Peer-Reviewed Journal Details
Mandatory Fields
Hurley, D;Potter, CB;Walker, GM;Higginbotham, CL
2018
May
Journal Of Pharmaceutical Sciences
Investigation of Ethylene Oxide-co-propylene Oxide for Dissolution Enhancement of Hot-Melt Extruded Solid Dispersions
Published
8 ()
Optional Fields
GLASS-TRANSITION TEMPERATURES PHYSICOCHEMICAL CHARACTERIZATION AMORPHOUS INDOMETHACIN PHYSICAL STABILITY POLYMER BLENDS SOLUBLE DRUGS RELEASE CYCLODEXTRINS FORMULATIONS RECRYSTALLIZATION
107
1372
1382
The optimal design of amorphous solid dispersion formulations requires the use of excipients to maintain supersaturation and improve physical stability to ensure shelf-life stability and better absorption during intestinal transit, respectively. Blends of excipients (surfactants and polymers) are often used within pharmaceutical products to improve the oral delivery of Biopharmaceutical Classification System class II drugs. Therefore, in this study, a dissolution enhancer, poloxamer 407 (P407), was investigated to determine its effect on the dissolution properties and on the amorphous nature of the active pharmaceutical ingredient contained in the formulation. Phase solubility studies of indomethacin (INM) in aqueous solutions of P407 and poly(vinylpyrrolidone-vinyl acetate copolymer) showed an increase in the kinetic solubility of INM compared with the pure drug at 37 degrees C with a K-a value of 0.041 mu g/mL. The solid dispersions showed a higher dissolution rate when compared to pure and amorphous drugs when performed in pH buffer 1.2 with a kinetic solubility of 21 mg/mL. The stability data showed that the amorphous drug in solid solutions with poly(vinylpyrrolidone-vinyl acetate copolymer) and P407 remained amorphous, and the % P407 loading had no effect on the amorphous stability of INM. This study concluded that the amorphous solid dispersion contributed to the increased solubility of INM. (C) 2018 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
HOBOKEN
0022-3549
10.1016/j.xphs.2018.01.016
Grant Details