The prediction of urine antibacterial activity from pharmacological and microbiological parameters was assessed by using experimental urine levels and urine bactericidal titers determined up to 72 h after a 400-mg single dose of two quinolones in a phase I study. The area under the bactericidal curve (AUBC) was accurately predicted for norfloxacin but significantly (P < 0.001) underestimated for rufloxacin (actual value was four times higher than the predicted value against Escherichia coli and two times higher against Staphylococcus aureus). In vitro susceptibility differences between the two strains predicted the ex vivo AUBC differences for norfloxacin but not for rufloxacin, where ex vivo differences were greater than expected. Urine bactericidal titers for up to 72 h were accurately predicted for norfloxacin against E. coli and S. aureus and for rufloxacin against S. aureus, but experimental activity for up to 48 h was four times higher (P < 0.001) than the predicted activity for rufloxacin against E. coli. In the case of norfloxacin, the duration of adequate urine antibacterial activity against S. aureus was overestimated. Inaccurate estimations of ex vivo antibacterial activity of a suspected active metabolite (as with rufloxacin) when an adequate cutoff is not established may have dosing implications.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC163827 | PMC |
http://dx.doi.org/10.1128/AAC.41.5.927 | DOI Listing |
Medicina (Kaunas)
December 2024
School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Despite being one of the most common infectious diseases, urinary tract infections (UTIs) still represent a challenge for clinicians to diagnose and treat, especially in the era of growing antibiotic resistance among uropathogenic bacteria. Recent studies investigating the pathophysiology of UTIs have discovered the prominent role of antimicrobial peptides in the urinary tract defense system. Cathelicidin is an evolutionary conserved antimicrobial peptide encoded by one single gene in humans.
View Article and Find Full Text PDFIndian J Microbiol
December 2024
Technical Institute of Baquba, Middle Technical University, Baquba, 32001 Iraq.
Research for novel compounds that may block bacterial development has continued and prompted by antibiotic-resistant bacteria. The expenses of community for health care as a result of antibiotic resistance has indeed been remarkable during the last decades and demand immediate of medical attention. Consequently, this research presents the antibacterial effect of genuine metal oxide nanoparticles against () and that have been isolated from urinary tract infection patients.
View Article and Find Full Text PDFMicrob Drug Resist
October 2024
Infection Management Department, The Fifth Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Carbapenem-resistant (CRKP) infection has become a significant threat to global health. The application of chemical disinfectants is an effective infection control strategy to prevent the spread of CRKP in hospital environments. However, bacteria have shown reduced sensitivity to clinical disinfectants in recent years.
View Article and Find Full Text PDFWorld J Urol
August 2024
Neuro-Urology, Swiss Paraplegic Centre, Nottwil, Switzerland.
Animals (Basel)
June 2024
Center of Excellence for Food and Water Risk Analysis (FAWRA), Department of Veterinary Public Health, Faculty of Veterinary Science, Chulalongkorn University, Bangkok 10330, Thailand.
Fosfomycin is a bactericidal drug recommended as an alternative treatment for canine bacterial cystitis, particularly in cases involving multidrug-resistant (MDR) infections when no other options are available. In this study, minimum inhibitory concentration (MIC) and mutant prevention concentration (MPC) of fosfomycin were determined against 79 clinical isolates using the agar dilution method. The susceptibility rate of to fosfomycin was 86.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!