Determination of sunset yellow, allura red, and fast green using a novel magnetic nanoadsorbent modified with Elaeagnus angustifolia based on magnetic solid-phase extraction by HPLC

Abstract Sunset yellow (SY), allura red (AR) and fast green (FG) are frequently used in commercial food products, although they are considered to be hazardous to public health due to their toxic efficacy and high exposure risk potency. In this study, a new, rapid, and reliable method based on a magnetic solid-phase extraction (MSPE) was developed for the simultaneous determination of SY, AR, and FG. Fe3O4 modified with Elaeagnus angustifolia was used for the first time as an adsorbent (Fe3O4-EA) in MSPE. It was characterized with scanning electron microscopy, Brunauer Emmet Teller surface area analysis and X-ray diffraction. MSPE parameters were optimized in terms of pH, adsorption, and elution time and elution volume. High-performance liquid chromatography was used for dye quantitation. Analytical separation was performed by applying ammonium acetate buffer, acetonitrile, and methanol as the mobile phase to a C18 reverse-phase analytical column. Intraday and inter-day repeatability of the method performed at the concentration of 0.2, 1.0 and 2.0 µg/mL exhibited <8.1% RSD (n=3). The limit of detection values was between 0.05-0.1 µg/mL. The adsorption data of SY, AR and FG on Fe3O4-EA were fitted with the Langmuir model with qmax values of 45.0, 70.4 and 73.0 mg/g, respectively.

Autumn olive (Elaeagnus umbellata Thunb.) berry reduces fasting and postprandial glucose levels in mice

BACKGROUND/OBJECTIVES: Fasting and postprandial hyperglycemia should be controlled to avoid complications of diabetes mellitus. This study investigated the effects of autumn olive (Elaeagnus umbellata Thunb.) berry (AOB) on fasting and postprandial hyperglycemia in mice. MATERIALS/METHODS: In vitro α-glucosidase inhibitory effect of AOB was determined. Maltose solution (2 g/kg) with and without AOB extract at 500 mg/kg or acarbose at 50 mg/kg was orally administered to normal mice after overnight fasting and glucose levels were measured. To study the effects of chronic consumption of AOB, db/db mice received the basal diet or a diet containing AOB extract at 0.4% or 0.8%, or acarbose at 0.04% for 7 weeks. Blood glycated hemoglobin and serum glucose and insulin levels were measured. Expression of adiponectin protein in epididymal white adipose tissue was determined by Western blotting. RESULTS: In vitro inhibitory effect of AOB extract on α-glucosidase was 92% as strong as that of acarbose. The AOB extract (500 mg/kg) or acarbose (50 mg/kg) significantly suppressed the postprandial rise of blood glucose after maltose challenge and the area under the glycemic response curve in normal mice. The AOB extract at 0.4% or 0.8% of diet or acarbose at 0.04% of diet significantly lowered levels of serum glucose and blood glycated hemoglobin and homeostasis model assessment for insulin resistance values in db/db mice. The expression of adiponectin protein in adipose tissue was significantly elevated by the consumption of AOB at 0.8% of diet. CONCLUSIONS: Autumn olive (E. umbellata Thunb.) berry may reduce postprandial hyperglycemia by inhibiting α-glucosidase in normal mice. Chronic consumption of AOB may alleviate fasting hyperglycemia in db/db mice partly by inhibiting α-glucosidase and upregulating adiponectin expression.

Chemical constituents from traditional Uighur herbal medicine Elaeagnus angustifolia flowers / 中国中药杂志

Seven aromatic glycosides (1-7), including four phenylethanol glycosides, one phenylmethanol glycoside, one phenylpropane glycoside and one benzoside, were isolated from the methanolic extract of Uighur Medicine Elaeagnus angustifolia flowers. Their structures were elucidated based on the analysis of spectroscopic data (1D, 2D NMR and HR-MS). Compound 1 is a new compound, named as angustifol A. Six known compounds were identified as 2-phenylethyl-O-β-D-glucopyranoside(2), salidroside (3), vanillic acid 4-O-β-D-glucopyranoside(4), vanilloloside (5), (Z)-isoconiferin (6), 2-phenylethyl-6-O-α-L-arabinofuranosyl-β-D-glucopyranoside (7). Compounds 2-7 were isolated from the genus Elaeagnus for the first time. In vitro anti-inflammatory assays revealed that none of these compounds showed good COX inhibitory activities.

