Comparison of terpene components from flowers of Artemisia annua BJP

Terpene constituents of essential oils obtained by steam distillation from Artemisia annua flowers at the pre-, fulland post-flowering stage was investigated by gas chromatography (GC) and gas chromatography-mass spectrometric detector (GC-MS). The aim was to evaluate change the biosynthesis pathway of terpenes at different flowering stages. The samples studied showed that main components of essential oils were monoterpenes hydrocarbons (48.1%) and oxygenated monoterpenes (41%) in the preflowering, oxygenated monoterpenes (35.6%) and sesquiterpenes hydrocarbons (5.0%) in the full-flowering, and oxygenated monoterpenes (29.6%), sesquiterpenes hydrocarbons (32.2%) and oxygenated sesquiterpenes (25.3%) in the post-flowering, respectively. The relative content of monoterpenes decreased from pre-flowering to post-flowering, while that of sesquiterpenes increased. The results indicated that the biosynthesis pathway of terpenes might be changed at different flowering at stages, while the change of content and composition of terpenes might be a self-adaptation of A. annua. Article Info Received: 1 June 2012 Accepted: 12 June 2012 Available Online: 18 June 2012 DOI: 10.3329/bjp.v7i2.10815 Cite this article: Yang ZN, Zhu SQ, Yu ZW. Comparison of terpene components from flowers of Artemisia annua. Bangladesh J Pharmacol. 2012; 7: 114-19. Comparison of terpene components from flowers of Artemisia annua Zhan Nan Yang1,2, Shi Qiong Zhu1 and Zheng Wen Yu1 School of Life Sciences, Guizhou Normal University, Guiyang, Guizhou, 550 001, Peoples Republic of China; Key Laboratory for Information System of Mountainous Area and Protection of Ecological Environment of Guizhou Province, Guizhou Normal University, Guiyang, Guizhou 550 001, Peoples Republic of China. This work is licensed under a Creative Commons Attribution 4.0 License. You are free to copy, distribute and perform the work. You must attribute the work in the manner specified by the author or licensor. systemic study about the essential oils of the herb has not been previously mentioned in literature. The effect of flowering on terpenes content of A. annua flower essential oils at pre-, fulland post-flowering stage was investigated. In the present paper we report the analytical results of the essential oils at different flower developing stages. Materials and Methods A. annua cultivar Wuling-3938 plants were grown in the Artemisia GAP Cultivation Demonstration Site of Holleypharm, Chongqing, China. The flowers were harvested at pre-, fulland post-flowering stage in September to November 2007 on a same plant. The flowers were separated from other capitula organs, leaves and stem of A. annua, and identified by Mr. Rongchang Luo of Holley Natural Resource Exploiture Co. Ltd, Chongqing, China and deposited in the Herbarium, College of Bioengineering, Chongqing University, Chongqing, China. Shade-dried plant materials (50.0 g) were hydrodistilled separately in Clevenger-type equipment for 4h. The oils were collected and dried over anhydrous sodium sulfate and stored in a refrigerator at 4°C for analysis. GC analyses were performed using a Shimadzu GC2010 gas chromatograph equipped with an FID and an HP-5 fused silica column (30 m × 0.32 mm i.d., 0.25 μm film thickness) with a 5% phenyl-substituted methylpolysiloxane phase. The oven temperature was programmed at 40°C for 4 min and then increased to 240°C at a rate of 4°C/min. Injector and detector temperatures were 250 and 265°C, respectively. The carrier gas, helium (99.999%), was adjusted to a linear velocity of 43 cm/s. The essential oil samples were diluted 5-fold, and 1 μL of a diluted solution was injected into the GC/MS in the split mode with a split ratio of 1/20. MS analyses were performed using a Shimadzu MSQP2010 with ionization energy of 70 eV, a scan time of 0.5 s and a mass range of 33–450 amu. The percentages of compounds were calculated by the area normalization method without considering response factors. The components of the oil were identified by comparison of their mass spectra with those of the spectrometer database using the NIST147 mass spectral database and also with those of authentic compounds. The identifications were confirmed by comparison of the fragmentation patterns and Retention index with those reported in the literature (Divya et al., 2007a; Flora et al., 2007; Divya et al., 2007b). The retention index was found with a standard mixture of C8 to C22 compounds under chromatography conditions, consistent with those of the chromatography conditions of the samples analyzed. Results and Discussion The flower essential oils were obtained from A. annua at pre-, fulland post-flowering stage with 2.2, 1.4 and 1.3% yield (relative to dried weight), respectively. Three oils were pale yellow, and the results of the analysis of the essential oils are given in Table I. A total of sixty-three compounds were identified in three essential oil samples. The oils contain mainly monoterpenes and sesquiterpenes, representing 96.2, 98.9 and 99.3% of the oils in A. annua at pre-, fulland post-flowering stage, respectively. Monoterpenes hydrocarbons and oxygenated monoterpenes content was greater in the preliminary florescence oil, they were 48.1 and 41.0%. The main compounds in the oil were myrcene (37.7%), 1,8-cineole (16.1%) and camphor (15.0%). The oxygenated monoterpenes and sesquiterpenes hydrocarbons were dominants in the flourishing florescence oil (35.6 and 5.0%). The oil contained predominantly caryophyllene (19.4%), germacrene D (18.1%), camphor (15.8%), 1,8-cineole (10.6%), (Z)-farnesene (9.4%). The terminal florescence oil contains mainly oxygenated monoterpenes (29.6%), sesquiterpenes hydrocarbons (32.2%) and oxygenated sesquiterpenes (25.3%). The major constituents identified in the oil were camphor (16.6%), caryophyllene (16.3%), -caryophyllene oxide (15.8%), -farnesene (9.0%), (-)-spathulenol (7.2%). A significant difference was the absence of oxygenated sesquiterpenes in preliminary florescence, while the monoterpenes hydrocarbons were lacked in the terminal florescence oil. It is reported (Liu et al., 1988) that the inflorescence oil of A. annua from Changchun, China, contained Artemisia ketone (63.1%), 1,8-cineole (1.5%), -pinene (1.5%) and caryophyllene (1.9%). Another literature (Divya Goel et al., 2007) reported the major compounds of the cultivar A. annua petal oil were trans-sabinol (10.2%), paramentha-1, 4 (8)-dien-3-ol (10.1%) and 1,8cineole (6.8%). The influence of transplanting time on inflorescence essential oil yield and composition has been studied (Flora Haider et al., 2007). Their result shows that oil yield was found to range from 0.5 to 1.6% (w/v). Camphor (23.30-57.00%), 1,8-cineole (5.6021.40%) and -caryophyllene (2.5-8.7%) were key compounds. The percentage occurrence of rest of the compounds was found to vary with different transplanting time. Our results were more similar to that of Flora Haider. The content of the monoterpenes hydrocarbons were decreased sharply with flower developing, especially for -myrcene, it from 37.7% in the preliminary florescence oil to 0.2% in the flourishing florescence oil, the compound was lacked in the terminal florescence oil (Figure 1A). The oxygenated sesquiterpenes were Bangladesh J Pharmacol 2012; 7: 114-119 115

