ArticleSmall science2026
Reconfigurable Magnetic Nanopore Platform for Selective Trapping.
Article in Small science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Solid-state nanopores offer a powerful platform for nanoscale analysis of individual analytes, including biomolecules and functionalized nanoparticles, by confining them within a precisely defined sensing region. However, their inherently passive operation restricts practical applications, as they cannot precisely control particle position or dynamics inside the pore. Here, we introduce magnetic nanopore architectures that integrate a ferromagnetic layer into the nanopore system. Acting as a magnetic discontinuity within an otherwise uniformly magnetized film, the nanopore generates localized stray magnetic fields that enable magnetic tweezing of magnetic nanoparticles, which can be functionalized with fluorescent biomolecules. Importantly, the nanopore geometry is designed to reversibly switch between a nearly uniform magnetization state and a magnetic flux-closure state through the application of momentary magnetic fields of predetermined amplitude. This capability allows the magnetic tweezing effect to be selectively activated or deactivated, enabling controlled capture and release of tagged biomolecules on demand. As a proof of concept, we demonstrate the selective magnetic trapping of fluorescent magnetic particles. Our work establishes a robust and controllable approach for reconfigurable, on-chip magnetic nanopore platforms capable of selective trapping and high-throughput single-particle detection.
Indexed as
Identifiers
What OpenQuestion holds
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 OpenQuestion graph.