ArticleJournal of pharmaceutical analysis2026
Synergistic cell membrane-coated ECL-DNA biosensor for specificity-enhanced drug lead evaluation.
Article in Journal of pharmaceutical analysis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- Multidisciplinary cutting-edge technologies accelerating target-based drug discovery.Journal of pharmaceutical analysis · 2026Article
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cell membrane coating technology has recently emerged as a promising platform for drug activity assessment due to its unique biointerfacing capabilities. Nevertheless, its integration with conventional detection methods such as high performance liquid chromatography (HPLC) and fluorescence probe analysis remains limited by poor specificity and low accuracy, primarily resulting from non-specific adsorption of non-target membrane receptors and interference from background signals. In this study, we presented a collaborative strategy that integrates aptamers with cell membrane coating technology to establish a novel electrochemiluminescence (ECL)-DNA biosensor platform for specifically detecting drug-target receptor interactions. High specificity was achieved through competitive binding between aptamers and drug candidates for membrane receptors, while high accuracy was ensured by employing an ECL detection system incorporating signal cascade amplification and three-dimensional (3D) DNA walkers, enabling reliable performance even with complex biological samples. Using this approach, we demonstrated a linear dynamic range of 1 nmol/L to 2 μmol/L for the detection of desloratadine activity, with a limit of detection (LOD) of 0.16 nmol/L. Furthermore, the platform was successfully applied to evaluate the binding activity of eight drugs to angiotensin-converting enzyme 2 (ACE2), and their pharmacological activities were further characterized. Overall, this aptamer-cell membrane coating synergistic strategy offered excellent specificity and ultra-high sensitivity, making it a valuable tool for elucidating drug-receptor mechanisms of action and providing a robust reference for preclinical drug activity evaluation.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.