Validation of a levofloxacin HPLC assay in plasma and dialysate for pharmacokinetic studies.

Abstract:

:An HPLC method with fluorescence detection suitable for routine determination of levofloxacin in plasma and dialysate has been validated. Sample preparation was assured by one-step protein precipitation for plasma or direct injection of the dialysate solution, respectively. Separation occurred on an YMC Pro C18 RP column (150 mm x 2 mm) with an acidic binary gradient mobile phase and detection at excitation and emission wavelengths of 296 and 504 nm. The assay was linear between 0.1 and 6 microg/ml for plasma and 0.1 and 5 microg/ml for dialysate with intra- and inter-day precision and accuracy lower than 10%. No degradation of levofloxacin was observed under the applied conditions for both matrices. The method was successfully applied to an in vitro pharmacokinetic study and patient samples as well.

journal_name

J Pharm Biomed Anal

authors

Siewert S

doi

10.1016/j.jpba.2006.02.010

subject

Has Abstract

pub_date

2006-06-16 00:00:00

pages

1360-2

issue

4

eissn

0731-7085

issn

1873-264X

pii

S0731-7085(06)00181-6

journal_volume

41

pub_type

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