Ultrasonic Extraction Time Research Articles

Ultrasonic-assisted DES extraction optimization, characterization, antioxidant and in silico study of polysaccharides from Angelica dahurica Radix

In this study, polysaccharides from Angelica dahurica Radix (ADR) were extracted by using ultrasonic-assisted deep eutectic solvent (DES) extraction method. The DES consist of choline chloride (HBA, hydrogen bonding acceptor) and 1, 4-butanediol (HBD, hydrogen bonding donor) with the molar ratio of 1:3 was proved as the best system for polysaccharides extraction. A Box-Behnken design with three factors and three levels was utilized to optimize ultrasonic power, extraction time and temperature for increased polysaccharides yield. The optimal extraction parameters were determined as follows: DES water content of 20 %, liquid–solid ratio of 10:1 mL/g, ultrasonic time of 21 min, temperature at 60 °C, and ultrasonic power of 435 W. These conditions yielded an extraction rate nearly matching the theoretical predicted value of the response surface model, surpassing the traditional hot water extraction method by 1.33 times and requiring less time. The antioxidant polysaccharides was assessed using DPPH,ABTS and Hydroxyl methods, which indicated that ADRP extracted by ultrasound assisted DES had excellent antioxidant capacity and showed a dose–response relationship with drug concentration. Structural analysis identified ADR polysaccharides as a heteropolysaccharide rich in sugar aldonic acids—namely, fucose, rhamnose, arabinose, galactose and glucose—with molar ratios of 0.47:1.99:17.61:64.76:15.17. The polysaccharides’ number-average molecular weight was determined to be 97.422 kDa, with a weight-average molecular weight of 245.678 kDa. Network pharmacology and molecular docking analysis suggest that the monosaccharides Rha and Ara could potentially interact with the proteins GSR and GSTA1, respectively, indicating that ADRP had good antioxidant potential and could be applied in multiple fields with promising development prospects in the future.

Extraction, Identification, and Antioxidant Activity of Flavonoids from Hylotelephium spectabile (Boreau) H. Ohba.

The extraction of total flavonoids from Hylotelephium spectabile (Boreau) H. Ohba (H. spectabile) leaves was studied through the use of a double enzyme-assisted ultrasonic method, and the extraction process was optimized using the Box-Behnken design. Eight different macroporous resins were screened for purification in single-factorial experiments, and the flavonoid compounds in the extract of H. spectabile leaves were identified using HPLC-MS. Through the evaluation of the total reducing capacity and capacity for reducing 1,1-diphenyl-2-trinitrophenylhydrazine (DPPH), hydroxyl radicals (·OH), and 2,2'-biazobis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS), the in vitro antioxidant activities of the crude extracts of the total flavonoids and purified total flavonoids of H. spectabile leaves were investigated. The results showed that the most efficient conditions for flavonoid extraction were an ultrasonic extraction time of 60 min, an ethanol concentration of 35%, a liquid-to-material ratio of 20:1 mL/g, and an amount of enzyme (cellulose/pectinase = 1:1) of 1.5%, forming H. spectabile powder. Under these conditions, the total flavonoid extraction rate in the H. spectabile leaf extract was 4.22%. AB-8 resin showed superior performance in terms of purification, and the optimal adsorption and desorption times were 1.5 h and 3 h, respectively. The recommended parameters for purification included a liquid volume of 5.5 BV, a flow rate of 1.2 BV/min, a pH of 5, and a concentration of 0.8 mg/mL. The observed order for reducing capacity was ascorbic acid (VC) > rutin > purified total flavonoids > crude extract of total flavonoids. The purified total flavonoid extract from H. spectabile showed a good scavenging ability against DPPH, ·OH, and ABTS·+, suggesting strong antioxidant activity. Therefore, this study can serve as technical support and reference data for the further development and utilization of H. spectabile resources.

