Article ID Journal Published Year Pages File Type
1216414 Journal of Chromatography B 2006 5 Pages PDF
Abstract

A simple, rapid and precise HPLC method using ultrafiltration to remove plasma protein was developed to determine biapenem concentrations in human plasma. Plasma was separated by centrifugation at 4 °C from blood collected in heparinized vacuum tubes, and biapenem was stabilized by immediate mixing the plasma with 1 M 3-morpholinopropanesulfonic acid (MOPS) buffer (pH 7.0) (1:1). Biapenem was detected by ultraviolet absorbance at 300 nm with no interfering plasma peak. The calibration curve of biapenem in human plasma was linear from 0.04 to 50 μg/mL. The limit of detection was 0.01 μg/mL, which was more than 40-fold lower than that of conventional plasma protein precipitation using ammonium sulfate. The assay has been clinically applied to pharmacokinetic studies in patients.

Related Topics
Physical Sciences and Engineering Chemistry Analytical Chemistry
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