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A microarray chip for label-free detection of narcotics

机译:用于无毒品检测的微阵列芯片

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A protein array chip for label-free optical detection of low molecular weight compounds has been developed. As a proof of principle, the chip is proven capable of rapidly (approximately 1 min) determining hits from aqueous cocktails composed of four common narcotics, cocaine, ecstasy, heroin, and amphetamine, using imaging surface plasmon resonance (SPR) as the detection principle. The chip is produced by injecting a mixture of antibodies and letting them self-sort and bind to narcotic analog coupled proteins already present in a predefined pattern on the supporting substrate. An indirect detection method, where antibodies are displaced from the surface upon recognition of their corresponding narcotics, is used to obtain the optical contrast and thus a detectable SPR and/or ellipsometric signal. Two types of readouts are possible from the present setup: intensity SPR images and SPR/ellipsometric sensorgrams. Positive hits were routinely obtained for analyte concentrations of 50 pg/μL and the limit of detection, without any parameter optimizations, seems to fall in the range 0.5 pg/μL (1.4 nM) for heroin, 2.5 pg/μL (8.2 nM) for cocaine, and 5 pg/μL for the other two narcotics (26 nM for ecstasy and 37 nM for amphetamine). With improved readout possibilities (sampling frequency), signal evaluation algorithms, and antibody–antigen design strategies, we believe this limit can be further improved. The chip is shown to work for many measurement cycles with excellent reproducibility. Moreover, with a more advanced fluidic system, excess injected antibodies could be collected and reused for many cycles, which could make the running costs of the system very low. The chip is in no way limited to detection of narcotics. Other low molecular weight compounds could easily be detected on the same chip. For example, trinitrotoluene detection has already been demonstrated using our chip. Possible areas of application for the system are therefore envisaged in airport and underground transport security, customs, drug interdiction, forensics, and as warning alerts on military equipment and personnel.
机译:已开发出一种用于低分子量化合物的无标记光学检测的蛋白质阵列芯片。作为原理的证明,该芯片能够使用成像表面等离振子共振(SPR)作为检测原理,能够快速(约1分钟)确定由四种常见麻醉药,可卡因,摇头丸,海洛因和苯丙胺组成的水性混合物的命中率。该芯片是通过注射抗体混合物并使其自选并与已经以预定模式存在于支持基质上的麻醉类似物偶联蛋白结合而制成的。间接检测方法用于获得光学对比度,从而获得可检测的SPR和/或椭偏信号,在这种方法中,一旦识别出相应的麻醉剂,抗体就会从表面移开。从当前设置中可以读取两种类型:强度SPR图像和SPR /椭偏传感器图。常规分析物浓度为50 pg /μL时可得到阳性结果,而未经任何参数优化,检测限似乎落在海洛因0.5 pg /μL(1.4 nM),海洛因2.5 pg /μL(8.2 nM)的范围内。可卡因,其他两种麻醉品为5 pg /μL(摇头丸为26 nM,苯丙胺为37 nM)。通过提高读出的可能性(采样频率),信号评估算法和抗体-抗原设计策略,我们相信可以进一步改善这一限制。该芯片可在许多测量周期内工作,并具有出色的重现性。此外,在更先进的流体系统中,多余的注射抗体可以被收集并重复使用许多周期,这可以使系统的运行成本非常低。该芯片绝不限于检测毒品。其他低分子量化合物很容易在同一芯片上检测到。例如,已经使用我们的芯片演示了三硝基甲苯检测。因此,在机场和地下运输安全,海关,禁毒,法医以及对军事装备和人员发出警告时,可以设想该系统的可能应用领域。

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