Pharmacology for Dentistry

(Ben Green) #1

(Mode of Action of Drugs)


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Chapter


1.4


Chapter


9.6 Antiviral Agents


Viruses have no cell wall and made up of
nucleic acid core enclosed in a protein coat
which consists of identical subunits.
Viruses are of two types, DNA
(deoxyribonucleic acid) viruses and RNA
(ribonucleic acid) viruses. DNA viruses are
herpes simplex, small pox, hepatitis B,
varicellazoster etc. and RNA viruses are
rabies, measles, dengue, rubella, yellow
fever, poliomyelitis and HIV etc.


In viral infections, replication of viruses
are at peak, at or before the manifestation
of clinical symptoms. So, the treatment
generally depends either on early initiation
of therapy or prevention of infection i.e.
chemoprophylaxis.


The various antiviral agents are
classified as under (the doses for specific
infections is given in text) in table 9.6.1.


ANTI-HERPES AGENTS

IDOXURIDINE


It is chemically related to thymidine and
acts by competing with it in the
synthesis of DNA and ultimately
preventing the utilization of thymidine.


It prevents the replication of DNA
viruses and its clinical use is limited to
herpes simplex keratitis.
Toxicity includes alopecia, leucopenia,
thrombocytopenia and liver damage.
It is used in herpes simplex keratocon-
junctivitis in 0.1 to 0.5% solution/eye oint-
ment applied one to two hourly.

ACYCLOVIR
Acyclovir is a synthetic purine
nucleoside analogue with in vitro and in
vivo inhibitory activity against human
herpes viruses.
Acyclovir triphosphate interferes with
the viral DNA polymerase and inhibits
viral DNA replication with resultant chain
termination following its incorporation into
the viral DNA.
Acyclovir is only partially (20%)
absorbed from the gut.
Most of the drug is excreted un-
changed by the kidney by tubular secre-
tion and glomerular filtration.9-
Carboxymethoxymethylguanine is the
only significant metabolite of acyclovir re-
covered from the urine.

Antiviral Agents

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