Показать сокращенную информацию
dc.contributor.author | Ziyatdinova G. | |
dc.contributor.author | Budnikov G. | |
dc.contributor.author | Pogorel'tsev V. | |
dc.date.accessioned | 2018-09-18T20:14:29Z | |
dc.date.available | 2018-09-18T20:14:29Z | |
dc.date.issued | 2006 | |
dc.identifier.issn | 1061-9348 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/137860 | |
dc.description.abstract | A voltammetric procedure is developed for determining captopril in pharmaceuticals. It is based on the preliminary electrochemical accumulation of the captopril oxidation product on a platinum electrode in a 0.1 M HNO 3 solution at 1.2 V versus a saturated silver-silver chloride electrode. The reduction current of the oxidation product is a linear function of captopril concentration in the range from 1.2 × 10 -6 to 3.2 × 10 -4 M. The determination limit is 9.2 × 10 -7 M. The relative standard deviation is between 1 and 4%. © Pleiades Publishing, Inc., 2006. | |
dc.relation.ispartofseries | Journal of Analytical Chemistry | |
dc.title | Determination of captopril in pharmaceutical forms by stripping voltammetry | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 8 | |
dc.relation.ispartofseries-volume | 61 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 798 | |
dc.source.id | SCOPUS10619348-2006-61-8-SID33746609411 |