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Vol. 29 No. 6 (2017): Vol 29 Issue 6

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Characterization of Volatile and Polar Compounds of Jiaogulan Tea [Gynostemma pentaphyllum (Thunb.) Makino] by Hyphenated Analytical Techniques

https://doi.org/10.14233/ajchem.2017.20467
Eugene K. Blythe
Coastal Research and Extension Center, Mississippi State University, South Mississippi Branch Experiment Station, Poplarville, Mississippi 39470, USA
Betul Demirci
Department of Pharmacognosy, Faculty of Pharmacy, Anadolu University, Eskisehir, 26470, Turkey
Fatih Goger
Department of Pharmacognosy, Faculty of Pharmacy, Anadolu University, Eskisehir, 26470, Turkey
Nurhayat Tabanca
U.S. Department of Agriculture-Agricultural Research Service, Subtropical Horticulture Research Station, Miami, Florida 33158, USA

Corresponding Author(s) : Eugene K. Blythe

blythe@pss.msstate.edu

Asian Journal of Chemistry, Vol. 29 No. 6 (2017): Vol 29 Issue 6

Abstract

Jiaogulan [Gynostemma pentaphyllum (Thunb.) Makino] is a Chinese medicinal plant from southern Asia that has rapidly gained popularity and interest for its health-promotive and therapeutic properties. The volatile composition of jiaogulan tea was analyzed by using headspace-solid phase microextraction (HS-SPME) coupled with gas chromatography-mass spectrometry (GC-MS). A total of 29 volatile components were detected in the jiaogulan tea, with major compounds being benzaldehyde (15.3 %), 1,8-cineole (8.7 %), 6-methyl-5-hepten-2-one (7.8 %), (Z)-3-hexenal (7.6 %) and a-ionone (6.3 %). The chemical characterization of methanolic extract and 5 % infusion from the G. pentaphyllum leaves was determined by using LC-ESI-MS/MS systems. Chlorogenic acids, flavonoids and gypenosides were determined. The compounds quercetin 3-O-hexoside, isorhamnetin rutinoside and kaempferol dimethyl ether were identified in the extracts for the first time. Phenolic content was determined by gallic acid equivalents and antioxidant activity of the extracts was evaluated by DPPH, b-carotene/linoleic acid and ABTS radical scavenging assays. Both extracts showed weak antioxidant activity.

