Cao Jie, Chen Xiao-Ying
Scientific Research and Experiment Center, Fujian Police College, Fuzhou, China.
Fuzhou University Postdoctoral Research Station of Chemistry, Fuzhou University, Fuzhou, China.
Front Bioeng Biotechnol. 2024 Feb 9;12:1329129. doi: 10.3389/fbioe.2024.1329129. eCollection 2024.
Estrone (E1), as an endogenous estrogen, has a variety of physiological functions in human body and is of great significance to human health. On the other hand, it is a widely distributed and highly disturbing environmental endocrine disruptor in water. Therefore, there is an urgent need to develop a sensitive, rapid, and inexpensive method for the on-site determination of E1, which is not only for clinical diagnosis and treatment, but also for the investigation and monitoring of endogenous estrogen pollution in environmental water. In this study, Ru(bpy) /MWCNTs/Nafion/gold electrodes were prepared by surface electrostatic adsorption and ion exchange. A molecularly imprinted membrane (MIP) with the capability to recognize E1 molecules was prepared by sol-gel method, and the electrodes were modified with MIP to form an electrochemical luminescence sensor (MIP-ECL). This method simultaneously possesses ECL's advantage of high sensitivity and MIP's advantage of high selectivity. Moreover, the addition of carboxylated multi-walled carbon nanotubes (MWCNT-COOH) improved the functionalization of the gold electrode surface and increased the binding sites of MIP. Meanwhile, the good conductivity of MWCNTs promoted electron transfer and further improved the sensitivity of the sensor. The sensor showed a wide linear interval in which the E1 concentrations can range from 0.1 μg/L to 200 μg/L, along with a high linear correlation coefficient ( = 0.999). The linear regression equation of the sensor was Y = 243.64x-79.989, and the detection limit (LOD) was 0.0047 μg/L. To validate our sensor, actual samples were also measured by the reference method (LC-MS/MS), and it was found that the relative deviation of quantitative results of the two different methods was less than 4.1%. This indicates that the quantitative results obtained by this sensor are accurate and can be used for rapid determination of E1 in clinical samples and environmental water.
雌酮(E1)作为一种内源性雌激素,在人体中具有多种生理功能,对人类健康具有重要意义。另一方面,它是一种在水中广泛分布且极具干扰性的环境内分泌干扰物。因此,迫切需要开发一种灵敏、快速且廉价的现场测定E1的方法,这不仅用于临床诊断和治疗,还用于环境水体中内源性雌激素污染的调查和监测。在本研究中,通过表面静电吸附和离子交换制备了Ru(bpy)/多壁碳纳米管(MWCNTs)/Nafion/金电极。采用溶胶 - 凝胶法制备了具有识别E1分子能力的分子印迹膜(MIP),并用MIP对电极进行修饰,形成电化学发光传感器(MIP - ECL)。该方法同时具备电化学发光的高灵敏度优势和分子印迹的高选择性优势。此外,羧基化多壁碳纳米管(MWCNT - COOH)的加入改善了金电极表面的功能化,增加了MIP的结合位点。同时,MWCNTs良好的导电性促进了电子转移,进一步提高了传感器的灵敏度。该传感器呈现出较宽的线性区间,E1浓度范围为0.1μg/L至200μg/L,线性相关系数较高( = 0.999)。传感器的线性回归方程为Y = 243.64x - 79.989,检测限(LOD)为0.0047μg/L。为验证我们的传感器,还采用参考方法(液相色谱 - 串联质谱法,LC - MS/MS)对实际样品进行了测定,发现两种不同方法的定量结果相对偏差小于4.1%。这表明该传感器获得的定量结果准确,可用于临床样品和环境水体中E1的快速测定。