Evidence-Based Complementary and Alternative Medicine

Evidence-Based Complementary and Alternative Medicine / 2014 / Article

Research Article | Open Access

Volume 2014 |Article ID 873803 | 8 pages | https://doi.org/10.1155/2014/873803

Evaluation of Bioactive Compounds, Pharmaceutical Quality, and Anticancer Activity of Curry Leaf (Murraya koenigii L.)

Academic Editor: Hamid Reza Sadeghnia
Received02 Oct 2013
Revised12 Dec 2013
Accepted01 Jan 2014
Published16 Feb 2014


In this study, we investigated some bioactive compounds and pharmaceutical qualities of curry leaf (Murraya koenigii L.) extracts from three different locations in Malaysia. The highest TF and total phenolic (TP) contents were observed in the extracts from Kelantan (3.771 and 14.371 mg/g DW), followed by Selangor (3.146 and 12.272 mg/g DW) and Johor (2.801 and 12.02 mg/g DW), respectively. High quercetin (0.350 mg/g DW), catechin (0.325 mg/g DW), epicatechin (0.678 mg/g DW), naringin (0.203 mg/g DW), and myricetin (0.703 mg/g DW) levels were observed in the extracts from Kelantan, while the highest rutin content (0.082 mg/g DW) was detected in the leaves from Selangor. The curry leaf extract from Kelantan exhibited higher concentration of gallic acid (0.933 mg/g DW) than that from Selangor (0.904 mg/g DW) and Johor (0.813 mg/g DW). Among the studied samples, the ones from Kelantan exhibited the highest radical scavenging activity (DPPH, 66.41%) and ferric reduction activity potential (FRAP, 644.25 μm of Fe(II)/g) followed by those from Selangor (60.237% and 598.37 μm of Fe(II)/g) and Johor (50.76% and 563.42 μm of Fe(II)/g), respectively. A preliminary screening showed that the curry leaf extracts from all the locations exhibited significant anticarcinogenic effects inhibiting the growth of breast cancer cell line (MDA-MB-231) and maximum inhibition of MDA-MB-231 cell was observed with the curry leaf extract from Kelantan. Based on these results, it is concluded that Malaysian curry leaf collected from the North (Kelantan) might be potential source of potent natural antioxidant and beneficial chemopreventive agents.

1. Introduction

Plant-derived substances have recently attracted great interest, owing to their versatile applications. Medicinal plants are the richest source of bioactive compounds used in traditional and modern medicine as nutraceuticals and food supplements, pharmaceutical intermediates, and chemical entities for synthetic drugs [1]. Flavonoids are an important group of plant secondary metabolites with a wide range of biological activities [2]. These natural products have been shown to have antioxidant properties and are capable of scavenging free superoxide radicals, thus providing antiaging benefits as well as reducing the risk of cancer. Park et al. [3] showed that some flavonoid components in green tea were effective in inhibiting cancer by inducing the mechanisms that cause cancer cell death and inhibit tumor invasion. It has been found that flavonoids reduce the lipid and glucose levels in blood and support the human immune system [4, 5]. The health-promoting effects of flavonoids are the result of their ability to induce the activity of protective enzyme systems [6]. Breast cancer is the most common cancer in women and men, diagnosed in more than 1.2 million women worldwide and accounting for approximately 23% of all cancers reported. This cancer was reported as a most common form of cancers among Malaysian women since 2003 (18% of all cancers cases). A woman in Malaysia had a 1 in 20 chance of developing breast cancer in her lifetime [7]. Several studies have suggested that flavonoids such as catechin and quercetin are able to control the growth of cancer cells in human body [8, 9]. The plant Murraya koenigii (L.) Spreng, commonly known as curry leaf or Pokok kari (Daun kari) in Malaysia, belongs to the family of Rutaceae, which is native to India and now distributed in most of Southern and Southeast Asia [10]. Curry leaf has a slightly pungent, bitter, and feebly acidulous taste and is widely used for cooking in Malaysia and other Asian countries. It is also one of the traditional folk remedies that contains several interesting bioactive compounds with health-promoting properties [10]. Different parts of M. koenigii have been used in traditional Ayurveda medicine for the treatment of cough, hypertension, hysteria, hepatitis, rheumatism, poisonous bites, and skin eruptions. In addition, curry leaf has been reported to have antitumor [11], antioxidant [12], anti-inflammatory [13], antihyperglycemic [14], and hypoglycemic effects [15]. Nevertheless, the information about the secondary metabolite content and the antioxidant and anticancer activity of Malaysian curry leaf is still scarce. Additional research in this direction would help to further elucidate health benefits provided by this functional food additive.

The present investigation was undertaken to determine the bioactive compounds and antioxidant activity in the leaf extracts of M. koenigii collected from three different locations in Malaysia. In addition, anticancer properties of the curry leaf extracts have been investigated in vitro by using a breast cancer cell line.

