Improved Extraction Efficiency Research Articles

Current Status of Mining, Modification, and Application of Cellulases in Bioactive Substance Extraction.

Cellulases have been used to extract bioactive ingredients from medical plants; however, the poor enzymatic properties of current cellulases significantly limit their application. Two strategies are expected to address this concern: (1) new cellulase gene mining strategies have been promoted, optimized, and integrated, thanks to the improvement of gene sequencing, genomic data, and algorithm optimization, and (2) known cellulases are being modified, thanks to the development of protein engineering, crystal structure data, and computing power. Here, we focus on mining strategies and provide a systemic overview of two approaches based on sequencing and function. Strategies based on protein structure modification, such as introducing disulfide bonds, proline, salt bridges, N-glycosylation modification, and truncation of loop structures, have already been summarized. This review discusses four aspects of cellulase-assisted extraction. Initially, cellulase alone was used to extract bioactive substances, and later, mixed enzyme systems were developed. Physical methods such as ultrasound, microwave, and high hydrostatic pressure have assisted in improving extraction efficiency. Cellulase changes the structure of biomolecules during the extraction process to convert them into effective ingredients with better activity and bioavailability. The combination of cellulase with other enzymes and physical technologies is a promising strategy for future extraction applications.

Extraction optimization of luteolin, antioxidant compound, from Arachis hypogaea L. hull using response surface methodology

Luteolin is the most abundant phytochemical phenolic compound contained within peanut hulls and has broad pharmacological characteristics and high bioavailability. In this study, the extraction conditions for luteolin from peanut hulls were optimized. The effects of methanol concentration and reaction temperature on luteolin solubility were determined using the central composite design (CCD) under response surface methodology. Luteolin content within in the extracts increased with increasing temperature and organic solvent-to-water ratios. The optimal conditions for luteolin extraction were 81°C and 87.5% methanol for a predicted extraction value of 174.51 mg/100 g, which was within 1.25% of the experimental value of 172.35 mg/100 g, confirming the predicted model. Additionally, compared to conventional stirring, the luteolin content of reflux-extracted peanut hull had a higher extraction efficiency by 42.50%. The antioxidant compound contents and antioxidant capacity of the extracts were also determined, with the effects of temperature and solvent concentration increasing along with the extracted luteolin. In this study, CCD optimized the conditions for obtaining luteolin from peanut hulls, suggesting that the improved extraction efficiency of the bioactive compound can expand the use of peanut shells in the nutraceutical and food industries.

Study on the Mechanism of Ionic Liquids Improving the Extraction Efficiency of Essential Oil Based on Experimental Optimization and Density Functional Theory: The Fennel (Foeniculi fructus) Essential Oil Case.

In this work, microwave-assisted ionic liquids treatment, followed by hydro-distillation (MILT-HD), as an efficient extraction technology, was used to extract essential oil. The purpose for this was to use multivariate analysis (MVA) models to investigate the effects of potential critical process parameters on the extraction efficiency of essential oil, and explore the mechanism of ionic liquids (ILs). According to the design of experiment (DoE), under optimal process conditions, the extraction efficiency of essential oil was dramatically enhanced, and had low energy demands. Since little is known regarding those mechanisms, according to the non-covalent interaction analysis, the underlying mechanism for ILs improving extraction efficiency was explored based on the density functional theory (DFT). The results showed that ILs could form intense non-covalent bond interaction with cellulose. It helped destroy the network hydrogen bond structure of cellulose in plant cells and caused the essential oils in the cells to be more easily exposed to the extraction solution, thereby accelerating extraction efficiency. Based on this work, it is conducive to understand the MILT-HD process better and gain knowledge of the mechanism of ILs.

Highly Efficient Semi-Continuous Extraction and In-Line Purification of High β-O-4 Butanosolv Lignin.

