[A Hydride Generation-Catalytic Resonance Rayleigh Scattering Method for Detection of Trace Arsenic].

Arsenic is a toxic metal element and the establishment of a highly sensitive and selective method for As has great significance to human health and environment protection. In sulfuric acid medium, As(Ⅲ) was reduced by NaBH4 to form AsH3 gas that was trapped by the Ce(Ⅳ)-I- catalytic absorption solution to cause Ce(Ⅳ) concentration decreased and As particle increased, which resulted in the resonance Rayleigh scattering (RRS) and fluorescence increased at 370 and 351 nm respectively. The increased RRS and fluorescence intensities were linear to As(Ⅲ) concentration in the range of 0.

[A Facile Nanogold Surface Plasmon Resonance Absorption Method for CO Tracing].

The detection of gas pollutants in atmosphere and indoor air is very important to human health and safety. Monoxide carbon (CO) is a common gas pollutant with high toxicity that mainly comes from the inadequacy oxidization of carbon such as oil, coal and petrol inadequacy combustion, auto-gas and some natural disasters whose limit value in air is lower than 6.0 mg·m-3 in the national standard.

[Determination of Trace Boron Based on Gold Nanorod Plasmonic Resonance Rayleigh Scattering Energy Transfer to the Coordinate].

B is a necessary trace element for human and animals, but the excess intake of B caused poison. Thus, it is very important to determination of B in foods and water. The target of this study is development of a new, sensitive and selective resonance Rayleigh scattering energy transfer (RRS-ET) for the determination of B.

[Fluorescence Determination of Trace Se with the Hydride-K13-Rhodamine 6G System].

Se is a necessary trace element for human and animals, but the excess intake of Se caused poison. Thus, it is very important to determination of Se in foods and water. The target of this study is development of a new, sensitive and selective hydride generation-molecular fluorescence method for the determination of Se.

[Resonance Rayleigh scattering determination of trace tobramycin using aptamer-modified nanogold as probe ].

Nanogold (NG) was prepared using NaBH4 reduction of HAuCl4. The NG was modified by the tobramycin-aptamer to obtain a stable Apt-NG probe for tobramycin. The three aptamers containing 15, 21 and 27 bases were examined, and results showed that the aptamer with 21 bases was best and was chosen for use.

[Resonance Rayleigh scattering determination of trace ozone based on the cationic surfactant association particles].

In the presence of pH 4.0 HAC-NaAC buffer solution, using H3BO3-KI (BKI) as absorption solution, O3 oxidized KI to produce I2, and it reacted with excess I- to form I3- that combined with the cationic surfactant (CS) such as cetylpyridinium chloride (CPCl), tetradecyl pyridinium bromide (TPB), cetyl trimethyl ammonium bromide (CTMAB), and tetradecyl dimethylbenzyl ammonium chloride (TDMAC) to produce stable (CS-I3)n association particles, which exhibited a strong resonance Rayleigh scattering (RRS) peak at 470 nm. Under the chosen conditions, as the concentration of O3 (C) increased, the concentration of I3- increased, and the RRS intensity at 470 nm (1470 nm) increased due to more association particles forming.

Supramolecular sky-blue phosphorescent polymer iridium complexes for single-emissive-layer organic light-emitting diodes.

Novel supramolecular phosphorescent polymers (SPPs) are synthesized as a new class of solution-processable electroluminescent emitters. The formation of these SPPs takes advantage of the efficient non-bonding assembly between bis(dibenzo-24-crown-8)-functionalized iridium complex monomer and bis(dibenzylammonium)-tethered co-monomer, which is monitored by (1) H NMR spectroscopy and viscosity measurements. These SPPs show good film morphology and an intrinsic glass transition with a Tg of 94-116 °C.

[DNAzyme cracking-nanogold resonance Rayleigh scattering spectral method for the determination of trace Cu2+].

In the condition of pH 7.0 HEPES buffer solution and 0.19 mol x L(-1) NaCl, the substrate strand DNA (SS) and the enzyme strand DNA (ES) hybridized into a double-stranded DNA (dsDNA) at 80 degrees C.

[Resonance scattering detection of trace Hg2+ using aptamer modified AuSe nanoalloy].

