There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.
Abstract
The development of
electrochemical sensors for flutamide detection
is a crucial step in biomedical research and environmental monitoring.
In this study, a composite of
Actinidia-derived carbon particles (CPs) and tungsten disulfide (WS
2) was formed and used as an electrocatalyst for the electrochemical
detection of flutamide. The CPs had an average diameter of 500 nm
and contained surface hydroxyl and carbonyl groups. These groups may
help anchor the CPs onto the WS
2 platelets, resulting in
the formation of a CPs-WS
2 nanocomposite with a high surface
area and a conducting network, enabling electron transfer. Using the
CPs-WS
2 composite supported at a glassy carbon electrode,
a linear concentration range extending from 1 nM to 104 μM,
a limit of detection of 0.74 nM, and a sensitivity of 26.9 ±
0.7 μA μM
–1 cm
–2 were
obtained in the detection of flutamide in a phosphate buffer. The
sensor showed good recovery, ranging from 88.47 to 95.02%, in river
water samples, and exhibited very good selectivity in the presence
of inorganic ions, including Al
3+, Co
2+, Cu
2+, Fe
3+, Zn
2+, NO
3–, SO
42–, CO
32–, and Cl
–.
Carbon nanotubes (CNTs) promise to advance a number of real-world technologies. Of these applications, they are a particularly attractive for uses in chemical sensors for environmental and health monitoring. However, chemical sensors based on CNTs are often lacking in selectivity and the elucidation of their sensing mechanisms remains challenging. This review is a comprehensive description of the parameters that give rise to the sensing capabilities of CNT-based sensors and the application of CNT-based devices in chemical sensing. This Review begins with the discussion of the sensing mechanisms in CNT-based devices, the chemical methods of CNT functionalization, architectures of sensors, performance parameters, and theoretical models used to describe CNT-sensors. It then discusses the expansive applications of CNT-based sensors to multiple areas including environmental monitoring, food and agriculture applications, biological sensors, and national security. The discussion of each analyte focuses on the strategies used to impart selectivity and the molecular interactions between the selector and the analyte. Finally, the Review concludes with a brief outlook over future developments in the field of chemical sensors and their prospects for commercialization.
Biosensors with high sensitivity, selectivity and a low limit of detection, reaching nano/picomolar concentrations of biomolecules, are important to the medical sciences and healthcare industry for evaluating physiological and metabolic parameters. Over the last decade, different nanomaterials have been exploited to design highly efficient biosensors for the detection of analyte biomolecules. The discovery of graphene has spectacularly accelerated research on fabricating low-cost electrode materials because of its unique physical properties, including high specific surface area, high carrier mobility, high electrical conductivity, flexibility, and optical transparency. Graphene and its oxygenated derivatives, including graphene oxide (GO) and reduced graphene oxide (rGO), are becoming an important class of nanomaterials in the field of biosensors. The presence of oxygenated functional groups makes GO nanosheets strongly hydrophilic, facilitating chemical functionalization. Graphene, GO and rGO nanosheets can be easily combined with various types of inorganic nanoparticles, including metals, metal oxides, semiconducting nanoparticles, quantum dots, organic polymers and biomolecules, to create a diverse range of graphene-based nanocomposites with enhanced sensitivity for biosensor applications. This review summarizes the advances in two-dimensional (2D) and three-dimensional (3D) graphene-based nanocomposites as emerging electrochemical and fluorescent biosensing platforms for the detection of a wide range of biomolecules with enhanced sensitivity, selectivity and a low limit of detection. The biofunctionalization and nanocomposite formation processes of graphene-based materials and their unique properties, surface functionalization, enzyme immobilization strategies, covalent immobilization, physical adsorption, biointeractions and direct electron transfer (DET) processes are discussed in connection with the design and fabrication of biosensors. The enzymatic and nonenzymatic reactions on graphene-based nanocomposite surfaces for glucose- and cholesterol-related electrochemical biosensors are analyzed. This review covers a very broad range of graphene-based electrochemical and fluorescent biosensors for the detection of glucose, cholesterol, hydrogen peroxide (H2O2), nucleic acids (DNA/RNA), genes, enzymes, cofactors nicotinamide adenine dinucleotide (NADH) and adenosine triphosphate (ATP), dopamine (DA), ascorbic acid (AA), uric acid (UA), cancer biomarkers, pathogenic microorganisms, food toxins, toxic heavy metal ions, mycotoxins, and pesticides. The sensitivity and selectivity of graphene-based electrochemical and fluorescent biosensors are also examined with respect to interfering analytes present in biological systems. Finally, the future outlook for the development of graphene based biosensing technology is outlined.
Permits the broadest form of re-use including for commercial purposes, provided that
author attribution and integrity are maintained (
https://creativecommons.org/licenses/by/4.0/).
History
Date
received
: 22
March
2024
Date
accepted
: 14
June
2024
Date
revision received
: 08
May
2024
Funding
Funded by: Science Foundation Ireland, doi 10.13039/501100001602;
Award ID: SFI/20/FFP-P/8793
Funded by: Irish Research Council, doi 10.13039/501100002081;
scite shows how a scientific paper has been cited by providing the context of the citation, a classification describing whether it supports, mentions, or contrasts the cited claim, and a label indicating in which section the citation was made.