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Evaluation of in vitro antimalarial activity of different extracts of Artemisia aucheri Boiss. and A. armeniaca Lam. and fractions of the most potent extracts.

1. Introduction

Malaria is one of the most common infectious diseases that are caused by parasites of the genus Plasmodium and kills more than one million individuals in the tropical and subtropical zones annually [1, 2]. This situation has been complicated by the appearance of drug-resistant parasites especially to the existing cheap drugs like chloroquine [3]; hence, there has been increasing attempts to identify other alternatives especially plant-derived antimalarial drugs. The genus Artemisia (Compositae) is one of the most popular herbs in traditional medicines and mostly used for the treatment of diseases like malaria, hepatitis, cancers, and inflammations [4]. It is a large genus with about 400 species, predominately distributed in the world (especially in Europe, North America, Asia, and South Africa) and 34 species are documented in the flora of Iran [5, 6]. There has been growing attention to this genus since the isolation of Artemisinin, obtained from A. annua, and its distinguished clinical effects as a potent antimalarial drug [7]. Artemisinin with an endoperoxide sesquiterpene lactone structure is unlike those of any other known antimalarials (mefloquine, amodiaquine, and chloroquine) that kills all stages of the parasite by a reductive interaction with free heme, resulting in generation of some types of free radicals that could alkylate parasite proteins and damage membranes [8]. Artemisinin also acts byblocking free heme biocrystallization (like 4-aminoquinolines) and hemoglobin degradation [9]. In the last few years, artemisinin and its derivatives were the top of the list of antimalarial drugs against drug-resistant Plasmodium falciparum strains, but recently, the emergence of artemisinin-resistant parasites in some regions [10, 11] has led researchers to search for new sources of alternative therapies. In our previous study, dichloromethane extracts of Artemisia scoparia and A. spicigera were shown to possess antimalarial activity in [beta]-hemation formatin assay [12]. As a continuation of our research on Iranian Artemisia spp., we have now evaluated antimalarial effect of different extracts and fractions of Artemisia aucheri and A. armeniaca. In various studies, hypocholesterolemic and antiatherosclerotic effects of Artemisia aucheri in rabbits were confirmed [13-16]. Likewise, different extracts of A. aucheri have been reported to possess wound healing [17], leishmanicidal [18, 19] and antifungal [20] effects. In the case of A. armeniaca, phytochemical evaluations on extracts and essential oil have been carried out and the presence of two new coumarin-hemiterpene ether glycosides [21], four prenylated coumarins, and some known flavonoids [22, 23] was reported. The main constituent of the oil extracted from the aerial parts of A. armeniaca was found to be [alpha]-pinene [24, 25]. The objectives of this study were to investigation of the antimalarial activity of different extracts of these Artemisia species (I), fractionation of the most potent extract (II), and determination of the most potent fractions (III).

2. Materials and Methods

2.1. Chemicals. Hematin porcine, chloroquine diphosphate, sodium dodecyl sulfate (SDS), sodium acetate, magnesium sulfate, sodium hydrogen phosphate, sodium chloride, potassium chloride, sodium hydroxide, glucose, and sodium bicarbonate were purchased from Sigma-Aldrich Chemical Company, oleic acid from Fluka, dimethylsulfoxide, hydrochloric acid, and silica gel 60 (0.040-0.063 mm) from Merck, and all the solvents used for extraction and fractionation from Caledon and Scharlau.

2.2. Plant Material. The aerial parts of Artemisia armeniaca Lam. were collected from Arasbaran, East Azarbaijan province (Iran), in August 2008. The identity of the plant was confirmed by morphological examination in comparison to the herbarium specimens. Voucher number TBZfph 528 is retained in the School of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran. Aerial parts of Artemisia aucheri Boiss. were collected from Chahar Bagh region, Golestan province (Iran), in December 2011 and authenticated by Mr. S. A. Hosseini, Agricultural and Natural Resources Research Center of Golestan Province, Gorgan, Iran. A voucher specimen (number 2383) is deposited in the herbarium.

