Formulation, Characterization, and in Vivo Evaluation of Celecoxib-PVP Solid Dispersion Nanoparticles Using Supercritical Antisolvent Process

Molecules

Eun-Sol Ha²  Gwang-Ho Choo²  In-Hwan Baek¹  Min-Soo Kim² 

[1] College of Pharmacy, Kyungsung University, Busan 608-736, Korea; E-Mail:;College of Pharmacy, Pusan National University, Busan 609-735, Korea; E-Mails:

关键词: solid dispersion;    bioavailability;    celecoxib;    nanoparticles;    supercritical antisolvent;   

DOI  :  10.3390/molecules191220325

来源: mdpi

【 摘 要 】

The aim of this study was to develop celecoxib-polyvinylpyrrolidone (PVP) solid dispersion nanoparticles with and without surfactant using the supercritical antisolvent (SAS) process. The effect of different surfactants such as gelucire 44/14, poloxamer 188, poloxamer 407, Ryoto sugar ester L1695, and d-α-tocopheryl polyethylene glycol 1000 succinate (TPGS) on nanoparticle formation and dissolution as well as oral absorption of celecoxib-PVP K30 solid dispersion nanoparticles was investigated. Spherical celecoxib solid dispersion nanoparticles less than 300 nm in size were successfully developed using the SAS process. Analysis by differential scanning calorimetry and powder X-ray diffraction showed that celecoxib existed in the amorphous form within the solid dispersion nanoparticles fabricated using the SAS process. The celecoxib-PVP-TPGS solid dispersion nanoparticles significantly enhanced in vitro dissolution and oral absorption of celecoxib relative to that of the unprocessed form. The area under the concentration-time curve (AUC_{0→24 h}) and peak plasma concentration (C_max) increased 4.6 and 5.7 times, respectively, with the celecoxib-PVP-TPGS formulation. In addition, in vitro dissolution efficiency was well correlated with in vivo pharmacokinetic parameters. The present study demonstrated that formulation of celecoxib-PVP-TPGS solid dispersion nanoparticles using the SAS process is a highly effective strategy for enhancing the bioavailability of poorly water-soluble celecoxib.

【 授权许可】

CC BY   
© 2014 by the authors; licensee MDPI, Basel, Switzerland.