2. Materials and Methods

2.1. Plant Material

Fresh leaves of curry leaf were collected locally from three different province of Malaysia, namely, Kelantan (Bachok, North), Selangor (BFK, Central), and Johor (Nasuha, South). The samples were identified by Malaysian Agriculture Research and Development Institute (MARDI). Voucher specimens of M. koenigii Kelantan (MTM0018/1), Selangor (MTM0018/3), and Johor (MTM0018/2) were collected. Malaysian Agriculture Research and Development Institute (MARDI) verified and kept samples. The leaves were shade-dried and were powdered using mechanical grinder. These powered materials were used for further analysis.

2.2. Preparation of Extract

Leaf samples (0.25 g) were extracted with 20 mL of methanol on a shaker for 2 h at room temperature. The extract solution was treated with 5 mL of hydrochloric acid (6 M) and refluxed for 2 h at 90°C. The hydrolysed samples were cooled to room temperature and filtered through a 0.45 μm membrane [16].

2.3. Determination of Total Phenolic Content

The content of total phenolics from the curry leaf was evaluated by the Folin-Ciocalteu method [17]. Briefly, 1 mL of extract was added to deionized water (10 mL) and Folin-Ciocalteu phenol reagents (1.0 mL). After 5 min, 20% sodium carbonate (2.0 mL) was added to the mixture. The solution was kept in total darkness, and the absorbance was measured at 750 nm using a spectrophotometer (U-2001, Hitachi Instruments Inc., Tokyo, Japan). Gallic acid was used for the calibration curve.

2.4. Determination of Total Flavonoids

The total flavonoid content of the curry leaf extract was determined using a modified colourimetric method [18]. Briefly, extracts of each plant material (1 mL) were diluted with 4 mL water in a 10 mL volumetric flask. Initially, 5% NaNO2 solution (0.3 mL) was added to each volumetric flask; after 5 min, 10% AlCl3 (w/v) was added; and at 6 min, 1.0 M NaOH (2 mL) was added. Absorbance of the reaction mixture was read at 430 nm. Quercetin was used for the calibration curve.

2.5. Separation and Analysis of Flavonoids and Phenolic Acids by HPLC

Reversed-phase HPLC was used to assay flavonoid composition. The Agilent HPLC system used consisted of a Model 1100 pump equipped with a multisolvent delivery system, an L-7400 (Hitachi) ultraviolet (UV) detector, and fitted with an Agilent C18 (5 μm,  mm) column. The mobile phase consisted of (A) 0.03 M phosphoric acid in water and (B) methanol. The mobile phase was filtered under vacuum through a 0.45 um membrane filter before use. The flow rate was maintained at 1 mL/min and UV absorbance was measured at 260–360 nm. The operating temperature was maintained at room temperature [19, 20]. Identification of the compounds was achieved by comparison of retention times with standards, UV spectra, and UV absorbance ratios after coinjection of samples and standards.

2.6. Determination of Antioxidant Activity
2.6.1. Ferric Reducing Antioxidant Potential (FRAP) Assay

The stock solutions consisted of 300 mM acetate buffer, 10 mM TPTZ (2,4,6-tripyridyl-S-triazine) solution in 40 mM HCl, and 20 mM FeCl3 solution. Acetate buffer (25 mL) and TPTZ (2.5 mL) were mixed, and 2.5 mL FeCl3 was added. Leaf extract (150 μL) was added to 2850 μL of the FRAP solution and kept for 30 min in the dark place. The absorbance of solution was measured at 593 nm using a spectrophotometer (U-2001, Hitachi Instruments Inc., Tokyo, Japan) [21].

2.6.2. 1,1-Diphenyl-2-picrylhydrazyl (DPPH) Assay

The radical scavenging ability was determined using the method described by Mensor et al. [22]. Briefly, an alcohol solution of DPPH (1 mL, 3 mg/mL) was added to 2.5 mL samples containing different concentrations of extracts. The samples were first kept in the dark at room temperature and their absorbance was read at 518 nm after 30 min. The antiradical activity was determined using the following formula: where is the absorbance value of the blank sample or control reaction and is the absorbance value of the test sample. The optic densities of the samples and controls were measured in comparison to ethanol. BHT (butylhydroxytoluene) and α-tocopherol were used as positive controls.

2.7. Determination of Anticancer Activity
2.7.1. Cell Culture and Treatment

Human breast carcinoma cell lines (MDA-MB-231) and normal human mammary epithelial cell (MCF-10A) were cultured in 100 μL of RPMI 1640 media (Roswell Park Memorial Institute) containing 10% fetal bovine serum (FBS). Cell lines were incubated overnight at 37°C in 5% CO2 for cell attachment.

