Centre for Nanoscience and Nanotechnology, Department of Chemistry, The Gandhigram Rural Institute, Gandhigram-624 302, Dindigul, Tamilnadu, India.
Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
J Mater Chem B. 2020 Oct 28;8(41):9502-9511. doi: 10.1039/d0tb01681k.
In purine metabolism, the xanthine oxidoreductase enzyme converts hypoxanthine (HXN) to xanthine (XN) and XN to uric acid (UA). This leads to the deposition of UA crystals in several parts of the body and the serum UA level might be associated with various multifunctional disorders. The dietary intake of caffeine (CF) and ascorbic acid (AA) decreases the UA level in the serum, which leads to cellular damage. Hence, it is highly needed to monitor the UA level in the presence of AA, XN, HXN, and CF and vice versa. Considering this sequence of complications, the present paper reports the fabrication of an electrochemical sensor using low-cost N-doped carbon dots (CDs) for the selective and simultaneous determination of UA in the presence of AA, XN, HXN, and CF at the physiological pH. The colloidal solution of CDs was prepared by the pyrolysis of asparagine and fabricated on a GC electrode by cycling the potential from -0.20 to +1.2 V in a solution containing CDs and 0.01 M H2SO4. Here, the surface -NH2 functionalities of CDs were used to make a thin film of CDs on the GC electrode. FT-IR spectroscopy confirmed the involvement of the -NH2 group in the formation of the CD film. HR-TEM analysis depicts that the formed CDs showed spherical particles with a size of 1.67 nm and SEM analysis exhibits the 89 nm CD film on the GC electrode surface. The fabricated CD film was successfully used for the sensitive and selective determination of UA. The determination of UA was achieved selectively in a mixture consisting of AA, XN, HXN, and CF with 50-fold high concentration. The CDs-film fabricated electrode has several benefits over the bare electrode: (i) well-resolved oxidation peaks for five analytes, (ii) boosted sensitivity, (iii) shifted oxidation as well as on-set potentials toward less positive potentials, and (iv) high stability. The practical utility of the present sensor was tested by simultaneously determining the multifactorial disorders-causing agents in human fluids. The electrocatalyst developed in the present study is sustainable and can be used for multiple analyses; besides, the electrochemical method used for the fabrication of the CD film is environmentally benign.
在嘌呤代谢中,黄嘌呤氧化还原酶将次黄嘌呤(HXN)转化为黄嘌呤(XN),然后将 XN 转化为尿酸(UA)。这导致 UA 晶体在身体的几个部位沉积,血清 UA 水平可能与各种多功能障碍有关。咖啡因(CF)和抗坏血酸(AA)的饮食摄入会降低血清中的 UA 水平,从而导致细胞损伤。因此,在 AA、XN、HXN 和 CF 存在的情况下监测 UA 水平非常重要,反之亦然。考虑到这种并发症的顺序,本论文报道了一种使用低成本氮掺杂碳点(CDs)制造电化学传感器的方法,用于在生理 pH 下选择性和同时测定 AA、XN、HXN 和 CF 存在下的 UA。CDs 的胶体溶液通过天冬酰胺的热解制备,并通过在包含 CDs 和 0.01 M H2SO4 的溶液中循环电位从-0.20 到+1.2 V 在 GC 电极上制造。在这里,CDs 的表面-NH2 官能团用于在 GC 电极上形成 CDs 的薄膜。傅里叶变换红外光谱(FT-IR)证实了-NH2 基团在 CD 薄膜形成中的参与。高分辨率透射电子显微镜(HR-TEM)分析表明形成的 CDs 显示出 1.67nm 的球形颗粒,扫描电子显微镜(SEM)分析显示 GC 电极表面上有 89nm 的 CD 薄膜。所制备的 CD 薄膜成功地用于 UA 的灵敏和选择性测定。在包含 AA、XN、HXN 和 CF 的混合物中,可以选择性地测定 UA,其浓度高 50 倍。与裸电极相比,CD 薄膜修饰电极具有以下几个优点:(i)五个分析物的氧化峰得到很好的分离,(ii)提高了灵敏度,(iii)氧化和起始电位向更负的电位移动,以及(iv)高稳定性。本研究开发的电催化剂可持续且可用于多种分析;此外,用于制备 CD 薄膜的电化学方法对环境友好。