Traditionally, drugs were extracted from plants or microorganisms such as moulds
Digitalis and digoxin are drugs extracted from foxglove. Aspirin originates from a compound found in the bark of willow trees, its properties first recorded in 400 BC
In 1982, AlexanderFleming was growing bacteria. After returning from holiday, he noticed moulds growing on his plates
He noticed a clear ring in the agar around the spots of mould and realised something had killed the bacteria
Fleming called the substance penicillin after the penicillium mould that produced it
There is a drive to find new medicines but it is difficult to find chemicals that kill bacteria without damaging human cells
A good medicine is:
effective - it must prevent or cure a disease
safe - it must not be too toxic or have serious side effects
stable - you must be able to use the medicine under normal conditions and store it for some time
Testing a new drug can take up to 12 years and cost 1.7 billion pounds
Pre-clinical trials
New drugs are tested in the lab on cells and tissues for efficacy (effective - cures the disease) and toxicity. If they pass the test, they are tested on animals
Clinical trials
The drug is now tested on healthy volunteers and patients at low dose for side effects
Then on small number of patients for efficacy
Larger number of patients to find the optimum dosage
Trials on humans involve double-blind trials where half the patients are given the drug and half are given a placebo (e.g. a pill that does not contain the new drug).
Neither the patient nor the doctor know who has received the drug or the placebo to avoid bias.
If both groups improve in a similar way, the patients improved because of the placebo effect (when the patients improve simply because they think they are being treated for the illness)
The results are published in scientific journals after being scrutinised by peer-review, which means other scientists can check the results