Extraction of Total Phenolics of Sour Cherry Pomace by High Pressure Solvent and Subcritical Fluid and Determination of the Antioxidant Activities of the Extracts

Abstract

High pressure liquid extraction (HPE) and subcritical fluid (CO₂+ethanol) extraction (SCE) were used for the extraction of total phenolic compounds (TPC) from sour cherry pomace. Antiradical efficiency (AE) of the extracts was also determined. Ethanol was the solvent for HPE and co‐solvent for SCE. Combinations of pressure (50, 125, 200 MPa), temperature (20, 40, 60°C), solid/solvent ratio (0.05, 0.15, 0.25 g/ml) and extraction time (10, 25, 40 min) were variables for HPE according to the Box‐Behnken experimental design. The variables used for SCE were pressure (20, 40, 60 MPa), temperature (40, 50, 60°C), ethanol concentration (14, 17, 20 wt%) and extraction time (10, 25, 40 min). For HPE, TPC, and AE at the optimum conditions (176–193 MPa, 60°C, 0.06–0.07 g solid/ml solvent, 25 min) were found as 3.80 mg gae/g sample and 22 mg DPPH^?/g sample, respectively. TPC and AE at the optimum conditions (54.8–59 MPa, 50.6–54.4°C, 20 wt% ethanol, 40 min) for SCE were determined as 0.60 mg gae/g sample and 2.30 mg DPPH^?/g sample for sour cherry pomace, respectively.     

Optimization of microwave-assisted extraction of bioactive compounds from pistachio (Pistacia vera L.) hull

ABSTRACT

Phenolic compounds were extracted from pistachio hull using microwave-assisted solvent extraction (MASE). The effects of four parameters, microwave power, extraction time, solvent to sample ratio, and ethanol concentration were evaluated. The extraction conditions were optimized by response surface methodology to enhance the total phenolic content (TPC). Optimal conditions were found as 140 W microwave power, 4.5 min extraction time, 19:1 (v/w) solvent to sample ratio, and 56% ethanol concentration to get maximum TPC (62.24 mg GAE/g dry hull). Also, MASE was compared with conventional solvent extraction (CSE) and MASE gave higher TPC, yield, and antioxidant activity.     

OBTAINING SCARLET SAGE (SALVIA COCCINEA) EXTRACT THROUGH HOMOGENIZER- AND ULTRASOUND-ASSISTED EXTRACTION METHODS

Scarlet sage (Salvia coccinea) leaves were extracted with water, ethanol, methanol, and aqueous mixtures of those solvents by homogenizer-assisted extraction (HAE) and ultrasound-assisted extraction (UAE) methods, which are novel technologies used for this purpose. The best results were compared with those obtained by the conventional Soxhlet method (SM). Total phenolic content was expressed in gallic acid equivalent (GAE) per g of dried leaf. Free radical scavenging activity for the antioxidant capacity was tested by 1,1-diphenyl-2-picryl hydrazyl (DPPH) radical. The greatest amount of extraction was achieved by pure water with the value of 368.87 mg/g dried matter and the highest total phenolic content was observed by 100% methanol as 43.18 mg-GAE/g dried matter, both obtained by the HAE method. The mint leaves extracted by SM exhibited the highest antioxidant capacity, with a value of 90.55% for inhibition of DPPH radical.     

Optimization of ultrasound-assisted extraction of bioactive compounds from B. forficata subsp. Pruinosa

Extracts containing bioactive compounds were obtained from Bauhinia forficata leaves by ultrasound-assisted extraction (UAE) with three different solvents (n-hexane, ethyl acetate, and ethanol) and were compared with those obtained by a conventional method (maceration). Box-Behnken experimental design was applied to examine and optimize the effect of the extraction temperature (40°C-60°C), power (20%-80%), and sample to solvent ratio (1:10 to 1:20 (w/v)) on the total phenolic content (TPC), total flavonoid content (TFC), and the ferric reducing antioxidant power (FRAP) of B. forficata leaf extracts. This experimental design generated second-order polynomial models, which accurately describe the experimental data, allowing the prediction of optimal conditions for the investigated responses. Optimal extraction was achieved under the following conditions: 80% power, temperature of 41°C, and a 1:20 sample to solvent ratio. Under these conditions, the experimental yield was 8.33 ± 0.32%, total phenolic content was 59.47 ± 0.71 mg GAE · g_extract⁻¹, total flavonoid content was 62.30 ± 3.38 mg QE · g_extract⁻¹, and the ferric reducing antioxidant power was 726.7 ± 15.7 μmol Fe(II)EQ · g_extract⁻¹, which were close to the predicted values, which validated the models. The major compounds found in B. forficata extracts were tocopherols, phytol, heneicosane, and β-Sitosterol.     

