Label-free Sensor Research Articles

Label-Free Chemiresistive Sensors Based on Self-Assembled Ti3C2Tx MXene Films for Monitoring of Microcystin-LR in Water Samples.

Herein, we propose a label-free chemiresistive sensor for the highly sensitive and selective detection of microcystin (MC)-LR in water samples. The sensor uses a layer-by-layer (LBL) assembled conductive film consisting of Ti3C2Tx nanosheets as the sensing channel. It is further modified by using an aptamer for the specific recognition of MC-LR. The response signal is based on the change in resistance of the conductive channel upon binding of MC-LR with the aptamer. Our novel strategy is the first concept proposed for immobilizing the aptamer containing -SH on the channel surface through a Ti-S bond under weakly alkaline condition. The resulting sensor is highly sensitive and stable for the detection of MC-LR, with a detection limit of 0.18 ng L-1 and a wide linear range from 1 to 104 ng L-1. We used the sensor to continuously monitor MC-LR released by cultivated Microcystis aeruginosa, showing a strong relationship between MC-LR and cell density. Furthermore, the sensor was successfully used to measure MC-LR in freshwater lakes with moderate algal blooms, and the results agreed well with those obtained by liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis. The present study provides a reliable method for highly sensitive and selective detection of MC-LR in environmental waters.

Comparing nanobody and aptamer-based capacitive sensing for detection of interleukin-6 (IL-6) at physiologically relevant levels

A major societal challenge is the development of the necessary tools for early diagnosis of diseases such as cancer and sepsis. Consequently, there is a concerted push to develop low-cost and non-invasive methods of analysis with high sensitivity and selectivity. A notable trend is the development of highly sensitive methods that are not only amenable for point-of-care (POC) testing, but also for wearable devices allowing continuous monitoring of biomarkers. In this context, a non-invasive test for the detection of a promising biomarker, the protein Interleukin-6 (IL-6), could represent a significant advance in the clinical management of cancer, in monitoring the chemotherapy response, or for prompt diagnosis of sepsis. This work reports a capacitive electrochemical impedance spectroscopy sensing platform tailored towards POC detection and treatment monitoring in human serum. The specific recognition of IL-6 was achieved employing gold surfaces modified with an anti-IL6 nanobody (anti-IL-6 VHH) or a specific IL-6 aptamer. In the first system, the anti-IL-6 VHH was covalently attached to the gold surface using a binary self-assembled-monolayer (SAM) of 6-mercapto-1-hexanol (MCH) and 11-mercaptoundecanoic acid. In the second system, the aptamer was chemisorbed onto the surface in a mixed SAM layer with MCH. The analytical performance for each label-free sensor was evaluated in buffer and 10% human serum samples and then compared. The results of this work were generated using a low-cost, thin film eight-channel gold sensor array produced on a flexible substrate providing useful information on the future design of POC and wearable impedance biomarker detection platforms.

Single-Particle Plasmon Sensor to Monitor Proteolytic Activity in Real Time.

We have established a label-free plasmonic platform that monitors proteolytic activity in real time. The sensor consists of a random array of gold nanorods that are functionalized with a design peptide that is specifically cleaved by thrombin, resulting in a blueshift of the longitudinal plasmon. By monitoring the plasmon of many individual nanorods, we determined thrombin's proteolytic activity in real time and inferred relevant kinetic parameters. Furthermore, a comparison to a kinetic model revealed that the plasmon shift is dictated by a competition between peptide cleavage and thrombin binding, which have opposing effects on the measured plasmon shift. The dynamic range of the sensor is greater than two orders of magnitude, and it is capable of detecting physiologically relevant levels of active thrombin down to 3 nM in buffered conditions. We expect these plasmon-mediated label-free sensors to open the window to a range of applications stretching from the diagnostic and characterization of bleeding disorders to fundamental proteolytic and pharmacological studies.

A smartphone-assisted colorimetric aptasensor based on aptamer and gold nanoparticles for visual, fast and sensitive detection of ZEN in maize.

