Ethanol Reflux Method Research Articles

Effects and mechanisms of Salvia miltiorrhiza Bunge extract on myocardial cell apoptosis in rat heart failure model.

This work aimed to investigate the effects of Tanshinone IIA (Tan IIA) on myocardial cell (MC) apoptosis in a rat model of heart failure (HF). Tan IIA was extracted from Salvia miltiorrhiza Bunge (SMB) using an ethanol reflux method. Fifty rats were randomly divided into five groups: sham (no treatment), mod (HF model establishment), low dose (LD: 0.1 mL/kg Tan IIA), medium dose (MD: 0.3 mL/kg Tan IIA), and high dose (HD: 0.5 mL/kg Tan IIA), with 10 rats in each group. The effects of different doses of Tan IIA on cardiac function, MC apoptosis, and the levels of proteins associated with the PI3K/Akt/mTOR signaling pathway were compared. Mod group showed a significant decrease in systolic arterial pressure, mean arterial pressure, heart rate, left ventricular systolic pressure, left ventricular ejection fraction, left ventricular fractional shortening, and the levels of p-PI3K, p-Akt, and p-mTOR proteins versus sham group (p < 0.05). Additionally, the left ventricular end-diastolic diameter (LVIDd), end-systolic diameter, diastolic pressure, and MC apoptosis were significantly increased (p < 0.05). LD, MD, and HD groups exhibited significant improvements across various indicators of cardiac function and MC apoptosis versus mod group (p < 0.05). Tan IIA may improve cardiac function and inhibit MC apoptosis in rats with HF by modulating the PI3K/Akt/mTOR signaling pathway.

Fabrication of Magnetic Silica Nanomaterials and Their Effects on Algal Harvesting

Harmful algal blooms are a global problem in water environments, and their explosive growth endangers the health of aquatic ecosystems. Magnetic nanomaterials for the harvesting of microalgae have received a lot of attention because of their high efficiency, low cost, and ease of operation. In this study, magnetic mesoporous silica nanomaterials were prepared using Fe3O4 as a carrier and harvesting on Chlorella sp. HQ. It was found that silica coated with magnetic Fe3O4 microspheres has good dispersion. The harvesting of Chlorella sp. HQ via magnetic mesoporous silica could be maintained over a wide pH range (4 to 12). After the removal of organic components from the surface of the material, the magnetic mesoporous silica obtained a better porous structure. The ethanol reflux method was more beneficial than the calcination method in maintaining the stable structure of the material, thus improving the harvesting efficiency of the material for the microalgae Chlorella sp. HQ by a maximum of 17.8% (65.9% to 83.7%). When the molar ratio of active agent cetyltrimethylammonium bromide (CTAB) and stabilizer polyvinylpyrrolidone (PVP) was 1: 0.092 at pH 4 and algal concentration of 0.5 g/L, the materials showed the maximum harvesting efficiency of Chlorella sp. HQ was 84.2%.

Osmanthus-Loaded PVP/PVA Hydrogel Inhibits the Proliferation and Migration of Oral Squamous Cell Carcinoma Cells CAL-27.

Conventional medical agents for oral squamous cell carcinoma (OSCC) with some adverse effects no longer meet the needs of the public. In this study, the prognosis-related hub genes of osmanthus-targeted therapy for OSCC were predicted and analyzed by network pharmacology and molecular docking. Osmanthus was extracted using the ethanol reflux method and osmanthus-loaded PVP/PVA (OF/PVP/PVA) hydrogel was prepared by electron beam radiation. The molecular structure, crystal structure and microscopic morphology of hydrogels were observed by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. OSCC cells CAL-27 were cultured with OF/PVP/PVA hydrogel at different concentrations of extract to discover cell proliferation by MTT assay. The scratching test and JC-1 staining were used to observe the migration and mitochondrial membrane potential. Through experimental exploration, we found that a total of six prognosis-related targets were predicted, which are PYGL, AURKA, SQLE, etc., and osmanthus extract had good binding activity to AURKA. In vitro, except for proliferation inhibition, OF/PVP/PVA hydrogel prevented cell migration and changed the mitochondrial membrane potential of CAL-27 cells at a concentration equal to or greater than 50 μg/mL (p < 0.05). The addition of autophagy inhibitor chloroquine and 3-methyladenine weakened the migration inhibition of hydrogel (p < 0.05).

Osmanthus Fragrans Loaded NIPAAM Hydrogel Promotes Osteogenic Differentiation of MC3T3-E1.