The impacts of Elaeagnus umbellata Thunb. leaf and fruit aqueous extracts on mice hepatic, extrahepatic antioxidant and drug metabolizing enzymes related structures

ABSTRACT In this work, the potential chemopreventive activities of Elaeagnus umbellata fruit aqueous (EUFA) and leaf aqueous (EULA) extracts focusing on the modulatory influence of xenobiotic metabolizing enzymes (XMEs), antioxidant enzymes, glucose-6-phosphate dehydrogenase (G6PD), 6-phosphogluconate dehydrogenase (6PGD), lactate dehydrogenase (LDH) activity, lipid peroxidation (LP), sulfhydryl groups were investigated in the hepatic and extrahepatic organs of Swiss albino mice (50 and 100 mg/kg body wt given orally for 14 days) and compared with BHA (0.75 % in diet). The modulatory and chemopreventive properties of two different doses EUFA and EULA were observed for cytochrome P450, cytochrome b5, sulfhydryl groups, NADPH-cytochrome P450 reductase, NADH-cytochrome b5 reductase, 7-ethoxyresorufin-deethylase and N,N-dimethylaniline N-oxidase activities in the liver and compared with BHA as a standard. The activities of glutathione S-transferase (GST) and DT-diaphorase (DTD) showed a significant increase in the kidney, forestomach, heart and brain at both doses of EUFA and EULA. The results of EULA-treated groups were found a notable increase in LDH, G6PD, 6PGD, GST and DTD activities. Superoxide dismutase level in liver, kidney and heart exhibited a significant increase at both doses of EULA. Glutathione reductase activity was a remarkable level at high dose of EUFA in liver, kidney and EULA in kidney. Both doses of EUFA were effective in inducing glutathione peroxidase activitiy in heart. The levels of LP at low and high doses of EULA-treated and EUFA-treated were effective in liver and kidney, respectively. The present results demonstrate that significant effects in the level of XMEs and antioxidant enzymes of EUFA and EULA are remarkable for modulating roles and natural chemoprevention properties and therefore is considered for a valuable natural source.

Chemical constituents from leaves of Elaeagnus mollis / 中草药

Objective: To study the chemical constituents in the leaves of Elaeagnus mollis. Methods: Their structures were identified on the basis of silica gel column chromatography and Sephadex LH-20 gel column chromatography, and HPLC methods were used for the separation and purification of chemical constituents. Results: Sixteen compounds were isolated from 70% ethanol extracts of the leaves of E. mollis. The structures were identified as kaempferol-3-O-β-D-glucopyranoside (1), kaempferol-3-O-(6″-O-trans-p-coumaroyl)-β-D- glucopyranoside (2), kaempferol-3-O-(6″-O-cis-p-coumaroyl)-β-D-glucopyranoside (3), quercetin-3-O-α-L-arabinopyranoside (4), kaempferol-7-O-α-L-rhamnopyranoside (5), kaempferol-3,7-di-O-α-L-rhamnopyranoside (6), kaempferol-3-O-β-D-galactopyranosyl-7- O-α-L-rhamnopyranoside (7), kaempferol-3-O-α-Larabinofuranosyl-7-O-α-L-rhamnopyranoside (8), hippophamide (9), L-tryptophan (10), arjunolicacid (11), ursolicacid (12), kaempferol (13), rutin (14), adenosine (15), and β-daucosterol (16). Conclusion: Compounds 3-10 and 15 are isolated from the plants of Elaeagnus L. for the first time. Compounds 1, 2, 11, and 12 are isolated from this plant for the first time.

A new phenolic glycoside from Li medicine Lihua Bidou Yan Prescription / 中草药

Objective: To study the chemical constituents of Li medicine Lihua Bidou Yan prescription. Methods: Chemical constituents were isolated by using various column chromatography. The structures were elucidated on the basis of physicochemical constants and spectral analysis. The anti-inflammatory activities of compound 1 were evaluated using LPS-induced RAW 264.7 cells. Results: Two compounds were obtained from Lihua bidou yan Prescription and identified as rhyncoside A-4-methly ether (1) and rhyncoside C (2), respectively. The NO production in LPS-induced RAW264.7 cells was slightly inhibited by compound 1 at a concentration of 50 μmol/L. Conclusion: Compound 1 is a new phenolic glycoside; Compound 2 is obtained from the prescription for the first time. Rhyncoside A-4-methyl ether has anti-inflammatory activity.

Evaluation of phytochemical constituents and antioxidant activity of selected actinorhizal fruits growing in the forests of Northeast India.

