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Development and Evaluation of a Chloramphenicol Hypertonic Ophthalmic Solution
Hypertonic ophthalmic solutions are used to treat ocular diseases associated with edema. In this study, we developed a chloramphenicol hypertonic ophthalmic solution. These drops were developed based on the cosolvency and additional dielectric constant concepts. Two different solvents: PEG 300 and g...
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Formato: | Texto |
Lenguaje: | English |
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Medknow Publications
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2852064/ https://www.ncbi.nlm.nih.gov/pubmed/20390083 http://dx.doi.org/10.4103/0250-474X.40334 |
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author | Jithan, A. V. Mohan, C. Krishna Vimaladevi, M. |
author_facet | Jithan, A. V. Mohan, C. Krishna Vimaladevi, M. |
author_sort | Jithan, A. V. |
collection | PubMed |
description | Hypertonic ophthalmic solutions are used to treat ocular diseases associated with edema. In this study, we developed a chloramphenicol hypertonic ophthalmic solution. These drops were developed based on the cosolvency and additional dielectric constant concepts. Two different solvents: PEG 300 and glycerol were used as cosolvents. Solubility curves were plotted. Based on the solubility curves, two different solutions were selected. These solutions were evaluated for physical parameters and accelerated stability. The results indicated that chloramphenicol was stable in these formulations. The selected blend of solutions was hypertonic. Thus, the solubility and stability of chloramphenicol was enhanced using a cosolvency technique so as to develop a chloramphenicol hypertonic ophthalmic solution. |
format | Text |
id | pubmed-2852064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-28520642010-04-13 Development and Evaluation of a Chloramphenicol Hypertonic Ophthalmic Solution Jithan, A. V. Mohan, C. Krishna Vimaladevi, M. Indian J Pharm Sci Research Paper Hypertonic ophthalmic solutions are used to treat ocular diseases associated with edema. In this study, we developed a chloramphenicol hypertonic ophthalmic solution. These drops were developed based on the cosolvency and additional dielectric constant concepts. Two different solvents: PEG 300 and glycerol were used as cosolvents. Solubility curves were plotted. Based on the solubility curves, two different solutions were selected. These solutions were evaluated for physical parameters and accelerated stability. The results indicated that chloramphenicol was stable in these formulations. The selected blend of solutions was hypertonic. Thus, the solubility and stability of chloramphenicol was enhanced using a cosolvency technique so as to develop a chloramphenicol hypertonic ophthalmic solution. Medknow Publications 2008 /pmc/articles/PMC2852064/ /pubmed/20390083 http://dx.doi.org/10.4103/0250-474X.40334 Text en © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Jithan, A. V. Mohan, C. Krishna Vimaladevi, M. Development and Evaluation of a Chloramphenicol Hypertonic Ophthalmic Solution |
title | Development and Evaluation of a Chloramphenicol Hypertonic Ophthalmic Solution |
title_full | Development and Evaluation of a Chloramphenicol Hypertonic Ophthalmic Solution |
title_fullStr | Development and Evaluation of a Chloramphenicol Hypertonic Ophthalmic Solution |
title_full_unstemmed | Development and Evaluation of a Chloramphenicol Hypertonic Ophthalmic Solution |
title_short | Development and Evaluation of a Chloramphenicol Hypertonic Ophthalmic Solution |
title_sort | development and evaluation of a chloramphenicol hypertonic ophthalmic solution |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2852064/ https://www.ncbi.nlm.nih.gov/pubmed/20390083 http://dx.doi.org/10.4103/0250-474X.40334 |
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