Determination of Pharmaceuticals Based on Indole Alkaloids with Amperometric DNA-Sensors and Enzyme Immunoassay Test-System

2011 ◽  
Vol 44 (5) ◽  
pp. 837-849 ◽  
Author(s):  
Sofya S. Babkina ◽  
Nikolay A. Ulakhovich
1991 ◽  
Vol 74 (1) ◽  
pp. 43-46 ◽  
Author(s):  
Bhanu P Ram ◽  
Prithipal Singh ◽  
Lorelei Martins ◽  
Teri Brock ◽  
Nikolai Sharkov ◽  
...  

Abstract A high-volume enzyme immunoassay (EIA) system for slaughterhouse screening of sulfamethazine In swine plasma/ serum has been developed. The system Includes a robotic sample processor that performs most of the liquid handling requirements in the assay. The assay gives good correlation with the widely used thin layer chromatographic method for determination of sulfamethazine in serum and plasma (r = 0.826). Inter- and Intra-assay coefficients of variation are less than 10%. Approximately 2,400 serum/ plasma samples can be analyzed In a normal working day (8 h) with this system.


2019 ◽  
Vol 27 (1) ◽  
pp. 35-40
Author(s):  
Tatyana V. Zhestkova ◽  
Mikhail A. Butov ◽  
Yulian Yu. Lymar ◽  
Sergey V. Papkov

Aim. Determination of the prevalence of Helicobacter pylori (H. pylori) infection among the population of the Ryazan region. Materials and Methods. 833 individuals (809 adults and 24 children) were examined for presence of IgG class antibodies using the enzyme immunoassay (2017-2018). The criteria for inclusion into the study were: a desire of a patient to undergo examination for the presence of antibodies to H. pylori in blood. Criteria for exclusion: past treatment for helicobacteriosis. The presence of helicobacteriosis was determined by enzyme immunoassay for quantitative detection of IgG class antibodies (anti-H. pylori IgG) using BCM Diagnostics Helicobacter pylori IgG (USA) test system and for qualitative determination of IgG antibodies to H. pylori in blood serum on IMMULITE 2000 (Germany; test IMMULITE 2000 H. pylori IgG). Sensitivity of the used test systems was 95.0%, specificity 98.0%. Results. High contamination of adult residents of Ryazan with H. pylori 65.6% was found (70.6% of males, 64.4% of females). Prevalence of H. pylori infection among adults in 2017 was 64.4% and in 2018 70.2%, however, the observed increase in the number of infected individuals was not statistically significant (p0.05). The highest prevalence of H. pylori infection was observed in individuals 40 years of age (67.2%). Gender-related differences in the prevalence of Helicobacter pylori infection were revealed in individuals of 40 years and older. H. pylori infection in males of 40 years was 75.2%, against 65.5% in females of the same age (p0.05). In children of 4-16 years, the share of individuals with positive serological test with anti-H. pylori IgG reached 20.8%. All H. pylori infected children were above 9 years of age. Individuals with positive serological tests received consultation of a gastroenterologist, and on indications underwent additional examination with administration of eradication treatment. In patients with indefinite results the examination was repeated after a week and/or the presence of H. pylori antigen in feces was determined. Conclusion. The data obtained indicate a high level of infection with H. pylori in the adult population in the Ryazan region 65.6%. The incidence of detection of anti-H. pylori IgG in the population was maximal in individuals 40 years (67.2%).