There is an urgent need to find long-acting, natural osteogenesis-promoting drug systems. In this study, first the potential targets and mechanism of osmanthus fragrans (O. fragrans) extract in regulating osteogenic differentiation based on autophagy were analyzed by network pharmacology and molecular docking. Then, osmanthus fragrans was extracted using the ethanol reflux method and an osmanthus fragrans extract loaded Poly N-isopropylacrylamide (OF/NIPAAM) hydrogel was prepared by electron beam radiation. The chemical components of the osmanthus fragrans extract and the microstructure of OF/NIPAAM hydrogels were characterized by ultraviolet-visible spectrophotometry (UV-Vis) and X-ray diffraction (XRD), respectively. Mouse embryonic osteoblast precursor cells MC3T3-E1 were cultured with different concentrations of OF/NIPAAM hydrogel to discover cell proliferation activity by CCK-8 assay. Alkaline phosphatase (ALP) staining and alizarin red staining were used to observe the differentiation and calcification. Through experimental exploration, we found that a total of 11 targets were predicted, which are TP53, CASP3, SIRT1, etc., and osmanthus fragrans had good binding activity to TP53. In vitro, except for proliferation promotion, OF/NIPAAM hydrogel enhanced ALP activity and formation of mineralized nodules of MC3T3-E1 cells at a concentration equal to or less than 62.5 μg/mL (p < 0.05). The addition of autophagy inhibitor 3-methyladenine (3-MA) reduced ALP activity and mineralized nodule formation.

Antioxidative Activity Evaluation of High Purity and Micronized Tartary Buckwheat Flavonoids Prepared by Antisolvent Recrystallization.

Tartary buckwheat, a healthy food, is associated with a reduced risk of certain human chronic diseases. However, the bioactive component flavonoids in Tartary buckwheat have poor solubility and low absorption in vivo. To improve these points, 60.00% Tartary buckwheat total flavonoids (TFs) were obtained by ethanol refluxing method, which were purified and micronized by antisolvent recrystallization (ASR) using methanol as a solvent and deionized water as an antisolvent. By using High Performance Liquid Chromatography (HPLC) and electrospray ionized mass spectrometry (ESI-MS), the main flavonoid in pure flavonoids (PF) were rutin (RU), kaempferol-3-O-rutinoside (KA) and quercetin (QU); the content of TF is 99.81% after purification. It is more worthy of our attention that micronized flavonoids contribute more to antioxidant activity because of good solubility. These results provide a theoretical reference for the micronization of other flavonoids.

Optimization of extraction process of Children's Qingfei Zhisou Syrup based on pharmacodynamics

This study determined the extraction rates of indirubin in Indigo Naturalis by ethanol reflux extraction method and water extraction method. The pharmacodynamic study against cough induced by ammonia water in the mouse model and the cough induced by citric acid in the guinea pig model were performed to optimize the extraction process of the sovereign medicinal Indigo Naturalis and the whole prescription of Children's Qingfei Zhisou Syrup. The extraction rate of indirubin by the ethanol reflux method was 51.89%, and indirubin was not detected in the product of water extraction. Two samples of Children's Qingfei Zhisou Syrup prepared with different methods can prolong the incubation period of cough and suppress the frequency of coughs in pharmacodynamic experiments. In terms of prolonging the incubation period of cough, the two samples prepared with different methods had no significant difference. In terms of reducing the frequency of coughs, the high-dose Five kinds of ethanol extracts such as indigo naturalis and three kinds of water extracts such as gypsum had better effect against the citric acid-induced cough of guinea pigs than other samples(P&lt;0.05). The extraction rate of indirubin in Children's Qingfei Zhisou Syrup sample prepared with ethanol was higher than that with water. The two samples of Children's Qingfei Zhisou Syrup prepared with the two methods showed good antitussive effects. The sample prepared with 5 ingredients(including Indigo Naturalis) extracted with ethanol and 3 ingredients(including Gypsum Fibrosum) extracted with water had better alleviation effect on the citric acid-induced cough of guinea pig than the whole water extract sample. In conclusion, the optimum extraction scheme is ethanol extraction for 5 ingredients including Indigo Naturalis in combination with water extraction for 3 ingredients including Gypsum Fibrosum, and the Children's Qingfei Zhisou Syrup produced in this manner has better antitussive efficacy.

