Engineering Research Center of Nano-Geomaterials of Ministry of Education, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430074, China.
Anal Chem. 2020 Sep 15;92(18):12437-12441. doi: 10.1021/acs.analchem.0c02205. Epub 2020 Aug 27.
Electrochemical aptamer-based (E-AB) biosensors suffer from sensor-to-sensor signal variations due to the variation of the total number and the heterogeneity of probes immobilized on the electrode surface, with the former attracting more attention. As such, a calibration process to correct for such variations is required for this type of sensor, causing inconvenience and inaccessibility in harsh sensing environments such as blood samples, which has dramatically limited the widespread clinical use of biosensors. In response, here, we have adopted E-AB sensors to achieve calibration-free measurements of small biological/drug molecules. Specifically, we employ one probe-attached redox reporter and a second intercalated redox reporter to generate two signals, achieving good sensor-to-sensor reproducibility and thus obviating the need for calibration. We first demonstrated the capability of E-AB sensors for the accurate measurement of kanamycin, tobramycin, and adenosine triphosphate (ATP) in phosphate-buffered saline (PBS) buffer, achieving concentration ranges of approximately 4.7 × 10-, 2.0 × 10-, and 12.7-fold, respectively. Then, we applied this calibration-free approach to the measurement of these three target molecules directly in undiluted serum, achieving a concentration precision of a few micromolars.
电化学适体基(E-AB)生物传感器由于固定在电极表面上的探针总数和异质性的变化而存在传感器间信号变化的问题,其中前者更受关注。因此,这种类型的传感器需要进行校准过程来校正这些变化,这在血液样本等苛刻的传感环境中造成了不便和不可及,这极大地限制了生物传感器的广泛临床应用。有鉴于此,在这里,我们采用 E-AB 传感器来实现对小分子生物/药物分子的无校准测量。具体来说,我们使用一个附着有氧化还原报告探针和第二个嵌入的氧化还原报告探针来产生两个信号,从而实现良好的传感器间重现性,从而无需进行校准。我们首先展示了 E-AB 传感器在磷酸盐缓冲盐水(PBS)缓冲液中准确测量卡那霉素、妥布霉素和三磷酸腺苷(ATP)的能力,分别实现了约 4.7×10-、2.0×10-和 12.7 倍的浓度范围。然后,我们将这种无校准方法应用于直接在未稀释的血清中测量这三种目标分子,实现了几个微摩尔浓度的精度。