The late detection of cardiotoxic side effects, such as QT prolongation, in
duced by compounds of pharmacological interest can dramatically impede drug
discovery and development projects, and consequently increase their cost.
The launch of new drugs with undetected cardiotoxic side effects could have
hazardous consequences and could trigger lethal cardiac dysrhythmias in pa
tients. It is desirable, therefore, to test for the potential cardiotoxic s
ide effects of compounds at an early stage of drug development. Electrophys
iological test systems and cellular-based fluorometric high-throughput assa
ys are now available for cloned human cardiac ion channels. These test syst
ems are important fools in the preclinical safety evaluation of drugs and n
ewly developed compounds.