Comparative Study of Essential Oils Extracted from Egyptian Basil Leaves (Ocimum basilicum L.) Using Hydro-Distillation and Solvent-Free Microwave Extraction

Solvent-free microwave extraction (SFME) and conventional hydro-distillation (HD) were used for the extraction of essential oils (EOs) from Egyptian sweet basil (Ocimum basilicum L.) leaves. The two resulting EOs were compared with regards to their chemical composition, antioxidant, and antimicrobial activities. The EO analyzed by GC and GC-MS, presented 65 compounds constituting 99.3% and 99.0% of the total oils obtained by SFME and HD, respectively. The main components of both oils were linalool (43.5% SFME; 48.4% HD), followed by methyl chavicol (13.3% SFME; 14.3% HD) and 1,8-cineole (6.8% SFME; 7.3% HD). Their antioxidant activity were studied with the 2,2-diphenyl-1-picrylhydrazyl (DPPH•) radical scavenging method. The heating conditions effect was evaluated by the determination of the Total Polar Materials (TPM) content. The antimicrobial activity was investigated against five microorganisms: two Gram-positive bacteria, Staphylococcus aureus and Bacillus subtilis, two Gram-negative bacteria, Escherichia coli and Pseudomonas aeruginosa, and one yeast, Candida albicans. Both EOs showed high antimicrobial, but weak antioxidant, activities. The results indicated that the SFME method may be a better alternative for the extraction of EO from O. basilicum since it could be considered as providing a richer source of natural antioxidants, as well as strong antimicrobial agents for food preservation.


Introduction
Aromatic plants and EOs have been used since ancient times and are still widely used for their biological properties [1,2] and their applications in various industries: food, cosmetics, perfumery, and pharmacy [3]. Nowadays, EOs are attracting substantial interest from scientists because of their use in the treatment of certain infectious diseases for which synthetic antibiotics are becoming less and less active, or for preserving food against oxidation as alternatives to synthetic chemicals.
Ocimum basilicum L., named commonly as sweet basil, is a popular culinary herb belonging to the Lamiaceae family. O. basilicum known as lahbeq in Algeria [4] and called rehan in Arabic [5], is originally Traditionally, the basil leaves are used in folk medicine as a remedy for a large number of diseases, including cancer, convulsion, diarrhea, epilepsy, gout, nausea, sore throat, toothaches, and bronchitis [7][8][9]. It is also a source of EO containing biologically-active constituents which possess antioxidant and antimicrobial properties [3,[5][6][7][8][9]. The chemical composition of basil oil has been the subject of several studies. Basil oils have been classified into four chemotypes according to their chemical composition and geographical source. The European type, cultivated in Europe, USA, and Africa, is characterized by linalool and methyl chavicol as the major oil constituents. The Reunion type, located in the Comoros and Seychelles Islands, Africa, and Reunion Island, is characterized by a high concentration of methyl chavicol. Tropical type originated from India, Pakistan, Guatemala, Haiti, and Africa is rich in methyl cinnamate. Another basil chemotype, with eugenol as the main component, is common in North Africa, Russia, Eastern Europe, and parts of Asia [6,[10][11][12]. In addition to these, other basil oils have also been reported which contained various quantities of linalool, camphor, methyl chavicol, methyl cinnamate, and eugenol [13]. EOs are obtained from plants by various conventional and unconventional processes, such as mechanical pressing, maceration, solvent extraction, supercritical fluid and subcritical water extractions, and HD [14,15]. An original method, the solvent-free microwave extraction (SFME), has been developed and was patented in 2004 [16,17]. SFME is one of the newest techniques for EOs extraction assisted by microwaves, without any solvent or water, at atmospheric pressure. The advantages of using microwave energy are correlated to its effective heating and faster energy transfer and the fact that it is environmentally friendly [18][19][20]. To the best of our knowledge, there are no previous reports about the comparison of the chemical composition, antioxidant, and antimicrobial activities of the EO of O. basilicum L. leaves isolated by SFME and HD. Therefore, the aim of the present study is to provide data from the comparison between SFME and conventional HD in terms of extraction time, yield, chemical composition, antioxidant, and antimicrobial activities of EO extracted from Egyptian basil leaves.

