Preparation and release characteristics of polymer-coated and blended alginate microspheres

D. W. Lee, Sung Joo Hwang, J. B. Park, H. J. Park

Research output: Contribution to journalReview article

89 Citations (Scopus)

Abstract

To prevent a rapid drug release from alginate microspheres in simulated intestinal media, alginate microspheres were coated or blended with polymers. Three polymers were selected and evaluated such as HPMC, Eudragit RS 30D and chitosan, as both coating materials and additive polymers for controlling the drug release. This study focused on the release characteristics of polymer-coated and blended alginate microspheres, varying the type of polymer and its concentration. The alginate microspheres were prepared by dropping the mixture of drug and sodium alginate into CaCl 2 solution using a spray-gun. Polymer-coated microspheres were prepared by adding alginate microspheres into polymer solution with mild stirring. Polymer-blended microspheres were prepared by dropping the mixture of drug, sodium alginate and additive polymer with plasticizer into CaCl 2 solution. In vitro release test was carried out to investigate the release profiles in 500ml of phosphate buffered saline (PBS, pH 7.4). As the amount of polymer in sodium alginate or coating solution increase, the drug release generally decreased. HPMC-blended microspheres swelled but withstood the disintegration, showing an ideal linear release profiles. Chitosan-coated microspheres showed smooth and round surface and extended the release of drug. In comparison with chitosan-coated microspheres, HPMC-blended alginate microspheres can be easily made and used for controlled drug delivery systems due to convenient process and controlled drug release.

Original languageEnglish
Pages (from-to)179-192
Number of pages14
JournalJournal of Microencapsulation
Volume20
Issue number2
DOIs
Publication statusPublished - 2003 Mar 1

Fingerprint

Alginate
Microspheres
Polymers
drugs
preparation
polymers
Sodium alginate
Pharmaceutical Preparations
Chitosan
sodium
alginic acid
Spray guns
Controlled drug delivery
plasticizers
Plasticizers
Coatings
disintegration
stirring
Disintegration
profiles

All Science Journal Classification (ASJC) codes

  • Bioengineering
  • Pharmaceutical Science
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Colloid and Surface Chemistry

Cite this

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abstract = "To prevent a rapid drug release from alginate microspheres in simulated intestinal media, alginate microspheres were coated or blended with polymers. Three polymers were selected and evaluated such as HPMC, Eudragit RS 30D and chitosan, as both coating materials and additive polymers for controlling the drug release. This study focused on the release characteristics of polymer-coated and blended alginate microspheres, varying the type of polymer and its concentration. The alginate microspheres were prepared by dropping the mixture of drug and sodium alginate into CaCl 2 solution using a spray-gun. Polymer-coated microspheres were prepared by adding alginate microspheres into polymer solution with mild stirring. Polymer-blended microspheres were prepared by dropping the mixture of drug, sodium alginate and additive polymer with plasticizer into CaCl 2 solution. In vitro release test was carried out to investigate the release profiles in 500ml of phosphate buffered saline (PBS, pH 7.4). As the amount of polymer in sodium alginate or coating solution increase, the drug release generally decreased. HPMC-blended microspheres swelled but withstood the disintegration, showing an ideal linear release profiles. Chitosan-coated microspheres showed smooth and round surface and extended the release of drug. In comparison with chitosan-coated microspheres, HPMC-blended alginate microspheres can be easily made and used for controlled drug delivery systems due to convenient process and controlled drug release.",
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Preparation and release characteristics of polymer-coated and blended alginate microspheres. / Lee, D. W.; Hwang, Sung Joo; Park, J. B.; Park, H. J.

In: Journal of Microencapsulation, Vol. 20, No. 2, 01.03.2003, p. 179-192.

Research output: Contribution to journalReview article

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