Amounts of studies show that proprotein convertase subtilisin/kexin type 9 (PCSK9) can increase the low-density lipoprotein cholesterol ((LDL-C), leading to the progression and development of atherosclerosis. Hence, design an effective method to detect serum PCSK9 is meaningful for the prevention, monitor and diagnosis of cardiovascular diseases. Here, we reported a dual-signal method for detecting PCSK9 using a signal label, sulphur-doped palladium nanoflowers (s-PdNFs), inspired by its multifunctional properties of quenching and catalysis, which would simultaneously achieve electrochemiluminescence (ECL) analysis and electrochemical detection. For the ECL analysis, s-PdNFs could effectively quench the ECL intensity of peroxydisulfate/oxygen (SO/O) system via ECL resonance energy transfer (ECL-RET). Importantly, the donor-acceptor pair (s-PdNFs-SO pair) was firstly reported in the ECL-RET field. For the electrochemical detection, s-PdNFs with peroxidase-like activity, produce electric signals by catalyzing HO. Herein, a novel light-electricity dual signal immunosensor based on s-PdNFs was developed, and with a broad linear range of 5 fg mL to 50 ng mL (ECL channel) and 500 fg mL to 50 ng mL (electrochemical channel). Furthermore, the ECL channel and electrochemical channel can achieve the detection respectively which can meet different testing instruments. The two channels can also be combined to improve the accuracy of the detection. More importantly, the immunosensor realized the detection of PCSK9 in real serum samples demonstrated by good correlations with ELISA method. Our findings can promote the application of multifunctional materials in sensor and biomedicine field and provide a novel strategy for the detection of serum molecular.
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http://dx.doi.org/10.1016/j.bios.2019.111575 | DOI Listing |
J Am Chem Soc
September 2024
Department of Chemistry, National Taiwan University, Taipei 10617, Taiwan.
A novel series of excited-state intramolecular proton transfer (ESIPT) emitters, namely, , , and , endowed with dual intramolecular hydrogen bonds, were designed and synthesized. In the condensed phase, exhibit unmatched absorption and emission spectral features, where the minor 0-0 absorption peak becomes a major one in the emission. Detailed spectroscopic and dynamic approaches conclude fast ground-state equilibrium among enol-enol (EE), enol-keto (EK), and keto-keto (KK) isomers.
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2024
Sauvage Laboratory for Smart Materials, The School of Integrated Circuits, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.
Adv Mater
May 2024
School of Materials Science & Engineering, Jiangsu Collaborative Innovation Center of Photovoltaic Science and Engineering, Jiangsu Engineering Laboratory of Light-Electricity-Heat Energy-Converting Materials and Applications, Changzhou University, Changzhou, 213164, P. R. China.
Exciplex systems are promising candidates for thermally activated delayed fluorescence (TADF) molecules because of the small energy difference between the lowest singlet and triplet excited states (ΔE). However, realizing high-efficiency and low-external-quantum-efficiency (EQE) roll-off in solution-processed organic light-emitting diodes (OLEDs) using an exciplex system remains a formidable challenge. In this study, two (HLCT)-type isomers with a spiro skeleton, 2-BuspoCz-TRZ and 10-BuspoCz-TRZ, are designed and synthesized as acceptors of exciplexes, where tert-butylspirofluorene indole is regarded as a donor and the triazine unit as an acceptor.
View Article and Find Full Text PDFMater Horiz
April 2024
Jiangsu Collaborative Innovation Center of Photovoltaic Science and Engineering, Jiangsu Engineering Laboratory of Light-Electricity-Heat Energy-Converting Materials and Applications, School of Materials Science & Engineering, Changzhou University, Changzhou 213164, China.
Achieving both high emission efficiency and exciton utilization efficiency () in hot exciton materials is still a formidable task. Herein, a proof-of-concept design for improving in hot exciton materials is proposed elaborate regulation of singlet-triplet energy difference, leading to an additional thermally activated delayed fluorescence (TADF) process. Two novel dendrimers, named D-TTT-H and D-TTT-Bu, were prepared and characterized, in which diphenylamine derivatives were used as a donor moiety and tri(triazolo)triazine (TTT) as an acceptor fragment.
View Article and Find Full Text PDFMater Horiz
March 2024
School of Materials Science & Engineering, Jiangsu Collaborative Innovation Center of Photovoltaic Science and Engineering, Jiangsu Engineering Laboratory of Light-Electricity-Heat Energy-Converting Materials and Applications, Changzhou University, Changzhou 213164, P. R. China.
Achieving a high emission efficiency and a large luminescence asymmetry factor () in a single molecule exhibiting circularly polarised thermally activated delayed fluorescence (CP-TADF) remains a formidable challenge. In this work, a proof-of-concept, liquid-crystalline CP-TADF molecule is proposed to realise high by taking advantage of the order inherent in liquid crystals. Employing a chiral dinaphthol-based CP-TADF molecule as the emissive unit, a pair of liquid-crystalline CP-TADF molecules (R/S-4) is synthesised the introduction of six mesogenic moieties.
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