Abstract
A reversed-phase high-performance liquid chromatographic procedure has been developed: it is a simple and specific method for the determination of fifteen pentacyclic triterpenic compounds (α-boswellic acid, 3-O-acetyl-α-boswellic acid, β-boswellic acid, 3-O-acetyl-β-boswellic acid, α-amyrin, β-amyrin, lupeol, 3-epi-α-amyrin, 3-epi-β-amyrin, 3-epi-lupeol, α-amyrenone, β-amyrenone, lupenone, lupeolic acid and 3-O-acetyl-lupeolic acid) found in the most commonly traded frankincense, usually called “Eritrean-type” olibanum. In addition, the chromatographic comparison between fresh commercial resins and botanically certified ones was described in order to determine the geographical and/or the botanical origins of commercial frankincense. According to previous botanical studies, it appears difficult to make an unequivocal distinction between Boswellia carteri and B. sacra. On the other hand, Boswellia frereana (considered as a source of high-grade frankincense) shows a characteristic chromatogram and could be unambiguously distinguished from the other producing species of commercial frankincense. In a chemical point of view, Boswellia carteri and B. sacra were more especially characterized by the presence of lupeolic acid, boswellic acids and their respective O-acetyl derivatives, whereas 3-epi-lupeol was the major compound in B. frereana methanolic extracts.
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References
Tücker AO (1986) Econ Bot 40:425–433
Thulin M, Warfa AM (1987) Kew Bull 42:487–500
Dupéron J (1993) Rev Cytol Biol Végét Bot 16:185–209
Coppens JJW (1995) Olibanum (frankincense), myrrh and opopanax resins and oils. In: Flavours and Fragrances of Plant Origin. Non-Wood Forest Products, FAO – Food and Agriculture Organization of the United Nations, Rome, 1
Archier P, Vieillescazes C (2000) Analusis 2:233–237
Culioli G, Mathe C, Archier P, Vieillescazes C (2003) Phytochem 62:537–541. DOI 10.1016/S0031-9422(02)00538-1
Mathe C, Culioli G, Archier P, Vieillescazes C (2004) J Chromatogr A 1023:277–285. DOI 10.1016/j.chroma.2003.10.016
Badria FA, Mikhaeil BR, Maatooq GT, Amer MMA (2003) Z Naturforsh 58C:505–516
Büchele B, Zugmaier W, Simmet T (2003) J Chromatogr B 791:21–30. DOI 10.1016/S1570-0232(03)00160-0
Shweizer S, von Brocke AFW, Boden SE, Bayer E, Ammon HPT, Safayhi H (2000) J Nat Prod 63:1058–1061. DOI 10.1021/np000069k
Ganzera M, Khan IA (2001) Planta Med 67 :778–780. DOI: 10.1055/s-2001-18346
Tawab MA, Kaunzinger A, Bahr U, Karas M, Wurglics, Schubert-Zsilavecz M (2001) J Chromatogr B 761:221–227. DOI 10.1016/S0378-4347(01)00335-8
Hairfield EM, Hairfield Jr HH, McNair HM (1989) J Chromatogr Sci 27:127–133
Papageorgiou V, Bakola-Christianopoulou MN, Apazidou KK, Psarros EE (1997) J Chromatogr A 769:263–273. DOI 10.1016/S0021-9673(96)01032-1
Mills JS, White R (1994) In : The organic chemistry of museum objects, A Oddy, D Linstrum (Eds.), 2nd ed., Butterworth-Heinemann, Oxford
Acknowledgement.
The authors wish to thank Mr M. Pryet for the supply of samples of commercial frankincense, and Mr J.-M. Bel, Pr M. Thulin and Dr J. Dupéron for the botanically certified resins.
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Mathe, C., Culioli, G., Archier, P. et al. High-Performance Liquid Chromatographic Analysis of Triterpenoids in Commercial Frankincense. Chromatographia 60, 493–499 (2004). https://doi.org/10.1365/s10337-004-0417-3
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DOI: https://doi.org/10.1365/s10337-004-0417-3
Keywords
- Column liquid chromatography
- Lupane, oleanane and ursane triterpenes
- Boswellic acids
- Boswellia carteri, Boswellia sacra and Boswellia frereana