Journal
INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 644, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.ijpharm.2023.123294
Keywords
Hydrogenated phospholipids; Amorphous solid dispersions; Fenofibrate; Polymers; Supersaturation; Enabling formulations
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This study aimed to evaluate the feasibility and potential role of hydrogenated phospholipid as a matrix material and solubilizing additive for binary or ternary solid dispersions. It was found that hydrogenated phospholipid has the potential to enhance dissolution and bioavailability, and may be a viable formulation strategy to mitigate the food effect of fenofibrate.
Amorphous solid dispersions (ASD) represent a viable formulation strategy to improve dissolution and bioavailability of poorly soluble drugs. Our study aimed to evaluate the feasibility and potential role of hy-drogenated phospholipid (HPL) as a matrix material and solubilizing additive for binary (alone) or ternary (in combination with polymers) solid dispersions, using fenofibrate (FEN) as the model drug. FEN, incorporated within ASDs by melting or freeze-drying (up to 20% m/m), stayed amorphous during short-term stability studies. The solubility enhancing potential of HPL depended on the dissolution medium. In terms of enhancing in vitro permeation, solid dispersions with HPL were found equally or slightly more potent as compared to the polymer-based ASD. For studied ASD, in vitro permeation was found substantially enhanced as compared to a suspension of crystalline FEN and at least equal compared to marketed formulations under comparable conditions (literature data). Additionally, while the permeation of neat FEN and FEN in binary solid dispersions was affected by the dissolution medium (i.e., the prandial state), for ternary solid dispersions the permeation was independent of the prandial state (FaSSIF = FeSSIF). This suggests that ternary solid dispersions containing both polymer and HPL may represent a viable formulation strategy to mitigate fenofibrate's food effect.
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