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  • The Electrochemical Society  (4)
  • Unknown  (4)
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  • The Electrochemical Society  (4)
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  • Unknown  (4)
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  • 1
    Online Resource
    Online Resource
    The Electrochemical Society ; 2021
    In:  Journal of The Electrochemical Society Vol. 168, No. 5 ( 2021-05-01), p. 057506-
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 168, No. 5 ( 2021-05-01), p. 057506-
    Abstract: In this work, a label-free electrochemical immunosensor was structured for detecting alpha fetal protein (AFP) effectively. The proposed electrochemical immunosensor was structured by gold silver platinum nanodendrites loaded on amino-functionalized MoO 2 nanosheets (AuAgPt NDs/NH 2 -MoO 2 NSs). The AuAgPt NDs with rich dendrite structure provided abundant specific surface area for effective capture antibody. MoO 2 possessed the satisfactory catalytic ability in terms of H 2 O 2 reduction and charge transfer capacity. AuAgPt NDs possessed favourable catalytic performance to H 2 O 2 reduction. Therefore, the prepared AuAgPt NDs/NH 2 -MoO 2 NSs was better than AuAgPt NDs and NH 2 -MoO 2 NSs in H 2 O 2 reduction on account of a synergistic effect. The constructed electrochemical immunosensor possessed a satisfying detection limit of 3.3 fg ml −1 and a broad detection range which was from 10 fg ml −1 to 100 ng ml −1 (S/N = 3) for the AFP detection under optimal conditions. The constructed electrochemical immunosensor possessed favourable detection performance in sensitivity, stability, selectivity and reproducibility, which indicated that it possessed a practical application in the aspect of clinical detection.
    Type of Medium: Online Resource
    ISSN: 0013-4651 , 1945-7111
    RVK:
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2021
    Location Call Number Limitation Availability
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  • 2
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 168, No. 5 ( 2021-05-01), p. 057530-
    Abstract: Changes in the concentration of neuron-specific enolase (NSE) can be used as an indicator for many diseases. Electrochemical immunosensor is a reliable tool for early diagnosis, but achieving ultrasensitive analysis is a pressing problem. In this work, graphene oxide doped poly (3,4-ethylenedioxythiophene) (PEDOT/GO) spindle-like nanorods prepared by liquid/liquid interface polymerization method have good stability and high conductivity. The sulfur atoms on the thiophene ring combine with gold nanoparticles (Au NPs) to further improve the efficiency of interface electron transfer. Besides, the exposed carboxyl groups and Au NPs on the surface of PEDOT/GO can effectively couple with the capture antibody (Ab 1 ). Double-shelled Cu 2 O hollow spheres (Pd NPs@DSHSs-Cu 2 O) modified with palladium nanoparticles (Pd NPs) are used as signal markers. The abundant catalytic active sites and detection antibody (Ab 2 ) binding sites rely on the double-shell hollow spheres to increase the specific surface area. The combined effect of Cu 2 O and Pd NPs can efficiently catalyze H 2 O 2 to realize the amplification of electrical signals. The detection range of the immunosensor prepared by the above-mentioned sensing strategy was 50.0 fg ml −1 ∼ 100.0 ng ml −1 , and the detection limit was 7.54 fg ml −1 , which provides potential reference value for early clinical diagnosis.
    Type of Medium: Online Resource
    ISSN: 0013-4651 , 1945-7111
    RVK:
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2021
    Location Call Number Limitation Availability
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  • 3
    Online Resource
    Online Resource
    The Electrochemical Society ; 2013
    In:  ECS Transactions Vol. 50, No. 3 ( 2013-03-15), p. 333-339
    In: ECS Transactions, The Electrochemical Society, Vol. 50, No. 3 ( 2013-03-15), p. 333-339
    Abstract: High power internally-matched 4H-SiC MESFET with a total gate width of 4×27mm was demonstrated. The double p-type buffer layers were used for preventing electrons from entering the buffer and reaching the substrate traps. The peak of the electric field in the edge of the gate is restrained by the double recess gate structure, which is advantageous to the high break down voltage. A thermal oxide layer was grown and subsequently etched to remove etch-induced damage. The ohmic contact resistivity of 2 ×10-6Ω•cm2 was achieved. The pulsed output power, gain and drain efficiency of the internally-matched 4x27mm SiC MESFET measured at 2GHz were 300W, 9.2dB, and 24.8%, respectively.
    Type of Medium: Online Resource
    ISSN: 1938-5862 , 1938-6737
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2013
    Location Call Number Limitation Availability
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  • 4
    Online Resource
    Online Resource
    The Electrochemical Society ; 2022
    In:  Journal of The Electrochemical Society Vol. 169, No. 6 ( 2022-06-01), p. 067509-
    In: Journal of The Electrochemical Society, The Electrochemical Society, Vol. 169, No. 6 ( 2022-06-01), p. 067509-
    Abstract: Neuron-specific enolase (NSE) is a reliable biomarker for the diagnosis of small cell lung cancer (SCLC). Effective detection of NSE plays an important role in the clinical diagnosis, treatment, and prediction of disease recurrence of SCLC. Herein, a simple label-free electrochemical immunosensor based on reduced graphene oxide/Cu 8 Ni 2 (rGO/Cu 8 Ni 2 ) nanocomposite was reported to detect the neuron-specific enolase (NSE). The rGO/Cu 8 Ni 2 nanocomposite was prepared by loading optimized CuNi (8:2) alloy on the reduced graphene oxide through electrostatic-adsorption interactions and in situ simultaneous reductions. As a noble-metal-free alloy, Cu 8 Ni 2 exhibits favorable catalytic activity. Combining the CuNi alloys with graphene can effectively keep off the aggregation of the alloy and further maintain its high catalytic activity. Simultaneously with the huge surface area and conductivity of rGO, rGO/Cu 8 Ni 2 showed increased bound antibodies and enhanced catalytic activity, which makes the fabricated immunosensor exhibit enhanced performance. Under the optimal conditions, the designed electrochemical immunosensor for detecting NSE showed a wide linear range from 500 fg ml −1 to 50 ng ml −1 and the low detection limit was 137 fg ml −1 . The proposed immunosensor in this study provides an effective method for the detection of NSE and may be expected to be applied in clinical diagnosis and treatment.
    Type of Medium: Online Resource
    ISSN: 0013-4651 , 1945-7111
    RVK:
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2022
    Location Call Number Limitation Availability
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