Publication | Closed Access
Molecularly imprinted superparamagnetic iron oxide nanoparticles for rapid enrichment and separation of cholesterol
57
Citations
35
References
2013
Year
NanoparticlesSpiked Human SerumGeneral ProtocolEngineeringPolymer NanotechnologyMetal NanoparticlesResponsive PolymersPolymer-based MagnetMagnetic ResonancePolymer NanocompositesChemistryBiomedical EngineeringPolymersMagnetismChemical EngineeringHybrid MaterialsPolymer ChemistryNanoparticle CharacterizationSaturation MagnetizationNanotechnologyRapid EnrichmentMolecular ImprintingMolecule-based MagnetNanomaterialsDrug Delivery SystemsMedicineFunctional MaterialsNanomagnetism
A general protocol to prepare surface molecularly imprinted polymer core-shell superparamagnetic Fe3O4 nanoparticles (Fe3O4@MIP SPNPs), using a surface-mediated RAFT polymerization approach, is described. Cholesterol-imprinted Fe3O4@MIP SPNPs were obtained by oleic acid-stabilized Fe3O4 nanoparticles with a trithiocarbonate agent and subsequently by polymerizing thin molecularly imprinted layers composed of dimethylacrylamide and N,N'-methylene(bis)acrylamide units. The surface-mediated RAFT polymerization approach allows the synthesis of ∼20 nm hybrid composite particles with a ∼6 nm MIP shell, exhibiting superparamagnetic properties (saturation magnetization = 35.4 emu g(-1)) and specific molecular recognition of cholesterol. The Fe3O4@MIP SPNPs show the capability of rapid enriching and separating cholesterol (∼3.1% in weight) and are renewable and cyclically exploited due to their monodispersive and superparamagnetic features. Moreover, under optimal conditions, the Fe3O4@MIP SPNP recoveries of spiked human serum, milk, yolk and beef were 91.6%, 93.6%, 92.4% and 91.2%, respectively. Finally, the method of molecular imprinting on superparamagnetic particles can be extended to a wide range of applications for cell sorting, biomolecule enrichment and separation, and drug delivery.
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