2.7.2. MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium Bromide) Assay

The assay was conducted as follows: cancer cells were seeded in 96-well plates at a density of cells/well in 100 μL RPMI. At 24 h after seeding, the medium was removed and the cells were incubated for 3 days with RPMI in the absence or presence of various concentrations of curry leaf extracts. Extracts concentrations used ranged between 20, 40, 80, 160, 320, and 640 μg/mL. After incubation, 20 μL of MTT reagent was added into each well. The plate was incubated again in a CO2 incubator at 37°C for 4 h. The resulting MTT-products were determined by measuring the absorbance at 570 nm using ELISA reader [23]. Each point represents the mean of triplicate experiments. The cell viability was determined using the formula

2.8. Statistical Analysis

All analytical values shown represent the means of three replicates. Data were analysed using analysis of variance by Statistical Analysis System (SAS 9.0). Mean separation test between treatments was performed using Duncan multiple range test and a was regarded as significant.

3. Results and Discussion

3.1. Total Flavonoid Content and Composition

The results obtained from a preliminary analysis of flavonoid compounds are shown in Table 1. There was a significant difference in the total flavonoid (TF) content among the extract of curry leaf originated from different locations. The highest TF content was observed in the curry leaf from Kelantan ( mg/g DW) followed by that from Selangor ( mg/g DW) and Johor ( mg/g DW). In this study, six flavonoid compounds were identified in curry leaf extracts. The highest rutin concentration was observed in the plants from Selangor ( mg/g DW). Zhang et al. [24] identified rutin in the concentration of 0.356 mg/100 g DW in the curry leaf from Florida, USA. The samples from Kelantan showed a high quercetin content ( mg/g DW), but there was no significant location-specific difference in this parameter. As shown in Table 1, epicatechin was detected in the plants from two locations, Kelantan and Selangor, with the highest level observed in those from Kelantan ( mg/g DW).


Epicatechin ND
Naringin NDND

All analyses are the mean of triplicate measurements ± standard deviation. Results expressed in mg/g DW. Means not sharing a common letter were significantly different at .

Contrary to epicatechin, catechin was detected in the curry leaf from all locations and the highest catechin concentration was observed in the curry leaf extract from Kelantan ( mg/g DW). Naringin was detected only in the Kelantan extract ( mg/g DW). Myricetin is a flavonoid found in many herbs, fruits, and vegetables as well as other plants [25]. Myricetin exerts powerful biological effects including anticancer and antioxidant activities [26, 27]. The results showed that myricetin was the most abundant flavonoid in curry leaf and a high myricetin concentration was detected in the samples from Kelantan ( mg/g DW) followed by those from Selangor ( mg/g DW) and Johor ( mg/g DW). Figure 1 shows the HPLC chromatogram of curry leaf extracts from Kelantan location.

3.2. Total Phenolic Content and Identification of Phenolic Acids

Phenolics that exhibit antioxidant activity are known to be mainly flavonoids and phenolic acids. Phenolic acids are the major class of phenolic compounds widely occurring in the plant kingdom, especially in herbs and vegetables. As shown in Table 2, the curry leaf from Kelantan had the highest total phenolic (TP) content ( mg/g DW) followed by that from Selangor ( mg/g DW) and Johor ( mg/g DW). A significant difference () was observed between Kelantan and Selangor, while the difference between Selangor and Johor was insignificant. Wong et al. [28] investigated the TP content in 25 tropical plants and reported that curry leaf was the second after petai beans (26.4 mg/g DW) in regard to TP concentration. However, compared to some other medicinal herbs such as Melisa officinalis (13.2 mg/g DW), Taraxacum officinale (12.6 mg/g DW), Acorus calamus (12.45 mg/g DW), Echinacea purpurea (15.1 mg/g DW), Syzygium aromaticum (8.96 mg/g DW), and Salvia officinalis (8.25 mg/g DW), curry leaf exhibited a substantial TP content (12.02–14.37 mg/g DW) [29]. It is evident that the TP content measured by the Folin-Ciocalteu method does not reveal quality or quantity of the individual phenolic compounds present in plant extracts [30]. In the current study, three phenolic acids including gallic acid, cinnamic acid, and ferulic acid were identified in the curry leaf extracts from three locations. The curry leaf extract from Kelantan exhibited the highest concentration of gallic acid ( mg/g DW) compared to that from Selangor ( mg/g DW) and Johor ( mg/g DW). In addition, no significant difference was observed in the concentration of gallic acid between Kelantan and Selangor plants.


Gallic acid
Cinnamic acidND
Ferulic acid NDND
Vanillic acid

All analyses are the mean of triplicate measurements ± standard deviation. Results are expressed in mg/g DW. Means not sharing a common letter were significantly different at .

As Table 2 shows, cinnamic acid was not detected in the curry leaf from Kelantan, while the plants from Selangor exhibited a higher cinnamic acid content ( mg/g DW) than those from Johor ( mg/g DW). Ferulic acid in high concentrations was shown to inhibit photoperoxidation of linoleic acid [31]. The most interesting finding here was that ferulic acid could be detected only in the curry leaf extracts from Kelantan, which has not been previously reported. Vanillic acid was detected in curry leaf extracts from all locations and extracts from Kelantan exhibited the highest concentration of vanillic acid ( mg/g DW) compared to Selangor () and Johor ().

