Adverse effects   

      Drug Interactions 

      Pharmacological outline of Sparfloxacin

      FUTURE DEVELOPMENTS  of Quinolones 

      Conclusion

Adverse Drug Effects

1. Gastro Intestinal Tract – All quinolones have varying degrees of  GIT irritation ranging from mild nausea to severe gastritis which can be limited by administering ½ hr after food.

Antacids / Divalent cations /H2 antagonists reduce  GIT absorption and hence should not be used for treating  GIT adverse effects.

2. Central Nervous System effects-  The mechanism is not known  probably interfering with  GABA activity ?  A direct pharmacological effect.

• The Pharmacodynamic Drug interactions with  NSAIDs manifest sometimes as  convulsions (enoxacin X fenbufen)

• The Pharmacokinetic drug- drug interaction with Theophylline.

• Sparfloxacin is devoid of proconvulsant activity

• Proconvulsant activity with

• Pefloxacin > enoxacin  >  Ofloxacin > Norfloxacin > Cinoxacin >  

• Ciprofloxacin > Nalidixic acid  etc.,

3.  Cardio Vascular System Toxicity :- Both Sparfloxacin and Grepafloxacin are implicated in producing QT prolongation syndrome often mild but assumes significance when administered together with other agents like antiarrythmics, Macrolides, Cisapride, Azole antifungals, H1 antagonists like astemizole,cetrizine, terfinadine etc.,

4.  Phototoxicity:   Skin reactions like erythema,pruritus,urticaria and rashes with phototoxicity are often associated.  Sun burns occur when exposed to UV rays  of UVA 320-400nm especially transmitted by the clouds & window panes.

Sparfloxacin, Lomefloxacin Fleroxacin,  show increased incidence of phototoxicity while Trovafloxacin, Grepafloxacin,  and Moxifloxacin  have reduced potential for Phototoxicity. Quinolones exhibit Photomutagenic & even photocarcinogenic effect in animals.. The underlying mechanism appears to be due to the formation of photodegradation products and  leading to the generation of reactive oxygen species.

In this context Newer quinolones are synthesized with chiral modification. It is not definite whether Tocopherols have any protective effect on phototoxicity.

5.  Arthropathy- Interest has been focussed on proteoglycan synthesis and  mitochondrial function. Occurrence of this adverse effect precludes the use of very good antibacterials in paediatrics. Human data from the experience with 3 compound have revealed that Nalidixic acid has poor tissue penetrability and hence did not manifest chodrotoxicity and in the case of  ciprofloxacin and norfloxacin there was reduced AUC and therefore low systemic exposure. In case of Pefloxacin with 5-10  times higher systemic exposure ( Higher AUC) is well known to be associated with high incidence of arthropathy in humans because the drug affects articular cartilage & epiphyseal growth plate. The importance of this toxicity is that it is irreversible and manifest later after the drug is discontinued. The use of Nalidixic acid in UTI and ciprofloxacin in cystic fibrosis (pseudomonal) are officially permitted to be used in paediatrics.  Recently many clinical studies revealed  that newer quinolones  might appear to be safer for paediatric use.

Review of 31 reports involving 7045 paediatric patients  use of  Ciprofloxacin,Nalidixic acid,Pefloxacin,Norfloxacin, Ofloxacin in paediatric cystic fibrosis, no arthropathy was observed.  

Similarly the use of Norfloxacin, Trovafloxacin, and Ciprofloxacin in shigellosis, Salmanellosis, Meningococcal  meningitis showed in incidence of arthropathy in paediatric group.   Trovafloxacin, Gatifloxacin, Clinafloxacin,  and Moxifloxacin  appears more promising for paediatric use.

Further studies are planned in selected paediatric age groups with quinolones before concluding for official use of quinolones (except those already approved) in paediatric infections.

6.  Tendinopthy:

In 1991 Flouroquinolone associated Tendinopathy and tendon rupture have been reported. More than 1000 cases of quinolone induced tendinitis have been reported as per French surveillance in 1997. Clinically manifested as congestion and /or inflammation and oedema of tendon leading to pain and swelling and in more than 50% of cases it was bilateral and then tendon ruptures. 400 cases with in 18 months of treatment with Ofloxacin, Norfloxacin, Ciprofloxacin and Pefloxacin. In more than 70% patients aged 60yrs or above and in 10% of patients receiving concurrent steroid medication. Achilles tendon rupture reported to have occurred 120 days after the start of treatment and can occur even after withdrawal of the drug. Pathologically there was ultrastructure alteration in tendinocytes. In animals ,Mg deficiency aggravated tendinopathy.

Drug Interactions:

           Primary drug-  Quinolones . Interact with

           X  Warfarin  = enhanced  anticoagulation

            X   H2 Antagonists =  quinolone absorption

            X   Cyclosporin  =   toxicity

           X   Rifampicins  = decreases serum concentration of quinolone

           X   NSAIDs  = Convulsions

           X   Insulin & oral hypoglycemics = hypoglycemia.

