| Revista: | Ecletica quimica |
| Base de datos: | PERIÓDICA |
| Número de sistema: | 000367024 |
| ISSN: | 0100-4670 |
| Autors: | Revanasiddappa, Hosakere Doddarevanna1 Veena, M.A |
| Institucions: | 1University of Mysore, Department of Chemistry, Manasagangotri, Mysore. India |
| Any: | 2008 |
| Període: | Jul-Sep |
| Volum: | 33 |
| Número: | 3 |
| Paginació: | 47-52 |
| País: | Brasil |
| Idioma: | Inglés |
| Tipo de documento: | Artículo |
| Enfoque: | Experimental |
| Resumen en inglés | Highly sensitive and selective spectrophotometric methods (A and B) were developed for the determination of micro amounts of olanzapine (OLZ). Method A (direct method) is based on the oxidation of olanzapine with a known excess of iodine monochloride (ICl) in an acidic medium. Under the same condition, thymol blue was iodinated by unreacted ICl, and the absorbance of uniodinated thymol blue was measured at 536 nm. The decrease in ICl concentration is a measure of drug concentration. In method B (indirect method), oxidation of OLZ by a known excess of Ce(IV) in sulfuric acid medium followed by the reaction of unreacted Ce(IV) with leuco crystal violet (LCV) to crystal violet (CV), which is measured in an acetate buffer medium ( pH 4.9) at 580 nm. These methods obey the Beer's law in the concentration range of 0.2-1.6 µg mL-1 (method A) and 0.1-1.4 µg mL-1 (method B). The developed procedures have been successfully applied to the determination of OLZ in pure and in dosage forms. The results exhibit no interference from the presence of excipients. The reliability of the methods was established by parallel determination of OLZ against the reference method |
| Disciplines | Química |
| Paraules clau: | Química analítica, Química farmacéutica, Olanzapina, Espectrofotometría, Farmacología |
| Keyword: | Chemistry, Analytical chemistry, Medicinal chemistry, Olanzapine, Spectrophotometry, Pharmacology |
| Text complet: | Texto completo (Ver PDF) |