3.3. Antioxidant Activity
3.3.1. Ferric Reducing Antioxidant Potential (FRAP) Assay

The FRAP assay is based on the reduction of ferric tripyridyltriazine (Fe(III)-TPTZ) to ferrous tripyridyltriazine (Fe(II)-TPTZ) at low pH. The FRAP assay has been widely used to estimate the antioxidant content/power of dietary polyphenols [32]. As Figure 2 shows, the reducing power in the curry leaf extracts was in the range between 644.25 (Kelantan) and 563.42 μm of Fe(II)/g (Johor). The FRAP values for all three curry leaf extracts were significantly lower than those shown by the standard antioxidants, butylated hydroxytoluene (BHT) and vitamin C (715.1 and 1232.24 μmol Fe (II)/g, resp.). In this study, we used the FRAP assay because it is quick and simple in measuring the antioxidant capacity of different products including plants, wines, and animal tissues [33]. Many previous studies highlighted the potential role of flavonoids and phenolic acids of herbs and spices which may act as antioxidants [2, 5, 9, 22, 26, 29]. In general, the antioxidant activity of flavonoids is defined by the substitution pattern and structure of hydroxyl groups. In the flavonoid chemical structure, the 3′,4′-orthodihydroxy configuration in the ring B and the 4-carbonyl group in the ring C define the radical scavenging activity. The presence of 3- and 5-OH groups provides a catechol-like structure in the ring C, which is also essential for the antioxidant activity of flavonoids [29]. Furthermore, the presence of the C2-C3 double bond conjugated with a 4-keto group is responsible for electron delocalization from the ring B and enhancement of the free radical scavenging activity. In the absence of the o-dihydroxy structure in the ring B, a catechol structure in the ring A can compensate for the flavonoid antioxidant activity [34].

3.3.2. 1,1-Diphenyl-2-picrylhydrazyl (DPPH) Assay

The DPPH radical scavenging by antioxidants is thought to be due to their hydrogen-donating ability. Among the studied locations, the curry leaf extracts from Kelantan exhibited the highest DPPH scavenging activity (66.41%) followed by those from Selangor (60.23%) and Johor (5.76%). In addition, a significant difference in the DPPH activity was observed among the three locations (Figure 3). The results of the current study showed that the DPPH radical scavenging of the curry leaf extracts was lower than that of BHT (83.7%) and vitamin C (92.3%) at 20 mg/mL. The IC50 (fifty percent free radical scavenging) values were 8.65, 10.4, and 10.88 mg/mL for Kelantan, Selangor, and Johor extracts, respectively. The DPPH scavenging activity observed in this study was comparable to that reported by Marinova et al. [35] but higher than that shown by Odukoya et al. [36]. Analysis of the data presented in Figures 3 and 4 indicates that in curry leaf extracts the FRAP activity did not markedly differ from the free radical scavenging activity measured by the DPPH assay because both of these assays work by the same mechanism (single-electron transfer). Antioxidant compounds such as polyphenols may be more efficient as ferric reducing agents than free radical scavenges because of steric hindrance [29].

Pulido et al. [37] reported that in most cases the ability of antioxidants to reduce the ferric ion is correlated with the antioxidant parameters assessed by other methods including the DPPH radical scavenging assay. Arnous et al. [38] reported a strong correlation between the DPPH free radical scavenging ability and ferric ion reduction in wines.

3.4. Correlations between TF, TP, FRAP, and DPPH Activity

Table 3 shows that the FRAP activity had a significant positive correlation with TP (; ) and TF (; ) suggesting that in curry leaf the increase in the FRAP activity might be due to the increase in the TP and TF. Furthermore, the DPPH scavenging activity in curry leaf extracts demonstrated a significant positive correlation with TP (; ) and TF (; ). An interesting finding (Table 3) is that the FRAP activity showed more correlation with TF than with TP, while the DPPH activity correlated more with TF than TP. A linear correlation between the TP content and antioxidant capacity has been demonstrated in some previous studies [3941], while other found poor or no linear correlation between the total antioxidant activity and TP content [28, 42]. Our results confirm the importance of flavonoids and phenolics as the antioxidant agents in curry leaf extracts that significantly contribute to the total antioxidant capacity.



Represents significance at .

3.5. Anticancer Activity

A preliminary screening showed that curry leaf extracts from the three locations exhibited a significant anticancer activity against MDA-MB-231 cancer cells, with the inhibition rate of 67.2, 59.8, and 53.6% at concentration of 320 μg/mL from Kelantan, Selangor, and Johor, respectively (Figure 4). MDA-MB-231 cells treated with tamoxifen (positive control) showed 87.2% inhibition at the same concentration. The IC50 values (fifty percent free radical scavenging) of the curry leaf extracts from Kelantan, Selangor, and Johor for MDA-MB-231 cells were 103.4, 149.6, and 194.3 μg/mL, respectively. Flavonoids are among the most potent ingredients that underlie the protective effect of diets rich in fruits and vegetables with respect to colorectal cancer [42]. Hence, flavonoid compounds could probably be responsible for the anticancer activity of curry leaf. The American National Cancer Institute recommends considering crude herbal extracts that do not decrease the viability of normal cells below 76% [43] as safe for human consumption. In the current study, the highest flavonoid content and anticancer activity against MDA-MB-231 cells were demonstrated for the Kelantan curry leaf suggesting that the high anticancer activity in curry leaf extracts may be attributed to the high concentration of flavonoids such as myricetin, epicatechin, and quercetin known as potent anticancer agents. However, more research is needed for a better understanding of the association between these flavonoids and anticancer activity in curry leaf extracts.

