Quinolones, such as ciprofloxacin and ofloxacin, have gained wide acce
ptance for the treatment of bacterial infections of the respiratory tr
act, urinary tract, skin and soft tissues, as well as sexually transmi
tted diseases. Good pharmacokinetic profiles and potent activities aga
inst a wide range of Gram-negative and Gram-positive pathogens result
in the use of these antibacterials in both hospital and community sett
ings. Although recently developed clinical quinolones dominate in the
chemotherapy of various bacterial infections, their use is restricted
by limited activities against a number of clinically-important Gram-po
sitive bacteria such as Streptococcus pneumoniae, Streptococcus pyogen
es, Staphylococcus aureus, and enterococci. Ciprofloxacin, the market
leader, also has low potency against anaerobes. Bacterial resistance (
such as in Pseudomonas aeruginosa and methicillin-resistant Staphyloco
ccus aureus) to ciprofloxacin is increasing rapidly. Many quinolone co
mpounds are being synthesised to address these drawbacks. The new quin
olones currently under development are characterised by enhanced activ
ities against streptococci, staphylococci, enterococci and anaerobes.
Although the treatment of traditional bacterial infections is at prese
nt the focus of quinolone research, the future role of quinolones will
extend current applications to include new indications of bacterial i
nfections and other non-bacterial diseases. This review will concentra
te on the more recently developed quinolones which possess significant
ly more therapeutic value than existing quinolones, and will provide i
nformation on those compounds under commercial development with major
therapeutic potential. Recent developments in research into the identi
fication of quinolones for the treatment of tuberculous, cancer, viral
, fungal infections and parasitic diseases will also be discussed.