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Development, characterization and solubility study of solid dispersions of Cefuroxime Axetil by the solvent evaporation method
Cefuroxime Axetil (Poorly water soluble drug), when prepared as solid dispersion showed improved solubility and dissolution. Therefore, the main purpose of this investigation was to increase the solubility and dissolution rate of Cefuroxime Axetil by the preparation of its solid dispersion with urea...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255422/ https://www.ncbi.nlm.nih.gov/pubmed/22247865 http://dx.doi.org/10.4103/0110-5558.72427 |
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author | Arora, S. C. Sharma, P. K. Irchhaiya, Raghuveer Khatkar, Anurag Singh, Neeraj Gagoria, Jagbir |
author_facet | Arora, S. C. Sharma, P. K. Irchhaiya, Raghuveer Khatkar, Anurag Singh, Neeraj Gagoria, Jagbir |
author_sort | Arora, S. C. |
collection | PubMed |
description | Cefuroxime Axetil (Poorly water soluble drug), when prepared as solid dispersion showed improved solubility and dissolution. Therefore, the main purpose of this investigation was to increase the solubility and dissolution rate of Cefuroxime Axetil by the preparation of its solid dispersion with urea, using the solvent evaporation method. Physical mixtures and solid dispersions of Cefuroxime Axetil were prepared by using urea as a water-soluble carrier in various proportions (1:1, 1:2, 1:3, 1:4, 1:5, 1:6, and 1:7 by weight), by employing the solvent evaporation method. The drug release profile was studied and it was found that the dissolution rate and the dissolution parameters of the drug from the physical mixture as well as solid dispersion were higher than those of the intact drug. The Fourier Transform Infrared (FTIR) spectra revealed no chemical incompatibility between the drug and urea. Drug-polymer interactions were investigated using differential scanning calorimetry (DSC) and Powder X-Ray Diffraction (PXRD). |
format | Online Article Text |
id | pubmed-3255422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-32554222012-01-13 Development, characterization and solubility study of solid dispersions of Cefuroxime Axetil by the solvent evaporation method Arora, S. C. Sharma, P. K. Irchhaiya, Raghuveer Khatkar, Anurag Singh, Neeraj Gagoria, Jagbir J Adv Pharm Technol Res Original Article Cefuroxime Axetil (Poorly water soluble drug), when prepared as solid dispersion showed improved solubility and dissolution. Therefore, the main purpose of this investigation was to increase the solubility and dissolution rate of Cefuroxime Axetil by the preparation of its solid dispersion with urea, using the solvent evaporation method. Physical mixtures and solid dispersions of Cefuroxime Axetil were prepared by using urea as a water-soluble carrier in various proportions (1:1, 1:2, 1:3, 1:4, 1:5, 1:6, and 1:7 by weight), by employing the solvent evaporation method. The drug release profile was studied and it was found that the dissolution rate and the dissolution parameters of the drug from the physical mixture as well as solid dispersion were higher than those of the intact drug. The Fourier Transform Infrared (FTIR) spectra revealed no chemical incompatibility between the drug and urea. Drug-polymer interactions were investigated using differential scanning calorimetry (DSC) and Powder X-Ray Diffraction (PXRD). Medknow Publications & Media Pvt Ltd 2010 /pmc/articles/PMC3255422/ /pubmed/22247865 http://dx.doi.org/10.4103/0110-5558.72427 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 Arora, S. C. Sharma, P. K. Irchhaiya, Raghuveer Khatkar, Anurag Singh, Neeraj Gagoria, Jagbir Development, characterization and solubility study of solid dispersions of Cefuroxime Axetil by the solvent evaporation method |
title | Development, characterization and solubility study of solid dispersions of Cefuroxime Axetil by the solvent evaporation method |
title_full | Development, characterization and solubility study of solid dispersions of Cefuroxime Axetil by the solvent evaporation method |
title_fullStr | Development, characterization and solubility study of solid dispersions of Cefuroxime Axetil by the solvent evaporation method |
title_full_unstemmed | Development, characterization and solubility study of solid dispersions of Cefuroxime Axetil by the solvent evaporation method |
title_short | Development, characterization and solubility study of solid dispersions of Cefuroxime Axetil by the solvent evaporation method |
title_sort | development, characterization and solubility study of solid dispersions of cefuroxime axetil by the solvent evaporation method |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255422/ https://www.ncbi.nlm.nih.gov/pubmed/22247865 http://dx.doi.org/10.4103/0110-5558.72427 |
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