Pharmacokinetics

Sutomo Tanzil
Dept.of Pharmacology, Faculty of
Medicine, Sriwijaya University
The movement of drug molecules
across cellular barriers (1)
 To traverse cellular barriers (e.g.GI mucosa,
renal tubule, blood-brain barrier, placenta),
drugs have to cross lipid membranes.
 Drugs cross lipid membranes mainly (a) by
passive diffusional transfer and (b) carrier-
mediated transfer
 The main factor t/ determines the rate of
passive diffusional transfer across membranes
is a drug‟s lipid solubility. Molecular weight is
a less important factor.



The movement of drug molecules
across cellular barriers (2)
 With weak acids or bases only the unionised
forms can diffuse across lipid membrane; this
gives rise to pH partition.
 pH partition means t/ weak acids tend to
accumulate in compartments of relatively high
pH, whereas weak bases do the reverse.(ion
trapping phenomenon)
 Carrier-mediated transport is important for
some drugs t/ are chemically related to
endogenous substances.

Passive diffusional transfer
 Lipid solubility
 pH & ionization
 Not selective, no energy required,
not saturable, cannot be inhibited
 pH partition & ion trapping
 Most drugs across cell membrane
by this transfer.
Carrier-mediated Transport(CMT)
 Carrier molecule: a protein which binds molecules or ions, and
releases them on the other side of the membrane.
 CMT may operate without energy by facilitating the process of
transfer in the direction of its electrochemical gradient and the
mechanism is called facilitated diffusion. Eg.the transfer of
glucose across a muscle cell membrane mediated by GLUT4.
 CMT can also occur against an electrochemical gradient and is
called active transport. Eg.: sodium pumps, Na-Ca exchange.
 CMT shows the characteristic of saturation, and can be inhibited
competitively by a second ligand that binds the carrier.





Intravenous administration (i.v)
 Absorption circumvented w/ potentially immediate
effects. Suitable for large volume & for irritating
substances.
 Valuable for emergency use
 Permits titration of dosage
 Usually required for high-molecular weight protein
and peptide drugs
 Increased risk of adverse effects
 The solution must be injected slowly as a rule
 Not suitable for oily solutions or poorly soluble
substances.
Subcutaneous administration (s.c)
 Absorption is prompt, from aqueous
solution, slow and sustained from
repository preparations.
 Suitable for poorly soluble
suspensions and for instillation of
slow-release implants
 Not suitable for large volumes
 Possible pain or necrosis from
irritating substances.
Intramuscular administration (i.m.)
 Absorption is prompt from aqueous
solution, slow and sustained from
repository preparations.
 Suitable for moderate volumes, oily
vehicles, and some irritating substances.
 Precluded during anticoagulant therapy,
and may interfere w/ interpretation of
certain diagnostic tests (e.g.creatine
kinase)
Oral/Enteral administration
 Absorption is variable, depends on many
factors
 Most common method of drug adminis-
tration.It is also the safest,most conve-
nient, and most economical.
Disadvantages include limitation of
absorption of some drugs because of their
physical characteristics (eg.water
solubility), it also requires patient
compliance
 Bioavailability is potentially erratic and
incomplete.
Drug absorption and bioavailability
 Drugs w/ low lipid solubility are poorly absorbed from the
gut.
 A few drugs (eg.levodopa) are absorbed by CMT.
 Absorption from the gut depends on: -GI motility, -GI pH,
particle size, -physicochemical interaction with gut
contents (eg. Ca and tetracycline antibiotics)
 Bioavailability is the fraction of an ingested dose of a
drug that gains acces to the systemic circulation. It may
be low because absorption is incomplete, or because the
drug is metabolised in the gut wall or liver before reaching
the systemic circulation.
 Bioequivalence implies that if one formulation of a drug
is substituted for another no clinical untoward
consequences will ensue.
Methods for delaying absorption
 Addition of adrenaline (epinephrine)
to a local anesthetic
 „slow-release‟ form : procaine-
penicillin,medroxyprogesterone
acetate, testosterone propionat,
flufenazine decanoate
 Insulin zinc suspensions
 Subcutaneous implantation of solid
pellets
Drug distribution (V
d
)
 V
d
: the volume of plasma that would contain the
total body content of the drug at a concentration
equal to that in the plasma.
 Lipid insoluble drugs :confined to plasma and the
interstitial fluids; most do not enter the brain .
 Lipid-soluble drugs reach all compartments, and
may accumulate in fat.
 For drugs that accumulate outside the plasma
compartment (eg. in fat, or being bound to tissues)
V
d
may exceed total body volume.
Drug metabolism
 Phase I reactions:oxidation,reduction & hydrolysis.
These usually form more reactive products,sometimes
pharmacologically active, toxic or carcinogenic. Phase I
oftenly involve cytochrome P450 enzymes.
 Phase II reactions : conjugation (eg.glucuronidation) of
a reactive group (often inserted during phase I) and
form inactive and readily excretable products.
 Some conjugated products are excreted via bile, are
reactivated in the intestine and then reabsorbed.
 Induction of enzymes by other drugs and chemicals
can greatly accelerate hepatic drug metabolism.
 Some drugs show rapid “first-pass” hepatic
metabolism, and thus poor oral bioavailability.
Inhibition of P450
 Ketoconazole (an antifungal) which
forms a complex with CYP3A4,
causes a non-competitive inhibition
with a risk of a fatal cardiac
arrhythmia if the drug is given
concomitantly with terfenadine (an
antihistamine).
Induction of P450
Enzyme inducers: ethanol,rifampicin,
carbamazepine,increase the activity of
microsomal oxidase and conjugating
systems when administered repeatedly