Kinetics of Essential Oils Extracted by SFME and HD
Figures 1 and 2 represent the kinetics of EO obtained by SFME and HD from dry basil leaves. During the extraction process, the system temperature is equal to the boiling temperature of water at atmospheric pressure (100 °C). To reach this temperature, and thus obtain the distillation of the first EO droplet, it is necessary to heat the sample for only 5 min with SFME against 20 min for HD ( Figure 1). As shown on Figure 2, an extraction time of 30 min with SFME provides similar yields (0.48%˘0.02%) to those obtained after 60 min by HD. The results show that SFME is clearly advantageous with respect to conventional HD in terms of rapidity, efficiency, and substantial energy savings.
As shown on Figure 2, an extraction time of 30 min with SFME provides similar yields (0.48% ± 0.02%) to those obtained after 60 min by HD. The results show that SFME is clearly advantageous with respect to conventional HD in terms of rapidity, efficiency, and substantial energy savings.

Evaluation of Physical and Organoleptic Properties
Physical properties (specific gravity, refractive index, and solubility) and sensory evaluation of EO extracted by SFME and HD from the basil samples are shown in Table 1. There are no significant differences observed between the physical constants of the EO obtained by these two methods. The only difference resides in the color of the EO extracted by SFME which was lighter than that isolated by the classical method. The SFME method offers the possibility for a better reproduction of natural aroma of basil essential oil than the HD method.

Chemical Composition of the Essential Oils Obtained by SFME and HD
The components identified by GC and GC-MS in basil (EOs) from both methods are reported in Table 2. The EO of basil leaves isolated either by SFME or HD contains the same dominant components. Among 65 compounds identified in basil EO, representing 99.3 and 99.0% of the total oils obtained by SFME and HD, respectively, monoterpene, sesquiterpene, and derivatives of phenylpropanoid compounds were identified. Monoterpenes are the main components in the EOs but the relative amounts differ for the two extraction methods. The oxygenated compounds: monoterpene alcohol linalool is the most abundant component in basil EO (43.5% for SFME and 48.4% for HD) followed by methyl chavicol (13.3% for SFME and 14.3% for HD) and 1,8-cineole (6.8% for SFME and 7.3% for HD). Slightly lower amounts of oxygenated compounds (89.8% vs. 89.6%) and higher amounts of hydrocarbons (9.7% vs. 9.2%) are present in the EO of basil extracted

Evaluation of Physical and Organoleptic Properties
Physical properties (specific gravity, refractive index, and solubility) and sensory evaluation of EO extracted by SFME and HD from the basil samples are shown in Table 1. There are no significant differences observed between the physical constants of the EO obtained by these two methods. The only difference resides in the color of the EO extracted by SFME which was lighter than that isolated by the classical method. The SFME method offers the possibility for a better reproduction of natural aroma of basil essential oil than the HD method.

