Background and Objectives: Lipid-based self-nanoemulsifying drug delivery systems\n(SNEDDS) have resurged the eminence of nanoemulsions by modest adjustments and o_er many\nvaluable opportunities in drug delivery. Chlorpromazine, an antipsychotic agent with poor aqueous\nsolubility--with extensive first-pass metabolism-can be a suitable candidate for the development of\nSNEDDS. The current study was designed to develop triglyceride-based SNEDDS of chlorpromazine\nto achieve improved solubility, stability, and oral bioavailability. Materials and Methods: Fifteen\nSNEDDS formulations of each short, medium, and long chain, triglycerides were synthesized and\ncharacterized to achieve optimized formulation. The optimized formulation was characterized for\nseveral in vitro and in vivo parameters. Results: Particle size, zeta potential, and drug loading of\nthe optimized SNEDDS (LCT14) were found to be������
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