Optimization of Microwave-Assisted Extraction of Cherry Laurel Fruit

Response surface methodology was used to optimize the influence of microwave power (300–600 W), plant material-to-solvent ratio (0.05–0.2 g/cm³), and extraction time (10–30 min) on the efficiency of microwave-assisted extraction of the cherry laurel (Prunus laurocerasus L.) fruit. From experimental data, a quadratic polynomial mathematical model (R² = 0.9949) was developed to predict the extract yield. All considered factors were statistically significant for extraction efficiency, while the most important factor was extraction time. Microwave power of 550 W, plant material-to-solvent ratio of 0.05 g/cm³, and time of 25 min were determined as optimal conditions with a maximum yield of 9.36 g/100 g fresh plant material, which was confirmed through laboratory experiments (9.12 ± 0.61 g/100 g fresh plant material). An economic condition for simultaneous maximum extract yield (7.58 g/100 g fresh plant material) with minimal energy and solvent consumption was determined by the desirability function method (18.2 min, 300 W, and 0.2 g/cm³). Additionally, the total phenol and flavonoid quantification and antioxidant activity of both extracts were tested. There is no statistically significant difference in the total flavonoid content in the extracts obtained under both proposed conditions, while the total phenolic content and antioxidant activity of the extract obtained under economic conditions were slightly lower.     

The Effect of Olive Leaf Addition on Antioxidant Content and Antioxidant Activity of “Memecik” Olive Oils at Two Maturity Stages

In this study, the effects of leaf addition, maturity stage and storage on the antioxidant content and activity of olive oils (cv. Memecik) were investigated in the 2008/09 and 2009/10 crop seasons. Olive fruits were harvested at two different maturity stages (early and late), and the leaves of the same cultivar were added at different rates (0, 1, and 3 %) prior to oil extraction. After extraction, the oil samples were stored for 18 months and total chlorophyll, α-tocopherol, total phenolic content and the antioxidant activity [DPPH^· (2,2-diphenyl-1-picrylhydrazyl) and ABTS^·+ (2,2-azino-bis(3-ethylbenzothiazoline)-6-sulfonic acid) radical scavenging] were determined at 6 month-intervals. Olive leaf addition induced a significant increase in total chlorophyll, α-tocopherol, total phenolic content, and antioxidant activities in both years (P < 0.001). During the storage period antioxidant content and antioxidant activities in the oils significantly decreased in both years (P < 0.001). However, the oils to which leaf material was added had higher antioxidant contents and activities than those without leaf material addition at the end of the 18-month storage period. After storage, the antioxidant content and DPPH^· radical scavenging activity of control (0 %) samples were lower than those in the leaf added samples (3 %). The data obtained from this study suggested that the addition of olive leaf to oils allowed more functional olive oils with higher antioxidant contents.     

Integrating Microwave-Assisted Extraction of Essential Oils and Polyphenols from Rosemary and Thyme Leaves

The extraction of essential oils (EOs) and polyphenols from rosemary and thyme has been done using an integrated process: microwave hydro-diffusion and gravity (MHG) for EOs and microwave-assisted extraction (MAE) for polyphenols. The innovative installation based on the MHG principle allows uniform microwave irradiation field due to a mechanical stirring and experiments done at low pressure. The results of quantitative analysis of the EOs extracted by MHG after 10?min were similar with those obtained by traditional methods (conventional hydro-distillation (CHD) and microwave-assisted hydro-distillation (MHD)) after 150 and 105?min, respectively. The specific energy for MHG was 5–15 times lower compared with these classical methods. The MHG extraction of EOs is also an effective method for plant material pretreatment before polyphenol extraction. Total phenolic content increased from 35 to 55?mg GAE/g DM for rosemary and from 23 to 38?mg GAE/g DM for thyme.     