Innovative biomass fractionation is of major importance for economically competitive biorefineries. Lignin is currently severely underutilized due to the use of high severity fractionation methodologies that yield complex condensed lignin that limits high-value applicability. Mild lignin fractionation conditions can lead to lignin with a more regular C-O bonded structure that has increased potential for higher value applications. Nevertheless, such extraction methodologies typically suffer from inadequate lignin extraction efficiencies and yield. (Semi)-continuous flow extractions are a promising method to achieve improved extraction efficiency of such C-O linked lignin. Here we show that optimized organosolv extraction in a flow-through setup resulted in 93–96% delignification of 40 g walnut shells (40 wt% lignin content) by applying mild organosolv extraction conditions with a 2 g/min flowrate of a 9:1 n-butanol/water mixture with 0.18 M H2SO4 at 120°C in 2.5 h. 85 wt% of the lignin (corrected for alcohol incorporation, moisture content and carbohydrate impurities) was isolated as a powder with a high retention of the β-aryl ether (β-O-4) content of 63 linking motifs per 100 C9 units. Close examination of the isolated lignin showed that the main carbohydrate contamination in the recovered lignin was butyl-xyloside and other butoxylate carbohydrates. The work-up and purification procedure were investigated and improved by the implementation of a caustic soda treatment step and phase separation with a continuous integrated mixer/separator (CINC). This led to a combined 75 wt% yield of the lignin in 3 separate fractions with 3% carbohydrate impurities and a very high β-O-4 content of 67 linking motifs per 100 C9 units. Analysis of all the mass flows showed that 98% of the carbohydrate content was removed with the inline purification step, which is a significant improvement to the 88% carbohydrate removal for the traditional lignin precipitation work-up procedure. Overall we show a convenient method for inline extraction and purification to obtain high β-O-4 butanosolv lignin in excellent yields.

The role of pKa, log P of analytes, and protein matrix in solid-phase extraction using native and coated nanofibrous and microfibrous polymers prepared via meltblowing and combined meltblowing/electrospinning technologies

Effect of physicochemical properties including dissociation constant (pKa) and partition coefficient (log P) of the compounds on their extraction efficiency in sample preparation using fibrous polymer sorbents has been demonstrated. Poly-ε-caprolactone as meltblown/electrospun composite fibers, and polypropylene, polyethylene, poly(3-hydroxybutyrate), poly(lactic acid), and polyamide 6 in the meltblown fiber format were used as sorbents in solid-phase extraction. In addition, the polycaprolactone fibers were coated with dopamine, dopamine combined with heparin, and tannin, respectively, to modify their extraction properties. These fibers that were not yet used for extractions and the unique combination of sorbents and analytes significantly extends the scope of nanofibrous extraction. The extraction efficiency was determined using model pharmaceuticals including acetylsalicylic acid, moxonidine, metoprolol, propranolol, propafenone, diltiazem, atorvastatin, and amiodarone. These model compounds displayed the widest differences in both pKa and log P values. The extraction efficiency of some of the fibers reached 96.64%. Coating of polycaprolactone fibers with dopamine significantly improved extraction efficiency of slightly retained metoprolol while moxonidine was not retained on any sorbent. The fibrous sorbents were also tested for extraction of pharmaceuticals in bovine serum albumin and human serum, respectively, to demonstrate their capability to extract them from a complex protein-containing matrix. The clean-up efficiency of our fibers was compared with that of a commercial restricted access media (RAM) C-18 alkyl-diol silica column. Our technique is in accordance with the requirements of modern sample preparation techniques.

