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.     

Study on Optimum Extraction Conditions for Olive Leaf Extracts Rich in Polyphenol and Flavonoid

Ultrasound-assisted extraction (UAE) of polyphenols and flavonoids from olive leaves was investigated. The effects of temperature (27?37°C), solvent concentration (10?70% ethanol (EtOH), v/v) and time (30?60 min) were determined by both experimental and Response Surface Methodology (RSM) techniques. Free radical scavenging activity for the antioxidant capacity was tested by 1,1-diphenyl-2-picryl hydrazyl (DPPH) radical. For total phenolic content (TPC), 43.8252 mg-GAE/g dried leaf was predicted at the optimum conditions (34.18°C, 43.61% (v/v) of EtOH, and 59.99 min). In case of total flavonoid content (TFC), 31.9920 mg-CE/g dried leaf was calculated at the optimum conditions (34.44°C, 70% (v/v) of EtOH, and 60 min).     

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.     

Extraction of phenolic compounds from spent blackberry pulp by enhanced-fluidity liquid extraction

This research describes an enhance-fluidity liquid extraction process for extracting total phenolic compounds (TPC) from spent blackberry pulp (SBP) using a modified solvent (CO₂–ethanol mixture). Effects of particle size (from 1,400 to 180 μm), pressure (150–300 bar), and cosolvent (ethanol)-to-solid ratio (64, 128, and 192 mL ethanol/32 g solid) on the extraction of TPC at 40°C were investigated. Experimental data was processed using the Sovova's model to obtain the solubility of TPC in the modified solvent. The Peng–Robinson equation of state was used to correlate the solubility of phenolic compounds at high pressures. Results indicated that particle sizes ranging from 600 to 850 μm and pressure of 300 bar allowed obtaining extracts with higher antioxidant activity (94.71% of inhibition) and TPC content (11.59 mg GA/g SBP). High pressure and the modified solvent increased the solubility up to 3.4 × 10⁻⁴ (mol fraction).     

Study on the microwave-assisted extraction of polyphenols from tea

This study demonstrated a promising method for quickly extracting tea polyphenol (TP) by microwave-assisted extraction (MAE) technology. Some influential parameters, including MAE temperature, microwave power, concentration of extraction solvent, MAE time and the solid/liquid ratio, were investigated. The optimum condition of MAE was obtained by dual extraction with 60% ethanol (v/v) and the solid/liquid ratio 1:12 g/mL at 80°C for 10 minutes under the microwave power 600W. The yield of TP was 96.5% under the described condition. Compared with traditional methods, including hot reflux extraction (HRE), ultrasound-assisted extraction (UAE) and supercritical fluid extraction (SFE), the extraction time was saved 8 times than that of HRE, and the yield was increased by 17.5%. The extraction time at comparable levels of production was saved 2 times, and the energy consumption was one fourth that of UAE. The extraction time was saved 5 times than that of SFE, and the yield of TP was increased by 40%. Moreover, compared with MAE of TP studied by others, it decreased the solid/liquid ratio from 1: 20 to 1: 12 g/mL without 90-min pre-leaching time, and the yield of TP was increased by 6%–40%.     

香椿叶中总黄酮的提取工艺研究

研究了溶剂法提取香椿叶总黄酮的工艺条件。在单因素试验的基础上,用正交实验法对香椿叶总黄酮的提取工艺进行优选,考察乙醇体积分数、固液比、提取时间、浸提温度对香椿叶总黄酮提取率的影响。结果表明,在浸提3次条件下,得到叶片总黄酮最佳工艺条件为:乙醇浓度80%、固液比为1∶10(g/mL)、提取温度80℃、提取时间2 h,在此条件下香椿叶片总黄酮提取率为61.13%;叶轴总黄酮最佳提取条件为:乙醇浓度70%、固液比为1∶10(g/mL)、提取温度80℃、提取时间1 h,在此条件下香椿叶轴总黄酮提取率为71.71%。     

Microwave-Assisted Batch Extraction of Polyphenols from Sea Buckthorn Leaves

Extraction of polyphenols from sea buckthorn leaves using microwave-assisted extraction (MAE) is described. The influence of different parameters on the extraction process (reactor type, stirring rate, extraction time, temperature, ethanol/water ratio) was studied. The polyphenolic extracts were analyzed in order to determine the total phenolic content (TPC) either by the Folin–Ciocalteu method or by differential pulse voltammetry (DPV), and the concentration of the main polyphenolic compounds by high-performance liquid chromatography (HPLC). The specific microwave energy was also determined. MAE resulted in a shorter extraction time (7.5 versus 30 min for the conventional method). The best results for MAE were obtained at a temperature of 90°C, using a solvent/plant ratio of 20/1 and 50% ethanol in the extraction solvent. The highest values of antioxidant capacity were obtained for polyphenolic extracts resulted from microwave extraction.     

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.     

