DOI QR코드

DOI QR Code

HPLC Separation of Isoquinoline Alkaloids for Quality Control of Corydalis species

  • Kim, Eun-Kyung (College of Pharmacy & Kyung Hee East-West Pharmaceutical Research Institute, Kyung Hee University) ;
  • Jeong, Eun-Kyung (College of Pharmacy & Kyung Hee East-West Pharmaceutical Research Institute, Kyung Hee University) ;
  • Han, Sang-Beom (College of Pharmacy, Choongang University) ;
  • Jung, Jee-H. (College of Pharmacy, Pusan National University) ;
  • Hong, Jong-Ki (College of Pharmacy & Kyung Hee East-West Pharmaceutical Research Institute, Kyung Hee University)
  • 투고 : 2011.05.12
  • 심사 : 2011.08.06
  • 발행 : 2011.10.20

초록

A simple and rapid analytical method was developed for the determination of eight isoquinoline alkaloids in Corydalis species. Eight isoquinoline alkaloids, including 2 aporphine alkaloids (isocorydine and glaucine) and 6 protoberberine alkaloids (coptisine, palmatine, berberine, canadine, corydaline, and tetrahydrocoptisine) were used as chemical markers which have a various biological activity and determined for quality control of Corydalis (C.) species (C. ternata, C. yanhusuo, and C. decumbens). To evaluate the quality of these herbal medicines, LC chromatographic separation of alkaloids were preferentially investigated on reversed-phase C18 column with pH variation and composition of mobile phase. In addition, the separation of these alkaloids in herbal extracts was found to be significantly affected on mobile phase composition using gradient elution. Especially for C. yanhusuo extract, berberine was seriously interfered with other alkaloid extracted from sample matrix when mobile phase composition was not optimized. As results, these compounds were successfully separated within 28 min using 10 mM ammonium acetate containing 0.2% triethylamine (adjusted at pH 5.0) as a mobile phase with gradient elution. On the basis of optimized HPLC conditions, 23 different Corydalis species samples were analyzed for the determination of alkaloid levels. In addition, principal component analysis (PCA) combined with the chromatographic data could be successfully classified the different geographic origin samples.

키워드

참고문헌

  1. Sturm, S.; Seger, C.; Stuppner, H. J. Chromatogr. A 2007, 1159, 42. https://doi.org/10.1016/j.chroma.2007.02.108
  2. Liden, M. Willdenowia 1996, 26, 23. https://doi.org/10.3372/wi.26.2602
  3. Chen, J.; Wang, F.; Liu, J.; Lee, F. S-C.; Wang, X.; Yang, H. Anal. Chim. Acta 2008, 613, 184. https://doi.org/10.1016/j.aca.2008.02.060
  4. Cheng, X.; Wang, D.; Jiang, L.; Yang, D. Phytochem. Anal. 2008, 19, 420. https://doi.org/10.1002/pca.1067
  5. Kim, K. H.; Lee, I. K.; Piao, C. J.; Choi, S. U.; Lee, J. H.; Kim, Y. S.; Lee, K. R. Bioorg. Med. Chem. Lett. 2010, 20, 4487. https://doi.org/10.1016/j.bmcl.2010.06.035
  6. Ding, B.; Zhou, T.; Fan, G.; Hong, Z.; Wu, Y. J. Pharm. Biomed. Anal. 2007, 45, 219. https://doi.org/10.1016/j.jpba.2007.06.009
  7. Wang, X.; Geng, Y.; Li, F.; Shi, X.; Liu, J. J. Chromatogr A 2006, 1115, 267. https://doi.org/10.1016/j.chroma.2006.03.103
  8. Grycová, L.; Dostál, J.: Marek, R. Phytochemistry 2007, 68, 150. https://doi.org/10.1016/j.phytochem.2006.10.004
  9. Yamada, Y.; Kitajima, M.; Kogure, N.; Wongseripipatana, S.; Takayama, H. Chem. Asian J. 2011, 6, 166. https://doi.org/10.1002/asia.201000538
  10. Tnahashi, T.; Zenk, M. H. J. Nat. Prod. 1990, 53, 579. https://doi.org/10.1021/np50069a007
  11. Suchomelova, J.; Bochorakova, H.; Paulova, H.; Musil, P.; Taborska, E. J. Pharm. Biomed. Anal. 2007, 44, 283. https://doi.org/10.1016/j.jpba.2007.02.005
  12. Chang-Qun, N.; Li-Yi, H. J. Chromatogr. A 1991, 542, 193. https://doi.org/10.1016/S0021-9673(01)88760-4
  13. Reinhart, P.; Harkrader, R.; Wylie, R.; Yewey, G.; Van Horne, K. C. J. Chromatogr. B 1991, 570, 425. https://doi.org/10.1016/0378-4347(91)80549-R
  14. Eva, T.; Hana, B.; Hana, Dostal, P. Planta Med. 1994, 60, 380. https://doi.org/10.1055/s-2006-959508
  15. Zhang, J.; Jin, Y.; Liu, Y.; Xiao, Y.; Feng, J.; Xue, X.; Zhang, X.; Liang, X. J. Sep. Sci. 2009, 32, 1401. https://doi.org/10.1002/jssc.200800729
  16. Perez-Arribas, L. V.; Manuel de Villena-Rueda, F. J.; Leon- Gonzalez, M. E.; Gonzalo-Lumbreras, R.; Polo-Diez, L. M. Anal. Bioanal. Chem. 2010, 396, 2647. https://doi.org/10.1007/s00216-010-3493-2
  17. Zhang, J.; Jin, Y.; Liu, Y.; Xiao, Y.; Feng, J.; Xue, X.; Zhang, X.; Liang, X. J. Sep. Sci. 2009, 32, 2084. https://doi.org/10.1002/jssc.200800703
  18. Lee, M. K.; Ahn, Y. M.; Lee, K. R.; Jung, J. H.; Jung, O-S.; Hong J. Anal. Chim. Acta 2009, 633, 271. https://doi.org/10.1016/j.aca.2008.12.038
  19. Chen, Y.; Zhu, S-B.; Xie, M-Y.; Nie, S.-P.; Liu, W.; Li, C.; Gong, X-F.; Wang, Y-X. Anal. Chim. Acta 2008, 623, 146. https://doi.org/10.1016/j.aca.2008.06.018
  20. Vespalec, R.; Bartak, P.; Simanek, V.; Vl kova, M. J. Chromatogr. B 2003, 797, 357. https://doi.org/10.1016/S1570-0232(03)00308-8
  21. www.chemicalize.org, www.chemspider.com
  22. Maulding, H. V.; Zoglio, M. A. J. Pharm. Sci. 1970, 59, 700. https://doi.org/10.1002/jps.2600590526
  23. Zhang, J.; Jin Y.; Dong J.; Xiao, Y.; Feng, J.; Xue X.; Zhang, X. Talanta 2009, 78, 513. https://doi.org/10.1016/j.talanta.2008.12.002