Ekstraksi berbantu gelombang ultrasonik dan fotodegradasi senyawa antosianin pada tangkai parijoto (Medinilla speciosa Blume)

Parijoto is an endemic plant widely found on the slopes of Mount Muria, Kudus Regency, Central Java. The local community often consumes parijoto fresh fruit and processes parijoto fruit such as syrup, dodol, candy, and tea. So far, the Parijoto stalk, which weighs 18.19% of the total weight of the parijoto stalk and fruit, has not been widely used, but it has great potential as a source of anthocyanin. Anthocyanin compounds have low stability to temperature and light. For this reason, extraction with a relatively low temperature and faster than conventional methods is required, one of which is Ultrasonic-assisted extraction. Ultrasonic waves produce cavitation bubbles, facilitating solvent penetration so that cell bioactive components can be extracted more effectively. This study aimed to determine the effect of ultrasonic wave-assisted extraction time of parijoto stalk anthocyanin and examine the effect of various light exposure intensities and exposure times (photodegradation) on Parijoto stalk anthocyanin extract. Ultrasonic-assisted extraction of parijoto stalk anthocyanins used a completely randomized design (CRD) with extraction time (5, 10, 15, 20, and 25 minutes) and three treatment repetitions. In photodegradation using a factorial complete randomized design with the treatment of light exposure intensity (2037 lux, 4259 lux, 6482 lux, and 9259 lux) and exposure time (6, 12, 18, and 24 hours). The results showed that the longer the extraction, up to 20 minutes, the total anthocyanin levels, redness (a*), and yellowness (b*) increased while lightness (L*) decreased. The higher the light intensity of the fluorescent lamp and the longer the light exposure, the lower the total anthocyanin content with a lower half-life. Ultrasonic-assisted extraction have proven to be quite effective for the anthocyanin extraction but need to attention with time and light exposure intensity.

Extraction and characterization of phenolic compounds from Commiphora gileadensis bark using ultrasonic-assisted extraction

Developing nations across the globe place significant importance on ensuring the complete protection, efficacy, and quality of herbal products and medicinal plants. Among these beneficial plants, Commiphora gileadensis stands out due to its diverse array of biological activities. The bark of this plant species offers numerous therapeutic advantages, including its potential for treating wounds, inflammatory conditions, and bacterial infections. To explore the process of extraction of biologically active components, this study employed ultrasonic-assisted extraction (UAE) on ethanolic extracts of C. gileadensis bark. Various variables of UAE process, such as ultrasonic frequency, extraction time, sample-to-solvent ratio, and ethanol concentration, were carefully investigated via the ‘’One-Factor-At-a-Time (OFAT)’’ method to understand their individual impacts on the extraction process. The obtained extracts underwent further analysis to identify the presence of different phytochemicals, employing techniques such as ‘’Gas Chromatography-Mass Spectroscopy (GC-MS) and Fourier Transform Infrared Spectroscopy (FTIR)’’. The experimental results demonstrated that the UAE process yielded promising outcomes, with the maximum extraction yields, total phenolic content (TPC), and total flavonoids content (TFC) of the ethanolic extract from C. gileadensis bark reaching 37.60 ± 0.31 %, 149.75 ± 3.23 mg GAE/g d.w., and 44.84 ± 3.02 mg QE/g d.w., respectively. Additionally, this study successfully identified a total of 30 phenolic compounds present in the C. gileadensis bark extract for the first time, highlighting the efficacy of UAE as a suitable method for efficiently extracting various groups of phytochemicals from the bark of C. gileadensis.

The application of deep eutectic solvents for protein extraction from bee bread (Perga)

Bee bread is one of the basic nutrients that bees use as a protein source and is formed as a result of the fermentation of bee pollen. In the last few years, this product has become increasingly recognized and consumed among bee products due to its functional properties. However, deep eutectic solvents (DES) have attracted great interest in recent years as promising green alternatives to replace traditional solvents due to their variable viscosity, low vapor pressure, application-specific adjustability, non-flammability and chemical stability. In this study, bee bread was extracted in 12 different DES with different hydrogen bond acceptor (HBA):hydrogen bond donor (HBD) combinations. The DES combination with the highest total protein content was determined to be choline chloride (ChCl)-urea. Then, ultrasonic extraction conditions were optimized for maximum bioactive extraction in extracts prepared with ChCl-urea. The optimum conditions were found as 31.3 %, 25 min, 35 °C for ultrasonic power, extraction time and temperature, respectively. The desirability value (d) of the model was 0.83. The extracts were analyzed for total phenolic content, total protein content, individual polyphenolics, individual amino acids and individual vitamins as well as antimicrobial and antioxidant activity tests. According to the results, total protein, total individual amino acids and total individual phenolics were higher in the extracts obtained with ChCl-urea compared to the extract prepared with conventional solvent (ethanol). In conclusion, all these findings showed that ChCl-urea combination can be an alternative to ethanol depending on the structural characteristics of the target compounds to be extracted from bee bread.

