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Author

Guifang Chen

Other affiliations: Nanjing University
Bio: Guifang Chen is an academic researcher from Shanghai University. The author has contributed to research in topics: Aptamer & Electron transfer. The author has an hindex of 12, co-authored 33 publications receiving 676 citations. Previous affiliations of Guifang Chen include Nanjing University.

Papers
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Journal ArticleDOI
Jing Zhao1, Jing Zhao2, Guifang Chen1, Li Zhu1, Genxi Li1, Genxi Li2 
TL;DR: Based on the strong interaction between single-stranded DNA (ssDNA) and graphene material, a simple but smart platform was designed in this article to fabricate electrochemical biosensors by using graphene quantum dots modified pyrolytic graphite electrode coupled with specific sequence ssDNA molecules as probes.

315 citations

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TL;DR: A colorimetric method that could be observed with naked eye and used copper nanoclusters for cost-effective detection of DNA in Hepatitis B virus, which has potential applications in correct diagnosis of genetic disease and monitoring of gene therapy in the poverty-stricken areas.

65 citations

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TL;DR: A novel nanozyme@DNA hydrogel architecture that may have a great potential for the utilization of nanozymes as well as the application of nanoZymes for biomedical analysis in complex physiological samples is fabricated.
Abstract: Nanozymes have received great attention owing to the advantages of easy preparation and low cost. Unlike natural enzymes that readily adapt to physiological environments, artificial nanozymes are apt to passivate in complex clinical samples (e.g., serum), which may damage the catalytic capability and consequently limit the application in biomedical analysis. To conquer this problem, in this study, we fabricated novel nanozyme@DNA hydrogel architecture by incorporating nanozymes into a pure DNA hydrogel. Gold nanoparticles (AuNPs) were adopted as a model nanozyme. Results indicate that AuNPs incorporated in the DNA hydrogel retain their catalytic capability in serum as they are protected by the hydrogel, whereas AuNPs alone totally lose the catalytic capability in serum. The detection of hydrogen peroxide and glucose in serum based on the catalysis of the AuNPs@DNA hydrogel was achieved. The detection limit of each reaches 1.7 and 38 μM, respectively, which is equal to the value obtained using natural enzymes. Besides the mechanisms, some other advantages, such as recyclability and availability, have also been explored. This nanozyme@DNA hydrogel architecture may have a great potential for the utilization of nanozymes as well as the application of nanozymes for biomedical analysis in complex physiological samples.

53 citations

Journal ArticleDOI
TL;DR: Surface-immobilized pure DNA hydrogels were formed using a surficial primer-induced strategy and adopted as scaffold materials for biosensing applications.
Abstract: Hydrogels are of great interest in the field of biosensing for their good biocompatibility, plasticity, and capability of providing 3D scaffolds. Nevertheless, the application of hydrogels has not been linked with broad surface biosensing systems yet. To overcome the limitations, here for the first time, surface-immobilized pure DNA hydrogels were synthesized using a surficial primer-induced strategy and adopted for biosensing applications. The DNA hydrogel 3D scaffold is successfully constructed on a transparent ITO electrode, which facilitates both colourimetric and electrochemical measurements. Results show that the hydrogel is able to wrap enzymes solidly and exhibits favourable stability under different conditions. Owing to the free diffusion of the micromolecular targets throughout the hydrogel, while isolating the enzymes from the macromolecular interferences outside the hydrogel, the direct colourimetric and electrochemical detection of hydrogen peroxide and bilirubin in serum is achieved. The detection limit of hydrogen peroxide in serum is 22 nM by colourimetric analysis and 13 nM by electrochemical measurement. The detection limit of bilirubin is 32 nM, a favourable limit that could be used in jaundice diagnosis. In addition, the enzyme@hydrogel can be easily regenerated and the catalytic activity is retained for a few cycles, thus allowing the recycling of the hydrogel-based biosensing system. The successful integration of DNA hydrogels with surface biosensing systems will greatly expand the applications of hydrogels for diagnostic and environmental monitoring purposes.

