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