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Structural determination of triterpenic acids in Prunellae Spica by fast atom bombardment tandem mass spectrometry

하고초의 생리활성 성분 Triterpenic Acids의 FAB-MS를 이용한 구조 규명

  • 안영민 (경희대학교 약학대학 나노의약생명과학과) ;
  • 이강노 (성균관대학교 약학대학 약학과) ;
  • 홍종기 (경희대학교 약학대학 나노의약생명과학과)
  • Received : 2008.05.20
  • Accepted : 2008.06.18
  • Published : 2008.08.25

Abstract

Five triterpenic acids as marker compounds were extracted and isolated from Prunellae Spica by column chromatography and reversed-phase high-performance liquid chromatography (HPLC), and their purity was determinated by HPLC (purity ${\geq}90%$). Molecular weight and elemental compositions of the five marker compounds were determined by fast atom bombardment high-resolution mass spectrometry (FAB-HRMS). The structural determination of the five marker compounds was carried out fast atom bombardment collision-induced dissociation tandem mass spectrometry (FAB-CID-MS/MS). The collision-induced dissociation (CID) of protonated molecules $[M+H]^+$ and deprotonated molecules $[M-H]^-$ produced diverse product ions due mainly to retro Diels-Alder reaction (RDA), dehydration and decarboxylation. Moreover, the CID-MS/MS spectra of the $[M-H]^-$ ions were observed charge-remote fragmentation (CRF) patterns. On the basis of interpretation of CID-MS/MS spectra, structural elucidation of triterpenic acids isolated from Prunellae Spica was clearly performed.

본 연구에서는 하고초의 지표성분인 triterpenic acids 5종을 컬럼 크로마토그래피와 역상 HPLC를 이용하여 추출 및 분리했고, 이들 성분의 순도는 90% 이상임을 HPLC를 이용하여 확인했다. 고속원자충돌 이온화법-고분해능 질량분석기(FAB-HRMS)를 사용하여 지표성분의 분자량 및 원소조성을 결정했으며, 지표성분의 구조 분석은 FAB-MS/MS 의해 음이온 및 양이온 모드에서 수행하였다. Triterpenic acid류의 충돌유발분해(collision-induced dissociation, CID) 탄뎀질량분석(MS/MS) 스펙트럼에서 protonated molecule인 $[M+H]^+$ 및 deprotonated molecule인 $[M-H]^-$ 이온의 CID는 주로 retro Diels-Alder (RDA), 탈수 (dehydration) 및 탈탄산(decarboxylation) 반응에 의한 다양한 생성이온들이 나타났다. 특히, $[M-H]^-$이온의 CID-MS/MS 스펙트럼에서는 charge-remote fragmentation (CRF) 현상에 의한 이온들도 특성이온으로 나타났다. 이들 CID-MS/MS 스펙트럼의 해석을 통하여 하고초의 지표성분인 triterpenic acids의 구조 규명을 수행하였다.

