scholarly journals Development of pharmacognostic parameters for the leaf of Bridelia scandens (Roxb.) Willd

2021 ◽  
Vol 10 (4) ◽  
pp. 230-235
Author(s):  
J. Preetham ◽  
◽  
S. Kiran ◽  
R. Sharath ◽  
P. Sivakami Sundari ◽  
...  
Keyword(s):  
Thick Layer ◽  
Fluorescence Analysis ◽  
Calcium Oxalate Crystals ◽  
Flavonoid Content ◽  
Quantitative Microscopy ◽  
Adaxial Side ◽  
Microscopic Studies ◽  
Dark Green ◽  
Pale Green

Background: Pharmacognostic study of medicinal plants is an important parameter for standardization and authentication of plants, with the help of which adulteration and substitution can be prevented. The present study deals with pharmacognostic profile of leaf of Bridelia scandens (Roxb).Willd. an important traditional plant, belonging to family Euphorbiaceae used to treat various ailments. Methods: The present study includes macroscopic and microscopic studies, quantitative microscopy, and physiochemical characters such as ash value, extractive values, fluorescence analysis, and total phenol and flavonoid content. Results: Macroscopically, the leaves are B. scandens are elliptic –oblong or obavate, dark green above, pale green below lateral veins. Microscopically, leaf consists of thick semicircular midrib and the lamina, cortical zone ending with thick continuous cylinder of sclerenchyma cells. Sclerenchyma cylinder completely enclosed the vascular cylinder of the midrib, consists of only continuous thick layer of phloem. Xylem cylinder consists of numerous short or long radial chains of vessels. The lateral vein is flat on the adaxial side and prominently projecting hemispherical body on the adaxial side. Powder microscopy of leaf revealed the presence of spiral xylem vessels, rosette and prismatic calcium oxalate crystals and trichomes. A Physiochemical characteristic was also determined. Conclusion: Existing literature revealed that so far, no Pharmacognostic study has been reported on the leaf of B. scandens. Findings from this investigation can be used for its identification and determination of quality and purity of medicinally important plant. Thus exploring the usefulness of pharmacognostic evaluation to validate and authenticate drug

Sorption of Se (IV) from aqueous solutions with subsequent determination by X-ray fluorescence analysis

2020 ◽  
Vol 86 (10) ◽  
pp. 5-9
Author(s):  
D. G. Filatova ◽  
A. A. Arkhipenko ◽  
M. A. Statkus ◽  
V. V. Es’kina ◽  
V. B. Baranovskaya ◽  
...  
Keyword(s):  
Inductively Coupled Plasma ◽  
Fluorescence Analysis ◽  
Standard Samples ◽  
Phase Contact Time ◽  
Sorbent Phase ◽  
X Ray ◽  
Fundamental Parameters ◽  
Inductively Coupled ◽  
Subsequent Determination

An approach to sorptive separation of Se (IV) from solutions on a novel S,N-containing sorbent with subsequent determination of the analyte in the sorbent phase by micro-x-ray fluorescence method is presented. The sorbent copolymethylenesulfide-N-alkyl-methylenamine (CMA) was synthesized using «snake in the cage» procedure and proven to be stable in acid solutions. Conditions for quantitative extraction of Se (IV) were determined: sorption in 5 M HCl or 0.05 M HNO3 solutions when heated to 60°C, phase contact time being 1 h. The residual selenium content in the solution was determined by inductively coupled plasma mass spectrometry (ICP-MS) using 82Se isotope. The absence of selenium losses is proved and the mechanism of sorption interaction under specified conditions is proposed. The method of micro-x-ray fluorescence analysis (micro-RFA) with mapping revealed a uniform distribution of selenium on the sorbent surface. The possibility of determining selenium in the sorbent phase by micro-RFA is shown. When comparing the obtained results with the results of calculations by the method of fundamental parameters, it is shown the necessity of using standard samples of sorbates to obtain correct results of RFA determination of selenium in the sorbent phase.

scholarly journals Determination of antioxidant activity and phenolic compounds for basic standardization of Turkish propolis

2021 ◽  
Vol 64 (1) ◽  
Author(s):  
Aslı Özkök ◽  
Merve Keskin ◽  
Aslı Elif Tanuğur Samancı ◽  
Elif Yorulmaz Önder ◽  
Çiğdem Takma
Keyword(s):  
Antioxidant Capacity ◽  
Caffeic Acid ◽  
Caffeic Acid Phenethyl Ester ◽  
Total Phenolic ◽  
Scaling Analysis ◽  
Flavonoid Content ◽  
Multidimensional Scaling Analysis ◽  
Flavonoid Quercetin ◽  
Phenolic And Flavonoid