2.3. Extract Preparation. The plant samples were air-dried at room temperature under shade, finely ground, and extracted by cold maceration method. 100 g of each plant sample was extracted successively with petroleum ether (PE), dichloromethane (DCM), ethyl acetate (EtOAC), ethanol, and ethanol-water (1: 1 v/v) at room temperature (sequential maceration with ca. 3 x 1L of each solvent). All the extracts were separately concentrated using a rotary evaporator at a maximum temperature of 45[degrees]C.

2.4. Fractionation. DCM extracts of plants (1.54 g of A. armeniaca and 1.56 g of A. aucheri) were fractionated by vacuum liquid chromatography (VLC) over silica gel (20 g for each) with solvent mixtures of increasing polarities: EtOAC/PE (10 : 90), EtOAC/PE (20 : 80), EtOAC/PE (40 : 60), EtOAC/PE (60: 40), EtOAC/PE (80: 20), EtOAC/PE (100 : 0), and methanol. All the fractions were fully dried using a rotary evaporator at a maximum temperature of 45[degrees]C.

2.5. TLCAnalysisofExtractsand Fractions. The identification of main chemical groups was carried out by TLC on silica gel 60 [F.sub.254] Merck (layer thickness 0.25 mm) as follows: for methoxylated flavonoids, chloroform/ethylacetate (60 : 4) and for methylated coumarins, toluene/ether (1 : 1/saturated with 1% acetic acid) were used as solvent system. They were detected under UV 366 nm.

2.6. In Vitro [beta]-Hematin Formation Assay. The potential antimalarial activity of plant extracts was evaluated by the method described by Afshar et al. [12] with some modifications. Briefly, varying concentrations (0-2 mg/mL in DMSO) of the extracts and fractions were incubated with 3 mM of hematin, 10 mM oleic acid, and 1M HCl. The final volume was adjusted to 1 mL using sodium acetate buffer, pH 5. Chloroquine diphosphate was used as a positive control. The reaction mixtures were incubated overnight at 37[degrees]C with constant gentle shaking. After incubation, samples were centrifuged (14,000 rpm, 10 min, at 21[degrees]C) and the hemozoin pellet was repeatedly washed with incubation (15 min at 37[degrees]C with regular shaking) in 2.5% (w/v) SDS in phosphate buffered saline followed by a final wash in 0.1 M sodium bicarbonate until the supernatant was clear (usually 3-8 washes). After the final wash, the supernatant was removed and the pellets were dissolved in 1mL of 0.1 M NaOH before determining the hemozoin content by measuring the absorbance at 400 nm (Beckman DU640 spectrophotometer). The results were recorded as %inhibition (I%) of heme crystallization compared to negative control (DMSO) using the following equation: I% = [(AN-AS)/AN]x100, where AN: absorbance of negative control and AS is absorbance of test samples.

2.7. Statistical Analysis. All experiments were conducted in triplicate measurements and presented as the Mean [+ or -] SD. Data were analyzed by Excel 2010 Microsoft. The [IC.sub.50] and [IC.sub.90] values were calculated from nonlinear regression analysis.

3. Results

The results from the in vitro [beta]-hematin formation assay of five different extracts from A. armeniaca and A. aucheri and seven fractions of their respective DCM extracts as well as the extraction and fractionation yields are listed in Table 1. The inhibition of [beta]-hematin formation expressed as percentage (I%) and standard deviations (n = 3) are given for each extract/fraction. [IC.sub.50] and [IC.sub.90] values were measured graphically by plotting concentrations versus percentage of inhibition. Three extracts (EtOAC, ethanol, and hydroethanol) of both plants had no anti-malarial activity at all while the DCM extracts of A. armeniaca and A. aucheri compared to the standard anti-malarial compound, chloroquine ([IC.sub.50] = 0.04 [+ or -] 0.002, [IC.sub.90] = 0.35 [+ or -] 0.006), showed the most potent anti-malarial activity with [IC.sub.50] values of 1.36 [+ or -] 0.01 and 1.83 [+ or -] 0.03 mg/mL and [IC.sub.90] values of 2.12 [+ or -] 0.04, 2.62 [+ or -] 0.09 mg/mL, respectively. PE extracts possessed a weak activity with [IC.sub.50] values of 3.51 [+ or -] 0.11 and 4.79 [+ or -] 0.92 mg/mL and [IC.sub.90] values of 7.96 [+ or -] 0.17, 10.25 [+ or -] 2.91 mg/mL for A. armeniaca and A. aucheri, respectively. Among the seven different polarity fractions obtained from the DCM extract of A. armeniaca, 80% EtOAC/PE and 100% EtOAC fractions showed considerable anti-malarial activity with [IC.sub.50] values of 0.47 [+ or -] 0.006 and 0.94 [+ or -] 0.006 mg/mL and [IC.sub.90] values of 0.71 [+ or -] 0.006,1.26 [+ or -] 0.02 mg/mL, respectively. In the case of fractions separated from DCM extract of A. aucheri four polar fractions (60% EtOAC/PE, 80% EtOAC/PE, 100% EtOAC, and 100% MeOH fractions) showed remarkable anti-malarial effects with close [IC.sub.50] and [IC.sub.90] values (Table 1 and Figure 1).

