ReviewMaterials today. Bio2026
Tailoring virus-inspired nanoparticles for advanced drug and gene delivery.
Review in Materials today. Bio, 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
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Viruses, as naturally evolved gene delivery systems, exhibit exceptional efficiency in overcoming biological barriers, targeting specific cells, and inducing robust immune responses. Inspired by these characteristics, virus-mimicking nanocarriers have become a promising strategy for enhancing drug and gene delivery. This review provides a detailed exploration of virus-inspired nanodelivery systems, with particular emphasis on their structural and functional biomimetic properties. We first focus on natural viral delivery platforms, such as viral nanoparticles and virus-like particles. Then, we discuss the application of biomimetic strategies that mimic viral morphology and topological structure in overcoming multiple physiological barriers in the body. Particularly, we examine bioinspired strategies that mimic key viral infection functions, including overcoming physiological barriers, cell adhesion and surface recognition, membrane fusion and cellular internalization, environmental perception and endosomal escape, intracellular trafficking and organelle targeting, and immune modulation. Additionally, we highlight the integration of intelligent strategies to optimize delivery efficiency. Finally, we discuss the current challenges and future opportunities in the field, aiming to advance virus-inspired nanomedicine toward clinical applications.
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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 OpenQuestion graph.