Ultrasonic Extraction Research Articles

Optimization of Ultrasound‐Assisted Deep Eutectic Solvent Extraction and Bioactivities of Polysaccharide from Porphyra haitanensis

AbstractIn this paper, ultrasound‐assisted method and deep eutectic solvent (DES) are used to extract polysaccharides from Porphyra haitanensis. The single‐factor experiment is carried out first, and then the response surface experiment is designed to obtain the optimal process conditions. The optimal extraction conditions are the molar ratio of choline chloride to oxalate of 1:1, the water content of DES of 60%, the solid–liquid ratio of 1:60 g mL−1, the time of 120 min, the power of 200 W, and the temperature of 80 °C, with the extraction yield of 4.42%. And the yield of P. haitanensis polysaccharides (PHPs) is 3.14% and 3.31% by water immersion and ultrasonic water extraction, respectively, indicating that the DES extraction method is superior to these two methods, and the optimization effect is good. The extracted polysaccharides are tested for biological activity after separation and purification on DEAE and Sephadex G‐75 columns. The results of α‐glucosidase inhibitory activity and α‐amylase inhibitory activity show that PHPs have certain antioxidant activity. 1,1‐Diphenyl‐3‐nitrophenylhydrazine (DPPH) and 2,2‐diazo‐di‐3‐ethylbenzothiazolin‐6‐sulfonic acid (ABTS) free radical scavenging assays show that PHPs have certain antiglycemic activity.

Ionic liquid based ultrasonic assisted extraction of flavonoids from Artemisia vulgaris and in vitro evaluation of anticancer activity

This study was focused on an effective technique of flavonoids extraction from Artemesia vulgaris using ionic liquids (ILs) as green solvents. The findings showed that the hydrophilic IL, [Bmim][Br] coupled with ultrasonic-assisted extraction (UAE) was able to extract flavonoids better than hydrophobic IL, [Bmim][PF6]. Single-factor experiments reported that the optimum extraction time, 30 min and solid-to-liquid ratio, 1:10 could obtain high extraction yield (9.3 %) and flavonoid content (5.30 mg/g). With the assistance of ultrasonic energy, [Bmim][Br] was successfully to lysis cells and leach out flavonoids as explained by the morphological observation of SEM and functional groups in FTIR spectrum. UHPLC-MS/MS detected few intense flavonoids such as rutin, kaempferol-3-rutinoside, and quercetin-3-glucopyranoside in the extract. The monitoring of Kamlet-Taft parameters such as polarity, acidity and basicity explained the formation of hydrogen bonding between IL, cellulose and flavonoids. The extraction of flavonoids in [Bmim][Br] based UAE followed Peleg’s kinetic model satisfactorily (R2 > 0.95). [Bmim][Br] could be reused up to 5 cycles before lost its extractability. The recovered flavonoids extract exhibited high anticancer activity against HeLa cells (IC50 = 347.37 µg/mL) without any significant cytotoxic effect on normal cervical cells at the concentration up to 300 µg/L. Therefore, this technique was likely to be an efficient extraction of plant flavonoids.

Optimization of extraction of crude polysaccharide from Cassia seed via ultrasonic assisted cellulase and study on its antioxidant activity

In order to improve the current low extraction rate of cassia polysaccharide and improve its extraction efficiency, the ultrasonic wave assisted cellulase extraction method of cassia polysaccharide is first proposed and optimized. Orthogonal test is conducted to analyze the influence of six factors related to cellulase and ultrasonic wave on the extraction of cassia polysaccharide, and at the same time to explore the antioxidant activity of the extracted polysaccharide in vitro. The results show that the main and secondary factors affecting the extraction rate of cassia polysaccharide are pH > ultrasonic power > enzyme dosage > enzymatic hydrolysis temperature > enzymatic hydrolysis time > ultrasonic time. The optimal conditions are: enzyme dosage: 1.6%, enzymatic hydrolysis time: 80 min, enzymatic hydrolysis temperature: 52 ℃, enzymatic hydrolysis pH: 6.4, ultrasonic time: 30 min, ultrasonic power: 276 W, the polysaccharide yield under the optimal conditions is 12.29%, which is 5.31% and 14.43% higher than the single enzyme extraction method and ultrasonic extraction method reported in the literature, respectively, indicating that the composite extraction method is superior to the single extraction method. The antioxidant activity analysis shows that the half inhibitory concentrations of cassia polysaccharide against DPPH·, ABTS·+, ·OH, ·O2- free radicals are 0.894 mg/mL, 1.175 mg/mL, 1.908 mg/mL and 7.601 mg/mL, respectively, which shows good antioxidant activity in vitro. Therefore, ultrasonic assisted cellulase extraction of crude polysaccharide from cassia seed is a new efficient and rapid extraction method.

