Detailed Information

Cited 20 time in webofscience Cited 23 time in scopus
Metadata Downloads

Preparation and characterization of pH-independent sustained release tablet containing solid dispersion granules of a poorly water-soluble drug

Authors
Huyen Thi Thanh TranPark, Jun BomHong, Ki-HyukChoi, Han-GonHan, Hyo-KyungLee, JaehwiOh, Kyung TaekLee, Beom-Jin
Issue Date
Aug-2011
Publisher
ELSEVIER SCIENCE BV
Keywords
Solid dispersion granules; Surface adsorption; Sustained release tablet; pH-independent release; EDS imaging
Citation
INTERNATIONAL JOURNAL OF PHARMACEUTICS, v.415, no.1-2, pp 83 - 88
Pages
6
Journal Title
INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume
415
Number
1-2
Start Page
83
End Page
88
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/21328
DOI
10.1016/j.ijpharm.2011.05.052
ISSN
0378-5173
1873-3476
Abstract
Sustained release (SR) tablets containing solid dispersions (SD) granules of a poorly water-soluble drug were prepared to investigate the controlled pH-independent release of the drug. Losartan potassium (LST), an anti-hypertensive agent was chosen as a model drug because of its pH-dependent solubility and short elimination half-life. Poloxamer 188 was used as an SD carrier. A free-flowing SD granule was prepared by adsorbing the melt of the drug and poloxamer 188 onto the surface of an adsorbent. Aerosil 300 (fumed silicon dioxide), followed by direct compression with polyethylene oxide (PEO, 5 x 10(6)) to obtain an SD-loaded SR (SD-SR) matrix tablet. Differential scanning calorimetry (DSC) and powder Xray diffraction (PXRD) revealed partially amorphous structures of the drug in the SD granules. Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS) images indicated adsorption of SD granules onto the surface of the adsorbent. The SD granules dissolved completely within 10 min, a dissolution rate much higher than that of pure LST. Moreover, pH-independent sustained release of LST from the SD-SR tablet was achieved for 2 h in gastric fluid (pH 1.2) and for 10 h in intestinal fluid (pH 6.8). A combination of SD techniques using surface adsorption and SR concepts is a promising approach to control the release rate of poorly water-soluble drugs in a pH-independent manner. (C) 2011 Elsevier B.V. All rights reserved.
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Pharmacy > School of Pharmacy > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher Oh, Kyung Taek photo

Oh, Kyung Taek
대학원 (글로벌혁신신약학과)
Read more

Altmetrics

Total Views & Downloads

BROWSE