Glomerular filtration
 Drugs w/ MW <20,000 can cross
the glomerular filter, but plasma
albumin (MW 68,000) cannot.
 If a drugs is highly bound to plasma
albumin (eg. Warfarin 98% bound),
its concentration in glomerular
filtrate is very low (only 2%
warfarin).
Tubular secretion
 20% of renal plasma flow is filtered through the
glomerulus, leaving 80% of the delivered drug to pass
on to the peritubular capillaries of the proximal tubule.
Here drug molecules are transferred to the tubular
lumen by 2 independent carrier systems.One of these
transport acidic drugs, while the other handles organic
bases.
 These active transport can transport drug molecules
against an electrochemical gradient and can, therefore
, reduce the plasma concentration nearly to zero. Since
80% of the drug delivered to the kidney is presented to
the carrier, tubular secretion is potentially the most
effective mechanism of renal drug elimination, even
when most of the drug is bound to plasma protein (e.g.
penicillin)
Diffusion across the renal tubule
 As the glomerular filtrate traverses the
tubule, water is reabsorbed, so that the
volume of urine only about 1% of the
filtrate.
 High-lipid soluble drugs are excreted
slowly,while polar &low lipid soluble drugs
remain in the tubule & its concentration in
the urine is 100 times >than in plasma.
 The ion-trapping effect :a basic drug is
more rapidly excreted in an acid urine,
because the low pH within the tubule
favours ionization and thus inhibits
reabsorption.
Biliary excretion and enterohepatic
circulation
 Liver cells transfer various substances, including
drugs, from plasma to bile by means of transport
systems similar to those of the renal tubule and
which involve P-glycoprotein.
 Drug conjugates (particularly glucoronides) are
concentrated in the bile and delivered to the
intestine where the glucuronide is usually
hydrolysed, releasing active drug once more. Free
drugs can then be reabsorbed and the cycle
repeated (enterohepatic circulation).
 Examples :morphine, ethinylestradiol, and
rifampicin.
Effect of variation in rate of absorption
 Absorption rate constant , k
abs
, is
directly proportional to the amount
of drug which is still unabsorbed
 Area under the curve (AUC) is
directly proportional to the total
amount of drug that enters the
plasma.
 Oral Bioavailability = AUC
oral
/ AUC
iv
 Intravenous bioavailability = 100%
Saturation kinetics
 E.g. Ethanol, phenytoin, salicylate
 The rate of disappearance of ethanol
from the plasma is constant at about 4
mmol/L per hour irrespective of its
plasma concentration.
 Also oftenly termed as „zero-order
kinetics‟
 The rate of drug metabolism by hepatic
enzymes reaches a maximum at low
plasma concentration.
References and Further Reading
 Brunton,L.L.; et al.(2006). Goodman &
Gilman‟s The Pharmacological Basis of
Therapeutics, 11
th
Ed.,McGraw-Hill
Medical Publishing Division, USA.
 Katzung,B.G.(2007).Basic&Clinical
Pharmacology,10
th
Ed., McGraw-Hill,USA.
 Rang & Dale (2003). Pharmacology, 5
th

Ed.,Churchill Livingstone, London, UK.
 Staf Pengajar Dep.Farmakologi FK Unsri
(2008). Kumpulan Kuliah Farmakologi,
Edisi 2, EGC,Jakarta.