Quinolones and fluoroquinolones

Pharmacology of quinolones and fluoroquinolones

2. Quinolones were first developed in the 1960s
and can be classified into generations based
on antimicrobial activity.
First Nalidixic acid in 1962.

3. Quinolones

4. First Generation
Gram-negative, but
Pseudomonas spp.
Second Generation
Gram-negative, some gram-
positive and mycobacteria.
Third and Fourth Generation
Have increased activity against
gram-positive pathogens
including S. pneumoniae. They
are also active against many
agents causing zoonotic
infection and against
mycobacteria.

5. First Generation
Cinoxacin
Nalidixic Acid
Oxolinic acid
Second Generation
Ciprofloxacin
Enoxacin
Fleroxacin
Lomefloxacin
Levofloxacin
Norfloxacin
Ofloxacin
rulfloxacin
Third Generation
Gatifloxacin
Grepafloxacin
Pazufloxacin
Sparfloxacin
Tosufloxacin
Fourth Generation
Clinafloxacin
Gemifloxacin
Moxifloxacin
Trovafloxacin

6. Quinolones

7. The fluoroquinolones act
by inhibiting type 2
bacterial DNA
topoisomerases, DNA
gyrase and
topoisomerase IV. They
bind to and trap the
enzyme-DNA complex.
This blocks DNA
synthesis and cell
growth and ultimately
has a lethal effect on the
cell.

8. Quinolones

9. The fluoroquinolones are potent bactericidal agents against:
 E. coli and various species of Salmonella, Shigella, Enterobacter,
Campylobacter, and Neisseria
Ciprofloxacin is more active than norfioxacin against P. aeruginosa
Fluoroquinolones also have good activity against staphylococci,
including methicillin­resistant strains
Several intracellular bacteria are inhibited by
fluoroquinolones these include species of Chlamydia,
Mycoplasma, Legionella, Brucella, and
Mycobacterium (including Mycobacterium tuberculosis)

10. Quinolones

11. Resistance to quinolones may develop during
therapy via mutations in the bacterial
chromosomal genes encoding DNA gyrase or
topoisomerase IV, or by active transport of the
drug out of the bacteria.

13. Quinolones

14. Agent AdministrationAbsorption Half-Life (hrs)Disposition
Norfloxacin Oral 50% 4 (8 in anuria)M (20%)
R (27%)
CiprofloxacinOral, IV 75% 4 (10 in anuria)R (50%) M
Levofloxacin Oral, IV 98% 7 R (80%)
Gatifloxacin Oral, IV 96% 7-8 R (70%)
Moxifloxacin Oral, IV 89% 10-14 R (20%)
M (25%) (in liver)
NitrofurantoinOral Adequate 0.6-1.2 R, M (in tissue)
Polymyxin B Topical, oral, IVNot absorbed in
adults; absorbed
in children
6 by IV R
M, Metabolized; R, renal excretion as unchanged drug.

15. Quinolones

16. Disease Recommendations
RESPIRATORY TRACT INFECTIONS
Pharyngitis, otitis media Not appropriate
Necrotizing otitis Ciprofloxacin for Pseudomonas
aeruginosa
Sinusitis Third-generation fluoroquinolone
Community-acquired pneumoniaThird-generation fluoroquinolone
Hospital-acquired pneumonia Ciprofloxacin, for susceptible gram-
negative pathogens
URINARY TRACT INFECTIONS
Cystitis, uncomplicated All effective (second generation
most appropriate)
Pyelonephritis All effective (second generation
most appropriate)
Prostatitis All effective
SKIN STRUCTURE INFECTIONS
Primary cellulitis Not appropriate as first line therapy
Anaerobic soft-tissue infectionsNot appropriate

17. Disease Recommendations
OSTEOMYELITIS
Gram-negative bacterial infectionsCiprofloxacin
BACTERIAL DIARRHEAL
DISEASES
Ciprofloxacin used most commonly;
all considered likely to be effective
SEXUALLY TRANSMITTED DISEASES
Gonorrhea Resistance testing required
Chlamydia Ofloxacin, levofloxacin
Chancroid All likely to be effective
Mycoplasma Ofloxacin, levofloxacin
Syphilis Not appropriate
MYCOBACTERIAL DISEASES
Disseminated M. avium complexCiprofloxacin, ofloxacin as fourth
agent if needed
M. tuberculosis Ofloxacin, levofloxacin for drug-
resistance or intolerance to first-
line agents

18. Quinolones

19. Gastrointestinal effects
Central nervous system agitation (rarely seizures)
Damage to growing cartilage (not recommended for use in
children)
Theophylline interaction (with ciprofloxacin)