- 标题
- 摘要
- 关键词
- 实验方案
- 产品
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Fully Packaged Portable Thin Film Biosensor for the Direct Detection of Highly Pathogenic Viruses from On-Site Samples
摘要： The thin film transistor (TFT) is a promising biosensor system with great sensitivity, label-free detection, and a quick response time. However, even though the TFT sensor has such advantageous characteristics, the disadvantages hamper the TFT sensor's application in the clinical field. The TFT is susceptible to light, noise, vibration, and limited usage, and this significantly limits its on-site potential as a practical biosensor. Herein, we developed a fully packaged, portable TFT electrochemical biosensor into a chip form, providing both portability through minimizing the laboratory equipment size and multiple safe usages by protecting the semiconductor sensor. Additionally, a safe environment that serves as a miniature probe station minimizes the previously mentioned disadvantages, while providing the means to properly link the TFT biosensor with a portable analyzer. The biosensor was taken into a biosafety level 3 (BSL-3) laboratory setting to analyze highly pathogenic avian influenza virus (HPAIV) samples. This virus quickly accumulates within a host, and therefore, early stage detection is critical to deterring the further spread of the deadly disease to other areas. However, current on-site methods have poor limits of detection (105?106 EID50/mL), and because the virus has low concentration in its early stages, it cannot be detected easily. We have compared the sample measurements from our device with virus concentration data obtained from a RT-PCR (virus range: 100?104 EID50/mL) and have identified an increasing voltage signal which corresponds to increasing virus concentration.
关键词： avian influenza virus,label-free detection,portable biosensor,chip sensor,rapid detection
更新于2025-09-23 15:23:52
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Exploiting electrostatic shielding-effect of metal nanoparticles to recognize uncharged small molecule affinity with label-free graphene electronic biosensor
摘要： Label-free electronic biosensors as the non-electrochemical analytical tools without requirement of sophisticated instrumentation have become attractive, although their application in competitive affinity sensing of uncharged small molecules is hindered by a difficulty in the development of competing analogues. To break through this bottleneck, we report a novel analogue made by epitope-modified metal nanoparticles to enable the electronic signaling of small-molecule analyte recognition via competitive affinity. While the electronic signaling capability of metal nanoparticle analogues is demonstrated by a graphene field-effect transistor bioassay of small-molecule glucose as a proof-of-principle, interestingly, we discover a new electronic signaling mechanism in the metal nanoparticle affinity, different to the intuitive charge accumulation expectation. On the basis of Kelvin-probe force microscopic potential characterization and theoretical discussion, we fundamentally elucidated the signaling mechanism as a seldom used electrostatic shielding-effect, that is, in the analogue-receptor affinity, metal nanoparticles with the charge density lower than receptor biomolecules can reduce the collective electrical potential via charge dispersion. Further consider the convenient epitope-modifiability of metal nanoparticles, the easy-to-develop analogues for diverse target analyte might potentially be predictable in the future. And the application of label-free electronic biosensors for the competitive affinity bioassay of range-extended small molecules may thus be promoted based on the electrostatic shielding-effect.
关键词： electrostatic shielding-effect,competitive affinity,graphene field-effect transistor biosensor,uncharged small molecule,metal nanoparticle analogue
更新于2025-09-23 15:23:52
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Morpholino Oligonucleotide Cross-Linked Hydrogels as Portable Optical Oligonucleotide Biosensors
摘要： Morpholino Oligonucleotides (MOs), an uncharged DNA analogue, are functionalized with an acrylamide moiety and incorporated into polymer hydrogels as responsive crosslinks for microRNA sequence detection. The MO crosslinks can be selectively cleaved by a short target analyte single-stranded DNA (ssDNA) sequence based on microRNA, inducing a distinct swelling response measured optically. The MO crosslinks offer significant improvement over DNA based systems through improved thermal stability, no salt requirement and 1000-fold improved sensitivity over a comparative biosensor, facilitating a wider range of sensing conditions. Analysis was also achieved using a mobile phone camera, demonstrating portability.
