4.8 Article

Enzyme-free impedimetric biosensor-based molecularly imprinted polymer for selective determination of L-hydroxyproline

Journal

BIOSENSORS & BIOELECTRONICS
Volume 191, Issue -, Pages -

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2021.113387

Keywords

L-hydroxyproline; Molecularly imprinted polymer; Electrochemical impedance spectroscopy; Non-enzymatic sensor; Bone diseases

Funding

  1. National Research Council of Thailand (NRCT)
  2. Science Achievement Scholarship of Thailand (SAST)
  3. 90th Anniversary of Chulalongkorn University Fund [GCUGR1125633048D]
  4. Electrochemistry and Optical Spectroscopy Center of Excellence (EOSCE), Chulalongkorn University
  5. Department of Chemistry, Faculty of Science, Chulalongkorn University

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This study reported a novel enzyme-free impedimetric biosensor for the selective and sensitive determination of the biomarker L-hydroxyproline for early diagnosis of bone diseases. By using a mixture of monomers for coelectropolymerization, the biosensor showed high selectivity and sensitivity, and successfully detected L-hydroxyproline in human serum samples.
This study first reported enzyme-free impedimetric biosensor-based molecularly imprinted polymers for selective and sensitive determination of L-hydroxyproline (L-hyp), a biomarker for the early diagnosis of bone diseases. In recent study, utilizing a single 3-aminophenylboronic acid (3-APBA) to create imprinted surfaces could result in a strong interaction and difficulty in removal of a template molecule. Hence, a mixture of monomer solution containing 3-APBA and o-phenylenediamine (OPD) in the presence of the L-hyp molecule was coelectropolymerized onto the screen-printed electrode using cyclic voltammetry (CV) to eradicate this mentioned limitation. The detection principle of this sensor is relied on alteration of mediator's charge transfer resistance (R-ct) that could be obstructed by L-hyp occupied in imprinted surface. The successfully fabricated biosensor was explored by scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), and confocal scanning microscopy. Furthermore, the effect of polymer composition on the R-ct response was systematically investigated. The result exhibited that the mixture of monomers could provide the highest change of R-ct due to high selectivity from esterification of 3-APBA and from hydrogen bond of OPD surrounding the template. The sensor showed a significant increase in 11, in the presence of L-hyp, whereas no observable resistance change was detected in the absence thereof. The calibration curve was obtained in the range from 0.4 to 25 mu tg mL(-1) with limits of detection (3SD(blank)/Slope) and quantification (10SD(blank)/Slope) of 0.13 and 0.42 mu tg mL(-1) , respectively. This biosensor exhibited high selectivity and sensitivity and was successfully applied to determine L-hyp in human serum samples with satisfactory results.

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