Colorimetric determination of copper ions based on the catalytic leaching of silver from the shell of silver-coated gold nanorods

We have developed a method for the colorimetric determination of copper ions (Cu2+) that is based on the use of silver-coated gold nanorods (Au@Ag NRs). Its outstanding selectivity and sensitivity result from the catalytic leaching process that occurs between Cu2+, thiosulfate (S2O3 (2-)), and the surface of the Au@Ag NRs. The intrinsic color of the Au@Ag NRs changes from bright red to bluish green with decreasing thickness of the silver coating. The addition of Cu2+ accelerates the leaching of silver from the shell caused in the presence of S2O3 (2-). This result in a decrease in the thickness of the silver shell which is accompanied a change in color and absorption spectra of the colloidal solution. The shifts in the absorption maxima are linearly related to the concentrations of Cu2+ over the 3-1,000 nM concentration range (R = 0.996). The method is cost effective and was applied to the determination of Cu2+ in real water samples.We have developed a method for the colorimetric determination of copper ions (Cu2+) that is based on the use of silver-coated gold nanorods (Au@Ag NRs). Its outstanding selectivity and sensitivity result from the catalytic leaching process that occurs between Cu2+, thiosulfate (S2O3 (2-)), and the surface of the Au@Ag NRs. The intrinsic color of the Au@Ag NRs changes from bright red to bluish green with decreasing thickness of the silver coating. The addition of Cu2+ accelerates the leaching of silver from the shell caused in the presence of S2O3 (2-). This result in a decrease in the thickness of the silver shell which is accompanied a change in color and absorption spectra of the colloidal solution. The shifts in the absorption maxima are linearly related to the concentrations of Cu2+ over the 3-1,000 nM concentration range (R = 0.996). The method is cost effective and was applied to the determination of Cu2+ in real water samples

Highly sensitive label-free colorimetric sensing of nitrite based on etching of gold nanorods

A simple colorimetric method with high sensitivity and selectivity was developed for sensing of nitrite as low as 4.0 mu M by naked eyes, which is based on etching of gold nanorods accompanied by shape changes in aspect ratios (length/width) and a visible color change from bluish green to red and then to colorless with the increase of nitrite

SERS Tags: Novel Optical Nanoprobes for Bioanalysis

CONTENTS1. Introduction1.1. Fundamental Theory of Surface-Enhanced Raman Scattering1.2. Optical Properties of SERS Tags2. Synthesis of SERS Tags2.1. Noble Metal Nanosubstrates2.1.1. Single Particle-Based SERS Substrates2.1.2. Nanoparticle Cluster-Based Substrates2.2. Raman Reporter Molecules2.2.1. Selection Principles and Reporter Types2.2.2. Self-Assembled Monolayer Coverage Strategy2.3. Surface Coating for Protection2.3.1. Biomolecule Coating2.3.2. Polymer Coating2.3.3. Liposome Coating2.3.4. Silica Coating2.4. Attachment of Targeting Molecules3. Bioanalysis Applications3.1. Ionic and Molecular Detection3.2. Pathogen Detection3.3. Live-Cell Imaging3.3.1. Cancer Marker Detection3.3.2. Intercellular Microenvironment Sensing3.4. Tissue SERS Imaging3.5. In Vivo SERS Imaging4. Challenges and Perspectives4.1. Reproducible Signal of SERS Tags4.1.1. Precisely Controlled Hot Spots for Nanosubstrates4.1.2. Calibration of SERS Intensities and Enhancements4.2. Improving Multiplexing Capability4.3. Reduced Size for Subcellular Imaging4.4. Development of Multifunctional Nanoplatforms4.4.1. Magnetic SERS Dots4.4.2. Multimodal Imaging Dots4.4.3. SERS Tag-Based Therapeutic Systems4.5. Biocompatibility5. Conclusions and Remarks</ul

Colorimetric sensing of copper(II) based on catalytic etching of gold nanoparticles

