Sagar Pinky, Srivastava Monika, Prakash Rajiv, Srivastava S K
Department of Physics, Institute of Science, Banaras Hindu University, Varanasi, 221005, India.
School of Materials Science and Technology, IIT (BHU) Varanasi, 221005, India.
Anal Methods. 2020 Jun 18;12(23):3014-3024. doi: 10.1039/d0ay00899k.
Herein, we report a voltammetric method for the nanomolar detection of cefixime, a third-generation antibiotic. The determination of cefixime is validated on a glassy carbon electrode (GCE) as well as on a screen-printed carbon electrode (SPCE). In the present study, we have reported a facile "one step simple hydrothermal synthesis" of MoS2 quantum dots and with the oxidation of aurochloric acid for the further formation of an MoS2 QD-AuNP composite. The as-synthesized nanocomposite was characterized via UV-Vis spectroscopy, FTIR spectroscopy, XRD, TEM and EDX techniques, and further applied in the modification of working electrodes, showing excellent electroactivity. The sensing of cefixime was done via cyclic and differential pulse voltammetry techniques. The presence of the only anodic peak in the voltammogram reveals the irreversible oxidation of cefixime in the potential range of about 1.3 ± 0.1 V vs. Ag/AgCl. The study was also performed at different scan rates, which indicate a diffusion-controlled mechanism. The proposed cefixime sensor showed a linear response in the concentration range of 0.33-90.82 μM (at S/N = 3) with a limit of detection (LOD) of 3.9-4.5 nm. The electrochemical sensitivity is calculated as 8.63 μA μM-1 cm-2 and 7.07 μA μM-1 cm-2 in buffer and pharmaceutical formulation (commercially available cefixime tablet), respectively. The effects of several interferents were also investigated. The proposed sensor is effectively used for estimating cefixime in phosphate buffer and the commercially available cefixime tablets with no cross-reactivity or matrix effects and shows a promising prospect for real applications.
在此,我们报告了一种用于纳摩尔级检测第三代抗生素头孢克肟的伏安法。头孢克肟的测定在玻碳电极(GCE)以及丝网印刷碳电极(SPCE)上得到验证。在本研究中,我们报道了一种简便的二硫化钼量子点“一步简单水热合成法”,并通过氯金酸氧化进一步形成二硫化钼量子点-金纳米粒子复合材料。通过紫外-可见光谱、傅里叶变换红外光谱、X射线衍射、透射电子显微镜和能谱技术对合成的纳米复合材料进行了表征,并进一步应用于工作电极的修饰,显示出优异的电活性。通过循环伏安法和差分脉冲伏安法技术对头孢克肟进行传感检测。伏安图中仅出现一个阳极峰,表明头孢克肟在相对于Ag/AgCl约1.3±0.1 V的电位范围内发生不可逆氧化。该研究还在不同扫描速率下进行,结果表明是扩散控制机制。所提出的头孢克肟传感器在0.33 - 90.82 μM的浓度范围内呈现线性响应(信噪比S/N = 3),检测限(LOD)为3.9 - 4.5 nM。在缓冲液和药物制剂(市售头孢克肟片剂)中的电化学灵敏度分别计算为8.63 μA μM⁻¹ cm⁻²和7.07 μA μM⁻¹ cm⁻²。还研究了几种干扰物的影响。所提出的传感器有效地用于估算磷酸盐缓冲液和市售头孢克肟片剂中的头孢克肟,无交叉反应或基质效应,在实际应用中显示出广阔的前景。