An Improved Ultrasound-Assisted Alkali Extraction Process of Perilla Seed Meal Polysaccharide

The quantitative effects of extraction time, extraction temperature, concentration of alkali solution, and ratio of solid to liquid on yield of perilla seed meal polysaccharides were investigated using response surface methodology (RSM). The experimental data obtained were fitted to a second-order polynomial equation using multiple regression analysis and also analyzed by appropriate statistical methods. By solving the regression equation and also by analyzing the response surface contour plots, the optimal ultrasound-assisted (ultrasonic power was 70 W) extraction conditions of polysaccharides were determined: Extraction time of 29.4 min, extraction temperature of 42.8°C, concentration of NaOH of 4.5 mol/L, and ratio of liquid to solid of 22 g/mL. These predicted values were also verified by validation experiments.     

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.     

Ultrasound-assisted extraction of natural antioxidants from betel leaves (Piper betle): Extraction kinetics and modeling

Present study investigated the extraction kinetics of antioxidants from Piper betle by ultrasound-assisted extraction for three extraction variables: temperature, solute to solvent ratio and ethanol concentration. Based on the results of yield, total phenolic content and antioxidant activity, the optimum results were obtained at 50°C, 1:20 g/mL and 80% ethanol, respectively. Statistical coefficients of R² ≥ 0.961 and RMSE ≤ 0.508 for two-site kinetic model confirm the use of proposed models for simulation and prediction purpose. Comparison with ascorbic acid and butylated hydroxytoluene solidifies the use of Piper betle as feasible source of natural antioxidants. The presence of hydroxychavicol and eugenol was affirmed by high-performance liquid chromatography assay.     

Development of the ultrasonic conditions as an advanced technique for extraction of phenolic compounds from Eucalyptus robusta

This study is designed to develop ultrasonic conditions as an advanced technique for optimal recovery of phenolics and antioxidants from Eucalyptus robusta leaf and to evaluate the impact of solvents, temperature, sonication time and power on ultrasound-assisted extraction of these compounds. Temperature has the greatest impact on the total phenolic content (TPC) yield followed by time and power. A yield of 163.68 ± 2.13 mg GAE/g of TPC is observed using 250 W ultrasonic power for 90 min at 60°C with water. This study validates UAE as an efficient, green, and sustainable technique for extracting phenolics from E. robusta.     

Optimization of Ultrasound-Assisted Extraction of Artemisinin from Artemisia annua L. by Response Surface Methodology

Artemisinin is a compound extracted from Artemisia annua L. with a remarkable curative effect against malaria. It can be extracted using ultrasound-assisted extraction (UAE) and then detected via HPLC. In this study, response surface methodology (RSM) was used to optimize UAE conditions for obtaining the maximum yield of artemisinin. Three independent variables (ratio of solvent to material, extraction temperature, and ultrasonic power) were evaluated using the Box-Behnken experimental design, with the yield of artemisinin as a response variable. Experimental data were highly fitted to a mathematical-regression model using multiple linear regression (MLR). Based on response surface plots, the three independent variables exhibited interactive effects on the yield of artemisinin. The optimal extraction conditions were as follows: 42.71 mL/g ratio of solvent to material, 41.86°C extraction temperature and 120 W ultrasonic power. The predicted yield of artemisinin by model was 0.7848%, whereas the actual yield in the extracts was 0.7826% ± 0.0790% in adjusted optimal conditions, with a relative error of 0.28%. The results undoubtedly demonstrated that RSM could be used to explore the optimum conditions of artemisinin extraction.     

Study on the microwave-assisted extraction of polyphenols from tea

This study demonstrated a promising method for quickly extracting tea polyphenol (TP) by microwave-assisted extraction (MAE) technology. Some influential parameters, including MAE temperature, microwave power, concentration of extraction solvent, MAE time and the solid/liquid ratio, were investigated. The optimum condition of MAE was obtained by dual extraction with 60% ethanol (v/v) and the solid/liquid ratio 1:12 g/mL at 80°C for 10 minutes under the microwave power 600 W. The yield of TP was 96.5% under the described condition. Compared with traditional methods, including hot reflux extraction (HRE), ultrasound-assisted extraction (UAE) and supercritical fluid extraction (SFE), the extraction time was saved 8 times than that of HRE, and the yield was increased by 17.5%. The extraction time at comparable levels of production was saved 2 times, and the energy consumption was one fourth that of UAE. The extraction time was saved 5 times than that of SFE, and the yield of TP was increased by 40%. Moreover, compared with MAE of TP studied by others, it decreased the solid/liquid ratio from 1 ∶ 20 to 1 ∶ 12 g/mL without 90-min pre-leaching time, and the yield of TP was increased by 6%–40%.     