Hippophae salicifolia, Elaeagnus pyriformis, Myrica esculenta and M. nagi are actinorhizal plants growing in the sacred forests of Northeast India with multipurpose uses. The present investigation was undertaken to determine the phenol, flavonoid and flavonol contents of the fresh fruit juice of these plant species including the antioxidant potential by means of DPPH, H2O2 and NO scavenging activity and FRP. The total phenolic, flavonoid and flavonol contents of fruit juice ranged from 321.68±0.06 to 76.67±0.01 mg/g GAE, 272.92±0.07 to 20.12±0.02 mg/g QE and 258.92±0.08 to 18.72±0.02 mg/g QE, respectively. At 2.0 mg/mL concentration, DPPH scavenging activity was found to be the highest in M. esculenta (89.62%) and the lowest in E. pyriformis (17.58%). The reducing power activity was found significantly higher in H. salicifolia juice, which increased with increase in concentration. The H2O2 scavenging activity of H. salicifolia juice was found to be as high as 98.78%, while Elaeagnus juice was found to be less effective with just 48.90%. Juice of H. salicifolia showed the greatest NO scavenging effect of 75.24% as compared to juice of E. pyriformis, where only 37.54% scavenging was observed at the same concentration. Taking into account all the experimental data, it can be said that the fruits of H. salicifolia and both M. nagi and M. esculenta have good antioxidant activity compared to fruits of E. pyriformis.

Micromonospora is a normal occupant of actinorhizal nodules.

Actinorhizal plants have been found in eight genera belonging to three orders (Fagales, Rosales and Cucurbitales). These all bear root nodules inhabited by bacteria identified as the nitrogen-fixing actinobacterium Frankia. These nodules all have a peripheral cortex with enlarged cells filled with Frankia hyphae and vesicles. Isolation in pure culture has been notoriously difficult, due in a large part to the growth of fast-growing contaminants where, it was later found, Frankia was slow-growing. Many of these contaminants, which were later found to be Micromonospora, were obtained from Casuarina and Coriaria. Our study was aimed at determining if Micromonospora were also present in other actinorhizal plants. Nodules from Alnus glutinosa, Alnus viridis, Coriaria myrtifolia, Elaeagnus x ebbingei, Hippophae rhamnoides, Myrica gale and Morella pensylvanica were tested and were all found to contain Micromonospora isolates. These were found to belong to mainly three species: Micromonospora lupini, Micromonospora coriariae and Micromonospora saelicesensis. Micromonospora isolates were found to inhibit some Frankia strains and to be innocuous to other strains.

Effect of Elaeagnus pungens leaves on contraction of isolated guinea pig tracheal smooth muscle / 中草药

Objective: To investigate the effect of n-butanol fraction from Elaeagnus pungens leaves (BFEP) on the contraction of isolated guinea pig tracheal smooth muscle under the basal tonus or spasmogens. Methods: Guinea pig tracheal smooth muscle spiral strips were isolated. Under the normal state or the condition treated with acetylchohne (Ach), histamine (Hist), or KCl, Ca2+ release in cells without calcium, and extracellular Ca2+ influx at the high concentration of Ca2+, the effect of BFEP on the tension of isolated trachea was observed. Results: BFEP relaxed the tracheal strip significantly in the concentration-dependent manner under the basal tonus. The tested drug produced an unparallel rightward shift of the cumulative concentration-response curve of Hist or Ach. The contraction induced by high K+ and extracellular Ca2+ influx was inhibited. Conclusion: BFEP could inhibit the contraction of isolated guinea pig tracheal smooth muscle under the basal tonus or spasmogens.

Study on the enrichment technology of total flavonoids in Elaeagnus angustifolia flower by macroporous adsorption resin / 中国药学杂志

OBJECTIVE: To screen the best macroporous adsorptive resin for separation and purification of flower Elaeagnus angustifolia flavonoids and to establish the purification process parameters. METHODS: Using macroporous adsorption resin adsorption rate and desorption rate as the indexes, the best resin was screened out for enriching flower Elaeagnus angustifolia flavonoids. The optimal process conditions were investigated through single factor test. RESULTS: DA201 resin showed good adsorption and separation property for Elaeagnus angustifolia flavonoids. The detailed process conditions were as follows: the ratio of diameter to height of resin column was 1:8, sample loading rate was 0.5 mL·min-1, sample concentration was 20 mg·mL-1, pH was adjusted to 4, with elution rate of 0.5 mL·min-1, the largest sample load was 4.5 BV, eluent concentration was 80% and the dosage was 12 BV. CONCLUSION: DA201 type resin, showed good purification effect for flavonoids Elaeagnus angustifolia in the defined process conditions with a yield of 85.23%. The purity of total flavonoids achieved 14.95%, which was 3 times of that by coarse extraction (4.901%). Copyright 2012 by the Chinese Pharmaceutical Association.

