Influence of drying and extraction methods on yield and chemical composition of the essential oil of Satureja hortensis

The aerial parts of Satureja hortensis, cultivated in Iran (Research Station of Alborz, Karaj), were collected at the full-flowering stage and dried by three different drying methods (sun-drying, shade-drying and oven-drying at 45 °C). The essential oils of every treatment were obtained by hydro-distillation of the aerial parts. In addition, the essential oil of shade-dried sample was obtained by two other distillation methods (water- and steam-distillation and direct steam-distillation). The oils were analyzed by capillary GC and GC–MS. Statistical analysis showed no significant difference between oil yield (w/w) of the oven-dried sample (1.06%) compared to shade-dried (0.94%) and sun-dried (0.87%). The oil content of the shade-dried sample, obtained by hydro-distillation, was higher (0.94%) than that of the steam-distilled (0.27%). Twenty-three components were identified in the oil of S. hortensis in the different drying methods, including carvacrol (46.0–48.1%) and γ-terpinene (37.7–39.4%) as main components. Seventeen compounds were characterized in the oils of different distillation methods, including carvacrol (12.3–46%) and γ-terpinene (37.7–70.4%). Although the drying methods had no significant effect on oil composition of S. hortensis, the distillation changed the percentage of main components sharply (significant at 1%). The steam-distillation method produced the lowest amount of carvacrol and highest amount of γ-terpinene. The results showed that extraction by hydro-distillation gave the best results for S. hortensis, based on oil yield and carvacrol percentage.     

Drying Sage (Salvia officinalis L.) Plants and Its Effects on Content, Chemical Composition, and Radical Scavenging Activity of the Essential Oil

Chemical composition and antioxidant activity of Salvia officinalis essential oil (EO) were studied under different drying methods of plant material. Results obtained showed that dried plant material yielded more essential oils than did the fresh one. The highest EO yields were obtained by infrared drying at 45?°C (0.39%) followed by air drying (0.30%) and oven drying at 45?°C (0.26%). The analysis of EOs by gas chromatography?Cmass spectrometry, showed in each of 55 identified compounds belonging mostly to oxygenated monoterpenes. This class of compounds was significantly affected by following drying methods: oven at 65?°C, microwave (500?W), and infrared at 45?°C. The main components of sage EO, 1,8-cineole, ?? and ??-thujone, camphor, viridiflorol, and manool showed significant variation (p?<?0.05) with drying methods. Their concentrations increased significantly, particularly when drying sage at ambient air. Finally, the screening of antioxidant activity of the different sage EOs using the di(phenyl)-(2,4,6-trinitrophenyl)iminoazanium radical (DPPH) assay showed an appreciable reduction of the stable radical DPPH, although microwave drying was the most efficient method with an IC50 of 1.60% as compared with fresh plant (IC50?=?5.32).     

Composition of oregano essential oil (Origanum vulgare) as affected by drying method

The influence of the drying method on volatile compounds of Origanum vulgare was evaluated. The drying methods tested were convective (CD) at 60 °C and vacuum-microwave (VMD), as well as a combination of convective pre-drying and VM finish-drying (CPD–VMFD). The volatile compounds of fresh and dried oregano were extracted by steam-hydrodistillation and analyzed by GC–MS. Oregano drying kinetics was described by a simple exponential model for CD and CPD–VMFD, while VMD kinetics consisted of two periods: linear until a critical point and exponential beyond that point. Thirty-four compounds were tentatively identified, with carvacrol, thymol, and γ-terpinene, being the major components. The total volatiles concentration of fresh oregano (33.0 g kg⁻¹) decreased significantly during drying, independently of the method used (CD: 10.2 g kg⁻¹, CPD–VMFD: 13.1 g kg⁻¹, and VMD: 27.9 g kg⁻¹). The final conclusion was that VM dehydrated Polish oregano was of better aromatic quality than that dried using hot air.     

Effects of drying methods on qualitative and quantitative properties of essential oil of two basil landraces