Optimizing Ultrasonic Extraction and Purification of Nuciferine With Response Surface Method

Background Lotus leaves are obtained from plants belonging to the genus Nelumbo in the Nymphaeaceae family. They serve both as agricultural produce and traditional Chinese medicinal herbs. Nuciferine, an amorphine alkaloid found in lotus leaves, holds significance due to its anti-inflammatory, lipid-lowering, and hypoglycemic properties. Objective The factors influencing nuciferine extraction from lotus leaves using the dipping-acid-assisted ultrasonic extraction method (DAUEM) have received limited attention. This study aims to optimize DAUEM conditions (ethanol concentration, solvent-to-material ratio, and ultrasonic extraction time) through a Box-Behnken response surface design. Methods Nuciferine purification from lotus leaves is achieved using D101 macroporous adsorptive resin. A single-factor test, with ethanol concentration ( V/V), solvent-to-material ratio ( V/M), and ultrasonic extraction time as variables, serves as a basis for optimizing the nuciferine extraction process via the response surface methodology. Results The highest nuciferine yield (0.1035 ± 0.005)% was obtained using 74% ethanol ( V/V), a 26:1 solvent-to-material ratio, and an 82min extraction time. Nuciferine purity reached 67.14% using 70% ethanol as the eluent and high-performance liquid chromatography for determination. DAUEM effectively extracts nuciferine from lotus leaves, with optimization achieved using Box-Behnken response surface methodology. D101 macroporous adsorption resin efficiently separates and purifies nuciferine in lotus leaves. Conclusion This experiment demonstrates good precision and accuracy, making it suitable for the extraction, separation, and purification of nuciferine in lotus leaves. The method lays the foundation for the development and utilization of nuciferine.

Enhanced extraction of clove essential oil by ultrasound and microwave assisted hydrodistillation and their comparison in antioxidant activity

Clove essential oil (CEO) is recognized for its variety of bioactivities and is widely used in the fields of food and pharmaceuticals. Eugenol is the main component that causes the oil's effectiveness. This study included a bibliometric analysis to demonstrate the novelty of the CEO extraction method. A combination of ultrasound and microwave techniques was utilized to enhance the efficiency of hydrodistillation (HD) extraction of essential oil from clove bud in terms of extraction yield, extraction rate, and eugenol composition, which is a strong antioxidant agent. Meanwhile, the effects of ultrasonic extraction temperature and time, microwave distillation power and time, and the ratio of clove to water were also investigated. The optimum conditions were as follows: ultrasonic extraction was at 40 °C for 45 min, microwave distillation power was 400 W for 45 min, and the clove to water ratio was 1:20 (g/mL). The ultrasound pretreatment prior to microwave-assisted hydrodistillation (U-MHD) method obtained the CEO, which had a significantly higher extraction yield (16.80 ± 0.26 %) and a greater amount of eugenol (78.49 %) than the CEOs obtained by traditional HD and MHD methods. Corresponding to the antioxidant activity of CEO from U-MHD, it possessed the strongest DPPH radical scavenging activity with an IC50 value of 2.79 ± 0.05 μg/mL, and it was comparable to the activity of eugenol. This is the first occurrence of CEO extraction employing the U-MHD procedure. This process could be used to enhance the bioactivity of CEO as well as its extraction efficiency, easy operation, rapid extraction, and eco-friendly technique. In terms of cost-analysis, MHD stands out as the most economically viable extraction method, boasting the lowest cost per 100 g product. The obtained results serve as fundamental data for implementing the scaling up of extraction processes to an industrial level.