51 citations

Journal ArticleDOI
TL;DR: In this paper, a supermolecular composite consisting of a binding peptide that is able to bind to the target CD44 and a self-assembled diphenylalanine (FF) nanostructure that provides a template for deposition of gold nanoparticles (AuNPs), is elaborately constructed on the surface of an electrode through the linkage of cucurbit[8]urils.

37 citations


Cited by
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TL;DR: In this article, a review of the photo and electron properties of carbon nanodots is presented to provide further insight into their controversial emission origin and to stimulate further research into their potential applications, especially in photocatalysis, energy conversion, optoelectronics, and sensing.
Abstract: Carbon nanodots (C-dots) have generated enormous excitement because of their superiority in water solubility, chemical inertness, low toxicity, ease of functionalization and resistance to photobleaching. In this review, by introducing the synthesis and photo- and electron-properties of C-dots, we hope to provide further insight into their controversial emission origin (particularly the upconverted photoluminescence) and to stimulate further research into their potential applications, especially in photocatalysis, energy conversion, optoelectronics, and sensing.

2,262 citations

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TL;DR: Electronic networks comprised of flexible, stretchable, and robust devices that are compatible with large-area implementation and integrated with multiple functionalities is a testament to the progress in developing an electronic skin akin to human skin.
Abstract: Human skin is a remarkable organ. It consists of an integrated, stretchable network of sensors that relay information about tactile and thermal stimuli to the brain, allowing us to maneuver within our environment safely and effectively. Interest in large-area networks of electronic devices inspired by human skin is motivated by the promise of creating autonomous intelligent robots and biomimetic prosthetics, among other applications. The development of electronic networks comprised of flexible, stretchable, and robust devices that are compatible with large-area implementation and integrated with multiple functionalities is a testament to the progress in developing an electronic skin (e-skin) akin to human skin. E-skins are already capable of providing augmented performance over their organic counterpart, both in superior spatial resolution and thermal sensitivity. They could be further improved through the incorporation of additional functionalities (e.g., chemical and biological sensing) and desired properties (e.g., biodegradability and self-powering). Continued rapid progress in this area is promising for the development of a fully integrated e-skin in the near future.

1,950 citations

Journal ArticleDOI
TL;DR: Recent developments in preparation of GQDs are discussed, focusing on the main two approaches (top-down and bottom-down).

1,796 citations

Journal ArticleDOI
TL;DR: A simple electrochemical approach to luminescent and electrocatalytically active nitrogen-doped GQDs (N-GQDs) with oxygen-rich functional groups is reported, which allows them to be used for biomedical imaging and other optoelectronic applications.
Abstract: Graphene quantum dots (GQDs) represent a new class of quantum dots with unique properties. Doping GQDs with heteroatoms provides an attractive means of effectively tuning their intrinsic properties and exploiting new phenomena for advanced device applications. Herein we report a simple electrochemical approach to luminescent and electrocatalytically active nitrogen-doped GQDs (N-GQDs) with oxygen-rich functional groups. Unlike their N-free counterparts, the newly produced N-GQDs with a N/C atomic ratio of ca. 4.3% emit blue luminescence and possess an electrocatalytic activity comparable to that of a commercially available Pt/C catalyst for the oxygen reduction reaction (ORR) in an alkaline medium. In addition to their use as metal-free ORR catalysts in fuel cells, the superior luminescence characteristic of N-GQDs allows them to be used for biomedical imaging and other optoelectronic applications.

1,796 citations

Journal ArticleDOI
01 Apr 2015-Small
TL;DR: The properties and synthesis methods of these carbon nanodots are reviewed and emphasis is placed on their biological (both fundamental and theranostic) applications.
Abstract: The emerging graphene quantum dots (GQDs) and carbon dots (C-dots) have gained tremendous attention for their enormous potentials for biomedical applications, owing to their unique and tunable photoluminescence properties, exceptional physicochemical properties, high photostability, biocompatibility, and small size. This article aims to update the latest results in this rapidly evolving field and to provide critical insights to inspire more exciting developments. We comparatively review the properties and synthesis methods of these carbon nanodots and place emphasis on their biological (both fundamental and theranostic) applications.

1,665 citations