PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Powiadomienia systemowe
  • Sesja wygasła!
  • Sesja wygasła!
  • Sesja wygasła!
Tytuł artykułu

Study on the separation of triterpene saponins from Panax notoginseng by off-line two-dimensional supercritical fluid chromatography–ultrahigh-performance liquid chromatography

Autorzy
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The off-line two-dimensional supercritical fluid chromatography (SFC)–ultrahigh-performance liquid chromatography (UHPLC) was selected to separate the triterpene saponins from Panax notoginseng. The separation by SFC was performed on an Atlantis® HILIC silica column. Methanol was selected as a modifier, and the most time-saving gradient was developed. The decrease of the column temperature and the increase of the back pressure could shorten the retention time but had no effect on the separation selectivity. Then, the back pressure, column temperature, and flow rate were set as 131 bar, 45 °C, and 4.0 mL min−1, respectively. The retention behavior of the saponins from P. notoginseng was different between SFC and reversed-phase liquid chromatography (RPLC), which facilitated to construct an off-line SFC/RPLC–mass spectrometry (MS) system. In first dimension, a total of eight fractions were collected under SFC and further analyzed by RPLC–MS in second dimension. The result indicated that the retention behavior of triterpene saponins was mainly controlled by the hydrogen bonding interactions which were affected by the number and types of sugars, as well as the aglycone in the structure of triterpene saponins. Thus, the presence of “clustering effect” under SFC was observed, namely, one SFC peak always contained several saponins with same number of sugars and similar structure of aglycone. The clustering effect of triterpene saponins promised SFC to be used as first dimension to complete the preliminary crude separation in the two-dimensional liquid chromatography.
Rocznik
Strony
497--502
Opis fizyczny
Bibliogr. 37 poz., rys., tab.
Twórcy
autor
  • Engineering Research Center of Pharmaceutical Process Chemistry, Ministry of Education, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China
autor
  • Engineering Research Center of Pharmaceutical Process Chemistry, Ministry of Education, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China
autor
  • Engineering Research Center of Pharmaceutical Process Chemistry, Ministry of Education, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China
Bibliografia
  • 1. Cicero, A. F. G. ; Vitale, G. ; Savino, G. ; Arletti, R. Phytother. Res. 2003, 17, 174–178.
  • 2. Dong, T. T. X. ; Cui, X. M. ; Song, Z. H. ; Zhao, K. J. ; Ji, Z. N. ; Lo, C. K. ; Tsim, K. W. K. J. Agri. Food Chem. 2003, 51, 4617–4623.
  • 3. Ma, W. G. ; Mizutani, M. ; Malterud, K. E. ; Lu, S. L. ; Ducrey, B. ; Tahara, S. Phytochemistry 1999, 52, 1133–1139.
  • 4. Yoshikawa, M. ; Murakami, T. ; Ueno, T. ; Hirokawa, N. ; Yashiro, K. ; Murakami, N. ; Yamahara, J. ; Matsuda, H. ; Saijoh, R. ; Tanaka, O. Chem. Pharm. Bull. 1997, 45, 1056–1062.
  • 5. Yoshikawa, M. ; Murakami, T. ; Ueno, T. ; Yashiro, K. ; Hirokawa, N. ; Murakami, N. ; Yamahara, J. ; Matsuda, H. ; Saijoh, R. ; Tanaka, O. Chem. Pharm. Bull. 1997, 45, 1039–1045.
  • 6. Zhao, P. ; Liu, Y.-Q. ; Yang, C.-R. Phytochemistry 1996, 41, 1419–1422.
  • 7. Vincken, J. P. ; Heng, L. ; de Groot, A. ; Gruppen, H. Phytochem. 2007, 68, 275–297.
  • 8. Bondoc, K. G. V. ; Lee, H. ; Cruz, L. J. ; Lebrilla, C. B. ; Juinio-Menez, M. A. Comp. Biochem. Physiol. B-Biochem. Mol. Biol. 2013, 166, 182–193.
  • 9. Colorado-Rios, J. ; Munoz, D. ; Montoya, G. ; Marquez, D. ; Marquez, M. E. ; Lopez, J. ; Martinez, A. Mar. Drugs 2013, 11, 4815–4833.
  • 10. Kim, S. N. ; Ha, Y. W. ; Shin, H. ; Son, S. H. ; Wu, S. J. ; Kim, Y. S. J. Pharm. Biomed. Anal. 2007, 45, 164–170.
  • 11. Li, L. ; Zhang, J. L. ; Sheng, Y. X. ; Guo, D. A. ; Wang, Q. ; Guo, H. Z. J. Pharm. Biomed. Anal. 2005, 38, 45–51.
  • 12. Liu, C. ; Han, J. Y. ; Duan, Y. Q. ; Huang, X. ; Wang, H. Sep. Purif. Technol. 2007, 54, 198–203.
