Juanjuan Lu

Electrochemical biosensor based on graphene oxide-Au nanoclusters composites for l-cysteine analysis

In this paper, a linker-free connected graphene oxide/Au nanocluster (GO-Au NCs) composite was prepared under sonication through electrostatic interactions, and characterized by transmission electron microscope (TEM), atomic force microscope (AFM), ultraviolet-visible (UV-vis) and FT-IR spectrum. The morphological and structural characterizations evidence that the Au NCs can be efficiently decorated on the GO. The electrochemical investigations indicated that GO-Au NCs composite has an important role in the electrocatalytic activity towards the oxidation of L-cysteine (CySH). The GO-Au NCs composite modified electrode shows a large determination range from 0.05 to 20.0 μmol/L, a remarkably low detection limit is 0.02 μmol/L and low oxidation potential (+0.387). It was found that metal ions, carbohydrates, nucleotide acids and amino acids had no distinct effect on the determination of L-cysteine. In addition, the sensor has some important advantages such as simple preparation, fast response, good stability and high reproducibility. The direct determination of free reduced and total CySH in human urine samples has been successfully carried out without the assistance of any separation techniques.

Ultrasensitive electrochemical immunosensor based on Au nanoparticles dotted carbon nanotube–graphene composite and functionalized mesoporous materials

A facile and sensitive electrochemical immunosensor for detection of human chorionic gonadotrophin (hCG) was designed by using functionalized mesoporous nanoparticles as bionanolabels. To construct high-performance electrochemical immunosensor, Au nanoparticles (AuNPs) dotted carbon nanotubes (MWCNTs)-graphene composite was immobilized on the working electrode, which can increase the surface area to capture a large amount of primary antibodies (Ab(1)) as well as improve the electronic transmission rate. The as-prepared bionanolabels. composed of mesoporous silica nanoparticles (MCM-41) coated with AuNPs through thionine linking, showed good adsorption of horseradish peroxidase-labeled secondary anti-hCG antibody. Interlayer thionine was not only a bridging agent between MCM-41 and AuNPs but also an excellent electron mediator. The approach provided a good linear response range from 0.005 to 500 mIU mL(-1) with a low detection limit of 0.0026 mIU mL(-1). The immunosensor showed good precision, acceptable stability and reproducibility. Satisfactory results were obtained for determination of hCG in human serum samples. The proposed method provides a new promising platform of clinical immunoassay for other biomolecules.

Electrochemiluminescence of blue-luminescent graphene quantum dots and its application in ultrasensitive aptasensor for adenosine triphosphate detection.

A simple approach based on exfoliating and disintegrating treatments for graphite oxide, followed by hydrothermal synthesis, was developed to prepare water-soluble graphene quantum dots (GQDs). The as-prepared GQDs exhibited bright blue emission under ultraviolet irradiation (∼365nm), and showed an excitation-independent photoluminescence feature. More importantly, a newly anodic electrochemiluminescence (ECL) was observed from the water-soluble GQDs with H2O2 as coreactant for the first time, and the ECL induced a strong light emission at a low potential (ca. 0.4V vs. Ag/AgCl). The ECL mechanism is investigated in detail. Employing SiO2 nanospheres as signal carrier, a novel SiO2/GQDs ECL signal amplification labels were synthesized based on which a ultrasensitive ECL aptamer sensor was proposed. Under the optimized experimental conditions, the proposed ECL aptamer sensor exhibited excellent analytical performance for adenosine triphosphate (ATP) determination, ranging from 5.0×10(-12) to 5.0×10(-9)molL(-1) with the detection limit of 1.5×10(-12)molL(-1). Due to the low cytotoxicity and excellent biocompatibility, GQDs are demonstrated to be an eco-friendly material as well as excellent ECL labeling agents for biosensor.

Ultrasensitive electrochemical immunoassay for carcinoembryonic antigen based on three-dimensional macroporous gold nanoparticles/graphene composite platform and multienzyme functionalized nanoporous silver label.

Three-dimensional macroporous gold nanoparticles/graphene composites (3D-AuNPs/GN) were synthesized through a simple two-step process, and were used to modify working electrode sensing platform, based on which a facile electrochemical immunoassay for sensitive detection of carcinoembryonic antigen (CEA) in human serum was developed. In the proposed 3D-AuNPs/GN, AuNPs were distributed not just on the surface, but also on the inside of graphene. And this distribution property increased the area of sensing surface, resulting in capturing more primary antibodies as well as improving the electronic transmission rate. In the presence of CEA, a sandwich-type immune composite was formed on the sensing platform, and the horseradish peroxidase-labeled anti-CEA antibody (HRP-Ab2)/thionine/nanoporous silver (HRP-Ab2/TH/NPS) signal label was captured. Under optimal conditions, the electrochemical immunosensor exhibited excellent analytical performance: the detection range of CEA is from 0.001 to 10 ng mL(-1) with low detection limit of 0.35 pg mL(-1) and low limit of quantitation (LOQ) of 0.85 pg mL(-1). The electrochemical immunosensor showed good precision, acceptable stability and reproducibility, and could be used for the detection of CEA in real samples. The proposed method provides a promising platform of clinical immunoassay for other biomolecules.

