Sulfur nanoparticle-encapsulated MOF and boron nanosheet-ferrocene complex modified electrode platform for ratiometric electrochemical sensing of adriamycin and real-time monitoring of drug release

材料科学 纳米片 电极 化学工程 电化学 纳米颗粒 电化学气体传感器 检出限 二茂铁 纳米技术 化学 色谱法 工程类 物理化学 冶金
作者
Meng Yang,Zejun Sun,Hui Jin,Rijun Gui
出处
期刊:Microchemical Journal [Elsevier BV]
卷期号:177: 107319-107319 被引量:34
标识
DOI:10.1016/j.microc.2022.107319
摘要

This work developed a modified electrode platform for dual-channel applications in ratiometric electrochemical sensing and real-time monitoring of drug release. In the presence of cobalt ions and sulfur nanoparticles (SNPs), 2-methylimidazole was polymerized to form SNPs-encapsulated cobalt metal–organic framework (MOF), [email protected] Boron nanosheets (BNSs) were prepared through ultrasound-assisted liquid-phase exfoliation, followed by loading ferrocene (Fc) to form BNSs-Fc complex. A clean glassy carbon electrode (GCE) was modified with Nafion on the surface, followed by drop-casting of BNSs-Fc and [email protected] to construct a modified electrode platform, [email protected] MOF/BNSs-Fc/GCE. The morphologies, microstructures, spectra and properties of products were characterized systematically. The platform was used as a new ratiometric electrochemical sensor to detect adriamycin (ADR), due to stable Fc signal output and content-dependent ADR signal output during the electrochemical redox process of Fc and ADR. Under optimal conditions, the sensor can perform effective detection of ADR in a broad range of 0.01–10 μM, with a low limit of detection of 2 nM. The sensor was verified to possess high detection selectivity, sensitivity and stability, and enabled successful detection of ADR in biological fluid samples, indicating potential reliability and practicability. Besides, the prepared BNSs-ADR carriers in electrolyte solution have the capability of spontaneous and pH-regulatable release of ADR. By means of the platform-based sensor, linear relationships of ADR/Fc redox-peak current ratio (or concentration of released ADR) versus release time were well constructed, which thus realized ratiometric electrochemical real-time monitoring of ADR release by the sensor.
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