Chemical Composition of the Essential Oils Obtained by SFME and HD
The components identified by GC and GC-MS in basil (EOs) from both methods are reported in Table 2. The EO of basil leaves isolated either by SFME or HD contains the same dominant components. Among 65 compounds identified in basil EO, representing 99.3 and 99.0% of the total oils obtained by SFME and HD, respectively, monoterpene, sesquiterpene, and derivatives of phenylpropanoid compounds were identified. Monoterpenes are the main components in the EOs but the relative amounts differ for the two extraction methods. The oxygenated compounds: monoterpene alcohol linalool is the most abundant component in basil EO (43.5% for SFME and 48.4% for HD) followed by methyl chavicol (13.3% for SFME and 14.3% for HD) and 1,8-cineole (6.8% for SFME and 7.3% for HD). Slightly lower amounts of oxygenated compounds (89.8% vs. 89.6%) and higher amounts of hydrocarbons (9.7% vs. 9.2%) are present in the EO of basil extracted by SFME in comparison with HD. The chemical profile of the basil EO, isolated by SFME and HD in our study, was comparable to that reported by Figueredo et al. [21].   1 Compounds are listed in order of their classes. Compositional values less than 0.1% are denoted as traces (tr). Presence of a compound is indicated by its GC-FID percentage with S.D. = standard deviation, absence is indicated by "-"; 2 RI = retention indices are determined on HP-1 and INNOWAX column using the homologous series of n-alkanes (C8-C24); 3 Correct isomer not identified.
A substantial number of studies conducted on the composition of the EO of basil revealed a huge diversity in the constituents of its oil with different chemotypes from many regions of the world. It can be described from Table 3 that the major constituents which have been isolated from different O. basilicum oils include linalool, methyl chavicol, eugenol, methyl cinnamate, 1,8-cineole, bergamotene, limonene, camphor, α-cardinol, geraniol, etc. [22]. In the Brazilian basil leaf EOs [23], linalool, geraniol, and 1,8-cineole are the major compounds corroborating with Oman basil [5], as well as Poland [24] basil. For Czech Republic [25], Guinea [26], and Reunion [18], the major compounds of basil EO are linalool and eugenol. Marotti et al. [10] reported the presence of linalool, methyl chavicol, and eugenol as main components of Italian basil EO. It was also reported that four major compounds characterize the basil EO of Austria: linalool, methyl chavicol, methyl cinnamate, and α-cadinol [27]. These results are consistent with those obtained in previous works in Bulgaria [28] and USA [29]. In O. basilicum EO from Romania [30], linalool was reported as the main component. The major compounds of EO extracted from Algeria [31] leaves of basil, were linalool, linalyl acetate, elemol, and geranyl acetate. However, the first major compound from French Polynesia basil leaf EOs [32] is methyl cinnamate. Regarding Pakistan basil [33], four major compounds were found: linalool, epi-α-cardinol, α-bergamotene, and γ-cadinene. In the case of Egypt basil oils, Ismail [34] has reported linalool, 1,8-cineole, eugenol, and methyl cinnamate as dominant components. Concerning basil from Turkey, Chalchat et al. [35] cited three major compounds: methyl chavicol, limonene, and p-cymene. Additionally, the EO from Madagascar [36], Iran [37], and Thailand [38] is rich in methyl chavicol. On the other hand, Purkayastha [39] reported that camphor, followed by limonene and β-selinene were the major compounds in O. basilicum EO from Northeast India. According to Simon et al. [6], the Egyptian basil is very similar to the European, characterized by linalool and methyl chavicol as the major oil constituents that were in agreement to our results that the essential oil of basil belonged to the linalool-rich type. The observed difference in the constituents of basil EOs between countries may be probably due to environmental conditions and genetic factors, different chemotypes, and the nutritional elements of the plants, as well as other factors that can influence the oil composition.