A simple, fast, low cost, sensitive, intuitive, visual, label-free, and smartphone-assisted aptamer sensor based on colorimetric assay for the measurement of zearalenone was constructed. The nucleic acid aptamer of zearalenone was used as the recognition element and gold nanoparticles were used as the indicator. Several factors that could influence sensitivity, including the concentration of aptamer and NaCl, and incubation time, and specificity, have been investigated. The results showed that under the optimal conditions, the signal had a good linear relationship when zearalenone concentration is 5-300ng/mL. A linear regression equation is Y=0.0003X+0.5128 (R2=0.9989) and a limit of detection is 5ng/mL. The specificity of the sensor was good. Zearalenone in maize samples were successfully measured. The recoveries of Zearalenone are 81.3 %-96.4 %. The whole process takes only 15min to complete. The smartphone assisted colorimetric aptamer sensor can be used for the detection of zearalenone in maize.

Highly sensitive label-free biosensor: graphene/CaF2 multilayer for gas, cancer, virus, and diabetes detection with enhanced quality factor and figure of merit

One of the primary goals for the researchers is to create a high-quality sensor with a simple structure because of the urgent requirement to identify biomolecules at low concentrations to diagnose diseases and detect hazardous chemicals for health early on. Recently graphene has attracted much interest in the field of improved biosensors. Meanwhile, graphene with new materials such as CaF2 has been widely used to improve the applications of graphene-based sensors. Using the fantastic features of the graphene/CaF2 multilayer, this article proposes an improvement sensor in the sensitivity (S), the figure of merit (FOM), and the quality factor (Q). The proposed sensor is based on the five-layers graphene/dielectric grating integrated with a Fabry–Perot cavity. By tuning graphene chemical potential (µc), due to the semi-metal features of graphene, the surface plasmon resonance (SPR) waves excited at the graphene/dielectric boundaries. Due to the vertical polarization of the source to the gratings and the symmetry of the electric field, both corners of the grating act as electric dipoles, and this causes the propagation of plasmonic waves on the graphene surface to propagate towards each other. Finally, it causes Fabry–Perot (FP) interference on the surface of graphene in the proposed structure's active medium (the area where the sample is located). In this article, using the inherent nature of FP interference and its S to the environment's refractive index (RI), by changing a minimal amount in the RI of the sample, the resonance wavelength (interferometer order) shifts sharply. The proposed design can detect and sense some cancers, such as Adrenal Gland Cancer, Blood Cancer, Breast Cancer I, Breast Cancer II, Cervical Cancer, and skin cancer precisely. By optimizing the structure, we can achieve an S as high as 9000 nm/RIU and a FOM of about 52.14 for the first resonance order (M1). Likewise, the remarkable S of 38,000 nm/RIU and the FOM of 81 have been obtained for the second mode (M2). In addition, the proposed label-free SPR sensor can detect changes in the concentration of various materials, including gases and biomolecules, hemoglobin, breast cancer, diabetes, leukemia, and most alloys, with an accuracy of 0.001. The proposed sensor can sense urine concentration with a maximum S of 8500 nm/RIU and cancers with high S in the 6000 nm/RIU range to 7000 nm/RIU. Also, four viruses, such as M13 bacteriophage, HIV type one, Herpes simplex type 1, and influenza, have been investigated, showing Maximum S (for second resonance mode of λR(M2) of 8000 nm/RIU (λR(M2) = 11.2 µm), 12,000 nm/RIU (λR(M2) = 10.73 µm), 38,000 nm/RIU (λR(M2) = 11.78 µm), and 12,000 nm/RIU (λR(M2) = 10.6 µm), respectively, and the obtained S for first resonance mode (λR(M1)) for mentioned viruses are 4740 nm/RIU (λR(M1) = 8.7 µm), 8010 nm/RIU (λR(M1) = 8.44 µm), 8100 nm/RIU (λR(M1) = 10.15 µm), and 9000 (λR(M1) = 8.36 µm), respectively.

A Label-Free and Ultrasensitive Prussian Blue-Based Dipstick Sensor for Bacterial and Biofilm Detection.

Water and food contamination has become the major contributor to infections and deaths. However, rapid and sensitive bacterial detection still remains an unmet demand that has attracted widespread attention. Often water and food samples are sent out for laboratory testing to detect the presence of contamination, which is time-consuming and laborious. Herein, we have developed a highly sensitive, tenable, affordable, and robust (STAR) paper-based colorimetric dipstick sensor based on the principle of Prussian blue (PB) synthesis as an indicator of bacterial contamination. In the presence of bacteria, it leads to the formation of PB, a dye that acts as a colorimetric indicator. The intensity of the PB is the direct measure of the degree of contamination. The fabrication of the STAR dipstick sensor involves a simple and cost-effective process. The STAR dipstick sensor is ultrasensitive and can detect up to 101 CFU/mL of bacteria within minutes of contact with the test sample. The STAR dipstick sensor is fabricated using biodegradable components, which is speculated to facilitate quick and environmentally friendly degradation after each use. The sensor has been validated for its properties and capabilities at different pH to detect both Gram-positive and Gram-negative bacterial strains in real-time samples. The stability and degradation were also monitored. Comprehensively, the proposed STAR dipstick sensor can serve as a point-of-care device to detect bacterial contamination in a swift and sensitive manner.