피인용 문헌

  1. A simple approach to quantitative analysis using three-dimensional spectra based on selected Zernike moments vol.138, pp.2, 2013, https://doi.org/10.1039/C2AN36139F
  2. Simultaneous Determination of Structurally Diverse Compounds in Different Fangchi Species by UHPLC-DAD and UHPLC-ESI-MS/MS vol.18, pp.5, 2013, https://doi.org/10.3390/molecules18055235
  3. UHPLC Separation of Structurally Diverse Markers in Fangchi Species vol.34, pp.3, 2013, https://doi.org/10.5012/bkcs.2013.34.3.975
  4. (Pall.) Fisch by HPLC vol.36, pp.13, 2013, https://doi.org/10.1002/jssc.201300036
  5. Adsorption of Berberine Hydrochloride, Ligustrazine Hydrochloride, Colchicine, and Matrine Alkaloids on Macroporous Resins vol.58, pp.5, 2013, https://doi.org/10.1021/je400057w
  6. (Maxim) Fedde and the effective fractionation of the alkaloids by high-performance liquid chromatography with diode array detection vol.38, pp.1, 2014, https://doi.org/10.1002/jssc.201400905
  7. Simultaneous Determination of Isoquinoline Alkaloids in Medicinal Asiatic Plants by Ultrasound-Assisted Extraction and High-Performance Liquid Chromatography – Mass Spectrometry with Principal Component Analysis vol.51, pp.16, 2018, https://doi.org/10.1080/00032719.2018.1439050
  8. Identification of structurally diverse alkaloids in Corydalis species by liquid chromatography/electrospray ionization tandem mass spectrometry vol.26, pp.15, 2011, https://doi.org/10.1002/rcm.6272
  9. Study on pharmacokinetics and tissue distribution of the isocorydine derivative (AICD) in rats by HPLC-DAD method vol.5, pp.3, 2015, https://doi.org/10.1016/j.apsb.2015.03.012
  10. Simultaneous screening and analysis of antiplatelet aggregation active alkaloids from Rhizoma Corydalis vol.54, pp.12, 2011, https://doi.org/10.1080/13880209.2016.1211714
  11. Determination of isoquinoline alkaloids by UPLC-ESI-Q-TOF MS: Application to Chelidonium majus L. vol.30, pp.6, 2011, https://doi.org/10.5806/ast.2017.30.6.379
  12. Palmatine-loaded electrospun poly(ε-caprolactone)/gelatin nanofibrous scaffolds accelerate wound healing and inhibit hypertrophic scar formation in a rabbit ear model vol.35, pp.7, 2021, https://doi.org/10.1177/0885328220950060
  13. Solanum vegetable‐based diets improve impairments in memory, redox imbalance, and altered critical enzyme activities in Drosophila melanogaster model of neurodegeneration vol.45, pp.3, 2011, https://doi.org/10.1111/jfbc.13150