4. Discussion

The malaria parasite, Plasmodium, degrades hemoglobin within the infected erythrocytes to use the catabolic products as the chief source of nutrition for its development and proliferation [26, 27]. Free heme is released as a toxic byproduct of this process which could affect cellular metabolism by peroxidizing membranes and inhibiting a variety of enzymes [28]. To protect itself, the malaria parasite uses several detoxification pathways to get rid of excess heme. Polymerization of heme into an insoluble, nontoxic crystalline compound, hemozoin (also called malaria pigment) is believed to be the prominent way of detoxification [29]. Thus, the inhibition of hemozoin formation is an attractive target for development of several antimalarial drugs such as 4-aminoquinolines (quinine, mefloquine, and chloroquine) and is therefore considered as a suitable target for drug screening programs [30]. Many in vitro assays based on spectral characteristics and differential solubility of monomeric heme and [beta]-hematin (synthetic analogue of hemozoin) have been described and used for screening of novel synthetical [31, 32] and natural [33] antimalarial compounds. In this study, 10 extracts and 14 fractions of A. armeniaca and A. aucheri were evaluated for their antimalarial activity by an in vitro [beta]-hematin formation assay developed by Afshar et al. [12]. As shown from the results presented in Table 1 and Figure 1, among the different polarity extracts of A. armeniaca, DCM extract showed the most potent activity ([IC.sub.50] = 1.36 [+ or -] 0.01 and [IC.sub.90] = 2.12 [+ or -] 0.04 mg/mL) and indicated that compounds with strongest antimalarial activity have medium polarity. Subsequent bioactivity-guided fractionation of DCM extract by VLC over silica gel with solvent mixtures of increasing polarities afforded seven fractions. The activity of 80% EtOAC/PE and 100% EtOAC fractions was observed to be significantly higher than that of DCM extract and 80% EtOAC/PE fraction was determined the most active fraction. The inhibitory activity of these two fractions was comparable with that of standard drug chloroquine ([IC.sub.50] = 0.04 [+ or -] 0.002 and [IC.sub.90] = 0.35 [+ or -] 0.006 mg/mL) while the remaining fractions were considered inactive. TLC analysis of the DCM extract and its fractions indicated the presence of terpenes, fatty acids, methylated coumarins, and methoxylated flavonoids as major constituents. Previous investigations showed that methoxylated flavonoids [34], terpens, steroids [35], saponins [36], and methylated coumarins [37] exhibited antiplasmodial activity in different antimalarial assays. In 80% EtOAC/PE and 100% EtOAC fractions, methoxylated flavonoids and methylated coumarins were identified by TLC analysis and could be considered as the major active constituents. Therefore, it seems that the potent antimalarial activity of A. armeniaca DCM extract and its active fractions might be related to the presence of these compounds. As observed in Table 1, similar findings were illustrated in case of A. aucheri extracts and fractions. DCM extract was found to be more potent ([IC.sub.50] = 1.83 [+ or -] 0.03, [IC.sub.90]= 2.62 [+ or -] 0.09 mg/mL) than the corresponding PE extract ([IC.sub.50] = 4.79 [+ or -] 0.92, [IC.sub.90] = 10.25 [+ or -] 2.91 mg/mL) while the other three polar extracts were inactive. The DCM extract was selected for further investigation because of its potent activity and subjected to fractionation by the above-mentioned procedure. Among the seven different polarity fractions, 10% EtOAC/PE, 20% EtOAC/PE, and 40% EtOAC/PE fractions revealed no activity in this assay system, while the last four polar fractions showed the potent activity with close [IC.sub.50] and [IC.sub.90] values (Table 1). Methoxylated flavonoids and methylated coumarins were identified by TLC analysis from 60% EtOAC/PE, 80% EtOAC/PE, 100% EtOAC, and 100% MeOH fractions. Furthermore, in previous phytochemical study, two endoperoxide derivatives were isolated from the aerial parts of A. aucheri [38] that structurally similar to artemisinin. Additionally, in recent study, the presence of amorpha-4,11-diene synthase, a key enzyme in artemisinin production, was demonstrated in A. aucheri [39]. Therefore, the possibility that the antimalarial activity displayed by DCM extract and its active fractions reported here would be due to the presence of these types of compounds could not be excluded. Overall, the results from this investigation showed that both DCM extracts of these Artemisia species act as inhibitors of heme crystallization pathway and A. armeniaca illustrated more potent activity than A. aucheri. A comparison of DCM fractions of two tested plants based on [IC.sub.50] and [IC.sub.90] values (Figure 1) revealed that 80% EtOAC/PE fraction of A. armeniaca were about 3-fold and 4-fold more potent than 80% EtOAC/PE fraction of A. aucheri, respectively. This difference might have been derived from the high concentration of antimalarial components in this fraction and removing as much the lipid-like compounds from it. As shown in Figures 2 and 3, at lower concentrations of the active extracts and fractions, the observed absorbance was higher than the negative control which might be due to the presence of other fatty acids and lipids causing synergistic effect with oleic acid in the assay. It was demonstrated that the [IC.sub.50] and [IC.sub.90] values could be reduced by completely removing the lipids and purifying the active antimalarial principles.