Sweet basil, a plant that is extensively cultivated in some countries, is used to enhance the flavour of salads, sauces, pasta and confectioneries as both a fresh and dried herb. To determine the effect of drying methods on qualitative and quantitative characteristics of the plant and essential oil of basil, two landraces, Purple and Green, were dried in sunlight, shade, mechanical ovens at 40 °C and 60 °C, a microwave oven at 500 W and by freeze-drying. For comparison, the essential oils of all samples were extracted by hydrodistillation and analyzed using GC and GC–MS. The highest essential oil yields (v/w on dry weight basis) were obtained from shade-dried tissue in both landraces followed by the freeze-dried sample of the purple landrace and the fresh sample of green landrace. Increasing the drying temperature significantly decreased the essential oil content of all samples. Significant changes in the chemical profile of the essential oils from each of the landrace were associated with the drying method, including the loss of most monoterpene hydrocarbons, as compared with fresh samples. No significant differences occurred among several constituents in the extracted essential oils, including methyl chavicol (estragole), the major compound in the oil of both landraces, whether the plants were dried in the shade or sun, oven at 40 °C or freeze-dried, as compared with a fresh sample. The percentage methyl chavicol in the oil, however, decreased significantly when the plant material was dried in the oven at 60 °C or microwaved. In addition, linalool, the second major compound in the purple landrace, and geranial and neral, major compounds in the green landrace, decreased significantly when the plant tissue was dried in the oven at 60 °C or microwaved.     

Composition of peel essential oils from four selected Tunisian Citrus species: Evidence for the genotypic influence

The peel essential oils from four selected Tunisian Citrus species: sweet orange (Citrus sinensis Osbeck), mandarin (Citrus reticulata Blanco); sour orange (Citrus aurantium L.) and pummelo (Citrus grandis Osbeck), cultivated under the same pedoclimatic and cultural conditions have been analysed by gas chromatography (GC) and gas chromatography–mass spectrometry (GC–MS). The essential oils content ranged from 1.06% to 4.62% (w/w) in pummelo and mandarin, respectively. The qualitative and quantitative analysis led to the identification of 70 components in all oil samples. The analysed oils consist mainly in monoterpene hydrocarbons (97.59–99.3%), with limonene (92.52–97.3%) and β-pinene (1.37–1.82) being the major constituents. The remaining chemical classes were weakly represented (<1%). Both qualitative and quantitative differences between oil samples have been observed and numerous components have been proposed as marker compounds. Since the influence of different environmental factors has been eliminated, the observed chemical variability between the studied species and cultivars seems likely to results from the genetic variability.     

Loss of essential oil of tarragon (Artemisia dracunculus L.) due to drying

The effect of hot air‐drying on the essential oil constituents and yield in French and Russian tarragon (Artemisia dracunculus L.) leaves was studied. The tarragon leaves were dried at air temperatures ranging from 40 to 90 °C. The drying stopped when the moisture content of the samples reached 10% or for some of the treatments reached 7, 20 and 30%. The essential oil of the fresh and dried leaves was isolated by hydrodistillation and analysed by capillary gas chromatography and gas chromatography–mass spectrometry. The decrease of oil during the drying process was highest at 60 °C drying temperature. For French tarragon the decrease in the amount of oil was significantly lower at 90 °C. The effect of the relative humidity of the drying air at each temperature was not significant. The main compounds were estragole in French tarragon (69%) and sabinene in Russian tarragon (40%). The drying process changed the relative percentage of the constituents in the oil; for instance, the relative percentages of estragole decreased and sabinene increased in French tarragon. Copyright © 2006 Society of Chemical Industry     

Comparison of essential oils of clove buds extracted with supercritical carbon dioxide and other three traditional extraction methods

Supercritical fluid extraction (SFE) of essential oil from clove buds with CO₂ was explored. The effect of different parameters, such as temperature (30 °C, 40 °C, 50 °C), pressure(10 MPa, 20 MPa, 30 MPa) and particle size (three degree index), on the extraction yield and the content of eugenol in extracts was investigated using three-level orthogonal array design. The experimental results show that the temperature has the largest effect on the eugenol content of the extracts, and particle size has the maximum effect on the oil yield. The essential oil of 19.56% yield, in which the maximum content of eugenol in extracts is 58.77%, can be extracted from clove buds at pressure of 10 MPa and temperature of 50 °C. Essential oil of clove buds obtained by SFE, hydrodistillation, steam distillation and Soxhlet extraction were further analyzed by gas chromatography/mass spectrometric detection to compare the extraction methods. Twenty three compounds in the clove oils have been identified, showing that the composition of the clove oil extracted by different methods is mostly similar, whereas relative concentration of the identified compounds is apparently different. General characteristics of the clove oils obtained by different methods were further compared, and SFE is considered as the optimum process among the four processes for obtaining clove oil with high quality.     

