scholarly journals Isolation and Bioactivity Analysis of Ethyl Acetate Extract fromAcer tegmentosumUsing In Vitro Assay and On-Line Screening HPLC-ABTS+System

2014 ◽  
Vol 2014 ◽  
pp. 1-15 ◽  
Author(s):  
Kwang Jin Lee ◽  
Na-Young Song ◽  
You Chang Oh ◽  
Won-Kyung Cho ◽  
Jin Yeul Ma
Keyword(s):  
Phenolic Compounds ◽  
Ethyl Acetate ◽  
Silica Gel ◽  
Hot Water ◽  
Assay Method ◽  
Vitro Assay ◽  
Chemical Structures ◽  
Freeze Dried ◽  
On Line

TheAcer tegmentosum(3 kg) was extracted using hot water, and the freeze-dried extract powder was partitioned successively using dichloromethane (DCM), ethyl acetate (EA), butyl alcohol (n-BuOH), and water. From the EA extract fraction (1.24 g), five phenolic compounds were isolated by the silica gel, octadecyl silica gel, and Sephadex LH-20 column chromatography. Based on spectroscopic methods such as1H-NMR,13C-NMR, and LC/MS the chemical structures of the compounds were confirmed as feniculin (1), avicularin (2), (+)-catechin (3), (−)-epicatechin (4), and 6′-O-galloyl salidroside (5). Moreover, a rapid on-line screening HPLC-ABTS+system for individual bioactivity of the EA-soluble fraction (five phenolic compounds) was developed. The results indicated that compounds1and2were first isolated from theA. tegmentosum. The anti-inflammatory activities and on-line screening HPLC-ABTS+assay method of these compounds in LPS-stimulated murine macrophages were rapid and efficient for the investigation of bioactivity ofA. tegmentosum.

scholarly journals CONSTITUENTS AND INHIBITORY EFFECT ON HUMAN PATHOGENIC BACTERIA OF THE ROOTS OF SCUTELLARIA BAICALENSIS

2019 ◽  
Vol 57 (1) ◽  
pp. 7
Author(s):  
Duc Long Le ◽  
Huu Tung Nguyen ◽  
Thi Thom Nguyen ◽  
Gyung Ja Choi ◽  
Dinh Hoang Vu ◽  
...  
Keyword(s):  
Ethyl Acetate ◽  
Pathogenic Bacteria ◽  
Inhibitory Effect ◽  
Scutellaria Baicalensis ◽  
Plant Materials ◽  
Chemical Structures ◽  
Human Pathogenic Bacteria ◽  
Antibiotic Effect ◽  
Study Results

Abstract-HCTN_16Methanol extract of the roots of Scutellaria baicalensis effectively inhibited the bacterial growth of human pathogenic bacteria Staphylococcus aureus ATCC 6538, Bacillus cereus ATCC 21768 and Bacillus subtilis ATCC 6633 at MICs of 2,000 µg/mL. n-Hexane, ethyl acetate and aqueous residues were prepared by successively partitioning the methanol extract with n-hexane and ethyl acetate. Among them, only ethyl acetate layer showed antibiotic effect; whereas n-hexane and aqueous layers were inactive against tested bacteria. The ethyl acetate residue was fractionated by silica gel column chromatography to afford three flavonoids and an oligosaccharide. Their chemical structures were elucidated as wogonin (SB1), baicalein (SB4), baicalin (SB5) and tetrasaccharide (SB10) on the basis of the analysis of NMR and MS spectroscopic data. The isolates were evaluated for in vitro inhibitory effect against human pathogenic bacteria using micro dilution bioassay method. Baicalein (SB4) showed a broad-spectrum inhibition against various human pathogenic bacteria. In particular, it was found to potently inhibit S. aureus ATCC 6538 and B. cereus ATCC 21768 with MICs of 9.5 and 38 µg/mL, respectively. The study results demonstrated antibiotic effect of the extracts from the roots of S. baicalensis and characterization of compounds isolated from the plant materials.

AN IN VITRO ASSAY OF CORTICOTROPHIN

1955 ◽  
Vol 33 (2) ◽  
pp. 209-216 ◽  
Author(s):  
K. W. McKerns ◽  
E. Nordstrand
Keyword(s):  
Dose Response ◽  
In Vitro Assay ◽  
Assay Method ◽  
Response Curves ◽  
Vitro Assay ◽  
Rat Adrenals ◽  
Assay Design ◽  
Dose Response Curves ◽  
Gland System

The ability of corticotrophin to increase the corticoid output of rat adrenals in an isolated gland system has been developed as a useful assay method for the measurement of corticotrophin potency. The extra corticoids produced by stimulation are measured in terms of cortisone. Log dose response curves are presented for corticotrophin levels from 0.002 to 0.135 I.U./100 mgm. adrenals. A four point assay design, the precision of corticoid measurements, and the characteristics of the log dose response curves for a number of types of corticotrophin are given. With four measurements of each dose level the average lambda s/b for 20 assays was 0.209 ± 0.085 (S.D.).

