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Kwiecień, Anna
2004
Praca doktorska
A new chromatographic-densitometric method for the simultaneous identification and quantitation of some chosen betablockers has been developed and used for quantitative determination of atenolol, acébutolol, propranolol and bisoprolol in pharmaceutical preparations. The stability of the most hydrophilic atenolol, less hydrophilic acébutolol and the most lipophilic propranolol has been investigated under the influence of temperature in acid and basic solutions of four concentrations. The chemical structures of the degradation products have been established by comparing Rf values, absorption spectra and ’H NMR. Correlation between kinetic or thermodynamic parameters describing degradation process of chosen betablockers and their polarity has been investigated. It was stated that with increasing polarity (atenolol, acébutolol, propranolol) the stability of these substances increases. Moreover, the problem of degradation of betablockers in solutions of different pH may be important for technology of producing drugs and for their effectiveness and safety of using.
Kraków
2 - studia doktoranckie
farmakologia
Wydział Farmaceutyczny
Krzek, Jan
oai:dl.cm-uj.krakow.pl:1351
ZB-99182
pol
tylko w bibliotece
Jan 23, 2023
Nov 21, 2012
31
0
http://dl.cm-uj.krakow.pl:8080/publication/1351
RDF
OAI-PMH
Ekiert, Radosław
Hubicka, Urszula
Szybka-Hrynkiewicz, Przemysław
Piotrowska, Joanna
Kępczyńska, Elżbieta
Wrzosek, Anna
Dudzik, Barbara
Citation style: chicago-author-date iso690-author-date
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