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Development of a Gradient HPLC Method for the Simultaneous Determination of Sotalol and Sorbate in Oral Liquid Preparations Using Solid Core Stationary Phase

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11160%2F15%3A10294607" target="_blank" >RIV/00216208:11160/15:10294607 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064203:_____/15:10294607

  • Result on the web

    <a href="http://www.hindawi.com/journals/jamc/2015/806736/" target="_blank" >http://www.hindawi.com/journals/jamc/2015/806736/</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1155/2015/806736" target="_blank" >10.1155/2015/806736</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Development of a Gradient HPLC Method for the Simultaneous Determination of Sotalol and Sorbate in Oral Liquid Preparations Using Solid Core Stationary Phase

  • Original language description

    A selective and sensitive gradient HPLC-UV method for quantification of sotalol hydrochloride and potassium sorbate in five types of oral liquid preparations was developed and fully validated. The separation of an active substance sotalol hydrochloride,potassium sorbate (antimicrobial agent), and other substances (for taste and smell correction, etc.) was performed using an Ascentis Express C18 (100 x 4.6 mm, particles 2.7 mu m) solid core HPLC column. Linear gradient elution mode with a flow rate of 1.3 mL min(-1) was used, and the injection volume was 5 mu L. The UV/Vis absorbance detector was set to a wavelength of 237 nm, and the column oven was conditioned at 25 degrees C. A sodium dihydrogen phosphate dihydrate solution (pH 2.5; 17.7 mM) was used as the mobile phase buffer. The total analysis time was 4.5 min (+ 2.5 min for reequilibration). The method was successfully employed in a stability evaluation of the developed formulations, which are now already being used in the thera

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FR - Pharmacology and apothecary chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/EE2.3.20.0235" target="_blank" >EE2.3.20.0235: Establishment of Research Team Focused on Experimental and Applied Biopharmacy</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Analytical Methods in Chemistry

  • ISSN

    2090-8865

  • e-ISSN

  • Volume of the periodical

    2015

  • Issue of the periodical within the volume

    March

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    6

  • Pages from-to

  • UT code for WoS article

    000352380300001

  • EID of the result in the Scopus database

    2-s2.0-84926637040