Title page for ETD etd-12152005-213148


Type of Document Dissertation
Author Zhang, Yan
URN etd-12152005-213148
Title Miniature fiber-optic multicavity Fabry-Perot interferometric biosensor
Degree PhD
Department Electrical and Computer Engineering
Advisory Committee
Advisor Name Title
Anbo Wang Committee Chair
Ahmad Safaai-Jazi Committee Member
Gary R. Pickrell Committee Member
Ira Jacobs Committee Member
James R. Heflin Committee Member
Keywords
  • Temperature compensation
  • Polyelectrolyte self-assembly
  • Fiber optic biosensor
  • Fabry-Perot interferometry
Date of Defense 2005-12-06
Availability unrestricted
Abstract
Fiber-optic Fabry-Perot interferometric (FFPI) sensors have been widely used due to their high sensitivity, ease of fabrication, miniature size, and capability for multiplexing. However, direct measurement of self-assembled thin films, receptor immobilization process or biological reaction is limited in the FFPI technique due to the difficulty of forming Fabry-Perot cavities by the thin film itself. Novel methods are needed to provide an accurate and reliable measurement for monitoring the thin-film growth in the nanometer range and under various conditions.

In this work, two types of fiber-optic multicavity Fabry-Perot interferometric (MFPI) sensors with built-in temperature compensation were designed and fabricated for thin-film measurement, with applications in chemical and biological sensing. Both the tubing-based MFPI sensor and microgap MFPI sensor provide simple, yet high performance solutions for thin-film sensing. The temperature dependence of the sensing cavity is compensated by extracting the temperature information from a second multiplexed cavity. This provides the opportunity to examine the thin-film characteristics under different environment temperatures.

To demonstrate the potential of this structure for practical applications, immunosensors were fabricated and tested using these structures. Self-assembled polyelectrolytes served as a precursor film for immobilization of antibodies to ensure they retain their biological activity. This not only provides a convenient method for protein immobilization but also presents the possibility of increasing the binding capacity and sensitivity by incorporating multilayers of antibodies into polyelectrolyte layers. The steady-state measurement demonstrated the surface concentration and binding ratio of the immunoreaction. Analysis of the kinetic binding profile provided a fast and effective way to measure antigen concentration. Monitoring the immunoreaction between commercially available immunoglobulin G (IgG) and anti-IgG demonstrated the feasibility of using the MFPI sensing system for immunosensing applications.

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