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Automation and Analytical Techniques |
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 (
I) was proportional to concentration at 0.008330.3333 mg/L ApoAI and 0.001970.1972 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.
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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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