Resonance Rayleigh Scattering Effect of Immunonanosilver Aggreagations and its Application to Rapid Determination of Trace Hg(II)

2013 ◽  
Vol 664 ◽  
pp. 749-753
Author(s):  
Li Li Xu ◽  
Zhi Liang Jiang ◽  
Ai Hui Liang
Keyword(s):  
Phosphate Buffer ◽  
Rayleigh Scattering ◽  
Sodium Citrate ◽  
Rapid Determination ◽  
Phosphate Buffer Solution ◽  
Resonance Rayleigh Scattering ◽  
Buffer Solution ◽  
Scattering Effect ◽  
Large Particles

Using PEG-10000 and sodium citrate as stabilizer, and NaBH4 as reducer, a stable nanosilvers (AgNPs) sol was prepared. In pH 6.6 phosphate buffer solution containing NaCl, the AgNPs were aggregated to large particles, which lead to resonance Rayleigh scattering (RRS) peak at 350 nm enhancement. Upon addition of cysteine, the peak decreased. The decreased value ΔI is linear to cysteine concentration in the range of 5-60×10-8 mol/L. Thus, a new RRS method was proposed for detection of cysteine.

A Nanosilver Resonance Rayleigh Scattering Method for the Determination of Trace Cysteine

2013 ◽  
Vol 664 ◽  
pp. 741-745
Author(s):  
Xin Hui Zhang ◽  
Yan Yan Wei ◽  
Chi Zhang ◽  
Miao Miao Chi ◽  
Jian Zhang ◽  
...  
Keyword(s):  
Phosphate Buffer ◽  
Rayleigh Scattering ◽  
Sodium Citrate ◽  
Phosphate Buffer Solution ◽  
Resonance Rayleigh Scattering ◽  
Scattering Method ◽  
Buffer Solution ◽  
Large Particles

Using PEG-10000 and sodium citrate as stabilizer, and NaBH4 as reducer, a stable nanosilver (AgNPs) sol was prepared. In pH 6.6 phosphate buffer solution containing NaCl, the AgNPs were aggregated to large particles, which lead to resonance Rayleigh scattering (RRS) peak at 350 nm enhancement. Upon addition of cysteine, the peak decreased. The decreased value ΔI is linear to cysteine concentration in the range of 5.0×10-8-6.0×10-7 mol/L. Thus, a new RRS method was proposed for detection of cysteine.

An Aptamer-Modified Nanogold Method for the Determination of Trace Ag+ Using Resonance Rayleigh Scattering as Detection Technique

2013 ◽  
Vol 647 ◽  
pp. 618-622
Author(s):  
Zhi Liang Jiang ◽  
Chen Yin Lin ◽  
Ai Hui Liang
Keyword(s):  
Gold Nanoparticle ◽  
Rayleigh Scattering ◽  
High Sensitivity ◽  
Resonance Rayleigh Scattering ◽  
Buffer Solution ◽  
Hepes Buffer ◽  
Large Particles ◽  
Ethanesulfonic Acid ◽  
Hepes Buffer Solution

Aptamer was modified the gold nanoparticle (AuNP) to form stable aptamer-AuNP probe that was not gathered in the pH 7.2 2-[4-(2-hydroxyethyl)-1-piperazinyl]ethanesulfonic acid (HEPES) buffer solution and in the presence of NaCl. The Ag+ react with the aptamer-AuNP probe to fold a hairpin structure complex of Ag+-aptamer and release AuNPs that were aggregated to large particles, which lead to resonance Rayleigh scattering (RRS) peak at 596 nm enhancement. The enhanced value ΔI596nm is linear to Ag + concentration in the range of 6.7×10-8-1.33×10-6 mol/L. Thus, a new RRS methods were proposed for detection of Ag+, with high sensitivity, good selectivity and simplicity.

