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Zhike He

Publications and source records attributed to Zhike He.

14 recordsLinked to original sources
PubMed2006

A hydrogen peroxide biosensor based on the direct electrochemistry of hemoglobin modified with quantum dots.

Direct electron transfer of hemoglobin modified with quantum dots (QDs) (CdS) has been performed at a normal graphite electrode. The response current is linearly dependent on the scan rate, indicating the direct electrochemistry of hemoglobin in that case is a surface-controlled electrode process. UV-vis spectra suggest that the conformation of hemoglobin modified with CdS is little different from that of hemoglobin alone, and the conformation changes reversibly in the pH range 3.0-10.0. The hemoglobin in a QD film can retain its bioactivity and the modified electrode can work as a hydrogen peroxide biosensor because of its peroxidase-like activity. This biosensor shows an excellent response to the reduction of H2O2 without the aid of an electron mediator. The catalytic current shows a linear dependence on the concentration of H2O2 in the range 5x10(-7)-3x10(-4) M with a detection limit of 6x10(-8) M. The response shows Michaelis-Menten behavior at higher H2O2 concentrations and the apparent Michaelis-Menten constant is estimated to be 112 microM.

Biosensing Techniques↗
PubMed2006

In vitro selection of DNA aptamer against abrin toxin and aptamer-based abrin direct detection.

Abrin toxin as the target protein, belongs to class II ribosome-inactivating proteins family, has high toxicity to eukaryotic cells. Here, we firstly report the DNA aptamers, isolated by in vitro selection, recognize abrin toxin with high affinity and specificity, and have the advantage of no cross-reaction with structure-similar protein ricin toxin over antibodies. Then, a highly selective and sensitive aptamer-based abrin assay was established using a molecular light switching reagent [Ru(phen)(2)(dppz)](2+) with a limit of detection of 1 nM and a wide linear range from 1 to 400 nM with the correlation coefficient of 0.993. This assay can be successfully directly performed not only in physiological buffer but also in more complicated biological matrix, such as diluted serum.

Abrin↗
PubMed2006

Hybrid silica monolithic column for capillary electrochromatography with enhanced cathodic electroosmotic flow.

A hybrid silica monolithic stationary phase for RP CEC was prepared by in situ co-condensation of (3-mercaptopropyl)-trimethoxysilane (MPTMS), phenyltriethoxysilane (PTES), and tetraethoxysilane (TEOS) via a sol-gel process. The thiol groups on the surface of the stationary phase were oxidized to sulfonic acids by peroxytrifluoroacetic acid. The introduced sulfonic acid moieties on the monoliths were characterized by a strong and relatively stable EOF in a broad pH range from 2.35 to 7.0 in CEC. Aromatic acids and neutral compounds can be simultaneously separated in this column under cathodic EOF. The CEC column exhibited a typical RP chromatographic mechanism for neutral compounds due to the introduced phenyl groups.

Amino Acids, Aromatic↗
PubMed2006

Quantum dot-mediated detection of gamma-aminobutyric acid binding sites on the surface of living pollen protoplasts in tobacco.

gamma-Aminobutyric acid (GABA) is an inhibitory transmitter in the central nervous system of mammals. Recent investigations showed that it also plays an important role in regulating pollen tube growth and orientation in plants. To determine whether GABA receptors are also present on the membrane of pollen protoplasts, a fluorescence probe of quantum dots (QDs) was constructed and applied. The water-soluble CdSe-ZnS (core-shell) QDs were first synthesized and verified to possess good optical properties. GABA was then bioconjugated to the QDs in the presence of 1-ethyl-3-(3)-dimethylaminopropyl carbodiimide (EDC) and N-hydroxysuccinimide (NHS) to make the fluorescence probe. Using the probe, GABA binding sites were detected on the protoplast membrane of both pollen and somatic cells. Both the fluorescent signals on the surface of the protoplasts and the Ca(2+) oscillation assayed via the Ca(2+) probe Fluo-3/AM inside the protoplasts provided evidence that the potential GABA(B) receptors are present on the plant protoplast membrane.

Aniline Compounds↗
PubMed2005

Electrochromatographic evaluation of a silica monolith capillary column for separation of basic pharmaceuticals.

A silica-based monolithic capillary column was prepared via a sol-gel process. The continuous skeleton and large through-pore structure were characterized by scanning electron microscopy (SEM). The native silica monolith has been successfully employed in the electrochromatographic separation of beta-blockers and alkaloids extracted from traditional Chinese medicines (TCMs). Column efficiencies greater than 250 000 plates/m for capillary electrochromatography (CEC) separation of basic compounds were obtained. It was observed that retention of basic pharmaceuticals on the silica monolith was mainly contributed by a cation-exchange mechanism. Other retention mechanisms including reversed-phase and normal-phase mechanisms and electrophoresis of basic compounds also played a role in separation. A comparison of the differences between CEC and capillary zone electrophoresis (CZE) separation was also discussed.

Adrenergic beta-Antagonists↗
PubMed2005

Preparation of monolithic silica column with strong cation-exchange stationary phase for capillary electrochromatography.

A monolithic silica based strong cation-exchange stationary phase was successfully prepared for capillary electrochromatography. The monolithic silica matrix from a sol-gel process was chemically modified by treatment with 3-mercaptopropyltrimethoxysilane followed by a chemical oxidation procedure to produce the desired function. The strong cation-exchange stationary phase was characterized by its substantial and stable electroosmotic flow (EOF), and it was observed that the EOF value of the prepared column remained almost unchanged at different buffer pH values and slowly decreased with increasing phosphate concentration in the mobile phase. The monolithic silica column with strong cation-exchange stationary phase has been successfully employed in the electrochromatographic separation of beta-blockers and alkaloids extracted from traditional Chinese medicines (TCMs). The column efficiencies for the tested beta-blockers varied from 210,000 to 340,000 plates/m. A peak compression effect was observed for atenolol with the mobile phase having a low phosphate concentration.

