Multiple Compartment PK Flashcards
General Information
- Time course and extent of distribution and elimination of drug from body determines its disposition
- Body may be viewed as a number of kinetic compartments between which drug distributes and from which elimination occurs
- Rarely do these kinetic compartments have true physiological basis
- Blood, readily available fluid, and well-perfused tissues may be treated as a homogeneous unit known as central compartment (brain may or may not be included here depending on the lipophilicity of the drug)
- Drug levels in poorly perfused tissues (muscles, lean tissue, fat) may be treated kinetically as peripheral compartment
Representation of Data
- 3 possible Models
- Always have k12 and k21
- Can leave central compartment only (k10), peripheral compartment only (k20), or both compartments (10 & 20)
- Difficult to determine which model is correct
- Most common: leaving central compartment only
Z
-Number of solvable rate constants when sampling from a central compartment
Z = 2(n-1) + 1
-For a two compartment model, Z = 3, but one of the models has four rate constants
IV: Two Compartment Model Variables
Xc = amount of drug in central compartment Xp = amount of drug in peripheral compartment k12 = transfer rate constant of central ==> peripheral K21 = transfer rate constant of peripheral ==> central k10 = elimination rate constant from central
IV Assumptions
- Drug elimination occurring from central compartment only
- There is time required for drug to equilibriate between two compartments
- Drug elimination and distribution is governed by first order kinetics
Order to Solve Rate Constants
K21 ==> K10 ==> K12
Are lambda2 and K10 the same parameter?
No. Lambda includes both distribution and elimination while K10 is only elimination from the central compartment.
Vc - IV
Volume of distribution in central compartment
Vc = Dose / (C1 + C2)
Css Volume - IV
Rate of drug entry into both compartments form the other are equal at Css
Vss = Vc * [1 + K12/K21]
- *Function of transfer rates, NOT effected by elimination changes, true volume of distribution**
- Useful when seeing is a disease or drug-drug interaction affects the body’s ability to eliminate drug or space for drug distribution
Clearance
Cl = F * Dose / AUC
Same equation for oral and IV
AUC - IV
2-compartment : AUC = C1/lambda1 + C2/lambda2
Continue pattern for as many compartments in model
AUMC
- Area under first moment curve
- t * C = first moment, since C is multiplied by time raised to power of 1
- AUMC is calculated as t*C is intergrated from 0 to infinity
MRT
- Mean Residence Time
- Average time drug resides in the body
- Only parameter that requires multiple half lives
- Useful when comparing 2 systems (health v.s. disease)
Multiple Compartment Models: Oral
- Difficulties in modeling since 3 biological processes are included: absorption, distribution, and elimination
- Overall representation of equations and models are more complex and require special computers to calculate the parameters
- Visual determination of 2-compartment characterisitcs of oral medication are not always possible and need curve-fitting software to determine
- Drug usually given IV to determine if it follows the 2-compartment system
Oral Multiple Compartment Variables
Xa = amount of drug in absorption compartment
Ka = absorption rate constant
All other variables are the same as IV
Vc - Oral
F * Dose / AUC *k10
Vss - Oral
F * Dose / AUC * lambda2
Are transfer constants calculated the same way in oral and IV compartment models?
Yes, they are unaffected by absorption.
Equations not included
Equations not included were too complicated to type out and should be included on the equation sheet, make sure you are familiar with them for the exam.