基于spion -活性炭纳米复合界面的抗高血压药物阿替洛尔的先进电化学检测与表征。

IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Ananya S Agnihotri, Nidhin M
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引用次数: 0

摘要

采用简单的水热法合成了超顺磁性氧化铁纳米颗粒(SPIONs)、活性炭(AC)和SPION-AC纳米复合材料。合成材料的表征包括动态光散射、x射线衍射、场发射扫描电镜、高分辨率透射电镜和振动样品磁强计,以及电化学表征研究,如电化学阻抗谱。在SPION-AC纳米复合材料中,SPION-15%AC用于修饰玻碳电极(GCE)。SPION和AC之间的协同作用显著增强了体系的电化学性能,从而为抗高血压药物阿替洛尔(ATN)的商业片剂样品的高效检测提供了平台。该传感器性能优良,线性检测范围为1.21 μM ~ 285 μM。该传感器具有0.401 μM的低检测限(LOD),可精确量化ATN,使其成为改善患者护理的有前途的工具。高选择性、可重复性和在复杂药物基质中的良好回收率进一步突出了该传感器在生物医学和临床应用中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advanced electrochemical detection and profiling of the antihypertensive drug atenolol via a SPION-activated carbon nanocomposite interface.

This study reports the synthesis of superparamagnetic iron oxide nanoparticles (SPIONs), activated carbon (AC) and SPION-AC nanocomposites using a simple hydrothermal method. Characterization of the synthesized materials includes dynamic light scattering, X-ray diffraction, field emission scanning electron microscopy, high resolution transmission electron microscopy, and vibrating sample magnetometry, along with electrochemical characterization studies such as electrochemical impedance spectroscopy. Among the SPION-AC nanocomposites, SPION-15%AC was employed to modify a glassy carbon electrode (GCE). The synergistic interaction between SPION and AC significantly enhanced the electrochemical properties of the system, leading to the development of a highly efficient platform for the detection of the antihypertensive drug atenolol (ATN) in commercial tablet samples. The sensor demonstrated excellent performance, with a linear detection range from 1.21 μM to 285 μM. With a low detection limit (LOD) of 0.401 μM, the sensor offers precise quantification of ATN, making it a promising tool for improving patient care. High selectivity, reproducibility, and excellent recovery in complex pharmaceutical matrices further highlight the potential of this sensor for biomedical and clinical applications.

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来源期刊
Nanoscale Advances
Nanoscale Advances Multiple-
CiteScore
8.00
自引率
2.10%
发文量
461
审稿时长
9 weeks
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