Investigating the possibility of using subcritical water for extracting polycyclic aromatic hydrocarbons from soils of the dry-steppe zone

In the course of the model experiment, extraction conditions of 16 priority PAHs in subcritical water medium were selected for soils of the chestnut-solonetz complex. For low molecular weight 2-ringed naphthalene and 3-ringed acenaphthene, acenaphthylene, anthracene, phenanthrene and fluorene, the optimal extraction conditions correspond to 10 minutes at a temperature of 200°C. For high molecular weight 4- and 5-ring benz(a)anthracene, fluoranthene, pyrene, chrysene, benz(b)fluoranthene, benz(k)fluoranthene, dibenz(a,h)anthracene, as well as the pollutant of the first hazard class - benz(a)pyrene, the optimal extraction time reached 20 minutes at a temperature of 250°C. For 6-ring benz(g,h,i)perylene and indeno(1,2,3-cd)pyrene, the optimum extraction time increased to 30 minutes and the temperature to 300°C. When comparing the methods of extraction of pollutants from soils, it is shown that the extraction methods can be placed in the following descending order by the value of the extraction coefficient of priority PAHs from the studied types of soils: ultrasonic extraction (1.05) > subcritical extraction (1.13) > saponification method (1.25). Using multivariate analysis of dispersion it is shown that the efficiency of subcritical aqueous extraction decreases with increasing number of benzene rings in the PAH molecule, as well as with increasing soil salinity in the following order: Gleyic Kastanozems < Endosalic Kastanozems < Kastanozems Sodic < Solonets.

Ultrasound-Assisted Extraction of Atractylodes chinensis (DC.) Koidz. Polysaccharides and the Synergistic Antigastric Cancer Effect in Combination with Oxaliplatin.

Oxaliplatin (OXA) is recognized as a first-line drug for gastric cancer. However, low accumulation of the OXA in the target site and the development of drug resistance directly led to treatment failure. In the present study, an ultrasonic extraction method for Atractylodes chinensis (DC.) Koidz. polysaccharides (AKUs) and the combination treatment with OXA in vitro were studied. Results showed that when the pH level was 11, the ultrasound power at 450 W, the solid-liquid ratio was 1:20, and the ultrasound treatment for 30 min, the yield of AKUs was significantly increased to 13.20 ± 0.35%. The molecular weights of the AKUs ranged from 7.21 to 185.94 kDa, and its monosaccharides were mainly composed of arabinose (Ara), galactose (Gal), and glucose (Glu) with a ratio of 58.36, 16.90, and 15.49%, respectively. Cell experiments showed that, compared to OXA alone (2 μg/mL, inhibition rate of 18%), the treatment of OXA with AKUs had a significant synergistic inhibitory effect on MKN45 proliferation, which increased to 33, 41, and 45% with increasing AKUs concentrations (5-50 μg/mL), respectively, representing a 2.5-fold inhibition. Inductively coupled plasma-mass spectrometry (ICP-MS) determination confirmed that AKUs significantly increased the intracellular uptake of OXA by 29%, compared to that of OXA alone. We first demonstrated that the combined synergistic inhibitory effect of AKUs and OXA on gastric cancer cells was mediated by reducing the expression of efflux proteins (MRP1 and MRP2) and increasing the expression of ingested protein (OCT2). As a result of the above, AKUs deserved to be an effective adjuvant combined with chemotherapeutics in a clinical setting.

