Molecularly imprinted polymers for chemical agent detection in multiple water matrices

被引:40
作者
Jenkins, AL
Bae, SY
机构
[1] Jasco Inc, Easton, MD 21601 USA
[2] USA, Geoctr Inc, Edgewood Chem Biol Command, Aberdeen Proving Ground, MD 21010 USA
关键词
molecularly imprinted polymers; chemical agents; luminescence; detection;
D O I
10.1016/j.aca.2004.12.088
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the past few years concerns over the possibility of terrorist actions against domestic and military water supplies has become paramount. Antibodies, peptides, and enzymes have been used as molecular recognition elements in chemical sensors; however, such devices often have storage and operational stability issues that limits their success. Molecularly imprinted polymers (MIPs), have been successfully demonstrated an alternative in pesticide applications [A.L. Jenkins, R. Yin, J.J. Jensen, Analyst 126 (2001) 798-802]. The MIP materials possess selective molecular recognition properties that are comlementary to the analyte in the shape and positioning of functional groups. These polymers p have high selectivity and affinity constants while maintaining excellent thermal and mechanical stability. In this study, direct imprinting of chemical agents EA2192, VX, sarin, and soman (the "G" agents), was performed and the limits of detection calculated. The ability of these sensors to work in various water matrices including tap, deionized and reverse osmosis water with residual chlorine was also evaluated. Typical detection limits for these MIP sensors are approximately 50 ppt with wide linear dynamic ranges (ppt-ppm). Sensor response time is approximately 15 min. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 37
页数:6
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