Optimization of Heat Pump–Assisted Intermittent Drying

In the present study, heat pump–assisted drying of salak fruit was optimized by dividing the dehydration process into three distinct phases, namely, the initial, intermittent, and final stages. Drying variables considered for the optimization were the intermittent duration (X ₁), intermittent ratio (X ₂), and intermittent cycle (X ₃); the response variables studied were the total drying time (Y ₁), total heating time during intermittent drying (Y ₂), total heating time after intermittent drying (Y ₃), total color change (Y ₄), ascorbic acid content (Y ₅), and total phenolic content (Y ₆). Response surface methodology was used to determine the best combination of the drying variables that could provide the shortest drying period and premium product quality. Experimental results showed that all of the response variables were improved under the optimized intermittent drying conditions compared to the conventional method using constant drying conditions. The optimized heat pump–assisted intermittent drying reduced the drying time by 36% and improved phytochemicals retention with ascorbic acid and total phenolic content recorded at 18.4 ± 1.8 mg ascorbic acid/100 g dw and 43.3 ± 2.2 mg gallic acid equivalent (GAE)/g dw, respectively. The color change of the final product was minimum with a ΔE* value of 7.26 ± 2.03.     

Microwave-assisted extraction as an advanced technique for optimization of saponin yield and antioxidant potential from Phyllanthus amarus

The objective of this study was to apply microwave-assisted extraction (MAE) as an advanced technique for optimization of saponin yield and antioxidant potential from Phyllanthus amarus. The findings indicated that the optimal MAE parameters consisted of 100% methanol, irradiation time 4 s/min, extraction time 50 min, and solvent to sample ratio 50 mL/g. Under these optimal parameters, saponin content (SC), saponin extraction efficiency (SEE), and total phenolic content (TPC) of P. amarus were 229.5 mg escin equivalents (EEs)/g dried sample, 82.8%, and 40.7 mg gallic acid equivalents (GAEs)/g dried sample, respectively. The antioxidant capacity of P. amarus in terms of 2,2ˊ-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid) radical scavenging capacity (ARSC), 2,2-diphenyl-1-picryl-hydrazil radical scavenging capacity (DRSC), and ferric reducing antioxidant power (FRAP) were 487.3, 330.6, and 233.5 mg trolox equivalents (TEs)/g dried sample, respectively. These measured values were not significantly different from the predicted values by response surface methodology (227.9 mg EE/g dried sample, 82.1%, and 39.2 mg GAE/g dried sample for SC, SEE, and TPC and 484.8, 297.3, and 226.6 mg TE/g dried sample for ARSC, DRSC, and FRAP, respectively). Hence, the optimal MAE parameters are suggested for effective extraction of saponins from P. amarus for further investigations and applications.     

Antioxidants from a heated histidine-glucose model system. I: Investigation of the antioxidant role of histidine and isolation of antioxidants by high-performance liquid chromatography

The radical-combining activity of Maillard reaction products [MRP_(aq)], produced by heating d-glucose and l-histidine (3:1) in a 0.1 M phosphate buffer for 10 h at 105°C (final pH 6.53), was estimated directly by means of a diphenylpicrylhydrazyl radical (DPPH^·) method. Additionally, the indirect methods of peroxide values changes (oven test), hexanal formation, and protection factors (Rancimat method) were determined on a lipid model system that consisted of sunflower seed oil/water (1:2), emulsified with 3% (w/w) Tween 40. Results from the DPPH^· method showed a potential antioxidant activity of MRP_(aq), which was confirmed by the indirect methods. Surprisingly, histidine in solution alone (heated or not) exhibited an antioxidant activity greater than or similar to the MRP_(aq) activity in the indirect methods with the lipid model system, in contrast to the results from the DPPH^· method. The suitability of various solvents for extraction of potential antioxidant compounds from freeze-dried MRP_(aq) was examined, and ethanol extracts showed the greatest activity by the DPPH^· method. Consequently, the ethanol extract of freeze-dried MRP_(aq) was separated by means of preparative reverse-phase high-performance liquid chromatography (HPLC) with a 0.05 M phosphate buffer (pH 4.4)/water/acetonitrile gradient system. The antioxidant activity of the eluate was measured through the DPPH^· method, and a fraction (Fraction A) with antiradical activity was further purified by preparative HPLC. Fraction B was collected, and its freeze-dried residue exhibited potent antiradical activity, significantly greater than that of the same level of n-propyl gallate.     