Electrochemically controlled solid phase microextraction based on nanostructured polypyrrole film for selective extraction of sunset yellow in food samples

Solid-phase microextraction (SPME) is extensively employed in analytical chemistry to improve extraction efficiency. The development of SMPE methods is still a great challenge thanks to its poor selectivity. Herein, we have reported the application of electrochemically controlled solid-phase microextraction (EC-SPME) based on a conducting molecularly imprinted polymer (CMIP) film for the selective extraction and determination of sunset yellow (SY) in food samples using a UV–Vis spectrophotometer. The CMIP film was electrochemically prepared in the presence of SY anions as the template anions during the electropolymerization of pyrrole onto the stainless steel fiber surface using the potentiostat method. The imprinting process was carefully investigated via FESEM, CV, and EIS approaches. In the developed EC-SPME method, the extraction of SY occurred at CMIP when the potential was applied, and as a consequence, the sensing performance was dramatically enhanced as compared to that obtained via SPME. The film template with SY showed high selectivity for SY compared to studied interferents. The EC-SPME method responded linearly to SY with a limit of detection of 0.34 µmol L−1. Also, the developed method had a sufficient sensitivity level to determine analyte in food samples. Finally, the suitability of the proposed method for the analysis of orange-flavored jelly powder, peach juice powder, and beverage samples was demonstrated. To validate the proposed method, the results were compared with those obtained through HPLC–UV analysis.

Reduced graphene oxide coated nickel foam for stir bar sorptive extraction of benzotriazole ultraviolet absorbents from environmental water

The use of porous carrier and coating sorbents in stir bar sorptive extraction (SBSE) contributes to the improvement of extraction efficiency and dynamics. Herein, porous nickel foam (NF) with large surface area and magnetic property was used as the carrier of stir bar. NF was added into the mixture of graphene oxide (GO) and reducing agent, and reduced graphene oxide (RGO) coating was obtained on the surface of NF substrate by in situ hydrothermal reduction. The characterization results of Fourier transform infrared spectroscopy, X-ray power-diffraction and scanning electron microscope showed that GO was partially reduced into RGO, and the RGO coating was uniformly loaded on the NF surface. The obtained RGO-NF composite was used as the stir bar coating for the analysis of six benzotriazole (BZTs) UV absorbents. The extraction efficiency was between 48 and 64% for six BZTs. RGO-NF stir bar exhibited faster adsorption/desorption kinetics than commercial polydimethylsiloxane coated stir bar (50 min vs 120/360 min) due to its porous structure and large specific surface area. On this basis, a method of RGO-NF coated stir bar sorptive extraction combined with high performance liquid chromatography (HPLC)-DAD was established for the determination of six BZTs. Under the optimized conditions, the limits of detection were 0.33–0.50 μg/L for six target BZTs, and the linear range was 1–100 μg/L. The proposed method merits good ability to resist matrix and was used to analyze six BZTs in environmental water samples. The recoveries of target BZTs were obtained within 83.0–112% in the spiked East Lake water and 97.0–111% in the spiked Yangtze River water, respectively.

A New Method for Improving Extraction Efficiency and Purity of Urine and Plasma Cell-Free DNA.

This study assessed three commercially available cell-free DNA (cfDNA) extraction kits and the impact of a PEG-based DNA cleanup procedure (DNApure) on cfDNA quality and yield. Six normal donor urine and plasma samples and specimens from four pregnant (PG) women carrying male fetuses underwent extractions with the JBS cfDNA extraction kit (kit J), MagMAX Cell-Free DNA Extraction kit (kit M), and QIAamp Circulating Nucleic Acid Kit (kit Q). Recovery of a PCR product spike-in, endogenous TP53, and Y-chromosome DNA was used to assess kit performance. Nucleosomal-sized DNA profiles varied among the kits, with prominent multi-nucleosomal-sized peaks present in urine and plasma DNA isolated by kits J and M only. Kit J recovered significantly more spike-in DNA than did kits M or Q (p < 0.001) from urine, and similar amounts from plasma (p = 0.12). Applying DNApure to kit M- and Q-isolated DNA significantly improved the amplification efficiency of spike-in DNA from urine (p < 0.001) and plasma (p ≤ 0.013). Furthermore, kit J isolated significantly more Y-chromosome DNA from PG urine compared to kit Q (p = 0.05). We demonstrate that DNApure can provide an efficient means of improving the yield and purity of cfDNA and minimize the effects of pre-analytical biospecimen variability on liquid biopsy assay performance.