Label-free electrochemical biosensor based on Ng-PCL polymer signal amplification for the detection of carcinoembryonic antigen

Carcinoembryonic antigen (CEA) is the related antigen first extracted from embryonic tissue and is an acidic glycoprotein with human embryonic antigenic properties. It is an important biomarker for the detection of many malignancies. In this paper, we have developed a signal amplified sandwich-type electrochemical impedance biosensor based on naringin initiated poly(ε-caprolactone) (Ng-PCL) polymer for highly sensitive and rapid determination of CEA. The polymer Ng-PCL is a macromolecular polymer that can increase the sensitivity of biosensor. First, SH-functionalized CEA-aptamer 1 (Apt1) was attached to the electrode surface as a recognition probe by Au-S bonds in order to form a self-assembly monolayer (SAM). Then, the one end of CEA antigen could recognize the Apt1 modified on the electrode surface, the other end could recognize the COOH-functionalized CEA-aptamer 2 (Apt2) forming a sandwich structure. Finally, polymer Ng-PCL as a signal amplification unit, which was connected to Apt2 by ester bonds. As a result, the electron transfer in the electrode interface was hindered effectively and a label-free electrochemical impedance sensor was constructed successfully. The high sensitivity and selectivity of biosensor relied on the SAM, polymer Ng-PCL, and specific recognition of CEA. Under the optimum experimental conditions, we proposed electrochemical impedance biosensor had wide detection range between 5 pg/mL and 200 ng/mL, and the sensitivity can reach 0.675 pg/mL. Moreover, the electrochemical impedance biosensor performed high specificity, good stability and satisfactory reproducibility as well. Thus, this strategy will provide new path for the detection of other biomarkers in early clinical diagnosis.

Chemical Sensing and Analysis with Optical Nanostructures

Nanostructures and nanomaterials, especially plasmonic nanostructures, often show optical properties that conventional materials lack and can manipulate light, as well as various light–matter interactions, in both their near-field and far-field regions with a high efficiency. Thanks to these unique properties, not only can they be used to enhance the sensitivity of chemical sensing and analysis techniques, but they also provide a solution for designing new sensing devices and simplifying the design of analytical instruments. The earliest applications of optical nanostructures are surface-enhanced spectroscopies. With the help of the resonance field enhancement of plasmonic nanostructures, molecular signals, such as Raman, infrared absorption, and fluorescence can be significantly enhanced, and even single-molecule analysis can be realized. Moreover, the resonant field enhancements of plasmonic nanostructures are often associated with other effects, such as optical forces, resonance shifts, and photothermal effects. Using these properties, label-free plasmonic sensors, nano-optical tweezers, and plasmonic matrix-assisted laser desorption/ionization have also been demonstrated in the past two decades. In the last few years, the research on optical nanostructures has gradually expanded to non-periodic 2D array structures, namely metasurfaces. With the help of metasurfaces, light can be arbitrarily manipulated, leading to many new possibilities for developing miniaturized integrated intelligent sensing and analysis systems. In this review, we discuss the applications of optical nanostructures in chemical sensing and analysis from both theoretical and practical aspects, aiming at a concise and unified framework for this field.

