研究目的
To design and fabricate a self-powered biosensing device based on a TiO2 NSs@MoS2 QDs heterojunction for quantitative detection of exosomal RNA (HOTTIP) as a biomarker for gastric cancer.
研究成果
The self-powered device based on TiO2 NSs@MoS2 QDs heterojunction successfully enables ultrasensitive detection of HOTTIP with a wide linear range and low detection limit, demonstrating high selectivity and reproducibility. It holds promise for portable and economical biosensing applications in cancer diagnostics.
研究不足
The device relies on visible light excitation, which may limit performance in low-light conditions. The regeneration process requires heating, which could affect long-term stability. Specificity was tested against a limited set of interfering genes, and real-sample applications may face matrix effects.
1:Experimental Design and Method Selection:
The study involves creating a heterojunction structure between TiO2 nanosilks (NSs) and MoS2 quantum dots (QDs) to form a Type I band alignment for enhanced photoelectrochemical performance. Methods include synthesis of nanomaterials, fabrication of the biosensing device, and application for RNA detection using hybridization with a capture probe.
2:Sample Selection and Data Sources:
Exosomes were isolated from serum using an ExoQuick kit, and exosomal RNA (HOTTIP) was extracted using a miRNeasy Micro Kit. Synthetic gene fragments were used for specificity tests.
3:List of Experimental Equipment and Materials:
Instruments include SEM (JEOL JSM-6700F), TEM (JEOL JEM-1400), XRD (Bruker D8 focus), FT-IR (Perkin-Elmer 580B), XPS (ThermoFisher ESCALAB 250), electrochemical workstation (Zahner Zennium PP211), PL spectrometer (Perkin Elmer LS-45/55), UV-vis spectrometer (Perkin-Elmer Lambda 35), and a pressure steam sterilizer (Shanghai ShenAn LDZX-30KBS). Materials include TiO2 NSs, MoS2 QDs, primer probes, and various chemicals like ascorbic acid.
4:Experimental Procedures and Operational Workflow:
Synthesis of TiO2 NSs and MoS2 QDs, hybridization to form TiO2 NSs@MoS2 QDs, fabrication of the biosensing device on ITO electrodes, incubation with primer probe and HOTTIP, and measurement of photocurrent and power output under visible light irradiation. Regeneration involved heating the anode in ultrapure water.
5:Data Analysis Methods:
Data were analyzed using electrochemical techniques (i-t and EIS), with parameters fitted using ZSimpWin software. Statistical analysis included calculation of RSD and recovery rates for accuracy and precision.
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SEM
JSM-6700F
JEOL
Characterization of morphology and microstructure of nanomaterials
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TEM
JEM-1400
JEOL
Imaging of nanomaterial structures
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XRD
D8 focus
Bruker
Analysis of crystallization of materials
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FT-IR
580B
Perkin-Elmer
Spectroscopic analysis of functional groups
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XPS
ESCALAB 250
ThermoFisher Scientific
Surface chemical analysis
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PL Spectrometer
LS-45/55
Perkin Elmer
Photoluminescence measurements
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UV-vis Spectrometer
Lambda 35
Perkin-Elmer
Ultraviolet-visible spectroscopy
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Electrochemical Workstation
Zennium PP211
Zahner
Electrochemical tests including EIS and i-t measurements
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Pressure Steam Sterilizer
LDZX-30KBS
Shanghai ShenAn
Sterilization of equipment and water
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ExoQuick Kit
System Biosciences
Isolation of exosomes from serum
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miRNeasy Micro Kit
QIAGEN
Extraction of exosomal RNA
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High Capacity cDNA Reverse Transcription Kit
Takara
Generation of first-strand cDNA
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