Optimization of Microwave-Assisted Extraction of Astaxanthin from Haematococcus Pluvialis by Response Surface Methodology and Antioxidant Activities of the Extracts

Abstract

Microwave-assisted extraction (MAE) was applied for the extraction of astaxanthin from Haematococcus pluvialis and response surface methodology (RSM) was used to optimize extraction parameters to the content of astaxanthin. Four independent variables such as microwave power (W), extraction time (sec), solvent volume (mL), and the number of extraction were optimized in this paper. The optimal conditions were determined and tri-dimensional response surfaces were plotted from the mathematical models. The F-test and p-value indicated that microwave power, extraction time, the number of extraction, and their quadratic had a highly significant effect on the response value (p <0.01), then the solvent volume and the interaction effects of microwave power and the number of extraction also displayed significant effect (p <0.05). Considering the extraction efficiency, the optimized conditions of MAE were as follows: microwave power was 141 W, extraction time 83 sec, solvent volume 9.8 mL, the number of extraction four times. About 594 ± 3.02 µg astaxanthin was extracted from Haematococcus pluvialis the dried powders (100 mg) under the optimal conditions, and it close to the predicted contents (592 µg). The antioxidant activities of the extracts obtained under optimal conditions were analyzed, and the results showed that the extracts presented strong ability of inhibiting the peroxidantion of linoleic acid, exhibited strong radical-scavenging properties against the DPPH, as well as strong reducing power.     

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.     

Kinetic study of nordihydroguaiaretic acid recovery from Larrea tridentata by microwave‐assisted extraction

BACKGROUND: Nordihydroguaiaretic acid (NDGA) is a powerful antioxidant with biological activities of great interest in several health areas, including antiviral, cancer chemopreventive, and antitumorgenic. Little information is available on extraction methods of NDGA from Larrea tridentata. Hence, the aim of this study was to develop a rapid and effective microwave‐assisted extraction (MAE) method for NDGA recovery from Larrea tridentata leaves, and to compare the results obtained with those found using conventional heat‐reflux extraction (HRE). RESULTS: Extraction time for similar NDGA yields was significantly reduced from 18 to 1 min when MAE was used instead of HRE. Optimum conditions for NDGA extraction (3.79 ± 0.65%) consisted in using 50% methanol as extraction solvent in a solid/liquid ratio of 1/10 g mL^?1. Micrographs demonstrated that the improvement in NDGA extraction by MAE might be related to a greater extent of cell rupture of the plant material. Extracts obtained by MAE exhibited antiradical activity only slightly lower than those obtained by HRE. CONCLUSIONS: MAE proved to be a faster and more efficient method for NDGA extraction from Larrea tridentata leaves than HRE. The better results for NDGA extraction by MAE might be explained by the greater extent of cell rupture of plant material during the extraction process. Copyright © 2010 Society of Chemical Industry     

Recovery of Anti-Cancer Damnacanthal from Roots of Morinda citrifolia by Microwave-Assisted Extraction

Abstract

This study investigated the effects of material particle size, irradiation time, extraction temperature, type of solvents, ethanol composition, and the ratio of liquid-to-sample on microwave-assisted extraction (MAE) of roots of Morinda citrifolia to obtain the most important anti-cancer compound, damnacanthal. The highest recovery of the compound was obtained after 5 min of MAE of small particle size material at 100 and 120°C. Longer extraction time caused the decrease in percent recovery due to the decomposition of the compound. Among the pure solvents tested, acetone and methanol gave the highest recovery. However, the use of ethanol-water solution (80% v/v) could considerably improve the yield of damnacanthal extracted. MAE was found to give the highest extraction efficiency when compared with other extraction methods such as extraction with electrical heating, soxhlet extraction, and ultrasound-assisted extraction (UAE).     

