TY - JOUR
T1 - Laser scribed graphene: A novel platform for highly sensitive detection of eletroactive biomolecules
AU - Ghanam, Abdelghani
AU - Ait Lahcen, Abdellatif
AU - Beduk, Tutku
AU - Alshareef, Husam N.
AU - Amine, Aziz
AU - Salama, Khaled N.
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: The authors would like to express their acknowledgements to the financial support of funding from King Abdullah University of Science and Technology (KAUST), Saudi Arabia. Also, we thank the KAUST Sensor Initiative and KAUST Visiting Student Program for supporting this work. In addition, we would like to thank Dr Sakandar Rauf, Dr Veerappan Mani, Dr Sandeep G. Surya and Saravanan Yuvaraja for their suggestions and comments.
PY - 2020/8/19
Y1 - 2020/8/19
N2 - Laser-scribed graphene electrodes (LSGEs) have recently shown a potential for the development of electrochemical biosensors thanks to their electronic properties, porous structures, and large surface area that can support the charge transfer. In this paper, the authors present a comparative study of the electrochemical performances of LSGEs with the conventional screen-printed carbon electrodes (SPCEs) toward the detection of most commonly used phenolic compounds and biomolecules. Cyclic voltammetry measurements showed a significant enhancement in the electron transfer rate of all tested electroactive species at LSGEs compared to conventional SPCE. We have suggested, for the first time, a mechanistic study for catecholamine redox reactions at LSGE as the electron transfer–chemical reaction–electron transfer mechanism. Moreover, the excellent performances of LSGE were observed in terms of the electrocatalytic detection of paracetamol (PCM). Therefore, the second part of this study compared the analytical performances of LSGE and SPCE with respect to the detection of PCM. The LSGE allows a fast and reversible system for PCM with a low ΔEp of 88 mV while the SPCE exhibits a quasi-reversible system with a higher ΔEp of 384 mV. The LSGE demonstrated a PCM linear range of concentration between 0.1 μM and 10 μM, with a detection limit of 31 nM. In addition, the LSGE showed a successful applicability with good selectivity and sensitivity for PCM determination in real samples of pharmaceutical tablets. Hence, LSGEs could be an excellent platform for simple and low-cost electrochemical biosensor applications.
AB - Laser-scribed graphene electrodes (LSGEs) have recently shown a potential for the development of electrochemical biosensors thanks to their electronic properties, porous structures, and large surface area that can support the charge transfer. In this paper, the authors present a comparative study of the electrochemical performances of LSGEs with the conventional screen-printed carbon electrodes (SPCEs) toward the detection of most commonly used phenolic compounds and biomolecules. Cyclic voltammetry measurements showed a significant enhancement in the electron transfer rate of all tested electroactive species at LSGEs compared to conventional SPCE. We have suggested, for the first time, a mechanistic study for catecholamine redox reactions at LSGE as the electron transfer–chemical reaction–electron transfer mechanism. Moreover, the excellent performances of LSGE were observed in terms of the electrocatalytic detection of paracetamol (PCM). Therefore, the second part of this study compared the analytical performances of LSGE and SPCE with respect to the detection of PCM. The LSGE allows a fast and reversible system for PCM with a low ΔEp of 88 mV while the SPCE exhibits a quasi-reversible system with a higher ΔEp of 384 mV. The LSGE demonstrated a PCM linear range of concentration between 0.1 μM and 10 μM, with a detection limit of 31 nM. In addition, the LSGE showed a successful applicability with good selectivity and sensitivity for PCM determination in real samples of pharmaceutical tablets. Hence, LSGEs could be an excellent platform for simple and low-cost electrochemical biosensor applications.
UR - http://hdl.handle.net/10754/664689
UR - https://linkinghub.elsevier.com/retrieve/pii/S0956566320305017
U2 - 10.1016/j.bios.2020.112509
DO - 10.1016/j.bios.2020.112509
M3 - Article
C2 - 32877778
SN - 0956-5663
SP - 112509
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
ER -