Light extraction efficiency improvement through double sided periodic photonic structures for deep UV light emitting diodes

Polarization-dependent light extraction efficiency (LEE) of AlGaN based flip-chip deep ultraviolet light emitting diode (peak emission at 280 nm) with embedded periodic photonic structure (PPS), surface PPS and double-sided PPS configuration have been studied by utilizing three-dimensional finite-difference time-domain (3D FDTD) method. Among the three considered configurations, double-sided PPS has been found to possess the maximum improvement in LEE, followed by embedded PPS configuration. The surface PPS offers the least LEE improvement among the three configurations with reference to the conventional deep-UV LED structure. The respective improvements for TE, TM and overall LEE have been found to be around 128.37%, 59.18% and 99% for the double-sided PPS as compared to the conventional deep-UV LED.

Facile fabrication of composited solid phase microextraction thin membranes for sensitive detections of trace hydroxylated polycyclic aromatic hydrocarbons in human urine

Solid phase microextraction (SPME) has potential to be used for the high-performance enrichments of hydroxylated polycyclic aromatic hydrocarbons (OH-PAHs), which are important biomarkers of PAH exposure. By choosing suitable adsorbent, it is conducive to fabricate new-type of SPME device for improved extraction efficiencies towards OH-PAHs. In this study, a novel method of surface solvent evaporation has been proposed to fabricate SPME thin membrane, integrating the advantages of polydimethylsiloxane (PDMS) and different porous adsorbents. The powdery metal organic framework (Uio66-NH2), porous polymer (powdery polymer aerogel, PPA) and ordered mesoporous carbon (OMC) have been chosen as typical adsorbents and fabricated as thin membranes successfully, indicating the universality of the proposed method for membrane fabrication. Comparing the extraction efficiencies of three prepared membranes towards OH-PAHs, the OMC-PDMS membrane has demonstrated best enrichment efficiencies. The OMC-PDMS membrane was used for the enrichments of trace OH-PAHs in human urine of both smokers and nonsmokers, combining with liquid chromatographic tandem mass spectrometry (LC-MS/MS). The detection limits were in the range of 0.15–0.39 ng L−1, and satisfactory recoveries were found to be 82.1%–115%. It can be seen that the universal strategy to fabricate SPME membrane is helpful to achieve broad-spectrum or selective enrichments of target analytes from complex matrix by simple modulation of membrane components.

Fault diagnosis method of rare earth extraction production line based on wavelet packet and alexnet transfer learning

In rare earth production, improving the fault detection of extraction equipment has a key impact on improving extraction efficiency and product quality. The traditional method is based on the observation of the liquid level, the efficiency and accuracy can’t be guaranteed. In this paper, a fault diagnosis and recognition method for rare earth extraction production line based on wavelet packet and alexnet transfer learning is proposed. Taking six fault states of rare earth extraction production line as the research object, the fault signal is extracted by wavelet packet decomposition, and the corresponding target data set of time-frequency diagram is generated. Then, the pre trained alexnet model is trained and fine tuned on the generated target data set, and finally applied to fault diagnosis of rare earth extraction production line. The results show that the proposed method is more accurate than the traditional convolution neural network, which verifies the effectiveness of the method.

Magnetic Dispersive Solid Phase Extraction Using Recycled-graphite for GO-Fe3O4-dithizone Composite Combined with FAAS for Determination of Lead in Environmental Samples.