5. Conclusion

From the selection of 10 extracts with different polarity, results showed that the DCM extract of A. armeniaca was the most active extract in [beta]-hematin formation assay followed by the DCM extract of A. aucheri. This preliminary study and its data persuade us to focus on purifying the active components of these extracts and investigating further on animal models for in vivo evaluation.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.


This work was performed in partial fulfillment of the requirements for Pharm. D. of Ali Shiravand, Kermanshah University of Medical Sciences, Kermanshah, Iran.


[1] A. R. Bilia, D. Lazari, L. Messori, V. Taglioli, C. Temperini, and F. F. Vincieri, "Simple and rapid physico-chemical methods to examine action of antimalarial drugs with hemin: its application to Artemisia annua constituents," Life Sciences, vol. 70, no. 7, pp. 769-778, 2002.

[2] D. Rathore, D. Jani, R. Nagarkatti, and S. Kumar, "Heme detoxification and antimalarial drugs--known mechanisms and future prospects," Drug Discovery Today, vol. 3, no. 2, pp. 153-158, 2006.

[3] A. Ishih, C. Ikeya, M. Yanoh, H. Takezoe, T. Miyase, and M. Terada, "A potent antimalarial activity of Hydrangea macrophylla var. Otaksa leaf extract against Plasmodium yoelii 17XL in mice," Parasitology International, vol. 50, no. 1, pp. 33-39, 2001.

[4] K. D. Yoon, Y.-W. Chin, M. H. Yang, and J. Kim, "Separation of anti-ulcer flavonoids from Artemisia extracts by high-speed countercurrent chromatography," Food Chemistry, vol. 129, no. 2, pp. 679-683, 2011.

[5] A. A. Mahmoud and A. A. Ahmed, "a-Pinene-type monoterpenes and other constituents from Artemisia suksdorfii," Phytochemistry, vol. 67, no. 19, pp. 2103-2109, 2006.

[6] V. Mozaffarian, A Dictionary of Iranian Plant Names, Farhang Moaser, Tehran, Iran, 2007.

[7] L. Ferchichi, J. Merza, A. Landreau et al., "Occurrence of isocoumarinic and phenolic derivatives in Artemisia campestris L. subsp. campestris," Biochemical Systematics and Ecology, vol. 34, no. 11, pp. 829-832, 2006.

[8] S. de Ridder, F. van der Kooy, and R. Verpoorte, "Artemisia annua as a self-reliant treatment for malaria in developing countries," Journal of Ethnopharmacology, vol. 120, no. 3, pp. 302-314, 2008.