Variations in essential oil and fatty acid composition during Myrtus communis var. italica fruit maturation

The essential oil and fatty acid composition of Myrtus communis var. italica fruit during its ripening was determined. The effect of the harvesting time on some physical properties of Myrtus fruits, fruit weight and moisture content, were significant. The increase of fruit weight (from 2.54 to 8.79 g% fruits) during ripeness was correlated positively with that of moisture content (from 28% to 72%). Fruit essential oil yields varied from 0.003% to 0.01% and showed a remarkable increase at 60 days after flowering to reach a maximum of 0.11%. Forty-seven volatile compounds were identified in fruit essential oils; 1,8-cineole (7.31–40.99%), geranyl acetate (1.83–20.54%), linalool (0.74–18.92%) and α-pinene (1.24–12.64%) were the main monoterpene compounds. Total fatty acid contents varied from 0.81% to 3.10% during fruit maturation and the predominant fatty acids were linoleic (12.21–71.34%), palmitic (13.58–37.07%) and oleic (6.49–21.89%) acids. The linoleic acid proportions correlated inversely with palmitic and oleic acids during all the stages of ripening.     

Changes produced in the aroma compounds and structural integrity of basil (Ocimum basilicum L) during drying

The influence of drying on the aroma compounds, from a chemical and sensory standpoint, and on the structural integrity of basil (Ocimum basilicum L) was evaluated. The drying methods tested were oven drying at 45 °C, air drying at room temperature and freeze‐drying. The volatile compounds of fresh and dried basil were extracted and concentrated by simultaneous distillation/extraction and analysed by gas chromatography/mass spectrometry. In all, 27 volatile components were identified, linalool being the major component, followed by eugenol. The total quantity of volatiles of fresh basil decreased considerably during oven drying and freeze‐drying, whereas air drying of basil at room temperature brought about only small losses of volatile components. The cell damage produced on basil leaves during drying was evaluated by scanning electron microscopy. From a sensory standpoint, fresh basil was described as having a fresh, herbaceous and floral odour, while the dried samples had a mentholated, spicy, hay‐like and earthy odour. Copyright © 2004 Society of Chemical Industry     

Chemical diversity in curry leaf (Murraya koenigii) essential oils

Wild and cultivated Murraya koenigii leaf essential oils collected from ten Indian locations were investigated for their chemical diversity. The essential oil yields ranged from 1.2–2.5 ml/kg biomass. GC and GC-MS analyses revealed ninety compounds, constituting 93.8–99.9% of the essential oils. The highest concentrations of α-pinene (55.7%) and β-pinene (10.6%) were found in the essential oil of wild plants. α-Pinene (13.5–35.7%) and/or β-phellandrene (14.7–50.2%) were the dominant essential oil constituents of seven locations. (E)-Caryophyllene (26.5%, 31.5%) and α-selinene (9.5%, 10.4%) were the principal essential oil components of two locations. The odour profiles of the essential oils were distinctly different. Tetradecanoic acid, hexadecanoic acid, piperitone, cada-1,4-diene,1,10-di-epi-cubenol, γ-eudesmol, α-muurolol, (Z,E)-farnesol and (Z,Z)-farnesol are identified for the first time in curry leaf essential oil. The chemical diversity of the oils offers opportunity to flavourists to choose curry leaves and essential oils with preferential flavour composition.     

不同干燥方式对橘皮精油和黄酮的影响

采用晒干、阴干、烘干及真空干燥4种方式对橘皮进行处理,研究不同干燥方式对橘皮精油含量、精油组分和黄酮含量的影响。结果表明,烘干得到的橘皮精油含量最高为2.11%,其次是晒干(1.91%)、真空干燥(1.95%)和阴干(1.65%)。通过GC-MS分析,新鲜及4种干燥方式得到的橘皮精油共鉴定出23种组分,主要成分为D-柠檬烯。橘皮中的精油组分主要分为6类,分别是萜烯类、醇类、醛类、酚类、醚类及苯类。干燥之后橘皮中的黄酮含量均有所下降,其中阴干橘皮中黄酮含量最高为15.73 mg/g,其次是烘干为15.49 mg/g。综合比较四种干燥方法,烘干干燥时间短,不受天气影响,得到的橘皮精油及黄酮含量均比较高,因此烘干更适合橘皮的干燥。     

Isomerisation kinetics and antioxidant activities of β-carotene in carrots undergoing different drying techniques and conditions

Carrots are known as a natural source of β-carotene. In order to preserve the latter, carrots must generally be processed, and drying is one of the most common methods for processing carrots. During drying β-carotene in carrots suffers degradation. β-Carotene degradation is generally due to thermal degradation and isomerisation. In this work, the drying kinetics as well as the isomerisation kinetics and antioxidant activities of β-carotene in carrots undergoing hot air drying, vacuum drying and low-pressure superheated steam drying (LPSSD) were determined within the temperature range of 60–80 °C and, in the case of vacuum drying and LPSSD, at a pressure of 7 kPa. A high performance liquid chromatography (HPLC) method was used to determine the β-carotene contents and its isomerisation kinetics, while the antioxidant activities of various combinations of all-trans- and cis-forms of β-carotene in carrots were evaluated using the Trolox equivalent antioxidant capacity (TEAC) assay.     

