AI Article Synopsis

  • Developed a new method using a molecularly imprinted polymer (MIP) for effectively extracting and concentrating warfarin from biological samples through solid-phase extraction (SPE).
  • The optimal MIP was created with a specific ratio of warfarin, pyrrole, and a cross-linker, and its performance was compared to a nonimprinted polymer (NIP).
  • Characterization and testing showed high sensitivity and accuracy with detection limits around 0.0035-0.0050 µg/mL and recoveries over 95% for both plasma and urine samples.

Article Abstract

The aim of this work was to develop a method for the clean-up and preconcentration of warfarin from biological sample employing a new molecularly imprinted polymer (MIP) as a selective adsorbent for solid-phase extraction (SPE). This MIP was synthesized using warfarin as a template, pyrrole as a functional monomer and vinyl triethoxysilane as a cross-linker. The molar ratio of 1:4:20 (template-functional monomer-cross-linker) showed the best results. Nonimprinted polymers (NIPs) were prepared and treated with the same method, but in the absence of warfarin. The prepared polymer was characterized by Fourier transmission infrared spectrometry and scanning electron microscopy. An adsorption process (SPE) for the removal of warfarin using the fabricated MIPs and NIPs was evaluated under various conditions. Effective parameters on warfarin extraction, for example, type and volume of elution solvent, pH of sample solution, breakthrough volume and maximum loading capacity, were studied. The limits of detection were in the range of 0.0035-0.0050 µg mL(-1). Linearity of the method was determined in the range of 0.0165-10.0000 µg mL(-1) for plasma and 0.0115-10.0000 µg mL(-1) for urine with coefficients of determination (R(2)) ranging from 0.9975 to 0.9985. The recoveries for plasma and urine samples were >95%.

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http://dx.doi.org/10.1002/bmc.3469DOI Listing

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