Advances in Pharmacological and Pharmaceutical Sciences

Advances in Pharmacological and Pharmaceutical Sciences / 2016 / Article

Research Article | Open Access

Volume 2016 |Article ID 6392656 |

Meryem El Jemli, Rabie Kamal, Ilias Marmouzi, Asmae Zerrouki, Yahia Cherrah, Katim Alaoui, "Radical-Scavenging Activity and Ferric Reducing Ability of Juniperus thurifera (L.), J. oxycedrus (L.), J. phoenicea (L.) and Tetraclinis articulata (L.)", Advances in Pharmacological and Pharmaceutical Sciences, vol. 2016, Article ID 6392656, 6 pages, 2016.

Radical-Scavenging Activity and Ferric Reducing Ability of Juniperus thurifera (L.), J. oxycedrus (L.), J. phoenicea (L.) and Tetraclinis articulata (L.)

Academic Editor: Robert Gogal
Received21 Oct 2015
Accepted14 Apr 2016
Published16 May 2016


Objective. The aim of this work is to study and compare the antioxidant properties and phenolic contents of aqueous leaf extracts of Juniperus thurifera, Juniperus oxycedrus, Juniperus Phoenicea, and Tetraclinis articulata from Morocco. Methods. Antioxidant activities of the extracts were evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical-scavenging ability, Trolox equivalent antioxidant capacity (TEAC), and ferric reducing antioxidant power (FRAP) assays. Also the total phenolic and flavonoids contents of the extracts were determined spectrophotometrically. Results. All the extracts showed interesting antioxidant activities compared to the standard antioxidants (butylated hydroxytoluene (BHT), quercetin, and Trolox). The aqueous extract of Juniperus oxycedrus showed the highest antioxidant activity as measured by DPPH, TEAC, and FRAP assays with IC50 values of μg/mL, μg/mL, and μg/mL, respectively. The strong correlation observed between antioxidant capacities and their total phenolic contents indicated that phenolic compounds were a major contributor to antioxidant properties of these plants extracts. Conclusion. These results suggest that the aqueous extracts of Juniperus thurifera, Juniperus oxycedrus, Juniperus phoenicea, and Tetraclinis articulata can constitute a promising new source of natural compounds with antioxidants ability.

1. Introduction

Researchers are now looking for natural antioxidants which do not have any side effects on human health. The search is underway to find out newer, effective, and safe antioxidants, in order to use them in foods and pharmaceutical preparations to replace the synthetic ones.

Medicinal plants are the major source of chemical compounds exhibiting antioxidant activity. Several studies have reported the interesting composition of Moroccan medicinal plants, including phenolic acids, flavonoids, and tannins, which are known for their health benefits as antioxidants [13].

The Moroccan flora contains more than 4200 vascular plant species. However, few ones were screened for pharmacological or chemical properties [4]. Among them, the Cupressaceae is the most common family of conifers (gymnospermae) throughout the world. In fact, they make a striking impression on the plant landscape of the mediterranean basin and are one of world’s biodiversity hotspots. The Cupressaceae grows up from the coast up to high altitudes, also able to develop in extreme ecological conditions and considered among the most important aromatic plants in the Moroccan traditional medicine.

Recent investigation has reaffirmed the validity of many of their traditional uses and reported that the extracts from Cupressaceae contain most of the important phenolic compounds, especially flavonoids, neolignans, and phenylpropanoids [57]. In this context and based on taxonomic criteria indicating close similarities between the four chosen species (Juniperus thurifera, Juniperus phoenicea, Juniperus oxycedrus, and Tetraclinis articulata), it is interesting to evaluate the chemotaxonomic and pharmacological differences characterizing this plant family. These species have many uses in traditional medicine in several parts of the world. Juniper berries are used as a spice, particularly in European cuisine, which are the only spice derived from conifers. In Morocco, Cupressaceae tar, leaves, and fruits are widely used to treat different hair and skin problems like dandruff, eczema, itchiness, and fungal infections [8]. Additionally, infusions of Cupressaceae species of dried leaves are used internally to treat rheumatism, diarrhea, and diabetes mellitus. These health benefits could be in part attributed to the potential effects of their antioxidants such as phenolic compounds on the reactive oxygen species produced in the human body [9, 10].