关键词： microRNA,Biosensor,Oligonucleotide sensor,Morpholino oligonucleotide,Hydrogel
更新于2025-09-23 15:23:52
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Ultrasensitive detection of miRNA with an antimonene-based surface plasmon resonance sensor
摘要： MicroRNA exhibits differential expression levels in cancer and can affect cellular transformation, carcinogenesis and metastasis. Although fluorescence techniques using dye molecule labels have been studied, label-free molecular-level quantification of miRNA is extremely challenging. We developed a surface plasmon resonance sensor based on two-dimensional nanomaterial of antimonene for the specific label-free detection of clinically relevant biomarkers such as miRNA-21 and miRNA-155. First-principles energetic calculations reveal that antimonene has substantially stronger interaction with ssDNA than the graphene that has been previously used in DNA molecule sensing, due to thanking for more delocalized 5s/5p orbitals in antimonene. The detection limit can reach 10 aM, which is 2.3–10,000 times higher than those of existing miRNA sensors. The combination of not-attempted-before exotic sensing material and SPR architecture represents an approach to unlocking the ultrasensitive detection of miRNA and DNA and provides a promising avenue for the early diagnosis, staging, and monitoring of cancer.
关键词： surface plasmon resonance,biosensor,antimonene,cancer diagnosis,miRNA detection
更新于2025-09-23 15:23:52
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A label-free aptamer-based nanogap capacitive biosensor with greatly diminished electrode polarization effects
摘要： A significant impediment to the use of impedance spectroscopy in bio-sensing is the electrode polarization effect that arises from the movement of free ions to the electrode–solution interface, forming an electrical double layer (EDL). The EDL screens the dielectric response of the bulk and its large capacitance dominates the signal response at low frequency, masking information particularly relevant for biological samples, such as molecular conformation changes and DNA hybridization. The fabrication of nanogap capacitors with electrode separation less than the EDL thickness can significantly reduce electrode polarization effects and provide enormous improvement in sensitivity due to better matching of the sensing volume with the size of the target entities. We report on the fabrication of a horizontal thin-film nanogap capacitive sensor with electrode separation of 40 nm that shows almost no electrode polarization effects when measured with water and ionic buffer solutions, thereby allowing direct quantification of their relative permittivity at low frequencies. Surface modification of the electrodes with thiol-functionalized single strand DNA aptamers transforms the device into a label-free biosensor with high sensitivity and selectivity towards the detection of a specific protein. Using this approach, we have developed a biosensor for the detection of human alpha thrombin. In addition, we also examine frequency dependent permittivity measurements on high ionic strength solutions contained within the nanogap and discuss how these support recent experimental observations of large Debye lengths. A large shift in the Debye relaxation frequency to lower frequency is also found, which is consistent with water molecules being in a rigid-like state, possibly indicating the formation of an ordered ‘‘ice-like’’ phase. Altogether, this work highlights the need for better understanding of fluids in confined, nanoscale geometries, from which important new applications in sensing may arise.
关键词： electrode polarization,aptamer,nanogap,capacitive biosensor,dielectric spectroscopy,thrombin
更新于2025-09-23 15:23:52
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Poly(azomethine-urethane) and zeolite-based composite: Fluorescent biosensor for DNA detection
摘要： In the present paper, a highly selective and sensitive fluorescent biosensor based on poly(azomethine-urethane) and zeolite for the determination of DNA molecules was developed. Zeolite was chosen to enhance with anionic or cationic functional groups in polymer matrix and interaction between polymer and DNA. Several parameters such as polymer concentration, pH and incubation time effect on the sensitivity of the fluorescent biosensor were optimized. Linear range was determined between 2.50 and 25.00 nmol/L DNA concentration and limit of detection (LOD) of the biosensor was calculated as 0.095 nmol/L under the optimal conditions. Interference study were also performed in the presence of different amino acids, cations and organic compounds. The results clearly indicated that the tested cations and compounds were not induced a significant fluorescence change and the proposed zeolite-based biosensor was shown a good selectivity for DNA.
关键词： fluorescent sensor,DNA,Zeolite,biosensor
更新于2025-09-23 15:23:52
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An automatic multi-thread image segmentation embedded system for surface plasmon resonance sensor
摘要： In order to reduce the uncertainties associated with manual selection of regions of interest (ROIs) commonly used in Surface Plasmon Resonance (SPR) imaging system, we proposed and implemented an automatic image segmentation method in an embedded system to facilitate the potential real-time applications. Intuitive marker-controlled watershed algorithm is developed to segment ROIs (reaction, blank, and background regions) from images acquired from an experimental image SPR system. The marker assignment algorithms and pre-processing algorithms are executed in parallel by multi-threading programming on the multi-core embedded system to both real-time and good quality of segmentation. This method exhibited a good robustness in a series of ROIs segmentation test. Furthermore, the intensity response from triplicate detection of glucose standard solutions indicated a good reproducibility of data. The linear range was from 2.5 mg/mL to 20.4 mg/mL, with a correlation coefficient (R2) of 0.999 and sensitivity of 2.69 a.u./mg/mL. In conclusion, the proposed automatic image segmentation method effectively makes the measurement more precise and simplified.