Keywords

Gypenosides Gynosaponins Volatiles HS-SPME LC-ESI-MS/MS Antioxidant activity
Blythe, E. K., Demirci, B., Goger, F., & Tabanca, N. (2017). Characterization of Volatile and Polar Compounds of Jiaogulan Tea [Gynostemma pentaphyllum (Thunb.) Makino] by Hyphenated Analytical Techniques. Asian Journal of Chemistry, 29(6), 1285–1290. https://doi.org/10.14233/ajchem.2017.20467
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References
  1. J.F. Cui, P. Eneroth and J.G. Bruhn, Eur. J. Pharm. Sci., 8, 187 (1999); https://doi.org/10.1016/S0928-0987(99)00013-5.
  2. R.N. Mishra and D. Joshi, Int. J. Res. Pharm. Biomed. Sci., 2, 1483 (2011).
  3. M. Blumert and J. Liu, Jiaogulan: China’s Immortality Herb, Torchlight Publishing, Badger, California, USA, pp. 12-18 (1999).
  4. Y. Zhao, Y. Niu, Z. Xie, H. Shi, P. Chen and L. Yu, J. Funct. Foods, 5, 1288 (2013); https://doi.org/10.1016/j.jff.2013.04.013.
  5. D.J. Chen, H.M. Liu, S.F. Xing and X.L. Piao, Bioorg. Med. Chem. Lett., 24, 186 (2014); https://doi.org/10.1016/j.bmcl.2013.11.043.
  6. J.J. Lin, H.Y. Hsu, J.S. Yang, K.W. Lu, R.S.C. Wu, K.C. Wu, T.Y. Lai, P.Y. Chen, C.Y. Ma, W.G. Wood and J.G. Chung, Phytomedicine, 18, 1075 (2011); https://doi.org/10.1016/j.phymed.2011.03.009.
  7. V.T.T. Huyen, D.V. Phan, P. Thang, N.K. Hoa and C.G. Ostenson, Horm. Metab. Res., 42, 353 (2010).
  8. T.H. Kao, S.C. Huang, B.S. Inbaraj and B.H. Chen, Anal. Chim. Acta, 626, 200 (2008); https://doi.org/10.1016/j.aca.2008.07.049.
  9. Z. Xie, Y. Zhao, P. Chen, P. Jing, J. Yue and L. Yu, J. Agric. Food Chem., 59, 3042 (2011).
  10. Y. Lv, X. Yang, Y. Zhao, Y. Ruan, Y. Yang and Z. Wang, Food Chem., 112, 742 (2009); https://doi.org/10.1016/j.foodchem.2008.06.042.
  11. X.Y. Shang, Y. Zhang, Y.L. Bai, C.L. Xu, W.N. Niu and C.G. Qin, Asian J. Chem., 25, 9092 (2013); https://doi.org/10.14233/ajchem.2013.15010.
  12. W. Yan, Y. Niu, J. Lv, Z. Xie, L. Jin, W. Yao, X. Gao and L. Yu, Carbohydr. Polym., 92, 2111 (2013); https://doi.org/10.1016/j.carbpol.2012.11.074.
  13. F. Yang, H. Shi, X. Zhang, H. Yang, Q. Zhou and L. Yu, Food Chem., 141, 3606 (2013); https://doi.org/10.1016/j.foodchem.2013.06.015.
  14. F. Aktan, S. Henness, B.D. Roufogalis and A.J. Ammit, Nitric Oxide, 8, 235 (2003); https://doi.org/10.1016/S1089-8603(03)00032-6.
  15. A. Attawish, S. Chivapat, S. Phadungpat, J. Bansiddhi, Y. Techadamrongsin, O. Mitrijit, B. Chaorai and P. Chavalittumrong, Fitoterapia, 75, 539 (2004); https://doi.org/10.1016/j.fitote.2004.04.010.
  16. N. Chiranthanut, S. Teekachunhatean, A. Panthong, P. Khonsung, D. Kanjanapothi and N. Lertprasertsuk, J. Ethnopharmacol., 149, 228 (2013); https://doi.org/10.1016/j.jep.2013.06.027.
  17. P. Escoubas, L. Lajide and J. Mitzutani, Entomol. Exp. Appl., 66, 99 (1993); https://doi.org/10.1111/j.1570-7458.1993.tb00697.x.
  18. J. Liang, P. Geng, H. Ni, A. Ma and Z. Xiong, J. Hubei Univ. Nat. Sci., 4, 438 (2010).
  19. F.W. McLafferty and D.B. Stauffer, The Wiley/NBS Registry of Mass Spectral Data, J. Wiley & Sons, New York, USA (1989).
  20. W.A. Koenig, D. Joulain and D.H. Hochmuth, MassFinder 3, Hamburg, Germany (2004).
  21. D. Joulain and W.A. Koenig, The Atlas of Spectra Data of Sesquiterpene Hydrocarbons, EB-Verlag, Hamburg, Germany (1998).
  22. ESO, 2000, The Complete Database of Essential Oils, Boelens Aroma Chemical Information Service, The Netherlands (1999).
  23. V.L. Singleton, R. Orthofer and R.M. Lamuela-Raventós, in ed.: L. Packer, Methods in Enzymology, Academic Press, San Diego, California, USA, vol. 299 p. 152 (1999).
