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Clinical Chemistry 52: 1389-1394, 2006; 10.1373/clinchem.2005.061176
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Right arrow Automation and Analytical Techniques
(Clinical Chemistry. 2006;52:1389-1394.)
© 2006 American Association for Clinical Chemistry, Inc.


Automation and Analytical Techniques

Gold-Labeled Nanoparticle-Based Immunoresonance Scattering Spectral Assay for Trace Apolipoprotein AI and Apolipoprotein B

Zhiliang Jiang1,2,a, Shuangjiao Sun1, Aihui Liang2, Wenxin Huang1 and Aimiao Qin2

1 Department of Resource and Environmental Science, Guangxi Normal University, Guilin, China.
2 Department of Material and Chemical Engineering, Guilin University of Technology, Guilin, China.

aAddress correspondence to this author at: Department of Resource and Environmental Science, Guangxi Normal University, Guilin 541004, China.

Background: Apolipoprotein AI (ApoAI) and ApoB are risk indicators of cardiovascular disease. We describe the use of immunoresonance scattering to measure the ApoAI and ApoB in serum.

Methods: We used a trisodium citrate method to prepare 9.0-nm gold nanoparticles labeled with goat anti-human ApoAI and ApoB antibodies. The immune reaction between gold-labeled antibodies and antigens took place in Na2HPO4-NaH2PO4 buffer solution (pH 6.4 for ApoAI and pH 6.0 for ApoB) in the presence of 75 g/L polyethylene glycol (PEG). We used a transmission electron microscope to observe the shape of the gold nanoparticles. Results were compared with those obtained by immunoturbidimetric methods. Twenty-five human serum samples were assayed by the immunoresonance scattering assay preset with the data indicated and by an immunoturbidimetric assay.

Results: The presence of PEG greatly enhanced the intensity of resonance-scattering peaks at 560 nm. The intensity ({Delta}I) was proportional to concentration at 0.00833–0.3333 mg/L ApoAI and 0.00197–0.1972 mg/L ApoB. The detection limits were 2.04 and 0.96 µg/L for ApoAI and ApoB, respectively. The results for human serum samples were in agreement with those obtained with an immunoturbidimetric method. Linear regression analysis revealed a correlation coefficient, slope, and intercept of 0.915, 0.966, and 68.53 mg/L, respectively, for ApoAI and 0.919, 0.996, and 15.46 mg/L for ApoB.

Conclusion: This method showed high sensitivity and good selectivity for quantitative determination of ApoAI and ApoB in human serum, with satisfactory results.




The following articles in journals at HighWire Press have cited this article:


Home page
J Biomol ScreenHome page
Z. Jiang, L. Wei, M. Zou, A. Liang, and M. Meng
Rapid Assay of Trace Immunoglobulin M by a New Immunonanogold Resonance Scattering Spectral Probe
J Biomol Screen, April 1, 2008; 13(4): 302 - 308.
[Abstract] [PDF]


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Clin. Chem.Home page
Z. Jiang, W. Huang, J. Li, M. Li, A. Liang, S. Zhang, and B. Chen
Nanogold Catalysis Based Immunoresonance-Scattering Spectral Assay for Trace Complement Component 3
Clin. Chem., January 1, 2008; 54(1): 116 - 123.
[Abstract] [Full Text] [PDF]




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