Evidence map›Paper›PMID 42524176›Full record

ReviewSmall science2026

Advances in Polyethyleneimine-Derived Nanoformulations.

Mohamed S Attia, Mariusz Skwarczynski, Waleed M Hussein

Abstract readReview
In one paragraph

Review 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.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Mohamed S AttiaSchool of Pharmacy and Medical Sciences Griffith University Southport Queensland Australia.ORCID https://orcid.org/0000-0003-1964-3420
Mariusz SkwarczynskiSchool of Chemistry and Molecular Biosciences The University of Queensland St Lucia Queensland Australia.ORCID https://orcid.org/0000-0001-7257-807X
Waleed M HusseinMonash Institute of Pharmaceutical Sciences Monash University Parkville Victoria Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Formulations derived from polyethyleneimine (PEI) serve as versatile and efficient vehicles for the delivery of genes, drugs, and vaccines that are low-immunogenic and viable alternatives to viral vectors. PEI ensures efficient endosomal escape, preventing the therapeutic cargo from degradation, enhancing uptake, and facilitating effective cytoplasmic release via the proton sponge effect. By combining PEI with tailor-made delivery vehicles, such as polymeric assemblies, lipid-based systems, and inorganic nanomaterials, enhanced targeting, safety, and therapeutic efficacy can be accomplished. PEI-based systems are capable of delivering a wide range of drugs; in particular, they are suited to delivering drugs with a negative charge. A further function of PEI is to activate antigen-presenting cells and stimulate cytokine production in order to enable the delivery of vaccines. In spite of the promise of PEI-based formulations, biocompatibility remains a substantial concern. The most effective ways to increase PEI biocompatibility include optimizing charge density, molecular weight, and branching, developing targeted and responsive delivery systems, and using chemical modifications. To pave the way for future clinical applications, we discuss strategies to increase PEI safety, as well as recent advances and prospects in PEI-based delivery approaches for gene, drug, and vaccine delivery.

Indexed as

adjuvantdrug deliverygene deliverypolyethyleneiminevaccine delivery

Identifiers

PMID42524176
PMCPMC13410413

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.