Based on the catalytic etching of gold nanoparticles (AuNPs), a label-free colorimetric probe was developed for the detection of Cu2+ in aqueous solutions. AuNPs were first stabilized by hexadecyltrimethylammonium bromide in NH3-NH4Cl (0.6 M/0.1 M) solutions. Then thiosulfate (S2O32-) ions were introduced and AuNPs were gradually dissolved by dissolved oxygen. With the further addition of Cu2+, Cu(NH3)(4)(2+) oxidized AuNPs to produce Au(S2O3)(2)(3-) and Cu(S2O3)(3)(5-), while the later was oxidized to Cu(NH3)(4)(2+) again by dissolved oxygen. The dissolving rate of AuNPs was thereby remarkably promoted and Cu2+ acted as the catalyst. The process went on due to the sufficient supply of dissolved oxygen and AuNPs were rapidly etched. Meanwhile, a visible color change from red to colorless was observed. Subsequent tests confirmed such a non-aggregation-based method as a sensitive (LOD= 5.0 nM or 032 ppb) and selective (at least 100-fold over other metal ions except for Pb2+ and Mn2+) way for the detection of Cu2+ (linear range, 10-80 nM). Moreover, our results show that the color change induced by 40 nM Cu2+ can be easily observed by naked eyes, which is particularly applicable to fast on-site investigations. (C) 2013 Elsevier B.V. All rights reserved.Based on the catalytic etching of gold nanoparticles (AuNPs), a label-free colorimetric probe was developed for the detection of Cu2+ in aqueous solutions. AuNPs were first stabilized by hexadecyltrimethylammonium bromide in NH3-NH4Cl (0.6 M/0.1 M) solutions. Then thiosulfate (S2O32-) ions were introduced and AuNPs were gradually dissolved by dissolved oxygen. With the further addition of Cu2+, Cu(NH3)(4)(2+) oxidized AuNPs to produce Au(S2O3)(2)(3-) and Cu(S2O3)(3)(5-), while the later was oxidized to Cu(NH3)(4)(2+) again by dissolved oxygen. The dissolving rate of AuNPs was thereby remarkably promoted and Cu2+ acted as the catalyst. The process went on due to the sufficient supply of dissolved oxygen and AuNPs were rapidly etched. Meanwhile, a visible color change from red to colorless was observed. Subsequent tests confirmed such a non-aggregation-based method as a sensitive (LOD= 5.0 nM or 032 ppb) and selective (at least 100-fold over other metal ions except for Pb2+ and Mn2+) way for the detection of Cu2+ (linear range, 10-80 nM). Moreover, our results show that the color change induced by 40 nM Cu2+ can be easily observed by naked eyes, which is particularly applicable to fast on-site investigations. (C) 2013 Elsevier B.V. All rights reserved

Label free colorimetric sensing of thiocyanate based on inducing aggregation of Tween 20-stabilized gold nanoparticles

Based on inducing the aggregation of gold nanoparticles (AuNPs), a simple colorimetric method with high sensitivity and selectivity was developed for the sensing of thiocyanate (SCN-) in aqueous solutions. Citrate-capped AuNPs were prepared following a classic method and Tween 20 was subsequently added as a stabilizer. With the addition of SCN-, citrate ions on AuNPs surfaces were replaced due to the high affinity between SCN- and Au. As a result, Tween 20 molecules adsorbed on the AuNPs surfaces were separated and the AuNPs aggregated. The process was accompanied by a visible color change from red to blue within 5 min. The sensing of SCN- can therefore be easily achieved by a UV-vis spectrophotometer or even by the naked eye. The potential effects of relevant experimental conditions, including concentration of Tween 20, pH, incubation temperature and time, were evaluated to optimize the method. Under optimized conditions, this method yields excellent sensitivity (LOD = 0.2 mu M or 11.6 ppb) and selectivity toward SCN-. Our attempt may provide a cost-effective, rapid and simple solution to the inspection of SCN- ions in saliva and environmental aqueous samples

Highly Sensitive Surface-Enhanced Raman Scattering Sensing of Heparin Based on Antiaggregation of Functionalized Silver Nanoparticles

