Chem. J. Chinese Universities ›› 2009, Vol. 30 ›› Issue (12): 2381.

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Optical Detection of Immunoreaction Based on the Porous Silicon Bragg Reflector

LÜ Xiao-Yi1, QINGGeLe Tu2, XIANG Mei3, JIA Zhen-Hong4*, LI Rui5, ZHONG Fu-Ru3, LI Jiang-Wei2, ZHANG Fu-Chun2   

  1. 1. School of Electronic and Information Engineer, Xi′an Jiaotong University, Xi′an 710049, China;
    2. Key Laboratory of Xinjiang Biological Resources and Gene Engineering, College of Life Sciences and Technology,
    3. College of Chemistry and Chemical Engineering,
    4. College of Information Science & Engineering,
    5. School of Physics, Xinjiang University, Urumqi 830046, China
  • Received:2009-06-22 Online:2009-12-10 Published:2009-12-10
  • Contact: JIA Zhen-Hong. E-mail: jzhh@xju.edu.cn
  • Supported by:

    国家自然科学基金(批准号: 60968002)、教育部新世纪优秀人才支持计划(批准号: NCET-05-0897)和新疆维吾尔自治区高校科学研究计划(批准号: XJEDU2006I10)资助.

Abstract:

Porous silicon has attracted considerable attention for sensor application due to its remarkable optical properties and the easy fabrication. In this study, an optical immunoassay was developed by the optic reflectance spectroscopy of the porous silicon Bragg reflectors. The artificial immunogen of hydroxysafflor yellow A(HSYA-BSA) and the polyclonal anti-HSYA antibodies were employed as the target and probe, respectively. HSYA is the main chemical component of the flower of the safflower, which is widely used in traditional Chinese medicine for treatment of cerebrovascular and cardiovascular diseases. First, porous silicon Bragg reflector was functionalized using oxidation and silanization. Then, the polyclonal anti-HSYA antibodies were immobilized to the porous silicon Bragg reflector surface used a crosslink method. After the antigen-antibody reaction, the reflection spectrum red shifts and the red shift of spectrum increases with the increase of HSYA-BSA concentration. It is showing the red shifts of the reflectance spectrum as function of HSYA-BSA concentrations. Control experiments were also presented with negative serum and the result suggests that the reflection spectrum red shift is due to selective antigen-antibody binding and this porous silicon Bragg reflector immunosensor possess high specificity. Compared to conventional ELISA, the procedures are label-free and detection time is reduced. Thus, this research lays a foundation of exploiting label-free porous silicon Bragg reflector immunosensor and could be further developed for component detection of safflower of a quick and accurate determination.

Key words: Porous silicon Bragg reflector; Optical detection; Hydroxysafflor yellow A; Reflectances pectrum

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