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Designing a Dosing Regimen for Aminophylline: Calculating Plasma Levels, Assignments of Health sciences

A case study on designing a dosing regimen for a patient named mr. Jm who is to be treated with aminophylline for asthma. Calculations to determine the dosing interval, dose, and steady-state peak and trough levels based on the patient's weight, bioavailability, and pharmacokinetic parameters. The document also discusses the importance of considering the therapeutic window and the need for a loading dose.

Typology: Assignments

Pre 2010

Uploaded on 03/18/2009

koofers-user-blv
koofers-user-blv 🇺🇸

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Download Designing a Dosing Regimen for Aminophylline: Calculating Plasma Levels and more Assignments Health sciences in PDF only on Docsity! Diskette #2/Case Studies/Designing.. 1 PHA 5127 Designing A Dosing Regimen Answers provided by Jeffrey Stark Mr. JM is to be started on aminophylline for the treatment of asthma. He is a non-smoker and weighs 60 kg. Design an oral dosing regimen for this patient such that the theophylline plasma levels are within the therapeutic window. Assume very fast absorption of the tablet. The following information is provided: F(bioavailability) = 1 Aminophylline is 85% theophylline by weight Vd = 0.5 L/kg 100 mg aminophylline tablets are available Cl = 40 ml/hr/kg therapeutic window is 10-20 mg/L 1) Determine Vd and Cl for this patient based on the normal values given above. Calculate ke. 2) Determine the dosing interval using the relationship between τ and the fluctuation factor F. The dosing interval should be practical (i.e. some factor of a 24-hour period). 3) Use the average steady-state equation to determine the dose. Note that only 100 mg tablets of aminophylline are available here. 4) Calculate the steady-state peak and trough levels based on this dosing regimen to verify that the theophylline levels are within the therapeutic range. 5) What information is needed to better design a dosing regimen for this patient? 6) How many doses will it take to reach steady-state plasma levels? If the dose or the dosing interval is changed, how long will it take to again reach the steady-state? 7) Suggest a loading dose to decrease the amount of time required to reach a therapeutic level. What would be the peak concentration after this loading dose? Working through this problem should help you understand where many of the equations we have seen come into play. Diskette #2/Case Studies/Designing.. 2 Answers by Jeffrey Stark 1) Vd, Cl, and ke may be estimated for this patient using the average values given as per kilogram. Vd = (0.5 L/kg)(60 kg) = 30 L Cl = (40 ml/hr/kg)(60 kg) x (1L/1000ml) = 2.4 L/hr It is now possible to calculate ke: Cl = ke Vd Which rearranges to give 1080.0 30 /4.2 −=== hr L hrL V Clk d e 2) The dosing interval τ can be determined using the equation: ek Fln=τ , where F is the fluctuation factor that relates the Cpss (peak) and the Cpss (trough) (min) (max) ss ss Cp Cp F = Since we want the dosing regimen to produce plasma levels within the therapeutic window, we can use Cpss(max) = 20 mg/L And Cpss(min) = 10 mg/L Then, 2 /10 /20 == Lmg LmgF The dosing interval should be: hr hrk F e 66.8 08.0 2lnln 1 === −τ We can round this number down to 8 in order to dose three thimes per day τ = 8 hr
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