scholarly journals 6,7- AND 7,8-DIHYDROXYBENZOPYRYLIUM DERIVATIVES: SYNTHESIS, PROPERTIES AND ANALYTICAL APPLICATION (REVIEW)

2021 ◽  
Vol 26 (2(78)) ◽  
pp. 48-55
Author(s):  
A. N. Chebotarev ◽  
S. V. Toporov ◽  
D. V. Snigur ◽  
D. A. Barbalat

The present review is devoted to a class of organic analytical reagents 6,7- and 7,8-dihydroxybenzopyrylium derivatives: their synthetic pathways, physicochemical properties, state in solutions, and analytical applications are described. Anion nature influence on spectral characteristics and some physico-chemical properties of 6,7-dihydroxybenzopyrylium derivatives was noted. Pathways of acid-base transformations in aqueous solutions of 6,7-dihydroxybenzopyrylium derivatives were described. It has been shown that derivatives of 6,7- and 7,8-dihydroxybenzopyrylium are capable for complexation with a number of p-, d-, and f-elements (Cu (II), Ga (III), In (III), Tl (III), Ge (IV), La (III), titanium subgroup, Bi (III), Mo (VI), W(VI) and others). Information on their composition, structure and analytical characteristics is summarized. It is noted that with the 6,7-dihydroxybenzopyrylium derivatives the simple and highly sensitive methods for the direct spectrophotometric and extraction-photometric determination of Ga(III), In(III), Tl(III), Ti(IV), Zr(IV), Hf(IV), Mo(VI), Ge(IV), Bi(III), Cu(II) have been developed. It is noted that 6,7-dihydroxybenzopyrilium derivatives complexes with Mo(VI) and Cu(II) are effectively extracted by Triton X‑100 micellar phase, which forms the basis for highly sensitive combined spectrophotometric and atomic absorption methods for their determination. The simplicity of targeted synthesis of 7,8- and 6,7-dihydroxybenzopyrylium derivatives opens the way to their use in the development of combined cloud point extraction and liquid-liquid microextraction with spectrophotometric or atomic absorption detection methods for the determination of a number of p- and d-elements.

Eisei kagaku ◽  
1971 ◽  
Vol 17 (6) ◽  
pp. 393-397
Author(s):  
KATSUHIKO TANAKA ◽  
KATSUHISA FUKAYA ◽  
KIYOSHI YOSHITANI ◽  
SYOZO FUKUI ◽  
SABURO KANNO

2016 ◽  
Vol 183 (11) ◽  
pp. 3035-3041 ◽  
Author(s):  
Sujin Lee ◽  
Yun-Sik Nam ◽  
Sung-Hee Choi ◽  
Yeonhee Lee ◽  
Kang-Bong Lee

Molecules ◽  
2020 ◽  
Vol 26 (1) ◽  
pp. 174
Author(s):  
Gregor Marolt ◽  
Mitja Kolar

From the early precipitation-based techniques, introduced more than a century ago, to the latest development of enzymatic bio- and nano-sensor applications, the analysis of phytic acid and/or other inositol phosphates has never been a straightforward analytical task. Due to the biomedical importance, such as antinutritional, antioxidant and anticancer effects, several types of methodologies were investigated over the years to develop a reliable determination of these intriguing analytes in many types of biological samples; from various foodstuffs to living cell organisms. The main aim of the present work was to critically overview the development of the most relevant analytical principles, separation and detection methods that have been applied in order to overcome the difficulties with specific chemical properties of inositol phosphates, their interferences, absence of characteristic signal (e.g., absorbance), and strong binding interactions with (multivalent) metals and other biological molecules present in the sample matrix. A systematical and chronological review of the applied methodology and the detection system is given, ranging from the very beginnings of the classical gravimetric and titrimetric analysis, through the potentiometric titrations, chromatographic and electrophoretic separation techniques, to the use of spectroscopic methods and of the recently reported fluorescence and voltammetric bio- and nano-sensors.


2020 ◽  
pp. 179-186
Author(s):  
Dzhavgarat Ruslanovna Imachuyeva ◽  
Fatima Kazbekovna Serebryanaya ◽  
Ifrat Nazimovich Zilfikarov

Preparing of the antiviral and antibacterial medicinal plants is a promising task of native pharmacy. In this regard, it is interesting to study species of the genus penny, namely Hedysarum caucasicum M.Bieb., Hedysarum grandiflorum Pall., Hedysarum daghestanicum Rupr. ex. Boiss., the regions of distribution, chemical composition and known pharmacological properties will allow to justify directions of their rational use, as well as creation of new phytopreparations of antiviral action on the basis of medicinal raw materials. During the complex pharmacognostic studies of three species of Hedysarum L. we have developed the method for isolation and quantitative determination of the sum of xanthones in terms of mangiferin by UV spectrophotometry. The technique takes into account the basic physical and chemical properties of xanthones, is characterized by reproducibility, high accuracy, simplicity of implementation, allows to carry out both screening evaluation of various raw objects containing mangiferin derivatives, as well as standardization of the prepared medicinal plant raw material of the penny. The developed methods are tested on the aerian organs of Hedysarum L. species, collected and dried taking into account the rules and requirements of drug raw material procurement. As a result, Hedysarum caucasicum M.Bieb herb (0.624%) was found to be the highest quantitative amount of xanthone sum in terms of mangiferin. The obtained results show the prospect of further research of the aerian part of the Hedysarum caucasicum M.Bieb. as an additional source of mangiferin. The method of quantitative determination of xanthone sum in the list for mangiferin in the above-ground part of Hedysarum caucasicum M.Bieb; Based on the obtained data, it has been found that the proposed technique is highly sensitive, reproducible and usable.


