M. Kamberi et al., Influences of urinary pH on ciprofloxacin pharmacokinetics in humans and antimicrobial activity in vitro versus those of sparfloxacin, ANTIM AG CH, 43(3), 1999, pp. 525-529
The impact of acidification and alkalinization of urine on the pharmacokine
tics of ciprofloxacin was investigated after single 200-mg oral doses were
administered to nine healthy male volunteers. In addition, the effect of hu
man urine on the MICs of ciprofloxacin and sparfloxacin against some common
urinary tract pathogens such as Escherichia coli and Pseudomonas aeruginos
a was investigated. Acidic and alkaline conditions were achieved by repeate
d oral doses of ammonium chloride or sodium bicarbonate, respectively, Plas
ma ciprofloxacin levels in all subjects were adequately described in terms
of two-compartment model kinetics with first-order absorption. Acidificatio
n and alkalinization treatments had no effect on ciprofloxacin absorption,
distribution, or elimination. The total amount of unchanged ciprofloxacin e
xcreted over 24 h under acidic conditions was 88.4 +/- 14.5 mg (mean +/- st
andard deviation) (44.2% of the oral dose) and 82.4 +/- 16.5 mg (41.2% of t
he oral dose) under alkaline conditions, while the total amount of unchange
d drug excreted over 24 h in volunteers receiving neither sodium bicarbonat
e nor ammonium chloride was 90.53 +/- 9.8 mg (45.2% of the oral dose). The
mean renal clearance of ciprofloxacin was 16.78 +/- 2.67, 16.08 +/- 3.2, an
d 16.31 +/- 2.67 liters/h with acidification, alkalinization, and control,
respectively, Renal clearance and concentrations of ciprofloxacin in urine
were not correlated with urinary pH, The antibacterial activity of ciproflo
xacin and sparfloxacin against E. coli NIHJ JC-2 and P, aeruginosa ATCC 278
53 was affected by human urine and in particular by its pH. The activities
of both quinolones against E, coli NIHJ JC-2 were lower at lower urinary pH
and rather uniform, while in the case of P, aeruginosa ATCC 27853 ciproflo
xacin was more active than sparfloxacin.