  • 13. Wan, J. B. ; Li, P. ; Li, S. P. ; Wang, Y. T. ; Dong, T. T. X. ; Tsim, K. W. K. J. Sep. Sci., 29, 2190–2196.
  • 14. Liu, Y. Y. ; Li, J. B. ; He, J. M. ; Abliz, Z. ; Qu, J. ; Yu, S. S. ; Ma, S. G. ; Liu, J. ; Du, D. Rapid Commun. Mass Spectrom. 2009, 23, 667–679.
  • 15. Guo, X. J. ; Zhang, X. L. ; Guo, Z. M. ; Liu, Y. F. ; Shen, A. J. ; Jin, G. W. ; Liang, X. M. J. Chromatogr. A 2014, 1325, 121–128.
  • 16. Poole, C. F. J. Chromatogr. A 2012, 1250, 157–171.
  • 17. Taylor, L. T. Anal. Chem. 2010, 82, 4925–4935.
  • 18. Lesellier, E . J. Chromatogr. A 2012, 1228, 89–98.
  • 19. Jiang, C. W. ; Ren, Q. L. ; Wu, P. D. J. Chromatogr. A 2003, 1005, 155–164.
  • 20. Lee, J. W. ; Nishiumi, S. ; Yoshida, M. ; Fukusaki, E. ; Bamba, T. J. Chromatogr. A 2013, 1279, 98–107.
  • 21. Lesellier, E. ; Destandau, E. ; Grigoras, C. ; Fougere, L. ; Elfakir, C. J. Chromatogr. A 2012, 1268, 157–165.
  • 22. Abrahamsson, V. ; Rodriguez-Meizoso, I. ; Turner, C. J. Chromatogr. A 2012, 1250, 63–68.
  • 23. Bamba, T. ; Shimonishi, N. ; Matsubara, A. ; Hirata, K. ; Nakazawa, Y. ; Kobayashi, A. ; Fukusaki, E. J. Biosci. Bioeng. 2008, 105, 460–469.
  • 24. Matsubara, A. ; Bamba, T. ; Ishida, H. ; Fukusaki, E. ; Hirata, K. J. Sep. Sci. 2009, 32, 1459–1464.
  • 25. Ashraf-Khorassani M. ; Taylor, L. T. J. Sep. Sci. 2010, 33, 1682–1691.
  • 26. Patel, M. A. ; Riley, F. ; Ashraf-Khorassani, M. ; Taylor, L. T. J. Chromatogr. A 2012, 1233, 85–90.
  • 27. Taylor, L. T. J. Chromatogr. A 2012, 1250, 196–204.
  • 28. Zheng, J. ; Taylor, L. T. ; Pinkston, J. D. Chromatographia 2006, 63, 267–276.
  • 29. Zhao, Y. ; McCauley, J. ; Pang, X. ; Kang, L. P. ; Yu, H. S. ; Zhang, J. ; Xiong, C. Q. ; Chen, R. ; Ma, B. P. J. Sep. Sci. 2013, 36, 3270–3276.
  • 30. Agrawal, H. ; Kaul, N. ; Paradkar, A. ; Mahadik, K. Acta Chromatographica 2006, 17, 125.
  • 31. Scoparo, C. T. ; de Souza, L. M. ; Dartora, N. ; Sassaki, G. L. ; Gorin, P. A. J. ; Iacomini, M. J. Chromatogr. A 2012, 1222, 29–37.
  • 32. Slonecker, P. J. ; Li, X. ; Ridgway, T. H. ; Dorsey, J. G. Anal. Chem. 1996, 68, 682–689.
  • 33. Xing, Q. Q. ; Liang, T. ; Shen, G. B. ; Wang, X. L. ; Jin, Y. ; Liang, X. M. Analyst 2012, 137, 2239–2249.
  • 34. Guo, X. ; Zhang, X. ; Feng, J. ; Guo, Z. ; Xiao, Y. ; Liang, X. Anal. Bioanal. Chem. 2013, 405, 3413–3421.
  • 35. Sandra, P. ; Medvedovici, A. ; David, F. LC GC Eur. 2003, 16, 32–34.
  • 36. Novakova, L. ; Perrenoud, A. G. G. ; Francois, I. ; West, C. ; Lesellier, E. ; Guillarme, D. Analytica Chimica Acta 2014, 824, 18–35.
  • 37. Khater, S. ; West, C. ; Lesellier, E. J. Chromatogr. A 2013, 1319, 148–159.
Uwagi
PL
Opracowanie rekordu w ramach umowy 509/P-DUN/2018 ze środków MNiSW przeznaczonych na działalność upowszechniającą naukę (2018).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-f06c6bf0-3d29-4770-bb50-2df1b5480b29
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.