SPARFLOXACIN:

Sparfloxacin is an orally effective and it is a new diflourinated quinolone with structure similar to ciprofloxacin  with broad antibacterial spectrum  including improved activity against Grampositive, Mycobacteriae, Chlamydiae, Mycoplasmae, and anaerobes with good tissue penetration and long elimination half life.  Its effect is superior against Staphylococci epidermides, E.fecalis, Streptococci pneumonia, C.perfringes & other anaerobes. It is the most appropriate agent for treatment of Urinary Tract Infection, Respiratory tract infection and other systemic infection having both improved patient compliance and greater efficacy .

Clinical trials with Sparfloxacin:

1. Sparfloxacin is well tolerated and effective against obstetric & gynecological  infection

2. Sparfloxacin  exerted strong antimicrobial activity against  Shigellae, Salmonellae, Camphylobacter,  and marked clinical efficacy against enteritis induced by the above organisms.

3. Sparfloxacin found to be very useful in post- surgical infections.

4. Sparfloxacin  in respiratory infections – Excellent activity against S.aureus, Streptococci pneumoniae, Br.catarrhalis,H.influenzae, Mycoplasmae and therefore indicated in URI, ACEB, Diffuse panbronchiolitis, Bronchiectasis, & pneumonia.

5. Sparfloxacin has excellent activity in the following dermatological conditions viz., Folliculitis, Pustular acne, Furunculosis, carbuncles, Impetigo, Erysipelas, Cellulitis, Felon, Lymphangitis, paronychia,SC abscess, Hidradenitis, Infected atheroma, Infected pilinoidal sinus  etc.,

6. Sparfloxacin in Leprosy:

   • Radio respirometric  activity undetectable  after 4 weeks of therapy

   • Serum phenolic glycolipid 1 antigen diminished in all patients

   • Among 20 quinolones, Sparfloxacin was the most active in leprosy

7. Sparfloxacin exerted very good effect in Mycobacterial infections with the exception of M.scrofulaceum and M.chelonae.

8. Sparfloxacin  exhibits highest antimicrobial  potency against Legonellairs infection because of its enhanced penetration into human neutrophils with Intra Cellular concentrations exceeding extracellular concentrations several times. Therefore sparfloxacin is superior bactericidal against M.homins, M.pneumoniae, M.genitaklium, U.urealyticum, M.fermentans.

9. Sparfloxacin has good activity against MAC infection but the role of quinolones in multi- drug regimen for opportunistic infections by MAC in AIDS remains unclear.  

Recent Advances with Newer Quinolones:

1. Grepafloxacin in o/d regimen is superior to ciprofloxacin in Streptococci pneumoniae

2. Gatifloxacin o/d is highly effective in Respiratory & UTI and did not exhibit any phototoxicity.

3. Sitfloxacin useful in treatment of Catheter associated  nosocomial and other infections by Pseudomonas species with less chance for resistance induction .

4. Oral Trovafloxacin is very effective against MDR respiratory pathogen because of its greater penetration into respiratory fluids and secretion.

5. Moxifloxacin is highly effective in  M. catrrhalis, Chlamydiae, Mycoplasmae, Legionellae because of its 10 fold Intra Cellular concentrations  on oral administration.

6. Moxifloxacin is highly active against str. peumoniae (Penicillin/macrolide resistant)

7. Newer quinolones  have greater activity than macrolide or cephalosporins against common respiratory pathogens and therefore useful in;                

-         community acquired pneumonia

-         Penicillin resistant Streptococci pneumonia

-         Beta-lactamase resistant H.influenzae

-         Beta-lactamase resistant Mor.catarrhalis.

H.  Once /day alatrovafloxacin/Trovafloxacin  IV to oral treatment is clinically effective as twice/day IV to oral ciprofloxacin for treatment of nosocomial infections with no additional anaerobic coverage.

Future Quinolones:

·        Greater potency

·        Reduced frequency of resistance selection

·        Better CNS/CSF penetration

·        Improved safety & tolerability

·        Greater activity against gram+ve species

·        Effective against IC pathogens

·        Enhanced activity against anaerobes

·        Suitable for paediatric use.

Conclusion:

NEWER QUINOLONES APPEAR TO HAVE A HEALTHY FUTURE ?

Glossary

MBC - Min bactericidal concentration @ which no colony forms after 24 hrs of incubation @ 35’ C

MIC – Defined as the lowest concentration of antibacterial agent that inhibits the development of visible growth in the broth.

PAE – Post Antibiotic Effect is the term used to describe suppression of bacterial growth that persists after short exposure of organism to antimicrobial agent. PAE may have a clinical effect on antimicrobial dosage.