泰国罗勒挥发油的提取工艺优化、组成分析及感官评价

该研究考察SO3微热爆（SO3 Micro-Thermal Explosion,STEX）预处理辅助提取泰国罗勒挥发油的工艺,并对所得挥发油化学成分和香气轮廓进行比较分析。结果表明：阴干和SD（水上蒸馏）法是最优的干燥方式和提取方法;STEX预处理的最佳工艺为SO3与干物质质量比1:3、预处理温度50 ℃、预处理时间30 min,此条件下挥发油得率为0.56%,相比于SD法和WD（水中蒸馏）法分别提高了41.41%和90.48%;放大验证实验中挥发油得率可进一步提高至0.60%;扫描电镜观察发现STEX预处理后的罗勒表面微观结构发生明显改变,表面皱缩严重,气孔扩张明显;元素和红外分析结果显示,STEX预处理会显著提高罗勒S元素含量（p<0.05）,但不影响其化学官能团构成;经GC-MS鉴定,WD、SD和STEX-SD来源的挥发油均以甲基胡椒酚和甲基丁香酚为主,其中,STEX-SD来源的挥发油可鉴定化合物31种,种类最多;感官评价结果表明,三种挥发油均以茴香和柠檬香为主,但STEX-SD来源的挥发油具有更明显的香气。STEX可作为一种预处理方法用于提高罗勒等芳香性植物挥发油的得率和香气品质。     

Essential oil composition of Pterospartum tridentatum grown in Portugal

The essential oils, isolated by hydrodistillation and distillation-extraction, from the aerial parts of different populations of Pterospartum tridentatum collected during the flowering phase, at different locations in Portugal, were analysed by GC and GC–MS. All the P. tridentatum populations studied afforded a yellowish oil in a yield <0.05% (v/w). cis-Theaspirane (2–14%), trans-theaspirane (2–17%) and octen-3-ol (2–37%) were, in variable amounts, the dominant components of the oils. Cluster analysis of the essential oil compositions from the nine populations studied, confirmed a major chemical variability.     

Phytochemical composition and antimicrobial activities of the essential oils from Satureja subspicata Vis. growing in Croatia

The present study describes the phytochemical profile and antimicrobial activity of Satureja subspicata Vis. essential oils, collected in Dalmatia (Croatia). Three samples of essential oils were obtained from the aerial parts of the plant by hydrodistillation and analyzed by GC–MS. From the 24 compounds representing 97.47% of the oils, carvacrol (16.76%), α-pinene (13.58), p-cymene (10.76%), γ-terpinene (9.54%) and thymol methyl ether (8.83%) appear as the main components. The oils also contained smaller percentages of myrcene, linalool, β-caryophyllene, limonene, geranyl acetate, 1-Octen-3-ol, nerol, thymol and borneol. Furthermore, antimicrobial activity of the oil was evaluated using agar diffusion and broth microdilution methods. The antimicrobial test results showed that the oils had a great potential antimicrobial activity against all 13 bacteria and 9 fungal strains. Gram-positive bacteria are more sensitive to the investigated oil, with a range of 0.09 to 6.25 μl/ml than Gram-negative bacteria in the range which is significantly higher from 1.56 to 25.00 μl/ml. Results presented here may suggest that the essential oil of S. subspicata possesses antimicrobial properties, and is therefore a potential source of antimicrobial ingredients for the food and pharmaceutical industry.     

Chemical composition and antioxidant and antimicrobial activity of two Satureja essential oils

Hydro-distilled volatile oils from the aerial parts of Satureja montana L., and Satureja subspicata Bartl. ex Vis., growing wild in Bosnia and Herzegovina, were analyzed by GC/MS. More than one hundred compounds were identified in both plant oils, representing 92.4–98.1% of the total oil. The major constituents of essential oils obtained from the plant material of S. montana, collected from two different localities, were thymol (31.7%), and geraniol (22.3%), respectively. The most abundant compounds in essential oils of S. subspicata, collected at two different stages of development, were thymol (28.6%), and spathulenol (37.6%), respectively. The screening of antimicrobial activity of essential oil samples was individually evaluated against Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Pseudomonas aeruginosa and Bacillus subtilis using a paper disc diffusion method. All tested microorganisms were inhibited by essential oil samples. Antioxidant activity was tested using the DPPH radical-scavenging method. All samples showed activity comparable to thymol, which was used as a positive probe.     