[9] K. Borstnik, I. H. Paik, T. A. Shapiro, and G. H. Posner, "Antimalarial chemotherapeutic peroxides: artemisinin, yingzhaosu A and related compounds," International Journal for Parasitology, vol. 32, no. 13, pp. 1661-1667, 2002.

[10] A. M. Dondorp, F. Nosten, P. Yi et al., "Artemisinin resistance in Plasmodium falciparum malaria," The New England Journal of Medicine, vol. 361, no. 5, pp. 455-467, 2009.

[11] F. Astelbauer, M. Gruber, B. Brem et al., "Activity of selected phytochemicals against Plasmodium falciparum" Acta Tropica, vol. 123, no. 2, pp. 96-100, 2012.

[12] F. H. Afshar, A. Delazar, O. Janneh et al., "Evaluation of antimalarial, free-radicalscavenging and insecticidal activities of Artemisia scoparia and A. spicigera, Asteraceae," Brazilian Journal of Pharmacognosy, vol. 21, no. 6, pp. 986-990, 2011.

[13] N. Jafari Dinani, S. Asgary, H. Madani, G. H. Naderi, and P. Mahzoni, "Hypocholesterolemic and antiatherosclerotic effect of Artemisia aucheri in hypercholesterolemic rabbits," Pakistan Journal of Pharmaceutical Sciences, vol. 23, no. 3, pp. 321-325, 2010.

[14] N. Jafari Dinani, S. Asgari, H. Madani, G. H. A. Naderi, and P. Mahzuni, "Effect of Artemisia aucheri on regression of atherosclerotic plaque in rabbits," Journal of Medicinal Plants, vol. 8, no. 29, pp. 72-79, 2009.

[15] S. Asgary, N. Jafari Dinani, H. Madani, and P. Mahzouni, "Ethanolic extract of Artemisia aucheri induces regression of aorta wall fatty streaks in hypercholesterolemic rabbits," Pharmazie, vol. 63, no. 5, pp. 394-397, 2008.

[16] D. N. Jafari, S. Asgary, H. Madani, P. Mahzoni, and G. Naderi, "Effect of Artemisia aucheri extract on atherogenic lipids and atherogenesis in hypercholesterolemic rabbits," Journal of Medicinal Plants, vol. 6, no. 23, pp. 20-28, 2007

[17] M. Allahtavakoli, F. A. B. Asad, M. Mahmoudi et al., "Effect of hydro-alcoholic extract of Artemisia aucheri on healing of skin wound in rat," Journal of Mazandaran University of Medical Sciences, vol. 20, no. 77, pp. 69-76, 2010.

[18] M. Sharif, A. Daryani, M. Rostami, H. Nahrevanian, and M. Azadbakht, "Evaluation of anti-leishmanial efficacy by in vivo administration of herbal extract artemisia auchery on leishmania major in Balb/c mice," Pharmacologyonline, vol. 2, pp. 1136-1144, 2009.

[19] M. Sharif, H. Ziaei, M. Azadbakht, A. Daryani, A. Ebadattalab, and M. Rostami, "Effect of methanolic extracts of Artemisia aucheri and Camellia sinensis on Leishmania major (in vitro)," Turkish Journal of Medical Sciences, vol. 36, no. 6, pp. 365-369, 2006.

[20] G. Amin, A. Dehmoobed-Sharifabadi, M. H. Salehi Surmaghi et al., "Screening of Iranian plants for antifungal activity: part 1," Daru, vol. 10, no. 1, pp. 38-48, 2002.

[21] M. Mojarrab, A. Delazar, M. Hamburger, and O. Potterat, "New coumarin-hemiterpene ether glucosides and a structurally related phenylpropanoic acid derivative from Artemisia armeniaca," Natural Product Communications, vol. 5, no. 10, pp. 1619-1622, 2010.

[22] M. Mojarrab, A. Delazar, S. B. Moghadam et al., "Armenin and isoarmenin--two prenylated coumarins from the aerial parts of Artemisia armeniaca," Chemistry and Biodiversity, vol. 8, no. 11, pp. 2097-2103, 2011.

[23] K. S. Rybalko, O. A. Konovalova, V. I. Sheichenko, and P. I. Zakharov, "Armin--a new coumarin from Artemisia armeniaca," Chemistry of Natural Compounds, vol. 12, no. 3, pp. 262-265, 1976.