We report a simple and sensitive surface-enhanced Raman scattering (SERS) platform for the detection of heparin, based on antiaggregation of 4-mercaptopyridine (4-MPY) functionalized silver nanoparticles (Ag NPs). Here, protamine was employed as a medium for inducing the aggregation of negatively charged 4-MPY functionalized Ag NPs through surface electrostatic interaction, which resulted in significantly enhanced Raman signal of the Raman reporter. However, in the presence of heparin, the interaction between heparin and protamine decreased the concentration of free protamine, which dissipated the aggregated 4-MPY functionalized Ag NPs and thus decreased Raman enhancement effect. The degree of aggregation and Raman enhancement effect was proportional to the concentration of added heparin. Under optimized assay conditions, good linear relationship was obtained over the range of 0.5-150 ng/mL (R-2 = 0.998) with a minimum detectable concentration of 0.5 ng/mL in standard aqueous solution. Furthermore, the developed method was also successfully applied for detecting heparin in fetal bovine serum samples with a linear range of 1-400 ng/mL.We report a simple and sensitive surface-enhanced Raman scattering (SERS) platform for the detection of heparin, based on antiaggregation of 4-mercaptopyridine (4-MPY) functionalized silver nanoparticles (Ag NPs). Here, protamine was employed as a medium for inducing the aggregation of negatively charged 4-MPY functionalized Ag NPs through surface electrostatic interaction, which resulted in significantly enhanced Raman signal of the Raman reporter. However, in the presence of heparin, the interaction between heparin and protamine decreased the concentration of free protamine, which dissipated the aggregated 4-MPY functionalized Ag NPs and thus decreased Raman enhancement effect. The degree of aggregation and Raman enhancement effect was proportional to the concentration of added heparin. Under optimized assay conditions, good linear relationship was obtained over the range of 0.5-150 ng/mL (R-2 = 0.998) with a minimum detectable concentration of 0.5 ng/mL in standard aqueous solution. Furthermore, the developed method was also successfully applied for detecting heparin in fetal bovine serum samples with a linear range of 1-400 ng/mL

Controlling Capillary-Driven Fluid Transport in Paper-Based Microfluidic Devices Using a Movable Valve

This paper describes a novel, strategy for fabricating the movable valve on paper-based microfluidic devices to manipulate capillary-driven fluids. The movable valve fabrication is first realized using hollow rivets as the-holding center it, control the paper channel in different layer movement that Jesuits in the :channel&#39;s connection or disconnection. The relatively simple Valve fabrication procedure is robust, Versatile, and, compatible with microfluidic paper-based analytical devices (mu PADs) with differing levels of complexity. It is remarkable that the movable valve can be convenient and free to control fluid without the timing setting; advantages that make it user-friendly for untrained users to carry out the complex multistep operations. For the, performance of the Movable valve to be-verified, several different designs of mu PADs were tested and obtained with satisfactory results. In addition; in the proof-of-concept enzyme-linked immunosorbent assay experiments, we demonstrate the use of these valves in mu PADs for the successful analysis of samples of carcino-embryonic antigen, showing good sensitivity and reproducibility. We hope this technique will open new avenues for the fabrication of paper-based valves in an easily adoptable and widely available way on mu PADs and provide potential point-of-Care applications in the future.This paper describes a novel, strategy for fabricating the movable valve on paper-based microfluidic devices to manipulate capillary-driven fluids. The movable valve fabrication is first realized using hollow rivets as the-holding center it, control the paper channel in different layer movement that Jesuits in the :channel&#39;s connection or disconnection. The relatively simple Valve fabrication procedure is robust, Versatile, and, compatible with microfluidic paper-based analytical devices (mu PADs) with differing levels of complexity. It is remarkable that the movable valve can be convenient and free to control fluid without the timing setting; advantages that make it user-friendly for untrained users to carry out the complex multistep operations. For the, performance of the Movable valve to be-verified, several different designs of mu PADs were tested and obtained with satisfactory results. In addition; in the proof-of-concept enzyme-linked immunosorbent assay experiments, we demonstrate the use of these valves in mu PADs for the successful analysis of samples of carcino-embryonic antigen, showing good sensitivity and reproducibility. We hope this technique will open new avenues for the fabrication of paper-based valves in an easily adoptable and widely available way on mu PADs and provide potential point-of-Care applications in the future

Fluorescent sensing of mercury(II) based on formation of catalytic gold nanoparticles

A fluorescence assay for the highly sensitive and selective detection of Hg2+ using a gold nanoparticle (AuNP)-based probewas proposed. The assay was based on the formation of Hg-Au alloys, which accelerated the oxidization of o-phenylenediamine by dissolved oxygen to produce 2,3-diaminophenazine, a fluorescent product.;A fluorescence assay for the highly sensitive and selective detection of Hg2+ using a gold nanoparticle (AuNP)-based probewas proposed. The assay was based on the formation of Hg-Au alloys, which accelerated the oxidization of o-phenylenediamine by dissolved oxygen to produce 2,3-diaminophenazine, a fluorescent product

A uracil nitroso amine based colorimetric sensor for the detection of Cu²⁺ ions from aqueous environment and its practical applications