Study on the extraction process, chemical compositions, and anti-inflammatory activity of total saponins extract from Anemone raddeana Regel

Anemone raddeana Regel. is mainly distributed in the northeast of China, and its rhizomes part is rich in saponins, which is commonly used for treatment of pain, inflammatory and rheumatic illnesses. However, there are few reports on saponins from Anemone raddeana Regel. This research had investigated the extraction process, chemical compositions, and anti-inflammatory activity in vitro of total saponins extract from Anemone raddeana Regel. The extraction process was optimized by the single factor experiment and response surface methodology, and the anti-inflammatory activities were evaluated by determination of the nitric oxide content and cytophagocytic activity in LPS induced RAW 264.7 cells. The optimized extraction parameters for the total saponins extract were as follows: ethanol concentration 50 %, the ratio of liquid to material 43:1 mL/g, ultrasonic extraction time 70 min, and the yield of the total saponin was 1.74 % under these extraction conditions. Forty-three components were preliminarily separated and analyzed from the total saponins fraction by UPLC-QTOF-MS method. In addition, it was found that the total saponins extract could exert the anti-inflammatory effect by reducing the nitric oxide content and inhibiting the phagocytic activity. This study suggested that the total saponins extract from Anemone raddeana Regel. could exhibit the superior anti-inflammatory activity, and be developed as a green and natural anti-inflammatory drug.

Establishment and Optimization of Flavonoid Extraction and Detection System for Hemerocallis

Hemerocallis is a characteristic vegetable with outstanding edible and medicinal value. Flavonoids are important bioactive components of Hemerocallis. To improve the extraction efficiency and detection accuracy of flavonoids from Hemerocallis, we established a high-performance liquid chromatography (HPLC) detection system, which can simultaneously detect multiple flavonoids. In addition to the previously developed organic solvent extraction method, an ultrasonic-assisted extraction technique that uses fewer samples was established to extract flavonoids from Hemerocallis. The extraction conditions of the ultrasonic-assisted extraction were optimized via a single-factor experiment and a response surface experiment. The HPLC system detected and determined the contents of rutin, isoquercetin, myricetin, quercetin, apigenin, and diosmetin from 70 Hemerocallis germplasm resources. In addition, we evaluated the antioxidant activity of flavonoids in Hemerocallis using DPPH free radical scavenging capacity with ascorbic acid (Vc) as a positive control. The results showed that the optimum conditions for the ultrasonic extraction process were as follows: sample weight of 0.25 g, ethanol volume fraction of 72%, ethanol volume of 2.5 mL, and ultrasonic extraction time of 17 min. Under these conditions, flavonoid extraction had a strong scavenging effect on DPPH. With the increase in the sample solutions’ concentrations, its antioxidant capacity was gradually enhanced, and the DPPH scavenging rate reached 70.2%. The optimized ultrasonic-assisted extraction technology can increase the total content of six flavonoids in day lily bud by 59.01%, especially the content of rutin (increased by 64.41%) in Hemerocallis flower buds. Among 70 Hemerocallis plant resources, we selected materials H0087 and H0059 with high and stable flavonoid content, with the total content of six substances being 4390.54 ug/g and 3777.13 ug/g. Thus, this study provides a reference for extracting and determining flavonoid contents in Hemerocallis materials. It also provides a theoretical basis for high-quality individual plant breeding.

Microwave and ultrasound-assisted extraction of bioactive compounds from Papaya: A sustainable green process

The demand for sustainable and eco-friendly extraction methods for bioactive compounds from natural sources has increased significantly in recent years. In this study, we investigated the effectiveness of the microwave pretreated ultrasound-assisted extraction (MPUAE) process for the extraction of antioxidants (TPC, DPPH, and FRAP) from papaya pulp and peel. The optimized variables for the MPUAE process were determined using the Box-Behnken design tool of response surface methodology. Our results showed that the optimized variables for pulp and peel were 675.76 and 669.70 W microwave power, 150 s of irradiation time, 30 °C ultrasound temperature, and 19.70 and 16.46 min of ultrasonic extraction time, respectively. Moreover, the MPUAE process was found to be more energy-efficient and environmentally friendly compared to the conventional ultrasound-associated extraction (UAE) technique. The MPUAE process emitted less CO2 to the environment and had a shorter extraction time, resulting in a more sustainable and cost-effective extraction process. Our study suggests that the MPUAE process has the potential to be a promising and eco-friendly alternative for the industrial extraction of bioactive compounds from papaya and other natural sources.