[24] M. Mojarrab, A. Delazar, S. Asnaashari, and F. H. Afshar, "Chemical composition and general toxicity of essential oils extracted from the aerial parts of Artemisia armeniaca Lam. and A. incana (L.) Druce growing in Iran," Research in Pharmaceutical Sciences, vol. 8, no. 1, pp. 65-69, 2013.

[25] M. Kazemi, M. R. Zand, K. Roshanaei, M. Mehrzad, and A. Rustaiyan, "Composition of the volatile oils of Artemisia armenica lan. and Artemisia splendens willd. from Iran," Journal of Essential Oil Research, vol. 22, no. 2, pp. 126-128, 2010.

[26] T. J. Egan, "Haemozoin formation," Molecular and Biochemical Parasitology, vol. 157, no. 2, pp. 127-136, 2008.

[27] N. T. Huy, D. T. Uyen, M. Sasai et al., "A simple and rapid colorimetric method to measure hemozoin crystal growth in vitro," Analytical Biochemistry, vol. 354, no. 2, pp. 305-307, 2006.

[28] K. V. Sashidhara, S. P. Singh, S. V Singh et al., "Isolation and identification of b-hematin inhibitors from Flacourtia indica as promising antiplasmodial agents," European Journal of Medicinal Chemistry, vol. 60, pp. 497-502, 2013.

[29] P. Sonnet and C. Mullie, "In vitro antimalarial activity of ICL670: a further proof of the correlation between inhibition of [beta]-hematin formation and of peroxidative degradation of hemin," Experimental Parasitology, vol. 128, no. 1, pp. 26-31, 2011.

[30] A. Alam, M. Goyal, M. S. Iqbal et al., "Novel antimalarial drug targets: hope for new antimalarial drugs," Expert Review of Clinical Pharmacology, vol. 2, no. 5, pp. 469-489, 2009.

[31] K. Toth, N. I. Wenzel, N. Chavain et al., "Antimalarial versus cytotoxic properties of dual drugs derived from 4-aminoquinolines and mannich bases: interaction with DNA," Journal of Medicinal Chemistry, vol. 53, no. 8, pp. 3214-3226, 2010.

[32] B. L. Tekwani and L. A. Walker, "Targeting the hemozoin synthesis pathway for new antimalarial drug discovery: technologies for in vitro [beta]-hematin formation assay," Combinatorial Chemistry and High Throughput Screening, vol. 8, no. 1, pp. 63-79, 2005.

[33] S. Vargas, K. Ndjoko Ioset, A.-E. Hay, J.-R. Ioset, S. Wittlin, and K. Hostettmann, "Screening medicinal plants for the detection of novel antimalarial products applying the inhibition of [beta]-hematin formation," Journal of Pharmaceutical and Biomedical Analysis, vol. 56, no. 5, pp. 880-886, 2011.

[34] L. Tona, R. K. Cimanga, K. Mesia et al., "In vitro antiplasmodial activity of extracts and fractions from seven medicinal plants used in the Democratic Republic of Congo," Journal of Ethnopharmacology, vol. 93, no. 1, pp. 27-32, 2004.

[35] C. Kraft, K. Jenett-Siems, K. Siems et al., "In vitro antiplasmodial evaluation of medicinal plants from Zimbabwe," Phytotherapy Research, vol. 17, no. 2, pp. 123-128, 2003.

[36] F. Traore, R. Faure, E. Ollivier et al., "Structure and antiprotozoal activity of triterpenoid saponins from Glinus oppositifolius," Planta Medica, vol. 66, no. 4, pp. 368-371, 2000.

[37] F. W. Muregi, A. Ishih, T. Miyase et al., "Antimalarial activity of methanolic extracts from plants used in Kenyan ethnomedicine and their interactions with chloroquine (CQ) against a CQ-tolerant rodent parasite, in mice," Journal of Ethnopharmacology, vol. 111, no. 1, pp. 190-195, 2007.

[38] A. Rustaiyan, A. Bamonieri, M. Raffatrad, J. Jakupovic, and F. Bohlmann, "Eudesmane derivatives and highly oxygenated monoterpenes from Iranian Artemisia species," Phytochemistry, vol. 26, no. 8, pp. 2307-2310, 1987.