2017 ◽  
Vol 2017 ◽  
pp. 1-8
Author(s):  
Felisberto G. Santos ◽  
Boaventura F. Reis

A highly sensitive analytical procedure for photometric determination of molybdenum in plant materials was developed and validated. This procedure is based on the reaction of Mo(V) with thiocyanate ions (SCN−) in acidic medium to form a compound that can be monitored at 474 nm and was implemented employing a multicommuted flow analysis setup. Photometric detection was performed using an LED-based photometer coupled to a flow cell with a long optical path length (200 mm) to achieve high sensitivity, allowing Mo(V) determination at a level of μg L−1 without the use of an organic solvent extraction step. After optimization of operational conditions, samples of digested plant materials were analyzed employing the proposed procedure. The accuracy was assessed by comparing the obtained results with those of a reference method, with an agreement observed at 95% confidence level. In addition, a detection limit of 9.1 μg L−1, a linear response (r=0.9969) over the concentration range of 50–500 μg L−1, generation of only 3.75 mL of waste per determination, and a sampling rate of 51 determinations per hour were achieved.


Author(s):  
E. V. Moiseeva ◽  
I. A. Potapova

Mercury is one of the most common in various industries and at the same time dangerous chemicals. It is able to be deposited in the body and have a toxic effect for a long time after the cessation of contact. Under the influence of mercury, workers can develop various intoxications, as a result of which pathological changes in the nervous, cardiovascular, endocrine, immune and reproductive systems are possible.Under production conditions, mercury enters the body, usually in the form of vapors (absorbed about 80%) and suspended particles. Inorganic forms of mercury are excreted mainly in the urine (60%). However, insufficient attention is currently being paid to the problem of determining the mercury content in urine samples. To date, in world practice there is no systematic approach to the determination of small doses of mercury in the body, as a result of which it is difficult to timely identify public health disorders. This is largely due to the lack of highly sensitive and highly effective methods of analysis, allowing routine measurements with minimal cost and high accuracy. The methods currently used are either quite expensive or have low accuracy/sensitivity.The aim of the study was to develop a method of atomic absorption determination of mercury in urine by cold steam, which would allow at minimal cost to increase the accuracy and sensitivity of mercury detection in the body.Materials and methods. Quantitative measurement of mercury in urine samples was carried out on an atomic absorption spectrometer with a mercury-hydride prefix using model solutions of different concentrations.Results. The study determined the optimal conditions for sample preparation of urine samples, set the range of concentrations for the construction of the calibration schedule, studied the effect of the matrix on the accuracy of the analysis by the “introduced-found” method. The lower limit of detection of the developed technique was 0.05 mcg/l, the upper limit–100 mcg/l (if necessary, it can be increased by additional dilution). The relative error of determination depending on the concentration varied from 3 to 15%.Conclusions. A highly sensitive, affordable and relatively inexpensive method for the determination of mercury in urine has been developed, which will allow to diagnose with high accuracy the background contents of mercury in urine, which is especially important when inspecting workers of industries associated with the use of mercury and its compounds, as well as the population living in areas close to these industries.


2008 ◽  
Vol 62 (4) ◽  
Author(s):  
Suling Feng ◽  
Limin Guo

AbstractIn a hydrochloric acid medium, benzhexol hydrochloride, cyproheptadine hydrochloride, and maprotiline hydrochloride, can react with ammonium molybdate to form ion-association complexes by virtue of electrostatic attraction and hydrophobic interaction which result in a significant enhancement of the resonance light scattering intensity. The maximum scattering wavelengths were found at 364 nm, 364 nm, and 381 nm for benzhexol hydrochloride, cyproheptadine hydrochloride, and maprotiline hydrochloride systems, respectively. Spectral characteristics of the three systems, influencing factors, and optimum conditions were investigated. The reason of resonance light-scattering enhancement and the mechanism of interactions between the drugs and ammonium molybdate were also discussed. Based on the linear relationship between the enhanced intensity of resonance light scattering and the concentration of drugs, a highly sensitive method for the determination of the three drugs was developed, the detection limits being 0.0110 μmol L−1, 0.0038 μmol L−1, and 0.0155 μmol L−1 for benzhexol hydrochloride, cyproheptadine hydrochloride, and maprotiline hydrochloride, respectively. The method was successfully applied to the determination of the investigated drugs in pharmaceutical, serum, and urine samples.


2008 ◽  
Vol 73 (5) ◽  
pp. 569-576 ◽  
Author(s):  
Mohamed Issa ◽  
Mahmoud Nejem ◽  
Monzer Al-Kholy ◽  
Said El-Abadla ◽  
Sobhi Helles ◽  
...  

A highly sensitive indirect atomic absorption spectrophotometric (AAS) method has been developed for the determination of very low concentrations of ciprofloxacin, amoxycillin and diclofenac sodium. The method is based on the oxidation of these drugs with iron(III). The excess of iron(III) was extracted into diethyl ether and then the iron(II) in the aqueous layer was aspirated into an air-acetylene flame and determined by AAS. The linear concentration ranges were 25-400, 50-500 and 60-600 ng ml-1 for ciprofloxacin, amoxycillin and diclofenac sodium, respectively. The results were statistically compared with the official method using t- and f-test at p < 0.05. There were insignificant interferences from most of the excipients present. The intra- and inter-day assay coefficients of variation were less than 6.1 % and the recoveries ranged from 95 to 103 %. The method was applied for the analysis of these drug substances in their commercial pharmaceutical formulations.


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