High sensitivity ELISA determination of taxol in various human biological fluids

1999 ◽  
Vol 20 (3) ◽  
pp. 549-555 ◽  
Author(s):  
Stan R Svojanovsky ◽  
Kamal L Egodage ◽  
Jun Wu ◽  
Milan Slavik ◽  
George S Wilson
Kardiologiia ◽  
2019 ◽  
Vol 59 (11) ◽  
pp. 66-75 ◽  
Author(s):  
A. M. Chaulin ◽  
L. S. Karslyan ◽  
E. V. Bazyuk ◽  
D. A. Nurbaltaeva ◽  
D. V. Duplyakov

The article is devoted to problems of clinical-diagnostic value of determination of cardio-specific troponins in human biological fluids. Improvement of laboratory instrumentation and emergence of high sensitivity methods of analysis have allowed to identify troponins in urine, dialysate, and oral fluid. In the review we present actual information related to measurement of troponins in blood serum, data on testing of cardio-specific troponins in urine, dialysate, and oral fluid. Special attention is paid to determination of some cardiomarkers in oral fluid with thorough analysis of diagnostic value and effectiveness of the conducted studies.


Sensors ◽  
2019 ◽  
Vol 19 (23) ◽  
pp. 5298 ◽  
Author(s):  
Lee ◽  
Sung ◽  
Kang ◽  
Parameswaran ◽  
Choi ◽  
...  

The level of human serum albumin (HSA) in biological fluids is a key health indicator and its quantitative determination has great clinical importance. In this study, we developed a selective and sensitive fluorescent HSA probe by fluorescence-based high-throughput screening of a set of fluorescent thieno[3,2-b]pyridine-5(4H)-one derivatives against major plasma proteins: HSA, bovine serum albumin (BSA), globulin, fibrinogen, and transferrin. The fluorophore chosen finally (4 in Scheme 1) showed noticeable fluorescence enhancement in the presence of HSA (160-fold increase), and it exhibited rapid response, high sensitivity (detection limit 8 nM), and the ability to clearly distinguish HSA from BSA in pH 9 buffer condition. Moreover, the probe could be applicable to detect trace amounts of HSA in an artificial urine sample; further, it might be applied to the determination of the HSA concentration in complex biological samples for pre-clinical diagnosis.


Fire Safety ◽  
2018 ◽  
pp. 74-79
Author(s):  
O. Scherbyna

The methods of isolation, purification and qualitative and quantitative determination of phenol in air and biological fluids of an organism are offered. Isolation was carried out by distillation with water vapor, purification by extraction with chloroform, and identification by qualitative reactions, by chromatography in a thin layer of sorbent and by liquid chromatography. The quantitative determination of phenol was carried out by liquid chromatography in a reverse phase (chromatograph "Tsvet-304" with an ultraviolet detector). Calculation of the quantitative content of phenol was carried out by the method of absolute calibration. As a result of the research, it was found that by using the molecular liquid chromatography method, it is possible to determine 17-20% of phenol isolated from urine and 21-24% isolated from the air. The retention time of phenol 1h.14s, the results of the analysis are well reproducible. The worked out techniques have high resolution, high sensitivity and speed of analysis.


2008 ◽  
Vol 62 (4) ◽  
Author(s):  
Ahmad Alghamdi

AbstractThe square-wave voltammetric technique was used to explore the adsorption properties of the astemizole drug. The analytical methodology used was based on the adsorptive preconcentration of the drug on a hanging mercury drop electrode (HMDE), followed by the electrochemical reduction process which yielded a well-defined cathodic peak at −1.184 V (vs. the Ag/AgCl electrode). To achieve high sensitivity, various experimental and instrumental variables were investigated such as the supporting electrolyte, pH, accumulation time and potential, drug concentration, scan rate, SW frequency, pulse amplitude, convection rate, and the working electrode area. Under the optimized conditions, the AdSV peak current was proportional over the analyte concentration range of 5 × 10−7 to 2.5 × 10−6 mol L−1 (r = 0.998) with the detection limit of 1.4 × 10−8 mol L−1 (6.4 ng mL−1). The precision of the proposed method in terms of RSD was 2.4 %, whereas the method accuracy was indicated by the mean recovery of 100.1 %. Possible interferences of several substances usually present in the pharmaceutical tablets and formulations were also evaluated. The applicability of this electroanalytic approach was illustrated by the determination of astemizole in tablets and biological fluids.


