ArticlePolymer science & technology (Washington, D.C.)2026
Polymeric Gene Delivery at Sub-Stoichiometric N/P Ratios.
Article in Polymer science & technology (Washington, D.C.), 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
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Efficient cytosolic delivery remains a major challenge for the clinical translation of nucleic acid therapeutics. While cationic polymers are promising gene carriers, they suffer from an inherent trade-off between transfection efficiency and cytotoxicity: high nitrogen-to-phosphorus (N/P) ratios can enhance gene delivery efficacy but inevitably increase cellular toxicity due to excess free cationic polymers. Here, we report a fluorinated polymer that achieves potent gene transfection at an unprecedentedly low N/P ratio below 1. Mechanistic studies demonstrate that the obtained polymer completely condenses DNA into stable nanoparticles at an N/P ratio around 0.4, with negligible unbound polymers remaining in the polyplexes. Detailed intracellular trafficking analysis revealed that the polymer/DNA complexes are primarily internalized via scavenger-receptor-mediated endocytosis, followed by rapid endosomal escape and efficient nuclear entry within 4 h. The polymer successfully delivered multiple protein-expressing plasmids across diverse cell lines, demonstrating broad applicability. Our findings establish this fluorinated polymer as a novel class of highly efficient gene vectors that function without requiring excess free cationic polymers. This study provides valuable insights for the rational design of next-generation gene delivery systems with enhanced efficiency and minimized cytotoxicity.
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.