Preparation and quality evaluation of Ibuprofen and Piphenhydramine hydrochloride orally disintegrating tablets

The present study was designed to evaluate the preparation and quality of ibuprofen and diphenhydramine hydrochloride orally disintegrating tablets. The formulation was optimized with disintegration time and taste as reference parameters by single-factor and orthogonal experiments. Then the hardness...

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Autores principales: Luo, Y.H., Ge, Z. K., Zhao, X.Y., Chen, Q., Bourkaib, Nadia, Luo, M., Luo, L.Y., Wu, Lei, Hu, B. X.
Formato: Articulo
Lenguaje:Inglés
Publicado: 2012
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/25696
http://www.latamjpharm.org/resumenes/31/6/LAJOP_31_6_1_9.pdf
Aporte de:
id I19-R120-10915-25696
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Farmacia
diphenhydramine HCl
formulation
orally disintegrating tablet
Ibuprofeno
spellingShingle Farmacia
diphenhydramine HCl
formulation
orally disintegrating tablet
Ibuprofeno
Luo, Y.H.
Ge, Z. K.
Zhao, X.Y.
Chen, Q.
Bourkaib, Nadia
Luo, M.
Luo, L.Y.
Wu, Lei
Hu, B. X.
Preparation and quality evaluation of Ibuprofen and Piphenhydramine hydrochloride orally disintegrating tablets
topic_facet Farmacia
diphenhydramine HCl
formulation
orally disintegrating tablet
Ibuprofeno
description The present study was designed to evaluate the preparation and quality of ibuprofen and diphenhydramine hydrochloride orally disintegrating tablets. The formulation was optimized with disintegration time and taste as reference parameters by single-factor and orthogonal experiments. Then the hardness, disintegrating time and dissolution were examined. The best prescription was found to contain: ibuprofen 200 mg, diphenhydramine HCl 25 mg, citric acid 30 mg, microcrystalline cellulose 115 mg, mannitol 48.5 mg, polyvinylpolypyrrolidone 40 mg, sodium lauryl sulphate 10 mg, magnesium Stearate 3.5 mg, gum arabic 1.5 mg, aspartame 15 mg, steviosin 1.5 mg, and sodium bicarbonate 10 mg. The orally disintegrating tablets were congruent and smooth with pleasant taste in mouth. The disintegration time was less than 60 s, and more than 80 % of ibuprofen and diphenhydramine HCl were dissolved within 10 min. Consequently, the formulation design is reasonable and the process of preparation is feasible.
format Articulo
Articulo
author Luo, Y.H.
Ge, Z. K.
Zhao, X.Y.
Chen, Q.
Bourkaib, Nadia
Luo, M.
Luo, L.Y.
Wu, Lei
Hu, B. X.
author_facet Luo, Y.H.
Ge, Z. K.
Zhao, X.Y.
Chen, Q.
Bourkaib, Nadia
Luo, M.
Luo, L.Y.
Wu, Lei
Hu, B. X.
author_sort Luo, Y.H.
title Preparation and quality evaluation of Ibuprofen and Piphenhydramine hydrochloride orally disintegrating tablets
title_short Preparation and quality evaluation of Ibuprofen and Piphenhydramine hydrochloride orally disintegrating tablets
title_full Preparation and quality evaluation of Ibuprofen and Piphenhydramine hydrochloride orally disintegrating tablets
title_fullStr Preparation and quality evaluation of Ibuprofen and Piphenhydramine hydrochloride orally disintegrating tablets
title_full_unstemmed Preparation and quality evaluation of Ibuprofen and Piphenhydramine hydrochloride orally disintegrating tablets
title_sort preparation and quality evaluation of ibuprofen and piphenhydramine hydrochloride orally disintegrating tablets
publishDate 2012
url http://sedici.unlp.edu.ar/handle/10915/25696
http://www.latamjpharm.org/resumenes/31/6/LAJOP_31_6_1_9.pdf
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