2020 ◽  
Vol 16 (8) ◽  
pp. 996-1009
Author(s):  
Khadijeh Ghanbari ◽  
Ashraf Sivandi

Background: Hypertension is a major risk for morbidity and mortality, while hypertension is associated with cardiovascular disease and organ damage. Recent research efforts have focused on the development of highly selective angiotensin receptor blockers. In which losartan (LOS) is considered as a new generation of an effective oral drug product against arterial hypertension. Therefore, the determination of drugs in biological fluids, pharmaceuticals (tablets), and wastewater is of critical importance for clinical applications, forensics, quality control, and environmental protection that call for the development of analytical methods. Many ranges of methods such as spectroscopic methods and chromatographic techniques have been developed to determine LOS in pharmaceutical formulations and biological fluids. However, there are crucial interference problems in these methods. For these reasons, more sensitive, desirable, portable, low-cost, simple, and selective nanocomposite-based sensors are needed in terms of health safety. Nanomaterials such as reduced graphene oxide, chitosan, and metal nanoparticles are used to improve the sensitivity in the development of electrochemical sensors. Objective: In this study, a novel reduced graphene oxide (RGO), chitosan (Chit), gold (Au), and zinc oxide (ZnO) nanocomposite (RGO/Chitosan/Au/ZnO) was synthesized and used to develop a sensitive and efficient electrochemical sensor for LOS detection. Methods: Modification of electrode by RGO/Chit/Au/ZnO nanocomposite was performed in four stages with GO (at -2.0 V for 150 s), Chitosan (at -3.0 V for 300 s), Au nanoparticles (at -0.4 V for 400 s), and Zn nanoflowers like (at -0.7 V for 1200 s). The RGO/Chitosan/Au/ZnO nanocomposite was characterized by field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR). Cyclic Voltammetry (CV) and Differential Pulse Voltammetry (DPV) were used to detect LOS, and the influence of pH value, scan rate, accumulation potential, and time also losartan concentration on the performance of ZnO/Au/Chitosan/RGO/GCE were investigated. In order to investigate the selectivity of the modified electrode for the determination of LOS, the effect of possible interfering species was evaluated and showed that these species are not interferences. Also, the reproducibility of the modified electrode was investigated and implying that the RGO/Chit/Au/ZnO nanocomposite was highly reproducible. Results: The modified electrode was used as a sensor for the selective and sensitive determination of LOS with a detection limit of 0.073 μM over the dynamic linear range of 0.5μM to 18.0 μM. In addition, electrochemical oxidation of LOS was well recovered in pharmaceutical formulations. Conclusion: LOS is used to treat high blood pressure, taking into account the oxidation of this compound, the use of electrochemical based sensors, ideally suited to a specific chemical species, can be fully selectable and High-sensitivity answer is very important. In this study, the electrodes with RGO/Chit/Au/ZnO nanocomposite were modified by the electrochemical method. Nanocomposites were characterized by various methods such as FE-SEM, FT-IR, XRD, Raman, and XPS. The electrocatalytic activity of the modified electrode was then investigated for measuring LOS. According to the results of the modified electrode, high sensitivity, reproducibility, and selectivity have been shown to oxidize this composition.


2019 ◽  
Vol 85 (2) ◽  
pp. 12-16
Author(s):  
I. V. Saunina ◽  
E. N. Gribanov ◽  
E. R. Oskotskaya

The sorption of Hg (II), Cd (II), and As (III) by natural aluminosilicate is studied. It is shown that the mineral absorbs those toxicants in a rather wide pH range, quantitative extraction of analytes being achieved in a neutral or close to neutral medium (pH values range within 7.0 - 8.0; 6.3 - 7.5; 7.4 - 8.5 for Hg (II), As (III), and Cd (II), respectively). The effect of the time of phase contact on the degree of extraction of elements is shown. The sorption capacity of the mineral in optimal conditions of the medium acidity (0.06 mmol/g for mercury, 0.31 mmol/g for cadmium, and 0.52 mmol/g for arsenic) is determined. The distribution coefficients attain values of aboutnX 103-nX 104. A new combined method for determination of Hg (II), Cd (II), and As (III) in natural and waste water is developed and tested. The method consists in a preliminary group sorption concentration of the analytes by aluminosilicate, desorption of the analytes from the surface of the mineral and their subsequent atomic absorption determination. The correctness of the method is verified in analysis of spiked samples. The method is easy to use and exhibits high sensitivity, reproducibility and accuracy of analyte determination. The relative standard deviation does not exceed 0.13. Economic availability and possibility of using domestic sorption materials are the important advantages of the proposed procedure which can be used in the practice of laboratories monitoring the quality and safety of environmental objects.


2020 ◽  
Vol 25 (42) ◽  
pp. 4464-4485 ◽  
Author(s):  
Katarzyna Kluszczyńska ◽  
Liliana Czernek ◽  
Wojciech Cypryk ◽  
Łukasz Pęczek ◽  
Markus Düchler

Background: Exosomes open exciting new opportunities for advanced drug transport and targeted release. Furthermore, exosomes may be used for vaccination, immunosuppression or wound healing. To fully utilize their potential as drug carriers or immune-modulatory agents, the optimal purity of exosome preparations is of crucial importance. Methods: Articles describing the isolation and purification of exosomes were retrieved from the PubMed database. Results: Exosomes are often separated from biological fluids containing high concentrations of proteins, lipids and other molecules that keep vesicle purification challenging. A great number of purification protocols have been published, however, their outcome is difficult to compare because the assessment of purity has not been standardized. In this review, we first give an overview of the generation and composition of exosomes, as well as their multifaceted biological functions that stimulated various medical applications. Finally, we describe various methods that have been used to purify small vesicles and to assess the purity of exosome preparations and critically compare the quality of these evaluation protocols. Conclusion: Combinations of various techniques have to be applied to reach the required purity and quality control of exosome preparations.


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