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Next generation planar waveguide detection of microcystins in freshwater and cyanobacterial extracts, utilising a novel lysis method for portable sample preparation and analysis

机译:利用新型裂解方法进行便携式样品制备和分析的下一代平面波导检测淡水和蓝细菌提取物中的微囊藻毒素

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摘要

The study details the development of a fully validated, rapid and portable sensor based method for the on-site analysis of microcystins in freshwater samples. The process employs a novel lysis method for the mechanical lysis of cyanobacterial cells, with glass beads and a handheld frother in only 10min. The assay utilises an innovative planar waveguide device that, via an evanescent wave excites fluorescent probes, for amplification of signal in a competitive immunoassay, using an anti-microcystin monoclonal with cross-reactivity against the most common, and toxic variants. Validation of the assay showed the limit of detection (LOD) to be 0.78ngmL and the CCß to be 1ngmL. Robustness of the assay was demonstrated by intra- and inter-assay testing. Intra-assay analysis had % C.V.s between 8 and 26% and recoveries between 73 and 101%, with inter-assay analysis demonstrating % C.V.s between 5 and 14% and recoveries between 78 and 91%. Comparison with LC-MS/MS showed a high correlation (R=0.9954) between the calculated concentrations of 5 different Microcystis aeruginosa cultures for total microcystin content. Total microcystin content was ascertained by the individual measurement of free and cell-bound microcystins. Free microcystins can be measured to 1ngmL, and with a 10-fold concentration step in the intracellular microcystin protocol (which brings the sample within the range of the calibration curve), intracellular pools may be determined to 0.1ngmL. This allows the determination of microcystins at and below the World Health Organisation (WHO) guideline value of 1µgL. This sensor represents a major advancement in portable analysis capabilities and has the potential for numerous other applications.
机译:这项研究详细介绍了一种经过充分验证的,快速且基于便携式传感器的方法,用于现场分析淡水样品中的微囊藻毒素。该方法采用新颖的裂解方法对蓝细菌细胞进行机械裂解,只需10分钟即可完成玻璃珠和手持起泡器的裂解。该测定利用一种创新的平面波导装置,该装置通过van逝波激发荧光探针,从而在竞争性免疫测定中使用抗微囊藻毒素单克隆抗体对最常见的毒性变体具有交叉反应,从而放大信号。该方法的验证显示检测限(LOD)为0.78ngmL,CCß为1ngmL。通过测定内和测定间测试证明了测定的鲁棒性。批内分析的C.V.%在8%至26%之间,回收率在73%至101%之间,批间分析表明C.V.s在5%至14%之间,回收率在78%至91%之间。与LC-MS / MS的比较显示,计算出的5种铜绿微囊藻培养物的总微囊藻毒素含量之间的高度相关性(R = 0.9954)。总微囊藻毒素含量通过分别测量游离和与细胞结合的微囊藻毒素来确定。游离微囊藻毒素的含量可以测量为1ngmL,而在细胞内微囊藻毒素方案中将浓度提高10倍(使样品在校准曲线的范围内),则可将细胞内池确定为0.1ngmL。这样就可以测定等于或低于世界卫生组织(WHO)指导值1µgL的微囊藻毒素。该传感器代表了便携式分析功能的重大进步,并具有许多其他应用的潜力。

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