大多生物分子在各種溫度下會有不同的活性反應，故本研究以干涉式相位量測的表面電漿感測器為基礎，加入溫度控制裝置，進行P極化光、不同濃度的鹽水實驗及免疫球蛋白IgG與Anti-IgG之鍵結實驗，並用五步演算法進行解相分析。以純水及鹽水實驗量測系統表現，得到的系統穩定度為0.4667度，系統靈敏度為1.617x10^3 (Degree/RIU)，系統折射率解析度可達2.886x10^-4 (RIU)。
本研究將IgG附著於金膜上，通入Anti-IgG進行鍵結，並討論在常溫下及有使用溫度控制，亦即生物體溫度(36 )下的實驗情況，在有使用溫度控制下的IgG及Anti-IgG之結合所產生的相位變化為6.72度，未使用溫度控制的相位變化為3.04度，兩者差異為3.68度。使用溫度控制裝置將溫度固定於實際生物分子的生存溫度時，將能從實驗過程中得到更接近於現實的生物分子活性反應，因此結合溫度控制裝置於表面電漿共振系統，將適用於進行更多種類的生物分子檢測。

Most biomolecules have different reaction activities at various temperatures. In this study, a temperature control apparatus was incorporated into a surface plasmon resonance (SPR) sensor, which is based on the interferometric phase measurements. Three kinds of experiments were performed, including P-polarized light measurements, salt-water mixture measurements and antibody-antigen binding experiments. The acquired temporal intensity signals were processed by the Schwider-Hariharan five-step phase-shifting algorithm to obtain the phases. The achieved phase-detection stability was 0.4667 degrees, and the system sensitivity was 1.617x10^3 degrees/RIU (refractive index unit). In addition, the corresponding system sensitivity was 2.886x10^-4 RIU.
In the third experiment, IgG was first binded on the Au film, and then anti-IgG was pumped into the flow cell to bind with IgG. The experiments were performed at two temperatures: at room temperature and at 36 degrees Celsius. The phase changes during the binding process were 6.72 degrees at 36 degrees Celsius, and 3.04 degrees at room temperature. The difference in phase changes between the two temperatures was 3.68 degrees. By using temperature control, the experiment results would be closer to the reality, which enables more varieties of biomolecular reactions to be detected by this SPR system.

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