AN IN VITRO ASSAY OF CORTICOTROPHIN

1955 ◽  
Vol 33 (1) ◽  
pp. 209-216
Author(s):  
K. W. McKerns ◽  
E. Nordstrand
Keyword(s):  
Dose Response ◽  
In Vitro Assay ◽  
Assay Method ◽  
Response Curves ◽  
Vitro Assay ◽  
Rat Adrenals ◽  
Assay Design ◽  
Dose Response Curves ◽  
Gland System

The ability of corticotrophin to increase the corticoid output of rat adrenals in an isolated gland system has been developed as a useful assay method for the measurement of corticotrophin potency. The extra corticoids produced by stimulation are measured in terms of cortisone. Log dose response curves are presented for corticotrophin levels from 0.002 to 0.135 I.U./100 mgm. adrenals. A four point assay design, the precision of corticoid measurements, and the characteristics of the log dose response curves for a number of types of corticotrophin are given. With four measurements of each dose level the average lambda s/b for 20 assays was 0.209 ± 0.085 (S.D.).

Influence of the assay method used on the selection of the most active forms of FSH from the human pituitary

1986 ◽  
Vol 113 (1) ◽  
pp. 17-22 ◽  
Author(s):  
Leif Wide ◽  
Bruce Hobson
Keyword(s):  
Biological Properties ◽  
Dominant Factor ◽  
Assay Method ◽  
Major Influence ◽  
Human Pituitary ◽  
Vitro Assay ◽  
Molecular Charge ◽  
In Vivo Bioassay

Abstract. The biological properties of different forms of human pituitary FSH, varying in their molecular charge, were investigated. FSH in two individual human pituitaries and a pool of 30 human pituitaries was extracted and subjected to electrophoresis. From each electrophoresis 14 consecutive fractions with the highest RIA activity were examined with in vitro and in vivo bioassays. The in vitro assay was based upon the estimation of oestradiol produced by cultured Sertoli cells from 10 day old rats. The in vivo bioassay was an hCG augmented test using immature female mice injected on 3 consecutive days. The increase in ovarian weight was the index of response. Both in the individual and in the pooled pituitary material the less negatively charged forms had the highest activity in the in vitro bioassay. In contrast, the more negatively charged forms had the highest activity in the in vivo bioassay. Forms of FSH from each of the two individual pituitary extracts were pooled according to their migration rate and injected iv into mice. The amount of FSH remaining in the circulation of the mouse after 1 h was related to the molecular charge. The highest value was obtained with the pool containing the more negatively charged forms of the hormone. The results indicate that the disappearance rate of the FSH molecule is a dominant factor in the in vivo bioassay. A consequence of these observations will be that the assay method chosen to monitor the purification of FSH will have a major influence on the biological properties of the final preparation.

Phenylalanine ammonia-lyase, flavanone 3β-hydroxylase and flavonol synthase enzyme activity by a new in vitro assay method in berry fruits

2014 ◽  
Vol 153 ◽  
pp. 130-133 ◽  
Author(s):  
Gema Flores ◽  
Fernando De la Peña Moreno ◽  
Gracia Patricia Blanch ◽  
Maria Luisa Ruiz del Castillo
Keyword(s):  
Enzyme Activity ◽  
Phenylalanine Ammonia Lyase ◽  
In Vitro Assay ◽  
Assay Method ◽  
Vitro Assay ◽  
Flavonol Synthase ◽  
Berry Fruits

scholarly journals Phenolic Compounds from Psidium guajava (Linn.) Leaves: Effect of the Extraction-Assisted Method Upon Total Phenolics Content and Antioxidant Activity

2020 ◽  
Vol 11 (2) ◽  
pp. 9346-9357
Keyword(s):  
Antioxidant Activity ◽  
Phenolic Compounds ◽  
Phenolic Content ◽  
Crosslinking Agent ◽  
Psidium Guajava ◽  
Total Phenolic ◽  
Vitro Assay ◽  
Ultrasound Assisted ◽  
Guava Leaves

