Abstract

A new and selective sorbent for molecularly imprinted polymer solid-phase extraction (MIP-SPE) was prepared to extract meropenem from plasma and urine samples. The extracted analyte was analyzed by high-performance liquid chromatography (HPLC) coupled with photodiode array detection. Methacrylic acid (MAA) as functional monomer, ethylene glycol dimethacrylate (EGDMA) as cross-linker, azobisisobutyronitrile (AIBN) as an initiator and meropenem as a template molecule were used for the MIP preparation. Imprinted meropenem molecule was removed from the polymeric structure using acetonitrile in water (1:9, v/v), as the eluent solvent. Under the optimized conditions, the limit of detection (LOD) and limit of quantification (LOQ) were 35 and 120μg L-1, respectively. The developed MIP-SPE method demonstrates that it could be applied for the determination of meropenem in plasma and urine samples. Keywords: Molecularly imprinted polymer, solid-phase extraction, meropenem, human urine and plasma, high-performance liquid chromatography.

Highlights

  • Meropenem is a broad-spectrum carbapenem antibiotic.[1]

  • As announced in the scientific notice,[5] the MIC for the meropenem is very different from one bacteria to another, but very often it is effective in the range 0.5–4 μg mL–1 against most sensitive germs

  • Selectivity Test Ceftazidime, cefixime and isoniazid were selected as competitive compounds to estimate the selectivity of Molecularly imprinted polymers (MIPs) for meropenem

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Summary

Introduction

Meropenem is a broad-spectrum carbapenem antibiotic.[1]. It is active against Gram-positive and Gram-negative bacteria.[2]. Meropenem has advantages in the intensive care unit (ICU), notably in critically ill patients with renal failure, a population at risk for accumulating co-administered drugs or metabolites.[8]

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