Therefore, the present study aims to determine and compare the antioxidant potential of aqueous leaf extracts of Juniperus thurifera, Juniperus phoenicea, Juniperus oxycedrus, and Tetraclinis articulata using DPPH free radical-scavenging activity (DPPH), Trolox equivalent antioxidant capacity (TEAC), and ferric reducing antioxidant power (FRAP) assays and moreover to determine their total phenolic contents and investigate the relationship between total phenolic content and antioxidant activity.

2. Material and Methods

2.1. Plant Materials

In February 2014, leaves of J. thurifera, J. Phoenicea, J. oxycedrus, and T. articulata were collected from wild populations located in Oukaimeden, Essaouira, Ourika, and Ait Issi Ihahan regions, respectively. The characteristics of collection sites are shown in Table 1. The leaves were identified by Pr. Fennane, and vouchers specimens were deposited at the herbarium of the Scientific Institute of Rabat and referred to as 79594 (J. thurifera), 79592 (J. phoenicea), 79588 (J. oxycedrus), and 79589 (T. articulata). The collected plant material was air-dried at room temperature (20–24°C). Leaves of dried plant were separated from plant and stored in tight-seal dark containers until use.

SpeciesCollection siteVoucher specimensLatitude/longitudeAltitude (m)Yield % (v/w)

JTOukaimeden79594N 31°14′/W 07°41′2700
JPEssaouira79592N 31°10′/W 09°30′724
JOOurika79588N 31°13′/W 08°03′1170
TAAit Issi Ihahan79589N 30°91′/W 09°43′1300

2.2. Preparation of Plant Extracts

To prepare the water extract, 10 g of dry powdered plant material was soaked in 100 mL of boiling distilled water and left to stand at room temperature for 30 min. The hot infusions were then filtered using Whatman filter paper and concentrated under vacuum on a rotary evaporator at 60°C and stored at 4°C for further use.

2.3. Antioxidant Activity
2.3.1. DPPH Free Radical-Scavenging Activity

The ability of water extracts of J. thurifera, J. Phoenicea, J. oxycedrus, and T. articulata to scavenge the DPPH radical was estimated using the method described by Şahin et al. [11]. An aliquot of 50 μL of various sample concentrations was added to a volume of 2 mL from the DPPH methanolic solution (60 μM). The reaction mixture was well shaken and incubated for 20 min at room temperature in the dark and the absorbance was recorded at 517 nm. The blank was constituted by methanol instead of the extract. Butylated hydroxytoluene (BHT) and quercetin were used as positive controls. The percentage inhibition of the DPPH radical by the samples was calculated using the following equation:where is the absorbance of control sample and is the absorbance of the test sample. The sample concentration providing 50% of inhibition (IC50) was determined from the plotted curve of inhibition using several concentrations.

2.3.2. Trolox Equivalent Antioxidant Capacity (TEAC) Assay

The ABTS free radical-scavenging activity of each sample was determined according to the method described by Loizzo et al. [12]. The ABTS radical cation was produced by reacting ABTS with potassium per sulfate. A mixture of ABTS (2 mM) and potassium persulfate (70 mM) was allowed to stand overnight at room temperature in the dark to form the radical cation ABTS, 16 h prior to use. The ABTS solution was then diluted with 80% methanol to obtain an absorbance of at 734 nm. 100 μL of appropriately diluted samples was added to 2 mL of ABTS solution and the absorbance was recorded at 734 nm after 1 min of incubation at room temperature. A standard curve was obtained by using Trolox standard solution at various concentrations (ranging from 0 to 0.24 μg/mL). The scavenging activity of different concentrations of extracts and fractions against ABTS radical were also measured to calculate IC50, and the procedure was similar to the DPPH scavenging method described above.

2.3.3. Reducing Power Determination

The ferric reducing capacity of extracts was investigated by using the potassium ferricyanide-ferric chloride method [13]. Briefly, 0.2 mL of each of the extracts at different concentrations, 2.5 mL of phosphate buffer (0.2 M, pH 6.6), and 2.5 mL of potassium ferricyanide K3Fe(CN)6 (1%) were mixed and incubated at 50°C for 20 min, to reduce ferricyanide into ferrocyanide. The reaction was stopped by adding 2.5 mL of 10% (w/v) trichloroacetic acid followed by centrifugation at 1000 rpm for 10 min. Finally, 2.5 mL of the upper layer was mixed with 2.5 mL of distilled water and 0.5 mL of FeCl3 (0.1%) and the absorbance was measured at 700 nm. The sample concentration providing 0.5 of absorbance (IC50) was calculated by plotting absorbance against the corresponding sample concentration. BHT and quercetin were used as a reference compound.

