Analytical Division, Department of Chemistry, Institute of Science, Banaras Hindu University, Varanasi, 221005, India.
Analytical Division, Department of Chemistry, Institute of Science, Banaras Hindu University, Varanasi, 221005, India.
Anal Chim Acta. 2017 Jun 29;974:75-86. doi: 10.1016/j.aca.2017.04.001. Epub 2017 Apr 10.
A new ultra sensing molecularly imprinted polymer beads modified pencil graphite electrode was fabricated, with the help of the inverse suspension polymerization technique, for ascertaining the adequate supplementation of dacarbazine in the cancer treatment. The inverse suspension polymerization technique was beneficial in obtaining surface imprinted polymer-based electrocatalytic nanospheres with narrow size distribution. These nanospheres were found to be superior to the corresponding microspheres and planar films, in terms of electrode kinetics and sensitivity, with the differential pulse anodic stripping voltammetric transduction. Herein, multiwalled carbon nanotubes functionalized ester links were invoked in between the imprinted nanospheres and the pencil graphite electrode surface to secure a stable coating and better electrodics. The proposed electrochemical sensor showed the imprinting factor and the analyte adsorption coefficient as high as 24.3 and 1.06 × 10 L mol, respectively. Furthermore, 16-fold and 4-fold faster electron transfer kinetics were observed with the imprinted nanospheres than the corresponding imprinted planar film and the microspheres based electrodes, respectively. The limits of detection [0.02 (aqueous), 0.02 (plasma), 0.01 (urine), and 0.03 ng mL (pharmaceutics), (3σ, RSD ≤ 0.23%)] of dacarbazine, realized with the imprinted polymer nanospheres, were free from any cross-reactivity and false-positive complications in aqueous, blood plasma, urine, and pharmaceutical samples.
一种新型的超灵敏分子印迹聚合物珠修饰的铅笔芯石墨电极被制备出来,借助反相悬浮聚合技术,以确定在癌症治疗中补充达卡巴嗪的适当剂量。反相悬浮聚合技术有利于获得表面印迹聚合物基的电催化纳米球,具有较窄的粒径分布。与相应的微球和平面膜相比,这些纳米球在电极动力学和灵敏度方面具有优势,采用差分脉冲阳极溶出伏安法进行电信号转换。在此,在印迹纳米球和铅笔芯石墨电极表面之间引入了功能化的酯键连接的多壁碳纳米管,以确保稳定的涂层和更好的电导率。所提出的电化学传感器显示出高达 24.3 的印迹因子和 1.06×10 L mol 的分析物吸附系数。此外,与相应的印迹平面膜和基于微球的电极相比,印迹纳米球的电子转移动力学分别快 16 倍和 4 倍。印迹聚合物纳米球实现的达卡巴嗪的检测限[0.02(水溶液)、0.02(血浆)、0.01(尿液)和 0.03 ng mL(药物),(3σ,RSD≤0.23%)]在水溶液、血浆、尿液和药物样品中均无交叉反应和假阳性并发症。