Use of pectin as a carrier for intragastric floating drug delivery: Carbonate salt contained beads

Pectin has been investigated as a carrier for an intragastric floating drug delivery by a means of calcium pectinate gel (CaPG) beads. The CaPG beads containing carbonate salt, as a gas-forming agent, were prepared by dispersing carbonate salt in pectin solution and then extruding into either neutra...

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Main Authors: Pornsak Sriamornsak, Srisagul Sungthongjeen, Satit Puttipipatkhachorn
Other Authors: Silpakorn University
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/24035
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spelling th-mahidol.240352018-08-24T08:43:28Z Use of pectin as a carrier for intragastric floating drug delivery: Carbonate salt contained beads Pornsak Sriamornsak Srisagul Sungthongjeen Satit Puttipipatkhachorn Silpakorn University Naresuan University Mahidol University Agricultural and Biological Sciences Biochemistry, Genetics and Molecular Biology Pectin has been investigated as a carrier for an intragastric floating drug delivery by a means of calcium pectinate gel (CaPG) beads. The CaPG beads containing carbonate salt, as a gas-forming agent, were prepared by dispersing carbonate salt in pectin solution and then extruding into either neutral or acidified solution of calcium chloride. The effect of selected factors, such as type of carbonates, percentage of carbonates, degree of methylesterification (DE) of pectin, type of gelation medium, drug loading and drying method, on morphology, floating and release properties was investigated. Incorporation of sodium bicarbonate into pectin solution resulted in porous structured beads. Acidity of gelation medium increased the pores in the structure of beads containing calcium carbonate. This is due to carbon dioxide generated from reaction of carbonate salts with acid. Drug release from CaPG beads is clearly dependent upon the formulation and processing variables studied. It is obvious that the highly porous of the freeze-dried beads showed a good floating ability with fast drug release. The drug release could be prolonged by using pectin with lower DE, 10% calcium carbonate, acidified gelation medium, and high drug loading. However, their floating ability seemed to be decreased. It is suggested that the optimization of formulation and processing variables is further needed to obtain a good floating ability and a prolonged drug release. © 2006 Elsevier Ltd. All rights reserved. 2018-08-24T01:38:28Z 2018-08-24T01:38:28Z 2007-02-01 Article Carbohydrate Polymers. Vol.67, No.3 (2007), 436-445 10.1016/j.carbpol.2006.06.013 01448617 2-s2.0-33845331381 https://repository.li.mahidol.ac.th/handle/123456789/24035 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33845331381&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Agricultural and Biological Sciences
Biochemistry, Genetics and Molecular Biology
spellingShingle Agricultural and Biological Sciences
Biochemistry, Genetics and Molecular Biology
Pornsak Sriamornsak
Srisagul Sungthongjeen
Satit Puttipipatkhachorn
Use of pectin as a carrier for intragastric floating drug delivery: Carbonate salt contained beads
description Pectin has been investigated as a carrier for an intragastric floating drug delivery by a means of calcium pectinate gel (CaPG) beads. The CaPG beads containing carbonate salt, as a gas-forming agent, were prepared by dispersing carbonate salt in pectin solution and then extruding into either neutral or acidified solution of calcium chloride. The effect of selected factors, such as type of carbonates, percentage of carbonates, degree of methylesterification (DE) of pectin, type of gelation medium, drug loading and drying method, on morphology, floating and release properties was investigated. Incorporation of sodium bicarbonate into pectin solution resulted in porous structured beads. Acidity of gelation medium increased the pores in the structure of beads containing calcium carbonate. This is due to carbon dioxide generated from reaction of carbonate salts with acid. Drug release from CaPG beads is clearly dependent upon the formulation and processing variables studied. It is obvious that the highly porous of the freeze-dried beads showed a good floating ability with fast drug release. The drug release could be prolonged by using pectin with lower DE, 10% calcium carbonate, acidified gelation medium, and high drug loading. However, their floating ability seemed to be decreased. It is suggested that the optimization of formulation and processing variables is further needed to obtain a good floating ability and a prolonged drug release. © 2006 Elsevier Ltd. All rights reserved.
author2 Silpakorn University
author_facet Silpakorn University
Pornsak Sriamornsak
Srisagul Sungthongjeen
Satit Puttipipatkhachorn
format Article
author Pornsak Sriamornsak
Srisagul Sungthongjeen
Satit Puttipipatkhachorn
author_sort Pornsak Sriamornsak
title Use of pectin as a carrier for intragastric floating drug delivery: Carbonate salt contained beads
title_short Use of pectin as a carrier for intragastric floating drug delivery: Carbonate salt contained beads
title_full Use of pectin as a carrier for intragastric floating drug delivery: Carbonate salt contained beads
title_fullStr Use of pectin as a carrier for intragastric floating drug delivery: Carbonate salt contained beads
title_full_unstemmed Use of pectin as a carrier for intragastric floating drug delivery: Carbonate salt contained beads
title_sort use of pectin as a carrier for intragastric floating drug delivery: carbonate salt contained beads
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/24035
_version_ 1763493037649952768