Enzymatic and Mechanical Extraction of Virgin Coconut Oil

The effect of different processing methods namely enzymatic method using crude protease extract (CPE) from overripe pineapple, microwave‐assisted extraction (MAE) and ultrasound‐assisted extraction (UAE) methods on the recovery yield of virgin coconut oil (VCO) is evaluated. The physicochemical properties of VCOs namely color, iodine value (IV), refractive index, saponification value, moisture content, free fatty acid, p‐anisidine value, lipid peroxidation, fatty acid composition, triacylglycerol (TAG) composition, melting and crystallization profile are compared. The total phenolic compounds and scavenging activity of the extracted VCOs are also examined. Results reveal that enzymatic approach exhibits the highest VCO yield (77.7% ± 0.38) at 50 °C for 2 h, followed by MAE (58.6%±0.07), control without enzyme (24.1%±0.19) and UAE (24.1%±0.12). The physicochemical properties of the VCOs extracted are found to conform to APCC standards established except IV. The antioxidant activity of VCO extracted with CPE shows no significant difference with MAE and UAE methods (p > 0.05). Lauric acid appears to be the most abundant fatty acid detected in all VCO samples. Similar exotherms and endotherms are observed in both melting and crystallization profiles with two distinct peaks exhibited. The TAG compositions of the extracted VCOs are mainly LaLaLa, LaLaM, CLaLa, CCLa, and LaMM (C = Capric acid; La = Lauric acid; M = Myristic acid). Practical Applications: The results obtained from this study indicate that VCO extraction using CPE from overripe pineapple is feasible. The enzymatic extraction protocol presented here would be useful for VCO production at industrial scale with a promising oil yield.     

Large-Scale Preparative Isolation of Rosavin from Rhodiola rosea via Ion Liquids MAE and Subsequent Flash Adsorption Chromatography

Rosavin was a major active compound from Rhodiola rosea. It is known that it possesses stimulant, antidepressant, and anticancer properties. In the present study, a two-step flash column chromatography has been developed for the large-scale preparative separation and purification of rosavin from the extracts of Rhodiola rosea, which were obtained by microwave assisted extraction (MAE) using ion liquids (ILs) as extraction solvent under the optimized conditions (microwave power 1200 W, extraction time 6 min, solid-liquid ratio 1:20, microwave temperature 120°C) resulting from the analysis of the D-optimal design. In the first separation, the Rhodiola rosea extract was loaded into polyamide and HPD-200 macroporous resin flash columns in series for efficient enrichment of rosavin. In the second one, the rosavin-rich crude sample after the serial column chromatography was subjected to final purification by silica gel flash chromatography. After the two-step separation, 529.1 mg of rosavin was obtained at a purity of 98.2% and a recovery of 60.6%. The separation process can provide a new method for large-scale separation and purification of rosavin for its pharmaceutical and practical use.     

Determination of Anti-Tumor Constitute Mollugin from Traditional Chinese Medicine Rubia cordifolia: Comparative Study of Classical and Microwave Extraction Techniques

Abstract

Rubia cordifolia is a common traditional Chinese medicine (TCM) used for centuries for the treatment of cough, inflammation of the joints, uterine hemorrhage, and uteritis. Mollugin is a major active component present in R. cordifolia and recognized as a potential anti-tumor compound. In this work, a microwave-assisted extraction (MAE) method has been developed for extracting mollugin from R. cordifolia. Several variables that can potentially affect the extraction yield, namely extracting solvent, microwave power, extraction time, and solid-liquid ratio were optimized. The separation and quantitative determination of mollugin was carried out by HPLC with UV detection at 254 nm. Under appropriate MAE conditions, such as extraction time of 4 min, ethanol concentration of 70% (v/v), microwave power of 460 W, and solid-liquid ratio of 1:20 (g/mL), the extraction yield of mollugin from R. cordifolia with MAE was higher than conventional extraction methods such as Soxhlet extraction, heat reflux extraction, and ultrasonic-assisted extraction. Due to the considerable saving in time and its higher extraction yield, the proposed MAE procedure was obviously a more rapid and effective sample preparation technique.     

溶剂和提取方法对苍耳子油提取的影响(英文)

为了有效提高苍耳子油的提取效率,考察了提取溶剂和提取方法对其提取率的影响.在5种常用提取溶剂(乙醇、乙酸乙酯、丙酮、二氯甲烷和环己烷)中,采用索氏提取法时二氯甲烷的提取率最高,采用微波法时乙醇的提取率最高.另外,采用微波法提取的苍耳子油的得率略低于索氏提取法,但微波法的提取效率更高,提取时间节省近30倍,溶剂消耗节省2倍.综合考虑,微波法提取具有更大的优势.     

Extraction of Astaxanthin from Shrimp Waste using Response Surface Methodology and a New Hybrid Organic-Inorganic Monolith

A 17-run Box-Behnken design (BBD) with three factors was used to improve the conditions for extracting astaxanthin from shrimp waste. The astaxanthin level was determined by high performance liquid chromatography (HPLC) using a C₁₈ column and a UV detector at 476 nm. The mean extraction yield of astaxanthin at the improved conditions (extraction time 1.4 h, extraction temperature 72.4°C, and liquid-solid ratio 27.3) was 98.7 ± 2.6 µg g^?1. A solid-phase extraction (SPE)-HPLC method was developed with a new hybrid organic-inorganic hybrid monolith for further purification of astaxanthin from shrimp waste. The SPE recoveries were ranging from 81.3 ± 2.4% to 86.5 ± 3.3%, and the intra-day and inter-day relative standard deviations (RSDs) of the proposed method were less than 4.3 ± 0.5% and 4.8 ± 0.2%, respectively. BBD increased the extraction efficiency and shortened extraction times significantly. SPE-HPLC with hybrid monolith showed good selectivity and purified astaxanthin from shrimp waste.     

