Determination of impurities and degradation products from veterinary medicinal products by HPLC method
Journal Title: Medicamentul Veterinar / Veterinary Drug - Year 2014, Vol 8, Issue 1
Abstract
The organic or inorganic impurities in the veterinary medicinal product can derive from starting materials, manufacturing process, incomplete purification, inappropriate storage. The acceptable levels of impurities in pharmaceuticals are estimated by comparison with standard solutions, according to the appropriate monographs. Forced degradation studies determine the stability of the method of dosage for the active compounds and for the entire finished product under excessive accelerated degradation conditions. They also provide information on degradation pathways and selectivity of analytical methods applied. The information provided by the degradation studies on the active compound and finished pharmaceutical product should demonstrate the specificity of the analytical method regarding impurities. Forced degradation studies should demonstrate that the impurities and degradation products generated do not interfere with the active compound. The current forced degradation methods consist of acid hydrolysis, basic hydrolysis, oxidation, exposure of the medicinal product to temperature and light. HPLC methods are an integral analytical instrument for the analysis of the medicinal product. The HPLC method should be able to separate, detect and quantify various specific degradation products that can appear after manufacture or storage of the medicinal product, as well as new elements appearing after synthesis. FDA and ICH guidelines recommend the enclosure of the results, including the chromatograms specific to the forced degradation subjected medicinal product, in the documentation for marketing authorization. Using HPLC methods in forced degradation studies on medicinal products provides relevant information on the method of determination for the formulation of the medicinal product, synthesis product, packaging methods and storage.
Authors and Affiliations
Elena Oltean
Disinfection air and surfaces: contemporary fine by forming a 5 mm without wetting on the basis of hydrogen peroxide – nocolyse generated by nebulizer Nocospray
Nocospray is a revolutionary concept for bio professional disinfection, with bactericidal, virucidal, fungicidal and sporicidal effect using hydrogen peroxide as the active substance in combination with colloidal silver,...
Synergistic interaction between trimetazidine and ketoprophen in mice
Recent studies have demonstrated the antinociceptive, anti-inflammatory, and gastric protective effects of trimetazidine (TDZ) on various models in rats. The present study proposes to demonstrate the antinociceptive acti...
Dezvoltarea si validarea metodei RP- HPLC de determinare cantitativă a furazolidonei si metronidazol din produsul Enteroguard M
A fost dezvoltată si validată o metodă isocratică de lichid cromatografie de performantă înaltă pentru determinarea cantitativă a metronidazolului si furazolidonei din comprimate Enteroguard M. Separarea HPLC a fost real...
Eficacitatea pastei antihelmintice FENBENDAZOL 30% în ciatostominoza cabalinelor
Ciatostominoza cabalinelor este o helmintoză a intestinului gros produsă de paraziți din familia Strongylidae, subfamilia Cyathostominae. Ciatostominele (strongili nemigratori) reprezintă o provocare atât pentru paraz...
[b]Elemente teoretice ale terapeuticii veterinare[/b]
În referatul de față sunt descrise, sintetic și întro manieră logică, principalele elementele de terapeutică veterinară. În prima parte se face referire la noțiunea de doză precum și la factorii care influențează stabili...