One-pot dual product synthesis of hierarchical Co3O4@N-rGO for supercapacitors, N-GDs for label-free detection of metal ion and bio-imaging applications

2018 ◽  
Vol 44 (3) ◽  
pp. 2869-2883 ◽  
Author(s):  
Raji Atchudan ◽  
Thomas Nesakumar Jebakumar Immanuel Edison ◽  
Dasagrandhi Chakradhar ◽  
Namachivayam Karthik ◽  
Suguna Perumal ◽  
...  
Keyword(s):  
Metal Ion ◽  
Label Free ◽  
One Pot ◽  
Label Free Detection ◽  
Bio Imaging

scholarly journals Combination of Capped Gold Nanoslit Array and Electrochemistry for Sensitive Aqueous Mercuric Ions Detection

Nanomaterials ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 88
Author(s):  
Cheng-Chuan Chen ◽  
Shu-Cheng Lo ◽  
Pei-Kuen Wei
Keyword(s):  
Metal Ion ◽  
Water Solution ◽  
Resonant Peak ◽  
Label Free ◽  
Glycerol Water ◽  
Detection Range ◽  
Label Free Detection ◽  
Intensity Changes ◽  
Mercuric Ions ◽  
Nanoslit Arrays

Label-free surface plasmon resonance (SPR) detection of mercuric ions in various aqueous solutions, using capped gold nanoslit arrays combined with electrochemical (EC) sensing technique, is demonstrated. The nanoslit arrays are fabricated on flexible cyclo-olefin polymer substrates by a nanoimprinting lithography method. The EC and SPR signals for the investigation of current responses and transmission SPR spectra are simultaneously measured during metal ions electrodeposition. Glycerol–water solution is studied to evaluate the resonant peak wavelength sensitivity (480.3 nm RIU−1) with a FOM of 40.0 RIU−1 and the obtained intensity sensitivity is 1819.9%. The ferrocyanide/ferricyanide redox couple performs the diffusion controlled electrochemical processes (R2 = 0.99). By investigating the SPR intensity changes and wavelength shifts of various mercuric ion concentrations, the optical properties are evaluated under chronoamperometric conditions. The sensors are evaluated in the detection range between 100 μM and 10 nM with a detection limit of 1 μM. The time dependence of SPR signals and the selectivity of 10 μM Hg2+ in the presence of 10 μM interfering metal ion species from Ca2+, Co2+, Ni2+, Na+, Cu2+, Pb2 + and Mn2+ are determined. The capped gold nanoslit arrays show the selectivity of Hg2+ and the EC sensing method is effectively utilized to aqueous Hg2+ detection. This study provides a label-free detection technique of mercuric ions and this developed system is potentially applicable to detecting chemicals and biomolecules.

scholarly journals Biomass-derived Carbon Quantum Dots for Visible-Light-Induced Photocatalysis and Label-Free Detection of Fe(III) and Ascorbic acid

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Gouri Sankar Das ◽  
Jong Pil Shim ◽  
Amit Bhatnagar ◽  
Kumud Malika Tripathi ◽  
TaeYoung Kim
Keyword(s):  
Quantum Dots ◽  
Ascorbic Acid ◽  
Visible Light ◽  
Fluorescence Emission ◽  
Carbon Quantum Dots ◽  
Active Species ◽  
Label Free ◽  
One Pot ◽  
Label Free Detection ◽  
Visible Light Driven

Abstract Visible-light-driven photocatalysts prepared using renewable resources are crucial but challenging to develop for the efficient degradation of organic pollutants, which is required to solve ever-increasing water deterioration issues. In this study, we report a visible-light-responsive photocatalyst for the efficient degradation of methylene blue (MB) as a model pollutant dye. Green-emissive carbon quantum dots (CQDs) were synthesized from pear juice via a facile, scalable, one-pot solvothermal process. The as-synthesized CQDs exhibit superior photocatalytic activity under visible-light irradiation owing to their efficient light absorption, electron transfer, and separation of photogenerated charge carriers, facilitating ~99.5% degradation of MB within 130 min. A possible mechanism for the photocatalysis is proposed on the basis of comprehensive active species trapping experiments. Furthermore, the CQDs were used in a specific sensitive assay for Fe(III) and ascorbic acid (AA), even with interference from other metal ions. The fluorescence emission of CQDs was “turned off” specifically upon binding of Fe(III) and “turned on” with AA. The prepared CQDs represent efficient photocatalysts and fluorescent probes that are not restricted by toxicity, cost, or lack of scalability.