Antioxidant Activity
The free radical scavenging activity of basil EOs was measured by the DPPH assay. The DPPHr adical is one of the most commonly used substrates for the fast evaluation of antioxidant activity because of its stability in radical form and the simplicity of the assay. O. basilicum EOs were able to reduce the stable, purple-colored radical DPPH·into yellow-colored DPPH-H [40]. The results of antioxidant activity of O. basilicum EO are reported in Figure 3 (the experiments were done in triplicate). It can be seen that O. basilicum EO extracted by SFME exhibited a dose dependent increase with a radical scavenging effect of 86.13%˘2.8% at 20 mg/mL, which is higher than the DPPH% inhibition of the O. basilicum EO extracted by HD (76.13%˘2.6%) at the same concentration. The DPPH% inhibition of the α-tocopherol (90.74%˘0.2%) at 5 mg/mL is higher than the DPPH% inhibition of the O. basilicum. DPPH scavenging activity is usually presented by the value of IC 50 (concentration that inhibits 50% of the DPPH radical). A comparison between the DPPH scavenging activity of O. basilicum EOs (SFME-EO IC 50 = 3.6 mg/mL, HD-EO IC 50 = 8.1 mg/mL) and those expressed by α-tocopherol (IC 50 = 0.8 mg/mL) showed that the EO exhibited weakest antioxidant effects than α-tocopherol (vitamin E). Therefore, the antioxidant effect of the oil was about four times lower for SFME-EO and 10 times lower for HD-EO than that of the standard antioxidant. Previous studies have shown that O. basilicum has potent antioxidant properties [5,[41][42][43][44][45]. Our findings are in agreement with Hadj-Khelifa et al. [31] who reported that O. basilicum EO containing linalool as a major compound exhibited lower antioxidant effects (IC 50 = 83.4 mg/mL) than the vitamin E (IC 50 = 22.0 mg/mL). Hussain et al. [33] showed that sweet basil EO which is rich in linalool offered antioxidant activity comparable to synthetic antioxidant BHT. However, Bozin et al. [46] found that basil oil containing methyl chavicol (45.8%) and linalool (24.2%) as major components exhibited very strong RSA, reducing the DPPH radical formation (IC 50 ) in the range of 0.4 µg/mL, and indicated that the most responsible compounds were the oxygenated phenolic monoterpene methyl chavicol and the mixture of mono and sesquiterpene hydrocarbons. Quite a different situation was observed by Mahmoud et al. [47], which found that the main component methyl chavicol exhibit a moderate antioxidant activity (DPPH assay). Also, Dawidowicz et al. [48] which showed that the main component methyl chavicol, do not exhibit antioxidant properties. The antioxidant properties of basil EOs (I% about 46.1%˘1.3%) result from the properties of other components, especially methyl eugenol that was considered as the main contributors of the antioxidant activity in the EO of Myrtus communis L. [49]. Politeo et al. [27] clearly suggests that the antioxidant capacity (IC 50 values of 1.4 g/L) of total EO is due only or mainly to the presence of eugenol (5.9%) in its chemical composition and that other constituents do not have significant effect on eugenol capacity. The antioxidant activity of eugenol has been reported several times, tested on various systems [50][51][52]. In accordance, Pripdeevech et al. [53] reported that the EO of O. basilicum from Thailand (linalool/eugenol chemotype) exhibited high scavenging ability of DPPH radicals (IC 50 = 26.53˘0.94 µg/mL). The same finding was reported by Dabire et al. [54] who showed that the decrease in the rate of eugenol in EO of O. basilicum causes a decrease of its antioxidant power. Lee et al. [29] also found that eugenol (0.896 mg/g) was the main contributor of the antioxidant activity of volatile extract of basil than major components. Hence, the main component does not always determine the antioxidant activity of the examined EOs. It is possible that components present at lower concentrations might be involved in some type of synergy with other active compounds. Our study indicated than the antioxidant activity of SFME-EO was relatively more active than HD-EO. As a result, the antioxidant activity of O. basilicum EO may be attributed to the higher content of linalool, methyleugenol, eugenol, and other minor components.  [33] showed that sweet basil EO which is rich in linalool offered antioxidant activity comparable to synthetic antioxidant BHT. However, Bozin et al. [46] found that basil oil containing methyl chavicol (45.8%) and linalool (24.2%) as major components exhibited very strong RSA, reducing the DPPH radical formation (IC50) in the range of 0.4 μg/mL, and indicated that the most responsible compounds were the oxygenated phenolic monoterpene methyl chavicol and the mixture of mono and sesquiterpene hydrocarbons. Quite a different situation was observed by Mahmoud et al. [47], which found that the main component methyl chavicol exhibit a moderate antioxidant activity (DPPH assay). Also, Dawidowicz et al. [48] which showed that the main component methyl chavicol, do not exhibit antioxidant properties. The antioxidant properties of basil EOs (I% about 46.1% ± 1.3%) result from the properties of other components, especially methyl eugenol that was considered as the main contributors of the antioxidant activity in the EO of Myrtus communis L. [49]. Politeo et al. [27] clearly suggests that the antioxidant capacity (IC50 values of 1.4 g/L) of total EO is due only or mainly to the presence of eugenol (5.9%) in its chemical composition and that other constituents do not have significant effect on eugenol capacity. The antioxidant activity of eugenol has been reported several times, tested on various systems [50][51][52]. In accordance, Pripdeevech et al. [53] reported that the EO of O. basilicum from Thailand (linalool/eugenol chemotype) exhibited high scavenging ability of DPPH radicals (IC50 = 26.53 ± 0.94 μg/mL). The same finding was reported by Dabire et al. [54] who showed that the decrease in the rate of eugenol in EO of O. basilicum causes a decrease of its antioxidant power. Lee et al. [29] also found that eugenol (0.896 mg/g) was the main contributor of the antioxidant activity of volatile extract of basil than major components. Hence, the main component does not always determine the antioxidant activity of the examined EOs. It is possible that components present at lower concentrations might be involved in some type of synergy with other active compounds. Our study indicated than the antioxidant activity of SFME-EO was relatively more active than HD-EO. As a result, the antioxidant activity of O. basilicum EO may be attributed to the higher content of linalool, methyleugenol, eugenol, and other minor components.

