Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

Enhanced Solubility and Bioavailability of Sibutramine Base by Solid Dispersion System with Aqueous Medium

Authors
Li, Dong XunJang, Ki-YoungKang, WonkuBae, KyoungjinLee, Mann HyungOh, Yu-KyoungJee, Jun-PilPark, Young-JoonOh, Dong HoonSeo, Youn GeeKim, Young RanKim, Jong OhWoo, Jong SooYong, Chul SoonChoi, Han-Gon
Issue Date
Feb-2010
Publisher
Pharmaceutical Society of Japan
Keywords
solid dispersion; water; sibutramine base; solubility; pharmacokinetics
Citation
Biological and Pharmaceutical Bulletin, v.33, no.2, pp 279 - 284
Pages
6
Indexed
SCI
SCIE
SCOPUS
Journal Title
Biological and Pharmaceutical Bulletin
Volume
33
Number
2
Start Page
279
End Page
284
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/40004
DOI
10.1248/bpb.33.279
ISSN
0918-6158
1347-5215
Abstract
To develop a novel sibutramine base-loaded solid dispersion with improved solubility bioavailability, various solid dispersions were prepared with water, hydroxypropylmethyl cellulose (HPMC), poloxamer and citric acid using spray-drying technique. The effect of HPMC, poloxamer and citric acid on the aqueous solubility of sibutramine was investigated. The physicochemical properties of solid dispersion were investigated using scanning electron microscopy (SEM), differential scanning calorimetry (DSC) and X-ray powder diffraction. The dissolution and pharmacokinetics in rats of solid dispersion were evaluated compared to the sibutramine hydrochloride monohydrate-loaded commercial product (Reductil (R)). The sibutramine base-loaded solid dispersion gave two type forms. Like conventional solid dispersion system, one type appeared as a spherical shape with smooth surface, as the carriers and drug with relatively low melting point were soluble in water and formed it. The other appeared as an irregular form with relatively rough surface. Unlike conventional solid dispersion system, this type changed no crystalline form of drug. Our results suggested that this type was formed by, attaching hydrophilic carriers to the surface of drug without crystal change, resulting from changing the hydrophobic drug to hydrophilic form. The sibutramine-loaded solid dispersion at the weight ratio of sibutramine base/HPMC/poloxamer/citric acid of 5/3/3/0.2 gave the maximum drug solubility of about 3 mg/ml. Furthermore, it showed the similar plasma concentration, area under the curve (AUC) and C-max of parent drug, metabolite I and II to the commercial product, indicating that it might give the similar drug efficacy compared to the sibutramine hydrochloride monohydrate-loaded commercial product in rats. Thus, this solid dispersion system would be useful to deliver poorly water-soluble sibutramine base with enhanced bioavailability.
Files in This Item
Go to Link
Appears in
Collections
COLLEGE OF PHARMACY > DEPARTMENT OF PHARMACY > 1. Journal Articles

qrcode

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

Related Researcher

Researcher Choi, Han Gon photo

Choi, Han Gon
COLLEGE OF PHARMACY (DEPARTMENT OF PHARMACY)
Read more

Altmetrics

Total Views & Downloads

BROWSE