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A novel surface plasmon resonance sensor based on a functionalized graphene oxide/molecular-imprinted polymer composite for chiral recognition of <scp>l</scp> -tryptophan
摘要: Herein, a novel surface plasmon resonance (SPR) sensor based on a functionalized graphene oxide (GO)/molecular-imprinted polymer composite was developed for the chiral recognition of L-tryptophan (L-Trp). The composite's recognition element was prepared via a facile and green synthesis approach using polydopamine as both a reducer of GO and a functional monomer as well as a cross-linker for molecular imprinting. The composite was characterized via Fourier transform infrared spectroscopy, scanning electron microscopy, X-ray diffraction, and Raman spectroscopy. After attaching the composite onto the gold surface of an SPR chip, the sensor was characterized using contact-angle measurements. The sensor exhibited excellent selectivity and chiral recognition for the template (i.e., L-Trp). Density functional theory computations showed that the difference in hydrogen bonding between the composite element and L-Trp and D-Trp played an important role in chiral recognition.
关键词: molecular-imprinted polymer,graphene oxide,surface plasmon resonance,L-tryptophan,chiral recognition
更新于2025-09-19 17:15:36
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Preparation of erythromycin imprinted polymer by metal-free visible-light–induced ATRP and its application in sensor
摘要: Erythromycin (ERY) molecular imprinted polymer was prepared on the surface of Au electrode modified with Ni and Au nanoclusters (MIP/AuNCs/Ni/Au) via metal-free visible-light–induced atom transfer radical polymerization, which was very easy, controllable, and environmentally benign. MIP/AuNCs/Ni/Au was examined by energy dispersive spectrometer (EDS), scanning electron microscope (SEM), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). Further, MIP/AuNCs/Ni/Au was successfully used for the determination of ERY by differential pulse voltammetry (DPV). Under the optimal conditions, MIP/AuNCs/Ni/Au gave a linear correlation over the ERY concentration from 1.0 × 10?8 to 1.0 × 10?1 mg/L with the detection limit of 3.2 × 10?9 mg/L (S/N = 3). Comparing with the similar sensors, the larger linear range and lower detection limit indicated the promising prospect of this electrochemical sensor. Hence, this study was of great importance for the polymer-modified electrodes and the sensitive detection of ERY.
关键词: Molecular imprinted polymer (MIP),Metal-free visible-light–induced atom transfer radical polymerization (MVL ATRP),Erythromycin (ERY)
更新于2025-09-04 15:30:14