ArticleJournal of nanobiotechnology2026
Dual-responsive zwitterionic hydrogel microneedle patch for the on-site detection of two alzheimer's disease - related miRNAs.
Article in Journal of nanobiotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Structural color-based microneedle patch with NIR-triggered on-demand drug release for intelligent treatment of infected wounds.Journal of nanobiotechnology · 2026Article
- Tea-derived natural nanodrug simultaneously enables real-time fluorescent tracking and noninvasive treatment of neuroinflammation in Alzheimer's disease.Journal of nanobiotechnology · 2026Article
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Authors and funding
8 authors.
Funding
Abstract
Nowadays, specific biomarkers and detection methods for the early, rapid and non-invasive diagnosis of Alzheimer's disease (AD) are scarce. MiR-34a and miR-206 are both upregulated in the cerebrospinal fluid and peripheral fluids of AD patients. In view of the similar biochemical information between interstitial fluid (ISF) and blood and high proportions of RNAs in ISF, this work developed an integrated optical patch that combined hydrogel microneedles (MNs) extraction with on-site fluorescence detection for the simultaneous sensing of miR-34a and miR-206. A zwitterionic compound trimethylamine nitrogen oxide amphiphile (TMAO) was introduced to the matrix of MNs by co-modification with hyaluronic acid (HA) and methacrylic acid (MAA) to endow the novel MNs with adjustable swelling ability, as well as resistance to non-specific adsorption property. Moreover, to avoid signal interferences, we innovatively performed spatial average cutting on the MNs. By embedding two toehold-mediated strand displacement (TMSD) probes within MNs matrix, a dual-emission MNs optical patch for the two miRNAs was thereby constructed. As a potential non-invasive and accurate diagnostic tool of AD, the capability of the proposed optical patch was further demonstrated by simultaneously and on-site differentiating expression levels of miR-34a and miR-206 in ISF between normal and AD model mice.
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