Magnetic dispersive solid phase extraction (MdSPE) was developed to determine the concentration of lead (Pb) in real water samples, while graphene oxide-magnetite-dithizone (GO-Fe3O4-DTZ) from the used graphite tubes (recycled graphite) of electrothermal technique was simply employed as a new sorbent to improve extraction efficiency, separated by external magnetic field and analyzed with FAAS. The synthesized sorbent was evaluated for its surface property, functional group and surface morphology by Zeta potential, Fourier transform infrared spectrophotometer (FTIR), and scanning electron microscope (SEM), respectively. The relevant measurement parameters, such as pH, extraction time, type and concentration of eluent, sample volume and reusability, were optimized. Under the optimal conditions, preconcentration factor was 13.33. The limit of detection (LOD) and limit of quantitation (LOQ) obtained were 0.070 and 0.23 mg/L, respectively. The relative standard deviation (%RSD) was 3.41%. Recovery values were 90.1 - 123%. In addition, the robustness of the method was affirmed in terms of tolerance limit obtained from interference studies.

Review on Extraction of Phenolic Compounds from Natural Sources Using Green Deep Eutectic Solvents.

For more sustainable and environmentally friendly scientific research, it is essential to apply green chemistry principles in all areas of science. A possible area in which green chemistry principles can significantly influence the productivity and the quality of the outcome is extraction of natural products. The conventional toxic solvents can be replaced by environmentally friendly solvents known as deep eutectic solvents, which fortunately, due to their unique properties, can significantly improve extraction efficiency. In this literature review, the extraction of a specific class of natural products, phenolic compounds, using different types of green deep eutectic solvents has been reviewed. Within this review, the composition of those solvents used to extract different types of phenolic compounds has been discussed. In addition, the factors affecting their extraction, extracting solvent component structure, molar ratio of extracting solvent components, extraction temperature, solid to extraction solvent ratio, and water content, have been evaluated.

The effect of ultrasound treatment on the extraction of lycopene and β-carotene from cherry silverberry fruits

The aim of this study was to evaluate the effect of ultrasound treatment on the efficiency of carotenoid extraction from cherry silverberries. Fruits (except for the control group) were sonicated at three power levels: 200,400 and 600 W. Fruits were extracted in 95% ethyl alcohol. After extraction, the content of β-carotene and lycopene in the extract was determined by HPLC with the UV-Vis SPD-20A detector and an acetonitrile-methanol-dichloromethane (75:25:5) as mobile phase. The dry matter content of all three sonicated samples was lower than in the control sample. Sonication at 200 W significantly (p < 0.05) increased β-carotene yield (by 59%) relative to the control sample. Lycopene yield also increased significantly (p < 0.05) relative to the control group after sonication at 200 W, but further increase in power did not induce significant improvement in extraction efficiency. The results of this study indicate that ultrasound treatment at 200 W (0.25 W·cm−3) increases the efficiency of carotenoid extraction from cherry silverberries and higher power can lead to reduction of extraction efficiency.

LC–MS/MS method for determining picogram-level of zolpidem and its main metabolites in hair using a zirconia-based sorbent

Although urine and blood samples have been conventionally used for testing zolpidem (ZPD), a sedative-hypnotic, these matrices have limited application because they have a relatively short detection period and can be used only in case of recent drug exposure. Therefore, it is necessary to use an alternative biological sample to obtain the evidence of ZPD misuse. Herein, a liquid chromatography–tandem mass spectrometric (LC–MS/MS) method was developed for the determination of ZPD and its metabolites, zolpidem phenyl-4-carboxylic acid (ZPCA) and zolpidem 6-carboxylic acid (ZCA), in hair to resolve the above-mentioned problems. Mechanical pulverization of hair, methanol extraction with sonication, and the zirconia-based hybrid solid–phase extraction technique were used for obtaining improved extraction efficiency and effective sample purification. The treated hair sample was analyzed using the LC–MS/MS method with the electrospray ionization source in positive and multiple-reaction monitoring modes. The target analytes were separated and detected within 8 min using an Xselect HSS T3 column. Gradient elution was performed using 5 mM ammonium formate and acetonitrile. The lower limit of quantification of ZPD, ZPCA, and ZCA were 1.0, 0.5, and 1.0 pg mg−1, respectively. The calibration ranges were 1.0–1000.0 pg mg−1 for ZPD, 0.5–200.0 pg mg−1 for ZPCA, and 1.0–200.0 pg mg−1 for ZCA, with the determination coefficients (r2 ≥ 0.9986). The intraday accuracy and precision ranged from −7.1 to 9.0% and within 6.5%, respectively, and the interday accuracy and precision ranged from −6.1 to 7.9% and within 5.4%, respectively. The recovery, matrix effect, and process efficiency were 65.2–96.6%, 64.6–106.5%, and 44.3–100.5%, respectively, with the relative standard deviation of 4.0–5.0%. The developed method was successfully applied to analyze 13 forensic hair samples of ZPD abusers, and the concentration ratios of ZPD and its two main metabolites (ZPCA and ZCA) in the ZPD-positive samples were also presented. These results revealed that ZPCA and ZCA were not easily incorporated into hair, and demonstrated that their analysis in hair samples requires the employed method to have picogram-level sensitivity. Therefore, the developed method was suitable for simultaneous analysis of ZPD, ZPCA, and ZCA in hair samples, and it could provide clear evidence for illegal ZPD administration, including ZPD-facilitated sexual assault.

