Sanya Khursheed , Sumera Sarwar , Dilshad Hussain , Muhammad Raza Shah , Jiri Barek , Muhammad Imran Malik
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Unlike previously reported sensors, the developed creatinine sensor can be employed for all levels of creatinine in samples of real patients.</div></div><div><h3>Results</h3><div>In this study, an efficient voltammetric sensor for creatinine is developed by modifying a glassy carbon electrode (GCE) with poly (ethyleneimine) (PEI) capped silver nanoparticles at titanium dioxide (PEI-AgNPs)/TiO<sub>2</sub>, i.e., titanium dioxide (TiO<sub>2</sub>)/graphene oxide (GO) nanocomposites (Ag@GO/TiO<sub>2</sub>-GCE). The Ag@GO/TiO<sub>2</sub> nanocomposite was characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), thermal gravimetric analysis (TGA), X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic light scattering (DLS), zeta potential, Fourier transform infrared (FT-IR) spectroscopy, and UV–Vis spectrophotometry. Various voltammetric techniques namely cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), chronoamperometry (CA), and differential pulse voltammetry (DPV) were employed. The Ag@GO/TiO<sub>2</sub>-GCE demonstrated good selectivity, stability, and a quick response time of 1.0 s for creatinine. An extended linear dynamic range (LDR) of creatinine from 0.01 pM (DPV) to 1.0 M (CV) based on different voltammetric techniques is imperative for detecting diverse creatinine levels in various body fluids. The LOD and LOQ of the developed creatinine detection method were found to be 1.15 pM and 3.5 pM, respectively. The electrochemical sensor exhibited an exceptionally high sensitivity of 15.74 μApM<sup>−1</sup>cm<sup>−2</sup>.The body fluids from healthy volunteers were spiked with a known amount of creatinine to evaluate sensor efficiency in the context of recovery. Finally, blood serum, saliva, and urine samples of kidney patients were analyzed for creatinine levels.</div></div><div><h3>Significance</h3><div>An important merit of the developed creatinine sensor is its ability for non-invasive point-of-care diagnosis in saliva with more than 90 % recovery. The comparison of the developed method with the standard Jaffes' colorimetric method endorsed its reliability and extended ability for the samples where Jaffes’ method fails. 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引用次数: 0
摘要
背景:不同体液中肌酐水平可以作为与前列腺癌和慢性肾脏疾病(CKD)相关的肾脏功能的重要生物标志物。肌酐水平在不同体液中的浓度不同,如血液、尿液和唾液。与以前报道的传感器不同,开发的肌酐传感器可以用于真实患者样品中的所有水平的肌酐。结果本研究通过在二氧化钛(PEI- agnps)/二氧化钛(TiO2),即二氧化钛(TiO2)/氧化石墨烯(GO)纳米复合材料(Ag@GO/TiO2-GCE)上涂覆纳米银修饰玻碳电极(GCE),开发了一种高效的肌酸酐伏安传感器。采用扫描电子显微镜(SEM)、原子力显微镜(AFM)、热重分析(TGA)、x射线衍射(XRD)、透射电子显微镜(TEM)、动态光散射(DLS)、zeta电位、傅里叶变换红外光谱(FT-IR)和紫外可见分光光度法对Ag@GO/TiO2纳米复合材料进行了表征。采用了循环伏安法(CV)、电化学阻抗法(EIS)、计时伏安法(CA)和差分脉冲伏安法(DPV)等多种伏安技术。Ag@GO/TiO2-GCE对肌酐具有良好的选择性和稳定性,反应时间为1.0 s。基于不同伏安技术的肌酸酐线性动态范围(LDR)从0.01 pM (DPV)扩展到1.0 M (CV),对于检测各种体液中不同的肌酸酐水平是必要的。所建立的肌酐检测方法的LOD和LOQ分别为1.15 pM和3.5 pM。该电化学传感器具有15.74 μApM-1cm-2的超高灵敏度。健康志愿者的体液中加入一定量的肌酐,以评估传感器在恢复过程中的效率。最后,对肾脏患者的血清、唾液和尿液样本进行肌酐水平分析。所开发的肌酸酐传感器的一个重要优点是它能够在唾液中进行无创的即时诊断,回收率超过90%。将该方法与标准的Jaffes比色法进行比较,证实了该方法的可靠性和扩展能力,适用于Jaffes法失效的样品。低LOD、高灵敏度、延长LDR和低成本使得采用该方法进行即时诊断成为可能。
Electrochemical detection of creatinine at picomolar scale with an extended linear dynamic range in human body fluids for diagnosis of kidney dysfunction
Background
Creatinine levels in different body fluids can serve as an important biomarker for kidney functioning relevant to prostate cancer and chronic kidney disease (CKD). Creatinine levels vary in concentration in different body fluids, such as blood, urine, and saliva. Unlike previously reported sensors, the developed creatinine sensor can be employed for all levels of creatinine in samples of real patients.
Results
In this study, an efficient voltammetric sensor for creatinine is developed by modifying a glassy carbon electrode (GCE) with poly (ethyleneimine) (PEI) capped silver nanoparticles at titanium dioxide (PEI-AgNPs)/TiO2, i.e., titanium dioxide (TiO2)/graphene oxide (GO) nanocomposites (Ag@GO/TiO2-GCE). The Ag@GO/TiO2 nanocomposite was characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), thermal gravimetric analysis (TGA), X-ray diffraction (XRD), transmission electron microscopy (TEM), dynamic light scattering (DLS), zeta potential, Fourier transform infrared (FT-IR) spectroscopy, and UV–Vis spectrophotometry. Various voltammetric techniques namely cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), chronoamperometry (CA), and differential pulse voltammetry (DPV) were employed. The Ag@GO/TiO2-GCE demonstrated good selectivity, stability, and a quick response time of 1.0 s for creatinine. An extended linear dynamic range (LDR) of creatinine from 0.01 pM (DPV) to 1.0 M (CV) based on different voltammetric techniques is imperative for detecting diverse creatinine levels in various body fluids. The LOD and LOQ of the developed creatinine detection method were found to be 1.15 pM and 3.5 pM, respectively. The electrochemical sensor exhibited an exceptionally high sensitivity of 15.74 μApM−1cm−2.The body fluids from healthy volunteers were spiked with a known amount of creatinine to evaluate sensor efficiency in the context of recovery. Finally, blood serum, saliva, and urine samples of kidney patients were analyzed for creatinine levels.
Significance
An important merit of the developed creatinine sensor is its ability for non-invasive point-of-care diagnosis in saliva with more than 90 % recovery. The comparison of the developed method with the standard Jaffes' colorimetric method endorsed its reliability and extended ability for the samples where Jaffes’ method fails. The low LOD, high sensitivity, extended LDR, and low-cost render the possibility of adopting this method for point-of-care diagnosis.
期刊介绍:
Analytica Chimica Acta has an open access mirror journal Analytica Chimica Acta: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review.
Analytica Chimica Acta provides a forum for the rapid publication of original research, and critical, comprehensive reviews dealing with all aspects of fundamental and applied modern analytical chemistry. The journal welcomes the submission of research papers which report studies concerning the development of new and significant analytical methodologies. In determining the suitability of submitted articles for publication, particular scrutiny will be placed on the degree of novelty and impact of the research and the extent to which it adds to the existing body of knowledge in analytical chemistry.