This study produced results which corroborate the findings of a great deal of the previous work in this field. Mahenine, a carbazole alkaloid isolated from curry leaf, has been reported to induce apoptosis in human myeloid HL-60 cancer cells by downregulating cell survival factors and disrupting the cell cycle progression [4446]. Antitumorogenic activity of a curry leaf extract (stem bark) against MCF-7 breast cancer cells has been reported by Handral et al. [47].

Previous studies were focused on different varieties and species of Murraya koenigii from different sampling areas like India, Indonesia, and so forth. Environmental conditions such as soil, sunlight, temperature, rainfall, storage conditions, altitude as well as different harvesting procedures, method of collection and time, and manufacturing processes such as drying, selecting, extracting, and purifying can generate substantial variability in bioactive compounds and plant [48, 49]. Information about pharmaceutical quality of Malaysian curry leaf from different collection locations is rare and such data from current study could be useful for future studies. Meanwhile, the results of current study have shown that production of secondary metabolites and pharmaceutical quality of curry leaf was influenced by grown area in Malaysia.

In a herbal supplement, one ingredient may provide the desired therapeutic benefits while others may have toxic effects for humans. Malaysian herbs and spices may also contain certain toxic components which are not well investigated. In this study, the curry leaf extracts were evaluated as nontoxic for normal (MCF-10A) cells as the IC50 values were greater than 320 μg/mL (Figure 5). The viability of normal cells treated with the curry leaf extract from Kelantan at the IC50 (121.4 μg/mL) was 71.6%. According to the obtained results, all the curry leaf extracts showed toxic effects at the concentrations above 320 μg/mL: the IC50 values of Kelantan, Selangor, and Johor extracts for normal cells were 334.5, 352.8, and 377.2 μg/mL, respectively. Paranagama et al. [50] reported that the IC50 value for the toxic effect of curry leaf was 240 μg/mL.

4. Conclusions

The curry leaf with the highest TF and TP contents also showed the highest antioxidant activity as indicated by the FRAP and DPPH assays. Among the three studied locations, Kelantan plants which had high levels of phenolic acids (especially gallic acid) and flavonoids (especially myricetin, epicatechin, and quercetin) also exhibited a significant anticancer activity. Thus, the quantitative and qualitative analyses of major individual flavonoids and phenolics could provide an explanation for the correlation between the TP content and antioxidant capacity in curry leaf extracts. A wide concentration range of flavonoids and phenolic acids and variations in the antioxidant activity in curry leaf extracts could be due to several factors including growing location, altitude, climate, temperature, and diversity of natural vegetation in the area. Furthermore, the composition of phenolic acids and flavonoids and the related antioxidant activity can be useful for standardization of curry leaf extracts for further pharmaceutical applications. One of the more significant findings to emerge from this study is that the curry leaf extracts exhibited a promising anticancer activity on MDA-MB-231 human breast cancer cell line. The extracts contained substantial amounts of effective flavonoid compounds such as myricetin, epicatechin, and quercetin which showed potency in the growth inhibition of breast cancer cells. Subsequently, our MTT assay indicated that curry plants grown in the North of Malaysia (Kelantan) are a potential source of anticarcinogenic therapeutic compounds. More information on other bioactive components in curry leaf would help to further evaluate the anticancer activity of this medicinal plant.

Conflict of Interests

The authors declare that they have no conflict of interests.


The authors would like to thank the Ministry of Higher Education Malaysia and the Research Management Centre, University Putra Malaysia (UPM) for sponsoring this work. They are also grateful to the Malaysian Agriculture Research and Development Institute for collecting of plant samples. The authors would like to acknowledge all staff of Laboratory of Nutrition, Department of Nutrition and Dietetics, Faculty of Medicine and Health Sciences for all the help and guidance in order to accomplish this project.


