AptaSure™ brings engineered aptamer chemistry into a simple, instrument-free lateral-flow test — designed to identify dangerous infections in minutes, right where care happens.
Aptamers are short, synthetic nucleic-acid sequences that fold into precise three-dimensional shapes, letting them bind a chosen target — like a bacterial protein — with antibody-like specificity.
Because they're chemically synthesized rather than grown biologically, aptamers can offer advantages in stability, batch-to-batch consistency, and lower-cost manufacturing at scale — well suited to a test made in volume and used anywhere.
AptaSure™ MRSA detects pbp2a — the protein that makes Staphylococcus aureus methicillin-resistant — using a cognate pair of aptamers and gold-nanoparticle signal, read by eye like a rapid test.
A gold-nanoparticle–labeled aptamer binds the MRSA marker protein pbp2a in the sample.
A second, cognate aptamer binds pbp2a at a different site — a two-point lock that drives specificity and reduces false reads.
The complex concentrates at the test line, producing a visible result in minutes — no instrument required.
Methicillin-resistant S. aureus is one of the most consequential healthcare-associated infections. Conventional identification relies on culture that can take 1–3 days — time in which patients are treated empirically.
A rapid, point-of-care answer is designed to support earlier, more targeted decisions — the kind of difference that matters for both patient outcomes and cost of care.
to a visual result, vs. days for culture
refrigeration required — shelf-stable, single-use
| Lab culture | AptaSure™ (design goals) | |
|---|---|---|
| Time to result | 1–3 days | ~10 minutes |
| Where it runs | Central laboratory | Point of care |
| Instrument | Lab equipment | None — visual read |
| Cold chain | Often required | Not required |
| Binding chemistry | — | Dual aptamer to pbp2a |
Comparison reflects design goals for an investigational device in development. Confirm against final validated performance.
AptaSure™ MRSA is being developed with research and clinical partners, with assay optimization and specificity testing conducted during development. The program is advancing toward FDA 510(k) pre-market notification. State the current, accurate regulatory status and validation data here, reviewed by Dr. Lange.
We share development data and the regulatory roadmap with qualified partners and investors under NDA.
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