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Voltammetric determination of leucovorin in pharmaceutical preparations using a boron-doped diamond electrode

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F18%3A39913160" target="_blank" >RIV/00216275:25310/18:39913160 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388955:_____/18:00492515

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s00706-018-2200-4" target="_blank" >http://dx.doi.org/10.1007/s00706-018-2200-4</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00706-018-2200-4" target="_blank" >10.1007/s00706-018-2200-4</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Voltammetric determination of leucovorin in pharmaceutical preparations using a boron-doped diamond electrode

  • Original language description

    Method for voltammetric determination of leucovorin, a drug frequently applied to decrease some unfavorable effects of anticancer drugs such as methotrexate or to increase the therapeutic effect of 5-fluorouracil, has been developed employing a bare boron-doped diamond electrode. It is the first method for leucovorin determination based on its electrochemical oxidation. Although at least three anodic and three cathodic voltammetric peaks could be recorded under the used conditions, only the anodic response situated at about + 900 mV (vs. saturated Ag|AgCl electrode) was suitable, namely due to its shape and position, for analytical purposes. Using differential pulse voltammetry with optimized parameters and supporting electrolyte of pH 3.0, the linear dynamic range of leucovorin determination was recorded from 0.15 to 25 mu mol dm(-3). Under such conditions, low limit of quantification of 0.050 mu mol dm(-3) and limit of detection of 0.015 mu mol dm(-3) as well was reached. Relative standard deviation calculated from 11 repeated measurements amounted to 0.7% and calculated from five repeated determinations amounting less than 3.0%. Applicability of the developed method was verified by repeated analysis of the pharmaceutical preparation with excellent results (recovery 98.7-102.8%, relative standard deviation 1.81%).

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10406 - Analytical chemistry

Result continuities

  • Project

    <a href="/en/project/GA17-03868S" target="_blank" >GA17-03868S: New Methods of Electrochemical Monitoring of Biologically Active Organic Compounds in Environmental, Biological and Food Matrices</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Monatshefte fur Chemie

  • ISSN

    0026-9247

  • e-ISSN

  • Volume of the periodical

    149

  • Issue of the periodical within the volume

    9

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    8

  • Pages from-to

    1701-1708

  • UT code for WoS article

    000442501400028

  • EID of the result in the Scopus database

    2-s2.0-85051284989