Multiple Compartment PK Flashcards

1
Q

General Information

A
  • 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
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2
Q

Representation of Data

A
  • 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
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3
Q

Z

A

-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

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4
Q

IV: Two Compartment Model Variables

A
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
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5
Q

IV Assumptions

A
  • 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
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6
Q

Order to Solve Rate Constants

A

K21 ==> K10 ==> K12

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7
Q

Are lambda2 and K10 the same parameter?

A

No. Lambda includes both distribution and elimination while K10 is only elimination from the central compartment.

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8
Q

Vc - IV

A

Volume of distribution in central compartment

Vc = Dose / (C1 + C2)

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9
Q

Css Volume - IV

A

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
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10
Q

Clearance

A

Cl = F * Dose / AUC

Same equation for oral and IV

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11
Q

AUC - IV

A

2-compartment : AUC = C1/lambda1 + C2/lambda2

Continue pattern for as many compartments in model

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12
Q

AUMC

A
  • 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
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13
Q

MRT

A
  • 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)
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14
Q

Multiple Compartment Models: Oral

A
  • 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
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15
Q

Oral Multiple Compartment Variables

A

Xa = amount of drug in absorption compartment
Ka = absorption rate constant
All other variables are the same as IV

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16
Q

Vc - Oral

A

F * Dose / AUC *k10

17
Q

Vss - Oral

A

F * Dose / AUC * lambda2

18
Q

Are transfer constants calculated the same way in oral and IV compartment models?

A

Yes, they are unaffected by absorption.

19
Q

Equations not included

A

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.