2.3.4. Determination of Total Phenolic Content

The total phenolic contents (TPC) were determined spectrophotometrically according to the Folin-Ciocalteu colorimetric method [14]. Briefly, 20 μL aliquot of extract solution was mixed with 1.16 mL of distilled water and 100 μL of Folin-Ciocalteu reagent, followed by the addition of 300 μL of Na2CO3 solution (20%). After 30 min of incubation at 40°C, the absorbance of the reaction mixture was measured at 760 nm. Gallic acid was used as a reference standard, and the results were expressed as microgram gallic acid equivalent (μg GAE)/mg dry weight of plant extract (edw).

2.3.5. Determination of Total Flavonoid Content

Total flavonoid content was measured by the aluminum chloride colorimetric assay [15]. 0.5 mL of the extracts or standard solution of quercetin was mixed with 0.5 mL of 2% AlCl3. After 1 hour at room temperature, the absorbance was measured at 420 nm. Total flavonoid content was expressed as microgram quercetin equivalent (μg QE)/mg dry plant extract (edw).

2.4. Statistical Analysis

All the assays were carried out in triplicate. The means and standard deviation (SD) were determined using SPSS version 20, the results of antioxidant activities and phenolic compounds composition are expressed as mean values ± SD, and the analysis of variance was performed to determine significant differences.

3. Results

3.1. Antioxidant Activities

Antioxidant activity is a complex procedure usually happening through several mechanisms and is influenced by many factors, which cannot be fully described with one single method. Therefore, it is essential to perform more than one type of antioxidant capacity measurement to take into account the various mechanisms of antioxidant action [1618]. In this study, three complementary tests were used to assess the antioxidant activity of J. thurifera, J. phoenicea, J. oxycedrus, and T. articulata infusions: DPPH free radical-scavenging activity, Trolox equivalent antioxidant capacity (TEAC), and reducing power assays.

As summarized in Table 2, the rank order of antioxidant potency was the same for all assays, namely, in decreasing order, J. oxycedrus, followed by J. thurifera, T. articulata, and J. oxycedrus.

AssaysInfusionsPositive control
J. thuriferaJ. phoeniceaJ. oxycedrusT. articulataBHTQuercetinTrolox


Values represent means ± SD (standard deviations) for triplicate experiments.

All extracts were able to reduce the stable, purple-coloured radical DPPH into yellow-coloured DPPH-H. The water extract obtained from J. oxycedrus had the strongest free radical-scavenging activity with IC50 value of μg/mL (Table 2). On the other hand the lowest capacity to reduce DPPH was observed in J. phoenicea water extract (IC50 = μg/mL).

All water extracts were less effective than the synthetic antioxidant BHT (IC50 = μg/mL) and quercetin (IC50 = μg/mL). Similarly, J. oxycedrus extract exhibited the best performance in ABTS and reducing power assays with IC50 = μg/mL and μg/mL, respectively.

3.2. Total Phenolic Compounds

The aqueous extracts of J. thurifera, J. phoenicea, J. oxycedrus, and T. articulata were characterized by the presence of considerable amount of phenolic compounds (Figure 1). The highest amount of total phenolics was found in J. oxycedrus with () μg GAE/mg edw, followed by J. thurifera () μg GAE/mg edw, T. articulata () μg GAE/mg edw, and J. phoenicea () μg GAE/mg edw.

3.3. Total Flavonoid Content

Concentration of flavonoids in investigated species ranged from 6.70 to 20.81 μg (QE)/mg edw (Figure 2). A high concentration of flavonoids was determined in J. oxycedrus accounting for , , and μg (QE)/mg edw in J. thurifera and T. articulata, respectively. The lowest flavonoid concentration was determined for J. phoenicea (μg (QE)/mg edw).

3.4. Relationship between Total Antioxidant Capacity and Phenolic Content

To evaluate the suitability and reliability of the three assay methods used to determine the total antioxidant capacities of the four Cupressaceae species, we performed correlation analysis of the values of total antioxidant capacity obtained by these methods. As shown in Table 3, all values were positive at significance level, indicating that the values of antioxidant capacities assayed by the three different methods were highly correlative. DPPH values were strongly correlated with the ABTS activities () and reasonably well correlated with the FRAP values (). The correlation between the ABTS and FRAP values was also highly significant ().