scholarly journals Metal-Modified Montmorillonite as Plasmonic Microstructure for Direct Protein Detection

Sensors ◽  
2021 ◽  
Vol 21 (8) ◽  
pp. 2655
Author(s):  
Giorgia Giovannini ◽  
Denis Garoli ◽  
Patrick Rupper ◽  
Antonia Neels ◽  
René M. Rossi ◽  
...  
Keyword(s):  
Hybrid Materials ◽  
Optical Sensors ◽  
Metal Ion ◽  
Protein Detection ◽  
Fluorescein Isothiocyanate ◽  
Detection Methods ◽  
Sensor Technology ◽  
Label Free ◽  
Detection Mechanism ◽  
Label Free Detection

Thanks to its negative surface charge and high swelling behavior, montmorillonite (MMT) has been widely used to design hybrid materials for applications in metal ion adsorption, drug delivery, or antibacterial substrates. The changes in photophysical and photochemical properties observed when fluorophores interact with MMT make these hybrid materials attractive for designing novel optical sensors. Sensor technology is making huge strides forward, achieving high sensitivity and selectivity, but the fabrication of the sensing platform is often time-consuming and requires expensive chemicals and facilities. Here, we synthesized metal-modified MMT particles suitable for the bio-sensing of self-fluorescent biomolecules. The fluorescent enhancement achieved by combining clay minerals and plasmonic effect was exploited to improve the sensitivity of the fluorescence-based detection mechanism. As proof of concept, we showed that the signal of fluorescein isothiocyanate can be harvested by a factor of 60 using silver-modified MMT, while bovine serum albumin was successfully detected at 1.9 µg/mL. Furthermore, we demonstrated the versatility of the proposed hybrid materials by exploiting their plasmonic properties to develop liquid label-free detection systems. Our results on the signal enhancement achieved using metal-modified MMT will allow the development of highly sensitive, easily fabricated, and cost-efficient fluorescent- and plasmonic-based detection methods for biomolecules.

scholarly journals DNA nanotechnology assisted nanopore-based analysis

2020 ◽  
Vol 48 (6) ◽  
pp. 2791-2806 ◽  
Author(s):  
Taoli Ding ◽  
Jing Yang ◽  
Victor Pan ◽  
Nan Zhao ◽  
Zuhong Lu ◽  
...  
Keyword(s):  
Single Molecule ◽  
Dna Nanotechnology ◽  
Clinical Diagnostics ◽  
Dna Assembly ◽  
Label Free ◽  
One Pot ◽  
Dna Strand Displacement ◽  
Label Free Detection ◽  
Target Molecules ◽  
Dna Strand

Abstract Nanopore technology is a promising label-free detection method. However, challenges exist for its further application in sequencing, clinical diagnostics and ultra-sensitive single molecule detection. The development of DNA nanotechnology nonetheless provides possible solutions to current obstacles hindering nanopore sensing technologies. In this review, we summarize recent relevant research contributing to efforts for developing nanopore methods associated with DNA nanotechnology. For example, DNA carriers can capture specific targets at pre-designed sites and escort them from nanopores at suitable speeds, thereby greatly enhancing capability and resolution for the detection of specific target molecules. In addition, DNA origami structures can be constructed to fulfill various design specifications and one-pot assembly reactions, thus serving as functional nanopores. Moreover, based on DNA strand displacement, nanopores can also be utilized to characterize the outputs of DNA computing and to develop programmable smart diagnostic nanodevices. In summary, DNA assembly-based nanopore research can pave the way for the realization of impactful biological detection and diagnostic platforms via single-biomolecule analysis.

scholarly journals The Role of Surface Chemistry in the Efficacy of Protein and DNA Microarrays for Label-Free Detection: An Overview

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1026
Author(s):  
Elisa Chiodi ◽  
Allison M. Marn ◽  
Matthew T. Geib ◽  
M. Selim Ünlü
Keyword(s):  
Surface Chemistry ◽  
Surface Functionalization ◽  
Dna Microarrays ◽  
Label Free ◽  
Polymeric Coatings ◽  
Label Free Detection ◽  
Particle Imaging ◽  
Single Particle Imaging ◽  
The Impact