Rutin extraction from female Carica papaya Linn. using ultrasound and microwave-assisted extractive methods: Optimization and extraction efficiencies

Green extractive methods accompanied by resource conservation through process optimization are important in working towards sustainable processes. In the present paper, rutin was extracted from the leaf of female Carica papaya Linn using microwave-assisted extraction (MAE), ultrasound-assisted extraction (UAE), sequential microwave ultrasound-assisted extraction (MUAE), and sequential ultrasound microwave-assisted extraction (UMAE) methods. Subsequently, the effect of extraction parameters on rutin yield were analyzed and compared. In addition, the extraction efficiency and energy consumption of the extraction processes were measured and discussed. In the present study, solid-liquid (S/L) ratio was determined to be the most significant extraction variable. Under optimized conditions, MUAE and UMAE were determined to yield the highest amount of rutin extracted at 18.46 ± 0.64 mg/g and 18.43 ± 0.81 mg/g, respectively. However, MUAE was determined to be the least resource efficient method as it consumed the highest amount of energy due to its relatively long extraction time. UAE was determined to be the most efficient in resource utilization as it required the least amount of energy for every mg/g of yield extracted, while the yield obtained was, nonetheless, comparatively high. The optimal condition obtained for UAE was 20 min of ultrasonic extraction time (TU), 20 % of ethanol mixture concentration (C), 710 μm of particle size (S), and 1:650 wt/wt of solid-liquid (S/L) ratio (R).

Extraction technology, components analysis and anti-inflammatory activity in vitro of total flavonoids extract from Artemisia anomala S. Moore

Artemisia anomala S. Moore exerts many pharmacological activities, including the removing of the blood stasis, relieving of the fever and analgesia, reducing the swelling and dampness. In this study, the extraction technology, chemical compositions and anti-inflammatory effect in vitro and mechanism of total flavonoids extract from Artemisia anomala S. Moore were studied. The optimal yield rate of total flavonoids extract was optimized by single factor experiments and response surface method, and the chemical constituents were analyzed by UPLC-QTOF-MS method; and the anti-inflammatory activity of the extract was evaluated with lipopolysaccharide induced RAW 264.7 cells. The highest extraction rate was 2.02% under these conditions of the concentration of ethanol 50%, the ultrasonic extraction time 30 min, and the ratio of solvent volume to material weight 20:1 (ml/g). In addition, the main components of total flavonoid extract were preliminarily identified and deduced based on mass spectrometry information and relevant literatures, and its stronger anti-inflammatory activity was demonstrated by reducing the phagocytosis, the content of nitric oxide and the level of related cytokines (tumor necrosis factor-α, interleukin−10, interleukin-6). Furthermore, it was further revealed that the anti-inflammatory effect of the extract was closely connected with the activation of TLR4-MyD88-NF-κB signalling pathway. This study indicated that the total flavonoids extract from Artemisia anomala S. Moore may be a better candidate anti-inflammatory natural medicine.

Enhancing lutein extraction from marigolds through ultrasound-assisted optimization using response surface methodology

This research aimed to enhance and optimize the ultrasound-assisted extraction (UAE) of lutein from marigold flowers. The Response Surface Methodology (RSM) was the primary optimization technique. Three key independent variables were considered to determine the best conditions for the highest lutein yield: ultrasonic amplitude, extraction temperature, and extraction time. These variables were systematically varied following the Central Composite Design (CCD). Lutein quantitation was achieved using ultraviolet-visible spectrophotometry analysis. Using both the RSM and CCD frameworks, the study established specific ranges for the operational conditions: 21.6–38.4% for ultrasonic amplitude, 23.18–56.82 °C for extraction temperature and 3.18–36.82 minutes for extraction duration. The study determined the optimal extraction conditions to be 32.76% ultrasonic amplitude, 40.08 °C extraction temperature, and 25.82 minutes of extraction time. Under these optimized conditions, the experimental lutein yield closely matched the yield predicted by the RSM model, thus confirming the model's accuracy. The UAE demonstrated a notably superior lutein yield compared to traditional extraction techniques. The RSM is a robust tool for refining and determining optimal UAE conditions for lutein extraction from marigold flowers. With its efficiency, speed, and eco- friendliness, the optimized UAE technique presents significant potential for widespread industrial use.