Resonance Rayleigh Scattering Determination of Trace Hemin Basing on Aptamer-Modified Nanogold Catalysis of HAuCl4-Vitamine C

2013 ◽  
Vol 787 ◽  
pp. 400-403
Author(s):  
Jin Chao Dong ◽  
Ai Hui Liang ◽  
Zhi Liang Jiang
Keyword(s):  
Detection Limit ◽  
Rayleigh Scattering ◽  
Resonance Rayleigh Scattering ◽  
Serum Samples ◽  
Buffer Solution ◽  
Strong Resonance ◽  
Scattering Spectra ◽  
Vitamine C ◽  
Nanogold Catalysis

Hemin aptamer was used to modify gold nanoparticles (AuNPs) to obtain a stable aptamer-nanogold probe (AussDNA). In the condition of pH 8.0 Tris-HCl buffer solution containing 50mmol/L NaCl, the substrate chain of AussDNA was cracked by hemin to produce a short single-stranded DNA(ssDNA) and then further combined with hemin to form a stable hemin-ssDNA conjugate. The AuNPs released from AussDNA would be aggregated in the condition of 50mmol/L NaCl and exhibited a strong resonance Rayleigh scattering (RRS) peak at 368nm. Under the selected conditions, the increased RRS intensity (ΔI368nm) was linear to hemin concentration in the range of 5-750nmol/L, with a detection limit of 66 pmol/L. This RRS method was applied to determination of residual hemin in serum samples, with satisfactory results. The remnant AussDNA in the solution exhibited a strong catalytic activity on the gold particle reaction of HAuCl4-vitamine C (VC) that can be monitored by RRS technique at 368 nm. When the hemin concentration increased, the AussDNA decreased, the catalysis decreased, and the RRS intensity at 368nm decreased. The decreased RRS intensity ΔI368nmwas linear to the hemin concentration in the range of 1-200nmol/L, with a detection limit of 54 pmol/L. Accordingly, a sensitivity, selectivity, and simplicity new method of resonance Rayleigh scattering spectra to detect hemin using aptamer-modified nanogold as catalyst was established.

Electrocatalytic performance of a zinc sulphide nanoparticles-modified carbon paste electrode for the simultaneous determination of acetaminophen, guanine and adenine

2018 ◽  
Vol 10 (11) ◽  
pp. 1362-1371 ◽  
Author(s):  
Mallappa Mahanthappa ◽  
Nagaraju Kottam ◽  
Shivaraj Yellappa
Keyword(s):  
Carbon Paste Electrode ◽  
Phosphate Buffer ◽  
Phosphate Buffer Solution ◽  
Zinc Sulphide ◽  
Modified Carbon Paste Electrode ◽  
Carbon Paste ◽  
Buffer Solution ◽  
Guanine And Adenine ◽  
Paste Electrode

The simultaneous electroanalysis of acetaminophen (AC), guanine (G) and adenine (A) was successfully achieved on the zinc sulphide nanoparticles-modified carbon paste electrode (ZnS NPs/CPE) in phosphate buffer solution (PBS).

A Renewable Amperometric Immunosensor for hs-CRP Based on Functionalized Fe3O4@Au Magnetic Nanoparticles Attracted on Fe (III) Phthlocyanine/Chitosan-Membrane Modified Screen-Printed Carbon Electrode by a Magnet

2011 ◽  
Vol 110-116 ◽  
pp. 519-526 ◽  
Author(s):  
Ning Gan ◽  
Ling Hua Meng ◽  
Fu Tao Hu ◽  
Yu Ting Cao ◽  
Yuan Zhao Wu ◽  
...  
Keyword(s):  
Magnetic Nanoparticles ◽  
Rapid Determination ◽  
Phosphate Buffer Solution ◽  
Carbon Electrode ◽  
Buffer Solution ◽  
Chitosan Membrane ◽  
Screen Printed Carbon Electrode ◽  
Hs Crp ◽  
Screen Printed