Correlation is significant at .
3.5. Correlation between Total Phenolic Content, Flavonoid Content, and Antioxidant Activity

The correlation between antioxidant capacity and phenolic content of the four Moroccan Cupressaceae samples is described in Table 3. The antioxidant activity data obtained from the DPPH method were highly correlated with the total phenolic contents () and total flavonoids concentration (). The total phenolic and flavonoid content also correlated well with the ABTS (; ) and FRAP values (; ).

4. Discussion

Oxidative stress has been implicated in several diseases including diabetes, rheumatoid arthritis, cardiovascular diseases, atherosclerosis, neurodegenerative diseases (Parkinson, Alzheimer, and Huntington), cancer, and aging [1921]. Natural antioxidants such as phenolic acids and flavonoid compounds from plants may offer resistance against the oxidative stress by scavenging free radicals, inhibiting lipid peroxidation, and by other mechanisms [22, 23]. Thus the present study was undertaken with the aim to show the antioxidant potentials of four Cupressaceae species known to be used in folk medicine in Morocco using three widely known methods (DPPH, ABTS, and FRAP) and also to establish the possible correlations between the antioxidant activity and total phenolic and flavonoid contents of the extracts.

In fact the used methods have different reaction mechanisms [24]. For instance, DPPH and ABTS assays are based on electron and H atom transfer, while the FRAP assay is based on electron transfer reaction [2426]. However, the three methods clearly indicated that the studied plants possess considerable antioxidant and antiradical activities.

Furthermore, well-pronounced correlations were observed between these methods which confirm that the three assays were all suitable and reliable for assessing total antioxidant capacities of the plant extracts.

The results of our screening on the four Cupressaceae species growing in Morocco showed that the leaf water extracts of J. oxycedrus have the strongest scavenging activity against DPPH (μg/mL), ABTS (μg/mL), and the best performance reducing power activity (μg/mL) followed by the leaf extract of J. thurifera (μg/mL (DPPH); μg/mL (ABTS); μg/mL (FRAP)), T. articulata (μg/mL (DPPH); μg/mL (ABTS); μg/mL (FRAP)), and J. phoenicea (μg/mL (DPPH); μg/mL (ABTS); μg/mL (FRAP)) (Table 2). This work also showed that the main polyphenolic class (flavonoid and phenolic acids) was common among the different species and some polyphenolic compounds have been identified previously in various studies for different Cupressaceae species [2730].

There have been diverse reports on antioxidant activity of a number of Cupressaceae species. The leaves and berries of J. phoenicea showing a strong antioxidant activity in ABTS and DPPH radical-scavenging activity test afforded several phenolics (tannins, anthocyanins, and flavonoids), which were stated to be the free radical scavengers in this plant [31]. In a study on antioxidant activity of the Turkish Juniperus [32], the aqueous and ethanolic extracts of the fruits and leaves from J. oxycedrus were examined using two different tests of the ferric reducing antioxidant power assay and DPPH radical-scavenging activity and most of them showed a potent antioxidant effect under those systems, which is in accordance with our data. High DPPH scavenging activity of Tetraclinis articulata leaves collected in Tunisia was also reported [33].

The strong correlations between the total antioxidant capacity assayed by DPPH, ABTS, and FRAP methods and the phenolic content (Table 3) indicate that the phenolic compounds largely contribute to the antioxidant activities of these Cupressaceae species and therefore could play an important role in the beneficial effects of these important medicinal plants. The results were in accordance with other researches, several studies have found that phenolic compounds are major antioxidant constituents in selected plants, and there are direct relationships between their antioxidant activity and total phenolic content [3437].

5. Conclusion

The findings obtained in this study support the traditional uses of those plant species as therapeutic agents. The higher antioxidant potential of those Moroccan Cupressaceae is conferred by their high phenolic content. J. oxycedrus presented the highest TPC, TFC, and antioxidant capacity values. In addition, there was a good correlation between phenolic content and antioxidant capacity of the leaves extracts. These results suggest that the water infusion from the leaves of J. thurifera, J. oxycedrus, J. phoenicea, and T. articulata constitutes a valuable source of antioxidant metabolites. Further investigations are required to identify their active metabolites.


