A new fluorescent detection route for chloride ion was designed with Nitrogen-doped graphene quantum dots (N-GQDs), which were prepared by a traditional hydrothermal method with citric acid as carbon source and urea as nitrogen source. The prepared N-GQDs solution was light yellow, and the freeze-dried solid was black. It emitted blue light under ultraviolet light. Meanwhile, The N-GQDs were characterized by TEM, XRD, UV-Vis and fluorescence, the results indicated that the N-GQDs had good dispersibility, photostability and excitation independent emission fluorescence. After addition of Ag+ solution, Ag+ combined to the surface functional groups of N-GQDs, resulting in an obvious quenching of the fluorescence intensity of N-GQDs. Nevertheless, the fluorescence intensity recovered significantly with the addition of Cl- to the N-GQDs/Ag+ system, this was because of AgCl was formed due to the “soft hard acid base principle”. The change of fluorescence intensity had a linear response to the chloride ion concentration in the range of 8.5-300 μmol L-1, with a detection limit (LOD) of 0.1 μmol L-1. To authenticate the application, the proposed method has been successfully used for quantitative analysis of chloride ion in real samples, including artificial sweat and environmental water.

A novel dual-signal amplificatory electrochemiluminescence (ECL) deoxyribonucleic acid (DNA) biosensor was designed for the determination of Hg2+. One amplification unit was gold nanoparticles (AuNPs) modified on a glassy carbon electrode, and the other was single-stranded DNA (ssDNA) (with amino at the 3’ terminal and thiol at the 5’ terminal) labeled with a carboxyl-functionalized Ru@SiO2 nanoparticles (Ru1@SiO2) as a nanoprobe. The ECL biosensor was obtained through a strong gold-sulfur bond between Au on AuNPs modified electrode and thiol in the nanoprobe. In the presence of Hg2+, the ECL signal reduced because the T-Hg2+-T existed between the ECL nanoprobe and the complementary DNA (c-DNA), which exhibited a sensing platform for the detection of Hg2+. The results revealed that the reduced ECL intensity was linearly proportional to the logarithm of the Hg2+ concentration in the range of 1.0 pmol L-1-100 nmol L-1 with limit of detection 0.02 pmol L-1. The proposed method was applied for the analysis of Hg2+ in the river water and the results were in good agreement with that obtained by atomic fluorescence spectroscopy.

A novel electrochemiluminescence (ECL) biosensor for the determination of lipopolysaccharide (LPS), a biomarker of endotoxemia, was designed. The nanoprobe (Ru1@SiO2-peptide) with a specific peptide (CIGKLHSAGK) labeled with a carboxyl functionalized Ru@SiO2 (Ru1@SiO2) was prepared by the acylation reaction. The ECL peptide biosensor was obtained by the strong gold-sulfur bond between Au on the gold electrode (AuE) surface and thiol group in the peptide. In the present of LPS, the peptide on the ECL biosensor can capture effectively LPS and the LPS/peptide/AuE was fabricated. When the Ru1@SiO2-peptide nanoprobe was bound, a sandwich compound of Ru1@SiO2-peptide/LPS/peptide was formed, and Ru(bpy)32+, in the sandwich compound, will do the ECL performance. The effective ECL amplification of Ru1@SiO2 exhibited excellent analytical performance to LPS with a wide detection linear range of 1.0~500 ng mL-1 and the detection limit was 0.3 ng mL-1. The biosensor could provide an evaluate of LPS expression on the bacteria surface and guide a new path to the clinical analysis of LPS related diseases.