An aptasensor for sensitive detection of human breast cancer cells by using porous GO/Au composites and porous PtFe alloy as effective sensing platform and signal amplification labels

A novel aptamer biosensor for cancer cell assay has been reported on the basis of ultrasensitive electrochemical detection. The assay uses the aptamer as a capture probe to recognize and bind the tumor marker on the surface of the cancer cells, forming an aptamer-based sandwich structure for MCF-7 cells detection. Functionalized nanoporous materials, porous graphene oxide/Au composites (GO/Au composites) and porous PtFe alloy have been introduced into the biosensor. Owing to the large surface area and versatile porous structure, the use of nanoporous materials can significantly improve the analysis performance of the biosensors by loading of large amounts of molecules and accelerating diffusion rate. Under the optimized experimental conditions, the proposed aptamer biosensor exhibited excellent analytical performance for MCF-7 cells determination, ranging from 100 to 5.0×10(7) cells mL(-1) with the detection limit of 38 cells mL(-1). The biosensor showed good selectivity, acceptable stability and reproducibility, and developed a highly sensitive and selective method for cancer cells detection.

Development of a novel deltamethrin sensor based on molecularly imprinted silica nanospheres embedded CdTe quantum dots

A novel procedure for the determination of deltmethrin (DM) is reported. The water-soluble CdTe quantum dots (QDs) and highly fluorescent silica molecularly imprinted nanospheres embedded CdTe QDs (CdTe-SiO2-MIPs) were prepared and characterized by fluorescence spectroscopy, UV-vis spectroscopy, TEM and IR. The fluorescence nanosensor based CdTe-SiO2-MIPs is developed. The possible quenching mechanism is discussed by DM. Under optimal conditions, the relative fluorescence intensity of CdTe-SiO2-MIPs decreased with increasing DM by a Stern-Volmer type equation in the concentration range of 0.5-35.0 μg mL(-1), the corresponding detection limit is 0.16 μg mL(-1). The developed sensor based on CdTe-SiO2-MIPs was applied to determine DM in fruit and vegetable samples.

Magnetic graphene nanosheets based electrochemiluminescence immunoassay of cancer biomarker using CdTe quantum dots coated silica nanospheres as labels.

A highly sensitive electrochemiluminescence (ECL) immunosensor for the detection of prostate specific antigen (PSA) was designed using biofunctionalized magnetic graphene nanosheets (G@Fe(3)O(4)) as immunosensing probes and CdTe quantum dots coated silica nanospheres (Si/QDs) as signal amplification labels. In this work, a sandwich-type immunosensor was fabricated, which was assembled on the surface of indium tin oxide glass (ITO). The analyte was detected in a home-made flow injection ECL (FI-ECL) cell through the immunosensor. Owing to the signal amplification of G@Fe(3)O(4) composite and Si/QDs, the ECL measurement showed a great increase in detection signals compared with the unamplified method. Under optimal conditions, a wide detection range (0.003-50 ng mL(-1)) and a low detection limit (0.72 pg mL(-1)) were obtained through the sandwich-type immunosensor. The proposed strategy successfully demonstrated a reproducible, specific, and potent method that can be expanded to detect other proteins.

Ultrasensitive electrochemiluminescence detection of lengthy DNA molecules based on dual signal amplification

Aimed at the facile detection of lengthy DNA molecules, an easily operated sandwich-type electrochemiluminescence (ECL) DNA biosensor was constructed on a glassy carbon electrode (GCE) based on CdTe quantum dots coated hollow ZnO nanoparticles (CdTe-ZnO NPs)-S(2)O(8)(2-) ECL system in this work. To fabricate a high-performance protocol, the GCE surface was successively modified by graphene nanosheet (GS), carbon nanotube (CNT) and gold nanoparticles (AuNPs) to form AuNPs dotted CNT-GS composites (Au@CNT-GS) platform, which improved the electronic transmission rate as well as increased the amount of immobilized capture probe CMV-F (S(1)). For further ultrasensitive, stable and low-potential ECL detection, CdTe-ZnO NPs were synthesized, and employed to label signal probe T7 promoter (S(3)). Based on the hybridization effect, the immobilized capture probe S(1), target DNA and labeled signal probe S(3) formed a sandwich-type DNA complex, which produced the ECL emission in the presence with S(2)O(8)(2-) coreactant. Under optimal conditions, the DNA ECL biosensor showed a good linear range over 10(-14) M to 10(-19) M with a low detection limit of 0.61 × 10(-19) M. The proposed strategy demonstrates a reproducible, stable, and potent method that can be expanded to detect the genome which exists in living cells.

Detection of L‐phenylalanine using molecularly imprinted solid‐phase extraction and flow injection electrochemiluminescence

A novel flow injection electrochemiluminescence method combined with molecularly imprinted solid-phase extraction was developed for the determination of L-phenylalanine, in which

Electrochemical DNA sensor based on three-dimensional folding paper device for specific and sensitive point-of-care testing

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