DPPH:Free radical-scavenging activity
TEAC:Trolox equivalent antioxidant capacity
FRAP:Ferric reducing antioxidant power
BHT:Butylated hydroxytoluene
J. thurifera: Juniperus thurifera
J. phoenicea: Juniperus phoenicea
J. oxycedrus: Juniperus oxycedrus
T. articulata: Tetraclinis articulata
IC50:Concentration providing 50% inhibition
TPC:Total phenolic contents
TFC:Total flavonoid content
SD:Standard deviation.

Competing Interests

All contributing authors declare no competing interests.


The authors are thankful to Pr. Taoufik Jamal, Director of CeDoc, Faculty of Medicine and Pharmacy Rabat, for his kind support, encouragement, and interest in the research work, Dr. El Hassani Abdelmounaim, Engineer in the Regional Directorates of Water and Forests and Desertification Control, for his help to collect the plant material, Pr. Fennane Mohamed, Botanist of Scientific Institute, Rabat, for his help in identification of the species, and all members of the Laboratory of Pharmacology and Toxicology, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, Morocco, especially Pr. Zellou Amina and Doukkali Zohra, for their kind advice during the experimental work.


  1. L. Cherrat, L. Espina, M. Bakkali, R. Pagán, and A. Laglaoui, “Chemical composition, antioxidant and antimicrobial properties of Mentha pulegium, Lavandula stoechas and Satureja calamintha Scheele essential oils and an evaluation of their bactericidal effect in combined processes,” Innovative Food Science and Emerging Technologies, vol. 22, pp. 221–229, 2014. View at: Publisher Site | Google Scholar
  2. E. M. E. Ouariachi, I. Hamdani, A. Bouyanzer et al., “Chemical composition and antioxidant activity of essential oils of Thymus broussonetii Boiss. And Thymus algeriensis Boiss. From Morocco,” Asian Pacific Journal of Tropical Disease, vol. 4, no. 4, pp. 281–286, 2014. View at: Publisher Site | Google Scholar
  3. N. Chahmi, J. Anissi, S. Jennan, A. Farah, K. Sendide, and M. El Hassouni, “Antioxidant activities and total phenol content of Inula viscosa extracts selected from three regions of Morocco,” Asian Pacific Journal of Tropical Biomedicine, vol. 5, no. 3, pp. 228–233, 2015. View at: Publisher Site | Google Scholar
  4. F. Médail and P. Quéwel, “Biodiversity hotspots in the mediterranean basin: setting global conservation priorities,” Conservation Biology, vol. 13, no. 6, pp. 1510–1513, 1999. View at: Publisher Site | Google Scholar
  5. S. A. Abul'saeva and L. T. Pashinina, “Flavonoids of the needles of Juniperus sabina,” Chemistry of Natural Compounds, vol. 17, no. 6, p. 590, 1982. View at: Publisher Site | Google Scholar
  6. T. Nakanishi, Y. Inatomi, H. Murata et al., “Phytochemical study on American plants I. Two new phenol glucosides, together with known biflavones and diterpene, from leaves of Juniperus occidentalis Hook,” Chemical and Pharmaceutical Bulletin, vol. 50, no. 10, pp. 1358–1361, 2002. View at: Publisher Site | Google Scholar
  7. N. Iida, Y. Inatomi, H. Murata et al., “A new flavone xyloside and two new flavan-3-ol glucosides from Juniperus communis var. depressa,” Chemistry and Biodiversity, vol. 4, no. 1, pp. 32–42, 2007. View at: Publisher Site | Google Scholar
  8. Anon, “Final report on the safety assessment of Juniperus communis extract, Juniperus oxycedrus extract, Juniperus oxycedrus tar, Juniperus phoenicea extract, and Juniperus virginiana extract,” International Journal of Toxicology, vol. 20, no. 2, pp. 41–56, 2001. View at: Publisher Site | Google Scholar
  9. G. R. Schinella, H. A. Tournier, J. M. Prieto, P. M. De Buschiazzo, and J. L. Ríos, “Antioxidant activity of anti-inflammatory plant extracts,” Life Sciences, vol. 70, no. 9, pp. 1023–1033, 2002. View at: Publisher Site | Google Scholar
