4.4 Article

Preparation and In Vitro-In Vivo Evaluation of Sustained-Release Matrix Pellets of Capsaicin to Enhance the Oral Bioavailability

期刊

AAPS PHARMSCITECH
卷 17, 期 2, 页码 339-349

出版社

SPRINGER
DOI: 10.1208/s12249-015-0352-7

关键词

capsaicin; in vitro release; oral bioavailability; pharmacokinetic studies; sustained-release pellets

资金

  1. National Natural Science Foundation of China [30973677, 81373371]
  2. National Twelfth Five-Year Plan for Science & Technology Support [2012BAD36B01]
  3. Doctoral Fund of Ministry of Education of China [20113227110012, 2014M560410]
  4. Doctoral Fund of Ministry of Education of Jiangsu province [1401023B]
  5. Special Funds for 333 project [BRA2013198]
  6. Special Funds for 331 project
  7. Priority Academic Program Development of Jiangsu University [13JDG007]
  8. Industry-University-Research Institution Cooperation in Jiangsu Province and Zhenjiang City [JHB2012-37, CY2010023, GY2011028]

向作者/读者索取更多资源

Capsaicin has multiple pharmacological activities including antioxidant, anticancer, and anti-inflammatory activities. However, its clinical application is limited due to its poor aqueous solubility, gastric irritation, and low oral bioavailability. This research was aimed at preparing sustained-release matrix pellets of capsaicin to enhance its oral bioavailability. The pellets comprised of a core of solid-dispersed capsaicin mixed with microcrystalline cellulose (MCC) and hydroxypropyl cellulose (HPMC) and subsequently coating with ethyl cellulose (EC) were obtained by using the technology of extrusion/spheronization. The physicochemical properties of the pellets were evaluated through scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and X-ray diffractometry (XRD). Besides, the in vitro release, in vivo absorption, and in vitro-in vivo correlation were also assessed. More importantly, the relative bioavailability of the sustained-release matrix pellets was studied in fasted rabbits after oral administration using free capsaicin and solid dispersion as references. The oral bioavailability of the matrix pellets and sustained-release matrix pellets of capsaicin was improved approximately 1.98-fold and 5.34-fold, respectively, compared with the free capsaicin. A good level A IVIVC (in vitro-in vivo correlation) was established between the in vitro dissolution and the in vivo absorption of sustained-release matrix pellets. All the results affirmed the remarkable improvement in the oral bioavailability of capsaicin owing to the successful preparation of its sustained-release matrix pellets.

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