Changes in fatty acid and essential oil composition of sage (Salvia officinalis L.) leaves under NaCl stress

Fatty acids and essential oils from hydroponically cultivated Salvia officinalis leaves were analyzed by GC and GC–MS. Four different levels of NaCl (25, 50, 75 and 100 mM) were applied. The first results showed that salt treatment reduced significantly the plant growth by 61% and the total fatty acids (TFA) content by 32% at 100 mM NaCl. Alpha-linolenic, gadoleic, palmitic and oleic acids were the major fatty acids. Moreover, the polyunsaturated fatty acids decreased, while the monounsaturated ones increased with respect to increasing salinity. Regarding the essential oil composition, the main compounds were α-and β-thujone, 1,8-cineole, camphor, α-humulene, viridiflorol and manool at all salt treatments. The yield had a maximum increase at 75 mM NaCl. Hence, sage can be considered as moderately salt sensitive.     

Quantity and chemical composition of essential oil of peppermint (Mentha × piperita L.) leaves under different drying methods

This work was aimed at quantitative and qualitative analyses of the essential oil of peppermint leaves under different drying methods. Thin layer drying experiments of the leaves were performed in shade, hot air dryer (at temperatures of 50°C, 60°C, and 70°C), and microwave oven (at power levels of 200, 400, and 800 W). Essential oils of the fresh and dried samples were extracted by hydrodistillation and analyzed using gas chromatography-mass spectrometry (GC/MS). The highest (22.24 g/kg _{dry matter}) and the lowest (1.33 g/kg _{dry matter}) oil yields were obtained from the hot air-dried leaves at temperature of 50°C and microwave-dried leaves at power of 800 W, respectively. In general, increasing drying temperature decreased the essential oil content. The GC/MS analysis of essential oils showed that the chemical compounds belonged mostly to oxygenated monoterpenes class (72.34–86.41%). The chemical compounds group was significantly (p < 0.01) decreased by microwave drying at power levels of 200 and 400 W. The assessed drying methods caused significant (p < 0.05 and/or p < 0.01) variations in the main constituents of the peppermint leaves essential oil including menthol, menthone, menthofuran, 1,8-cineole, and menthyl acetate. The minimum (35.01%) and maximum (47.50%) concentrations of menthol, as the major compound of the oil, were found in hot air-dried leaves at temperature of 50°C and microwave-dried leaves at power of 400 W, respectively. The percentage of menthone, as the second constituent in the essential oil, was significantly lost (p < 0.01) under microwave drying.     

不同高温热泵干燥条件对龙眼干品质的影响

以龙眼为研究对象,考察了不同热泵干燥温度和干燥风速对龙眼干一般理化特性、色泽、质构和活性成分等品质的影响。结果表明：采用高温热泵干燥时,干燥温度越高,龙眼干的总酸含量越高,复水率越低;干燥风速相同时,龙眼干的pH值随着温度的升高而降低;龙眼干燥后总体色泽的变化主要在色泽的变暗及变黄,干燥温度的升高和干燥风速的增加都会导致龙眼色泽变化的增加;总体来说,不同高温热泵干燥条件下,龙眼干的弹性、回复性、硬度以及耐咀性的变化均不显著,干燥风速较低,龙眼干的黏性较大;当干燥温度为60 ℃时,龙眼干中保留的游离酚含量最高,不同干燥条件下,结合酚含量、多糖含量的差异不显著。     

Essential oil composition of the turpentine tree (Pistacia terebinthus L.) fruits growing wild in Turkey

Constituents of essential oils from fruit samples of the turpentine tree (Pistacia terebinthus L.) collected from fifteen different localities of Turkey on August 2001 were identified by GC–MS. Twenty-eight compounds representing 92.3–100.0% of turpentine fruit oils were identified. The oil yields varied between 0.06% and 0.16%. The highest yield of oil was obtained from fruits of Antalya origin (Akba?-Serik) (0.16%). α-Pinene (51.3%), limonene (39.0%), p-cymen-8-ol (40.0%) and caryophyllene oxide (51.0%) were found as major components for different localities in Turkey. The predominant constituents in most samples were α-pinene (9.5–51.3%), limonene (tr-39.0%) and caryophyllene oxide (tr-51.5). Except for one collection (Manavgat-Antalya), which contained spathulenol (20.7%) and p-cymen-8-ol (40.0%), all the other samples yielded oils rich in α-pinene and limonene. β-Caryophyllene oxide is the most abundant compound in Hisarönü (?zmir), Alanya (Antalya) and Yaylada? (Hatay) oils. Results confirm the effect of locality on the oil content and composition.