  1. World Health Organization, Monographs on Selected Medicinal Plants, vol. 1, World Health Organization, 2009.
  2. A. Ghasemzadeh and H. Z. E. Jaafar, “Profiling of phenolic compounds and their antioxidant and anticancer activity in pandan (Pandanus amaryllifolius Roxb.) extracts from different locations of Malaysia,” BMC Complementary and Alternative Medicine, vol. 13, article 341, 2013. View at: Google Scholar
  3. S. J. Park, H. Myoung, Y. Y. Kim et al., “Anticancer effects of genistein, green tea catechins, and cordycepin on oral squamous cell carcinoma,” Journal of Oral and Maxillofacial Surgery, vol. 34, pp. 1–10, 2008. View at: Google Scholar
  4. U. J. Jung, M.-K. Lee, Y. B. Park, M. A. Kang, and M.-S. Choi, “Effect of citrus flavonoids on lipid metabolism and glucose-regulating enzyme mRNA levels in type-2 diabetic mice,” International Journal of Biochemistry and Cell Biology, vol. 38, no. 7, pp. 1134–1145, 2006. View at: Publisher Site | Google Scholar
  5. A. K. Atoui, A. Mansouri, G. Boskou, and P. Kefalas, “Tea and herbal infusions: their antioxidant activity and phenolic profile,” Food Chemistry, vol. 89, no. 1, pp. 27–36, 2005. View at: Publisher Site | Google Scholar
  6. A. García-Lafuente, E. Guillamón, A. Villares, M. A. Rostagno, and J. A. Martínez, “Flavonoids as anti-inflammatory agents: implications in cancer and cardiovascular disease,” Inflammation Research, vol. 58, no. 9, pp. 537–552, 2009. View at: Publisher Site | Google Scholar
  7. M. Dahlui, S. Ramli, and A. M. Bulgiba, “Breast cancer prevention and control programs in Malaysia,” Asian Pacific Journal of Cancer Prevention, vol. 12, no. 6, pp. 1631–1634, 2011. View at: Google Scholar
  8. I. C. W. Arts, D. R. Jacobs Jr., M. Gross, L. J. Harnack, and A. R. Folsom, “Dietary catechins and cancer incidence among postmenopausal women: The Iowa Women's Health Study (United States),” Cancer Causes and Control, vol. 13, no. 4, pp. 373–382, 2002. View at: Publisher Site | Google Scholar
  9. D. W. Lamson and M. S. Brignall, “Antioxidants and cancer III: quercetin,” Alternative Medicine Review, vol. 5, no. 3, pp. 196–208, 2000. View at: Google Scholar
  10. G. V. Satyavati, A. K. Gupta, and N. Tendon, Medicinal Plants of India, vol. 2, Indian Council of Medical Research, New Delhi, India, 1987.
  11. C. Ito, M. Itoigawa, K. Nakao et al., “Induction of apoptosis by carbazole alkaloids isolated from Murraya koenigii,” Phytomedicine, vol. 13, no. 5, pp. 359–365, 2006. View at: Publisher Site | Google Scholar
  12. F. Mohd Nor, M. Suhaila, I. N. Aini, and I. Razali, “Antioxidative properties of Murraya koenigii leaf extracts in accelerated oxidation and deep-frying studies,” International Journal of Food Sciences and Nutrition, vol. 60, no. 2, pp. 1–11, 2009. View at: Publisher Site | Google Scholar
  13. P. Muthumani, S. Venkatraman, K. V. Ramseshu et al., “Pharmacological studies of anticancer, anti inflammatory activities of Murraya koenigii (Linn) Spreng in experimental animals,” Journal of Pharmaceutical Sciences and Research, vol. 1, no. 3, pp. 137–141, 2009. View at: Google Scholar
  14. B. Dineshkumar, A. Mitra, and M. Mahadevappa, “Antidiabetic and hypolipidemic effects of mahanimbine (carbazole alkaloid) from Murraya koenigii (rutaceae) leaves,” International Journal of Phytomedicine, vol. 2, no. 1, pp. 22–30, 2010. View at: Publisher Site | Google Scholar
  15. S. V. Tembhurne and D. M. Sakarkar, “Hypoglycemic effects of fruit juice of Murraya koenigii (L) in alloxan induced diabetic mice,” International Journal of PharmTech Research, vol. 1, no. 4, pp. 1589–1593, 2009. View at: Google Scholar
  16. A. Crozier, E. Jensen, M. E. J. Lean, and M. S. McDonald, “Quantitative analysis of flavonoids by reversed-phase high-performance liquid chromatography,” Journal of Chromatography A, vol. 761, no. 1-2, pp. 315–321, 1997. View at: Publisher Site | Google Scholar
  17. D.-O. Kim, O. I. Padilla-Zakour, and P. D. Griffiths, “Flavonoids and antioxidant capacity of various cabbage genotypes at juvenile stage,” Journal of Food Science, vol. 69, no. 9, pp. C685–C689, 2004. View at: Google Scholar
  18. B. Sultana, F. Anwar, and M. Ashraf, “Effect of extraction solvent/technique on the antioxidant activity of selected medicinal plant extracts,” Molecules, vol. 14, no. 6, pp. 2167–2180, 2009. View at: Publisher Site | Google Scholar
