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Abstract: We report a simple approach for the selectively electrochemical sensing of cysteine (CySH) using β-MnO2 nanowires modified glassy carbon (GC) electrode via a direct and facile electrochemical co-deposition process with chitosan hydrogel. The electrode showed excellent electrocatalytic effect toward cysteine oxidation. A possible reaction mechanism related to the formation of surface complexes was proposed: the –SH group is the reacting group in the reaction between cysteine and MnO2, while the –NH2 group acts as an anchor to stabilize the surface complexes. The electrocatalytic behavior is further developed as a sensitive detection scheme for cysteine by amperometric measurement, which shows a large determination range of 0.5–630μM and a low detection limit of 70nM. Other nineteen amino acids in a 20-fold concentration do not interfere in the detection of cysteine. Furthermore, other biological species containing –SH group or Ssuch as glutathione, cystine, and bovine serum albumin (BSA), show no interferences because of steric hindrance and inactive S/ce:simple-para> [Copyright &y& Elsevier]

Abstract: Using chitosan as an effective linker between CMK-3 and glassy carbon electrode surface, {Hb/CMK-3} n multilayer film-modified electrodes were constructed through layer-by-layer assembly. The morphology of thus-formed {Hb/CMK-3} n film was characterized by scanning electron micrographs, and the interaction of hemoglobin (Hb) with CMK-3 was studied by UV–vis spectroscopy and electrochemical methods. Under optimal conditions, {Hb/CMK-3}6 film showed a couple of stable and well-defined redox peaks at about −377 and −296mV in pH 7.0 buffers. Furthermore, the {Hb/CMK-3}6 film displayed excellent electrocatalysis to the reduction of both H2O2 and O2. Based on thus-formed film and its direct electron transfer behavior, a novel biosensor was presented for the determination of H2O2 ranging from 1.2 to 57μM with the detection limit of 0.6μM at S/N=3. CMK-3 provided a desirable matrix for protein immobilization and biosensor preparation. [Copyright &y& Elsevier]

Abstract: This work demonstrates an aptasensor for ultrasensitive electrochemiluminescence (ECL) detection of thrombin based on an “off–on–off” approach. The system is composed of an Eu3+-doped CdS nanocrystals (CdS:Eu NCs) film on glassy carbon electrode (GCE) as ECL emitter. Then gold nanoparticles (AuNPs) labeled hairpin-DNA probe (ssDNA1) containing thrombin-binding aptamer (TBA) sequence was linked on the NCs film, which led to ECL quenching (off) as a result of Förster-resonance energy transfer (FRET) between the CdS:Eu NC film and the proximal AuNPs. Upon the occurrence of hybridization with its complementary DNA (ssDNA2), an ECL enhancement (on) occurred owing to the interactions of the excited CdS:Eu NCs with ECL-induced surface plasmon resonance (SPR) in AuNPs at large separation. Thrombin could induce ssDNA1 forming a G-quadruplex and cause the AuNPs to be close to CdS:Eu NCs film again, which resulted in an enhanced ECL quenching (off). This “off–on–off” system showed a maximum 7.4-fold change of ECL intensity due to the configuration transformation of ssDNA1 and provides great sensitivity for detection of thrombin in a wide detection range from 50aM to 1pM. [Copyright &y& Elsevier]