Dual-signal ratiometric electrochemiluminescence biosensor based on Au NPs-induced low-potential emission of PFO Pdots and LSPR-ECL mechanism for ultra-sensitive detection of microRNA-141

• Published in: Biosensors & bioelectronics 2024-10, Vol.261, p.116495, Article 116495
• Main Authors: Wang, Yin-Zhu, Li, Yue-Rong, Zhang, Yu-Qi, Xiang, Yuan-Meng, Bai, Rong-Rui, Liu, Yan, Li, Meng-Li, Meng, Gong-Rui, Pan, Shun-Long, Zhang, Fang, Mi, Li, Hu, Yong-Hong
• Format: Article
• Language: English
• Subjects: Biosensing Techniques - methods; Dual-potential ratiometric; Electrochemical Techniques - methods; Electrochemiluminescence; Fluorenes - chemistry; Glucose Oxidase - chemistry; Gold - chemistry; Humans; Hydrogen Peroxide - chemistry; Limit of Detection; Luminescent Measurements - methods; Metal Nanoparticles - chemistry; microRNA; MicroRNAs - analysis; PFO Pdots; Quantum Dots - chemistry; S-BN QDs
• ISSN: 0956-5663; 1873-4235; 1873-4235
• DOI: 10.1016/j.bios.2024.116495

In this study, we have for the first time constructed a ratiometric ECL biosensor for the ultrasensitive detection of microRNAs (miRNAs) using gold nanoparticles (Au NPs) to trigger both the low-potential emission from conjugated polymer poly(9,9-dioctylfluorene-2,7-diyl) dots (PFO Pdots) and the LSPR-ECL effect with sulfur-doped boron nitride quantum dots (S-BN QDs). PFO Pdots were first applied to the Au NPs-modified electrode, followed by covalent binding to capture the hairpin H1. Immediately thereafter, a small amount of miRNA-141 was able to generate a large amount of output DNA (OP) by traversing the target cycle. OP, H3-S-BN QDs, and H4-glucose oxidase (H4-GOD) were then added sequentially to the Au NPs-modified electrode surface, and the hybridization chain reaction (HCR) was initiated. This resulted in the introduction of a large amount of GOD into the system, which catalyzed the in situ formation of the co-reactant hydrogen peroxide (H2O2) from the substrate glucose. Due to the electron transfer effect, the production of H2O2 led to the ECL quenching of PFO Pdots. Meanwhile, H2O2 served as a co-reactant of S-BN QDs, resulting in strong ECL emission of S-BN QDs at the cathode. Furthermore, the cathodic ECL intensity of S-BN QDs was further enhanced by an LSPR-ECL mechanism between Au NPs and S-BN QDs. By measuring the ratio of ECL intensities at two excitation potentials, this approach could provide sensitive and reliable detection of miRNA-141 in the range of 0.1 fM ∼10 nM, with a detection limit of 0.1 fM.