Oil Enrichment and Heating Test
All the samples containing OO displayed close TPM values before heating but the total heating times required to reach the maximal TPM value of 25% were quite different: 4.7 ± 0.1 h for OO, 6.6 ± 0.1 h for OO-HD-EO and 7.8 ± 0.1 h for OO-SFME-EO ( Figure 4). Hence, the efficient EO supplementation of OO would significantly prolong the OO shelf life. The results show a high level of stability of virgin OO enriched with basil EO, especially those isolated by SFME. These results are in good agreement with other findings in the literature [55][56][57], which TPM effect might be attributed to

Oil Enrichment and Heating Test
All the samples containing OO displayed close TPM values before heating but the total heating times required to reach the maximal TPM value of 25% were quite different: 4.7˘0.1 h for OO, 6.6˘0.1 h for OO-HD-EO and 7.8˘0.1 h for OO-SFME-EO ( Figure 4). Hence, the efficient EO supplementation of OO would significantly prolong the OO shelf life. The results show a high level of stability of virgin OO enriched with basil EO, especially those isolated by SFME. These results are in good agreement with other findings in the literature [55][56][57], which TPM effect might be attributed to the phenolic compounds present in the EO, although there is no specific report carried out about basil oils on fried OO.

Antimicrobial Activity
The antimicrobial activity of sweet basil oil was tested against five pathogenic microorganisms. The results obtained from disc diffusion method ( Figure 5), followed by measurement of minimum inhibitory concentration (MIC) represented in Table 4, indicated that S. aureus was the most sensitive microorganisms showing largest inhibition zones (38-33 mm) and lowest MIC values (18-25 μL/mL). The lowest activity was observed against E. coli with the smallest inhibition zones (26-22 mm) and highest MIC value (25-30 μL/mL). Furthermore, growth inhibition was also prone to fungi C. albicans with inhibition zones (34-31 mm) and MIC value (30-40 μL/mL). Overall, the EOs of basil displayed a broad antimicrobial spectrum and exerted a much stronger antimicrobial effect against Gram-positive than against Gram-negative bacteria. These results are in accordance with the literature data [41,46]. The antimicrobial activity of the basil EO obtained by SFME is relatively higher than that obtained with HD. The EO of O. basilicum has been reported previously to have a good antimicrobial activity against a wide range of microorganisms [28,37,46,58,59]. Many authors have linked basil antimicrobial effects to the presence of high content of linalool. Thereby, Hussain et al. [33] reported that O. basilicum EO and linalool showed greater activity against bacterial strains than antifungal strains. Additionally, Hanif et al. [5] showed that Omani basil EO founded with higher linalool exhibited strong antibacterial activity against all the bacteria tested except P. putida and P. aeruginosa. Ouibrahim et al. [60] studied the antibacterial activity of Algerian basil EO, which is rich in linalool, against a wide range of Gram-negative and Gram-positive bacteria. They found that this oil is efficient in all tested bacterial strains except P. aeruginosa. Sienkiewicz et al. [61] demonstrated that basil oils containing mainly methyl chavicol (86.4%) can be widely used to eliminate clinical strains of E. coli found in different clinical conditions. Moghaddam et al. [62] revealed that the EO predominantly contains methyl chavicol (87.6%), which has antibacterial activity against all of the tested bacteria. These findings contradict those obtained by Lopez et al. [63] who reported that methyl chavicol has no relevance in the antimicrobial effects of the tested basil EOs in the vapor phase. By comparing the results of other researchers, it is possible to notice that for EOs tested, no significant correlation between the antibacterial activity and the percentage of the major components has been found. The different antibacterial activity exhibited by the oils, can be explained by either the synergistic effect of the different components in the oil and/or by the presence of other components that may be active even in small concentrations [43,64,65]. The antibacterial activity of EO from O. basilicum may be due in part to the presence of high content of linalool and methyl chavicol as the main components. However, between the two extracts of sweet basil, SFME-EO was relatively more active than HD-EO, which