Microwave Assisted Extraction of Phenolic Compounds from Sour Cherry Pomace

Microwave assisted extraction of sour cherry pomace at different conditions were compared with conventional extraction in terms of total phenolic content and antiradical efficiency. Total phenolic content and antiradical efficiency at the optimum conditions (700 W, ethanol-water, 12 min, 20 mL solvent/ g solid) of microwave assisted extraction were 14.14 mg GAE/g sample and 28.32 mg DPPH^·/g sample, respectively. Total phenolic content and antiradical efficiency of extracts obtained by conventional extraction were 13.78 mg GAE/g sample and 24.74 mg DPPH^·/g sample, respectively. Microwave assisted extraction increased antiradical efficiency and concentration of phenolic acids and shortened extraction time significantly.     

Microwave-Assisted Extraction of Phenolic Compounds from Caper

In this study, it was aimed to extract phenolic compounds from caper by using microwave and to compare the results with conventional extraction. For microwave-assisted extraction, power, extraction time, solid to solvent ratio, and solvent type were selected as independent variables. Dependent variables were total phenolic content (TPC), antioxidant activity, and concentration of phenolic compounds. The increase in solvent amount increased TPC. The highest TPC was obtained by using extraction conditions of 5 min at 400 W, solid to solvent ratio of 1:30, and ethanol-water mixture at a ratio of 50:50. There was no significant difference between microwave and conventional extraction on TPC and antioxidant activity (AA). However, microwave-assisted extraction decreased extraction time significantly.     

SIMULTANEOUS EXTRACTION AND QUANTITATION OF OLEANOLIC ACID AND URSOLIC ACID FROM SCUTELLARIA BARBATA D. DON BY ULTRASOUND-ASSISTED EXTRACTION AND HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY

A modified ultrasound-assisted extraction (MUAE) method and an HPLC technique were developed to identify and quantify simultaneously the amount of oleanolic acid (OA) and ursolic acid (UA) in Scutellaria barbata D. Don. The optimal conditions for MUAE were observed when the particle size was 0.2–0.5 mm, the duty cycle was 75%, the extraction temperature was 55°C, the ratio of solvent to raw material was 12.0:1 (mL:g), the ethanol concentration was 60%, and the extraction time was 25 min. Compared to the traditional extraction method, MUAE reduced the extraction time, extraction temperature, and solvent consumption and achieved superior yields of OA and UA. Furthermore, the combined MUAE-HPLC method was successfully applied for the first time to investigate and compare the amounts of OA and UA in samples obtained from different geographical regions.     

Comparison between conventional and ultrasound-assisted extractions of natural antioxidants from walnut green husk

Agricultural industries produce substantial quantities of phenolic-rich by-products, which have gained much attention due to their antioxidant properties. Ultrasonic technology was applied for extraction of antioxidants from the walnut green husk using ethanol as a food grade solvent. Response surface methodology (RSM) was used to optimize experimental conditions. The responses were total phenolic content (TPC), ferric reducing antioxidant power (FRAP), scavenging activity of 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical and yield. TPC varied from 6.28 to 7.23mg GA g^?1 dry sample. FRAP and DPPH values varied from 0.33 to 0.46 mmol Fe²⁺ g^?1 of dry sample and 33.98% to 56.31% inhibition, respectively. Extraction yields ranged from 33.04% to 38.72%. The optimal conditions were 60% ethanolwater mixture as solvent, temperature of 60 °C and extraction time of 30 min. Comparison of ultrasonic-assisted extraction (UAE) and conventional extraction was shown that TPC, FRAP, DPPH and yield obtained by UAE during 30 min were significantly higher than by conventional extraction during 16 hours. The extract can be used as substitute of synthetic antioxidants for food products, color and oxidative stabilization.     

Oxidation and Colloidal Stability of Oil-in-Water Emulsion as Affected by Pigmented Rice Hull Extracts

Extracts from the hull of pigmented rice were prepared using a mixture of methanol–water (1:1, 2:1, and 3:1, v/v) for different extraction times (0–180 min). Total phenolic content (TPC) of the extracts increased with increasing concentration of methanol and extraction time (P < 0.05). A positive correlation between TPC and antioxidant activities, i.e., DPPH and ABTS radical scavenging activities and reducing power, was observed. The extracts prepared using methanol–water at the ratio of 3:1 for 180 min at 50 °C, referred as rice hull phenolic extract (RHPE), showed the highest TPC and free radical scavenging abilities and reducing power (P < 0.05). When the effects of RHPE on physicochemical stability of the emulsions stabilized by different emulsifiers, i.e., Tween 20 and bovine serum albumin (BSA), were examined, the collapse of emulsion was retarded when RHPE was applied in BSA‐based emulsions, whereas a negative effect was noticeable in Tween 20‐based counterpart. Lower oxidative degree was found for BSA stabilized emulsions, compared to Tween 20 containing system. RHPE (1–3 %) markedly improved the oxidative stability, particularly for BSA stabilized emulsions. Therefore, RHPE could be employed along with the selected protein to increase physicochemical stability of emulsion.