Journal Article↗
PubMed2004

Chemiluminescence detection of isoniazid using Ru(phen)3(2+)-isoniazid-Ce(IV) system.

In our experiment, it was observed that isoniazid could enhance the chemiluminescence (CL) emission of tris-(1,10-phenanthroline)ruthenium(II) (Ru(phen)3(2+))-cerium(IV) (Ce(IV)) system and this enhancement effect was dependent on the concentration of isoniazid, based on which, a novel CL system was established for the detection of isoniazid. Under the optimum experimental conditions, the dynamic range and detection limit are 7.0 x 10(-2) to 6.5 microg ml(-1) and 2.5 x 10(-2) microg ml(-1), respectively. The R.S.D. is 3.4% (n = 11). The proposed method has been applied to detect the content of isoniazid in the injection solution with satisfactory results. The possible mechanism of the CL reaction was studied.

Calibration↗
PubMed2004

Lead as own luminescent sensor for determination.

In our experiments, it was observed that adding bromide to Pb2+ solution of N,N'-dimethylformamide (DMF), the highly emissive cluster Pb4Br11(3-) can be formed and the fluorescence intensity of the formed cluster is proportional to the concentration of Pb2+, based on which, a novel, simple approach that uses the emission from itself as the sensor for determination of Pb2+ is proposed. Under the optimum conditions, the linear range and detection limit is 1.0 x 10(-7) to 1.0 x 10(-5) mol l(-1) (correlation coefficient r = 0.9997) and 7.6 x 10(-9) mol l(-1), respectively. Foreign substrates effects were also investigated. The proposed method has been successfully applied to the determination of lead in the synthetic samples. The mechanism of the reaction is also studied.

Cations, Divalent↗
PubMed2003

Structural basis for vapoluminescent organoplatinum materials derived from noncovalent interactions as recognition components.

The spectroscopic properties and crystal structures of a series of platinum(II) complexes bearing functionalized sigma-alkynyl groups, namely [(tBu(2)bpy)Pt(C triple bond CAr)(2)] (tBu(2)bpy = 4,4'-bis-tert-butyl-2,2'-bipyridine, Ar = 4-pyridyl, 1; 3-pyridyl, 2; 2-pyridyl, 3; 4-ethynylpyridyl, 4; 2-thienyl, 5; pentafluorophenyl, 6) have been studied. Solid-state emissions of 1 and 6 are dependent on their crystallinity. Reversible and selective vapoluminescence was observed for 1 and 6 in the presence of chlorocarbon vapors. For solid 1, dramatic enhancement of green luminescence is observed upon sorption of CH(2)Cl(2) or CHCl(3) vapor. The excimeric orange emission for solid 6 is switched to monomeric green emission upon exposure to CH(2)Cl(2) vapor. The luminescent responses of a thin film of 1 towards various organic vapors have also been examined. In the crystallographically determined structure of 1.CH(2)Cl(2), the bis(acetylide) moiety acts as the receptor berth for a CH(2)Cl(2) molecule through concerted C-H.pi(C triple bond C) interactions, while Cl.Cl interactions connect the CH(2)Cl(2) molecules into infinite linear chains. The observed crystal lattices are arranged into scaffolds of varying porosity by weak C-H...N(py) (1.CH(2)Cl(2), 1.CH(3)CN, 4.DMF) and C-H...F-C (6, 6.CH(3)CN) interactions. The correlation between the crystal structures of 1.CH(2)Cl(2), 1.CH(3)CN, 2, 4.DMF, 5, 6, and 6.CH(3)CN and their vapoluminescence suggests that weak nonconventional hydrogen-bonding interactions preside over the reversible sensing and signalling processes.

Journal Article↗
PubMed2003

Determination of DNA by Rayleigh light scattering enhancement of molecular "light switches".

Base on the enhancement of Rayleigh light scattering signals of molecular "light switches" by DNA under acidic condition, a sensitive and convenient method for DNA determination was proposed. The experiments indicated that, under optimum conditions, good linear relationships were obtained between the Rayleigh light scattering intensity and the concentration of nucleic acids. The detect limits of calf thymus DNA (ctDNA) were 13.0 ng ml(-1), 4.2 ng ml(-1), 51.5 ng ml(-1) and 3.0 ng ml(-1) with four "light switches", respectively. Plasmid DNA extracted from Bacillus subtilis were determined by the proposed method with satisfactory results, and the recovery rates of calf thymus DNA were in the range of 94.6-110.7%.

Animals↗
PubMed2002

Fluorometric determination of DNA using a new ruthenium complex Ru(bpy)2PIP(V) as a nucleic acid probe.

A new ligand, 2-phenyl(5-fluoro)imidazo[f]-1,10-phenanthroline (PIP(V)), and its coordination compounds, Ru(bpy)2PIP(V), were synthesized. The fluorescence spectrum of the interaction between Ru(bpy)2PIP(V) and DNA was studied, and a very strong fluorescence peak at a wavelength of 589 nm appeared. The optimum condition of analyzing DNA was decided. The method is simple, convenient and fast, and also has high sensitivity and good selectivity. It has been satisfactorily employed for determinations in synthesized samples.

DNA↗