Optimization of Ultrasonic-Assisted Extraction of Flavonoids from Ilex Latifolia Thunb by Response Surface Methodology and their Influence over the Activity of Xanthine Oxidase

We have examined the ultrasonic ethanol extraction of Ilex latifolia Thunb flavonoids and the inhibitory effect of these flavo¬noids on xanthine oxidase. Four single-factor extraction conditions were examined: ethanol concentration (%), solid–liquid ratio (g/mL), ultrasonic extraction temperature (°C), and ultrasonic extraction time (min). With these data, the response surface methodology was adopted to optimize the ultrasonic extraction parameters. The optimal ultrasonic extraction parameters were determined to be the ethanol concentration of 49%, the solid-to-liquid ratio of 1:27, the ultrasonic extraction temperature of 74°C, and the ultrasonic extraction time of 97 min. Under the optimal conditions described ear¬lier, the experimental yield of flavonoids was 6.367% with a relative standard deviation of 1.9%, which was comparable to the theoretical extraction rate. The half maximal inhibitory concentration of flavonoids for xanthine oxidase is 5.50 mg/mL. The inhibitory effect was competitive and reversible, with an inhibitory kinetic constant Ki of 2.35 mg/mL.

An Integrated Strategy of Chemical Fingerprint and Network Pharmacology for the Discovery of Efficacy-Related Q-Markers of Pheretima.

Pheretima, one of the animal-derived traditional Chinese medicines, has been wildly used in various cardiovascular and cerebrovascular diseases, including stroke, coronary heart disease, hyperlipidemia, and hyperglycemia. However, it was still a big challenge to select the quality markers for Pheretima quality control. The fingerprint and network pharmacology-based strategy was proposed to screen the efficiency related quality markers (Q-Markers) of Pheretima. The ratio of sample to liquid, ultrasonic-extraction time, temperature, and power were optimized by orthogonal design, respectively. The chemical fingerprint of forty batches of Pheretima was established, and six common peaks were screened. The network pharmacology was used to construct the Pheretima-Components-Targets-Pathways-Stroke network. It was found that six potential efficacy Q-markers in Pheretima could exert the relaxing meridians effect to treat stroke through acting on multiple targets and regulating various pathways. A simple HPLC-DAD method was developed and validated to determine the efficacy Q-markers. Grey relational analysis was used to further verify the relation of potential efficiency related quality markers with the anticoagulation activity of Pheretima, which indicated that the contents of these markers exhibited high relationship with the anticoagulation activity. It was concluded that hypoxanthine, uridine, phenylalanine, inosine, guanosine, and tryptophan were selected as quality markers related to relaxing meridians to evaluate the quality of Pheretima. The fingerprint and network pharmacology-based strategy was proved to be a powerful strategy for the discovery of efficiency related Q-markers of Pheretima.

Study on extraction and antibacterial activity of aucubin from Eucommia ulmoides seed-draff waste biomass

