scholarly journals ISOLATION AND IDENTIFICATION OF EUPHORBIA TRIODONTA PLANT POLYPHENOLS BY CHROMATO-MASS SPECTROMETRY

2020 ◽  
pp. 105-114
Author(s):  
Zhamollitdin Fazlitdinovich Ziyavitdinov ◽  
Rahima Abdulla ◽  
Yuliya Igorevna Oshchepkova ◽  
Nodira Gulyamzhanovna Abdulladzhanova ◽  
Shavkat Ismailovich Salikhov

The aim of this work is to study the composition of polyphenols contained in plants of Euphorbia triodontus Prokh., growing throughout the Republic of Uzbekistan, in particular the Ferghana Valley region, using a high-performance liquid chromatograph with a diode-matrix detector (HPLC-DAD) and a tandem chromato-mass spectrometer (HPLC – Q-TOF-MS/MS). The roots of the plant Euphorbia triodontus Prokh., growing on the territory of Uzbekistan, collected in the period after flowering, studied the polyphenolic composition. For the first time from this type of Euphorbia, the method of stepwise hydrophobic chromatography was used to isolate polyphenolic fractions. By HPLC, as a result of semi-preparative chromatography, 6 individual compounds were isolated from the fraction eluted with a 20% methanol solution in the amount of: E-20-1 – 7 mg, E-20-2 – 22 mg, E-20-3 – 14.2 mg, E-20-4 – 41 mg, E-20-5 – 11.4 mg and E-20-6 – 32 mg. As a result of mass spectrometric analyzes, it was established that the polyphenols isolated in an individual state consist of gallic acid and glucose linked by an ester bond: O-galloyl-β-D-glucose. The structure of individual compounds was determined: E-20-1 – 1-O-meta-trigalloyl-β-D-glucopyranosyl-(4-O-β-D)-1-O-meta-trigalloyl-β-D-glucose, E-20-2 – 1-O-meta-trihalloyl-β-D-glucose, E-20-3 – 1-O-meta-tetragalloyl-β-D-glucose, E-20-4 – 1-O-meta-trigalloyl-4-O-haloyl-β-D-glucose, E-20-5 – 2,3,6-tri-O-galloyl-β-D-glucose and E-20-6 – 1,2,3,4,6-penta-O-galloyl-β-D-glucose.

2020 ◽  
pp. 133-140
Author(s):  
Zhamollitdin Fazlitdinovich Ziyavitdinov ◽  
Yuliya Igorevna Oshchepkova ◽  
Nodira Gulyamzhanovna Abdulladzhanova ◽  
Shavkat Ismailovich Salikhov

The aim of this work is to study the composition and structural characteristics of the polyphenols of the tanning sumac Rhus coriaria L. of the Anacardiaceae family, growing in Uzbekistan, using a high-performance liquid chromatograph with a diode-matrix detector (HPLC-DAD) and a tandem temple mass-spectrometer (HPLC– Q-TOF-MS / MS). The phenolic compounds of the aerial part (leaves) of Rhus coriaria L. plants of the Anacardiaceae family were studied. For the first time, polyphenol fractions were isolated from tanning sumac leaves using stepwise hydrophobic chromatography. By HPLC, as a result of semi-preparative chromatography from the fraction eluted with 30% ethanol, 9 individual compounds were obtained, in the amount of: R-1 – 0.5 mg, R-2 – 0.8 mg, R-3 – 2.3 mg, R-4 – 12.6 mg, R-5 – 34.5 mg, R-6 – 15 mg, R-7 – 8 mg, R-8 – 7.1 mg, R-9 – 45.5 mg As a result of mass spectrometric analyzes and NMR spectroscopy for individual polyphenols, it was established that the polyphenols isolated in the individual state consist of gallic acid and glucose, interconnected by an ester bond: mono-, di-, tri-, tetra-, penta- , hexa-, hepta-, octa- and non-O-galloyl-β-D-glucose.


2006 ◽  
Vol 830 (2) ◽  
pp. 231-237 ◽  
Author(s):  
Lata Kaphalia ◽  
Bhupendra S. Kaphalia ◽  
Santosh Kumar ◽  
Mary F. Kanz ◽  
Mary Treinen-Moslen

1981 ◽  
Vol 27 (9) ◽  
pp. 1546-1550 ◽  
Author(s):  
B W Renoe ◽  
C E Shideler ◽  
J Savory

Abstract We describe an integrated, molecular-absorbance, atomic absorption instrument for studying metal/ligand binding in clinical samples. For an interface between the "high-performance" liquid chromatograph and the atomic absorption instrument we used a flow-injection sample manipulator, thus allowing both the chromatograph and the atomic absorption detector to operate at their separate optimum conditions. After specimen separation with a gel permeation column, we measured the molecular components of the column eluate by molecular absorbance spectrometry and the atomic components (calcium and magnesium) by flame atomic absorption spectrophotometry. This instrument system is capable of separating and analyzing multiple components within 20 min of injection of the sample on the column. The chromatograms presented demonstrate the utility of the system for investigating metal binding to a variety of ligands in clinical samples.


Sign in / Sign up

Export Citation Format

Share Document