Novel composites of nano-metal–organic frameworks (IRMOF-3) and silver nanoparticles for the ultra-sensitive performance of SERS sensing and optical fiber modes

Rapid chemical detection of drugs of abuse in biological fluids such as blood and saliva is a concern within medicine and law enforcement. As an outcome, a label-free detection platform takes biological fluid samples with concentrations ranging from extremely high to very low. We obtained experimentally the limit of detection (LOD) of glycerol concentration, corresponding to a minimum resolvable refractive index of 3.4 × 10−7 RIU (refractive index unit). We applied the microfluidic device sensors to the quantitating concentration dopamine solutions. The experiment was recorded in real-time as the concentration of analyte injected exposed to the fiber core surface resulted in a sensitive change in optical power transmission. The presented sensors also exhibited reasonably good reproducibility and higher sensitivity, providing the LOD as 1.02 × 10−11 M. A relatively simple scheme procedure is proposed for the simultaneous detection and quantitative assessment of rhodamine B using surface-enhanced Raman spectroscopy with a limit of detection of 10−12 M and a relative standard deviation of 5.78% across a detection concentration range mainly from 10−5 M to 10−12 M. The obtained results demonstrate the potential of nano-metal–organic framework materials as large-area, label-free optical fiber sensors and SERS-based platforms for biomedical sensing and environmental applications.

Smartphone-powered portable chemiresistive sensing system for label free detection of lead ions in water

Lead (Pb) is a toxic heavy metal that can contaminate water sources and cause serious health problems. Detecting Pb in water is essential for protecting public health and the environment. However, the current state of technology heavily depends upon traditional bench-top equipment for detecting toxic heavy metal ions dissolved in water. In this paper we report a portable, label-free chemiresistive sensor for the selective detection of Pb ions dissolved in water. Lithography patterned micro-ineterdigitated electrodes (µIDEs) modified with Graphene oxide (GO) is used as the transducing agent to capture the sensor’s electrical response on a portable readout platform with a smartphone interface. Graphene oxide functionalized with environment friendly oligosaccharide β- Cyclodextrin acts as the sensing material. The sensor’s electrical properties undergo variation in the presence of Pb ions, hence serving as a parameter for successfully detecting the targeted heavy metal ion. The designed sensor is highly selective towards Pb ions, even in the presence of other heavy metal ions, with the lowest detection concentration being 100 pico Molar (pM). The smartphone-powered portable readout circuit, along with the sensor, makes the entire system energy-efficient and cost-effective, providing a quick analysis of the sensor output. Further, an ML algorithm is used to enhance the data analysis and assist the classification based on sensor response.

Label-free colorimetric sensor for Pb2+ determination using catalytic activity of MnO2 nanoflowers and elongated aptamer

In this study, a label-free aptasensor utilizing colorimetric properties was developed to detect Pb2+ with high sensitivity. The approach involved applying modified aptamer which enhanced the oxidase-mimicking activity of MnO2 nanoflowers. This innovative method provides an efficient means for monitoring Pb2+ ions without requiring any labeling techniques. The fundamental principle of this aptasensor is based on the adsorption of a modified aptamer onto MnO2 nanoflowers' surface, which in turn increases their affinity for chromogenic substrates and enhances their catalytic activity. The proposed aptasensor exploits the high sensitivity due to the extension of the aptamer sequence length by terminal deoxynucleotidyl transferase (TdT). Under optimum experimental conditions, the developed colorimetric aptasensor indicated a linear detection range from 4 to 80 nM with a limit of detection (LOD) of 1.4 nM. Moreover, the aptasensor successfully monitored Pb2+ in the drinking water, milk and human serum samples. Henceforth, the colorimetric aptasensor exhibited in this study possesses several benefits such as uncomplicated operation, cost-effectiveness, label-free detection and remarkable sensitivity. Thus rendering it a suitable option for analyzing intricate samples.

A label-free photoelectrochemical sensor based on BiVO4@graphene oxide hybrid for analysis of the antioxidant capacity in food

Antioxidant can protect body from free radical and dietary intake is a major source of antioxidants for human body. Therefore, it is particularly important to evaluate the antioxidant capacity of food and drink in daily diet. Herein, a label-free photoelectrochemical (PEC) sensor based on BiVO4@graphene oxide (GO) hybrid has been developed for antioxidants analysis and applied it to antioxidant capacity detection of real samples. Five representative antioxidants including ascorbic acid (AA), caffeic acid (CA), chlorogenic acid (CHA), fisetin (FT) and quercetin (QT) were determined by this PEC sensor to acquire photocurrent response at different concentrations. This PEC sensor exhibited excellent sensitivity and anti-interference. Furthermore, antioxidant capacity of food samples was assessed utilizing this PEC sensor, indicating the practicability and accuracy of this PEC sensor. This study suggests that BiVO4@GO composites constructed PEC sensor can provide a practical and fast method for detecting antioxidant capacity in the field of food.