  24. M.A. Papandreou, C.D. Kanakis, M.G. Polissiou, S. Efthimiopoulos, P. Cordopatis, M. Margarity and F.N. Lamari, J. Agric. Food Chem., 54, 8762 (2006); https://doi.org/10.1021/jf061932a.
  25. Kumarasamy, M. Byres, P.J. Cox, M. Jaspars, L. Nahar and S.D. Sarker, Phytother. Res., 21, 615 (2007); https://doi.org/10.1002/ptr.2129.
  26. B. Oomah and G. Mazza, J. Agric. Food Chem., 44, 1746 (1996); https://doi.org/10.1021/jf9508357.
  27. M.N. Clifford, K.L. Johnston, S. Knight and N. Kuhnert, J. Agric. Food Chem., 51, 2900 (2003); https://doi.org/10.1021/jf026187q.
  28. M.N. Clifford, S. Knight and N. Kuhnert, J. Agric. Food Chem., 53, 3821 (2005); https://doi.org/10.1021/jf050046h.
  29. K.C. Tsui, T.H. Chiang, J.S. Wang, L.J. Lin, W.C. Chao, B.H. Chen and J.F. Lu, Molecules, 19, 17663 (2014); https://doi.org/10.3390/molecules191117663.
  30. Y. Zhao, Z.H. Xie, Y.G. Niu, H.M. Shi, P. Chen and L.L. Yu, Food Chem., 134, 180 (2012); https://doi.org/10.1016/j.foodchem.2012.02.090.
  31. E. Hvattum and D. Ekeberg, J. Mass Spectrom., 38, 43 (2003); https://doi.org/10.1002/jms.398.
  32. J. Wu, Z. Chen, C. Zhang, Y. Lu and H. Wang, Sep. Sci. Technol., 48, 909 (2013); https://doi.org/10.1080/01496395.2012.710887.
  33. L.H. Hu, Z.L. Chen and Y.Y. Xie, Phytochemistry, 44, 667 (1997); https://doi.org/10.1016/S0031-9422(96)00577-8.
  34. M.H. Chen, Q.F. Wang, L.G. Chen, J.J. Shee, J.C. Chen, K.Y. Chen, S.H. Chen, J.G.J. Su and Y.W. Liu, J. Ethnopharmacol., 126, 42 (2009); https://doi.org/10.1016/j.jep.2009.08.012.
  35. P.K. Wu, W.C.S. Tai, R.C.Y. Choi, K.W.K. Tsim, H. Zhou, X. Liu, Z.H. Jiang and W.L.W. Hsiao, Food Chem., 128, 70 (2011); https://doi.org/10.1016/j.foodchem.2011.02.078.
  36. J.X. Wei, Y.G. Che, X.L. Xu, H.L. Fang, G.C. Chen and M.F. Mackay, Acta Chim. Sin., 49, 932 (1991).
  37. M.J. Simirgiotis, Molecules, 18, 2061 (2013); https://doi.org/10.3390/molecules18022061.
  38. V. Spinola, J. Pinto and P.C. Castilho, Food Chem., 173, 14 (2015); https://doi.org/10.1016/j.foodchem.2014.09.163.
  39. M. Simirgiotis, G. Schmeda-Hirschmann, J. Bórquez and E. Kennelly, Molecules, 18, 1672 (2013); https://doi.org/10.3390/molecules18021672.
  40. Z. Xie, W. Liu, H. Huang, M. Slavin, Y. Zhao, M. Whent, J. Blackford, H. Lutterodt, H. Zhou, P. Chen, T.T.Y. Wang, S. Wang and L.L. Yu, J. Agric. Food Chem., 58, 11243 (2010); https://doi.org/10.1021/jf1026372.
  41. Y.C. Tsai, C.L. Lin and B.H. Chen, Phytomedicine, 18, 2 (2010); https://doi.org/10.1016/j.phymed.2010.09.004.
  42. C.F. Liu, Shipin Keji, 11, 236 (2013).
  43. J.F. Niu, Y.P. Xiao, D.L. Jiang, L. Wang, D.H. Lv and F.C. Li, Yaowu Fenxi Zazhi, 32, 578 (2012).
  44. V. Razmovski-Naumovski, T.H.-W. Huang, V.H. Tran, G.Q. Li, C.C. Duke and B.D. Roufogalis, Phytochem. Rev., 4, 197 (2005); https://doi.org/10.1007/s11101-005-3754-4.
  45. L. Lee, D.H. Chambers, E. Chambers IV, K. Adhikari and Y. Yoon, Molecules, 18, 10024 (2013); https://doi.org/10.3390/molecules180810024.
  46. A. Plotto, K.W. Barnes and K.L. Goodner, J. Food Sci., 71, S401 (2006); https://doi.org/10.1111/j.1750-3841.2006.00047.x.
  47. B. Maikhunthod and P.L. Marriott, Food Chem., 141, 4324 (2013); https://doi.org/10.1016/j.foodchem.2013.05.156.
  48. L.F. Wang, J.Y. Lee, J.O. Chung, J.H. Baik, S. So and S.K. Park, Food Chem., 109, 196 (2008); https://doi.org/10.1016/j.foodchem.2007.12.054.
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