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Comparison of Essential Oils Compositions of Boswellia carteri Birdwood as a Food and Non-food in Different Distillation from Iranian Market | ||
| Journal of Medicinal plants and By-products | ||
| مقاله 6، دوره 5، شماره 1، تیر 2016، صفحه 39-44 اصل مقاله (120.45 K) | ||
| شناسه دیجیتال (DOI): 10.22092/jmpb.2016.108922 | ||
| نویسندگان | ||
| Azam Ranjbar Dounchaly* 1؛ Kamkar Jaimand2؛ Shahla Mozaffari1 | ||
| 1Department of Chemistry, Payame Noor University, Tehran, Iran | ||
| 2Department of Medicinal Plants, Research Institute of Forests and Rangelands, Agricultural Research, Education and Extension Organization, Tehran, Iran | ||
| چکیده | ||
| The genus Boswellia is one of the 17 genera belonging to Burseraceae family. In this study resin of Boswellia carteri birdwoodcollected or purchased from Tehram herbal Market as a food and non-food for chemical analysis. The essential oils of the resins of Boswellia carteri birdwoodobtained by different methods of distillation (water distillation, steam distillation and hydro-steam distillation), the composition of essential oils was analyzed by gas chromatography (GC) and gas chromatography, coupled to mass spectrometry (GC-MS). The major components of the different methods of distillation oils of Boswellia carteri birdwood as a non-food by hydro-steam distillation were dihydro citronellol acetate (48%), 2-phenyl ethyl anthranilate (11.5%), α-santonine (7.7%), and with water distillation were dihydro citronellol acetate (48.2%), borneol (8.6%), methyl decanoate (7.9%), and with steam distillation were dihydro citronellol acetate (60.6%), borneol (9.7%), (Z)-β-ocimene (5.3%), respectively. Also the major components of Boswellia carteri birdwood as a food by hydro-steam distillation were dihydro citronellol acetate (55.6%), α-santonine (9%), 2-phenyl ethyl anthranilate (7.3%), and with water distillation were dihydro citronellol acetate (63.7%), borneol (9.1%), 2-phenyl ethyl anthranilate (3%), and with steam distillation were dihydro citronellol acetate (55.9%), (E)-phytol acetate (7.5%), borneol (7.3%), were the predominant major compounds respectively. | ||
| کلیدواژه‌ها | ||
| Boswellia carteri birdwood؛ Distillation؛ essential oil؛ chemical composition | ||
| مراجع | ||
|
1. Lipp FJ, Kräuter Heilkunde, Heilung und Harmonie, Symbolik, Rituale und Folklore Östliche und Westliche Traditionen . Duncan Baird Publishers Ltd., 2001.
2. Springer V, Sandermann W, Naturharze, Terpentinol, Tallol, 1960.
3. Vollesen K, Burseraceae. In: The Flora of Ethiopia, Vol. 3. Hedberg, I.; Edward, S. (eds.), AddisAbaba University, Addis Ababa, 1989, pp. 442-478.
4. Tucker AO, Frankincense and myrrh. Econo Botany, 1986;40:425-433.
5. Dekebo A,Phytochemical Studies on the Resin of some Commiphora and Boswelliaspp. Ph. D.Thesis, Addis Ababa University, Addis Ababa, Ethiopia, 2001.
6. Kindeya GH, Ecology and Management of Boswellia papyrifera (Del.) Hochst. Dry Forest in Tigray, Northern Ethiopia. Ph. D. Thesis, Culvillier Verlag, Gottingen, Germany, 2003.
7. Hamm A, Bleton J, Connan J, Tchapla A, chemical investigation by headspace SPME and GC-MS of volatile and semi volatile terpenes in various olibanum samples.Phytochem. 2005;66:1499-1514.
8. Proyan GJI, Alexander WPG, Monoterpenerich resins from someKenyan Burseraceae. J. Flavour Frag. 1987; 2:115-119.
9. Keller JC, Clark PH, Lofgren CS, Susceptibility of insecticide-resistant cockroachesto pyrethrins. Pest Control. 1956;24:14-15.
10. Kang HY,Matsushima N, Sameshima K, Takamura N. Termite resistance tests of hardwoods of Kochi growth: The strong termiticidal activity of kagonoki (Litsea coreanaL).Mokuzai Gakkaishi, 1990, 36: 78-84.