USE OF Prunus armeniaca L. SEED OIL AND PULP IN HEALTH AND COSMETIC PRODUCTS

Apricot (Prunus armeniaca L.) is grown at high altitudes. Apricot is a stone fruit that can grow at an altitude of 1000-2700 m (Khursheed et al., 2020). Apricot is widely used in the cosmetics industry, pharmaceutical industry and food industry. Apricots are valuable sources for functional foods and nutraceuticals. Apricot kernel and pulp are rich in polyphenols, fatty acids, carotenoids, minerals, vitamin A, ascorbic acid, thiamine, riboflavin, niacin and pantothenic acid and ascorbic acid. It also contains microelements such as Zn, Ca, Cu, Fe, Mg, Na, Mn, P and K. Apricotoil-based massage cream, moisturising cream, bleaching cream and skin mask are produced from apricot kernel pulp, contributing to recycling. In order to extract oil from apricot kernel, oils are extracted by cold press method. For the extraction of bioactive compounds from apricot kernels, various techniques such as solvent extraction, ultrasonication, enzyme assisted, microwave assisted and aqueous extraction are used. In general, our findings indicate that apricot kernels are a valuable source of oil with potential applications in food and cosmetic industries.

Effect of Extraction effectivity of Senna alata L. Leaves on the Total Phenolic, Antioxidative, Antimicrobial and Antigoat Activity

Phytochemicals from natural product such as part of plants have been widely used as a potential source of herbal medication due to their bioactivity. Ketepeng cina (Senna alata L) is a small shrub that lives in tropical and subtropical regions and commonly used as medicinal plant to cure various diseases from infectious microbes. The current research was aimed to evaluate the extraction effectivity of Senna alata L leaves and the influence of the parameter to the total phenolic content, antioxidative, antimicrobial and antigout activity. Extraction of Senna alata L leaves was conducted by several methods, i.e maceration, ultrasonication and hot water extraction. The study revealed that each method give different yield of extraction and the most effective among those method is maceration, which produce highest yields of extracts (19.4%). Ultrasonic-assisted extraction (UAE) method also resulted in high yield but lower than that of maceration. The maceration method increases the yield by about 170% compared to hot water method. The extracts obtained from maceration method contain highest content of total phenolic (278.39mg GAE/g dry mass), thus demonstrate highest antioxidant activity (IC50 25.68mg/L), but lowest anti uric activity (reducing uric acid level by 85.25%). Maceration method was able to increase total phenolic content by about 128% and improve antioxidant activity by about 41%, compared to hot water method. However, UAE was excellent in producing phytochemicals which were responsible in anti uric activity, thus have the highest percentage in reducing UA level (90.72%), or increases by about 6.4%. compared to hot water method.

Optimization of Ultrasonic Extraction Parameters for the Recovery of Phenolic Compounds in Brown Seaweed: Comparison with Conventional Techniques.

Seaweed, in particular, brown seaweed, has gained research interest in the past few years due to its distinctive phenolic profile that has a multitude of bioactive properties. In order to obtain the maximum extraction efficiency of brown seaweed phenolic compounds, Response Surface Methodology was utilized to optimize the ultrasound-assisted extraction (UAE) conditions such as the amplitude, time, solvent:solid ratio, and NaOH concentration. Under optimal conditions, UAE had a higher extraction efficiency of free and bound phenolic compounds compared to conventional extraction (stirred 16 h at 4 °C). This led to higher antioxidant activity in the seaweed extract obtained under UAE conditions. The profiling of phenolic compounds using LC-ESI-QTOF-MS/MS identified a total of 25 phenolics with more phenolics extracted from the free phenolic extraction compared to the bound phenolic extracts. Among them, peonidin 3-O-diglucodise-5-O-glucoside and hesperidin 5,7-O-diglucuronide are unique compounds that were identified in P. comosa, E. radiata and D. potatorum, which are not reported in plants. Overall, our findings provided optimal phenolic extraction from brown seaweed for research into employing brown seaweed as a functional food.

Ultrasound Image-Based Breast Cancer Detection

Breast cancer is the second most common cause of cancer-related death in women, the definition of breast cancer has drawn attention from the bioinformatics and healthcare communities. Only by removing a sample of breast tissue from the breast, examining, and analyzing it under a microscope would this type of research be possible. In the histopathology lab, issues are found by employing skilled pathologists to examine the specimens; these issues are then further investigated utilizing specialized procedures. However, because they have experience in this field, the ultrasonography may mistakenly reveal abnormal changes or diseases. Recent pattern recognition research has revealed several areas that could be improved, therefore there is now more of an emphasis on building strong image processing experiments to provide a highly-and enhancing current diagnosis. Let's employ deep learning approaches for the image feature and the image feature extraction methodology to detect the disease types of breast tissue using histology and image recognition techniques. Before using ultrasonic feature extraction and the final classification in ultrasound feature extraction, this image can be enlarged utilizing ultrasound processing and CNN approach. Index Terms— Machine learning algorithm, Ultra sound image, MRI.

