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Ultrasensitive Detection of Aesculetin Using a Ruthenium Nanoparticle-Modified Carbon Fiber Microelectrode and Mechanistic Investigation of Its Interaction with DNA

Ruiting TianSchool of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, ChinaMin ShiSchool of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, ChinaTao FANGSchool of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, ChinaUchkun ISHIMOVInstitute of Bioorganic Chemistry, Uzbekistan Academy of Sciences, Tashkent, UzbekistanAwais Ullah IhsanDepartment of Biosciences, COMSATS University Islamabad Sahiwal Campus, Sahiwal, PakistanJie LiSchool of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, ChinaSyed Aftab NaqviDepartment of Electrical Engineering, COMSATS University Islamabad Sahiwal Campus, Sahiwal, PakistanXue HuangSchool of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, ChinaHan ChengSchool of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, China
ABI

Аннотация

• A ruthenium nanoparticle-modified carbon fiber microelectrode (RuNPs/CFME) was developed for ultrasensitive detection of aesculetin. • The RuNPs/CFME exhibited a 2.2-fold decrease in charge transfer resistance and significantly enhanced electrocatalytic activity. • The sensor demonstrated a wide linear range (0.01-1 μM), with a low detection limit of 1.62 nM and excellent reproducibility (RSD < 2%). • The platform successfully investigated the interaction between aesculetin and DNA, revealing a dominant electrostatic binding mode. • Practical applicability was confirmed through high recovery rates (95.7-102.6%) in human serum samples. This study presents the development of an ultrasensitive electrochemical sensor based on a ruthenium nanoparticle-modified carbon fiber microelectrode (RuNPs/CFME) for the detection of aesculetin and investigation of its interaction with DNA. The RuNPs/CFME exhibited significantly enhanced electrocatalytic activity, attributed to the large specific surface area and excellent conductivity of RuNPs, resulting in 54.6% decrease in charge transfer resistance compared to the bare electrode. The sensor demonstrated a linear response to aesculetin in the concentration range of 0.01-1 μM, with a detection limit (LOD) of 1.62 nM and a quantification limit (LOQ) of 5.44 nM. The electrode process was adsorption-controlled and involved a two-electron transfer. The modified sensor displayed high selectivity against common interferents, excellent reproducibility (RSD < 2%), and stability (>95% signal retention after 10 days). Furthermore, the platform was applied to study the interaction between aesculetin and calf thymus dsDNA, revealing a binding mechanism dominated by electrostatic interactions, as evidenced by a negative shift in oxidation potential and current attenuation. The sensor was successfully employed for aesculetin detection in human serum samples, achieving recoveries of 95.7-102.6%, demonstrating its potential for pharmacological applications and drug-DNA interaction studies.

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