Recent development and challenges in extraction of phytonutrients from palm oil.

Phytonutrients are plant-derived bioactives which are widely utilized as colorants or supplements in food, cosmetic, and pharmaceutical products. To meet the global demand for phytonutrients, oil palm has emerged as a promising source of phytonutrients on account of its large-scale plantation worldwide and high oil productivity. Phytonutrients including carotenoids, tocols, sterols, squalene, phospholipids, coenzyme Q10, and polyphenols can be found in crude palm oil as well as in the byproducts (e.g. palm oil mill effluent and palm-pressed fiber oil) generated from the palm oil milling process. However, the high viscosity and semisolid properties of palm oil are problematic in phytonutrient extraction. Another major challenge is the retention of the sensitive phytonutrients during the extraction process. Over the years, the advances in the extraction methods have improved the extractability of phytonutrients. The emerging extraction methods can operate under mild conditions to mitigate the risk of phytonutrient degradation. This review outlines the types of phytonutrient in palm oil and their extraction strategies. The working principles and operating conditions of extraction methods are discussed along with their potential and limitations in terms of extraction efficiency and practicability. The methods for pretreatment of feedstocks for improving extraction efficiency are also highlighted. The challenges in the extraction of phytonutrient from palm oil feedstock are summarized. Lastly, we provide suggestions for overcoming the limitations and improving the performances of phytonutrient extraction.

Effect of ultrasound-assisted extraction on the structure and emulsifying properties of peanut protein isolate.

With an increasing demand for edible protein, research on new extraction methods is attracting more attention. The effects of such methods on functional properties are important. The present study aimed to evaluate the effect of ultrasound-assisted extraction on the extraction efficiency, structure, and the emulsifying properties of peanut protein isolate (PPI). Ultrasound-assisted extraction significantly improved extraction efficiency and shortened the processing time. The nanostructure, molecular weight distribution, and particle size of PPI were altered by ultrasound-assisted extraction. The emulsifying properties of the PPI from ultrasound-assisted extraction were significantly improved compared with alkaline extraction. Peanut protein isolate had lower molecular weight fractions, higher levels of hydrophobic amino acids, and the highest fluorescence intensity with ultrasound intensity, temperature, and time of 3.17 W cm-3 , 35 °C, and 30 min, respectively. These contributed to the higher emulsifying activity index and emulsifying stability index of the PPI emulsions. The uniform distribution of droplets and smaller particle size of the PPI emulsions was also observed. The results suggested that ultrasound can be used to induce the conformational changes to modify the interfacial association between protein-oil phases, thereby improving the emulsifying properties of peanut protein. © 2020 Society of Chemical Industry.

Improved Extraction Efficiency of Antioxidant Bioactive Compounds from Tetraselmis chuii and Phaedoactylum tricornutum Using Pulsed Electric Fields.