Penerapan Ultrasonik dalam Penelitian Aktivitas Antibakteri Staphylococcus epidermidis Ekstrak Daun Kelor (Moringa oleifera): Pendekatan Berbasis Sains dan Nilai Islam

This study reveals the potential of ultrasonic extraction method in yielding valuable extracts from Moringa oleifera leaves. Moringa oleifera, a versatile plant, takes center stage in this research. The concept aligned with the teachings of the Quran regarding the intricacies of Moringa and its application in acne treatment offers a secure and sustainable option. The utilization of ultrasonic extraction technique contributes to enhancing the benefits obtainable from Moringa. The antibacterial properties identified within Moringa position it as a promising candidate within the realm of medical applications, thereby aligning with the values propagated by the Quran, emphasizing the appreciation of nature's wonders.The methodology of this research involves ultrasonic extraction method and phytochemical analysis conducted in a laboratory setting, alongside evaluating the antibacterial potential through literature review. A bibliometric approach is employed to analyze relevant literature and Quranic verses concerning Moringa. This research falls within the qualitative research category and embodies the post-positivist perspective. Findings of the study indicate that the ultrasonic extraction method successfully yields approximately 22.22% of extract. Moreover, the phytochemical analysis reveals the presence of compounds such as flavonoids, saponins, tannins, alkaloids, triterpenoids, and steroids in the ethanol extract of Moringa leaves.

Lotus Leaf Extract Alleviates Lipopolysaccharide-Induced Intestinal Injury in Mice by Regulating Oxidative Stress and Inflammation.

Inflammatory bowel disease, a disease featured by intestinal epithelial barrier destruction and dysfunction, has been a constant threat to animal health. The primary objective of this research was to assess the impact of the extract derived from lotus leaves (LLE) on lipopolysaccharide (LPS) induced damage to the intestines in mice, as well as to investigate the fundamental mechanism involved. The LLE was prepared using ultrasonic extraction in this experiment, and the LLE total flavonoid content was 117.02 ± 10.73 mg/g. The LLE had strong antioxidant activity in vitro, as assessed by 2, 2-diphenyl-1-picrylhydrazyl, ferric reducing antioxidant power, and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) methods. In the vivo experiment, different doses of LLE (50, 100, and 200 mg/kg) were administered for 2 weeks before LPS treatment in mice. The results revealed that LLE alleviates intestinal tissue damage in LPS-induced mice. In the jejunum tissue, LLE significantly upregulated mRNA and protein expression levels of tight junction proteins, such as ZO-1, occludin, and claudin-1, and decreased the contents of the inflammatory cytokines, interleukin (IL)-1β, IL-6, and tumor necrosis factor-α. Furthermore, the malondialdehyde and lactate dehydrogenase contents increased by LPS in the liver were significantly reduced after administration of LLE, and the total antioxidant capacity, superoxide dismutase, and reduced glutathione decreased by LPS were remarkably increased by LLE. It was found that LLE could relieve LPS-induced oxidative stress by upregulating mRNA and protein expression of Nrf2 and HO-1 in jejunum tissue. In conclusion, LLE alleviates LPS-induced intestinal damage through regulation of the Nrf2/HO-1 signal pathway to alleviate oxidative stress, reducing inflammatory factors and increasing the expression of tight junction proteins in mice.

In silico molecular docking and dynamic simulation of anti-cholinesterase compounds from the extract of Catunaregam spinosa for possible treatment of Alzheimer's disease