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.     

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.     

Ultrasound-assisted extraction and adsorption of polyphenols from Ginger Rhizome (Zingiber officinale)

Ultrasound-assisted extraction followed by adsorption and desorption was performed successively for efficient recovery of polyphenols from ginger rhizome (Zingiber officinale). The maximum degree of extraction was observed in case of methanol (0.55 mg/ml) followed by acetone (0.52 mg/ml) and ethanol (0.37 mg/ml). At optimized conditions, the polyphenol recovery was found to be 19.2 mg. Amberlite XAD4 had shown the highest adsorption capacity (0.89 mg/ml). Kinetic studies indicated the adsorption equilibrium to be about 20 min. Adsorption capacity was achieved at 25 ± 2°C, and adsorption process exhibited exothermic nature. Freundlich isotherm fitted the data well. Ethanol had shown best desorption efficiency (93.44%).     

Assessment of Scale‐Up Parameters of Microwave‐Assisted Extraction via the Extraction of Flavonoids from Cocoa Leaves

Microwave‐assisted extraction (MAE) is a promising technique for the extraction of flavonoid compounds from plants. However, it is difficult to scale up due to the complex mass transfer involved. This has prompted the study of parameters for scaling up the system by considering energy‐related parameters, i.e. the nominal power density and the absorbed power density (APD). Modeling of MAE of flavonoid compounds from cocoa (Theobroma cacao L.) leaves using the film theory model was performed for this purpose. Operating parameters such as the sample particle size, the solvent‐to‐feed ratio, and the microwave irradiation power were also included in the kinetic study. The APD exhibited its aptitude as scaling‐up parameter as it can characterize both the extraction kinetics and the extraction yields of MAE. Furthermore, it can be used as a reference for predicting the optimum extraction time of MAE under various heating conditions.     

Extraction of Bioactive Compounds from Leaves of Lawsonia inermis by Green Pressurized Fluids

Supercritical carbon dioxide and microwave-assisted hydrothermal methods were investigated for extraction of bioactive components of leaves of Lawsonia inermis (henna), a world renowned source of natural hair dye component called lawsone (2-hydroxy-1,4-naphthoquinone). Results showed that the use of supercritical carbon dioxide was selective to extraction of non-polar compounds such as essential oils, and the recovery of lawsone was low. However, using hot and compressed water as a solvent, a maximum recovery of lawsone of about 76.2% could be obtained at 120°C and extraction time of 30 min. At higher temperatures and longer treatment time, the yield and recovery decreased due most likely to the degradation of the target compounds at severe conditions. Moreover, the highest composition of lawsone close to 24% was obtained at microwave power of 600 W in irradiation time of 1 min. Mild hydrothermal conditions assisted with microwave heating are recommended in order to obtain high recovery of lawsone. Direct microwave heating of the polar components and solvent could lead to rapid extraction of the target compounds.     

开放式超声微波协同萃取测定PVC塑料中邻苯二甲酸酯类增塑剂研究

概述了邻苯二甲酸酯类(PAEs)作为聚氯乙烯(PVC)增塑剂的应用、危害,说明了PAEs的理化性质,详细归纳了超声波、微波、超声.微波协同萃取技术的应用及PAEs分析测定方法.通过优化超声波、开放式微波和超声.微波等方式萃取PVC塑料样品中的PAEs的萃取条件,比较了3种不同萃取方式的萃取效率.结果表明,超声.微波协同萃取是比较理想的萃取方式.利用该方法对2种实际塑料样品中PAEs的萃取和分析,成功地定量测定了PVC塑料样品中DEHP、DINP和DBP等邻苯二甲酸酯类增塑剂的含量.该法可用于塑料制品中各类邻苯二甲酸酯类增塑剂的快速萃取和分析.     

