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be randomized to be administered orally (30 mg/kg) with either
nanoemulsion, microemulsion and control formulation, respectively. In
this instance, 3.0% w/w of captopril in olive oil, an emulsion formed
without the use of glycerol and sucrose ester surfactant will be use as a
control. Then, rats will be anesthetized with ketamine: xylazine; ratio of
2:1. Blood samples (0.25 ml) will be collected from the jugular vein using
heparinized syringes at predetermined time intervals of 0, 0.25, 0.5, 1.0,
1.5, 2.0, 3.0, 4.0, 5.0 and 6.0 h. Plasma samples will be treated with DA
prior to UPLC (Waters, USA) analysis.
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