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Vesna Vasić Katarina Krinulović Danijela Krstić Tatjana Momić Anica Horvat 《Monatshefte für Chemie / Chemical Monthly》2004,135(5):605-614
Summary. The possibility of using synaptic plasma membrane (SPM) enzymes Na+/K+-ATPase and Mg2+-ATPase, isolated from rat brain, as a biological component of multi-response sensing system for detection of different compounds (alkaline and heavy metal salts, organic compounds) was studied. The method is based on the spectrophotometric determination of inorganic ortho-phosphate (Pi) that serves as a measure of the enzymatic activity in the presence of various analytes. The concentration of Pi, liberated by enzyme catalysed hydrolysis of adenosinetriphosphate (ATP), was followed spectrophotometrically, by single exposure to analytes or in the mixture. Pi was dose dependent on the analyte concentration. Alkaline elements (Na, K, Mg), heavy metals (Pb, Cd, Hg, Cu, Fe, Co, Zn), toxic organic compounds (pyridine, urea, chlorpyrifos), and some drugs (digoxin, gitoxin) showed diverse effects, inducing the inhibition or stimulation of the enzymes activity. Development of simple test method for simultaneous detection of the investigated analytes based on the variation of medium assay composition was discussed. 相似文献
13.
Violeta D. Mitic Snezana D. Nikolic Vesna P. Stankov-Jovanovic 《Central European Journal of Chemistry》2010,8(3):559-565
A kinetic spectrophotometric method for hydrazine determination in the range of 9.36×10−7 to 4.37×10−5 mol dm−3, based on the inhibitory effect of hydrazine on the oxidation of Victoria Blue 4- R by KBrO3, was developed and validated. Kinetic parameters are reported for both the indicating and the inhibiting reaction. The detection
limit was established as 9.98×10−8 mol dm−3. The selectivity of the proposed method was tested considering the influence of different ions that may be present in real
samples. The method was successfully applied for hydrazine determination in various samples (very pure water from the water-steam
system of a power plant and Isoniazid tablets, a pharmaceutical product).
相似文献
14.
JPC – Journal of Planar Chromatography – Modern TLC - The behavior of 5,5-disubstituted hydantoin derivatives has been studied using four chromatographic systems, two normal-phase... 相似文献
15.
Mirjana Popsavin Miloš Svir?evLjilja Torovi? Gordana Bogdanovi?Vesna Koji? Dimitar JakimovSaša Spai? Lidija Aleksi?Velimir Popsavin 《Tetrahedron》2011,67(36):6847-6858
Synthesis of four new tiazofurin analogues has been accomplished starting from d-glucose. The key step of the synthesis was the three-step cascade that enabled an efficient hydrogen sulfide mediated one-pot conversion of 2-azido-3-O-acyl-ribofuranosyl cyanides to the corresponding 2-alkylamido ribofuranosyl thiocarboxamides. The resulting key intermediates were first converted to protected tiazofurin derivatives by cyclocondensation with ethyl bromopyruvate, and finally to target C-nucleosides by treatment with ammonia in methanol. In vitro cytotoxicities of tiazofurin analogues against a number of human tumour cell lines were recorded and compared with those observed for the parent molecule (tiazofurin), as well as the commercial antitumour agent doxorubicin (DOX). Analogues 2b-d have shown a potent in vitro cytotoxic activity against human myelogenous leukaemia K562. Among solid tumour cell lines, HT29 was sensitive only to 2d, while HeLa cells were sensitive to 2a, 2b and 2d. Only analogue 2a was highly cytotoxic against MCF-7 cells. No tiazofurin analogue exhibits any significant cytotoxicity towards normal foetal lung MRC-5 cells. Downregulation of Bcl-2, activation of caspase-3 and presence of cleavage product of PARP suggest that the cytotoxic effects of tiazofurin analogues 2a-d in K562 might be mediated by apoptosis in a caspase-dependent way. On the contrary, tiazofurin did not induce apoptosis of K562 cells, which suggests a different mechanism of action, most probably through the inhibition of IMPDH. Flow cytometry and Western blot analysis data agreed well with the results of MTT assay, and enabled identification of analogue 2c as the most promising antitumour agent that preferentially target cancer cells over normal cells and thus represents a new lead for further optimization. 相似文献
16.
Glavnik Vesna Simonovska Breda Vovk Irena Pavlović Dragana Mutavdžić Ašperger Danijela Babić Sandra 《平面色谱法杂志一现代薄层色谱法》2011,24(6):482-486
JPC – Journal of Planar Chromatography – Modern TLC - Validation of a method for the quantification of (−)-epicatechin and procyanidin B2 in chocolates is reported. After a simple... 相似文献
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Debayle Johan Ðogaš Vesna Gotovac Helisová Kateřina Staněk Jakub Zikmundová Markéta 《Methodology and Computing in Applied Probability》2021,23(2):471-490
Methodology and Computing in Applied Probability - The paper concerns a method for assessing similarity of realisations of random sets based on a construction of their morphological skeletons and a... 相似文献
19.
Marijana Petković Ana Vujačić Jürgen Schiller Živadin Bugarčić Jasmina Savić Vesna Vasić 《Rapid communications in mass spectrometry : RCM》2009,23(10):1467-1475
Attempts are being made to overcome the resistance of tumour cells to platinum (Pt) drugs by the synthesis of new generations of Pt complexes, and it is important to find appropriate and simple methods for the characterization of those novel complexes. The additional applicability of such a method for the analysis of the interactions of metal complexes with biomolecules would be advantageous. Matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry (MALDI‐TOFMS) seems to possess the capability to become this method of choice, since it could be applied to low‐mass complexes as well as for the analysis of large biomolecules. In this work the applicability of flavonoids – quercetin and rutin – as matrices for MALDI‐TOFMS analysis of dichlorido(ethylendiamine)platinum(II) ([PtCl2(en)]), dichlorido(diaminocyclohexane)platinum(II) ([PtCl2(dach)]) and chloride (diethylenetriamine) palladium(II) chloride ([PdCl(dien)]Cl) complexes is demonstrated. Spectra of Pt(II) and Pd(II) complexes recorded in the presence of quercetin and rutin are rather simple: Pt(II) complexes generate [M+Na]+ or [M+K]+ions, whereas the investigated Pd(II) complex gives ions generated by the loss of one Cl? or HCl. Flavonoids give a relatively small number of well‐defined ions in the low‐mass region (at m/z 303.3 for quercetin and m/z 633.5 for rutin). Quercetin and rutin can be applied in much lower concentrations than other common MALDI matrices and require rather low laser intensity. We speculate that flavonoids stabilize the structures of the metal complexes and that they may be useful for the analysis of other biologically active metal complexes, thus implying their broader applicability. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
20.
Correspondence analysis was used to classify the pattern-like FT-IR spectra of intact bacteria. The analysis was performed on a data set of approximately 80 normalized spectral derivatives of a selection of pathogenic bacteria. The correspondence analysis proved that the various different bacterial species were clustering in distinct regions of the correspondence maps suggesting that there do exist correlations between spectral data and biochemical/microbiological classification. 相似文献