Fluorophore-assisted green fabrication of flexible and cost-effective Ag nanoparticles decorated PVA nanofibers for SERS based trace detection

Detection and particularly quantitative analysis of organic pollutants such as rhodamine 6G (R6G), and p-nitrophenol (pNP) in water are very important for both human health and the ecological environment. In this study, we synthesized as a facile and low cost method silver nanoparticles on poly(vinyl alcohol) (PVA) nanofibers to prepare a film based surface enhancement Raman scattering (SERS) substrate for label free molecular detection. Detection of the R6G molecule with the obtained SERS substrate is possible even at concentrations as low as 10−12 M and therefore the obtained SERS substrate indicated excellent molecular sensitivity for R6G molecule. Limit of detection value (LOD) was determined as 1.07 × 10−13 M while the enhancement factor (EF) of the obtained SERS substrate was calculated as 1.06 × 109 for the R6G molecule. A fluorophore molecule named as 2,5-bis(4-hydroxyphenyl)thiazolo[5,4-d]thiazole (HPhTT) was effectively used for cross-linking of PVA nanofibers to use them as growth template for silver nanoparticles (AgNPs) formation on the surface without any reducing and stabilizing agent thanks to unique properties of HPhTT. Green and one pot preparation of such SERS substrates can pave the way for easily prepared commercial substrates.Moreover, AgNPs decorated PVA nanofiber-based SERS substrate has high reproducibility and good stability for SERS detection of organic pollutants. Obtained SERS substrate is expected to be applicable as a label-free sensor for various chemical and biological molecules.

SPR-Based Label-Free Sensor for RI-Based Detection of Urea Concentration

SPR-Based Label-Free Sensor for RI-Based Detection of Urea Concentration

Polished hollow core Bragg fiber sensor for simultaneous measurement of cortisol concentration and temperature.

Disturbance of surrounding temperature inevitably affects the accuracy of fiber biosensors. To that end, we propose a compact label-free optofluidic sensor based on a polished hollow core Bragg fiber (HCBF) that can simultaneously measure the cortisol concentration and surrounding temperature in real-time. The sensor is comprised of fusion splicing single mode fiber (SMF), multimode fiber (MMF) and HCBF. HCBF is side polished to remove part of the cladding that the suspended inner surface of the fiber can contact the external environment. After the incident light passes through the MMF from the SMF, it enters the hollow area, high refractive index (RI) layers, respectively, where the anti-resonant reflecting optical waveguide (ARROW) guiding mechanism and Mach-Zehnder interferometer (MZI) are simultaneously excited. Taking advantage of the high RI layers of HCBF, compared to the fiber with uniform cladding, the light can be more confined in the cladding and more sensitive to inner surface medium. The inner surface of sensor is immobilized with cortisol aptamer for the sake of achieving high sensitivity and specific sensing of cortisol with the limit of detection (LOD) to be 4.303 pM. The proposed sensor has a compact structure, enables temperature compensation, and can be fabricated at low cost making it highly suitable for in-situ monitoring and high-precision sensing of cortisol and other biological analytes.

Recognition of bovine hemoglobin protein on molecularly imprinted polymer surfaces using nonlinear vibrational spectroscopy

Advancement in molecularly imprinted biomimetics has aided in developing robust artificial recognition-based materials, which can be customized for bio/chemo-sensing of distinct molecules. The present study reports a simple one-step synthesis and analysis of protein-imprinted polymer thin films as a recognition element directly onto a solid support. Dopamine has been explored as a versatile functional monomer for a molecularly imprinted polymer (MIP) matrix to fabricate polydopamine (PDA) thin films with bovine hemoglobin as a template protein molecule. A detailed molecular-level insight into the recognition of the template molecule at each step has been investigated using vibrational sum frequency generation (VSFG) spectroscopy. A suitable PDA-coated thin film is selected based on the extent of polymerized intermediates formed after non-imprinted polymer fabrication at different time durations. An optimally prepared film of MIP is specified by observing the spectral signature of the methyl groups from protein molecules at the air–polymer interface. The template removal from MIP films after the washing procedure and subsequent re-binding of the protein molecules were evaluated by VSFG spectroscopy. The insightful molecular-level findings from SFG spectroscopy demonstrate the fabrication of an imprinted matrix as a label-free chemical sensor.

