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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...

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Autores principales: Inoue, Y., Takahashi, R., Okada, H., Iwasaki, Y., Murata, I., Kanamoto, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
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.
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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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