZHANG Qingbo, YANG Huibing, ZHANG Xue, ZHOU Nan. Studies on fingerprint of Shenkang injection[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(6): 543-547,576. doi: 10.3969/j.issn.1006-0111.2019.06.014
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