便携式流量免疫传感器的现场演示

Anne W. Kusterbeck, Paul T. Charles
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引用次数: 17

摘要

一种被称为FAST 2000的便携式生物传感器,由美国海军研究实验室(NRL)开发,由国际研究公司(Research International, Inc.)设计,已经对两种选定的炸药TNT和RDX进行现场分析的有效性进行了现场测试。该生物传感器利用抗体识别分析物分子和随后的荧光检测下游测量地下水和土壤中的污染物水平。在美国环境保护署确定为超级基金优先清理地点的军事基地进行的实地试验中,从不同地点的地下水监测井中收集了含有未知浓度爆炸物的样品,并在NRL传感器中进行了分析,没有对样品进行预处理或浓缩。测试地点包括志愿军弹药厂,查塔努加,田纳西州和乌马提拉陆军仓库活动,乌马提拉,俄勒冈州。现场样品采用便携式FAST 2000进行现场分析,裂片由美国epa认证的独立实验室使用HPLC SW846 Method 8330进行分析。结果表明,FAST 2000能够准确、准确地检测环境样品中的爆炸物。通过对FAST 2000法与HPLC法的回归曲线进行统计分析,结果显示两者具有较高的相关性,r2值在0.86 ~ 0.97之间。该检测系统样本量小(150 μl/次),样品分析时间小于3 min。传感器定量,方法检出限(MDL)为10 μl。除了受污染的现场样品外,还在实验室测试了适当的对照物、空白物和干扰物,以满足认证和验证数据的要求。结果评估基于准确性,精密度,成本,时间和废物产生。©1998 John Wiley &儿子,Inc。化学工程学报,2009,31 (2):341 - 335
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Field demonstration of a portable flow immunosensor

A portable biosensor known as the FAST 2000, developed by the Naval Research Laboratory (NRL) and engineered by Research International, Inc., has been field tested for effectiveness in performing on-site analyses for two selected explosives, TNT and RDX. The biosensor uses antibody recognition of analyte molecules and subsequent fluorescence detection downstream to measure contaminant levels in groundwater and soil. In field trials at military bases identified by the U. S. EPA as priority Superfund cleanup sites, samples containing unknown concentrations of explosives were collected from groundwater monitoring wells at various locations and analyzed in the NRL sensor with no sample pretreatment or concentration. Test sites included the Volunteer Army Ammunition Plant, Chattanooga, TN and Umatilla Army Depot Activity, Umatilla, OR. Field samples were analyzed on-site by the portable FAST 2000, and splits were analyzed by an independent U. S. EPA-certified laboratory with the use of HPLC SW846 Method 8330. Results demonstrated that the FAST 2000 can detect explosives in environmental samples with accuracy and precision. Statistical analyses based on regression curves comparing the FAST 2000 and HPLC methods showed a high degree of correlation, with r2 values between 0.86 and 0.97. The assay system required small sample volumes (150 μl/test) and samples were analyzed in less than 3 min. The sensor was quantitative, with a method detection limit (MDL) of 10 μg/l. Beyond contaminated field samples, appropriate controls, blanks, and interferents were tested in the lab for certification and validation data requirements. Results were evaluated based on accuracy, precision, cost, time, and waste generation. © 1998 John Wiley & Sons, Inc. Field Analyt Chem Technol 2: 341–350, 1998

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