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Ultra-rapid determination of andrographolide and dehydroandrographolide in Andrographis Herba by solid phase extraction and liquid chromatography with mass spektrometry

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
An ultra-rapid analytical method for determination of andrographolide and dehydroandrographolide in Andrographis Herba (AH) was developed by liquid chromatography with mass spectrometry (LC-MS). The sample was ultrasonically extracted with 10 mL 40% (v/v) methanol, and then purified with a C18 solid phase extraction column. The LC separation was performed on a Poroshell 120 EC-C18 column (3032.1 mm, 2.7 μm) and eluted with 0.5 mmol L1 ammonium acetate aqueous solution and acetonitrile (65:35) at a flow rate of 0.7 mL min1, and detected by mass spectrometry (MS). The LC-MS analytical time was less than 1 min. The new developed method presented a good linearity (r > 0.9900), precision and repeatability (RSD < 2.0%). The recoveries for andrographolide and dehydroandrographolide were 93.5% (RSD 5 2.2%) and 97.7% (RSD 5 2.4%), respectively. The developed method was successfully applied in determination of andrographolide and dehydroandrographolide in seven batches of AH samples, and the contents of analytes in all samples were complied with the relative acceptance criteria in Chinese Pharmacopeia (>0.8%). This new developed LC-MS method is an ultrarapid assay method for AH, which will help to improve the efficiency and reduce the cost of AH sample test.
Rocznik
Strony
279--–285
Opis fizyczny
Bibliogr. 26 poz., rys., wykr.
Twórcy
  • College of Medical Imaging Laboratory and Rehabilitation, Xiangnan University, Chenzhou 423000, P. R. China
  • Dongguan HEC Cordyceps R&D Co., LTD, Dongguan, Guangdong 523850, P. R. China
autor
  • College of Medical Imaging Laboratory and Rehabilitation, Xiangnan University, Chenzhou 423000, P. R. China
autor
  • Dongguan HEC Cordyceps R&D Co., LTD, Dongguan, Guangdong 523850, P. R. China
autor
  • Hong Zheng Dao (China) Traditional Chinese Medicine Research Co., LTD, Guangzhou, Guangdong 510665, P. R. China
autor
  • Dongguan HEC Cordyceps R&D Co., LTD, Dongguan, Guangdong 523850, P. R. China
autor
  • College of Medical Imaging Laboratory and Rehabilitation, Xiangnan University, Chenzhou 423000, P. R. China
autor
  • Dongguan HEC Cordyceps R&D Co., LTD, Dongguan, Guangdong 523850, P. R. China
Bibliografia
  • 1. The Chinese Pharmacopoeia. Committee of the Chinese Pharmacopoeia: Beijing, 2020, Vol. 1, p. 280.
  • 2. Li, W. K.; Xu, X. D.; Zhang, H. J.; Ma, C. Y.; Fong, H.; Breemen, R. V.; Fitzloff, J. Chem. Pharm. Bull. 2007, 55, 455.
  • 3. Rao, Y. K.; Vimalamma, G.; Rao, C. V.; Tzeng. Y. M. Phytochemistry 2004, 65, 2317.
  • 4. Jadhav, A. K.; Karuppayil, S. M. Phytotherapy 2021, 35, 5365.
  • 5. Hsieh, M. J.; Chen, J. C.; Yang, W. E.; Chien, S. Y.; Chen, M. K.; Lo, Y. S.; His, Y. T.; Chuang, Y. C.; Lin, C. C.; Yang, S. F. Biochem. Pharmacol. 2017, 130, 10.
  • 6. Tang, C. L.; Gu, G. L.; Wang, B.; Deng, X.; Zhu, X. Y.; Qian, H.; Huang, W. L. Chem. Biol. Drug Des. 2014, 83, 324.
  • 7. Chen, L. M.; Gao, H. M.; Zhu, J. J.; Feng, W. H.; Liu, X. Q.; Yan, L. H.; Meng, C. X. M.; Wang, Z. M.; Wang, D. Q. China J. Chin. Mater. Med. 2020, 45, 1717.
  • 8. Ding, L.; Luo, X. B.; Tang, F.; Yuan, J. B.; Guo, M. L.; Yao, S. Z. Talanta 2008, 74, 1344.
  • 9.Wang, Y. Q.; Wu, Z. F.; Ke, G.; Yang, M. Molecules 2015, 20, 430.
  • 10. Fu, S.; Du, L.; Yuan, Y.; He, X. J. Chromatogr. Sci. 2019, 57, 708.
  • 11. Karioti, A.; Timoteo, P.; Bergonzi, M. C.; Bilia A. R. Planta Med. 2017, 83, 1207.
  • 12. Song, Y. X.; Liu, S. P.; Jin, Z.; Qin J. F.; Jiang Z. Y. Molecules 2013, 18, 12192.
  • 13. Kureshi, A. A.; Dholakiya, C.; Hussain, T.; Mirgal, A.; Salvi, S. P.; Barua, P. C.; Talukdar, M.; Beena, C.; Kar, A.; Zachariah, T. J.; Kumari, P.; Dhanani, T.; Singh, R.; Kumar, S. Acta Chromatogr. 2020, 32, 179.
  • 14. Lee, J.; Han, H.; Yuan, X.; Park, E.; Kim, J. H.; Kim, J. H. Appl. Biol. Chem. 2021, 64, 13.
  • 15. Qian, Z. M.; Wu, Z.; Li, C. H.; Tan, G. Y.; Hu, H. K.; Li, W. J. Anal. Methods 2020, 12, 3337.
  • 16. Li, W. Q.; Li, W. J.; Qian, Z. M.; Chen, S. L.; Li, X. Chin. Herb. Med. 2014, 6, 217.
  • 17. Tanaka, N.; Mccalley, D. V. Anal. Chem. 2016, 88, 279.
  • 18. He, L. F.; He, X. Y.; Liu X. C.; Shi, W. J.; Xu, X. F.; Zhang, Z. C. Steroids 2020, 164, 108751.
  • 19. Li, W. Q.; Qian, Z. M.; Zou, Y. S.; Tan, G. Y.; Li, W. J.; Lei, Q. G.; Li, R. F.; Lan, D. M. Acta Chromatogr. 2022, https://doi.org/10.1556/1326.2022.01094.
  • 20. Li, W. Q.; Qian, Z. M.; Lei, Q. G.; Li, R. F.; Lian, Y. L.; Zou, Y. S.; Wang, Y. H.; Lan, D. M. J. Pharm. Biomed. Anal. 2023, 222, 115085.
  • 21. Bergeron, A.; Garofolo, F. Bioanalysis 2013, 5, 2331.
  • 22. Cortese, M.; Gigliobianco, M. R.; Magnoni, F.; Censi, R.; Martino, P. D. Molecules 2020, 25, 3047.
  • 23. Hajnos, W. M.; Wianowska, D.; Oniszczuk, A.; Dawidowicz, A. L. Acta Chromatogr. 2008, 20, 475.
  • 24. Asghari, A.; Barfi, B.; Barfi, A.; Saeidi, I.; Moud, G. F.; Peyrovi, M.; Babaei, A. B. Acta Chromatogr. 2014, 26, 157.
  • 25. Gao, L.; Wang, P.; Chen, Z. X.; Tang, S. Z.; Wu, S.; Li, G.; Qin, D. L. Acta Chromatogr. 2022, 34, 61.
  • 26. Yin, X.; Liu, Q.; Jiang, Y.; Luo, Y. Spectrochimica Acta Part A: Mol. Biomol. Spectrosc. 2011, 79(1), 191.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-9f7226aa-9c4e-453f-b319-03d65742ada1
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