[39] R. Hosseini, N. Yazdani, and G. A. Garoosi, "The presence of amorpha-4, 11-diene synthase, a key enzyme in artemisinin production in ten Artemisia species," DARU, Journal of Pharmaceutical Sciences, vol. 19, no. 5, pp. 332-337, 2011.

Mahdi Mojarrab, (1) Ali Shiravand, (1,2) Abbas Delazar, (3) and Fariba Heshmati Afshar (4)

(1) Novel Drug Delivery Research Center, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah 67346-67149, Iran

(2) Student Research Committee, Kermanshah University of Medical Sciences, Kermanshah 67346-67149, Iran

(3) Drug Applied Research Centre, Tabriz University of Medical Sciences, Tabriz 51656-65811, Iran

(4) Medical Philosophy and History Research Center, Tabriz University of Medical Sciences, Tabriz 371-51665, Iran

Correspondence should be addressed to Fariba Heshmati Afshar;

Received 7 August 2013; Accepted 24 October 2013; Published 14 January 2014

Academic Editors: Z. Liu and H. Verhoeven

TABLE 1: The 50% and 90% inhibition concentrations (mg/mL)
of different extracts and fractions of A. armeniaca and
A. aucheri in [beta]-hematin formation assay.

Plants                 Extracts/tractions   Yields (%)

                        Petroleum ether        1.11
                        Dichloromethane        4.46
Artemisia aucheri        Ethyl acetate         0.46
(aerial parts)              Ethanol            9.09
                         Ethanol-water         7.27

                        Petroleum ether        1.88
Artemisia armeniaca     Dichloromethane        1.97
(aerial parts)           Ethyl acetate         0.56
                            Ethanol            2.57
                         Ethanol-water        17.66

                          10% EtOAC/PE        16.86
                          20% EtOAC/PE         8.08
Artemisia aucheri         40% EtOAC/PE        24.68
(DCM tractions)           60% EtOAC/PE        15.06
                          80% EtOAC/PE         7.12
                           100% EtOAC          8.91
                         100% Methanol        10.51

                          10% EtOAC/PE         3.25
                          20% EtOAC/PE         3.90
                          40% EtOAC/PE        13.88
Artemisia armeniaca       60% EtOAC/PE         7.48
(DCM tractions)           80% EtOAC/PE        15.84
                           100% EtOAC          6.49
                         100% Methanol        40.91

Chloroquine                    --               --

Plants                     I[C.sub.50]           I[C.sub.90]
                           (mg/mL) (a)           (mg/mL) (a)

                       4.79 [+ or -] 0.92    10.25 [+ or -] 2.91
Artemisia aucheri      1.83 [+ or -] 0.03    2.62 [+ or -] 0.09
(aerial parts)                 --                    --
                               --                    --

                       3.51 [+ or -] 0.11    7.96 [+ or -] 0.17
                       1.36 [+ or -] 0.01    2.12 [+ or -] 0.04
Artemisia armeniaca            --                    --
(aerial parts)                 --                    --
                               --                    --

                               --                    --
                               --                    --
                               --                    --
Artemisia aucheri      1.23 [+ or -] 0.01    2.13 [+ or -] 0.07
(DCM tractions)        1.38 [+ or -] 0.05    2.70 [+ or -] 0.44
                       1.55 [+ or -] 0.01    2.01 [+ or -] 0.01
                       1.45 [+ or -] 0.03    2.26 [+ or -] 0.05

                               --                    --
                               --                    --
Artemisia armeniaca            --                    --
(DCM tractions)        0.47 [+ or -] 0.006   0.71 [+ or -] 0.006
                       0.94 [+ or -] 0.006   1.26 [+ or -] 0.02
                               --                    --

Chloroquine            0.04 [+ or -] 0.002   0.35 [+ or -] 0.006

(a) Experiment was performed in triplicate and expressed
as Mean [+ or -] SD.
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Title Annotation:Research Article
Author:Mojarrab, Mahdi; Shiravand, Ali; Delazar, Abbas; Afshar, Fariba Heshmati
Publication:The Scientific World Journal
Article Type:Report
Geographic Code:7IRAN
Date:Jan 1, 2014
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