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Fase de Disposición Lenta/eliminación: BETA: T (H) CP Real (Ug/ml) LN CP Real
Fase de Disposición Lenta/eliminación: BETA: T (H) CP Real (Ug/ml) LN CP Real
M
0 0 Err:502 C
0.5 20.6 3.02529107579554
1 13.4 2.59525470695687 20
2 7.3 1.98787434815435
3 5 1.6094379124341
4 3.7 1.30833281965018 15
6 2.2 0.78845736036427
Cp real (mg/L)
8 1.4 0.33647223662121
10 0.82 -0.1984509387238 10
12 0.5 -0.6931471805599
5
Fase de eliminación beta
r -0.9997541338681
r2 0.9995083281863
0
0 1 2 3 4
b 2.304280179274
B0 10.01696523751 ug/mL
m (beta) -0.24949341498 h -1
t 1/2 2.778218337459 h
Fase alfa
r -0.999981424412
r2 0.9999628491691
b 3.237303823599
A0 25.464971053 ug/mL
m (alfa) -1.52433883664 h -1
t 1/2 0.454719885039 h
PARÁMETROS FARMACOCINÉTICOS
Dosis 500000 ug
alfa 1.5243388366444 1/horas
beta 0.2494934149754 1/horas
A0 25.464971053001 ug/mL
B0 10.016965237505 ug/mL
t1/2 alfa 0.4547198850394 horas
t1/2 beta 2.7782183374589 horas
Cp0 35.481936290507 ug/mL
ABC 56.854801294064 ug/mL*h
CL 146.57220047665 mL/min
VD 14.09167740752 L
K21 0.6240798575126 1/horas t 1/2 k21 1.110670649302
K10 0.5403552194413 1/horas t 1/2 k10 1.282762071359
K12 0.6093971746659 1/horas t 1/2 k12 1.137430906108
Modelo Bicompartimental
Cp real (ug/mL) vs t(h)
3.5
2.5
Ln Cp real
1.5
0.5
0
0
-0.5
1 2 3 4 5 6 7 8 9 10 11 12 13 -1
t (h)
ln Cp extrap
0
0 0.5 1 1.5 2
t (h)
h
h
h
BETA
Modelo Bicompartimental
Ln Cp real vs t (h)
3.5
2.5
2
Ln Cp real
1.5
1
y=−0.2494x+2.3042
R2=0 .9995
0.5
0
0 2 4 6 8 10 12 14
-0.5
-1
t (h)
LFA
2.5
f(x) = − 1.52433883664435 x + 3.23730382359928
2 R² = 0.999962849169103
1.5
Ln Cp extrapol
0.5
0
0 0.5 1 1.5 2 2.5
-0.5
-1
1.5 2 2.5
-1.5
t (h)
t (h)
-1
-1.5
t (h)
partimental
l vs t (h)
+ 3.23730382359928
2 2.5 3 3.5
(h)
(h)
s de primer orden