Morphine electrochemical determination using SnO2 nanostructure-modified glassy carbon electrode in the presence of diclofenac.

IF 4.3 Q2 CHEMISTRY, MEDICINAL
ADMET and DMPK Pub Date : 2025-07-02 eCollection Date: 2025-01-01 DOI:10.5599/admet.2803
Zainab S Hadawi, Isam Ngaimesh Taeb, Rasha N Aljabery
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引用次数: 0

Abstract

In the present work, SnO2 nanostructures were synthesized and a sensitive voltammetric sensor on a glassy carbon electrode (GCE) was constructed to estimate morphine (MP) in the presence of diclofenac (DLF).

Background and purpose: Because diclofenac (DLF) is an NSAID, its administration can reduce postoperative morphine (MP) requirements in adults; for example, standard DLF dosing has been shown to decrease MP use after abdominal surgery. Hence, devising a simple, cost-effective, and swift assay for these compounds in biological and pharmaceutical specimens is indispensable.

Experimental approach: SnO2 nanostructures were synthesized, and a sensitive voltammetric sensor on a glassy carbon electrode (GCE) was constructed to estimate MP in the presence of DLF. Cyclic voltammetry was employed to evaluate the electrochemical response of the SnO2 nanostructures/GCE towards MP.

Key results: The SnO2 nanostructures exhibited a significant effect on the electrochemical reaction of the electrode toward the MP oxidation. The SnO2 nanostructures/GCE further exhibited a more sensitive detection platform for MP determination with a limit of detection of 0.006 μM using differential pulse voltammetry in a linear range of 0.01 to 340.0 μM.

Conclusion: The SnO2 nanostructures/GCE exhibited extremely high electrochemical activities towards the simultaneous oxidation of MP and DLF. Moreover, the SnO2 nanostructures/GCE provided reproducible and stable responses for MP quantitation. The platform prepared showed successful performance for MP and DLF determination in real samples. SnO2 nanostructures exhibited a significant effect on the electrochemical reaction of the electrode toward the MP oxidation. The SnO2 nanostructures/GCE further exhibited a more sensitive detection platform for MP determination with a limit of detection of 0.006 μM using differential pulse voltammetry in a linear range of 0.01 to 340.0 μM. Additionally, the SnO2 nanostructures/GCE exhibited extremely high electrochemical activities towards the simultaneous oxidation of MP and DLF. Moreover, the SnO2 nanostructures/GCE provided reproducible and stable responses for MP quantitation. The platform prepared showed successful performance for MP and DLF determination in real samples.

Abstract Image

Abstract Image

Abstract Image

双氯芬酸存在下,SnO2纳米结构修饰玻碳电极电化学测定吗啡。
在本工作中,合成了SnO2纳米结构,并在玻璃碳电极(GCE)上构建了一个灵敏的伏安传感器,用于在双氯芬酸(DLF)存在下估计吗啡(MP)。背景和目的:由于双氯芬酸(DLF)是一种非甾体抗炎药,给药可以减少成人术后吗啡(MP)的需求;例如,标准DLF剂量已被证明可以减少腹部手术后MP的使用。因此,设计一种简单、经济、快速的测定生物和药物样品中这些化合物的方法是必不可少的。实验方法:合成SnO2纳米结构,并在玻璃碳电极(GCE)上构建灵敏的伏安传感器来估计DLF存在时的MP。采用循环伏安法评价了SnO2纳米结构/GCE对MP的电化学响应。关键结果:SnO2纳米结构对电极对MP氧化的电化学反应有显著影响。在0.01 ~ 340.0 μM的线性范围内,差分脉冲伏安法的检测限为0.006 μM, SnO2纳米结构/GCE进一步为MP的测定提供了更灵敏的检测平台。结论:SnO2纳米结构/GCE对MP和DLF的同时氧化表现出极高的电化学活性。此外,SnO2纳米结构/GCE为MP定量提供了可重复性和稳定性的响应。所制备的平台在实际样品中具有良好的MP和DLF测定性能。SnO2纳米结构对电极对MP氧化的电化学反应有显著影响。在0.01 ~ 340.0 μM的线性范围内,差分脉冲伏安法的检测限为0.006 μM, SnO2纳米结构/GCE进一步为MP的测定提供了更灵敏的检测平台。此外,SnO2纳米结构/GCE对MP和DLF的同时氧化表现出极高的电化学活性。此外,SnO2纳米结构/GCE为MP定量提供了可重复性和稳定性的响应。所制备的平台在实际样品中具有良好的MP和DLF测定性能。
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来源期刊
ADMET and DMPK
ADMET and DMPK Multiple-
CiteScore
4.40
自引率
0.00%
发文量
22
审稿时长
4 weeks
期刊介绍: ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study
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