Cranfield Health, Cranfield University, Bedfordshire, England, UK.
Anal Chim Acta. 2011 Aug 12;699(2):223-31. doi: 10.1016/j.aca.2011.05.036. Epub 2011 Jun 1.
A membrane based heterogeneous competitive enzyme-linked immunosorbent assay (ELISA) was used in this work to develop an immunosensor for the detection of a common herbicide, isoproturon. A screen-printed carbon working electrode with carbon counter and silver-silver chloride pseudo-reference electrode was utilized incorporating a membrane fixed into intimate contact with the working electrode to facilitate signal transduction. The membrane containing an immobilized isoproturon-ovalbumin conjugate was laminated onto the carbon working electrode and horseradish peroxidase (HRP) labeled polyclonal antibody was then applied for the competitive assay. Two different amperometric systems, hydroquinone and o-phenylenediamine (OPD) mediation reduction were utilised and the properties of the resultant sensors were compared. A flow injection apparatus was also developed utilising the immunosensor. Limits of detection for isoproturon (LLD(90)) were found to be as low as 0.84 ng mL(-1). The senor was also validated using spiked extracted soil samples and also isoproturon contaminated samples.
本文采用基于膜的非均相竞争酶联免疫吸附测定(ELISA)方法,开发了一种用于检测常见除草剂异丙隆的免疫传感器。该免疫传感器采用带有碳对电极和银-氯化银参比电极的丝网印刷碳工作电极,其中包含与工作电极紧密接触的固定膜,以促进信号转导。含有固定化异丙隆-卵清蛋白结合物的膜被层压在碳工作电极上,然后应用辣根过氧化物酶(HRP)标记的多克隆抗体进行竞争性测定。使用了两种不同的电流测定系统,即对苯二酚和邻苯二胺(OPD)介导还原,并比较了所得传感器的性能。还利用该免疫传感器开发了一种流动注射装置。异丙隆的检测限(LLD(90))低至 0.84ng mL(-1)。该传感器还使用提取的污染土壤样品和含有异丙隆的污染样品进行了验证。