Spectrophotometric flow injection procedure to indirect determination of paracetamol in pharmaceutical formulations using o-tolidine as reagent

A spectrophotometric flow injection method for the determination of paracetamol in pharmaceutical formulations is proposed. The procedure was based on the oxidation of paracetamol by sodium hypochloride and the determination of the excess of this oxidant using o-tolidine dichloride as chromogenic re...

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Main Authors: Orlando Fatibello-Filho, Heberth Juliano Vieira
Format: Article
Language:English
Published: Universidade Estadual Paulista 2018-04-01
Series:Eclética Química
Online Access:https://revista.iq.unesp.br/ojs/index.php/ecletica/article/view/303
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spelling doaj-8cb5ddb026544503ac0d34f784204e0f2020-11-25T01:38:01ZengUniversidade Estadual PaulistaEclética Química1678-46182018-04-01332475310.26850/1678-4618eqj.v33.2.2008.p47-53303Spectrophotometric flow injection procedure to indirect determination of paracetamol in pharmaceutical formulations using o-tolidine as reagentOrlando Fatibello-Filho0Heberth Juliano Vieira1Departamento de Química, Centro de Ciências Exatas e de Tecnologia Universidade Federal de São CarlosDepartamento de Química, Centro de Ciências Exatas e de Tecnologia Universidade Federal de São CarlosA spectrophotometric flow injection method for the determination of paracetamol in pharmaceutical formulations is proposed. The procedure was based on the oxidation of paracetamol by sodium hypochloride and the determination of the excess of this oxidant using o-tolidine dichloride as chromogenic reagent at 430 nm. The analytical curve was linear in the paracetamol concentration range from 8.50 x 10-6 to 2.51 x 10-4 mol L-1 with a detection limit of 5.0 x 10-6 mol L-1. The relative standard deviation was smaller than 1.2% for 1.20 x 10-4 mol L-1 paracetamol solution (n = 10). The results obtained for paracetamol in pharmaceutical formulations using the proposed flow injection method and those obtained using a USP Pharmacopoeia method are in agreement at the 95% confidence level.https://revista.iq.unesp.br/ojs/index.php/ecletica/article/view/303
collection DOAJ
language English
format Article
sources DOAJ
author Orlando Fatibello-Filho
Heberth Juliano Vieira
spellingShingle Orlando Fatibello-Filho
Heberth Juliano Vieira
Spectrophotometric flow injection procedure to indirect determination of paracetamol in pharmaceutical formulations using o-tolidine as reagent
Eclética Química
author_facet Orlando Fatibello-Filho
Heberth Juliano Vieira
author_sort Orlando Fatibello-Filho
title Spectrophotometric flow injection procedure to indirect determination of paracetamol in pharmaceutical formulations using o-tolidine as reagent
title_short Spectrophotometric flow injection procedure to indirect determination of paracetamol in pharmaceutical formulations using o-tolidine as reagent
title_full Spectrophotometric flow injection procedure to indirect determination of paracetamol in pharmaceutical formulations using o-tolidine as reagent
title_fullStr Spectrophotometric flow injection procedure to indirect determination of paracetamol in pharmaceutical formulations using o-tolidine as reagent
title_full_unstemmed Spectrophotometric flow injection procedure to indirect determination of paracetamol in pharmaceutical formulations using o-tolidine as reagent
title_sort spectrophotometric flow injection procedure to indirect determination of paracetamol in pharmaceutical formulations using o-tolidine as reagent
publisher Universidade Estadual Paulista
series Eclética Química
issn 1678-4618
publishDate 2018-04-01
description A spectrophotometric flow injection method for the determination of paracetamol in pharmaceutical formulations is proposed. The procedure was based on the oxidation of paracetamol by sodium hypochloride and the determination of the excess of this oxidant using o-tolidine dichloride as chromogenic reagent at 430 nm. The analytical curve was linear in the paracetamol concentration range from 8.50 x 10-6 to 2.51 x 10-4 mol L-1 with a detection limit of 5.0 x 10-6 mol L-1. The relative standard deviation was smaller than 1.2% for 1.20 x 10-4 mol L-1 paracetamol solution (n = 10). The results obtained for paracetamol in pharmaceutical formulations using the proposed flow injection method and those obtained using a USP Pharmacopoeia method are in agreement at the 95% confidence level.
url https://revista.iq.unesp.br/ojs/index.php/ecletica/article/view/303
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