Response Surface Optimized Ultrasonic-Assisted Extraction of Quercetin and Isolation of Phenolic Compounds From Hypericum perforatum L. by Column Chromatography

The effects of ultrasonic-assisted extraction factors for the main phenolic compound (quercetin) from Hypericum perforatum L. were optimized using the Box–Behnken design (BBD) combined with response surface methodology. The BBD was employed to evaluate the effects of extraction temperature (30–70°C), extraction time (20–80 min), methanol concentration (20–80%, v/v), and HCl concentration (0.8–2.0 M) on the content of one of the major phenolic compounds of quercetin. The extracts were analyzed by high performance liquid chromatography (HPLC). The major phenolic compounds of H. perforatum were isolated and the antioxidant capacity and total phenol content were determined in crude extract and fractions. The optimum conditions were determined as extraction temperature 67°C, extraction time 67 min, methanol concentration 77% (v/v), and HCl concentration 1.2 M. The predicted content of quercetin was 10.81 mg/g dried plant under the optimal conditions and the subsequent verification experiment with 11.09 mg/g dried plant confirmed the validity of the predicted model. The isolated compounds were identified as quercetin, cyanidin, protocatechuic acid, and kaempferol.     

The role of drying methods on enzymatic activity and phenolics content of impregnated dried apple

Infusion of antioxidants into vegetables is a new food strategy managed by matrix processing. Raw and blanched apple were air- or freeze-dried. In the case of freeze-dried samples, different freezing methods were previously applied: conventional (?28°C), blast freezing (?30°C), and liquid N₂ (?196°C). Afterwards, air- and freeze-dried samples at different conditions were impregnated with a concentrated (40°Brix) tea extract and finally, air-dried for their stabilization. Total phenolic content (TPC), antioxidant capacity (AC), enzymatic activity, and microstructure were analyzed. Regardless of pretreatments, the impregnation and the further drying improved the antioxidant potential. Samples with the most porous microstructure free of degradative enzymes provided high AC (78.5?±?0.9?mg Trolox/g dried matter) and TPC (16.7?±?0.2?mg GAE/g dried matter).     

Optimization of Microwave‐Assisted Extraction of Flavonoid from Radix Astragali using Response Surface Methodology

Abstract

Response surface methodology (RSM) was applied to predict optimum conditions for microwave‐assisted extraction (MAE) of flavonoid from Radix Astragali. A central composite design was used to monitor the effect of temperature, extraction time, solvent‐to‐material ratio, and the ethanol concentration on yield of total flavanoid (TFA). Optimum extraction conditions were predicted as 108.2°C, 26.7 min, 23.1 ml/g solvent‐to‐material ratio and 86.2% ethanol. The maximum yield 1.234±0.031 mg/g was close to the yield of Soxhlet and higher than that of ultrasound assisted extraction and heat reflux extraction. MAE was an effective alternative to conventional extraction methods.     

Antioxidant Activity of Tannin Fractions Isolated from Buckwheat Seeds and Groats

