| Literature DB >> 25772420 |
Katja Čerpnjak1, Alenka Zvonar2, Franc Vrečer3, Mirjana Gašperlin4.
Abstract
The purpose of this study was to prepare solid SMEDDS (sSMEDDS) particles produced by spray-drying using maltodextrin (MD), hypromellose (HPMC), and a combination of the two as a solid carrier. Naproxen (NPX) as the model drug was dissolved (at 6% concentration) or partially suspended (at 18% concentration) in a liquid SMEDDS composed of Miglyol(®) 812, Peceol™, Gelucire(®) 44/14, and Solutol(®) HS 15. Among the sSMEDDSs tested, the MD-based sSMEDDSs (with a granular, smooth-surfaced, microspherical appearance) preserved the self-microemulsifying properties of liquid SMEDDSs and exhibited dissolution profiles similar to those of liquid SMEDDSs, irrespective of the concentration of NPX. In contrast, HPMC-based sSMEDDSs (irregular-shaped microparticles) exhibited slightly prolonged release times due to the polymeric nature of the carrier. Differential scanning calorimetry (DSC), X-ray powder diffraction (XRPD), and Raman mapping analysis confirmed molecularly dissolved NPX (at 6% of drug loading), whereas at 18% NPX loading drug is partially molecularly dissolved and partially in the crystalline state.Entities:
Keywords: DSC; Dissolution profile improvement; Microcapsules; Raman mapping; SEM; XRPD
Mesh:
Substances:
Year: 2015 PMID: 25772420 DOI: 10.1016/j.ijpharm.2015.03.015
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875