Chongqing, China, shares eighty percent of A. annua around the world, where an A. annua GAP Cultivation Demonstration Site has been built for three years.But systemic study about the essential oils of the herb has not been previously mentioned in literature.The effect of flowering on terpenes content of A. annua flower essential oils at pre-, full-and post-flowering stage was investigated.In the present paper we report the analytical results of the essential oils at different flower developing stages.Shade-dried plant materials (50.0 g) were hydro-distilled separately in Clevenger-type equipment for 4h.The oils were collected and dried over anhydrous sodium sulfate and stored in a refrigerator at 4°C for analysis.GC analyses were performed using a Shimadzu GC-2010 gas chromatograph equipped with an FID and an HP-5 fused silica column (30 m × 0.32 mm i.d., 0.25 μm film thickness) with a 5% phenyl-substituted methylpolysiloxane phase.The oven temperature was programmed at 40°C for 4 min and then increased to 240°C at a rate of 4°C/min.Injector and detector temperatures were 250 and 265°C, respectively.The carrier gas, helium (99.999%), was adjusted to a linear velocity of 43 cm/s.The essential oil samples were diluted 5-fold, and 1 μL of a diluted solution was injected into the GC/MS in the split mode with a split ratio of 1/20.MS analyses were performed using a Shimadzu MS-QP2010 with ionization energy of 70 eV, a scan time of 0.5 s and a mass range of 33-450 amu.The percentages of compounds were calculated by the area normalization method without considering response factors.The components of the oil were identified by comparison of their mass spectra with those of the spectrometer database using the NIST147 mass spectral database and also with those of authentic compounds.The identifications were confirmed by comparison of the fragmentation patterns and Retention index with those reported in the literature (Divya et al., 2007a;Flora et al., 2007;Divya et al., 2007b).The retention index was found with a standard mixture of C8 to C22 compounds under chromatography conditions, consistent with those of the chromatography conditions of the samples analyzed.

Results and Discussion
The flower essential oils were obtained from A. annua at pre-, full-and post-flowering stage with 2.2, 1.4 and 1.3% yield (relative to dried weight), respectively.Three oils were pale yellow, and the results of the analysis of the essential oils are given in Table I.
The content of the monoterpenes hydrocarbons were decreased sharply with flower developing, especially for -myrcene, it from 37.7% in the preliminary florescence oil to 0.2% in the flourishing florescence oil, the compound was lacked in the terminal florescence oil (Figure 1A).The oxygenated sesquiterpenes were  increased quickly with flower developing, the (-)spathulenol and -caryphyllene oxide were nice examples, both the compounds weren't detected in the preliminary florescence oil, there were only 1.8% and 3.0% in the flourishing florescence oil, they were added rapidly to 7.2 and 15.8% in the terminal florescence oil (Figure 1B).
In general, the oxygenated monoterpenes were declined slowly with flower developing, among major compounds, artemisia ketone, camphor, borneol and trans-3 (10)-Caren-2-ol were raised tendency, while 1,8-cineole was declined (Figure 1c).Interestingly, the sesquiterpenes hydrocarbons increased sharply from 8.9% at pre-flowering stage to 5.0% (at the top of content) at full -flowering stage, followly by, which decreased slowly to 32.2% at post-flowering stage.Among of these compounds, the change ofcaryophyllene and -farnesene was good examples.The content of former from 2.3% added to 19.4%, then decreased to 16.3%; and that of the later from 2.6% added to 9.4%, then decreased to 9.0% (Figure 1D).
As to the change of all terpenes in flower oils of A. annua at different flowering stage, the content of the monoterpenes hydrocarbons and oxygenated monoterpenes were the highest at the pre-flowering stage, and the sesquiterpenes hydrocarbons arrive to the top The present results have shown that the content of terpenes in the A annua oils has close relationship with flower developing.The flowering effect on monoterpenes content of plant oil has been reported elsewhere (Dudai et al., 1992).So flowering may be change the biosynthesis pathway of terpenes in the A. annua flower oil, in turn, the change of content of terpenes in the oils may be the self-adaptation for the physiological phenomenon of flowering.

Table I Chemical composition of the flower essential oils at pre-, full-and post-flowering stage of A. annua
(Cont.) TR = retention time; ND = not identified; (-) Not detected; aRI is the Retention index relative to C8-C22 n-alkanes on the HP-5ms column