Evidence map›Paper›PMID 40708387›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2025

Bypassing Endocytic Barriers: Visualizing Membrane Fusion and Endosomal Escape of Cubic Phase Lipid Nanoparticles (Cubosomes).

Sue Lyn Yap, Chaitali Dekiwadia, Enrico Della Gaspera, Calum J Drummond, Charlotte E Conn, Nhiem Tran

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 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. Article
  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

6 authors.

Sue Lyn YapSchool of Science, STEM College, RMIT University, 124 La Trobe St, Melbourne, VIC, 3000, Australia.
Chaitali DekiwadiaRMIT Microscopy & Microanalysis Facility (RMMF), STEM College, RMIT University, 124 La Trobe St, Melbourne, VIC, 3000, Australia.
Enrico Della GasperaSchool of Science, STEM College, RMIT University, 124 La Trobe St, Melbourne, VIC, 3000, Australia.ORCID 0000-0001-9948-5893
Calum J DrummondSchool of Science, STEM College, RMIT University, 124 La Trobe St, Melbourne, VIC, 3000, Australia.ORCID 0000-0001-7340-8611
Charlotte E ConnSchool of Science, STEM College, RMIT University, 124 La Trobe St, Melbourne, VIC, 3000, Australia.
Nhiem TranSchool of Science, STEM College, RMIT University, 124 La Trobe St, Melbourne, VIC, 3000, Australia.ORCID 0000-0002-0209-2434

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipid nanoparticles (LNPs) are versatile platforms for drug delivery, offering solutions for targeted therapeutics, gene therapy, and vaccines. Cubosomes - cubic phase lipid nanoparticles - exhibit unique structural properties that may allow direct cytosolic delivery, bypassing endocytic pathways that often limit intracellular drug delivery. Despite their potential, the mechanisms of cubosome interactions with mammalian cells, particularly their membrane fusion behavior, remain unclear. This study employs a multimodal microscopy-based approach to investigate cubosome interactions with cells, focusing on membrane fusion, lipid exchange, and endosomal escape. Advanced imaging techniques, including transmission, scanning, and cryogenic scanning electron microscopy, and live-cell fluorescence imaging, are used alongside tailored cubosome variants to examine interactions at micro- and nanoscale dimensions. Cubosome behaviors are compared to other nanoparticleslike liposomes and gold nanoparticles. For the first time, membrane fusion with mammalian plasma and endosomal membranes is visualized at the nanoscale, revealing how cubosomes bypass conventional endocytic pathways to deliver cargo directly into the cytosol. This work provides critical insights into LNP-cell interactions, establishing cubosomes as promising candidates for overcoming endosomal escape limitations in drug delivery. These findings will aid in developing next-generation lipid-based nanocarriers, particularly for RNA therapeutics, where efficient cytosolic delivery is essential for therapeutic efficacy.

Indexed as

EndocytosisEndosomesLipidsMembrane FusionNanoparticlesGoldHumansLiposomesGoldLipid NanoparticlesLipidsLiposomescubosomesendosomal escapelipid nanoparticlesmembrane fusionmicroscopynanoparticle–cell interactions

Identifiers

PMID40708387
PMCPMC12590531

What OpenQuestion holds

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LicenceCC BY
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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.