Under the condition of sodium citrate as stabilizer, the gold-selenium (AuSe) nano-alloy was prepared by sodium borohydride reduction procedure, and was modified by single-strand aptamer to obtain an aptamer nano-alloy probe (apta-AuSe) for Hg(II). In pH 6.8 Na2HPO4-NaH2PO4 buffer solution and in the presence of NaCl of 33 mmol L(-1), the Apta-AuSe probe is not aggregation.

[Resonance scattering spectral detection of trace K+ by aptamer-modified nanogold probe].

In pH 7.0 Na2HPO4-NaH2PO4 buffer solution, nanogold particles interacted with the aptamer to form a stable aptamer-nanogold complex that was not aggregation by NaCl. At 80 degrees C, K+ and aptamer folded to form a stable G-quadruplex that released nanogold particles, the uncombined nanogold particles aggregated to large nanogold clusters that caused the increase in resonance scattering (RS) intensity at 563 nm in high concentration of NaCl, and the laser scattering showed that the average diameter was 120 nm.

[Resonance scattering detection of trace Hg2+ using herring sperm DNA modified nanogold].

In pH 7.0 tris-HCl buffer solutions and in the presence of 0.017 mol x L(-1) NaCl, herring sperm DNA was combined with gold nanoparticles in size of 10 nm to form stable complex, and the NaCl did not cause the aggregation of the gold nanoparticles.

[Fluorescence analysis of trace glucose using glucose oxidase and horseradish peroxidase].

In acetate buffer solution and in the presence of glucose oxidase (GOD), glucose reduced the dissolved oxygen to form H2O2 that oxidized catalytically the excess KI to from I3- by horseradish peroxidase (HRP). The I3- combines respectively with rhodamine S (RhS), rhodamine 6G(Rh6G), butyl-rhodamine B(b-RhB) and rhodamine B(RhB) to form RhS-I3, Rh6G-I3, b-RhB-I3 and RhB-I3 associated particles that result in fluorescence quenching at 556, 556, 584 and 584 nm, respectively. Under the optimal conditions, the concentration of glucose in the range of 0.

[Fluorescence quenching assay of ultratrace horseradish peroxidase using rhodamine dye].

In acetate buffer solution, the reaction of H2O2 with KI was catalyzed by horseradish peroxidase (HRP) to form I3-. The I3- combined respectively with rhodamine S(RhS), rhodamine 6G(Rh6G), rhodamine B(RhB) and butyl-rhodamine B(b-RhB) to form RhS-I3, Rh6G-I3, RhB-I3 and b-RhB-I3 association particles, resulting in the fluorescence quenching at 580, 580, 554 and 554 nm, respectively. The effect of pH value, rhodamine dye concentration, KI concentration, H2O2 concentration, reaction temperature and time on the fluorescence quenching intensity (deltaF) of the four catalytic systems was considered respectively.

[Immunonanogold catalytic spectrophotometric determination of trace complement 3].

Gold nanoparticles about 10 nm in size were prepared by improved trisodium citrate reduction procedure, and were used to label goat anti-human C3 to obtain a sensitive spectral probe for complement 3 (C3) in the condition of pH 7.5. The immune reaction between nanogold-labeled C3 antibody (anti-C3) and the antigen C3 took place to form the nanogold immune complex in pH 5.

[Resonance scattering spectral properties of CdTe nanoparticles and its application].

In the present paper, CdTe quantum dots were prepared, and the resonance scattering, fluorescence and absorption spectral properties of CdTe quantum dots in aqueous solution were studied in details. The fluorescence spectral results showed that the CdTe quantum dots of 3.8, 4.

A simple and sensitive resonance scattering spectral method for determination of hydroxyl radical in Fenton system using rhodamine S and its application to screening the antioxidant.

Based on resonance scattering (RS) effect of rhodamine dye association particles, a new resonance scattering method for the determination of hydroxyl free radical from Fenton reaction was developed. In HCl-NaAc buffer solution, the OH of Fenton reaction oxidized the excess I(-) to I(3)(-). The I(3)(-) combined, respectively, with rhodamine B (RhB), butyl rhodamine B (b-RhB), rhodamine 6G (RhG) and rhodamine S (RhS) to form association particles that exhibit stronger resonance scattering effect at 420nm and 610nm.