A novel disposable screen-printed immunosensor for rapid determination of highly sensitive C reactiveprotein (hs-CRP) in human serum has been developed in the experiment. The sensor was constructed on one screen-printed carbon electrode (SPCE) with HRP labeled anti-hs-CRP antibody functionalized Fe3O4@Au magnetic nanoparticles (HRP labeled anti hs-CRP/ Fe3O4@Au) as the biorecognition probes attracted on the surface of Fe (III) phthalocyanine (FePc)/ chitosan membrane modified screen-printed carbon electrode (SPCE|FePc/Chit/chitosan) by external magnetic field. FePc was acted as electron immediate. The modified electrode shows an excellent electrocatalytic activity for hs-CRP in phosphate buffer solution (pH=7.0). After the immunosensor is incubated with hs-CRP antigen solution at 37°C for 20 min, the access of activity center of the HRP to electrode is partly inhibited, which leads to a linear decrease of the catalytic efficiency of the HRP to the reduction of immobilized FePc by H2O2 at –50 mV in hs-CRP’s concentration ranges from 1.2 to 200 ng/mL. The detection limit was 0.5ng/mL. The immunosensor was successfully utilized for determination of hs-CRP in real serum samples of heart disease patients, whose results were consistent with that by ELISA method. The accuracy and precision of the assay were 91.5-104.4% and 15.8-24.4%, respectively. The immunosensor was reusable once constructed and can be regenerated by adding new nanoprobes on the surface of basal electrode through magnet on its bottom. It can greatly reduce the detection cost which is valuable for the early diagnosis of tumors.

An Immunonanosilver Resonance Rayleigh Scattering Spectral Probe for Rapid Assay of Human Chorionic Gonadotrophin

2013 ◽  
Vol 680 ◽  
pp. 141-144 ◽  
Author(s):  
Qing Ye Liu ◽  
Gui Qing Wen ◽  
Kun Li ◽  
Ai Hui Liang
Keyword(s):  
Citric Acid ◽  
Optimal Condition ◽  
Rayleigh Scattering ◽  
Chorionic Gonadotrophin ◽  
Human Chorionic Gonadotrophin ◽  
Resonance Rayleigh Scattering ◽  
Serum Samples ◽  
Buffer Solution ◽  
Citric Acid Buffer

In pH 6.6 Na2HPO4- citric acid buffer solution and in the presence of KCl, the immunoreaction between hCG and nanosilver-labeled anti-hCG took place, the immunonanosilver-complex was formed and deposited, caused the resonance Rayleigh scattering (RRS) intensity at 510 nm decreased. In the optimal condition, the decreased RRS intensity responds linearly with the concentration of hCG over 0.125-1.75 µg/mL. Based on this, a new and simple RRS method has been proposed for the determination of hCG in serum samples, with satisfactory results.

Understanding the Endocrine Disruptor and Determination of Bisphenol A by Functional Cu-BTABB-MOF/rGO Composite as Facile Rapid Electrochemical Sensor: An Experimental and DFT Investigation

2022 ◽  
Author(s):  
Srikanth Ponnada ◽  
Demudu Babu Gorle ◽  
Maryam Sadat Kiai ◽  
Venkateswara raju Chikkili ◽  
M. Faraji ◽  
...  
Keyword(s):  
Bisphenol A ◽  
Electrochemical Sensor ◽  
Phosphate Buffer ◽  
Endocrine Disruptor ◽  
Phosphate Buffer Solution ◽  
Buffer Solution

A pioneering CuBTABB-MOF/rGO composite customized electrode is fabricated and utilized as a sensor towards identifying Bisphenol A (BPA) ina phosphate buffer solution of pH7.0. Composite is characterized by FTIR, Raman...

A Resonance Rayleigh Scattering Method for the Determination of Trace Benzotriazole Based on Complex Particle

2013 ◽  
Vol 830 ◽  
pp. 448-451
Author(s):  
Ling Ling Ye ◽  
Ai Hui Liang
Keyword(s):  
Detection Limit ◽  
Nitrogen Atom ◽  
Rayleigh Scattering ◽  
Hydroxylamine Hydrochloride ◽  
Regression Equation ◽  
Resonance Rayleigh Scattering ◽  
Scattering Method ◽  
Buffer Solution ◽  
Complex Particle

In pH 4.2 HAc-NaAc buffer solution, hydroxylamine hydrochloride reduced Cu2+ to Cu+ that coordinate the nitrogen atom of 1,2,3-benzotriazole (BTA) to form Cu-BTA complex particles with a resonance Rayleigh scattering (RRS) peak at 369 nm. Under the selected conditions, when the BTA concentration increased, the RRS intensity at 369 nm increased. The increased RRS intensity ΔI369nm was linear to BTA concentration in the range of 0.17-13.36 µg/mL, with a regression equation of ΔI369nm = 89.91C + 96.7, and the detection limit is 0.17 µg/mL. Accordingly, a new RRS method for BTA was established.

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