Electrochemical Olfactory Sensor for Odorants Using Porous Anodic Alumina (PAA) Nanochannels with Coupled Human Odorant Binding Proteins

By mimicking biological olifactory systems, sensors have been reported for the identification of important odorants at low concentration levels in complex environments. Herein a rapid and label-free olfactory sensor based on porous anodic alumina (PAA) nanochannels and the human odorant binding protein s(OBP2b) is reported for odorants. The OBP2b proteins were assembled on the surface of the PAA nanochannels by a Schiff base reaction and the recognition and connection of target with the OBP2b proteins led to steric hindrance inside the PAA nanochannels, resulting in a decreased anodic current due to the indicator, potassium ferricyanide. Using the PAA nanochannels with 55 nm pore diameter as the optimal reaction platform and the OBP2b proteins as the recognition element, the chronoamperometry allowed sensitive determination of ethyl acetate, lauric acid, and vanillin. Furthermore, odorants released by fruit samples were also detected by the developed sensor. Consequently, this sensitive and simple strategy provides an efficient and promising approach for environmental and biological sensing.

A Cytidine-Modified surfactant anchored liquid crystal Droplet-Based sensor for rapid and accurate detection of silver ions

Liquid crystal (LC) droplets exhibit unique and sensitive response behaviors to surface absorptions, making them promising candidates for sensing aplications. Here, we have developed a label-free, portable, and cost-effective sensor for the specific and rapid detection of silver ions (Ag+) in drinking-water samples. To achieve this, we have modified cytidine into a surfactant (denoted as C10–M–C) and anchored it onto the surface of LC droplets. The specific binding ability between cytidine and Ag+ enables LC droplets anchored with C10–M–C to respond rapidly and specifically to Ag+ ions. Furthermore, the sensitivity of the response meets requirements for the harmless concentration of Ag+ in drinking-water. The sensor we developed is label-free, portable, and cost-effectively. We believe that the sensor reported here can be applied to the detection of Ag+ in drinking-water and environmental samples.

Label-free electrochemiluminescence sensor based on magnetic nanoparticles modified with G-quadruplex DNA for detecting lead ions

Developing rapid and renewable sensors to detect heavy metal lead ions is a crucial and promising area of research. Herein, we constructed a label-free electrochemiluminescence (ECL) sensor for detecting Pb2+ using magnetic nanoparticles that were modified with a G-quadruplex probe. The aptamer probe was created by immobilizing a double-stranded DNA (dsDNA) onto the surface of Fe3O4@Au magnetic nanoparticles, with Ru(phen)32+ being intercalated into the dsDNA structure. Upon introduction of Pb2+, the dsDNA structure opened up to form the Fe3O4@Au-G-quadruplex-Pb2+ structure, resulting in the dissociation of single-stranded DNA (ssDNA) and Ru(phen)32+. The dissociated Ru(phen)32+ acted as an ECL probe, allowing for the construction of a highly sensitive sensing system that quantitatively relates Pb2+ concentrations to ECL signals. In the presence of the strong chelating agent EDTA, the hybridization of the two ssDNA strands back into the dsDNA structure allowed for the re-insertion of Ru(phen)32+ into the dsDNA structure, endowing the sensor with excellent renewability. The adapter sensor was characterized using cyclic voltammetry, electrochemiluminescence, and fluorescence spectroscopy. Over the range of 50 pM to 9 nM, the Pb2+ concentration exhibited a linear relationship with its corresponding ECL signal, with a detection limit of 1.2 pM. In addition, the biosensor demonstrated outstanding selectivity, stability, reproducibility, and potential for use in real-world sample applications.

Iron oxide/poly(3,4-ethylenedioxythiophene): poly(styrene sulfonate) glassy carbon electrode as a novel label-free electrochemical microRNA-21 sensor

MicroRNAs (miRNAs), a type of non-protein-coding and small RNAs, are encouraging molecular biomarkers for prior diagnosis of the certain diseases. Here, an electrochemical sensor based on iron oxide/poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate (Fe3O4/PEDOT:PSS) hybrid coated glassy carbon electrode (GCE) is reported to determine microRNA-21 (miRNA-21) as a biosensing platform based on hybridization event. The biosensor was characterized by cyclic voltammetry (CV) measurements. The Fe3O4/PEDOT:PSS demonstrated good sensing performance, including a wide detection range (0.1 pM-1 µM) and a low detection limit (0.023 pM) for potential medical applications.