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Formulation and evaluation of atenolol floating bioadhesive system using optimized polymer blends
INTRODUCTION: Oral sustained release gastro retentive dosage forms offer several advantages for drugs having absorption from the upper gastrointestinal tract to improve the bioavailability of medications which have narrow absorption window. The aim of the study was to develop a floating bioadhesive...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797488/ https://www.ncbi.nlm.nih.gov/pubmed/27051631 http://dx.doi.org/10.4103/2230-973X.177832 |
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author | Siddam, Haritha Kotla, Niranjan G. Maddiboyina, Balaji Singh, Sima Sunnapu, Omprakash Kumar, Anil Sharma, Dinesh |
author_facet | Siddam, Haritha Kotla, Niranjan G. Maddiboyina, Balaji Singh, Sima Sunnapu, Omprakash Kumar, Anil Sharma, Dinesh |
author_sort | Siddam, Haritha |
collection | PubMed |
description | INTRODUCTION: Oral sustained release gastro retentive dosage forms offer several advantages for drugs having absorption from the upper gastrointestinal tract to improve the bioavailability of medications which have narrow absorption window. The aim of the study was to develop a floating bioadhesive drug delivery system exhibiting a unique combination of floatation and bioadhesion to prolong the residence in the stomach using atenolol as a model drug. METHODS: Prior to compression, polymeric blend(s) were evaluated for flow properties. The tablets were prepared by direct compression method using bioadhesive polymer like Carbopol 934P and hydrophilic polymers like HPMC K4M, HPMC K15M, and HPMC K100M. The prepared tablets were evaluated for physical characteristics, bioadhesive strength, buoyancy lag time, swelling index and in vitro drug release studies. RESULTS: The mean bioadhesive strength was found to be in the range of 16.2 to 52.1 gm. The optimized blend (F11) showed 92.3% drug releases after 24 hrs. Whilst, increase in concentration of carbopol 934P, bioadhesive strength and swelling index was increased with slow release. The n values of optimized formulations were found in the range of 0.631-0.719 indicating non-fickian anomalous type transport mechanism. CONCLUSION: The study aided in developing an ideal once-a-day gastro retentive floating drug delivery system with improved floating, swelling and bioadhesive characteristics with better bioavailability. |
format | Online Article Text |
id | pubmed-4797488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47974882016-04-05 Formulation and evaluation of atenolol floating bioadhesive system using optimized polymer blends Siddam, Haritha Kotla, Niranjan G. Maddiboyina, Balaji Singh, Sima Sunnapu, Omprakash Kumar, Anil Sharma, Dinesh Int J Pharm Investig Original Research Article INTRODUCTION: Oral sustained release gastro retentive dosage forms offer several advantages for drugs having absorption from the upper gastrointestinal tract to improve the bioavailability of medications which have narrow absorption window. The aim of the study was to develop a floating bioadhesive drug delivery system exhibiting a unique combination of floatation and bioadhesion to prolong the residence in the stomach using atenolol as a model drug. METHODS: Prior to compression, polymeric blend(s) were evaluated for flow properties. The tablets were prepared by direct compression method using bioadhesive polymer like Carbopol 934P and hydrophilic polymers like HPMC K4M, HPMC K15M, and HPMC K100M. The prepared tablets were evaluated for physical characteristics, bioadhesive strength, buoyancy lag time, swelling index and in vitro drug release studies. RESULTS: The mean bioadhesive strength was found to be in the range of 16.2 to 52.1 gm. The optimized blend (F11) showed 92.3% drug releases after 24 hrs. Whilst, increase in concentration of carbopol 934P, bioadhesive strength and swelling index was increased with slow release. The n values of optimized formulations were found in the range of 0.631-0.719 indicating non-fickian anomalous type transport mechanism. CONCLUSION: The study aided in developing an ideal once-a-day gastro retentive floating drug delivery system with improved floating, swelling and bioadhesive characteristics with better bioavailability. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4797488/ /pubmed/27051631 http://dx.doi.org/10.4103/2230-973X.177832 Text en Copyright: © 2016 International Journal of Pharmaceutical Investigation http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Research Article Siddam, Haritha Kotla, Niranjan G. Maddiboyina, Balaji Singh, Sima Sunnapu, Omprakash Kumar, Anil Sharma, Dinesh Formulation and evaluation of atenolol floating bioadhesive system using optimized polymer blends |
title | Formulation and evaluation of atenolol floating bioadhesive system using optimized polymer blends |
title_full | Formulation and evaluation of atenolol floating bioadhesive system using optimized polymer blends |
title_fullStr | Formulation and evaluation of atenolol floating bioadhesive system using optimized polymer blends |
title_full_unstemmed | Formulation and evaluation of atenolol floating bioadhesive system using optimized polymer blends |
title_short | Formulation and evaluation of atenolol floating bioadhesive system using optimized polymer blends |
title_sort | formulation and evaluation of atenolol floating bioadhesive system using optimized polymer blends |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797488/ https://www.ncbi.nlm.nih.gov/pubmed/27051631 http://dx.doi.org/10.4103/2230-973X.177832 |
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