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  • 學位論文

開發梯度導模共振陣列感測晶片以應用於慢性腎臟病之快速篩檢

Development of gradient grating period guided-mode resonance microarray for chronic kidney disease

指導教授 : 黃正昇
本文將於2025/01/13開放下載。若您希望在開放下載時收到通知,可將文章加入收藏

摘要


隨著人口老化,慢性病越發盛行,若能及早發現便能及早給予治療,因此快速又準確的檢測便顯得極為重要,故本研究的目標在於開發快速、低成本、高靈敏度之生物感測器。 本研究應用週期梯度導膜共振開發一種感測器,利用生物分子鍵結後折射率改變的特性,從CCD上觀測光強度的分布圖,並由強度的偏移量來量測生物分子之濃度變化。為了驗證檢測生物分子的可行性,本研究以Albumin與Creatinine作為目標物進行量測,將導膜共振感測器結合微流道進行檢測,每次量測只需要60µl的檢體,Albumin與Creatinine的檢測極限分別為5.81 µg/ml與6.91µg/ml。 綜合上述所說,我們成功驗證了週期梯度導膜共振檢測生物分子的能力,並憑藉著其較小的尺寸與簡單的光路設計,可以進一步將GGP-GMR與智慧手機結合,並應用於定點照護。

並列摘要


As the population ages, chronic diseases become more prevalent. Treatment can be prescribed in time if detected early; therefore, rapid and accurate detection is extremely important. The goal of this study is to develop rapid, low-cost, and sensitive biosensors. In this study, a sensor based on gradient grating period guided-mode resonance (GGP-GMR) was developed. The change in refractive index upon adsorption of biomolecule causes the shift in intensity distribution at a CCD. The amount of intensity shift can be correlated to the sample concentration. To demonstrate its biosensing capability, a GGP-GMR was integrated with microfluidic channel for albumin and creatinine measurement. Only 60 µl of samples were required to achieve limit of detection of 5.81 and 6.91 µg/ml for albumin and creatinine, respectively. In summary, the GGP-GMR was successfully demonstrated for biomolecule detection. With its compact size and simple optical path design, a GGP-GMR can be further integrated with a smartphone for potential point of care applications.

參考文獻


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