本論文利用羧基化多壁奈米碳管(MWCNT-COOH)修飾網版印刷碳電極(SPCE),並用SPCE/MWCNT-COOH在pH 7.0環境下,於每次偵測前給予7分鐘的accumulation time (open circuit)來偵測鳥糞嘌呤(guanine, G)與腺嘌呤(adenine, A),並發現此修飾電極具有良好的催化活性。我們也利用穿透式電子顯微鏡與掃描式電子顯微鏡觀察MWCNT-COOH修飾溶液的分散情形與SPCE/MWCNT-COOH的地貌。 我們利用循環伏安法(CV)偵測guanine與adenine,在濃度範圍0.08 ~ 4.00 μM與0.24 ~ 4.00 μM之間,其濃度校正曲線斜率(靈敏度)為43.44 μA/μM與29.47 μA/μM,偵測極限為24.90 nM與56.17 nM。接著我們進一步利用差式脈衝伏安法(DPV)以降低其偵測極限,偵測guanine與adenine分別在濃度範圍0.04 ~ 1.15 μM與0.12 ~ 3.50 μM之間,其濃度校正曲線斜率(靈敏度)為14.53 μA/μM與10.79 μA/μM,偵測極限為8.90 nM與18.91 nM。使用小牛胸腺DNA作為真實樣品的實驗中,在濃度範圍為0.10 ~ 1.00 μg/mL DNA中所偵測到的(C+G)/(A+T)=67%,偵測極限為12.55 ng/mL。
In this work, we prepared carboxylated multi-walled carbon nanotubes modified screen-printed carbon electrodes (SPCE/MWCNT-COOH) by a simple deposition method. Electrochemical oxidation of guanine and adenine in pH 7.0 with 7 min. accumulation time (open circuit) were conducted, and showd excellent catalytic activity. The MWCNT-COOH modified solution and the SPCE/MWCNT-COOH modified electrodes were characterized by transmission electron microscopy(TEM) and scaning electron microscopy (SEM). A linear calibration plots of guanine (0.08 - 4.00 μM) and adenine (0.24 - 4.00 μM) were obtained by cyclic voltammetries, the sensitivities were 43.44 μA/μM and 29.47 μA/μM, and the detection limits were 24.90 nM and 56.17 nM, respectively. A linear calibration plots of guanine (0.04 - 1.15 μM) and adenine (0.12 – 3.50 μM) were obtained by difference pulse voltammetries, the sensitivities were 14.53 μA/μM and 10.79 μA/μM, and the detection limits were 8.90 nM and 18.91 nM, respectively.A linear calibration plots of calf thumus DNA (0.10 - 1.00 μg/mL) were obtained by difference pulse voltammetries, the (C+G)/(A+T)=67%, and the detection limit of calf thumus DNA was 12.55 ng/mL.