Pharmacokinetics: Two-Compartemet Model
Pharmacokinetics: Two-Compartemet Model
Two-compartemet Model
Ahmad Muhtadi
FACULTY OF PHARMACY
UNIVERSITAS PADJADJARAN
Two-compartemen
( intravascular)
Characteristics :
No absorption
All injected drug is in the systemic circulation
Slow distribution of drugs between blood stream and tissue
Equalibrium (stady state) is obatain some later time after
administration
Steep fall of first part of blood level curve due to distribution
Decline of second part of blood level curve depends on back
distribution of drug from tissue to the blood, exretion and
metabolism.
Two-compartemen
( intravascular)
Model :
PC
Cpo
C1’ C1 diff
A
C2 diff
B C2’
C1
C2
C1
C2
β
α
t1’ t2’ t1 t2
Time
Rate Constanta :
β = ( ln C1 – ln C2 ) hour -1
( t2 - t 1 )
k 21 = (A . β + B . α ) hour -1
( Cpo )
K 13 = ( Cpo )
( A + B)
hour -1
α β
Cpo = A + B ( μg/ mL)
A= ( α – k 21 ) ( μg/ mL)
(α–β)
B= ( k 21 – β) ( μg/ mL)
(α–β)
α . β = k21 . k13
Half life :
t½ α = 0,693 hour
α
t½ β = 0,693 hour
β
Volume Distribution :
Ve = D ( mL )
Cpo
Vd ss = Ve + Vt ( mL )
Vd ss = ( k 12 + k 21 ) . Ve ( mL )
k 21
Volume Distribution :
B = D. ( k21 – β ) ( mL )
Ve . ( α – β )
Vd ekstrapolasi = D = Ve. ( α – β ) ( mL )
B ( k21 – β )
Vd area = Vd ss + k13 – β . Ve ( mL )
k21– β
AREA UNDER CURVE (AUC)
Cp = B.e-βt + A.e-αt
Cp.dt = B.e-βt + A.e-αt
[ AUC ] = B + A
β α
[AUC] = ( B . β+ A . α )
(β.α)
[AUC] = ( B + A )
k13
[AUC] = D
( k13 . Ve )
Clirens :
Cl = D
[ AUC ]
BIOAVAIILABILITY (F) :
F absolut : { [AUC] po }
{ [AUC] iv }
F relatif : { [AUC] po }
{ [AUC] po* }
* = drug standard
Problem :