ROUTES OF ADMINISTRATION
ORAL ROUTE
FOR LOCAL EFFECT
Oral drug administration may be used to produce local effects
within the gastro-intestinal tract. Examples include antacids,
and sulphasalazine, which delivers 5-amino salicylic acid
(5-ASA) to the colon, thereby prolonging remission in patients
with ulcerative colitis (Chapter 34). Mesalazine has a pH-
dependent acrylic coat that degrades at alkaline pH as in the
colon and distal part of the ileum. Olsalazine is a prodrug con-
sisting of a dimer of two 5-ASA moieties joined by a bond that is
cleaved by colonic bacteria.
FOR SYSTEMIC EFFECT
Oral administration of drugs is safer and more convenient for
the patient than injection. There are two main mechanisms of
drug absorption by the gut (Figure 4.4).
Passive diffusion
This is the most important mechanism. Non-polar lipid-soluble
agents are well absorbed from the gut, mainly from the small
intestine, because of the enormous absorptive surface area
provided by villi and microvilli.
Active transport
This requires a specific carrier. Naturally occurring polar
substances, including sugars, amino acids and vitamins, are
absorbed by active or facilitated transport mechanisms. Drugs
that are analogues of such molecules compete with them for
transport via the carrier. Examples include L-dopa, methotrex-
ate, 5-fluorouracil and lithium (which competes with sodium
ions for absorption).
Other factors that influence absorption include:
- surgical interference with gastric function– gastrectomy
reduces absorption of several drugs;
2.disease of the gastro-intestinal tract(e.g. coeliac disease,
cystic fibrosis) – the effects of such disease are
unpredictable, but often surprisingly minor (see
Chapter 7);
3.the presence of food– the timing of drug administration in
relation to meal times can be important. Food and drink
dilute the drug and can bind it, alter gastric emptying and
increase mesenteric and portal blood flow;
ROUTES OFADMINISTRATION 19
Passive diffusion of a
water-soluble drug
through an aquas
channel or pore
Passive diffusion
of a lipid-soluble
drug
Carrier-mediated
active transport
of drug
Lumen
Drug
Epithelial
cell
membrane
ATP
D
D
D
D D
D
D
D
D D
D
D
D
D
Figure 4.4:Modes of absorption of drugs
from the gut.
PRODRUG DRUG
Relatively well-
absorbed and/or
good tissue
penetration
INACTIVE
Various
enzymes
in body
Relatively poorly
absorbed and/or
poor tissue
penetration
ACTIVE
Figure 4.3:Clinical use of prodrugs.
Table 4.1:Prodrugs
Prodrug Product
Enalapril Enalaprilat
Benorylate Aspirin and paracetamol
Levodopa Dopamine
Minoxidil Minoxidil sulphate
Carbimazole Methimazole
Vanciclovir Aciclovir