Evidence map›Paper›PMID 39636686›Full record

ArticleAngewandte Chemie (International ed. in English)2025

Self-Assembly and Biological Properties of Highly Fluorinated Oligonucleotide Amphiphiles.

Quentin Laurent, Beatrice L Bona, Jathavan Asohan, Marta Rosati, Sinan Faiad, Francesca Baldelli Bombelli, Pierangelo Metrangolo, Hanadi F Sleiman

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Quentin LaurentDepartment of Chemistry, McGill University, 801 Sherbrooke St. W, QC-H3A 0B8, Montreal, Canada.ORCID https://orcid.org/0000-0002-0814-5701
Beatrice L BonaSupraBioNano Lab, Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Via Luigi Mancinelli 7, MI-20131, Milano, Italy.ORCID https://orcid.org/0000-0002-7363-8756
Jathavan AsohanDepartment of Chemistry, McGill University, 801 Sherbrooke St. W, QC-H3A 0B8, Montreal, Canada.
Marta RosatiSupraBioNano Lab, Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Via Luigi Mancinelli 7, MI-20131, Milano, Italy.ORCID https://orcid.org/0000-0003-2141-1223
Sinan FaiadDepartment of Chemistry, McGill University, 801 Sherbrooke St. W, QC-H3A 0B8, Montreal, Canada.
Francesca Baldelli BombelliSupraBioNano Lab, Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Via Luigi Mancinelli 7, MI-20131, Milano, Italy.ORCID https://orcid.org/0000-0001-8138-9246
Pierangelo MetrangoloSupraBioNano Lab, Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Via Luigi Mancinelli 7, MI-20131, Milano, Italy.ORCID https://orcid.org/0000-0002-7945-099X
Hanadi F SleimanDepartment of Chemistry, McGill University, 801 Sherbrooke St. W, QC-H3A 0B8, Montreal, Canada.ORCID https://orcid.org/0000-0002-5100-0532

Funding

Canada Foundation for Innovation 42930European Union - NextGenerationEU P2022RBF5PFonds de recherche du Québec - Nature et technologies 284731Ministero della Salute PNC-E3-2022-23683266Natural Sciences and Engineering Research Council of Canada RGPIN-2024-06784Regione Lombardia 1175999Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung P500PN_206907
6 · The paper itself

Abstract

Nucleic acids, used as therapeutics to silence disease-related genes, offer significant advantages over small molecule drugs: they provide high specificity, the ability to target "undruggable" molecules, and adaptability to a wide range of disease phenotypes. However, their instability in biological media, as well their rapid clearance from the organism limit their applicability, necessitating the use of nanocarriers to overcome these challenges. Among these strategies, spherical nucleic acids (SNA)-composed of a densely packed corona of oligonucleotides around a nanoparticle-have emerged as a powerful tool, in particular when self-assembled from DNA amphiphiles. This non-covalent strategy however has caveats, especially when it comes to stability in complex biological media, where these SNAs disassemble in contact to serum proteins. Here, we developed highly fluorinated DNA amphiphiles that readily self-assemble into SNAs and have tunable stability profiles in biological media. They are made of branched fluorinated moieties with potentially improved biodegradability as compared to their linear counterparts. Depending on the number of fluorophilic interactions, the self-assembled SNAs can have excellent serum stabilities-up to days-and readily deliver nucleic acid therapeutics for gene silencing applications. These systems show great potential as promising candidates for nucleic acid-based therapies.

Indexed as

OligonucleotidesSurface-Active AgentsDNAHalogenationHumansNanoparticlesDNAOligonucleotidesSurface-Active Agentsdeliveryfluorinegene silencingoligonucleotidesself-assembly

Identifiers

PMID39636686
PMCPMC11811686

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.