High-Pressure Supercritical CO2 Extracts of Ganoderma lucidum Fruiting Body and Their Anti-hepatoma Effect Associated With the Ras/Raf/MEK/ERK Signaling Pathway.

As a noted medicinal mushroom, Ganoderma lucidum (G. lucidum) has been reported to have a number of pharmacological effects such as anti-tumor and liver protection. Compared with the common ethanol reflux method, supercritical CO2 extraction has obvious advantages in obtaining antitumor extracts from G. lucidum fruiting body such as short extraction time, low temperature and no solvent residue. However, Using high-pressure supercritical CO2 without entrainer to obtain the antitumor extracts from G. lucidum and studying their anti-hepatoma effect have not been reported. In this study, high-pressure supercritical CO2 extracts obtained under 65, 85, and 105 MPa pressure named as G65, G85, G105 respectively and ethanol reflux extract (GLE) were used to investigate their anti-hepatoma activity and the underlying molecular mechanism. The total triterpenoid content of G85 was significantly higher than that of G65 and GLE, but did not differ significantly from that of G105 by UV and high-performance liquid chromatography. GLE, G65, and G85 could inhibit cell proliferation, arrest cell cycle in G2/M phase, and induce apoptosis in two liver cancer cell lines (QGY7703 and SK-Hep1), of which G85 had the strongest effect. The results showed that the potency of their cytotoxicity of the high-pressure supercritical CO2 extracts on human hepatoma carcinoma cells in vitro was consistent with their total triterpenoid content. G85 exhibited significant anti-hepatoma effect with low toxicity In vivo. Further mechanistic investigation revealed that the anti-tumor effect of these extracts was associated with their inhibition of Ras/Raf/MEK/ERK signaling pathway. Our findings suggest that the high-pressure supercritical CO2 extraction of G. lucidum fruiting body can be used to obtain a triterpenoid-rich anti-tumor agent, which may have potential clinical significance for the treatment of human hepatoma.

Microwave-assisted green extraction of antioxidant components from Osmanthus fragrans (Lour) flower using natural deep eutectic solvents

Osmanthus fragrans (Lour) flower is a typical fragrant herb in eastern countries containing multiple bioactive compounds, the extract of which has been widely used as a natural antioxidant additive in food and cosmetics. However, the existing extraction methods use organic solvents during the extraction process, which is non-eco-friendly and harmful to human health. In this study, we introduce, to our knowledge for the first time, microwave-assisted deep eutectic solvent extraction (MA-DESE) to extract antioxidant components from O. fragrans flower. The MA-DESE procedure was optimised, validated, and compared with that of traditional solvent extraction by using response surface methodology. The maximum antioxidant activity of 101.81 mg Trolox equivalent/g of dry weight was achieved at the following optimum MA-DESE parameters: microwave power, 497.12 W; microwave treatment time, 59.03 s; and solid–liquid ratio, 31.14 mL/g. In addition, UPLC-MS analysis showed a greater variety of antioxidant components, such as olivil and osmanthuside H, in O. fragrans flower extract obtained by MA-DESE than by the traditional ethanol reflux method. These results demonstrated that MA-DESE, which is safe and eco-friendly, could substitute for the conventional solvent extraction process, which is time-consuming and tedious, for the extraction of antioxidant components from O. fragrans flower.

Synthesis, Crystal Structures and Catalytic Activities of Two Copper Coordination Compounds Bearing an N,N’-Dibenzylethylenediamine Ligand

Two copper coordination compounds bearing an N,N’-dibenzylethylenediamine ligand, namely [Cu3L(CH3COO)6]n (1) and [(CuCl4)∙(C6H5CH2NH2CH2)2] (2) (L = N,N’-dibenzylethylenediamine) were synthesized by the ethanol refluxing method. Powder X-ray diffraction (PXRD), infrared spectra (IR), elemental analyses, and single crystal X-ray diffraction were used to characterize and verify their structures. Structural analyses showed that the asymmetric unit of compound (1), composed of two Cu(II) cations, three acetate anions, and half of the ligand, was bridged by one acetate to obtain an infinite 1D chain structure. The analyses further showed that the asymmetric unit of compound (2), composed of two crystallographically independent [C6H5CH2NH2CH2]+ units, four chloride anions, and one central Cu(II) cation is connected into an infinite 2D network structure by the hydrogen bonding interactions. The copper compounds were used to catalyze the decomposition of H2O2, and the results showed that both of the compounds exhibited excellent catalytic activities under optimized conditions.