The importance of microarrays in diagnostics and medicine has drastically increased in the last few years. Nevertheless, the efficiency of a microarray-based assay intrinsically depends on the density and functionality of the biorecognition elements immobilized onto each sensor spot. Recently, researchers have put effort into developing new functionalization strategies and technologies which provide efficient immobilization and stability of any sort of molecule. Here, we present an overview of the most widely used methods of surface functionalization of microarray substrates, as well as the most recent advances in the field, and compare their performance in terms of optimal immobilization of the bioreceptor molecules. We focus on label-free microarrays and, in particular, we aim to describe the impact of surface chemistry on two types of microarray-based sensors: microarrays for single particle imaging and for label-free measurements of binding kinetics. Both protein and DNA microarrays are taken into consideration, and the effect of different polymeric coatings on the molecules’ functionalities is critically analyzed.

scholarly journals Label-Free Electrochemical Sensor for Rapid Bacterial Pathogen Detection Using Vancomycin-Modified Highly Branched Polymers

Sensors ◽  
2021 ◽  
Vol 21 (5) ◽  
pp. 1872
Author(s):  
Holger Schulze ◽  
Harry Wilson ◽  
Ines Cara ◽  
Steven Carter ◽  
Edward N. Dyson ◽  
...  
Keyword(s):  
Pathogen Detection ◽  
Electrochemical Impedance ◽  
Point Of Care ◽  
Branched Polymers ◽  
Label Free ◽  
Conformation Change ◽  
Gram Positive ◽  
Gram Positive Bacteria ◽  
Staphylococcus Carnosus ◽  
Label Free Detection

Rapid point of care tests for bacterial infection diagnosis are of great importance to reduce the misuse of antibiotics and burden of antimicrobial resistance. Here, we have successfully combined a new class of non-biological binder molecules with electrochemical impedance spectroscopy (EIS)-based sensor detection for direct, label-free detection of Gram-positive bacteria making use of the specific coil-to-globule conformation change of the vancomycin-modified highly branched polymers immobilized on the surface of gold screen-printed electrodes upon binding to Gram-positive bacteria. Staphylococcus carnosus was detected after just 20 min incubation of the sample solution with the polymer-functionalized electrodes. The polymer conformation change was quantified with two simple 1 min EIS tests before and after incubation with the sample. Tests revealed a concentration dependent signal change within an OD600 range of Staphylococcus carnosus from 0.002 to 0.1 and a clear discrimination between Gram-positive Staphylococcus carnosus and Gram-negative Escherichia coli bacteria. This exhibits a clear advancement in terms of simplified test complexity compared to existing bacteria detection tests. In addition, the polymer-functionalized electrodes showed good storage and operational stability.

scholarly journals A multicolor and ratiometric fluorescent sensing platform for metal ions based on arene–metal-ion contact

2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Anna Kanegae ◽  
Yusuke Takata ◽  
Ippei Takashima ◽  
Shohei Uchinomiya ◽  
Ryosuke Kawagoe ◽  
...  
Keyword(s):  
Metal Ions ◽  
Metal Ion ◽  
Near Infrared ◽  
Molecular Design ◽  
Theoretical Calculations ◽  
Probe Design ◽  
One Pot ◽  
Fluorescent Sensing ◽  
Sensing Platform ◽  
Ratiometric Detection

AbstractDespite continuous and active development of fluorescent metal-ion probes, their molecular design for ratiometric detection is restricted by the limited choice of available sensing mechanisms. Here we present a multicolor and ratiometric fluorescent sensing platform for metal ions based on the interaction between the metal ion and the aromatic ring of a fluorophore (arene–metal-ion, AM, coordination). Our molecular design provided the probes possessing a 1,9-bis(2′-pyridyl)-2,5,8-triazanonane as a flexible metal ion binding unit attached to a tricyclic fluorophore. This architecture allows to sense various metal ions, such as Zn(II), Cu(II), Cd(II), Ag(I), and Hg(II) with emission red-shifts. We showed that this probe design is applicable to a series of tricyclic fluorophores, which allow ratiometric detection of the metal ions from the blue to the near-infrared wavelengths. X-ray crystallography and theoretical calculations indicate that the coordinated metal ion has van der Waals contact with the fluorophore, perturbing the dye’s electronic structure and ring conformation to induce the emission red-shift. A set of the probes was useful for the differential sensing of eight metal ions in a one-pot single titration via principal component analysis. We also demonstrate that a xanthene fluorophore is applicable to the ratiometric imaging of metal ions under live-cell conditions.

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