  10. Y. Z. Cai, Q. Luo, M. Sun, and H. Corke, “Antioxidant activity and phenolic compounds of 112 traditional Chinese medicinal plants associated with anticancer,” Life Sciences, vol. 74, no. 17, pp. 2157–2184, 2004. View at: Publisher Site | Google Scholar
  11. F. Şahin, R. Çakmakçi, and F. Kantar, “Sugar beet and barley yields in relation to inoculation with N2-fixing and phosphate solubilizing bacteria,” Plant and Soil, vol. 265, no. 1-2, pp. 123–129, 2004. View at: Publisher Site | Google Scholar
  12. M. R. Loizzo, D. Pacetti, P. Lucci et al., “ Prunus persica var. platycarpa (Tabacchiera Peach): bioactive compounds and antioxidant activity of pulp, peel and seed ethanolic extracts,” Plant Foods for Human Nutrition, vol. 70, no. 3, pp. 331–337, 2015. View at: Publisher Site | Google Scholar
  13. R. Tundis, F. Menichini, M. Bonesi et al., “Antioxidant and hypoglycaemic activities and their relationship to phytochemicals in Capsicum annuum cultivars during fruit development,” LWT—Food Science and Technology, vol. 53, no. 1, pp. 370–377, 2013. View at: Publisher Site | Google Scholar
  14. S. Arabshahi-Delouee and A. Urooj, “Antioxidant properties of various solvent extracts of mulberry (Morus indica L.) leaves,” Food Chemistry, vol. 102, no. 4, pp. 1233–1240, 2007. View at: Publisher Site | Google Scholar
  15. A. A. L. Ordoñez, J. D. Gomez, M. A. Vattuone, and M. I. Isla, “Antioxidant activities of Sechium edule (Jacq.) Swartz extracts,” Food Chemistry, vol. 97, no. 3, pp. 452–458, 2006. View at: Publisher Site | Google Scholar
  16. K. Schlesier, M. Harwat, V. Böhm, and R. Bitsch, “Assessment of antioxidant activity by using different in vitro methods,” Free Radical Research, vol. 36, no. 2, pp. 177–187, 2002. View at: Publisher Site | Google Scholar
  17. O. I. Aruoma, “Methodological considerations for characterizing potential antioxidant actions of bioactive components in plant foods,” Mutation Research—Fundamental and Molecular Mechanisms of Mutagenesis, vol. 523-524, pp. 9–20, 2003. View at: Publisher Site | Google Scholar
  18. S. P. Wong, L. P. Leong, and J. H. W. Koh, “Antioxidant activities of aqueous extracts of selected plants,” Food Chemistry, vol. 99, no. 4, pp. 775–783, 2006. View at: Publisher Site | Google Scholar
  19. B. M. Hybertson, B. Gao, S. K. Bose, and J. M. McCord, “Oxidative stress in health and disease: the therapeutic potential of Nrf2 activation,” Molecular Aspects of Medicine, vol. 32, no. 4–6, pp. 234–246, 2011. View at: Publisher Site | Google Scholar
  20. D. Liang, Q. Zhou, W. Gong et al., “Studies on the antioxidant and hepatoprotective activities of polysaccharides from Talinum triangulare,” Journal of Ethnopharmacology, vol. 136, no. 2, pp. 316–321, 2011. View at: Publisher Site | Google Scholar
  21. J. L. Rains and S. K. Jain, “Oxidative stress, insulin signaling, and diabetes,” Free Radical Biology and Medicine, vol. 50, no. 5, pp. 567–575, 2011. View at: Publisher Site | Google Scholar
  22. R. Masella, R. Di Benedetto, R. Varì, C. Filesi, and C. Giovannini, “Novel mechanisms of natural antioxidant compounds in biological systems: involvement of glutathione and glutathione-related enzymes,” Journal of Nutritional Biochemistry, vol. 16, no. 10, pp. 577–586, 2005. View at: Publisher Site | Google Scholar
  23. J. Dai and R. J. Mumper, “Plant phenolics: extraction, analysis and their antioxidant and anticancer properties,” Molecules, vol. 15, no. 10, pp. 7313–7352, 2010. View at: Publisher Site | Google Scholar
  24. R. L. Prior, X. Wu, and K. Schaich, “Standardized methods for the determination of antioxidant capacity and phenolics in foods and dietary supplements,” Journal of Agricultural and Food Chemistry, vol. 53, no. 10, pp. 4290–4302, 2005. View at: Publisher Site | Google Scholar