  19. H. Bae, G. K. Jayaprakasha, J. Jifon, and B. S. Patil, “Extraction efficiency and validation of an HPLC method for flavonoid analysis in peppers,” Food Chemistry, vol. 130, no. 3, pp. 751–758, 2012. View at: Publisher Site | Google Scholar
  20. Standard Operating Protocol, HPLC Analysis of Phenolic Acids, CB0103, Botanical Center for Age-Related Diseases, West Lafayette, Ind, USA, 2001.
  21. I. F. F. Benzie and J. J. Strain, “The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: The FRAP assay,” Analytical Biochemistry, vol. 239, no. 1, pp. 70–76, 1996. View at: Publisher Site | Google Scholar
  22. L. Mensor, F. S. Menezes, G. G. Leitão et al., “Screening of Brazilian plant extracts for antioxidant activity by the use of DPPH free radical method,” Phytotherapy Research, vol. 15, no. 2, pp. 127–130, 2001. View at: Google Scholar
  23. C. B. S. Lau, C. Y. Ho, C. F. Kim et al., “Cytotoxic activities of Coriolus versicolor (Yunzhi) extract on human leukemia and lymphoma cells by induction of apoptosis,” Life Sciences, vol. 75, no. 7, pp. 797–808, 2004. View at: Publisher Site | Google Scholar
  24. M. Zhang, S. N. Hettiarachchy, R. Horax et al., “Phytochemicals, antioxidant and antimicrobial activity of Hibiscus sabdariffa, Centella asiatica, Moringa oleifera and Murraya koenigii leaves,” Journal of Medicinal Plants Research, vol. 5, no. 30, pp. 6672–6680, 2011. View at: Google Scholar
  25. K. H. Miean and S. Mohamed, “Flavonoid (myricetin, quercetin, kaempferol, luteolin, and apigenin) content of edible tropical plants,” Journal of Agricultural and Food Chemistry, vol. 49, no. 6, pp. 3106–3112, 2001. View at: Google Scholar
  26. F. Sun, X. Y. . Zheng, J. Ye, T. T. . Wu, Jl. Wang, and W. Chen, “Potential anticancer activity of myricetin in human T24 bladder cancer cells both in vitro and in vivo,” Nutrition and Cancer, vol. 64, no. 4, pp. 599–606, 2012. View at: Google Scholar
  27. R. Takasawa, A. Tao, K. Saeki et al., “Discovery of a new type inhibitor of human glyoxalase i by myricetin-based 4-point pharmacophore,” Bioorganic and Medicinal Chemistry Letters, vol. 21, no. 14, pp. 4337–4342, 2011. View at: Publisher Site | Google Scholar
  28. C.-C. Wong, H.-B. Li, K.-W. Cheng, and F. Chen, “A systematic survey of antioxidant activity of 30 Chinese medicinal plants using the ferric reducing antioxidant power assay,” Food Chemistry, vol. 97, no. 4, pp. 705–711, 2006. View at: Publisher Site | Google Scholar
  29. A. Wojdyło, J. Oszmiański, and R. Czemerys, “Antioxidant activity and phenolic compounds in 32 selected herbs,” Food Chemistry, vol. 105, no. 3, pp. 940–949, 2007. View at: Publisher Site | Google Scholar
  30. X. Wu, G. R. Beecher, J. M. Holden, D. B. Haytowitz, S. E. Gebhardt, and R. L. Prior, “Lipophilic and hydrophilic antioxidant capacities of common foods in the United States,” Journal of Agricultural and Food Chemistry, vol. 52, no. 12, pp. 4026–4037, 2004. View at: Publisher Site | Google Scholar
  31. S. Y. Wang, “Antioxidant capacity of berry crops, culinary herbs and medicinal herbs,” Acta Horticulture, no. 620, pp. 461–473, 2003. View at: Google Scholar
  32. A. Ghasemzadeh, H. Z. E. Jaafar, and A. Rahmat, “Antioxidant activities, total phenolics and flavonoids content in two varieties of malaysia young ginger (Zingiber officinale Roscoe),” Molecules, vol. 15, no. 6, pp. 4324–4333, 2010. View at: Publisher Site | Google Scholar
  33. A. Ghasemzadeh, H. Z. E. Jaafar, E. Karimi, and M. H. Ibrahim, “Combined effect of CO2 enrichment and foliar application of Salicylic acid on anthocyanin, flavonoids and isoflavonoids production and their antioxidant activity in ginger,” BMC Complementary and Alternative Medicine, vol. 12, article 229, 2012. View at: Google Scholar
  34. W. Bors, W. Heller, C. Michel, and M. Saran, “Radical chemistry of flavonoid antioxidants,” Advances in Experimental Medicine and Biology, vol. 264, pp. 165–170, 1990. View at: Google Scholar
  35. D. Marinova, F. Ribarova, and M. Atanassova, “Total phenolics and total flavonoids in Bulgaria fruits and vegetables,” Journal of the University of Chemical Technology and Metallurgy, vol. 40, pp. 255–260, 2005. View at: Google Scholar
  36. O. A. Odukoya, S. I. Inya-Agha, F. I. Segun, M. O. Sofidiyaand, and O. O. Ilori, “Antioxidant activity of selected Nigerian green leafy vegetables,” American Journal of Food Technology, vol. 2, no. 3, pp. 169–175, 2007. View at: Google Scholar