Aucubin (AU) is an active ingredient exerting strong antioxidant and anti-inflammatory effects in treating several diseases. This study evaluated the extraction of AU from Eucommia ulmoides seed-draff (EUSD) waste biomass using a series of solvents (methanol, ethanol, i-propanol, n-propanol, n-butanol, n-pentanol and cyclohexane) assisted with microwave and ultrasound, and proposed the optimized method for extraction. Five factors were investigated by Box-Behnken design (BBD) and response surface methodology (RSM). The optimized extraction conditions were as follows: liquid-solid ratio of 46.37 mL/g, methanol percentage of 89.56%, ultrasonic (extraction) time of 59.95 min, microwave power of 306.73 W, and microwave (extraction) time of 18.93 s. To this end, the AU extraction reached the maximum value (149.1 mg/g), which was consistent with the theoretical value (149.3 mg/g). Furthermore, the kinetics of extraction process were investigated by mathematic modeling. The extraction process analysis was also explored by 1H nuclear magnetic resonance (1H-NMR) spectroscopy, Fourier transform infrared (FTIR) spectroscopy and COSMOtherm program. This study found out that methanol provided better extraction efficiency than the conventional solvents (water, ethanol, i-propanol, n-propanol, n-butanol, n-pentanol, cyclohexane) due to possible interactions by the formation of hydrogen bond between AU and methanol, and ultrasound and microwave could significantly enhance mass transfer, which exhibited higher extraction efficiency and lower energy consumptions (149.1 mg/g and 0.102 kW·h vs. 73.4 mg/g and 0.700 kW·h for Soxhlet extraction). In the antibacterial activity study, the AU extract exerted strong antibacterial ability against 4 tested pathogens, and the antibacterial effect followed the order of: Staphylococcus aureus (35.9 ± 1.32 mm) >Escherichia coli (30.7 ± 1.38 mm) >Bacillus subtilis (20.5 ± 1.36 mm) >Salmonella (15.9 ± 1.39 mm) with the AU concentration of 40 mg/mL. Therefore, the development of this study will help to deepen the further understanding of natural product extraction by methanol-based ultrasonic and microwave, and has certain application value for the development and utilization of natural iridoid glycosides product.

Determination of Polycyclic Aromatic Hydrocarbons (PAHS) in Sewage Sludge and Compost by Dispersive Solid-Phase Microextraction (SPME) and Ultra-High Performance Liquid Chromatography (UHPLC) with Diode Array Detection (DAD)

Polycyclic aromatic hydrocarbons (PAHs) are carcinogenic that may degrade human health. Organic solvents are commonly used for the extraction of PAHs from solid samples and the analytes are determined chromatographically. This study describes the ultra-high performance iquid chromatography-diode array detection (UHPLC-DAD) determination of PAHs in sewage sludge and compost used as agricultural fertilizer. The PAHS may be transmitted to humans through the food chain. Analytes in the fertilizer were quantitatively extracted into the organic phase in water-dichloromethane-acetonitrile and determined liquid chromatographically. 16 PAHs were selectively extracted in a single clean-up step. For method development, the type and volume of organic solvent, pH of the water, and ultrasonic extraction time were optimized. For method validation, analytical figures of merit were obtained for the linearity, limit of detection (LOD), limit of quantification (LOQ), stability, intra- and inter-day precision, and accuracy. The developed and validated method was used for PAH determination in the fertilizers. Sample analyses were performed with 89–102% recovery values and 0.7–4.1% relative standard deviations.

Development of Green and Efficient Extraction of Bioactive Ginsenosides from Panax ginseng with Deep Eutectic Solvents.

The extraction of active constituents from natural sources in a green and efficient manner is considered an important field in the pharmaceutical industry. In recent years, deep eutectic solvents (DESs), a new type of green solvent, have attracted increasing attention. Therefore, we aimed to establish a green and high-efficiency extraction method for ginsenosides based on DESs. This study takes Panax ginseng as a model sample. Eighteen different DESs were produced to extract polar ginsenosides. Ultrasound-assisted extraction (UAE) was applied for simplicity and efficiency. A binary DES synthesized using choline chloride and urea at a proportion of 1:2 prepared by a heating stirring method is proven to be more effective than other solvents, such as the widely used 70% ethanol for the extraction of ginsenosides. Three variables that might affect the extraction, including the DES content in the extraction solvent, liquid/solid ratio, and ultrasound extraction time, were evaluated for optimization. The optimum extraction conditions for ginsenosides were determined as follows: DES water content of 20 wt%, liquid/solid ratio of 15 mL g−1, and an ultrasonic extraction time of 15 min. The extraction yield for the optimized method is found to be 31% higher than that for 70% ethanol, which achieves efficient extraction. This study shows that DESs are available to extract ginsenosides for use in traditional Chinese medicine. The discovery also contributes to further research into the green extraction of ginsenosides.