关键词： Optical sensor,Surface plasmon resonance (SPR),Biosensor,Watershed algorithm,Image segmentation
更新于2025-09-23 15:23:52
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A pyrophosphatase biosensor with photocurrent analysis
摘要： A light-induced photochemical biosensor was developed for the analysis of inorganic pyrophosphatase (PPase). PPase hydrolyzes pyrophosphate (PPi) into two independent o-phosphate ions. Two PPi units can chelate a copper ion (Cu2+), forming a PPi–Cu2+–PPi complex and preventing the Cu2+ triggers other reactions. A transparent indium tin oxide (ITO) electrode was coated with a layer of CdS quantum dots (QDs), and then 3,4-diaminobenzoic acid (DBA) was deposited as the anchor. A solution of the PPi–Cu2+–PPi complex and o-phenylenediamine (OPD) was mixed with the analytical sample and then a drop of the mixture was placed on the modified ITO electrode. In the absence of PPase, no reaction occurred between OPD and DBA. A photocurrent was obtained upon excitation of the CdS QDs under light. In the presence of PPase, Cu2+ was released from the complex, triggering the reaction of OPD with DBA on the electrode surface, thereby shielding the CdS QDs from excitation by the light. The observed photocurrent decreased. The difference in the two measured photocurrents corresponded to the activity of PPase. This photochemical biosensor had excellent sensitivity for PPase in the range from 0.8 to 5000 mU, with a limit of detection of 0.41 mU.
关键词： Quantum dots,Biosensor,o-Phenylenediamine,Photocurrent,PPase
更新于2025-09-23 15:23:52
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Multiphysics Simulation of Biosensors Involving 3D Biological Reaction-Diffusion Phenomena in a Standard Circuit EDA Environment
摘要： The topic of this paper is the development of biological models for 3D reaction–diffusion phenomena that can be used in any circuit electronic design automation environment for the simulation of biosensors. Biological systems that involve such 3D phenomena are described by partial differential equations. Our approach consists in discretizing these equations according to the finite-difference method and converting the resulting ordinary differential equations into an assembly of elementary electronic equivalent circuits that are directly simulated with SPICE. The main interest of this approach is the ability to couple such models with third-party SPICE models of electronic circuits, sensors, and transducers, i.e., models from any physical domain ruled by Kirchhoff laws, allowing modeling and simulation of any multi-physics systems in a conventional circuit design environment, here CADENCE. The tool is validated on simple problems for which analytical solutions are known. Then, the interest of the approach is illustrated on the study of a biosensor.
关键词： reaction-diffusion,Biosensor,virtual prototyping,biochemical reaction,ion-sensitive FET
更新于2025-09-23 15:22:29
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Optical enzymatic biosensor membrane for rapid in situ detection of organohalide in water samples
摘要： An optical biosensor employing immobilized haloalkane dehalogenase (HLD), the halide degrading enzyme for the detection of halogenated organic in environmental water and drinking water samples was developed. The enzymatic biosensor was fabricated by incorporating H+ ion selective chromoionophore ETH5294 and HLD enzyme in a stacked chitosan films system on a glass slide. Hydrolytic dehalogenation of dichloroethane (DCA) by the carbon-halide degrading HLD enzyme resulting in the release of a halogen, a proton and a primary alcohol. The halocarbon concentration was optically transduced by the pH transducer layer as a result of protonation reaction of the chromoionophore pH indicator dye embedded in the underneath layer. The resulting colour change of the protonated chromoionophore was measured by fiber optic reflectance spectrophotometry method. Under optimized conditions the detection limit of the proposed reflectance-based enzymatic biosensor membrane was estimated to be 1 mg L?1 with a wide dynamic linear concentration range of 5–60 mg L?1 DCA (R2 = 0.9792) and satisfactory reproducibility within the relative standard deviation (RSD) range of 3.4–4.3%. Validation test demonstrated that the optical halocarbon biosensor could be a promising tool for rapid (6 min) in situ and direct evaluation of organohalide in river water, tap water and bottled water samples without any sample pre-treatment or extraction steps.
关键词： Haloalkane dehalogenase,Biosensor,Halogenated hydrocarbon,Chitosan,Chromoionophore
更新于2025-09-23 15:22:29