Comparison of three different types of cilostazol-loaded solid dispersion: Physicochemical characterization and pharmacokinetics in rats

  • Mustapha, Omer; 
  • Kim, Kyung Soo; 
  • Shafique, Shumaila; 
  • Kim, Dong Shik; 
  • Jin, Sung Giu; 
  • ... Oh, Kyung Taek; 
  • 외 5명
Citations

WEB OF SCIENCE

34
Citations

SCOPUS

37

초록

The aim of this research was to compare three different types of cilostazol-loaded solid dispersion system including solvent-evaporated, solvent-wetted and surface-attached solid dispersion. The effect of polymers and surfactants on the aqueous solubility of cilostazol was investigated, leading to the selection of polyvinylpyrrolidone (PVP) and sodium lauryl sulphate (SLS). Employing a spray-drying technique, numerous surface-attached, solvent-evaporated and solvent-wetted solid dispersions were prepared with various amounts PVP and SLS using water, 90% ethanol and acetone, respectively. Their physicochemical properties, solubility, dissolution and oral bioavailability in rats were assessed, compared to the drug powder. Among each solid dispersion system tested, the surface-attached, solvent-evaporated and solvent-wetted solid dispersions composed of cilostazol, PVP and SLS at weight ratios of 3.0 : 0.75 :1.5, 3.0 :3.0 : 1.5 and 3.0 : 3.0 : 1.5, respectively, provided the highest drug solubility and dissolution. The solvent-evaporated solid dispersion gave homogeneous and very small spherical particles, in which the drug was changed to an amorphous state. In the solvent-wetted solid dispersion, the amorphous drug was attached to the polymer surface. Conversely, in the surface-attached solid dispersion, the carriers were adhered onto the surface of the unchanged crystalline drug. The solubility, dissolution and oral bioavailability were significantly increased in the order of solvent-evaporated > solvent-wetted > surface attached > drug powder. Thus, the type of solid dispersion considerably affected the physicochemical properties, aqueous solubility and oral bioavailability. Furthermore, the cilostazol-loaded solvent evaporated solid dispersion with the highest oral bioavailability would be actively recommended as a practical oral pharmaceutical product. (C) 2017 Elsevier B.V. All rights reserved.

키워드

Cilostazol; Solvent-evaporated solid dispersion; Solvent-wetted solid dispersion; Surface-attached solid dispersion; Solubility; Crystallinity; Oral bioavailability; IN-VIVO EVALUATION; SPRAY-DRYING TECHNIQUE; ORAL BIOAVAILABILITY; GELATIN MICROCAPSULE; ENHANCED SOLUBILITY; AQUEOUS SOLUBILITY; DRUG-DELIVERY; BEAGLE DOGS; TWEEN 80; FENOFIBRATE
제목
Comparison of three different types of cilostazol-loaded solid dispersion: Physicochemical characterization and pharmacokinetics in rats
저자
Mustapha, Omer; Kim, Kyung Soo; Shafique, Shumaila; Kim, Dong Shik; Jin, Sung Giu; Seo, Youn Gee; Youn, Yu Seok; Oh, Kyung Taek; Yong, Chul Soon; Kim, Jong Oh; Choi, Han-Gon
DOI
10.1016/j.colsurfb.2017.03.017
발행일
2017-06
유형
Article
저널명
Colloids and Surfaces B: Biointerfaces
권
154
페이지
89 ~ 95