RP-HPLC method for the quantitation of β-Sitosterol in Elaeagnus Gonyanthes Benth / 药物分析学报

Objective To establish an RP-HPLC method for the determination of β-Sitosterol in Elaeagnus Gonyanthes Benth. Methods The separation was performed on a luna C8 (2) (150 mm×4.6 mm, 5μm) column with the mobile phase of methanol-water (88∶12, v/v) at a flow rate of 1.0 mL/min, the detection wavelength was set at 210 nm, and the temperature of the column was maintained at 35 ℃. Results The calibration curve of β-Sitosterol was linear over the concentration range of 0.075-0.375 mg/mL (r=0.9999) and the average recovery of β-Sitosterol was 96.30% with RSD of 3.60%(n=3). Conclusion The method is simple, rapid, and accurate, and can be used for the quality control of Elaeagnus Gonyanthes Benth.

Comparative Study of Volatile Oil Extraction Process from Flowers of Elaeagnus angustifolia L.with Steam Distillation and Supercritical CO_2 Extraction / 中国中医药信息杂志

Objective To optimize the extraction process by determing the volatile oil yield of steam distillation and supercritical CO2 extraction from flowers of Elaeagnus angustifolia L..Methods Orthogonal test was carried out to compare two extraction effects between steam distillation and supercritical CO2 extraction by detecting the extraction ratio from flowers of Elaeagnus angustifolia L..Results Steam distillation time on volatile oil extraction has the greatest impaction,and the best condition of supercritical CO2 extraction was extraction pressure of 20 MPa,extraction temperature of 40 ℃,and flux of CO2 is 10 L/h.Conclusion Compared with steam distillation,supercritical CO2 extraction spends less time,has higher efficiency and less harm to the materiel after extracting.It adapts to batch process and is convenient for subsequent extraction technology.

Study on Extraction Process of Polysaccharides from Elaeagnus angustifolia L. by Enzymatic- assisted Ultrasonic Methods / 中国中医药信息杂志

Objective To optimize the technological conditions of polysaccharide extraction from Elaeagnus angustifolia L. by enzymatic-assisted ultrasonic. Methods The effects of different enzymes, enzymolysis temperature, enzyme dosage, enzymolysis time, material-water ratio, crushing degree, ultrasonic time and ultrasonic temperature on the extraction rate of Elaeagnus angustifolia L. polysaccharide was analyzed. Results The optimal technological condition was as follows:1.5% cellulase, 1.5% pectic enzyme, enzymolysis time 40 min, enzymolysis temperature 55 ℃, ultrasonic time 25 min, ultrasonic power 400 W, material- water ratio 1∶30, and temperature 60 ℃. In these conditions, the extraction efficiency of polysaccharide was 12.35%. Conclusion The process is simple and practicable, and can be used for the extraction of Elaeagnus angustifolia L. polysaccharide.

Studies on germination of dormant bud and seed of Elaeagnus mollis under tisssue culturing / 中草药

Object To study the factors causing the dormancy of seed and to broaden the scope in the choice of explant for the tissue culture of the rare and near extinct plant Elaeagnus mollis Diels.Methods Dormant buds from one-year old branch collected each month from Autumn to next Spring, and seed of the very year were selected and cultured on basic media with the addition of 6-BA, NAA and GA 3 Results The germination rate of dormant bud follows the regular order of the months when it was taken. Those taken in Autumn declined every month until next Spring, and the nrevived monthly with those taken in March showing the most prosperous germination.The dormant bud can germinate into shoots. When seed was cultured, there are several factors leading to its dormancy: hardness of the mesocarp, keratinization of periderm, refractory to water permeation and the presence of certain inhibitory subtances. Seed kernal is rich in nutrition, but susceptible to bacterial infection leading to its decay. But the germination rate was well over 70% which can be cultured to give bacteria free shoots. Conclusion Both dormant buds obtained in March and bacteria free shoots germinated from naked kernal can be used as new sources for the tissue culture of E mollis .

Liposoluble constituents of leaves of Elaeagnus pungens / 中成药

AIM: To study the chemical constituents of Elaeagnus pungens. METHODS: Chemical constituents were separated through chromatographic methods and their structures were elucidated by spectral analysis. RESULTS: Five compounds were isolated from the petroleum ether extract of leaves of Elaeagnus pungens Thunb.Their structures were elucidated as hentriantane(1),lupeol(2),?-sitosterol(3),oleanolic acid(4) and 3,5-dihydroxy4,7-dimethoxy flavone(5). CONCLUSION: Compounds hentriantane(1) and 3,5-dihydroxy-4,7-dimethoxyflavone(5) were isolated from this plant for the first time.