Questions
Questions
Multiple fill-in-the-blank

The pharmacokinetics of trastuzumab fit a two-compartment linear pharmacokinetic model. The estimated clearance is 0.225 L/day, volume of the central compartment is 2.95 L and the elimination half-life is long at 28.5 days.[Fill in the blank] What is the estimated volume of distribution during the elimination phase?[Fill in the blank] Is the volume of distribution during the elimination phase different to the volume of distribution of the central compartment? Why?[Fill in the blank] What is the expected initial plasma concentration in a 70 kg patient if the intravenous loading dose is 4 mg/kg?[Fill in the blank] What maintenance dose will required to maintain that plasma concentration?[Fill in the blank]

Question Image
View Explanation

View Explanation

Verified Answer
Please login to view
Step-by-Step Analysis
To approach this pharmacokinetics question, I’ll break down each blank and examine the details given and the standard two-compartment model relationships. 27a) What is the estimated volume of distribution during the elimination phase? - In a two-compartment model, the elimination-phase (β) volume of distribution Vdβ can be obtained from the relationship Vdβ = CL / ke, where ke is the elimination-rate constant. The elimination half-life t1/2β is 28.5 d......Login to view full explanation

Log in for full answers

We've collected over 50,000 authentic exam questions and detailed explanations from around the globe. Log in now and get instant access to the answers!

Similar Questions

Which of the following statements accurately describe the relationship between individual half-life and initial ("baseline") serum ChromoBzAc concentration?

Louise was given a single IV dose of 100 mg tramadol after the surgery for her wrist fracture. Blood samples were taken at various time intervals, and the plasma concentration-time data are given below. [table] Time (hr) | Plasma concentration (µg/mL) 0.25 | 11.1 0.5 | 10.7 1 | 10.0 3 | 7.5 6 | 4.9 12 | 2.1 [/table][Fill in the blank] Does tramadol display one or two compartment pharmacokinetics?[Fill in the blank] What is the plasma concentration at time zero?[Fill in the blank] What is the elimination rate constant?[Fill in the blank] Estimate the volume of distribution and elimination half-life.[Fill in the blank] What is the clearance?[Fill in the blank] If the fraction of tramadol excreted (fe) is 0.3, what is the renal clearance and hepatic clearance?[Fill in the blank] How much drug would be left in the body after 3 hours of dosing?[Fill in the blank] How long would it take for 99.9% of this drug to be eliminated?[Fill in the blank]

Clotgone® is first in class anti-coagulant for patients with atrial fibrillation to reduce the risk of clots forming and pulmonary embolisms and strokes. The pharmaceutical company who discovered and developed Clotgone® have produced population PK/PD modelling that demonstrates that the 40mg dose achieves therapeutic drug concentrations at the EC50 for all patients. The relationship between concentration and effect is immediate and reversible. They also describe via this population analysis that the population half-life of Clotgone is 4 hours. From this population PK analysis, the FDA approved dosing schedule for Clotgone ® is 40mg every 8 hours. You are presenting Clotgone® to a group of prescribers who will start using this new anti-coagulant in their patients. Please answer the following questions using pharmacokinetic/pharmacodynamic principles:[Fill in the blank] If I prescribe double the dose i.e. 80mg will I get double the anti-coagulation and therefore reduced risk of clotting?[Fill in the blank] If I give double the dose i.e.80mg, will I get double the duration of anticoagulation?[Fill in the blank] We know that there is greater compliance when people take medicines once daily. Also, all other anticoagulants on the market are currently a single daily dose. Would you get the same anti-coagulation relief if I prescribed 120mg (3 x 40mg tablets) once daily vs 40mg every 8 hours?[Fill in the blank]

Drug A and drug B each are administered as the same type of formulation (immediate-release table) and both have an elimination half-life of 3h. Drug B is affected by a genetic polymorphism while drug A is not. What can you conclude about the desired dosing interval?[Fill in the blank]

More Practical Tools for Students Powered by AI Study Helper

Join us and instantly unlock extensive past papers & exclusive solutions to get a head start on your studies!