Keywords

Acknowledgement

Grant : 한약재 평가기술 과학화 연구

Supported by : 식품의약품안전청

References

  1. N. K. Dubey, R. Kumar and P. Tripathi, Current Science, 86(1), 37-41(2004)
  2. M. M. W. B. Hendriks, L. C. Juarez, D. D. Bont and R. D. Hall, Anal. Chim. Acta, 545, 53-64(2005) https://doi.org/10.1016/j.aca.2005.04.026
  3. J. S. Kim, S. S. Kang, K. S. Lee, S.-Y. Chang and D. H. Won, Kor. J. Pharmacogn., 31(4), 416-420(2000)
  4. K. S. Nam and Y. H. Shon, Kor. J. Pharmacogn., 35(2), 147-151(2004)
  5. Y. H. Shon, K. T. Lee, S. H. Park, K. H. Cho, J. K. Lim and K. S. Nam, Kor. J. Pharmacogn., 32(4), 269- 273(2001)
  6. E. Nadinic, S. Gorzalczany, A. Rojo and C. V. Baren, Fototerapia, 70, 166-171(1999) https://doi.org/10.1016/S0367-326X(99)00020-9
  7. M. E. Alvarez, A. E. Rotelli, L. E. Pelzer, J. R. Saad and O. Giordano, II. Farmaco., 55, 502-505(2000) https://doi.org/10.1016/S0014-827X(00)00067-7
  8. C. Farina, M. Pinza and G. Pifferi, Il, Farmaco., 53, 22-32(1998) https://doi.org/10.1016/S0014-827X(97)00013-X
  9. N. Banno, T. Akihisa, H. Tokuda, K. Yasukawa, H. Higashihara, M. Ukiya, K. Watanabe, Y. Kimura, J. Hasegawa and H. Nishino, Biosci. Biotechnol. Biochem., 68(1), 85-90(2004) https://doi.org/10.1271/bbb.68.85
  10. L. Guo, S. Y. Cho, S. S. Kang, S. H. Lee, H. Y. Beak and Y. S. Kim, J. Ethnopharm., 113, 306-311(2007) https://doi.org/10.1016/j.jep.2007.06.013
  11. Y. C. Wang and Y. S. Yang, J. Chromatogr. B., 850, 392-399(2007) https://doi.org/10.1016/j.jchromb.2006.12.032
  12. J. Li, H. Qi, L.-W. Qi, L. Yi and P. Li, Anal. Chim. Acta, 596, 264-272(2007) https://doi.org/10.1016/j.aca.2007.05.016
  13. F. Modugno, E. Ribechini and M. P. Colombini, Rapid Commun. Mass Spectrom., 20, 1787-1800(2006) https://doi.org/10.1002/rcm.2507
  14. H. Heinzen, J. X. deVries, P. Moyna, G. Remberg, R. Martinez and L. F. Tietze, Phytochemical Analysis, 7, 237-244(1996) https://doi.org/10.1002/(SICI)1099-1565(199609)7:5<237::AID-PCA310>3.0.CO;2-M
  15. J.-Q. Gu, Y. Wang, S. G. Franzblau, G. Montenegro and B. N. Timmermann, Phytochem. Anal., 17, 102- 106(2006) https://doi.org/10.1002/pca.892
  16. G. A. van der Doelen, K. J. van den Berg, J. J. Boon, N. Shibayama, E. R. de la Rie and W. J. L. Genuit, J. Chromatogr. A, 809, 21-37(1998) https://doi.org/10.1016/S0021-9673(98)00186-1
  17. L. Huang, T. Chen, Z. Ye and G. Chen, J. Mass Spectrom., 42, 910-917(2007) https://doi.org/10.1002/jms.1228
  18. G. M. Cabrera, A. P. Vellasco, L. M. Levy and M. N. Eberlin, Phytochem. Anal., 18, 489-495(2007) https://doi.org/10.1002/pca.1005
  19. L. Lacikava, M. E. Abdel-Hamid, L. Novotny, I. Masterova and D. Grancai, Chromatographia, 63, 117- 122(2006) https://doi.org/10.1365/s10337-006-0724-y
  20. L. Novotny, M. E. Abdel-Hamid, H. Hamza, I. Masterova and D. Grancai, J. Pharm. Biomed. Anal., 31, 961- 968(2003) https://doi.org/10.1016/S0731-7085(02)00706-9
  21. M.-R. Lee, C.-M. Chen, B.-H. Hwang and L.-M. Hsu, J. Mass Spectrom., 34, 804-812(1999) https://doi.org/10.1002/(SICI)1096-9888(199908)34:8<804::AID-JMS835>3.0.CO;2-8
  22. R. K. Boyd, P. A. Bott, B. R. Beer, D. J. Harvan and J. R. Haas, Anal. Chem., 59, 189-193(1987) https://doi.org/10.1021/ac00128a039
  23. A. P. Bruins, K. R. Jennings and S. Evans, Int. J. Mass Spectrom. Ion Phys., 26, 395-404(1978) https://doi.org/10.1016/0020-7381(78)80058-8
  24. H. Kojima, H. Tominaga, S. Sato and H. Ogura, Phytochemistry, 26(4), 1107-1111(1987) https://doi.org/10.1016/S0031-9422(00)82359-6
  25. M. S. Ali, S. A. Ibrahim, S. Jalil and M. I. Choudhary, Phytother. Res., 21, 558-561(2007) https://doi.org/10.1002/ptr.2108
  26. T. Nakanishi, Y. Inatomi, H. Murata, S. Ishida, Y. Fujino, K. Miura, Y. Yasuno, A. Inada, F. A. Lang and J. Murata, Chem. Pharm. Bull., 55(2), 334-336(2007) https://doi.org/10.1248/cpb.55.334
  27. C. Cheng and M. L. Gross, Mass Spectrometry Reviews, 19, 398-420(2000) https://doi.org/10.1002/1098-2787(2000)19:6<398::AID-MAS3>3.0.CO;2-B
  28. N. J. Jensen, K. B. Tomer and M. L. Gross, J. Am. Chem. Soc., 107, 1863-1868(1985) https://doi.org/10.1021/ja00293a010
  29. J. Hong, K. Cho, Y. H. Kim, C. Cheong, K.-S. Lee and J. H. Jung, Rapid Commun. Mass Spectrom., 15, 1120-1126(2001) https://doi.org/10.1002/rcm.350
  30. J. H. Gil, J. Seo, K.-J. Kim, J. H. Jung, O.-S. Jung, M.- S. Kim and J. Hong, Rapid Commun. Mass Spectrom., 20, 1253-1256(2006) https://doi.org/10.1002/rcm.2421