Alzheimer's disease (AD), is characterized by a progressive loss of cognitive abilities as well as behavioral symptoms including disorientation, trouble solving problems, personality and mood changes. Acetylcholinesterase (AChE) is a promising target for symptomatic improvement in AD due to its consistent and early cholinergic deficit. This research has investigated the potential compounds from Catunaregam spinosa as AChE inhibitors as a treatment option for AD, aiming to enhance cholinergic neurotransmission and alleviate cognitive decline. Tacrine, the FDA's first approved treatment for AD, is no longer in use due to its hepatotoxicity. Box-Behnken design (BBD) modelling was used to optimise the ultrasonic extraction of alkaloids from the dried fruits of C. spinosa. GC-MS analysis revealed the presence of ninety phytoconstituents in the extract. Among them, eighty-nine new phytoconstituents are reported in this plant fruit for the first time. Out of ninety phytoconstituents, eight phytoconstituents showed the best binding affinity against the AChE enzyme, i.e., PDB IDs 1GQR, 1QTI and 4PQE of AD targets using iGEMDOCK. The lead hits were tested for their drug-like properties and atomistic binding mechanisms using in silico ADMET prediction, LigPlot analysis, and molecular dynamics simulation. The results suggest four compounds such as 1,4,7,10,13,16-hexaoxacyclooctadecane; butanoic acid, 3-methyl-2-[(phenylmethoxy)imino]-, trime; butane-1,2,3,4-tetraol; and D-(+)-ribonic acid.gamma-lactone as potent inhibitors of AChE for the possible treatment of AD.

Response Surface Modelling of Six Organic Acids from Pinellia ternata (Thunb.) Breit by Ultrasound-Assisted Extraction and Its Determination by High-Performance Liquid Chromatography Coupled to Triple Quadrupole Mass Spectrometry

Organic acids are a key active component of Pinellia ternata (Thunb.) Breit, and their concentration is closely associated with the quality of P. ternata. Developing an efficient and rapid method for detecting organic acids can offer a valuable technology for real-time assessment of P. ternata quality. In this work, a high-performance liquid chromatography coupled to triple quadrupole mass spectrometry (HPLC-QqQ-MS/MS) approach, combining the optimization of extraction conditions using response surface methodology (RSM), was developed for the simultaneous quantitative analysis of six organic acids in P. ternata. The optimal extraction conditions for organic acids in P. ternata were ultrasonic extraction with a solid–liquid ratio of 1:50, ultrasonic time of 60 min, and extraction temperature of 55 °C. Multiple-reaction monitoring (MRM) scanning was employed for quantification using HPLC-QqQ-MS/MS in negative ionization mode through a single run of 10 min, and the limit of detection (LLOD) and limit of quantification (LLOQ) for organic acids were as low as 0.138 ng/mL and 0.614 ng/mL, respectively. The relative standard deviations (RSDs) of reproducibility, precision, and stability were all lower than 5.0%, and recovery rates were 97.75–107.14%, with RSDs < 5.0%. Finally, this method was successfully applied to determine the investigated organic acids in 12 production regions of P. ternata, revealing significant differences between different production areas. This indicates that the optimized method is suitable for further accurate investigations of organic acids of P. ternata.

Total phenolic content and antioxidant activity of extracts obtained from tobacco waste seeds, grown under organic production

This study aimed to determine the total phenolic content of Oriental tobacco waste seeds, grown under organic production, and to evaluate their antioxidant activity by extraction with different solvents under different conditions. The extraction was performed with H2O, 99.9% CH3OH, 60% CH3OH, and 96% C2H5OH under maceration and ultrasonic extraction at 20°C and 40°C. All solvents were used in a volume of 4 mL, 5 mL, and 6 mL. The total phenolic content varied between 0.89 mg/g GAE (maceration; sample/solvent ratio 0.1g/5mL, C2H5OH) and 5.85 mg/g GAE (maceration; sample/solvent ratio 0.1g/6mL, C2H5OH). Ethanolic and 60% methanolic extracts had the highest antioxidant activity as determined by the DPPH method; 60% methanolic and water extracts had the highest antioxidant activity as determined by the ABTS method; while methanolic and 60% methanolic extracts had the highest antioxidant activity as determined by the FRAP method. In addition, the content of nicotine in tobacco seed extract was not detected.

Cell disruption of Chlorella sp. and Ecklonia maxima biomass for bioethanol production using Saccharomyces cerevisiae

The demand for bioethanol has increased over the years due to the high costs of fossil fuels, which have been associated with environmental deterioration, leading to the need for cheaper and cleaner biofuel sources. To address this issue, this study investigated micro (Chlorella sp.) and macroalgal (Ecklonia maxima) biomass cell disruption for subsequent bioethanol production using Saccharomyces cerevisiae. Different biomass concentrations of 1.25, 2.5, 3.75 and 5%w/v were prepared, and cell disrupted using ultrasonication and steam extraction for 10, 20, 30 and 40 mins. The samples were analysed for reducing sugar concentrations where the steam-extracted samples produced the highest reducing sugars of 8980 mg/L and 1800 mg/L for Chlorella sp. and E. maxima biomasses respectively. The extracts from ultrasonication and steam extraction were fermented for a period of 96 h where the steam-extracted extracts produced the highest ethanol concentrations from Chlorella sp. and E. maxima biomasses, at the maximum ethanol concentrations of 7 300 mg/L and 689.2 mg/L respectively. The findings of this paper showed that steam extraction is a preferred biomass pretreatment method since its extracts yielded higher ethanol concentrations while the ultrasonicated extracts produced lower ethanol concentrations.

