scholarly journals Research of polyphenolic compounds of Circaea lutetiana l.

Author(s):  
Akmaral Kozhantayeva ◽  
Sluken Rakhmadiyeva

One of the renewable sources of plant material is the plants of the Onagraceae L. family, growing on the territory of the Republic of Kazakhstan. The plant Circaea lutetiana L., (bipartite of Paris) of the genus Circaea L., (bipartite) of the family Onagraceae L., (fireweed), which belongs to medicinal, dyeing and food plants, was taken as an object of study. The presence of polyphenolic compounds was detected by paper chromatography in an ascending manner in solvent systems: butanol-acetic acid-water (BAW) (41:5), (40:12.5:29), 2%, 15% acetic acid with specific developers: diazotized sulfanilic acid (DZSA), diazotized para-nitroaniline (DZPNA), ammonia vapors, aluminum chloride (AlCl3), ferric chloride (FeCl3), ammonium-iron alum (AIA), vanillin reagent in sulfuric acid. The content of gallic and ferulic acids was determined in the roots and fruits of the plant, and ellagic acid in the leaves and fruits. Flavonoids and tannins of the hydrolyzable type were found in all plant organs, the largest number of them in fruits and the smallest in roots. Using the method of spectrophotometry in all plant organs, the content of flavonoids in terms of State standard sample (SSS) quercetin was determined (roots 0.96%, stems 2.03%, leaves 2.74%, fruits 3.67%), the content of tannins in terms of tannin (roots 0.005%, stems 1.19%, leaves 3.69%, fruits 5.99%).

2007 ◽  
Vol 111 (31) ◽  
pp. 9270-9280 ◽  
Author(s):  
Toshiyuki Takamuku ◽  
Yasuhiro Kyoshoin ◽  
Hiroshi Noguchi ◽  
Shoji Kusano ◽  
Toshio Yamaguchi

2011 ◽  
Vol 51 (5) ◽  
pp. 819-825 ◽  
Author(s):  
Housheng Hong ◽  
Longxiang Chen ◽  
Qingwen Zhang ◽  
Zheran Zhang

2011 ◽  
Vol 236-238 ◽  
pp. 2495-2498 ◽  
Author(s):  
Xue Song Huang ◽  
Xian Zhe Lin ◽  
Mo Ting Guo ◽  
Ya Zou

The solution of piperine in multiple solvent including ethanol, acetic acid, water and HCl were investigated to extract more piperine from piper fruit. Piperine was determined by reverse phase high-performance liquid chromatography with Diamonsil column (C18,5 μm ,250 mm×4. 6 mm) at 343 nm. Experiment data were simulated by Allometric model and the formula is Z=0.9+ 4.54×10-10×x5.675+1.8029×y2.12848+2.37×10-10×x5.675×y2.12848(Z:sample solution,mol/mL,x: the percentage of ethanol’s volume, ml/100mL,y: the acetic acid in the authentic sample solution, g/100mL), the adj·R2=0.997, the comparative deviation less than 2%. These results are good in agreement with experimental data. It reveals that the model can meet the requirements of the selection and design in extracting piperine from piper fruit.


1974 ◽  
Vol 52 (11) ◽  
pp. 1013-1017 ◽  
Author(s):  
William H. Cruickshank ◽  
Barry L. Malchy ◽  
Harvey Kaplan

Thiolysis of an O-dinitrophenyl-tyrosyl peptide results in an increased solubility in the stationary phase of a n-butanol – acetic acid – water – pyridine (15:3:12:10) (BAWP) paper chromatographic system. It is shown that this property can be used to form the basis of a diagonal paper chromatographic purification of tyrosyl peptides from enzymatic digests of proteins. The amino groups of the protein are first reacted with citraconic anhydride and then the citraconyl protein is reacted with 1-fluoro-2,4-dinitrobenzene. The dinitrophenyl-citraconyl protein is subjected to enzymatic digestion, applied to a strip of Whatman 3 MM paper, thiolyzed with 5% 2-mercaptoethanol in acetone, and subjected to chromatography using BAWP as solvent. A guide strip is removed, thiolyzed with 5% 2-mercaptoethanol in 25% pyridine, and resubjected to chromatography in BAWP at right angles to the original direction of chromatography. The tyrosyl peptides are displaced off the diagonal towards the origin. The off-diagonal peptides are isolated from the original chromatogram by thiolysis and chromatography using the diagonal chromatogram to locate the positions of the dinitrophenyl-tyrosyl peptides.


2021 ◽  
pp. 201-209
Author(s):  
Kamola Vakhabjanova Raimova ◽  
Nodira Gulomzhanovna Abdulladzhanova ◽  
Farrukh Nazimovich Toshpulatov ◽  
Nurali Azamovich Ergashev ◽  
Alimzhan Davlatbaevich Matchanov

The results of studies of the content of polyphenolic compounds and their antioxidant activity in the Pontic hawthorn plant Crataegus pontica K.Koch., growing in the mountainous regions of the Tashkent region of the Republic of Uzbekistan are presented. The collection of raw materials took place in the spring at the beginning of October 2019 and at the end of April 2020. The conditions for the isolation of polyphenolic compounds were selected under various conditions. It was shown that the optimal content of polyphenols is extracted with 70% acetone, followed by fractionation of the aqueous residue with ethyl acetate and precipitation with hexane. It was shown that in the plants harvested in spring, the amount of polyphenols was 4.28%, and the collected volume was 2.6%, of the air-dry mass of the raw material. Chromatographic methods (BC and TLC) revealed that the composition of plant leaves collected in spring contains more polyphenols than those collected in autumn. This plant contains compounds belonging to the class of flavonols, phenolic acids and flavan-3-ols. Polyphenols were identified by rutin, quercetin, quercetin-3-O-β-galactoside, catechin, and gallic acid by BC and TLC methods. The antioxidant activity of the sum of polyphenolic compounds was studied in the model of lipid peroxidation (LPO) in rat liver mitochondria. It was found that polyphenols have a protective effect on mitochondria, a reduced damaging effect of Fe2+ / ascorbate and antioxidant activity depends on the concentration of the studied polyphenolic substances. The introduction of rutin into the incubation medium in 5 μM medium inhibits LPO processes by 32.0%, and at 10 μM – by 85.9% and in 20 μM – by 96.8%, compared with the control.


Author(s):  
Olga V. Yatsenkova ◽  
Andrei M. Skripnikov ◽  
Boris N. Kuznetsov

The work describes a one-stage method of cellulose obtaining from fir wood based on peroxide delignification of wood under mild conditions (100 °C, atmospheric pressure) in the presence of acetic acid, water and catalyst of 2% wt. H2SO4. The possibility of obtaining cellulose with a residual lignin content <1% wt. at a low concentration of hydrogen peroxide (3% wt.) in the reaction medium was established. The optimal concentrations of reagents (Н2О2 – 3% wt., CH3COOH – 38.9% wt.) and the duration of the process (4 h) were determined by experimental and calculation methods. This conditions provide a high yield of cellulose product (≥45% wt.) with a low content of residual lignin (<1% wt.). The composition and structure of fir cellulose was studied by chemical analysis and by FTIR and SEM methods. The cellulosic product which was obtained in optimal process conditions is high-quality cellulose


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