11. Kalemba D, Kunicka A, Antibacterial and antifungal properties of essential oils. Curr. Med. Chem. 2003, 10: 813-829.
12. SandermannW, Chemie und Technologie, Springer-Verlag, Berlin, Gottingen, Heidel.Terpentinol, Tallol. 1960;118-122.
13. Vollesen K, Burseraceae. In:The Flora of Ethiopia, Vol. 3.Hedberg, I.;Edward,S. (eds.), AddisAbaba University, Addis Ababa, 1989, pp. 442-478.
14. Gamarda L, Dayton T, Di Stefano V, Pitonzo R, & Schillaci D, Chemical composition and antimicrobial activity of some oelegum resin essential oils from Boswellia spp. Annali di Chimica, 2007;97:837-844.
15. Hasson SS, Al-Balushi MS, Sallam TA, Idris MA, Habbal O, & Al-Jabri A, In vitro antibacterial activity of three medicinal plants-Boswellia (Luban) species. Asian Pacific J of Tropical Biomed, 2011;1:S178-S182.
16. Miller GA, & Morris M, Ethnoflora of the Soqotra Archipelago. Edinburgh, UK/Huddersfield, UK: The Royal Botanic Garden/Charlesworth Group.2004.
17. Tucker AO, Frankincense and myrrh.Economic Botany1986;40:425-433.
18. Dekebo A, Phytochemical Studies on the Resin of some Commiphora and Boswelliaspp. Ph. D. Thesis, Addis Ababa University, Addis Ababa, Ethiopia, 2001.
19. Kindeya GH, Ecology and Management of Boswellia papyrifera (Del.)Hochst. Dry Forest in Tigray, Northern Ethiopia. Ph. D. Thesis, Culvillier Verlag, Gottingen, Germany, 2003.
20. Al-Howiriny T, Alsheikh A, Alqasoumi S, Aghili Shirazi MH. Tehran: Tehran University of Medical Sciences; 2009. Makhzan-al-advia (Persian) pp. 105-801.
21. Badria FA, Mikhaeil BR, Maatooq GT, Amer MM. Immunomodulatory triterpenoids from the oleogum resin of Boswellia carterii Birdwood. Z Naturforsch C. 2003; 58: 505-516.
22. Yoshikawa M, Morikawa T, Oominami H, Matsuda H. Absolute stereostructures of olibanumols A, B, C, H, I, and J from olibanum, gum-resin of Boswellia carterii, and inhibitors of nitric oxide production in lipopolysaccharide-activated mouse peritoneal macrophages. Chem Pharm Bull. 2009;57: 957-964.
23. Chevrier MR, Ryan AE, Lee DY-W, Zhongze M, Wu-Yan Z, Via CS. Boswellia carterii extract inhibits TH1 cytokines and promotes TH2 cytokines in vitro. Clin Diagn Lab Immun. 2005;12:575-580.
24. Mothana RA, Hasson SS, Schultze W, Mowitz A, Lindequist U. Phytochemical composition and in vitro antimicrobial and antioxidant activities of essential oils of three endemic Soqotraen Boswellia species.Food Chem.2011; 126:1149-1154.
25. Adams RP, Identification of essential oils by ion trap mass spectroscopy. Academic Press: New York. 1989.
26. Shibamoto T, Retention indices in Essential oil analysis. In: Capillary Gas Chromatography in Essential oils analysis.Edits., Sandra P, and Bicchi C, , Dr. Alferd Huethig Verlag,New York. 1987. p. 259-274.
27. Davies NW, Gas chromatographic retention index of monoterpenes and sesquiterpenes on methyl silicon and carbowax 20M phases., Chromatogr.,1990. 503, 1-24.
28. Jauch J, In Weinrauchsymposium der DPhG: Phytomedicine, Tubingen, 2008.
29. Koch A, Basar S, Richter R, In Preparative Layer Chromatography (Kowalska T. and Sherma, J. Eds), CRC Press, Boca Raton, 2006; 391.
30. Mertens M, A Buettner; E Kirchhoff. Flavour Fragr. J., 2009;24:279.
31.World Health Organization. World Health Statistics[M]. 2010:64. | ||
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