Antimicrobial Activity
The antimicrobial activity of sweet basil oil was tested against five pathogenic microorganisms. The results obtained from disc diffusion method ( Figure 5), followed by measurement of minimum inhibitory concentration (MIC) represented in Table 4, indicated that S. aureus was the most sensitive microorganisms showing largest inhibition zones (38-33 mm) and lowest MIC values (18-25 µL/mL). The lowest activity was observed against E. coli with the smallest inhibition zones (26-22 mm) and highest MIC value (25-30 µL/mL). Furthermore, growth inhibition was also prone to fungi C. albicans with inhibition zones (34-31 mm) and MIC value (30-40 µL/mL). Overall, the EOs of basil displayed a broad antimicrobial spectrum and exerted a much stronger antimicrobial effect against Gram-positive than against Gram-negative bacteria. These results are in accordance with the literature data [41,46]. The antimicrobial activity of the basil EO obtained by SFME is relatively higher than that obtained with HD. The EO of O. basilicum has been reported previously to have a good antimicrobial activity against a wide range of microorganisms [28,37,46,58,59]. Many authors have linked basil antimicrobial effects to the presence of high content of linalool. Thereby, Hussain et al. [33] reported that O. basilicum EO and linalool showed greater activity against bacterial strains than antifungal strains. Additionally, Hanif et al. [5] showed that Omani basil EO founded with higher linalool exhibited strong antibacterial activity against all the bacteria tested except P. putida and P. aeruginosa. Ouibrahim et al. [60] studied the antibacterial activity of Algerian basil EO, which is rich in linalool, against a wide range of Gram-negative and Gram-positive bacteria. They found that this oil is efficient in all tested bacterial strains except P. aeruginosa. Sienkiewicz et al. [61] demonstrated that basil oils containing mainly methyl chavicol (86.4%) can be widely used to eliminate clinical strains of E. coli found in different clinical conditions. Moghaddam et al. [62] revealed that the EO predominantly contains methyl chavicol (87.6%), which has antibacterial activity against all of the tested bacteria. These findings contradict those obtained by Lopez et al. [63] who reported that methyl chavicol has no relevance in the antimicrobial effects of the tested basil EOs in the vapor phase. By comparing the results of other researchers, it is possible to notice that for EOs tested, no significant correlation between the antibacterial activity and the percentage of the major components has been found. The different antibacterial activity exhibited by the oils, can be explained by either the synergistic effect of the different components in the oil and/or by the presence of other components that may be active even in small concentrations [43,64,65]. The antibacterial activity of EO from O. basilicum may be due in part to the presence of high content of linalool and methyl chavicol as the main components. However, between the two extracts of sweet basil, SFME-EO was relatively more active than HD-EO, which might be attributed to the high contents of (E)-methyl cinnamate, methyl eugenol, eugenol, and other oxygenated compounds in SFME-EO. might be attributed to the high contents of (E)-methyl cinnamate, methyl eugenol, eugenol, and other oxygenated compounds in SFME-EO. 1 Diameter of inhibition zone (mm) including disc diameter of 6 mm; 2 Each value is the mean ± SD of three replications.

Plant Materials
Sweet basil broken leaves (9.4%˘0.4% of humidity) were purchased from Dios herbarium of organic agriculture product, F26410-Chatillon in Dios-France. Ocimum basilicum L. were collected from Egypt in 2011 and n˝28587.

Solvent-Free Microwave Apparatus and Procedure
SFME was performed in a Milestone "DryDist" microwave laboratory (Milestone, Bergamo, Italy). This is a multimode 2.45 MHz microwave reactor with a maximum delivered power of 1000 W. Temperature was monitored by use of an external infrared (IR) sensor. During experiments, time, temperature, pressure, and power can be controlled. The experiment was conducted at atmospheric pressure with 150 g of O. basilicum immersed in water (600 g) during 30 min at 600 W. The plant material was heated by using a fixed power density of 1.0 W¨g´1 for 30 min. A cooling system outside the microwave cavity condensed the distillate continuously with a Clevenger-type apparatus. Condensed water was returned to the flask and heating was continued at 100˝C until no more essential oil was obtained. The essential oil was collected, dried over anhydrous sodium sulfate, and stored at 4˝C until used.