Ultrasonically intensified extraction and emulsification of Azadirachtin and its bioactivity analysis for fenugreek crop growth

Azadirachtin and neem oil, renowned for medicinal and insecticidal properties, were studied for extraction and nanoemulsion synthesis, aiming to address inefficiencies of current extraction and emulsification techniques that impede the utilization of Azadirachtin. The novel aspects include an optimized ultrasonic extraction method for azadirachtin, utilizing a binary solvent system. Additionally, the emulsification of azadirachtin neem oil and its direct application as a bioinsecticide on fenugreek crops demonstrate unique advancements in the study. Response surface methodology and Box-Behnken design optimized extraction parameters such as 35 min time, 0.4 g/mL solid-to-solvent ratio, 40% amplitude, and binary-solvent ratio of 75:25 (v/v) (ethanol:n-hexane). Ultrasound demonstrated superior efficiency with process effectiveness 22 times greater than stirred extraction. The extracted azadirachtin neem oil, superior in yield and potency, underwent concentration and nanoemulsion synthesis via ultrasonication. Stable dispersions over 30 days affirmed nanoemulsion sustainability. Emulsification parameters optimized included stabilizer (acacia gum), stabilizer ratio (2:5:100, solid:oil:water, g:mL:mL), amplitude (40%), and time (40 min). Direct application of emulsion as a bioinsecticide on seasonal fenugreek crops exhibited significant efficacy, enhancing growth and nutritional values (60–100%). Ultrasonication emerged as a superior extraction and emulsification tool, yielding potent azadirachtin neem oil-based emulsions applicable across diverse sectors, including agriculture, food, and cosmetics industries.

In-situ adsorptive pyrolysis of e-waste using coal and rice husk fly ash as alternative adsorbents for energy and precious metal recovery by solvent extraction

This paper aims to use in-situ adsorptive pyrolysis combined with ultrasonication and solvent extraction for precious metal recovery from e-waste. The pyrolysis of discarded printed circuit board (PCB) and waste cable (WC) resulted in pyrolysis oil yields of 4.2–13.0 and 6.8–13.5%, respectively. Aliphatic and single-ring compounds were the major components of the pyrolysis oil. The pyrolysis char was ultrasonicated at 40 kHz for 20, 30, and 40 min at 35 °C to separate precious metals in pyrolysis char. The amounts of Au and Ag recovered by solvent extraction experiments with 2%vol HCl/2%vol HNO3, 2%vol HNO3 and 2%vol I2/2%vol H2O2 were 36.3–61.4 and 60.7–79.9%, respectively. The total energy recovery from the pyrolysis char, oil, and gas obtained from the pyrolysis of PCB was 9.0–9.2 MJ/kg. These results indicated that in-situ adsorptive pyrolysis with ultrasonication and solvent extraction could potentially facilitate e-waste conversion for energy and metal recovery processes at a lower cost.

Enzyme-Assisted Ultrasonic Extraction and Antioxidant Activities of Polysaccharides from Schizochytrium limacinum Meal.

Enzyme-assisted ultrasonic extraction (EAUE) was utilized and optimized for extracting polysaccharides from Schizochytrium limacinum meal (SLMPs) via the response surface methodology. The optimal EAUE conditions were determined as follows: enzyme concentration at 5.18%, ultrasonic temperature at 53 °C, ultrasonic duration of 40 min, ultrasonic power at 60 W, and a liquid-to-material ratio of 34 mL/g, achieving a polysaccharide extraction yield of 11.86 ± 0.61%. The purified polysaccharide component, SLMP1-1, isolated using DEAE Sepharose Fast Flow and Sephadex G-100 columns, exhibited potent antioxidant activity. SLMP1-1, with a molecular weight of 25.5 kDa, comprises glucose, mannose, arabinose, and galactose in a molar ratio of 16.39:14.75:1:693.03. 1H NMR analysis revealed the α configuration of SLMP1-1. Antioxidant assessments, including DPPH, ABTS, and ferric ion reduction assays, were detected with inhibitory values at 21.82-82.98%, 38.21-98.46%, and 3.30-20.30% at 0.2-1.0 mg/mL. This confirmed the effective antioxidant capacity of SLMP1-1, which is notably enhanced post oral and gastric digestion. The findings suggest that polysaccharides extracted from Schizochytrium limacinum meal hold significant promise as natural antioxidants.

