Development and evaluation of naproxen sodium 250 Mg effervescent tablets

Effervescent tablets have always been convenient, simple and measured dosage form. The phenomenon of carbonation, in this type of dosage form, accelerates the solubility and enhances the bioavailability of the drug and the addition of flavorant also masks the objectionable taste of the medicament in...

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Autores principales: Hanif, Muhammad, Muhammad, Iyad N., Effet, Wajhia, Yousuf, Rabia I., Ghiasuddin, Muhammad, Shoaib, Harris M.
Formato: Articulo
Lenguaje:Inglés
Publicado: 2011
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/8401
http://www.latamjpharm.org/resumenes/30/10/LAJOP_30_10_1_13.pdf
Aporte de:
id I19-R120-10915-8401
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Física
Comprimidos
Naproxeno
Evaluación de Medicamentos
spellingShingle Física
Comprimidos
Naproxeno
Evaluación de Medicamentos
Hanif, Muhammad
Muhammad, Iyad N.
Effet, Wajhia
Yousuf, Rabia I.
Ghiasuddin, Muhammad
Shoaib, Harris M.
Development and evaluation of naproxen sodium 250 Mg effervescent tablets
topic_facet Física
Comprimidos
Naproxeno
Evaluación de Medicamentos
description Effervescent tablets have always been convenient, simple and measured dosage form. The phenomenon of carbonation, in this type of dosage form, accelerates the solubility and enhances the bioavailability of the drug and the addition of flavorant also masks the objectionable taste of the medicament in a more patient compliant way. The present study focuses on developing a new, simple, cost effective formulation of naproxen sodium 250 mg as an effervescent tablet using direct compression technique. Nine different trial formulations of naproxen 250 mg were designed with varying proportions of sodium carbonate, sodium bicarbonate, citric acid and PEG 6000 and were prepared by direct compression method, and evaluated for pharmaceutical quality attributes. Quality assessment proved formulations F8 as a satisfactory one showing respectively mean weight of 2200 ± 50.52 having hardness and friability of 14.78421 ± 1.3791 kg and 1.241 %. Tablets took 4 min and 36 s to disintegrate completely. The average pH of the solution was within the range of 5.65 to 5.85. Dissolution profile comparison with the conventional formulation was carried out and maximum drug release by the trial formulation was observed within 15 min. spectrophotometric determination of drug content was found to be 99.82 ± 1.754. Stability characterization was also conducted on the formulations under stress (40 °C/75 % R.H.) that showed formulations remained stable throughout the study duration with acceptable difference in physical and chemical characteristics. Such formulations increases patient compliance and have possibly improved bioavailability. The work also emphasizes on the benefit of using direct compression method as a cost effective technique in terms of process, materials handling with productivity.
format Articulo
Articulo
author Hanif, Muhammad
Muhammad, Iyad N.
Effet, Wajhia
Yousuf, Rabia I.
Ghiasuddin, Muhammad
Shoaib, Harris M.
author_facet Hanif, Muhammad
Muhammad, Iyad N.
Effet, Wajhia
Yousuf, Rabia I.
Ghiasuddin, Muhammad
Shoaib, Harris M.
author_sort Hanif, Muhammad
title Development and evaluation of naproxen sodium 250 Mg effervescent tablets
title_short Development and evaluation of naproxen sodium 250 Mg effervescent tablets
title_full Development and evaluation of naproxen sodium 250 Mg effervescent tablets
title_fullStr Development and evaluation of naproxen sodium 250 Mg effervescent tablets
title_full_unstemmed Development and evaluation of naproxen sodium 250 Mg effervescent tablets
title_sort development and evaluation of naproxen sodium 250 mg effervescent tablets
publishDate 2011
url http://sedici.unlp.edu.ar/handle/10915/8401
http://www.latamjpharm.org/resumenes/30/10/LAJOP_30_10_1_13.pdf
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