Porous MnO as efficient catalyst towards the decomposition of Li2CO3 in ambient Li-air batteries

The undesirable formation and low-efficient decomposition of Li2CO3 on cathode of Li-air battery, is an insurmountable obstacle for its practical applications. High efficient cathode catalysts toward Li2CO3 decomposition still have not been thoroughly studied. Here, we report a porous MnO prepared by heating precursor using a facile ethanol refluxing method and employed as high efficient cathode catalyst in ambient Li-air battery for Li2CO3 decomposition. Compared with the pure carbon electrode, it demonstrated an improved electrochemical performance of more than 100 cycles in ambient air and low charging overpotential. At the 100th cycle, the discharge/charge terminal voltage of MnO cathode remains 2.65/4.00 V, which is much higher/lower than that of pure carbon electrode (2.36/4.44 V). These results reveal that the superior catalytic performance of MnO towards the Li2CO3 decomposition during charging. Additionally, we carefully examined the time- and depth-dependent discharge products distributions in the carbon-containing cathode, especially for the formation of Li2CO3, by X-ray photoelectron spectroscopy. The Li2CO3 was initially formed on the surface of Li2O2, and then gradually into the inner part of the Li2O2, which reveals that the Li2O2 is inclined to react with CO2 rather than the carbon based electrode materials. These results present essential information for the development of high efficient cathode catalysts toward the high-efficient decomposition of Li2CO3 for practical Li-air batteries in ambient air.

Solvent extraction of caffeoylquinic acids from Artemisia selengensis Turcz leaves and their in vitro inhibitory activities on xanthine oxidase

In this study, the caffeoylquinic acid (CQA) extract solution of the Artemisia selengensis Turcz (AST) leaves prepared by 70% ethanol reflux method was separated with petroleum ether, ethyl acetate, and water-saturated n-butanol to obtain the proper solvent to purify CQAs. Results showed that the ethyl acetate fraction (EAF) exhibited the highest total chlorogenic acid content (TCC) (241.46 ± 0.00 mg/g dry fraction), followed by the water-saturated n-butanol fraction (nBuF) (TCC = 62.30 ± 0.82 mg/g dry fraction). Ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry and high-performance liquid chromatography photodiode array were used to qualitatively and quantitatively determine the CQAs in these two fractions. In EAF, four CQAs, namely, 3-CQA, 3,5-diCQA, 3,4-diCQA, and 4,5-diCQA, were identified with the contents of 5.69 ± 0.03, 106.65 ± 0.83, 15.65 ± 0.24, and 28.08 ± 0.82 mg/g, respectively. Six CQAs, namely, 3-CQA, 4-CQA, 1,3-diCQA, 3,5-diCQA, 3,4-diCQA, and 4,5-diCQA, with contents of 16.57 ± 0.23, 3.22 ± 0.55, 4.49 ± 0.01, 16.86 ± 0.24, 7.35 ± 0.11, and 6.41 ± 0.13 mg/g, respectively, were identified in nBuF. Quantitative analysis of the six CQAs in AST leaves have not been reported, and 1,3-diCQA has been found in AST leaves for the first time. Moreover, either EAF or nBuF and the six CQA reference compounds showed certain inhibitory activity on xanthine oxidase (XOD) in vitro. EAF demonstrated a stronger XOD inhibitory effect (IC50 = 1.67 mg/mL) than nBuF. Among the six CQA compounds, 3,4-diCQA had the lowest IC50 of 12.80 μM, whereas 1,3-diCQA and 3-CQA had IC50 values of 23.69 and 28.29 μM, respectively. The inhibitory activity of 4-CQA was weak. These findings indicated that CQAs are the major components inhibiting the XOD activity in vitro in AST leaves.

PVP immobilized SiO2 nanospheres for high-performance shear thickening fluid

We develop a modified method to improve the rheological performance of SiO2-based shear thickening fluid (STF). Directly adding surfactant into STF is the most common method to improve the rheological performance of SiO2-based STF. However, the final viscosity increases quickly with the increase of shear rate, which is against for the practical applications. In this work, SiO2 nanospheres are firstly modified by PVP K30 through an ethanol refluxing method and the modified SiO2 nanospheres are used to prepare PVP@SiO2-STF. Compared with the unmodified SiO2 based STF (SiO2-STF), the PVP@SiO2-STF presents an obvious increase of shear thickening (ST) effects and the maximum viscosity increases by 7 times and the critical shear rates decrease about 10 times approximately. A reasonable explanation is proposed to interpret the influence of the modification methods on the rheological properties of STF. This work provides a new way to control the shear thickening behavior and also contributes to understand the mechanism of ST effect, which has an important significance to develop controllable STF.