AbstractThis study aimed to determine the standard amount of antioxidant content and compounds of the propolis for the standardization of propolis. For this purpose, the total flavonoids, total phenolic, CUPRAC antioxidant capacity content and the diversity of phenolic and flavonoid components of these propolis samples were found by HPLC determined at the 23 propolis samples which were collected different regions of Turkey. Beside that, the similarities and differences of these 23 provinces to each other according to their antioxidant capacities were investigated by multidimensional scaling analysis. The total flavonoid content in the propolis samples were determined between 21.28 and 152.56 mg CE/g. The total phenolic content in the propolis samples was found between 34.53 mg and 259.4 mg GAE/g. CUPRAC antioxidant capacity of the propolis samples and antioxidant range was found from 95.35 to 710.43 mg TE/g. Also, 4 flavonoid [Quercetin (min.1.12–max.4.14 mg/g), Galangin (min.0.72–max.40.79 mg/g), Apigenin (min.1.07–max.17.35 mg/g), Pinocembrin (min.1.32–max.39.92 mg/g] and 6 phenolic acid [Caffeic acid (min.1.20–max.7.6 mg/g), p-Coumaric acid (min.1.26–max.4.47 mg/g), trans-Ferulic acid (min.1.28–max.4.92 mg/g), Protocatechuic acid (1.78 mg/g), trans-Cinnamic acid (min.1.05–max.3.83 mg/g), Caffeic Acid Phenethyl Ester (CAPE) (min.1.41–max.30.15 mg/g)] components were detected as mg/g, in different ratios in propolis samples collected from different regions. The feature of this study, so far, is to have the maximum number of samples representing the Turkish propolis, and so is thought to help to national and international propolis standard workings.

Determination of the composition of binary chalcogenide glasses by X-ray fluorescence analysis

2010 ◽  
Vol 44 (1) ◽  
pp. 24-27 ◽  
Author(s):  
G. A. Bordovsky ◽  
A. V. Marchenko ◽  
P. P. Seregin ◽  
N. N. Smirnova ◽  
E. I. Terukov
Keyword(s):  
Chalcogenide Glasses ◽  
Fluorescence Analysis ◽  
X Ray

Validasi dari Spektrofotometri UV-Vis dan Kandungan Total Flavonoid Ekstrak Etanol dari Akar Alang-Alang (Imperata cylindrica) dan Daun Pegagan (Centella asiatica) Anita Puspa Widiyana

2021 ◽  
Vol 3 (2) ◽  
pp. 126-136
Author(s):  
Anita Puspa Widiyana ◽  
Keyword(s):  
Chemical Constituents ◽  
Centella Asiatica ◽  
Ethanol Extract ◽  
Chemical Compounds ◽  
Imperata Cylindrica ◽  
Total Flavonoid ◽  
Analysis Method ◽  
Flavonoid Content ◽  
Validation Testing

Validation as a quality control for the content of chemical compounds from natural ingredients. One of the chemical constituents is the flavonoids which are found in the Imperatacylindrica roots and Centella asiatica leaves. This study aims to ensure the analysis method meets the requirements and determines the levels of flavonoids. The research stages included extraction, validation and determination of total flavonoid. Extraction was carried out by immersing dry simplicia in 96% ethanol solvent for 3x24 hours. The solvent is evaporated using a rotary evaporator until a thick extract is formed. Validation testing includes linearity, accuracy, precision, LOD and LOQ. Determinationof the total flavonoid was carried out by measuring the absorption at a maximum wavelength of 428.2 nm. The validation results includethe correlation coefficient (R) of 0.998, precision % RSD <2 %, %accuracy 99,53-97,98%, LOD 3.02ppm and LOQ 9.15 ppm. The total flavonoid of the ethanol extract of Imperata cylindrica roots was 36.39 ± 0.08 mg/g QE and Centella asiatica leaves was 102.10 ± 0.08 mg/g QE. The conclusion is that the method used met the validation requirements and the total flavonoid content of the ethanol extract of Centella asiatica leaves was higher than Imperata cylindrica roots

Exploration of the forbidden regions of the Ramachandran plot (ϕ-ψ) with QTAIM

2017 ◽  
Vol 19 (38) ◽  
pp. 26423-26434 ◽  
Author(s):  
Roya Momen ◽  
Alireza Azizi ◽  
Lingling Wang ◽  
Yang Ping ◽  
Tianlv Xu ◽  
...  
Keyword(s):  
Amino Acids ◽  
Peptide Structure ◽  
Ramachandran Plot ◽  
Left Response ◽  
Forbidden Regions ◽  
Dark Green ◽  
Ramachandran Plots ◽  
Pale Green

Left: Response β is defined as: β = arccos(e̲2·y̲) with β* = arccos(e̲1·y̲). Right: QTAIM interpreted Ramachandran plots {(βϕ,βϕ*)-(βψ,βψ*)} ‘-’ is a hyphen and not a subtraction sign. Pale green and dark green crosses indicate the glycine, pink and red pluses represent the remaining amino acids (a.a.) in the magainin peptide structure.

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