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Design of sustained release pellets of ferrous fumarate using cow ghee as hot-melt coating agent
INTRODUCTION: The objective of the present study was to design ferrous fumarate (FF) sustained release (SR) pellets using of cow ghee (CG) as an important hot-melt coating (HMC) agent. MATERIALS AND METHODS: The pellets were coated by HMC technique using CG and ethyl cellulose composition by convent...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807982/ https://www.ncbi.nlm.nih.gov/pubmed/24167787 http://dx.doi.org/10.4103/2230-973X.119225 |
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author | Sakarkar, Dinesh M Dorle, Avinash K Mahajan, Nilesh Manoharrao Sudke, Suresh Gendappa |
author_facet | Sakarkar, Dinesh M Dorle, Avinash K Mahajan, Nilesh Manoharrao Sudke, Suresh Gendappa |
author_sort | Sakarkar, Dinesh M |
collection | PubMed |
description | INTRODUCTION: The objective of the present study was to design ferrous fumarate (FF) sustained release (SR) pellets using of cow ghee (CG) as an important hot-melt coating (HMC) agent. MATERIALS AND METHODS: The pellets were coated by HMC technique using CG and ethyl cellulose composition by conventional coating pan without the use of spray system. FF formulated as pellets and characterized with regard to the drug content and physico-chemical properties. Stability studies were carried out on the optimized formulation for a period of 6 months at 40 ± 2°C and 75 ± 5% relative humidity. RESULTS: Pellets with good surface morphology and smooth texture confirmed by stereo micrographs. HMC is easy, efficient, rapid and simple method since virtually no agglomeration seen during coating. In-vitro release from pellets at a given level of coating and for present pellet size was dependent upon the physico-chemical property of the drug and mostly aqueous solubility of the drug. The selection of optimized FF formulation was confirmed by comparing percent cumulative drug release with theoretical release profile. Formulation F2 had difference factor (f(1)) and similarity factor (f(2)) values was found to be 5 and 66 respectively. F2 showed SR of drug for 8 h with cumulative per cent release of 98.03 ± 4.49%. Release kinetics indicates approximately zero order release pattern. HMC pellets were stable during the course of stability study. CONCLUSIONS: By means of HMC using CG and ethyl cellulose, SR pellets containing FF were successfully prepared. |
format | Online Article Text |
id | pubmed-3807982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38079822013-10-28 Design of sustained release pellets of ferrous fumarate using cow ghee as hot-melt coating agent Sakarkar, Dinesh M Dorle, Avinash K Mahajan, Nilesh Manoharrao Sudke, Suresh Gendappa Int J Pharm Investig Original Research Article INTRODUCTION: The objective of the present study was to design ferrous fumarate (FF) sustained release (SR) pellets using of cow ghee (CG) as an important hot-melt coating (HMC) agent. MATERIALS AND METHODS: The pellets were coated by HMC technique using CG and ethyl cellulose composition by conventional coating pan without the use of spray system. FF formulated as pellets and characterized with regard to the drug content and physico-chemical properties. Stability studies were carried out on the optimized formulation for a period of 6 months at 40 ± 2°C and 75 ± 5% relative humidity. RESULTS: Pellets with good surface morphology and smooth texture confirmed by stereo micrographs. HMC is easy, efficient, rapid and simple method since virtually no agglomeration seen during coating. In-vitro release from pellets at a given level of coating and for present pellet size was dependent upon the physico-chemical property of the drug and mostly aqueous solubility of the drug. The selection of optimized FF formulation was confirmed by comparing percent cumulative drug release with theoretical release profile. Formulation F2 had difference factor (f(1)) and similarity factor (f(2)) values was found to be 5 and 66 respectively. F2 showed SR of drug for 8 h with cumulative per cent release of 98.03 ± 4.49%. Release kinetics indicates approximately zero order release pattern. HMC pellets were stable during the course of stability study. CONCLUSIONS: By means of HMC using CG and ethyl cellulose, SR pellets containing FF were successfully prepared. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3807982/ /pubmed/24167787 http://dx.doi.org/10.4103/2230-973X.119225 Text en Copyright: © 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Article Sakarkar, Dinesh M Dorle, Avinash K Mahajan, Nilesh Manoharrao Sudke, Suresh Gendappa Design of sustained release pellets of ferrous fumarate using cow ghee as hot-melt coating agent |
title | Design of sustained release pellets of ferrous fumarate using cow ghee as hot-melt coating agent |
title_full | Design of sustained release pellets of ferrous fumarate using cow ghee as hot-melt coating agent |
title_fullStr | Design of sustained release pellets of ferrous fumarate using cow ghee as hot-melt coating agent |
title_full_unstemmed | Design of sustained release pellets of ferrous fumarate using cow ghee as hot-melt coating agent |
title_short | Design of sustained release pellets of ferrous fumarate using cow ghee as hot-melt coating agent |
title_sort | design of sustained release pellets of ferrous fumarate using cow ghee as hot-melt coating agent |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807982/ https://www.ncbi.nlm.nih.gov/pubmed/24167787 http://dx.doi.org/10.4103/2230-973X.119225 |
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