College of Chemistry and Chemical Engineering, The Key Laboratory of Chongqing Modern Analytical Chemistry, Southwest University, Chongqing, 400715, P.R. China.
Analyst. 2012 Mar 7;137(5):1225-31. doi: 10.1039/c2an16105b. Epub 2012 Jan 19.
Here, we report a highly simple and general protocol for functionalization of the CoFe(2)O(4) NPs with chitosan polymers in order to make CoFe(2)O(4) NPs disperse and stable in solution. The functionalized CoFe(2)O(4) NPs (denoted as CF-CoFe(2)O(4) NPs) were characterized by scanning electron microscope (SEM), thermogravimetric (TG), X-ray diffraction (XRD) and FT-IR spectra. It was found that the CoFe(2)O(4) NPs were successfully decorated and uniformly dispersed on the surface of chitosan without agglomeration. The CF-CoFe(2)O(4) NPs were found to increase greatly the radiation emitted during the CL oxidation of luminol by hydrogen peroxide. Results of ESR spin-trapping experiments demonstrated that the CF-CoFe(2)O(4) NPs showed catalytic ability to H(2)O(2) decomposition into ˙OH radicals. On this basis, a highly sensitive and rapid chemiluminescent method was developed for hydrogen peroxide in water samples and glucose in blood samples. Under optimum conditions, the proposed method allowed the detection of H(2)O(2) in the range of 1.0 × 10(-9) to 4.0 × 10(-6) M and glucose in the range of 5.0 × 10(-8) to 1.0 × 10(-5) M with detectable H(2)O(2) as low as 500 pM and glucose as low as 10 nM, respectively. This proposed method has been successfully applied to detect H(2)O(2) in environmental water samples and glucose in serum samples with good accuracy and precision.
在这里,我们报告了一种非常简单和通用的方法,即用壳聚糖聚合物功能化 CoFe(2)O(4) NPs,以使 CoFe(2)O(4) NPs 在溶液中分散和稳定。功能化的 CoFe(2)O(4) NPs(表示为 CF-CoFe(2)O(4) NPs)通过扫描电子显微镜 (SEM)、热重 (TG)、X 射线衍射 (XRD) 和傅里叶变换红外光谱 (FT-IR) 进行了表征。结果发现,CoFe(2)O(4) NPs 成功地被修饰并均匀地分散在壳聚糖的表面上,没有团聚。发现 CF-CoFe(2)O(4) NPs 大大增加了过氧化物氢引发的鲁米诺 CL 氧化过程中发射的辐射。ESR 自旋捕获实验结果表明,CF-CoFe(2)O(4) NPs 表现出将 H(2)O(2) 分解为˙OH 自由基的催化能力。在此基础上,建立了一种用于水样中过氧化氢和血样中葡萄糖的高灵敏度、快速化学发光方法。在最佳条件下,该方法允许在 1.0 × 10(-9) 至 4.0 × 10(-6) M 的范围内检测 H(2)O(2),在 5.0 × 10(-8) 至 1.0 × 10(-5) M 的范围内检测葡萄糖,检测 H(2)O(2)的检出限低至 500 pM,检测葡萄糖的检出限低至 10 nM。该方法已成功应用于环境水样中 H(2)O(2)和血清样品中葡萄糖的检测,具有良好的准确性和精密度。