Hydro-Distillation Apparatus and Procedure
In this method, 150 g of O. basilicum immersed in 6 L water were submitted to hydro-distillation with a Clevenger-type apparatus for 1 h (until no more essential oil was obtained). The essential oil was collected, dried with anhydrous sodium sulfate, and stored at 4˝C until used.

Gas Chromatography by Flame Ionic Detector (FID)
GC analysis was carried out using an Agilent 6890N gas chromatograph, under the following operation conditions: vector gas, Helium; injector and detector temperatures, 250˝C; injected volume, 1.0 µL; split ratio 1/100; HP1 column (J and W Scientific, Folsom, CA, USA), polydimethylsiloxane (50 mˆ0.20 mm i.d., film thickness 0.33 µm; constant flow 1 mL/min) and INNOWAX (polyethyleneglycol, 50 mˆ0.20 mm i.d.ˆfilm thickness 0.4 µm; Interchim, Montluçon, France). Temperature program 45-250˝C at 2˝C/min and 250˝C for 60 min. Retention indices were determined with C5 to C24 alkane standards as reference. Relative amounts of individual components are based on peak areas obtained without FID response factor correction. Three replicates were performed for each sample. The average of these three values and the standard deviation were determined for each component identified.

Identification of the Components
Identification of the components was based on computer matching against commercial libraries (Wiley, MassFinder 2.1 Library, and NIST98), laboratory mass spectra libraries built up from pure substances, and MS literature data [66][67][68][69] combined with comparison of GC retention indices (RI) on apolar and polar column. RIs were calculated with the help of a series of linear alkanes C8-C24 on apolar and polar column (HP-1 and HP-INNOWAX). Compounds available in the laboratory were confirmed by external standard compound co-injection.

Physical Constants and Organoleptic Properties
Basil essential oils have been analyzed according to the standard method AFNOR [70]. The usual physical constants (specific gravity and refractive index) defining the EO have been determined at 20˝C. The organoleptic properties of the two basil EOs (SFME-EO and HD-EO) were analyzed by sensory evaluation. These tests were conducted by a panel comprising 10 graduate students from the University of Oran 1 Ahmed Benbella, Algeria. The samples presented to each panelist were evaluated as seen on Table 1 according to the following attributes: color, odor, and aspect.

Antioxidant Activity
The antioxidant activity of the O. basilicum EO was evaluated by the DPPH assay. DPPH (2,2-diphenyl-1-picrylhydrazyl) is a stable, highly-colored free radical that can abstract labile hydrogen atoms from phenolic antioxidants with concomitant formation of a yellow hydrazine (DPPH-H) [40]. The free radical-scavenging activity (RSA) of an extract can be expressed as the percentage of DPPH reduced by a given amount of extract. RSA was measured, following the modified method of Achat et al. [55]. Briefly, O. basilicum oil was subjected to serial dilutions in methanol to obtain different concentrations (2-20 mg/mL). 50 µL of each solution were added to 2 mL of a DPPH solution (2ˆ10´4 mol/L in methanol) and the mixture was left in the dark at room temperature for 30 min. The absorbance was then measured at 517 nm using a spectrophotometer. Free radical inhibition by DPPH was calculated in percent (%) according to the following equation: A 0 : absorbance of DPPH solution without any antioxidant. A i : absorbance of DPPH solution after reaction with EO. All experiments were performed in triplicate. The IC 50 value, which represents the EO concentration that caused neutralization of 50% DPPH radicals, was determined from the plot of the inhibition percentage against concentration. The capacity of each antioxidant was compared with the α-tocopherol (vitamin E) standard using the same methodology for various concentrations (0.2-5 mg/mL).

