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Transcript
CCP Main Text
25/10/06
1:06 pm
Page 2
1 Introduction to pharmacology
Pharmacology is the scientific study of the properties of drugs and their
interaction with living organisms, including viruses.1 The term ‘drug’ is in
common usage for any chemical used to treat disease or for recreational
purposes. Strictly speaking, the term describes any chemical that is used to
change the activity of a living cell.
Pharmacology has two main branches: pharmacodynamics and
pharmacokinetics. Pharmacodynamics is the study of the interaction of drugs
with cells. It can be thought of as how the drug affects the body.
Pharmacokinetics is the study of how the body handles the drug, including
how it is absorbed and distributed among the various compartments of the
body, how long it remains in the body in a therapeutically effective form, and
how it is metabolised and excreted. Pharmacology also embraces the study of
adverse reactions to drugs, drug–drug interactions and the consequences of
drug overdose. Pharmacology also covers toxicity of chemicals.
Clinical pharmacology is devoted mainly to the choice and use of drugs to
prevent and treat disease and to the consequences of drug misuse. Clinical
pharmacology is nowadays becoming more and more involved in the socioeconomic implications of clinical drug use. An example of this is the relatively
new science of pharmacovigilance, which is concerned with the follow-up of
drug use, and pharmacoeconomics, which examines the economic implications
of prescribing and dispensing increasingly more expensive treatments.
Drugs may originate from natural sources or be synthesised. Digoxin, for
example, was originally extracted from the foxglove, Digitalis purpurea, but is
now synthesised. Once a drug is identified as a possible treatment for a specific
condition, it undergoes an intensive battery of tests to determine its mechanism
of action, its potency, its specificity of action and its safety for the patient. The
drug’s fate in the body is studied, as well as its effects on the tissues and organs.
Its possible teratogenicity (ability to harm the unborn embryo or fetus) is also
investigated. Once a suitable dose and formulation are decided upon, the drug
undergoes rigorously controlled clinical trials, and if it passes all tests it may
be licensed for use in patients. Clinical pharmacology encompasses all aspects
of the drug’s use in patients, both before and after licensing.
Modern clinical pharmacology involves the expertise not only of doctors,
but also of nurses and pharmacists, who are involved in the choice of drug, and
dosage and administration, especially in hospitals. In outlying districts and in
developing countries, the pharmacist and nurse are often the only immediate
resource for patients, both for advice and for the monitoring of, for example,
adverse drug reactions and patient compliance. Pharmacists have prescribed
some remedies for hundreds of years. Nurses, both in hospital and in the
community, are now prescribing certain drugs and need pharmacological
knowledge to underpin their use of drugs for patients and to treat, for
example, adverse reactions and overdose.
2
CCP Main Text
25/10/06
1:06 pm
Page 3
natural
sources
extraction,
purification
biotechnology
chemical
synthesis
drug
pharmacodynamics
(what the drug does to the body)
pharmacokinetics
formulation
and delivery
mechanism
of action
absorption
distribution
receptors signal
transduction
metabolism
assays of the drug
bioassay
radioimmunoassay (RIA)
radioligand assay
ELISA (enzyme-linked
immunosorbent assay)
agonists and
antagonists
log10 dose–response
curves
excretion
half-life
compartmentalisation
excretion
toxicity studies
clinical trials
pharmacoeconomics
pharmacovigilance
Introduction to Pharmacology
3