Author(s):  
R Petrov ◽  
A. Fotin ◽  
O. Pidlubny

Introduction. The article deals with the results of the mycotoxicological analysis of feed samples of pond fish. There were found the T2-toxin and aflatoxins.The combined presence of aflatoxins B1, B2, G1 and G2 and T2-toxin was found in all samples of fish feed. Was also studied the impact of combination of several mycotoxins on organoleptic and physico-chemical characteristics of fish carcasses. Fish, affected by mycotoxins, can be classified to the category of doubtful freshness. Materials and methods of research. The studies were conducted between May and October 2019. The investigated materials were a large number of grain and grain mixtures, for feeding fish in six ponds in Nikolaevska settlement community of Sumy region. Preparation of grain samples were made according resolution of the Cabinet of Ministers of Ukraine, June 14, 2002, No. 833 «The order of the selection of samples animal, plant and biotechnological origin». The studies of the toxicity and persistent T2-toxin and full amount of aflatoxins B1, B2, G1 and G2 are conducted on the basis of the Sumy Regional Laboratory of Veterinary Medicine. Feed toxicity was investigated by bioassay on the Tetrahymena piriformis infusorium used the DSTU 3570-97. The RIDASCREEN test systems were used to investigate the aflatoxins B1, B2, G1 and G2 in grains and grain mixtures. Ichthyopathological studies were conducted in the department of Veterinary and Sanitary Examination, Microbiology, Zooghygiene, Safety and the Guality of Livestock Products of the Sumy National Agrarian University by the accepted methods. Results of research and discussion. In the territory of the Nikolaevska settlement community of Sumy region there are six ponds, in which hold fish, mainly crucian and carp. The fish are fed once a week. Feed mainly consists of grain waste (barley, wheat), which is supplied by local farmers. Food is stored in unsuitable premises. In the feed we noted the presence of remains of substandard grain, which was thrown out during separation. Grain samples are not sampled and laboratory tests are not carried out. The feed is shipped by transport to ponds, dumped from the shore into a pond, immersed in to the water, where consumed by the fish. Totaly 19 samples of feed were examined during this period. Organoleptic evaluation of grain and grain mixtures revealed that the color of the grain was natural, the smell of all the samples had a certain tinge of moldy-musty, some samples had signs of fermentation and mold. Aqueous solutions of the grain extracts and mixtures of the test samples caused a stopping of movement and death of all Tetrahymena piriformis infusions up to 60 minutes in 7 samples, that indicates the toxicity of these feeds. Low toxicity was detected in 11 samples of experimental feed. The absence of toxicity was evidenced by the activity of Tetrahymena piriformis infusoriums, which persisted for 1 hour after the action of aqueous extracts of the samples. The results of the determination of the toxicity of grain feed using infusorium Tetrahymena piriformis. To analyze the content of major mycotoxins was used competitive enzyme immunoassay. The RIDASCREEN FAST Aflatoxin test system and the RIDASCREEN FAST T-2 Toxin test system have a high sensitivity of 0.0017 mg / kg and 0.05 mg / kg, respectively, which made it possible to determine the content of T-2 toxin, the amounts of aflatoxins B1, B2, G1 and G2 in their lowest concentration. The results of analysis of feed samples using the amount of aflatoxins B1, B2, G1 and G2  That in all samples of grain and grain mixtures was established the presence of aflatoxins B1, B2, G1 and G2. In 7 samples its content exceeds the maximum permissible concentrations. In 10 samples, the combined presence of aflatoxins B1, B2, G1 and G2 and T2-toxin was found, in 5 samples - exceeding the maximum levels. It is known that the combination of several mycotoxins can lead to their synergistic interaction, which will have a more pronounced toxic effect. Unfortunately, it was not possible to determine the maximum content of aflatoxins B1, B2, G1 and G2 and T2-toxin, so further test kits with different reading ranges should be used, since highly sensitive mycotoxin detection kits make it impossible to determine up to 1 mg / kg. In the following research, we studied the chemical properties of fish meat: reaction to peroxidase (benzidine sample), amount of amino-ammonia nitrogen, reaction with copper sulfate, reaction with Eber reagent, determination of hydrogen sulfide, pH and reaction with Nesler reagent. When muscle is damaged by mycotoxin, the products protein breakdown appears, which promotes rapid breakdown of tissue elements and leads to rapid deterioration of fish. Analyzing changes in veterinary-sanitary and physico-chemical parameters of fish affected by mycotoxicosis, we can classify the affected fish in the category of doubtful freshness. Conclusions and prospects for further research. During the investigate of grain and grain mix for feeding pond fish it was found that 19 samples were highly toxic and 36.8% were law toxoc. 2. Using the competitive enzyme immunoassay the combined presence of aflatoxins B1, B2, G1 and G2 and T2-toxin was found in all samples In 7 samples its content exceeds the maximum permissible concentrations. T2-toxin was found was found in 16 samples, and in 10 samples its content exceeds the maximum permissible concentrations. Fish affected by mycotoxins for organoleptic and physico-chemical characteristics can be classified to the category of doubtful freshness.


