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Development of novel sibutramine base-loaded solid dispersion with gelatin and HPMC: Physicochemical characterization and pharmacokinetics in beagle dogs

Authors
Lim, Hyun-TaeBalakrishnan, PrabagarOh, Dong HoonJoe, Kwan HyungKim, Young RanHwang, Doo HyungLee, Yong-BokYong, Chul SoonChoi, Han-Gon
Issue Date
Sep-2010
Publisher
ELSEVIER SCIENCE BV
Keywords
Sibutramine base; Gelatin; Solid dispersion; Solubility; Bioavailability; Beagle dog
Citation
INTERNATIONAL JOURNAL OF PHARMACEUTICS, v.397, no.1-2, pp.225 - 230
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume
397
Number
1-2
Start Page
225
End Page
230
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/39548
DOI
10.1016/j.ijpharm.2010.07.013
ISSN
0378-5173
Abstract
To develop a novel sibutramine base-loaded solid dispersion with enhanced solubility and bioavailability, various solid dispersions were prepared using a spray drying technique with hydrophilic polymers such as gelatin, HPMC and citric acid. Their solubility, thermal characteristics and crystallinity were investigated. The dissolution and pharmacokinetics of the sibutramine base-loaded solid dispersion were then compared with a sibutramine hydrochloride monohydrate-loaded commercial product (Reductil (R)). The solid dispersions prepared with gelatin gave higher drug solubility than those prepared without gelatin, irrespective of the amount of polymer. The sibutramine base-loaded solid dispersions containing hydrophilic polymer and citric acid showed higher drug solubility compared to sibutramine base and sibutramine hydrochloride monohydrate. Among the formulations tested, the solid dispersion composed of sibutramine base/gelatin/HPMC/citric acid at the weight ratio of 1/0.8/0.2/0.5 gave the highest solubility of 5.03 +/- 0.24 mg/ml. Our DSC and powder X-ray diffraction results showed that the drug was present in an altered amorphous form in this solid dispersion. The difference factor (f(1)) values between solid dispersion and commercial product were 2.82, 6.65 and 6.31 at pH 1.2, 4.0 and 6.8, respectively. Furthermore, they had the similarity factor (f(2)) value of 65.68, 53.43 and 58.97 at pH 1.2, 4.0 and 6.8, respectively. Our results suggested that the solid dispersion and commercial product produced a similar correlation of dissolution profiles at all pH ranges. The AUC, C-max and T-max of the parent drug and metabolite land II from the solid dispersion were not significantly different from those of the commercial product, suggesting that the solid dispersion might be bioequivalent to the commercial product in beagle dogs. Thus, the sibutramine base-loaded solid dispersion prepared with gelatin, HPMC and citric acid is a promising candidate for improving the solubility and bioavailability of the poorly water-soluble sibutramine base. Crown Copyright (C) 2010 Published by Elsevier B.V. All rights reserved.
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