  25. B. Ou, D. Huang, M. Hampsch-Woodill, J. A. Flanagan, and E. K. Deemer, “Analysis of antioxidant activities of common vegetables employing oxygen radical absorbance capacity (ORAC) and ferric reducing antioxidant power (FRAP) assays: a comparative study,” Journal of Agricultural and Food Chemistry, vol. 50, no. 11, pp. 3122–3128, 2002. View at: Publisher Site | Google Scholar
  26. D. Huang, B. Ou, and R. L. Prior, “The chemistry behind antioxidant capacity assays,” Journal of Agricultural and Food Chemistry, vol. 53, no. 6, pp. 1841–1856, 2005. View at: Publisher Site | Google Scholar
  27. J. P. Lim, Y. C. Song, and J. W. Kim, “Free radical scavengers from the heartwood of Juniperus chinensis,” Archives of Pharmacal Research, vol. 25, no. 4, pp. 449–452, 2002. View at: Publisher Site | Google Scholar
  28. F. Martz, R. Peltola, S. Fontanay, R. E. Duval, J.-T. Riitta, and S. Stark, “Effect of latitude and altitude on the terpenoid and soluble phenolic composition of juniper (Juniperus communis) needles and evaluation of their antibacterial activity in the boreal zone,” Journal of Agricultural and Food Chemistry, vol. 57, no. 20, pp. 9575–9584, 2009. View at: Publisher Site | Google Scholar
  29. N. Miceli, A. Trovato, P. Dugo et al., “Comparative analysis of flavonoid profile, antioxidant and antimicrobial activity of the berries of Juniperus communis L. var. communis and Juniperus communis L. var. saxatilis Pall. from Turkey,” Journal of Agricultural and Food Chemistry, vol. 57, no. 15, pp. 6570–6577, 2009. View at: Publisher Site | Google Scholar
  30. M. M. Lesjak, I. N. Beara, D. Z. Orčić et al., “Juniperus sibirica Burgsdorf. as a novel source of antioxidant and anti-inflammatory agents,” Food Chemistry, vol. 124, no. 3, pp. 850–856, 2011. View at: Publisher Site | Google Scholar
  31. M. Ennajar, J. Bouajila, A. Lebrihi et al., “Chemical composition and antimicrobial and antioxidant activities of essential oils and various extracts of Juniperus phoenicea L. (Cupressacees),” Journal of Food Science, vol. 74, no. 7, pp. M364–M371, 2009. View at: Publisher Site | Google Scholar
  32. N. Orhan, I. E. Orhan, and F. Ergun, “Insights into cholinesterase inhibitory and antioxidant activities of five Juniperus species,” Food and Chemical Toxicology, vol. 49, no. 9, pp. 2305–2312, 2011. View at: Publisher Site | Google Scholar
  33. N. Herzi, S. Camy, J. Bouajila, P. Destrac, M. Romdhane, and J.-S. Condoret, “Supercritical CO2 extraction of Tetraclinis articulata: chemical composition, antioxidant activity and mathematical modeling,” The Journal of Supercritical Fluids, vol. 82, pp. 72–82, 2013. View at: Publisher Site | Google Scholar
  34. K. E. Heim, A. R. Tagliaferro, and D. J. Bobilya, “Flavonoid antioxidants: chemistry, metabolism and structure-activity relationships,” Journal of Nutritional Biochemistry, vol. 13, no. 10, pp. 572–584, 2002. View at: Publisher Site | Google Scholar
  35. Y.-Y. Soong and P. J. Barlow, “Antioxidant activity and phenolic content of selected fruit seeds,” Food Chemistry, vol. 88, no. 3, pp. 411–417, 2004. View at: Publisher Site | Google Scholar
  36. N. Balasundram, K. Sundram, and S. Samman, “Phenolic compounds in plants and agri-industrial by-products: antioxidant activity, occurrence, and potential uses,” Food Chemistry, vol. 99, no. 1, pp. 191–203, 2006. View at: Publisher Site | Google Scholar
  37. M. R. Loizzo, R. Tundis, M. Bonesi et al., “Radical scavenging, antioxidant and metal chelating activities of Annona cherimola Mill. (cherimoya) peel and pulp in relation to their total phenolic and total flavonoid contents,” Journal of Food Composition and Analysis, vol. 25, no. 2, pp. 179–184, 2012. View at: Publisher Site | Google Scholar

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