[Resonance scattering spectra of apolipoprotein immunocomplex particles and its analytical application].

In pH 6.8 Na2 HPO4-NaH2PO4 buffer solution and in presence of polyethylene glycol (PEG), apolipoprotein AI (ApoAI) and apolipoprotein B (ApoB) would combine with their corresponding antibody and produced immune complex particles in size of about 180 nm and 140 nm respectively, which exhibit stronger resonance scattering (RS) effect at 340 nm and 470 nm. The influence of pH, antisera volume, PEG concentration, incubation time and co-exists substances was considered.

[Immunoresonance scattering spectral assay of complement factor 4(C4)].

Based on resonance scattering (RS) effect of immune complex particles, a new resonance scattering method for the determination of C4 in the human blood serum was developed. It was based on the fact that goat anti-human C4 was combined with complement factor 4 (C4) in the pH 7.3 Na2 HPO4-KH2PO4 buffer solution.

A novel and highly sensitive resonance scattering spectral assay for horseradish peroxidase using cationic surfactant.

A novel and ultrasensitive resonance scattering (RS) spectral assay was proposed for detection of horseradish peroxidase (HRP) activity. It was based on that the HRP strongly catalyze H2O2 oxidation of excess I- to form I3-, the resulting I3- combined with four cationic surfactant (CS), including tetradecyl pyridinium bromide (TPB), cetyltrimethyl ammonium bromide (CTMA), cetylpyridinium chloride (CPCM) and tetradecyl dimethylbenzyl ammonium chloride (TDMBA) to produce association particles (TPB-I3)n, (CTMA-I3)m, (CPCM-I3)l and (TDMBA-I3)k, which exhibit a strongest resonance scattering peak at 478, 423, 538 and 491 nm, respectively. For the four systems of TPB, CPCM, CTMBA and TDMBA, the HRP activity determined was in the linear range of 0.

[Resonance scattering spectral study of IgA immune complex particles and its analytical application].

Based on the resonance scattering (RS) effect of immune complex particles, a new resonance scattering spectral method for the determination of trace IgA in the human blood serum was developed. It was based on that goat anti-human IgA was combined with the antigen of IgA. It is known that antibody has C-terminal and N-terminal and the N-terminal is binding site of antigen, and it could combine antigen.

An immunonanogold resonance scattering-quenching probe for rapid and sensitive assay of microalbumin.

A novel and sensitive immunonanogold resonance scattering (RS) spectral probe was obtained for rapid detection of microalbumin (Malb), using 10 nm gold nanaoparticle to label goat anti-human Malb. It was based on that the gold-labeled anti-Malb took place nonspecific aggregation and exhibited a strong RS peak at 577 nm in pH 5.2 C(6)H(8)O(7)-Na(2)HPO(4) buffer solution containing polyethylene glycol (PEG), and the immunocomplex formed after specific reaction of gold-labeled anti-Malb with Malb, which led to a decrease in the intensity of RS peak at 577 nm considerably.

An immunonanogold resonance scattering spectral probe for rapid assay of human chorionic gonadotrophin.

Background: Several assays for human chorionic gonadotrophin (hCG) such as radioimmunoassay and fluorescence immunoassays were reported. So far, there was no report about the immunonanogold resonance scattering spectral (ING-RSS) assay based on the immunoreaction and resonance scattering (RS) effect.

Methods: Three ING-RSS probes for hCG were prepared, using nanogold in size of 8, 10, 13 nm to label rabbit hCG antiserum (anti-hCG).

A new immune resonance scattering spectral assay for trace fibrinogen with gold nanoparticle label.

Gold nanoparticles in size of 9.0 nm was prepared by the trisodium citrate and used to label goat anti-human fibrinogen. In the pH 6.

[Resonance scattering spectral assay of papain enzymatic activity with sodium dodecyl benzene sulfonate].

In pH 6.5 phosphate buffer solutions, dodecyl benzene sulfonate (SDBS) was combined with casein to form association particles, which exhibited five Rayleigh scattering peaks at 470, 360, 400, 420 and 520 nm, respectively. Under suitable conditions, papain has catalytic effect on the hydrolysis of casein, and SDBS can stop the catalytic reaction and be combined with the excess casein to form association particles.