Phenolic compounds were extracted with 80% (v/v) aqueous acetone from buckwheat seeds and groats. Tannin fractions were obtained from the crude extracts by Sephadex LH-20 column chromatography. Total phenolic contents of isolated fractions from buckwheat seeds and groats were 477 and 371 mg catechin equiv/g, respectively. The analyzed samples were characterized by electrophoretic separations using capillary zone electrophoresis. Both fractions exhibited strong antioxidant activity. The tannin fraction of buckwheat seeds reduced 1,1-diphenyl-2-picrylhydrazyl radicals (DPPH^·) and [2,2′-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid)] diammonium salt radical cations (ABTS^·+) stronger than the fraction of buckwheat groats. The EC₅₀ values amounted to 0.019 and 0.020 mg while Trolox equivalent antioxidant capacity values were 4.06 and 3.55 mmol Trolox equiv/g for tannin fractions of buckwheat seeds and groats, respectively. Similarly, antioxidant activity of the tannin fraction of buckwheat seeds measured by photochemiluminescence assay, was higher than antioxidant activity noted for the fraction obtained from groats. However, both fractions inhibited oxidation to the same extent in applied lipid models: β-carotene-linoleic acid emulsion and l-α-lecithin liposomes. In β-carotene-linoleic acid emulsion system, 1 mg of tannin fractions exhibited similar antioxidant activity to 0.5 mg butylated hydroxyanisole (BHA).     

Cultivar Characterization of Tea Seed Oils by Their Active Components and Antioxidant Capacity

Cultivar characterization of tea seed oils based on their active components and antioxidant capacity was carried out, providing fundamental data for authentication. The seeds were collected from 28 cultivars grown under the same conditions in the region of Anxi county of Fujian province and their oils were analyzed. The results showed that total phenols content (TPC), total flavonoids content, α-tocopherol contents, γ-tocopherol content and δ-tocopherol content were 16.7–529.3 mg GAE/kg of oil, 4.4–208.7 mg rutin/kg of oil, 7.7–347.1 mg/kg of oil, 1.8–106.7 mg/kg of oil, 0.003–35.769 mg/kg of oil, respectively. The antioxidant capacity measured by DPPH radical scavenging activity (DPPH), oxygen radical absorbance capacity (ORAC), absorbance of protein carbonyl (APC) and the absorbance of protein hydroperoxides (APH) were 91.0–2,164.5 μmol/100 g of oil, 251.0–1,209.5 μmol/100 g of oil, 0.014–0.135, 0.034–0.458, respectively. The correlation analysis revealed that the presence of phenolic compounds was significantly correlated with the antioxidant capacity of tea seed oil. Principal Component Analysis revealed the first three components accounted for 81.31 % of the total variance within the data and the main contributor parameters were DPPH, ORAC, APC, APH and TPC. Hierarchical cluster analysis classified the cultivars into three groups, which were in line with the genetic relationship among the cultivars. Our results supplied basic data for the antioxidant mechanism research of tea seed oil and provided necessary information to develop a breeding program directed to tea seed cultivar selections with the high nutraceutical value of tea seed oil.     

Effect of the Drying Process on the Intensification of Phenolic Compounds Recovery from Grape Pomace Using Accelerated Solvent Extraction

In light of their environmental and economic interests, food byproducts have been increasingly exploited and valorized for their richness in dietary fibers and antioxidants. Phenolic compounds are antioxidant bioactive molecules highly present in grape byproducts. Herein, the accelerated solvent extraction (ASE) of phenolic compounds from wet and dried grape pomace, at 45 °C, was conducted and the highest phenolic compounds yield (PCY) for wet (16.2 g GAE/100 g DM) and dry (7.28 g GAE/100 g DM) grape pomace extracts were obtained with 70% ethanol/water solvent at 140 °C. The PCY obtained from wet pomace was up to two times better compared to the dry byproduct and up to 15 times better compared to the same food matrices treated with conventional methods. With regard to Resveratrol, the corresponding dry pomace extract had a better free radical scavenging activity (49.12%) than the wet extract (39.8%). The drying pretreatment process seems to ameliorate the antiradical activity, especially when the extraction by ASE is performed at temperatures above 100 °C. HPLC-DAD analysis showed that the diversity of the flavonoid and the non-flavonoid compounds found in the extracts was seriously affected by the extraction temperature and the pretreatment of the raw material. This diversity seems to play a key role in the scavenging activity demonstrated by the extracts. Our results emphasize on ASE usage as a promising method for the preparation of highly concentrated and bioactive phenolic extracts that could be used in several industrial applications.     

Prosopis farcta Seeds: Potential Source of Protein and Unsaturated Fatty Acids?