Pulsed electric fields (PEF) is a promising technology that allows the selective extraction of high-added value compounds by electroporation. Thus, PEF provides numerous opportunities for the energy efficient isolation of valuable microalgal bioactive substances (i.e., pigments and polyphenols). The efficiency of PEF-assisted extraction combined with aqueous or dimethyl sulfoxide (DMSO) solvents in recovering pigments and polyphenols from microalgae Tetraselmis chuii (T. chuii) and Phaeodactylum tricornutum (P. tricornutum) was evaluated. Two PEF treatments were applied: (1 kV/cm/400 pulses, 3 kV/cm/45 pulses), with a specific energy input of 100 kJ/kg. The total antioxidant capacity (TAC) was positively influenced by the use of DMSO. The highest TAC in the T. chuii culture was achieved at a lower extraction time and electric field than for P. tricornutum. The use of DMSO only improved the polyphenols′ extraction for P. tricornutum, whereas the PEF and extraction time were more important for T. chuii. Carotenoids and chlorophyll a were more efficiently extracted using DMSO, while chlorophyll b levels were higher following aqueous extraction for both microalgae. In P. tricornutum, the TAC and pigment extraction efficiency were in general higher at lower extraction times. It can be concluded that PEF may be a promising alternative for the enhancement of the selective extraction of antioxidant bioactive compounds from microalgae.

Microwave-Assisted Industrial Scale Cannabis Extraction

Cannabis is a flowering plant that has long been used for medicinal, therapeutic, and recreational purposes. Cannabis contains more than 500 different compounds, including a unique class of terpeno-phenolic compounds known as cannabinoids. Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD) are the most extensively studied cannabinoids. They have been associated with the therapeutic and medicinal properties of the cannabis plant and also with its popularity as a recreational drug. In this paper, an industrial method for cannabis extraction using 915 MHz microwaves coupled with continuous flow operation is presented. The main advantages of the microwave-assisted extraction (MAE) are associated to the continuous-flow operation at atmospheric pressure which allows for higher volumes of biomass to be processed in less time than existing extraction methods, with improved extraction efficiency leading to increased final product yields, improved extract consistency and quality because the process does not require stopping and restarting material flows, and ease of scale-up to industrial scale without the use of pressurised batch vessels. Moreover, due to the flexibility of changing the operation conditions, MAE eliminates additional steps required in most extraction methods, such as biomass decarboxylation or winterisation, which typically adds at least a half day to the extraction process. Another factor that sets MAE apart is the ability to achieve high extraction efficiency, i.e., up to 95% of the active compounds from cannabis biomass can be recovered at industrial scale.

Comparison of Different Extraction Methods for the Recovery of Olive Leaves Polyphenols

In the present study, advanced extraction techniques, microwave (MAE), ultrasound (UAE), and high pressure (HPAE)-assisted extraction, were applied to improve extraction efficiency of olive (Olea europaea L.) leaves polyphenols. The effect of sample mass (1.5 and 3 g), MAE—time (2, 8.5, and 15 min) and temperature (45 and 80 °C), UAE—time (7, 14, and 21 min) and amplitude (50 and 100%) and HPAE—time (1, 5.5, and 10 min) and pressure (300 and 500 MPa) on the concentration of each analyzed polyphenol compound was examined. Identified polyphenols were oleuropein, hydroxytyrosol, chlorogenic acid, caffeic acid, verbascoside, and rutin. All three advanced extraction techniques yielded higher content of total polyphenols when compared to the conventional heat-reflux extraction (CE) along with a significant reduction of extraction time from 60 (CE) to 2, 21, and 5.5 min in MAE, UAE, and HPAE, respectively. The most intensive values of tested parameters in each technique were the ones that promoted cell wall disruption, e.g., temperature of 80 °C in MAE, 100% amplitude in UAE and 500 MPa in HPAE. MAE and UAE were more efficient in total polyphenols’ recovery than HPAE.