A simple uracil nitroso amine based colorimetric chemosensor (UNA-1) has been synthesized and screened for its cation recognition ability. Sensor UNA-1 exhibited a high sensitivity and selectivity towards Cu²⁺ ions in aqueous medium in the presence of a wide range of other competing cations (Ag⁺, Al³⁺, Ba²⁺+, Ca²⁺, Cd²⁺, Co²⁺, Cr³⁺, Cs⁺, Fe²⁺, Fe³⁺, Li⁺, Mg²⁺, Mn²⁺, Na⁺, Ni²⁺, Pb²⁺, Zn²⁺, Hg²⁺ and Sr²⁺). With Cu²⁺, the sensor UNA-1 gave a distinct color change from colorless to dark yellow by forming a complex of 1:1 stoichiometry. Furthermore, sensor UNA-1 was successfully utilized in the preparation of test strips and supported silica for the detection of Cu²⁺ ions from aqueous environment

Dummy Molecularly Imprinted Polymers-Capped CdTe Quantum Dots for the Fluorescent Sensing of 2,4,6-Trinitrotoluene

Molecularly imprinted polymers (MIPs) with trinitrophenol (TNP) as a dummy template molecule capped with CdTe quantum dots (QDs) were prepared using 3-aminopropyltriethoxy silane (APTES) as the functional monomer and tetraethoxysilane (TEOS) as the cross linker through a seedgrowth method via a sol gel process (i.e., DMIP@QDs) for the sensing of 2,4,6-trinitrotoluene (TNT) on the basis of electron-transfer-induced fluorescence quenching. With the presence and increase of TNT in sample solutions, a Meisenheimer complex was formed between TNT and the primary amino groups on the surface of the QDs. The energy of the QDs was transferred to the complex, resulting in the quenching of the QDs and thus decreasing the fluorescence intensity, which allowed the TNT to be sensed optically. DMIP@QDs generated a significantly reduced fluorescent intensity within less than 10 min upon binding TNT. The fluorescence-quenching fractions of the sensor presented a satisfactory linearity with TNT concentrations in the range of 0.8-30 mu M, and its limit of detection could reach 0.28 mu M. The sensor exhibited distinguished selectivity and a high binding affinity to TNT over its possibly competing molecules of 2,4-dinitrophenol (DNP), 4-nitrophenol (4-NP), phenol, and dinitrotoluene (DNT) because there are more nitro groups in TNT and therefore a stronger electron-withdrawing ability and because it has a high similarity in shape and volume to TNP. The sensor was successfully applied to determine the amount of TNT in soil samples, and the average recoveries of TNT at three spiking levels ranged from 90.3 to 97.8% with relative standard deviations below 5.12%. The results provided an effective way to develop sensors for the rapid recognition and determination of hazardous materials from complex matrices.Molecularly imprinted polymers (MIPs) with trinitrophenol (TNP) as a dummy template molecule capped with CdTe quantum dots (QDs) were prepared using 3-aminopropyltriethoxy silane (APTES) as the functional monomer and tetraethoxysilane (TEOS) as the cross linker through a seedgrowth method via a sol gel process (i.e., DMIP@QDs) for the sensing of 2,4,6-trinitrotoluene (TNT) on the basis of electron-transfer-induced fluorescence quenching. With the presence and increase of TNT in sample solutions, a Meisenheimer complex was formed between TNT and the primary amino groups on the surface of the QDs. The energy of the QDs was transferred to the complex, resulting in the quenching of the QDs and thus decreasing the fluorescence intensity, which allowed the TNT to be sensed optically. DMIP@QDs generated a significantly reduced fluorescent intensity within less than 10 min upon binding TNT. The fluorescence-quenching fractions of the sensor presented a satisfactory linearity with TNT concentrations in the range of 0.8-30 mu M, and its limit of detection could reach 0.28 mu M. The sensor exhibited distinguished selectivity and a high binding affinity to TNT over its possibly competing molecules of 2,4-dinitrophenol (DNP), 4-nitrophenol (4-NP), phenol, and dinitrotoluene (DNT) because there are more nitro groups in TNT and therefore a stronger electron-withdrawing ability and because it has a high similarity in shape and volume to TNP. The sensor was successfully applied to determine the amount of TNT in soil samples, and the average recoveries of TNT at three spiking levels ranged from 90.3 to 97.8% with relative standard deviations below 5.12%. The results provided an effective way to develop sensors for the rapid recognition and determination of hazardous materials from complex matrices