SlipChip basado en códigos de barras para cuantificación digital multiplexada y de trazas de muestras con...

The development of the digital enzyme-linked immunosorbent assay (ELISA) has improved the detection of low-abundance protein biomarkers in biological samples, achieving a 1000-fold increase in sensitivity compared to conventional protein detection methods. However, existing digital ELISA technologies encounter difficulties in simultaneously identifying numerous protein biomarkers at ultralow concentrations, particularly in trace samples. This limitation calls for improvements in both detection multiplicity and sensitivity. Herein, a simple digital ELISA platform, the Barcodes Integrated SlipChip (BIS-chip), was developed for the ultrasensitive identification of multiple proteins from trace samples. The BIS-chip employs a two-step loading method that eliminates substrate precatalysis, thereby ensuring the specificity of 10-plex target detection. Additionally, its high bead-loading efficiency improves the assay sensitivity for each target. By counting digital "On" and "Off" signals, the BIS-chip quantifies a panel of 10 cytokines with low limits of detection (LoD) in the femtogram per milliliter (fg/mL) range, achieving a sensitivity improvement of several orders of magnitude compared with standard highly multiplexed suspension array technology. To validate its clinical applicability, the BIS-chip was used to simultaneously measure 10 cytokines from only 20 μL of intralesional plasma of patients diagnosed with oral lichenoid reactions (OLRs), a condition where cytokines are typically undetectable via commercial multiplexed immunoassays. Supported by machine-learning algorithms, the OLR diagnostic models were successfully developed with 95.7% sensitivity and 100% specificity. With its exceptional detection multiplicity, ultrasensitivity, and straightforward workflow, the BIS-chip provides an innovative solution for the quantitative analysis of clinical low-abundance biomarkers in trace samples.