The goal of this study is to evaluate the chemical composition of the Prosopis farcta seeds. The Kjeldahl method revealed that the level of the total protein was ca. 18 % on a dry weight basis (DW). Gas chromatographic analysis revealed the presence of six fatty acids. Linoleic acid with 57.55 % was the major fatty acid, followed by oleic and palmitic acids (24.58 and 12.91 %, respectively). Total phenolic content was 1.71 mg GAE/g DW (GAE = gallic acid equivalents). Methanolic extracts showed important antioxidant properties. This work highlights the importance of P. farcta seeds as natural and inexpensive sources of protein, unsaturated fatty acid, and phenolic compounds for both cosmetic and pharmaceutical uses.     

Extraction Kinetics and Anethole Content of Fennel (Foeniculum vulgare) and Anise Seed (Pimpinella anisum) Extracts Obtained by Soxhlet,Ultrasound, Percolation,Centrifugation, and Steam Distillation

Foeniculum vulgare (fennel) and Pimpinella anisum (anise) extracts were obtained by Soxhlet, cold percolation, ultrasound assisted extraction, and centrifugal extraction using ethanol as solvent; anise extracts were also obtained by steam distillation. Soxhlet presented the highest yields for both fennel and anise seed (16.8% and 23.3%, respectively). The highest anethole content among ethanolic extracts was obtained for centrifugal extraction (6.8 mg/g and 143 mg/g for fennel and anise extracts, respectively). Steam distillation presented low yield (0.26%), but high anethole content (68–98%, area). Anise ethanolic extracts also tested positive for flavonoids.     

Chemical Characterization of the Seed and Antioxidant Activity of Various Parts of <Emphasis Type="Italic">Salvadora persica</Emphasis>

This study investigated the fatty acid, tocopherol, sterol and total phenolic compounds of Salvadora percica seeds as well as the potential antioxidant activity of the leaves, bark and seedcake extracts. Two samples of S. persica seed collected from Kordofan (sandy soil) and Gezira (heavy clay soil) states in Sudan were used. The predominant fatty acids were 14:0, 16:0 and 18:1 representing 45.50, 35.12 and 10.20% for Kordofan and 45.20, 34.49 and 10.66% for Gezira samples. Gamma-tocopherol was the predominant tocopherol in both samples representing 61.3 and 61.7% of the total tocopherols, respectively, followed by α-tocopherol at 21.1 and 20.2%, respectively. Total sterol content was 3399.6 and 3385.3 mg/kg for Kordofan and Gezira samples, respectively. Beta-sitosterol, campesterol, stigmasterol and Δ5-avenasterol were predominant. The content of total phenolic compounds was determined in S. persica bark (SPB), S. persica leaves (SPL), and S. persica seedcake (SPC) extracts of each sample according to the Folin–Ciocalteau method as 111.70, 132.60, and 66.10 mg GAE/g extract for the Kordofan sample. They were found to be 105.90, 129.10 and 62.90 mg GAE/g extract in the Gezira sample, respectively. The two samples were significantly (P < 0.05) different in total phenolic content with SPL as the highest in both samples. The methanolic extracts of SPL, SPB, and SPC in both samples were markedly effective in inhibiting the oxidation of linoleic acid and subsequent bleaching of β-carotene in comparison with the control. But they were less effective than butylated hydroxyanisole.     

Intensification of phenolic extraction from yellow European plums by use of conventional,microwave-, and ultrasound-assisted extraction

ABSTRACT

In this study, microwave and ultrasound extraction were selected as process intensification tools to intensify the conventional heat reflux extraction process. Process efficiency was evaluated based on total phenolic content (ascorbic acid, neochlorogenic acid, and chlorogenic acid), scavenging ability of 2,2-diphenyl-1-picrylhydrazyl (DPPH) and ferric (Fe³⁺) free radicals, and process intensification principles and domains. Highest phenolic content and antioxidant activity were achieved using microwave extraction followed by heat reflux and ultrasound extraction. Microwave extraction was selected via decision matrix as a suitable process intensification approach based on results and its ability to satisfy process intensification principles.