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Cinoxacin in urinary tract infections. Theoretical and practical considerations
Urology
|May 1, 1981
Summary
Cinoxacin concentrations in canine prostate tissue and secretions were lower than serum levels. However, human prostatic tissue concentrations reached levels effective against urinary tract infection pathogens.
Area of Science:
- Pharmacology
- Urology
- Veterinary Medicine
Background:
- Cinoxacin is an antibiotic used for urinary tract infections.
- Understanding drug distribution in prostatic tissue is crucial for effective treatment.
Purpose of the Study:
- To determine cinoxacin concentrations in canine prostatic tissue, secretions, and interstitial fluid.
- To evaluate cinoxacin concentrations in human prostatic tissue.
- To assess cinoxacin's pharmacokinetic profile in humans with varying renal function.
Main Methods:
- Constant infusion experiments in dogs to measure cinoxacin levels in serum, prostatic tissue, secretion, and interstitial fluid.
- Administration of single or multiple 500 mg doses of cinoxacin to human subjects.
- Measurement of cinoxacin serum half-life in patients with normal and impaired renal function.
Main Results:
- In dogs, cinoxacin concentrations were consistently lower in prostatic tissue, secretion, and interstitial fluid compared to serum.
- Canine urethral and vaginal secretions showed cinoxacin concentrations approximately one-third to one-fourth of serum levels.
- Human prostatic tissue cinoxacin concentrations after 500 mg doses were within the minimum inhibitory concentration range for common urinary tract pathogens.
- Cinoxacin half-life was 2.7 hours in normal renal function and 8.5 hours in impaired renal function.
- Little to no drug accumulation was observed in patients with impaired renal function over seven days.
Conclusions:
- Cinoxacin exhibits limited distribution into canine prostatic tissue and secretions.
- Achieved cinoxacin concentrations in human prostatic tissue are therapeutically relevant for treating urinary tract infections.
- Cinoxacin's elimination is prolonged in patients with renal impairment, but accumulation is minimal with standard dosing regimens.