Copper oxide integrated perylene diimide self-assembled graphitic pencil for robust non-enzymatic dopamine detection. Issue 40 (19th July 2021)

• Record Type: Journal Article
• Authors: Amara, Umay; Riaz, Sara; Mahmood, Khalid; Akhtar, Naeem; Nasir, Muhammad; Hayat, Akhtar; Khalid, Muhammad; Yaqub, Muhammad; Nawaz, Mian Hasnain
• Is Part Of: RSC advances. Volume 11:Issue 40(2021)
• Page Start: 25084
• Page End: 25095
• Publication Date: 2021-07-19
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d1ra03908c
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Exploring a robust, extremely sensitive, cost-effective and reliable assay platform for the precise analysis of dopamine (DA) has become a big challenge predominantly at the clinical level. Abstract : Exploring a robust, extremely sensitive, cost-effective and reliable assay platform for the precise analysis of dopamine (DA) has become a big challenge predominantly at the clinical level. To participate in this quest, herein, we fabricated a perylene diimide (PDI) self-assembled graphitic surface of the graphitic pencil electrode (GPE) anchored copper oxide (CuO). The self-assembled N-rich PDI led to the fast movement of ions by decreasing the bandgap and improved the electron transport kinetics with more exposed catalytic active sites, thus resulting in the robust electrochemical sensing of DA. The designed sensor exhibited good sensitivity (4 μM −1 cm −2 ), high structural stability, repeatability and excellent reproducibility with an RSD value of 2.9%. Moreover, the developed system showed a wide linear range (5 μM to 500 μM) and reliable selectivity even in the presence of co-existing interferants, such as ascorbic acid and uric acid. The fabricated nanohybrid was eventually employed to analyze DA in spiked physiological fluids and provided satisfactory recoveries. The designed PDI-CuO based interface also showed a very low detection limit of 6 nM (S/N = 3), consequently confirming its suitability for clinical and biological applications.