Physicochemical Properties of Ursodeoxycholic Acid Dispersed in Controlled Pore Glass

The objective of this study was to reduce the crystallinity of ursodeoxycholic acid (UDCA) by solid dispersion with controlled pore glass (CPG). To evaluate the effect of pore diameter and pore volume of CPG on the crystalline properties of UDCA, we used powder X-ray diffractometry (PXRD) and differ...

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Main Authors: Okonogi S., Oguchi T., Yonemochi E., Puttipipatkhachorn S., Yamamoto K.
Format: Article
Language:English
Published: 2014
Online Access:http://www.ncbi.nlm.nih.gov/pubmed/3502482
http://cmuir.cmu.ac.th/handle/6653943832/4592
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spelling th-cmuir.6653943832-45922014-08-30T02:42:38Z Physicochemical Properties of Ursodeoxycholic Acid Dispersed in Controlled Pore Glass Okonogi S. Oguchi T. Yonemochi E. Puttipipatkhachorn S. Yamamoto K. The objective of this study was to reduce the crystallinity of ursodeoxycholic acid (UDCA) by solid dispersion with controlled pore glass (CPG). To evaluate the effect of pore diameter and pore volume of CPG on the crystalline properties of UDCA, we used powder X-ray diffractometry (PXRD) and differential scanning calorimetry (DSC). PXRD patterns and the DSC data indicated the presence of UDCA in a crystalline state in the physical mixtures. It was found that amorphous UDCA could be formed via solid dispersion with CPG obtained by a solvent method. The DSC thermograms of solid dispersions showed that there were two states of UDCA, amorphous and crystalline. The amount of crystalline fraction in the solid dispersions depended on the pore size, pore volume, and the specific surface area of CPG. When UDCA was mixed with different pore diameters of CPG, it was found that UDCA molecules preferentially interacted with pores of smaller size. Copyright 1999 Academic Press. 2014-08-30T02:42:38Z 2014-08-30T02:42:38Z 1999 JOURNAL ARTICLE 1095-7103 10421735 http://www.ncbi.nlm.nih.gov/pubmed/3502482 http://cmuir.cmu.ac.th/handle/6653943832/4592 ENG
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description The objective of this study was to reduce the crystallinity of ursodeoxycholic acid (UDCA) by solid dispersion with controlled pore glass (CPG). To evaluate the effect of pore diameter and pore volume of CPG on the crystalline properties of UDCA, we used powder X-ray diffractometry (PXRD) and differential scanning calorimetry (DSC). PXRD patterns and the DSC data indicated the presence of UDCA in a crystalline state in the physical mixtures. It was found that amorphous UDCA could be formed via solid dispersion with CPG obtained by a solvent method. The DSC thermograms of solid dispersions showed that there were two states of UDCA, amorphous and crystalline. The amount of crystalline fraction in the solid dispersions depended on the pore size, pore volume, and the specific surface area of CPG. When UDCA was mixed with different pore diameters of CPG, it was found that UDCA molecules preferentially interacted with pores of smaller size. Copyright 1999 Academic Press.
format Article
author Okonogi S.
Oguchi T.
Yonemochi E.
Puttipipatkhachorn S.
Yamamoto K.
spellingShingle Okonogi S.
Oguchi T.
Yonemochi E.
Puttipipatkhachorn S.
Yamamoto K.
Physicochemical Properties of Ursodeoxycholic Acid Dispersed in Controlled Pore Glass
author_facet Okonogi S.
Oguchi T.
Yonemochi E.
Puttipipatkhachorn S.
Yamamoto K.
author_sort Okonogi S.
title Physicochemical Properties of Ursodeoxycholic Acid Dispersed in Controlled Pore Glass
title_short Physicochemical Properties of Ursodeoxycholic Acid Dispersed in Controlled Pore Glass
title_full Physicochemical Properties of Ursodeoxycholic Acid Dispersed in Controlled Pore Glass
title_fullStr Physicochemical Properties of Ursodeoxycholic Acid Dispersed in Controlled Pore Glass
title_full_unstemmed Physicochemical Properties of Ursodeoxycholic Acid Dispersed in Controlled Pore Glass
title_sort physicochemical properties of ursodeoxycholic acid dispersed in controlled pore glass
publishDate 2014
url http://www.ncbi.nlm.nih.gov/pubmed/3502482
http://cmuir.cmu.ac.th/handle/6653943832/4592
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