  37. R. Pulido, L. Bravo, and F. Saura-Calixto, “Antioxidant activity of dietary polyphenols as determined by a modified ferric reducing/antioxidant power assay,” Journal of Agricultural and Food Chemistry, vol. 48, no. 8, pp. 3396–3402, 2000. View at: Publisher Site | Google Scholar
  38. A. Arnous, D. P. Makris, and P. Kefalas, “Correlation of pigment and flavanol content with antioxidant properties in selected aged regional wines from Greece,” Journal of Food Composition and Analysis, vol. 15, no. 6, pp. 655–665, 2002. View at: Publisher Site | Google Scholar
  39. A. Ghasemzadeh, H. Z. E. Jaafar, and E. Karimi, “Involvement of salicylic acid on antioxidant and anticancer properties, anthocyanin production and chalcone synthase activity in ginger (Zingiber officinale Roscoe) varieties,” International Journal of Molecular Science, no. 13, pp. 14828–14844, 2012. View at: Google Scholar
  40. A. Djeridane, M. Yousfi, B. Nadjemi, D. Boutassouna, P. Stocker, and N. Vidal, “Antioxidant activity of some algerian medicinal plants extracts containing phenolic compounds,” Food Chemistry, vol. 97, no. 4, pp. 654–660, 2006. View at: Publisher Site | Google Scholar
  41. V. Katalinic, M. Milos, T. Kulisic, and M. Jukic, “Screening of 70 medicinal plant extracts for antioxidant capacity and total phenols,” Food Chemistry, vol. 94, no. 4, pp. 550–557, 2006. View at: Publisher Site | Google Scholar
  42. A. Ghasemzadeh and H. Z. E. Jaafar, “Antioxidant potential and anticancer activity of Malaysian young ginger (Zingiber officinale Roscoe) varieties grown under different CO2 concentration,” Journal of Medicinal Plants Research, vol. 5, no. 14, pp. 3247–3255, 2011. View at: Google Scholar
  43. A. Itharat, P. J. Houghton, E. Eno-Amooquaye, P. J. Burke, J. H. Sampson, and A. Raman, “In vitro cytotoxic activity of Thai medicinal plants used traditionally to treat cancer,” Journal of Ethnopharmacology, vol. 90, no. 1, pp. 33–38, 2004. View at: Publisher Site | Google Scholar
  44. M. K. Roy, V. N. Thalang, G. Trakoontivakorn, and K. Nakahara, “Mechanism of mahanine-induced apoptosis in human leukemia cells (HL-60),” Biochemical Pharmacology, vol. 67, no. 1, pp. 41–51, 2004. View at: Publisher Site | Google Scholar
  45. K. Bhattacharya, S. K. Samanta, R. Tripathi et al., “Apoptotic effects of mahanine on human leukemic cells are mediated through crosstalk between Apo-1/Fas signaling and the Bid protein and via mitochondrial pathways,” Biochemical Pharmacology, vol. 79, no. 3, pp. 361–372, 2010. View at: Publisher Site | Google Scholar
  46. S. Parmar, A. Gangwal, and N. Sheth, “Mast cell membrane stabilization and anti-histaminic actions possible mechanism of action of anti-inflammatory action of Murraya koenigii,” Journal of Current Pharmaceutical Research, vol. 2, no. 1, pp. 21–25, 2010. View at: Google Scholar
  47. K. H. Handral, P. Anup, and S. D. Shruthi, “A review on Murraya koenigii: multipotential medicinal plant,” Asian Journal on Pharmaceutical and Clinical Research, vol. 5, no. 4, pp. 5–14, 2012. View at: Google Scholar
  48. M. S. Vaibhav, D. Kamlesh, P. Manohar, and R. M. Kakasaheb, “Application of quality control principles to herbal drugs,” International Journal of Phytomedicine, vol. 1, pp. 4–8, 2009. View at: Google Scholar
  49. I. F. F. Benzie and S. Wachtel-Galor, Herbal Medicine: Biomolecular and Clinical Aspects, CRC Press, Taylor and Francis, 2nd edition, 2011.
  50. P. A. Paranagama, A. A. C. K. Adhikari, K. P. Abeywickrama, and K. A. N. P. Bandara, “Toxicity and repellant activity of Cymbopogon citratus (D.C.) Stapf. and Murraya koenigii Sprang. against Callosobruchus maculatus (F.) (Coleoptera, Bruchidae),” Tropical Agricultural Research and Extension, vol. 5, no. 1-2, 2002. View at: Google Scholar

Copyright © 2014 Ali Ghasemzadeh et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

More related articles

6119 Views | 2836 Downloads | 31 Citations
 PDF  Download Citation  Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

We are committed to sharing findings related to COVID-19 as quickly and safely as possible. Any author submitting a COVID-19 paper should notify us at help@hindawi.com to ensure their research is fast-tracked and made available on a preprint server as soon as possible. We will be providing unlimited waivers of publication charges for accepted articles related to COVID-19. Sign up here as a reviewer to help fast-track new submissions.