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Set-up of a method using LC-UV to assay mometasone furoate in pharmaceutical dosage forms
dc.contributor.author | Ourique, Aline Ferreira | pt_BR |
dc.contributor.author | Contri, Renata Vidor | pt_BR |
dc.contributor.author | Guterres, Silvia Stanisçuaski | pt_BR |
dc.contributor.author | Beck, Ruy Carlos Ruver | pt_BR |
dc.contributor.author | Pohlmann, Adriana Raffin | pt_BR |
dc.contributor.author | Melero, Ana Z. | pt_BR |
dc.contributor.author | Schaefer, Ulrich F. | pt_BR |
dc.date.accessioned | 2013-07-02T01:43:21Z | pt_BR |
dc.date.issued | 2012 | pt_BR |
dc.identifier.issn | 0100-4042 | pt_BR |
dc.identifier.uri | http://hdl.handle.net/10183/72884 | pt_BR |
dc.description.abstract | A reliable method using LC-UV to assay mometasone furoate (MF) in creams or nasal sprays using the same chromatographic conditions was set up. Methanol:water 80:20 (v/v) (1.0 mL min-1) was used as mobile phase. MF was detected at 248 nm and analyzed in a concentration range from 1.0 to 20.0 μg mL-1. The method provided acceptable theoretical plates, peak simmetry, peak tailing factor and peak resolution a short run (5 min). The method showed specificity, good linearity (r = 0.9999) and the quantification limit was 0.379 μg mL-1. Furthermore, the method was precise (RSD < 2.0%), accurate (recovery > 97%) and robust. | en |
dc.format.mimetype | application/pdf | pt_BR |
dc.language.iso | eng | pt_BR |
dc.relation.ispartof | Química nova. São Paulo. Vol. 35, n. 4, (2012), p. 818-821 | pt_BR |
dc.rights | Open Access | en |
dc.subject | Pharmaceuticals | en |
dc.subject | Produtos farmacêuticos | pt_BR |
dc.subject | Cromatografia liquida | pt_BR |
dc.subject | Liquid chromatography | en |
dc.subject | Mometasona | pt_BR |
dc.subject | Mometasone | en |
dc.title | Set-up of a method using LC-UV to assay mometasone furoate in pharmaceutical dosage forms | pt_BR |
dc.type | Artigo de periódico | pt_BR |
dc.identifier.nrb | 000837761 | pt_BR |
dc.type.origin | Nacional | pt_BR |
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