Heating Conditions
The effect of heating conditions was studied through the determination of the amount of total polar materials (TPMs) which assemble the different groups of altered compounds (free fatty acids, mono and diglycerides) and the oxidation and polymeric derivatives, all formed at temperatures below 180˝C (French law No. 86-857) [71]. 200 µg of either SFME-EO or HD-EO were added to 200 g of virgin olive oil (OO). The samples were then heated under domestic frying conditions, i.e., at (180˘5)˝C during several hours [56]. The temperature was monitored by a thermocouple (ATC-300) inserted directly into the domestic deep-fat electric fryers. All samples were analyzed before the first heating session and then every hour until degradation of the oil. The end of the heating assay was reached according to the maximum TPM value of 25% as tolerated by the French law (Article 3-3 of decree No. 86-857 of 18/07/86) and as mandatory in several countries [71]. The TPM percentage is determined using a Testo probe which tests quickly the quality of oil via the measurement of the dielectric constant. All the measurements were performed in duplicate.

Disc Diffusion Method
Antimicrobial activities of the essential oils were determined by the paper disc diffusion method [72,73]. For these assays, cultures of the following microorganisms were used: two Gram-positive (Staphylococcus aureus ATCC 6538 and Bacillus subtilis ATCC 6633), two Gram-negative (Escherichia coli ATCC 25922 and Pseudomonas aeruginosa ATCC 14028) bacteria, and one yeast (Candida albicans ATCC 10231). All microorganisms were supplied by the Algerian Pasteur Institute. The cultures of microorganisms were maintained on nutrient agar (NA) medium. Briefly, suspensions of the tested microorganisms (10 7 -10 8 colony-forming units (CFU)/mL) were spread on the solid Muller-Hinton medium plates. Filter paper discs, 6 mm diameter (Whatman No. 1), were individually impregnated with 10 µL EO then placed onto the surfaces of the inoculated plates. A positive control containing microbial culture without the EO and a negative control containing only the medium were performed as well. At the end of the incubation time (24 h at 37˝C for bacteria and 25˝C for yeast), positive antibacterial and antifungal activities were established by the presence of a measurable inhibition zone and recorded in its width (mm) which includes the disc diameter. Each test was performed in three replicates.

Determination of the Minimum Inhibitory Concentration (MIC)
For the determination of the MIC, which represents the concentration that completely inhibits the growth of microorganisms, a micro dilution broth susceptibility assay was used as recommended by Chemat et al. [74]. Dilution series were made in a concentration range from 10 µL to 40 µL/mL of the EO in sterile test tubes containing nutrient broth (NB) medium. Using a vortex, each tube was vigorously stirred in order to perfectly disperse the EO in the culture medium. Then, 15 µL of the tested microorganism suspension (10 7 -10 8 colony-forming units (CFU)/mL) were inoculated into a test tube and incubated for 24 h in an oven at 37˝C for bacteria and 25˝C for yeast. A positive control containing microbial suspension without the EO and a negative control containing only the medium were performed. The MIC value was assimilated to the smallest concentration of the samples that did not become turbid. Each test was performed three times.

Conclusions
The solvent-free microwave extraction (SFME) technique has been compared with the conventional hydro-distillation (HD) method, for extraction of EO from Egyptian basil (O. basilicum L.) leaves. SFME was found to be highly effective enabling a considerable reduction in extraction time (30 min for SFME against 60 min for HD), providing an EO with yields similar to those of conventional HD. GC-MS results indicated that there were no significant differences between the constituents of EO obtained by SFME and those obtained by conventional HD. The results reported on the chemical composition of basil oil reveal that linalool represents the main compound in basil oil. Both essential oils SFME-EO and HD-EO indicate strong antimicrobial and low antioxidant activities and also a notable TPM effect. However, SFME-EO showed a better antimicrobial activity than HD-EO against all tested microorganisms, a greater antioxidant activity in the DPPH ‚ test and displayed an improved stability to virgin OO. SFME can be considered as a green technology that offers significant advantages over traditional hydro-distillation: shorter extraction times with similar yields, substantial energy and solvent saving, environmentally friendly approach, and lower cost. Thus, this method appears to be a good alternative for the extraction of EO from sweet basil for their applications in the food, pharmaceutical, and cosmetic industries.