The aim of this study was to investigate the influence of the extraction method on the dry extract yield of guava leaves, correlating the total phenolic content (TPC) with the antioxidant activity. The dry extracts were obtained from hydroethanolic (50 and 70%) extract using the ultrasound-assisted method. Folin-Ciocalteau reagent was used to determine the content of TPC. DPPH (2,2-diphenyl-1-picrylhydrazyl) in vitro assay was used to determine the ability to scavenge free radicals. The results analyses demonstrated that the ultrasound-assisted method produced a higher yield in both dry extracts (11%), in contrast to the conventional method. The 50% hydroethanolic solvent was more efficient in the extraction of bioactive compounds. Both extracts showed a positive correlation of phenolic content with antioxidant activity. The FTIR spectrograms showed changes in the chemical groups, as well as determining the aromaticity index of the extracts, indicating a higher aromatic prevalence to the solvent 50%, although it presented simpler phenolic structures. In conclusion, the results provide an important basis for the use of phenolic compounds extracted from guava leaves, not only due to the antioxidant activity exerted, however, for potential use as a crosslinking agent of sulfated and non-sulfated glycosaminoglycan (GAG).

scholarly journals Assessment of Antioxidant Potential and phytochemical screening of Phenolic Compounds of Gleditsia triacanthos L Pods

2018 ◽  
Vol 5 (3) ◽  
pp. 3648-3655
Author(s):  
Saidi Imène ◽  
Mahdjoub Bessam Hassiba ◽  
Benchaachoua Abbassia
Keyword(s):  
Antioxidant Activity ◽  
Phenolic Compounds ◽  
Ethyl Acetate ◽  
Total Antioxidant Capacity ◽  
Phytochemical Screening ◽  
Total Polyphenols ◽  
Gleditsia Triacanthos ◽  
Aqueous Fraction ◽  
Total Antioxidant

Objective: The present study aims at the phytochemical screening, the quantification of phenolic compounds of Gleditsia triacanthos L pods (Family Leguminosae) and the assessment of their antioxidant potential by in vitro assays. Subjects and Methods: The pods were extracted with 70% methanol and further partitioned with petroleum ether, chloroform, ethyl acetate, and n-butanol. The residual aqueous fraction has been also recovered. Colorimetric methods using Folin-Ciocalteu reagent, aluminum chloride and Folin-Denis were carried out to estimate total polyphenols, flavonoids and condensed tannins content of extracts. 2,2-diphenyl-1-picrylhydrazyl (DPPH) and total antioxidant capacity (TAC) were used to determine in vitro antioxidant activity. Results: In vitro phytochemical screening for all the extracts was tested and shown positive result for flavonoids, tannins, cardiac glycosides, sterols and terpenes, saponins and alkaloids. However, all the extracts were free of anthraquinones. The strongest activity against radical scavenging of DPPH was found in the ethyl acetate fraction (IC50= 16,288 ± 0,299 µg/ml) which contains highest amounts of flavonoids (25.160 ± 0.016 mg CE/g), whereas the chloroform fraction showed an important total antioxidant capacity (750,584 ± 129,793 mg AAE/g) with the highest amount of total polyphenols (131.667 ± 2.055 mg GAE/g). When compared to the other fractions, the aqueous fraction presented the lowest antioxidant activity for the two methods. Conclusion: These data suggest that the pods of Gleditsia triacanthos L can be a good natural source of antioxidants that can be beneficial for food and human health.

scholarly journals Araliachinoside A: A New Triterpene Glycoside From Aralia chinensis Leaves

2020 ◽  
Vol 15 (9) ◽  
pp. 1934578X2095275
Author(s):  
Pham Hai Yen ◽  
Nguyen Thi Cuc ◽  
Phan Thi Thanh Huong ◽  
Nguyen Xuan Nhiem ◽  
Nguyen Thi Hoai ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Nuclear Magnetic Resonance ◽  
High Resolution ◽  
Inhibitory Concentration ◽  
In Vitro Assay ◽  
Ionization Mass ◽  
Vitro Assay ◽  
Chemical Structures ◽  
Hepg2 Cell Lines

From the leaves of Aralia chinensis, 3 oleanane-type triterpene glycosides have been isolated, including 1 new glycoside, 3β,23 -dihydroxyolean-12-ene-28-oic acid 3 -O-β-d-glucopyranosyl-(1→3)- α-l-arabinopyranosyl-(1→3)-β-d-glucuronopyranoside 28 -O-β-d-glucopyranosyl ester (named as araliachinoside A, 1), and 2 known ones, 3β,23 -dihydroxyolean-12-ene-28-oic acid 3 -O-α-l-arabinopyranosyl-(1→3)- β-d-glucuronopyranoside 28 -O-β-d-glucopyronosyl ester (2) and 3β-hydroxyolean-12-ene-28-oic acid 3 -O-β-d-glucurono pyranoside 28 -O-β-d-glucopyronosyl ester (3). Their chemical structures were elucidated by using a combination of high-resolution electrospray ionization-mass spectrometry, 1-dimensional and 2-dimensional nuclear magnetic resonance spectral data, and by comparison with previous literature. Compounds 1-3 displayed cytotoxic activity toward KB and HepG2 cell lines with half-maximal inhibitory concentration values ranging from 8.1 ± 0.1 to 15.7 ± 0.3 µM in in vitro assay.

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