Floating tablets of minocycline hydrochloride: Formulation, in-vitro evaluation and optimization

Current study was aimed to formulate gastroretentive floating tablets of minocycline hydrochloride with desired floating properties, desired drug release rate, its local action in stomach for treatment of H. pylori infection and prevention of a side effect, pseudomembranous colitis. Simplex lattice...

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Main Authors: Ali Raza, Nadeem Irfan Bukhari, Sabiha Karim, Muhammad Ahsan Hafiz, Uzma Hayat
Format: Article
Language:English
Published: SpringerOpen 2017-12-01
Series:Future Journal of Pharmaceutical Sciences
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2314724516301789
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spelling doaj-80ca9696106b41e2947f11406638ac5d2020-11-24T22:10:07ZengSpringerOpenFuture Journal of Pharmaceutical Sciences2314-72452017-12-013213113910.1016/j.fjps.2017.05.001Floating tablets of minocycline hydrochloride: Formulation, in-vitro evaluation and optimizationAli RazaNadeem Irfan BukhariSabiha KarimMuhammad Ahsan HafizUzma HayatCurrent study was aimed to formulate gastroretentive floating tablets of minocycline hydrochloride with desired floating properties, desired drug release rate, its local action in stomach for treatment of H. pylori infection and prevention of a side effect, pseudomembranous colitis. Simplex lattice mixture design was used to get experimental layout. Methocel K100LV (X1), Methocel K15M (X2) and Carbopol 934 (X3) were selected as independent variables. Ten formulations (F1 to F10) were developed by direct compression and were evaluated for physical parameters, swelling index, floating lag time, floating time and in-vitro drug release rate. Furthermore, FTIR spectroscopic studies were performed to determine drug polymer interaction. Floating lag time (Y1), floating time (Y2), cumulative drug release at 3 h (Y3), 6 h (Y4) and 12 h (Y5) were selected as dependent variables. Results showed that floating lag time and floating time were decreased by presence of Carbopol 934 in formulation while increased by Methocel K100LV and Methocel K15M. Presence of Carbopol 934 also caused an increase in drug release rate while Methocel K100LV and Methocel K15M contributed in decreasing release rate. Except F1, all the other formulations showed floating time >12 h. On the basis of optimization criteria, composition of optimized formulation F0 (Methocel K100LV = 77.98 mg and Carbopol 934 = 82.02 mg) was determined by statistical analysis. FTIR spectroscopic studies showed that no interaction found between polymers and drug. Concisely, concluded that Carbopol 934 and Methocel 100LV can be used to fabricate gastroretentive floating tablets of minocycline hydrochloride with good buoyancy properties and sustained release action.http://www.sciencedirect.com/science/article/pii/S2314724516301789GRDDSFloating tabletsMinocyclineOptimization
collection DOAJ
language English
format Article
sources DOAJ
author Ali Raza
Nadeem Irfan Bukhari
Sabiha Karim
Muhammad Ahsan Hafiz
Uzma Hayat
spellingShingle Ali Raza
Nadeem Irfan Bukhari
Sabiha Karim
Muhammad Ahsan Hafiz
Uzma Hayat
Floating tablets of minocycline hydrochloride: Formulation, in-vitro evaluation and optimization
Future Journal of Pharmaceutical Sciences
GRDDS
Floating tablets
Minocycline
Optimization
author_facet Ali Raza
Nadeem Irfan Bukhari
Sabiha Karim
Muhammad Ahsan Hafiz
Uzma Hayat
author_sort Ali Raza
title Floating tablets of minocycline hydrochloride: Formulation, in-vitro evaluation and optimization
title_short Floating tablets of minocycline hydrochloride: Formulation, in-vitro evaluation and optimization
title_full Floating tablets of minocycline hydrochloride: Formulation, in-vitro evaluation and optimization
title_fullStr Floating tablets of minocycline hydrochloride: Formulation, in-vitro evaluation and optimization
title_full_unstemmed Floating tablets of minocycline hydrochloride: Formulation, in-vitro evaluation and optimization
title_sort floating tablets of minocycline hydrochloride: formulation, in-vitro evaluation and optimization
publisher SpringerOpen
series Future Journal of Pharmaceutical Sciences
issn 2314-7245
publishDate 2017-12-01
description Current study was aimed to formulate gastroretentive floating tablets of minocycline hydrochloride with desired floating properties, desired drug release rate, its local action in stomach for treatment of H. pylori infection and prevention of a side effect, pseudomembranous colitis. Simplex lattice mixture design was used to get experimental layout. Methocel K100LV (X1), Methocel K15M (X2) and Carbopol 934 (X3) were selected as independent variables. Ten formulations (F1 to F10) were developed by direct compression and were evaluated for physical parameters, swelling index, floating lag time, floating time and in-vitro drug release rate. Furthermore, FTIR spectroscopic studies were performed to determine drug polymer interaction. Floating lag time (Y1), floating time (Y2), cumulative drug release at 3 h (Y3), 6 h (Y4) and 12 h (Y5) were selected as dependent variables. Results showed that floating lag time and floating time were decreased by presence of Carbopol 934 in formulation while increased by Methocel K100LV and Methocel K15M. Presence of Carbopol 934 also caused an increase in drug release rate while Methocel K100LV and Methocel K15M contributed in decreasing release rate. Except F1, all the other formulations showed floating time >12 h. On the basis of optimization criteria, composition of optimized formulation F0 (Methocel K100LV = 77.98 mg and Carbopol 934 = 82.02 mg) was determined by statistical analysis. FTIR spectroscopic studies showed that no interaction found between polymers and drug. Concisely, concluded that Carbopol 934 and Methocel 100LV can be used to fabricate gastroretentive floating tablets of minocycline hydrochloride with good buoyancy properties and sustained release action.
topic GRDDS
Floating tablets
Minocycline
Optimization
url http://www.sciencedirect.com/science/article/pii/S2314724516301789
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