College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China.
Xiangjiang Laboratory, Changsha 410205, China.
Anal Chem. 2024 Jun 18;96(24):9909-9916. doi: 10.1021/acs.analchem.4c01044. Epub 2024 Jun 3.
The development of the Point-of-Care Testing (POCT) platform that combines convenience and cost-effectiveness is crucial for enabling the visual detection of disease biomarkers. In this work, a POCT platform for the sensitive detection of prostate specific antigen (PSA) with dual-signal output was constructed by functionalizing the Eppendorf (EP) tube. This was achieved through the modification of aptamer hairpin probes (AHPs) on the lid of the EP tube and the assembly of a nanoenzyme hydrogel film on its inner wall. The target could trigger the release of Ag by AHP and subsequently activate Ag-dependent DNAzyme (Ag-DNAzyme). This would initiate the cleavage of the DNA-Au/Pt NP hydrogel network, leading to the release of Au/Pt NPs. The released Au/Pt NPs exhibit both peroxidase (POD)-like and catalase (CAT)-like activity to produce a colorimetric response and induce liquid flow under pressure. Therefore, the target can be measured visually and quantitatively through colorimetric analysis and the measurement of total dissolved solids (TDS) using a pressure-triggered liquid flow device integrated into the platform. The designed platform is distinguished by its simplicity, specificity, cost-effectiveness, and remarkable sensitivity. It allows for the visual detection of PSA within concentration ranges of 0.5-100 ng/L (colorimetric) and 3-100 ng/L (TDS reading), boasting detection limits as low as 0.15 ng/L (colorimetric) and 0.57 ng/L (TDS reading). The strategy of target-triggered nanoenzyme release significantly enhances sensitivity and provides a guiding approach for visual biomarker detection.
开发兼具便利性和成本效益的即时检测(POCT)平台对于实现疾病生物标志物的可视化检测至关重要。在这项工作中,通过在 EP 管盖上修饰适体发夹探针(AHP)并在其内壁组装纳米酶水凝胶膜,构建了用于灵敏检测前列腺特异性抗原(PSA)的 POCT 平台,实现了双信号输出。靶标可以通过 AHP 触发 Ag 的释放,随后激活 Ag 依赖性 DNA 酶(Ag-DNAzyme)。这将引发 DNA-Au/Pt NP 水凝胶网络的切割,导致 Au/Pt NPs 的释放。释放的 Au/Pt NPs 具有过氧化物酶(POD)样和过氧化氢酶(CAT)样活性,可产生比色响应并在压力下诱导液体流动。因此,可以通过比色分析和使用集成到平台中的压力触发液体流动装置测量总溶解固体(TDS)来目视和定量测量靶标。设计的平台具有简单、特异性、成本效益和高灵敏度的特点。它可以在 0.5-100 ng/L(比色)和 3-100 ng/L(TDS 读数)的浓度范围内可视化检测 PSA,检测限低至 0.15 ng/L(比色)和 0.57 ng/L(TDS 读数)。靶标触发纳米酶释放的策略显著提高了灵敏度,为可视化生物标志物检测提供了一种指导方法。