Author(s):  
V. V Pisarev ◽  
Maria M Ulyashova ◽  
Gelia N Gildeeva

An integral part of preclinical pharmacokinetic studies is the development of a bioanalytical method for determination of the drug in a biological fluid.The aim of the research was to assess the suitability of the test system based on enzyme-linked immunosorbent assay (ELISA) for quantitative determination of rituximab in the blood serum of laboratory animals after intravenous administration of rituximab at a dose corresponding to the therapeutic dose in humans. Th test system was developed by the Scientific and Production Center Probiotech.Materials and methods: the determination of rituximab in biological samples was carried out using a two-stage sandwich-type ELISA, followed by detection based on horseradish peroxidase. The ELISA results were recorded using a microplate photometer at a wavelength of 450 nm.Results: the experiments helped to establish the detection limit (0.24 ng/mL) and the lower limit of quantitation (1.00 ng/mL) of rituximab in rabbit blood serum, they also demonstrated high selectivity of analyte determination in a multicomponent biological matrix. The mean rituximab concentration was within 14 % of the nominal value in the entire working range of the method. The within-run and between-run precision of the assay did not exceed 7.4 %, the total error of the method did not exceed 20.1 %. The linearity of dilution makes it possible to use the assay for the analysis of biological samples with a wide range of rituximab concentrations. The stability of the analyte in the rabbit blood serum was confirmed by storing samples for 6 hours at room temperature, for 50 days at —35 °C, and after 3 freeze-thaw cycles. The validated immunoassay was successfully used to determine the rituximab concentration in biological samples obtained in the rituximab pharmacokinetic trial in rabbits. The accuracy of the results was confirmed for the entire range of the determined concentrations; parallelism was demonstrated between the calibration curve and the results of analysis of serially diluted rabbit serum samples with the maximum concentration of rituximab.Conclusions: the proposed enzyme immunoassay test system can be used for quantitative determination of rituximab in the blood serum of laboratory animals, as it meets acceptance criteria for all validation parameters described in the international guidelines on validation of bioanalytical methods.


2021 ◽  
Vol 80 (Suppl 1) ◽  
pp. 1083.2-1084
Author(s):  
O. Rusanova ◽  
A. Trofimenko ◽  
N. Emelyanov ◽  
O. Emelyanova

Background:Production of antibodies to ceruloplasmin (CP) in rheumatoid arthritis is an issue that has not been studied well enough. It was not by chance that this copper–containing alpha 2-glycorpoteid of blood plasma showing multienzymatic properties was chosen as an object of investigation. Data on the content and activity of CP in the blood of rheumatoid arthritis patients are contradictory, which has to do with different approaches to selection of patients and different measuring methods.Objectives:Improving diagnosis of rheumatoid arthritis by determination of antibodies to CP as well as its amount and enzymatic activity.Methods:We studied the serum from 30 apparently healthy individuals, and 108 rheumatoid arthritis patients. Antibodies to CP were determined by enzyme immunoassay using immobilized granulated antigen preparations (modification by Gontar et al, 2002). The amount of CP was determined by enzyme immunoassay according to the method of I.S. Kuzmina et al (1991) using commercial diagnostic agent manufactured by Mechnikov Research Institute for Vaccines and Sera.Results:Enzyme immunoassay showed a mean level of CP antibodies in donor sera of 0,020±0,006 optical density units. The level of normal values of specific antibodies determined as M±2σ included an extinction value in the range 0 – 0,086. The mean value of oxidase activity and the amount of CP in healthy people was 716±26,3 and 921±32 ng/ml, correspondingly. In the process of study we revealed a reliable increase in CP antibody count, the activity and amount of CP in patients with rheumatoid arthritis while in all cases the parameters under study correlated with the degree of disease activity (p<0,05): at activity degree I CP antibodies were 0,098±0,011; CP activity was 954±48,1; CP amount was 1292±73,4. At activity degree II CP antibodies were 0,138±0,007; CP activity was 1163±39,6; CP amount was 1763±69,3. At activity degree III, CP antibodies were 0,182±0,015; CP activity was 1368±89,5; CP amount was 1794±102,8. After a course of hospital treatment was completed, we noted a reliable decrease in the activity and amount of CP (at degree I of rheumatoid arthritis activity p<0,001, at degree II of rheumatoid arthritis activity p<0,01for both parameters; at degree III, p<0,05) compared with baseline findings. A decrease in CP antibodies shows decelerated dynamics, especially in patients with pronounced disease activity, which indicates severe disorders in the immunity that cannot be cured completely within 30 – 40 days of hospital treatment course.Conclusion:Determination of CP antibodies, as well as quantitative content of CP and its oxidase activity can serve as indicators of the activity of rheumatoid arthritis, as well as an accessory criterion of the effectiveness of administered therapy.Disclosure of Interests:None declared


2014 ◽  
Vol 70 (4) ◽  
pp. 599-604 ◽  
Author(s):  
Bing Wang ◽  
Ivo Achu Nges ◽  
Mihaela Nistor ◽  
Jing Liu

In this work, biochemical methane potential (BMP) tests with cellulose as a model substrate were performed with the aid of three manually operated or conventional experimental setups (based on manometer, water column and gas bag) and one automated apparatus specially designed for analysis of BMP. The methane yields were 340 ± 18, 354 ± 13, 345 ± 15 and 366 ± 5 ml CH4/g VS obtained from experimental setups with manometer, water column, gas bag, and automatic methane potential test system, which corresponded to a biodegradability of 82, 85, 83 and 88% respectively. The results demonstrated that the methane yields of cellulose obtained from conventional and automatic experimental setups were comparable; however, the methane yield obtained from the automated apparatus showed greater precision. Moreover, conventional setups for the BMP test were more time- and labour-intensive compared with the automated apparatus.


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