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Formulation and evaluation of fast dissolving tablets of cinnarizine using superdisintegrant blends and subliming material
The aim of this investigation was to develop fast dissolving tablet of cinnarizine. A combination of super disintegrants, i.e., sodium starch glycolate (SSG) and crosscarmellose sodium (CCS) were used along with camphor as a subliming material. An optimized concentration of camphor was added to aid...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255354/ https://www.ncbi.nlm.nih.gov/pubmed/22247895 http://dx.doi.org/10.4103/2231-4040.90885 |
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author | Basu, Biswajit Bagadiya, Abhishek Makwana, Sagar Vipul, Vora Batt, Devraj Dharamsi, Abhay |
author_facet | Basu, Biswajit Bagadiya, Abhishek Makwana, Sagar Vipul, Vora Batt, Devraj Dharamsi, Abhay |
author_sort | Basu, Biswajit |
collection | PubMed |
description | The aim of this investigation was to develop fast dissolving tablet of cinnarizine. A combination of super disintegrants, i.e., sodium starch glycolate (SSG) and crosscarmellose sodium (CCS) were used along with camphor as a subliming material. An optimized concentration of camphor was added to aid the porosity of the tablet. A 3(2) full factorial design was applied to investigate the combined effect of two formulation variables: Amount of SSG and CCS. Infrared (IR) spectroscopy was performed to identify the physicochemical interaction between drug and polymer. IR spectroscopy showed that there is no interaction of drug with polymer. In the present study, direct compression was used to prepare the tablets. The powder mixtures were compressed into tablet using flat face multi punch tablet machine. Camphor was sublimed from the tablet by exposing the tablet to vacuum drier at 60°C for 12 hours. All the formulations were evaluated for their characteristics such as average weight, hardness, wetting time, friability, content uniformity, dispersion time (DT), and dissolution rate. An optimized tablet formulation (F 9) was found to have good hardness of 3.30 ± 0.10 kg/cm(2), wetting time of 42.33 ± 4.04 seconds, DT of 34.67 ± 1.53 seconds, and cumulative drug release of not less than 99% in 16 minutes. |
format | Online Article Text |
id | pubmed-3255354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-32553542012-01-13 Formulation and evaluation of fast dissolving tablets of cinnarizine using superdisintegrant blends and subliming material Basu, Biswajit Bagadiya, Abhishek Makwana, Sagar Vipul, Vora Batt, Devraj Dharamsi, Abhay J Adv Pharm Technol Res Original Article The aim of this investigation was to develop fast dissolving tablet of cinnarizine. A combination of super disintegrants, i.e., sodium starch glycolate (SSG) and crosscarmellose sodium (CCS) were used along with camphor as a subliming material. An optimized concentration of camphor was added to aid the porosity of the tablet. A 3(2) full factorial design was applied to investigate the combined effect of two formulation variables: Amount of SSG and CCS. Infrared (IR) spectroscopy was performed to identify the physicochemical interaction between drug and polymer. IR spectroscopy showed that there is no interaction of drug with polymer. In the present study, direct compression was used to prepare the tablets. The powder mixtures were compressed into tablet using flat face multi punch tablet machine. Camphor was sublimed from the tablet by exposing the tablet to vacuum drier at 60°C for 12 hours. All the formulations were evaluated for their characteristics such as average weight, hardness, wetting time, friability, content uniformity, dispersion time (DT), and dissolution rate. An optimized tablet formulation (F 9) was found to have good hardness of 3.30 ± 0.10 kg/cm(2), wetting time of 42.33 ± 4.04 seconds, DT of 34.67 ± 1.53 seconds, and cumulative drug release of not less than 99% in 16 minutes. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3255354/ /pubmed/22247895 http://dx.doi.org/10.4103/2231-4040.90885 Text en Copyright: © Journal of Advanced Pharmaceutical Technology & Research 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Basu, Biswajit Bagadiya, Abhishek Makwana, Sagar Vipul, Vora Batt, Devraj Dharamsi, Abhay Formulation and evaluation of fast dissolving tablets of cinnarizine using superdisintegrant blends and subliming material |
title | Formulation and evaluation of fast dissolving tablets of cinnarizine using superdisintegrant blends and subliming material |
title_full | Formulation and evaluation of fast dissolving tablets of cinnarizine using superdisintegrant blends and subliming material |
title_fullStr | Formulation and evaluation of fast dissolving tablets of cinnarizine using superdisintegrant blends and subliming material |
title_full_unstemmed | Formulation and evaluation of fast dissolving tablets of cinnarizine using superdisintegrant blends and subliming material |
title_short | Formulation and evaluation of fast dissolving tablets of cinnarizine using superdisintegrant blends and subliming material |
title_sort | formulation and evaluation of fast dissolving tablets of cinnarizine using superdisintegrant blends and subliming material |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255354/ https://www.ncbi.nlm.nih.gov/pubmed/22247895 http://dx.doi.org/10.4103/2231-4040.90885 |
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