Subcritical ethanol extraction of flavonoids from Moringa oleifera leaf and evaluation of antioxidant activity

A large-scale process to extract flavonoids from Moringa oleifera leaf by subcritical ethanol was developed and HPLC–MS analysis was conducted to qualitatively identify the compounds in the extracts. To optimize the effects of process parameters on the yield of flavonoids, a Box-Behnken design combined with response surface methodology was conducted in the present work. The results indicated that the highest extraction yield of flavonoids by subcritical ethanol extraction could reach 2.60% using 70% ethanol at 126.6°C for 2.05h extraction. Under the optimized conditions, flavonoids yield was substantially improved by 26.7% compared with the traditional ethanol reflux method while the extraction time was only 2h, and obvious energy saving was observed. FRAP and DPPH assays showed that the extracts had strong antioxidant and free radical scavenging activities.

Chemical constituents of ethyl acetate fraction from seed melon (Citrulluslanatus ssp. vulgaris var. megalaspermus)

In this paper, the chemical composition of ethyl acetate parts of seed melon were studied by using ethanol re-flux method, extraction method, and isolated by column chromatography oversilica gel and Sephadex LH-20 and HPLC. The structures of the separated compounds were identified by physical-chemical methods and spectral data such as MS, ¹H-NMR, ¹³C-NMR, etc. 12 compounds were got from the plant including one new compound, 4-hydroxymet-hyl-2-methoxyphenyl 1-O-β-D-[6'-O-(4″-hydroxybenzoyl)-glucopyranoside] (1) and 11 known compounds, uracil (2), thymine (3), 2'-deoxyuridine (4), 7,8-dimethylalloxazine (5), indole-3-carboxylic acid (6), β-adenosine (7), 4-hydroxybenzoic acid (8), p-coumaric acid (9), cucumegastigmanesⅠ (10), 3'-methoxyl-quercetin-7-O-β-D-glucopyranoside (11) and 3,3'-dimethyloxy-4,4'-dihydroxy-9,9'-monoepoxy lignan (12).

Polyvinylpyrrolidone-stabilized Pt colloidal catalysts in chloronitrobenzene hydrogenation and modification with rare earth ions

Polyvinylpyrrolidone (PVP)-stabilized Pt colloidal catalysts with hydrazine hydrate as a reductant were prepared in an H2PtCl6 water solution/PVP/n-butanol microemulsion system. With m-chloronitrobenzene (m-CNB) selective hydrogenation as a probe, we studied how the microemulsion composition as well as the reduction conditions would affect the hydrogenation performance of PVP-Pt. The effects of rare earth ions on the modification of PVP-Pt were further studied. The as-prepared PVP-Pt improved the m-CNB hydrogenation activity and significantly enhanced the reactive selectivity compared with the ethanol reflux method. The addition of a small amount of Pr3+-modified PVP-Pt/Pr (Pt:Pr molar ratio of 1:0.14) further improved the activity of the catalyst.

Isolation and purification of psoralen and isopsoralen and their efficacy and safety in the treatment of osteosarcoma in nude rats.