The pharmaceutical applications of total flavonoids extract from Isatis tinctoria L. leaves

Isatis tinctoria L. leaves (Folium isatidis), as dried leave of the isatis indigotica in the cruciferous family, has a variety of pharmacological effects, including regulation of immune function, anti-inflammatory, bacteriostasis, antipyretic effect. In this study, total flavonoids extract from Folium isatidis was systematically studied about extractive process, main components, antibacterial, antioxidant and anti-inflammatory activities. The total flavonoids extract yield was (7.65±0.07)% under the optimal extraction parameters of ethanol concentration 54.37%, ratio of solvent volume to material weight 40:1 ml/g, and ultrasonic extraction time 20 min. Nineteen chemical components were inferred and identified by UPLC-QTOF-MS method. Although the extract showed mild antibacterial and antioxidant effects with MIC values 31.25, 62.5, 125 and 125 mg/ml against Streptococcus, Salmonella, Staphylococcus aureus and Escherichia coli, and IC50 DPPH 12.64 µg/ml, IC50 ABTS 16.72 µg/ml and FRAP value at 0.11 mmol Fe2+/100 µg/ml compared with the positive control butylated hydroxytoluene with IC50 DPPH 8.13 µg/ml, IC50 ABTS 2.22 µg/ml and FRAP value at 0.16 mmol Fe2+/100 µg/ml. It exhibited better anti-inflammatory effects in LPS induced RAW 264.7 cell (50, 100 and 200 µg/ml of TFE) and ALI mice (100, 250, or 500 mg/kg•b•w of TFE), which was demonstrated by reducing cell phagocytic activity, decreasing the content of pro-inflammatory cytokine and inflammatory mediator, and improving lung tissue injury. Furthermore, the mechanism of anti-inflammatory action was further revealed to be related to the regulation of TLR4-TRIF-NF-κB signaling pathway. These studies revealed that total flavonoids extract could be used as a natural and green candidate for anti-inflammatory drugs and enrich the variety of clinical anti-inflammatory drugs.

Deep Eutectic Solvents (DESs)-Ultrasonic-Assisted Extraction of Paeoniflorin and Paeonol from Moutan Cortex

Deep eutectic solvents (DESs-)-ultrasonic-assisted extraction technology was used to evaluate and optimize the extraction process of paeoniflorin and paeonol in Moutan Cortex. First of all, 10 kinds of choline chloride-based DESs were selected as potential extraction solvents, and the DES extraction effect of choline chloride: lactic acid was determined to be the best. Then, single-factor experiments were conducted to explore the effects of DES composition (molar ratio, water content, and ratio of material to liquid) and ultrasonic treatment (ultrasonic power, extraction time, extraction temperature, and vortex time) on the yield of paeoniflorin and paeonol in Moutan Cortex. On this basis, the response surface method was used to optimize the process of ultrasonic-assisted extraction of paeoniflorin and paeonol from Moutan Cortex with DESs. The results showed that the optimum process parameters of DESs-ultrasonic-assisted extraction of paeoniflorin and paeonol from Moutan Cortex were as follows: molar ratio of choline chloride to lactic acid was 1 : 2, water content was 30%, ratio of material to liquid was 1 : 30 (g/mL), ultrasonic power was 300 W, extraction time was 33 min, extraction temperature was 50°C, and vortex time was 5 min. Under these conditions, the yield sum of paeoniflorin and paeonol in the obtained Moutan Cortex was 9.279 mg/g. The difference between the experimental value and the theoretical value was 0.333 mg/g. The results showed that the response surface method can simulate and predict the yield of paeoniflorin and paeonol in Moutan Cortex under different extraction conditions, and it was feasible to optimize the process parameters. The results of this study show that DES has great potential to replace traditional solvents in the extraction of active components of the Moutan Cortex. The study on the extraction of active components of traditional Chinese medicine by DES is helpful to expand the scope of the application of DES in traditional Chinese medicine.