Detection of Bromochloro Alkanes in Indoor Dust Using a Novel CP-Seeker Data Integration Tool.

Bromochloro alkanes (BCAs) have been manufactured for use as flame retardants for decades, and preliminary environmental risk screening suggests they are likely to behave similarly to polychlorinated alkanes (PCAs), subclasses of which are restricted as Stockholm Convention Persistent Organic Pollutants (POPs). BCAs have rarely been studied in the environment, although some evidence suggests they may migrate from treated-consumer materials into indoor dust, resulting in human exposure via inadvertent ingestion. In this study, BCA-C14 mixture standards were synthesized and used to validate an analytical method. This method relies on chloride-enhanced liquid chromatography-electrospray ionization-Orbitrap-high resolution mass spectrometry (LC-ESI-Orbitrap-HRMS) and a novel CP-Seeker integration software package for homologue detection and integration. Dust sample preparation via ultrasonic extraction, acidified silica cleanup, and fractionation on neutral silica cartridges was found to be suitable for BCAs, with absolute recovery of individual homologues averaging 66 to 78% and coefficients of variation ≤10% in replicated spiking experiments (n = 3). In addition, a total of 59 indoor dust samples from six countries, including Australia (n = 10), Belgium (n = 10), Colombia (n = 10), Japan (n = 10), Thailand (n = 10), and the United States of America (n = 9), were analyzed for BCAs. BCAs were detected in seven samples from the U.S.A., with carbon chain lengths of C8, C10, C12, C14, C16, C18, C24 to C28, C30 and C31 observed overall, though not detected in samples from any other countries. Bromine numbers of detected homologues in the indoor dust samples ranged Br1-4 as well as Br7, while chlorine numbers ranged Cl2-11. BCA-C18 was the most frequently detected, observed in each of the U.S.A. samples, while the most prevalent degrees of halogenation were homologues of Br2 and Cl4-5. Broad estimations of BCA concentrations in the dust samples indicated that levels may approach those of other flame retardants in at least some instances. These findings suggest that development of quantification strategies and further investigation of environmental occurrence and health implications are needed.

Development of ohmic-assisted green extraction technique with ultrasonic and microwave pretreatments: Burdock (Arctium lappa L.) root extract

The present study was carried out to investigate and optimize the recovery of Burdock (Arctium lappa L.) root extract (BRE) using Ohmic-assisted (OH) extraction method with ultrasonic (US-OH) and microwave (MW-OH) pretreatments. Initially the optimized OH condition was obtained with the aim of maximizing the extraction efficiency and total phenol content. Then, the effect of pretreatment time (20, 40 and 60 min), ultrasonic amplitude (50 and 100 %) and temperatures (30, 40 and 50 °C) in US-OH, and powers (100, 300 and 450 W) in MW-OH were investigated. Finally, optimized OH, US-OH, and MW-OH extraction methods were compared with the heat assisted extraction method (HAE). The results showed that all the main and interaction effects were significant in OH, US-OH, and MW-OH extraction methods (p < 0.05) and only the interaction effects on total phenolic content (TPC) were not significant in the OH method (p > 0.05). The voltage gradient equal to 12.8 V/cm, extraction time equal to 20.72 min and extraction temperature equal to 50 °C were obtained as optimal conditions in the OH extraction of BRE. Ultrasonic amplitude, extraction temperature and ultrasonic time 100 %, 50 °C and 40 min respectively were obtained as the optimum US-OH extraction method. According to the results of chemical compounds, microbial and morphological assays, extraction using pretreatment methods of ultrasound, microwave in ohmic heating, respectively, showed an improvement in the quality of the extraction compared to the conventional (HAE) method.