کلیدواژهها
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Magnetic nanoparticles, molecularly imprinted polymers (MIPs), tizanidine,
paracetamol, human plasma
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چکیده
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In this study, simple, effective, and general processes were used for the synthesis of a new
nano-molecularly imprinted polymers (MIPs) layer on magnetic Fe3O4 NPs with uniform coreshell
structure by combining surface imprinting and nanotechniques. The first step for synthesis
of the magnetic NPs was co-precipitation of Fe2+ and Fe3+ in an ammonia solution. Then, an
SiO2 shell was coated on the magnetic core with the Stöber method. Subsequently, the C=C
groups were grated onto the silica-modified Fe3O4 surface by 3-(Trimethoxysilyl) propyl
methacrylate. Finally, the MIPs films were formed on the surface of Fe3O4@SiO2 by the
copolymerization of C=C end groups with meth acrylic acid (the functional monomer), ethylene
glycol dimethacrylate (the cross-linker), 2, 2-azobisisobutyronitrile (the initiator), and tizanidine
(the template molecule). The products were characterized using techniques that included Fourier
transform infrared (FT-IR) spectroscopy, x-ray diffraction (XRD), thermo gravimetric analysis
(TGA), scanning electron microscopy (SEM), UVspectrophotometry, transmission electron
microscopy (TEM), and vibrating sample magnetometer (VSM). Measurement of tizanidine
through use of the core-shell magnetic molecularly imprinted polymers nanoparticles (MMIPs-
NPs) in human plasma samples compared to the paracetamol showed, synthesized nano-sized
MMIP for tizanidine has acted selectively.
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