Analytical interference of quinolone antibiotics and quinine derived drugs on urinary protein determined by reagent strips and the pyrogallol red-molybdate protein assay.
Author(s): da Silva AS, Falkenberg M
Publication: Clin Biochem, 2011, Vol. 44, Page 1000-4
PubMed ID: 21635881 PubMed Review Paper? No
Purpose of Paper
Conclusion of Paper
Studies
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Study Purpose
The purpose of this study was to determine the effects of quinolone antibiotics and anti-malarial drugs on the measurement of urine protein concentrations by two test strips and the PRM assay.
Summary of Findings:
False positives for urinary protein were found using the MultiStix 10 SG when therapeutic or supratherapeutic levels of the antimalarial drugs hydroxychloroquine sulfate and chloroquine diphosphate were added to urine or when supratherapeutic levels of quinine sulfate were added to urine. Supratherapeutic levels (350 mg/dL) of the quinolone antibiotics ofloxacin, ciprofloxacin hydrochloride, and norfloxacin also caused false positives for urine protein when using the MultiStix 10 SG test strips. Using the PRM assay, therapeutic and supratherapeutic levels (35 mg/dL or 350 mg/dL) of levofloxacin, ofloxacin, ciprofloxacin hydrochloride, and norfloxacin resulted in false positives for urine protein. All tested concentrations of the anti-malarial drugs (chloroquine diphosphate, hydroxychloroquine sulfate and quinine sulfate) interfered with urine protein measurement by the PRM assay. There were no false positives for urine protein when the Combur 10 test M was used.
Biospecimens
Preservative Types
- None (Fresh)
Diagnoses:
- Not specified
Platform:
Analyte Technology Platform Protein Clinical chemistry/auto analyzer Pre-analytical Factors:
Classification Pre-analytical Factor Value(s) Preaquisition Other drugs Levofloxacin
Ofloxacin
Ciprofloxacin hydrochloride
Norfloxacin
Chloroquine diphosphate
Hydroxychloroquine sulfate
Quinine sulfate
Clinical chemistry/auto analyzer Specific Detection method Multistix 10 SG
Combur 10 test M
Pyrogallol red-molybdate assay
