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The objective of this study was to formulate a self‐nanoemulsifying oral drug delivery system (SNEDDS) for the poorly water‐soluble trans‐Cinnamic acid (t‐CA SNEDDS) that could be evaluated for its antihyperglycemic efficacy in comparison to the parent t‐CA in an alloxan‐induced diabetic rat model. A SNEDDS formulation consisting of 60% surfactant (Kolliphor EL), 10% co‐surfactant (PEG 400) and 30%...
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