Publication date: Sep 11, 2025
A signal-on electrochemiluminescence (ECL) immunoassay was developed for the detection of the SARS-CoV-2 N protein using coreactant-encapsulated polymersomes as tags and a graphitic carbon nitride (g-CN) nanosheet-modified screen-printed carbon electrode (SPCE) as the working electrode. Poly(ether imide) (PEI)-modified g-CN nanosheets were prepared through ultrasonic exfoliation followed by a supramolecular covalent scaffold strategy. Spray coating, a scalable deposition technique, was employed to modify the SPCE surface with g-CN nanosheets. After thermal curing, the nanosheets adhered firmly to the electrode via binders in the carbon ink, yielding a stable modified SPCE. Immunosensors were constructed by immobilizing capture antibodies on the g-CN-modified SPCE. Potassium persulfate, (KSO), the coreactant of g-CN, was encapsulated in polymersomes to prepare ECL tags, and probes were fabricated by conjugating SARS-CoV-2 N protein binding aptamers to these polymersomes. Upon recognition of the target protein and sandwich complexes formed on the immunosensor, the subsequent addition of Triton X-100 disrupted the polymersomes, releasing large amounts of KSO, which markedly enhanced the ECL mission of g-CN nanosheets. This amplification enabled highly sensitive detection of the SARS-CoV-2 N protein. These findings demonstrate that controlled release of encapsulated coreactants from polymersome tags is an effective strategy to trigger g-CN-based ECL emission for sensitive viral protein detection.

| Concepts | Keywords |
|---|---|
| Electrochemiluminescence | Carbon |
| Immunosensor | Cn |
| Sandwich | Coreactant |
| Viral | Cov |
| Detection | |
| Ecl | |
| Electrode | |
| Encapsulated | |
| Modified | |
| Nanosheets | |
| Polymersomes | |
| Sars | |
| Spce | |
| Tags |
Semantics
| Type | Source | Name |
|---|---|---|
| drug | DRUGBANK | Activated charcoal |
| disease | IDO | protein |
| pathway | REACTOME | Release |