Ultrasound- and Microwave-Assisted Extractions Facilitate Oil Recovery from Gilthead Seabream (Sparus aurata) By-Products and Enhance Fish Oil Quality Parameters

This research aimed to analyze ultrasound (UAE) and microwave-assisted extraction (MAE) as novel technologies for utilizing gilthead seabream (Sparus aurata) by-products to produce high-quality fish oil for human consumption. The impacts of extraction parameters, namely, temperature, time, solvent-to-solid ratio, and their interactions on the extraction yield, are investigated using response surface methodology (RSM), and a central composite rotatable design. The optimized conditions are 15.47 mL g⁻¹ of solvent-to-solid ratio, 38 min, and 42 °C for UAE and 15.84 mL g⁻¹ of solvent-to-solid ratio, 18 min, and 40 °C for MAE. Under optimal conditions, the maximum extraction yields are 38.40 and 36.70% (g/g) for UAE and MAE, respectively. Both UAE and MAE have significantly higher mass transfer rates (61.70 and 121.58 g h⁻¹, respectively) than Soxhlet extraction (10.78 g h⁻¹). The fatty acid composition, physicochemical, and oxidation analyses of fish oils confirm the suitability of both UAE and MAE for the recovery of high-quality oils from fish processing by-products. The valorized oils mainly include unsaturated fatty acids (≈75%) and are rich in oleic acid. Furthermore, scanning electron microscopy analysis reveals that the key driving force for fast oil extraction is the structural degradation of fish by-products caused by ultrasound and microwave. Practical Applications: Due to environmental and economic viewpoints, the validation of fish oil from fish industry by-products has become a popular research topic recently. Alternative recovery techniques such as ultrasound- (UAE) and microwave-assisted extraction (MAE) protocols may have additional benefits in producing functional oils. Interactive effects of process parameters determine the success of the extraction technique; therefore optimization is a critical approach when applying the extraction protocols. This study shows that UAE and MAE techniques significantly enhanced oil extraction rate from gilthead seabream (Sparus aurota) by-products at lower temperatures and by using lower amounts of solvent. UVA and MAE increase oxidative stability and do not change the fatty acid composition. Hence, the by-product of the gilthead seabream can be a sustainable and food-grade fish oil source and UAE and MAE can be a good alternative to the conventional (Soxhlet) extraction by providing high yield and quality oil.     

Optimization of Microwave-Assisted Extraction of Tea Saponin and Its Application on Cleaning of Historic Silks

Microwave-assisted extraction (MAE) was utilized to extract tea saponin from oil-tea camellia seed cake. The factors influencing the extraction efficiency were studied, including the effects of microwave power, irradiation duration, temperature, ratio of solvent to material and aqueous ethanol concentration. By systematic orthogonal experiments, the optimal extraction technology was determined. Compared with a conventional extraction method, MAE shows great advantages with the extraction time reduced from 6 h to 4 min, 50 % organic solvent saved and about 14 % extraction yield enhanced. Fourier transform infrared spectroscopy testing and high performance liquid chromatography analysis proved that the extracted resultants were tea saponin with similar compounds as a standard tea saponin. The extracted tea saponin was applied on the cleaning of historic silks and showed good removal effect on the stains. This work provides useful information for fully use of oil-tea camellia seed cake and new applications of tea saponin at the protection of historic textiles.     

A novel process for extraction of tea oil from Camellia oleifera seed kernels by combination of microwave puffing and aqueous enzymatic oil extraction

The objective of this study was to extract the oil from Camellia oleifera seed kernels by aqueous enzymatic oil extraction (AEOE). We describe a novel process for extraction of tea oil preceded by tea saponin extraction from C. oleifera seed kernels. The extraction efficiency obtained with microwave‐assisted extraction (MAE) is very high, which the recovery yield is up to 83% in 30 s and the saponins in camellia seed kernels can be completely removed by the second MAE. Moreover, an important step in the process development has been the pretreatment by microwave puffing of camellia seed kernel residues followed by AEOE increased oil extraction yield from 53% to 95%, which will is comparable to hexane oil extraction yields from plant materials.     

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.     

Effect of ultrasound- and pulsed electric field-assisted enzymatic treatment on the recovery and quality of sunflower oil

The aim of this study was to evaluate the effect of cavitation and electroporation on enzymolysis extraction of sunflower oil. The optimum extraction conditions during 2 h under enzyme-assisted extraction (EAE) with a maximum oil yield of ≈23.70 ± 0.11% were as follows: cellulase/pectinase ratio 2:1, enzyme concentration 2%, pH 4.5, liquid/solid ratio 6:1 ml/g, and extraction temperature 40°C. Under the optimized enzymatic conditions, the application of ultrasound- (250 W) and pulsed electric field- (1.2 kV/cm; 52.4 kJ/kg) assisted enzymatic extraction for 30 min significantly increased the oil extraction yield by 91.1% and 18.6%, respectively, as compared with EAE.