Professional Documents
Culture Documents
com
108 Basic Pharmacokinetics
WFLDIOASFHILASDF
JIASDFHOASDFNIHI
OSDFNLSDFAHIOHA
SDFJIOHASDFLJASD
FIOHIOASFHIOHASD
FIOJNASDFIOHIOAS
DFJIOASDFHIOASDF
NIODFSHOASDFNDFI
SHASDFIONLSDFJHI
OADFASDFHIOASDF
HNIOSDFHSDFIOHS
DFIOHSDFIODFHIOS
DFHSDFIOAFHIODFS
HIOHSDFIOHSDFIOS
DFHIOSDFHSDFIOHS
DFIOHSDFIOHFDAP
´FIO'I4´9Q3435
´GI0NSG'I´KPFGISDF
Figure 6.2 Passage of drug in the gastrointestinal tract until transport across the membrane.
SCHEME:
Xa Ka (h–1) X K (h–1)
(drug in Xu
(Absorbable body or
drug at absorption Absorption Elimination
site) blood)
SETUP:
Ka K
Xa X Xu
Figure 6.3 Absorption of a one-compartment drug with first-order elimination, where Xa is the mass or amount of absorbable
drug remaining in the gut, or at the site of administration, at time t (i.e., drug available for absorption at time t); X is the mass or
amount of drug in the blood at time t; Xu is the mass or amount of drug excreted unchanged in the urine at time t; Ka is the
first-order absorption rate constant (h−1 or min−1 ); and K (or Kel ) is the first-order elimination rate constant (h−1 or min−1 ).