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Rheological Characterization of an Acetaminophen Jelly
The aim of this study was to prepare an inclusion complex of acetaminophen and β-cyclodextrin (molar ratio of 1:1). A jelly with inclusion complexes formed by kneading was prepared. The formation of inclusion complexes was assessed by powder X-ray diffraction patterns and Fourier transform-infrared...
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/PMC3831725/ https://www.ncbi.nlm.nih.gov/pubmed/24302798 http://dx.doi.org/10.4103/0250-474X.119825 |
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author | Inoue, Y. Takahashi, R. Okada, H. Iwasaki, Y. Murata, I. Kanamoto, I. |
author_facet | Inoue, Y. Takahashi, R. Okada, H. Iwasaki, Y. Murata, I. Kanamoto, I. |
author_sort | Inoue, Y. |
collection | PubMed |
description | The aim of this study was to prepare an inclusion complex of acetaminophen and β-cyclodextrin (molar ratio of 1:1). A jelly with inclusion complexes formed by kneading was prepared. The formation of inclusion complexes was assessed by powder X-ray diffraction patterns and Fourier transform-infrared spectroscopy. Jellies were prepared with xanthan gum, gelatin, and κ-carrageenan. The concentration of each jelling agent was 0.5, 1.0, and 1.5% w/v. Viscoelasticity and dissolution characteristics were determined and osmometry was performed. PGWater(™), a commercial jelly for fluid replacement, served as a reference for viscoelastic characteristics and dissolution. Powder X-ray diffraction measurement revealed a different diffraction pattern for the kneading than for acetaminophen and β-cyclodextrin. Fourier transform-infrared spectroscopy revealed an absorption peak (at around 1655 cm(−1)) due to the carbonyl group and benzene ring (at around 1610 cm(−1)) of acetaminophen. In contrast, the kneaded mixture (1:1) had a shift in the absorption peak due to the carbonyl group (at around 1650 cm(−1)) in acetaminophen's molecular structure, and the formation of an inclusion complex was noted. The viscosity of xanthan gum-1.0, gelatin-1.5, and carrageenan-0.5 resembled the viscoelasticity of PGWater(™). The acetaminophen in gelatin-1.0 and carrageenan-0.5 had dissolution behavior similar to that of commercial acetaminophen preparations. The osmolality of jellies prepared in different concentrations ranged from about 20-50 mOsm/kg. Results suggested that carrageenan-0.5 could serve as a useful jelly vehicle for acetaminophen. |
format | Online Article Text |
id | pubmed-3831725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38317252013-12-03 Rheological Characterization of an Acetaminophen Jelly Inoue, Y. Takahashi, R. Okada, H. Iwasaki, Y. Murata, I. Kanamoto, I. Indian J Pharm Sci Research Paper The aim of this study was to prepare an inclusion complex of acetaminophen and β-cyclodextrin (molar ratio of 1:1). A jelly with inclusion complexes formed by kneading was prepared. The formation of inclusion complexes was assessed by powder X-ray diffraction patterns and Fourier transform-infrared spectroscopy. Jellies were prepared with xanthan gum, gelatin, and κ-carrageenan. The concentration of each jelling agent was 0.5, 1.0, and 1.5% w/v. Viscoelasticity and dissolution characteristics were determined and osmometry was performed. PGWater(™), a commercial jelly for fluid replacement, served as a reference for viscoelastic characteristics and dissolution. Powder X-ray diffraction measurement revealed a different diffraction pattern for the kneading than for acetaminophen and β-cyclodextrin. Fourier transform-infrared spectroscopy revealed an absorption peak (at around 1655 cm(−1)) due to the carbonyl group and benzene ring (at around 1610 cm(−1)) of acetaminophen. In contrast, the kneaded mixture (1:1) had a shift in the absorption peak due to the carbonyl group (at around 1650 cm(−1)) in acetaminophen's molecular structure, and the formation of an inclusion complex was noted. The viscosity of xanthan gum-1.0, gelatin-1.5, and carrageenan-0.5 resembled the viscoelasticity of PGWater(™). The acetaminophen in gelatin-1.0 and carrageenan-0.5 had dissolution behavior similar to that of commercial acetaminophen preparations. The osmolality of jellies prepared in different concentrations ranged from about 20-50 mOsm/kg. Results suggested that carrageenan-0.5 could serve as a useful jelly vehicle for acetaminophen. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3831725/ /pubmed/24302798 http://dx.doi.org/10.4103/0250-474X.119825 Text en Copyright: © Indian Journal of Pharmaceutical Sciences 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 | Research Paper Inoue, Y. Takahashi, R. Okada, H. Iwasaki, Y. Murata, I. Kanamoto, I. Rheological Characterization of an Acetaminophen Jelly |
title | Rheological Characterization of an Acetaminophen Jelly |
title_full | Rheological Characterization of an Acetaminophen Jelly |
title_fullStr | Rheological Characterization of an Acetaminophen Jelly |
title_full_unstemmed | Rheological Characterization of an Acetaminophen Jelly |
title_short | Rheological Characterization of an Acetaminophen Jelly |
title_sort | rheological characterization of an acetaminophen jelly |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3831725/ https://www.ncbi.nlm.nih.gov/pubmed/24302798 http://dx.doi.org/10.4103/0250-474X.119825 |
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