A recent bioavailability study in adult human volunteers demonstrated that after the administration of a single enteric-coated aspirin granule product given with a meal, the plasma drug levels resembled the kinetics of a sustained-release drug product. In contrast, when the product was given to fasted subjects, the plasma drug levels resembled the kinetics of an immediate-release drug product. Give a plausible explanation for this observation.
Already registered? Login
Not Account? Sign up
Enter your email address to reset your password
Back to Login? Click here