Modern studies have shown that psoralen has a significant inhibitory effect on tumor growth in a variety of animals and humans. To obtain coumarin compounds - psoralen and isopsoralen - from traditional Chinese medicine Psoralea corylifolia L. using chromatographic techniques and isolation and purification methods, and to observe the transplanted tumor growth inhibitory effects and adverse reactions of psoralen and isopsoralen in nude rats with osteosarcoma. Dried ripe fruits of Psoralea corylifolia L. were taken as the raw material to prepare crude extract of Psoralea corylifolia L. by ethanol reflux method. Column chromatography was used to isolate the crude extract; compounds were structurally identified based on (1)H-NMR, (13)C-NMR spectra, the two compounds were identified as psoralen andisopsoralen, and their contents were 99.7% and 99.6, respectively. Nude rat model of osteosarcoma was established; the rats were randomized into: normal saline group, psoralen low- and high-dose groups, isopsoralen low- and high-dose groups, and cisplatin group. Osteosarcoma volume and weight inhibition rates in nude rats in each group were observed; radioimmunoassay was used to determine the serum alkaline phosphatase activity; peripheral blood cell and bone marrow nucleated cell counts were determined; light microscopy was used to observe heart, liver, spleen, lung, kidney, and tumor histopathology; and electron microscopy was used to observe the fine structure of tumor cells. Tumor volume inhibition rates were 43.75% and 40.18%, respectively, in the psoralen and isopsoralen low-dose groups, and tumor weight inhibition rates were 38.83% and 37.77%. Tumor volume inhibition rates were 67.86% and 66.96%, respectively, in the psoralen and isopsoralen high-dose groups, and tumor weight inhibition rates were 49.47% and 47.87%. Psoralen and ispsoralen markedly lowered serum AKP level. Psoralen and isopsoralen induced apoptosis or necrosis of osteosarcoma. After administration of high doses of psoralen and isopsoralen, toxic reactions such as writhing, lassitude, and hypoactivity were seen. Kidney histopathology showed tubulointerstitial dilatation and congestion, and inflammatory cell aggregation in the renal intercellular space. Psoralen and isopsoralen did not cause any significant toxic side effects to the bone marrow, or other organs such as heart, lung, liver, and spleen. Psoralen and isopsoralen have growth inhibitory effects on transplanted tumor in nude rats with osteosarcoma, and can induce tumor cell apoptosis or necrosis, without significant toxic effects.

Optimization of Extraction Technology of Favonoids from Kandelia Candel Leaves by Using Response Surface Methodology

This work is to extract flavonoids using ethanol refluxing method from the Kandelia candel leaves which are rich in flavonoids. Ethanol concentration, solid-liquid ratio, temperature and extraction time on the extraction rate were investigated by the single factor experiments. Box-Behnken design (BBD) based on response surface methodology (RSM) was adopted to optimize the parameters. The results showed the best extracting rate was more than 7.74%, when the extraction parameters were ethanol concentration 60%, extraction time 0.5 h and temperature 80°C.

Bench-scale preparation of Cu3(BTC)2 by ethanol reflux: Synthesis optimization and adsorption/catalytic applications

A metal organic framework, Cu3(BTC)2 was prepared in a 1L-capacity Pyrex reactor by ethanol reflux method. H3BTC (1,3,5-benzenetricarboxylic acid) ligand concentration of 1.01M with Cu salt/H3BTC mole ratio of 9:5 led to a product with excellent textural properties (>1700m2/g) in yield in the range of 40–76% − depending on the stirring rate − after 24h synthesis. Structural integrity was maintained after pelletizing the powder with a PVA binder, but textural properties deteriorated to some extent. The Cu3(BTC)2 powder was highly hydrophilic and water-sorption capacity decreased after pelletization. CO2 adsorption using the ground/sieved Cu3(BTC)2 pellets produced an improved breakthrough pattern despite a small reduction in saturation capacity compared with that of the powders. Tetralin oxidation reaction was then carried out for the Cu3(BTC)2 powder catalysts using TBHP as an oxidant. Tetralin conversions for three repeated runs remained almost constant and the heterogeneity of the Cu3(BTC)2 catalyst in the liquid phase oxidation was examined by hot-filtering experiment. Due to increased pore diffusion resistance, the pellets and its ground/sieved form showed lower catalytic properties than did the powder form of Cu3(BTC)2.

Preparation of octacosanol from filter mud produced after sugarcane juice clarification

Filter mud from sugarcane juice clarification containing 6.85 g/100 g waxes was used for octacosanol extraction by supercritical CO2 and hot ethanol reflux method, respectively. Comparing with hot ethanol reflux extraction, supercritical CO2 extraction provided a similar yield of waxes but a higher content of octacosanol in the waxes (29.65 g/100 g vs. 22.52 g/100 g). However, saponification of the waxes extracted by hot ethanol reflux extraction has significantly increased octacosanol content to 47.8 g/100 g. For high efficient preparation of octacosanol from filter mud, hot ethanol reflux extraction of waxes followed by saponification was the method of choice.

Extraction of Polysaccharides from &lt;i&gt;Cordyceps militaris&lt;/i&gt; by Ethanol Refluxing Method

The extraction of polysaccharides from cordyceps militaris by ethanol refluxing method was studied and the effected of solvent, solid-liquid ratio and time on the yields of polysaccharides were investigated and optimized conditions were determined through L9(34) orthogonal test at the same time. The yield of validate experiment was 33.50 % and the combination was 50 % ethanol + 1:15(g/ml) solid-liquid ratio + 7 h extraction time.