Unformatted text preview:

PHA 5127 Dose Optimization I Case Study IV 1. For the following situations, indicate whether the drug is: filtered, reabsorbed (if fully or if reabsorbed through transporters), or actively secreted (Assume GFR is 130mL/min, urine flow is 1.5mL/min) a. Drug with fu= 0.3 and a Clren=39mL/min b. Drug with fu=0.6 and a Clren=30mL/min c. Drug with fu=0.05 and a Clren=15mL/min d. Drug with fu=0.2 and a Clren=0.3mL/min e. Drug with fu=0.8 and a Clren=0.3mL/min 2. A 25 year old, 5’6’’, 80kg male patient with a serum creatinine concentration of 1.8mg/dL was given a drug treatment. Knowing this drug is mainly eliminated by glomerula filtration and has 60% plasma protein binding. Please estimate the Clearance of this drug (with Cockcroft-Gault equation) 3. TRUE (T) or FALSE (F) For a high extraction drug, liver blood flow is important to both hepatic clearance and oral bioavailability. T F For low extraction drug, fu (fraction of unbound drug in plasma) is important to both hepatic clearance and oral bioavailability. T F Basic drugs that are polar in their unionized form, the extent of re-absorption depends on the degree of its ionization. T F Secretion is indicated when renal clearance is larger than GFR*fu. T FIt is possible for renal clearance to be close to the kidney blood flow. T F Assuming no plasma protein binding, the renal clearance equals the urine flow when full re-absorption occurs. T


View Full Document

UF PHA 5127 - Dose Optimization I

Download Dose Optimization I
Our administrator received your request to download this document. We will send you the file to your email shortly.
Loading Unlocking...
Login

Join to view Dose Optimization I and access 3M+ class-specific study document.

or
We will never post anything without your permission.
Don't have an account?
Sign Up

Join to view Dose Optimization I 2 2 and access 3M+ class-specific study document.

or

By creating an account you agree to our Privacy Policy and Terms Of Use

Already a member?