Evidence map›Paper›PMID 40657043›Full record

ArticleDrug design, development and therapy2025

Development and Characterization of a Cationic Polyurethane Carrier for Enhanced Topical DNA Delivery.

Florin Borcan, Adel Len, Titus Vlase, Gabriela Vlase, Zoltan I Dudas, Roxana Popescu, Ramona C Albulescu, Cristina A Dehelean, Camelia A Szuhanek

Abstract read
In one paragraph

Article in Drug design, development and therapy, 2025. 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

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

9 authors.

Florin BorcanDepartment I, Faculty of Pharmacy, "Victor Babes" University of Medicine and Pharmacy, Timisoara, 300041, Romania.ORCID 0000-0003-3406-0303
Adel LenBudapest Neutron Centre, Institute for Energy Security and Environmental Safety, HUN-REN Centre for Energy Research, Budapest, 1121, Hungary.
Titus VlaseDepartment of Chemistry (Research Center "Thermal Analysis in Environmental Problems"), Faculty of Chemistry, Biology, Geography, West University Timisoara, Timisoara, 300115, Romania.
Gabriela VlaseDepartment of Chemistry (Research Center "Thermal Analysis in Environmental Problems"), Faculty of Chemistry, Biology, Geography, West University Timisoara, Timisoara, 300115, Romania.
Zoltan I DudasBudapest Neutron Centre, Institute for Energy Security and Environmental Safety, HUN-REN Centre for Energy Research, Budapest, 1121, Hungary.
Roxana PopescuDepartment II (Cellular and Molecular Biology), Faculty of Medicine, "Victor Babes" University of Medicine and Pharmacy, Timisoara, 300041, Romania.ORCID 0000-0002-9387-1141
Ramona C AlbulescuDepartment XI (Paediatrics II), Faculty of Medicine, "Victor Babes" University of Medicine and Pharmacy, Timisoara, 300594, Romania.
Cristina A DeheleanDepartment I, Faculty of Pharmacy, "Victor Babes" University of Medicine and Pharmacy, Timisoara, 300041, Romania.
Camelia A SzuhanekDepartment II (Research Center "Ortho-Center"), Faculty of Dental Medicine, "Victor Babes" University of Medicine and Pharmacy, Timisoara, 300041, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Nucleic acids are increasingly being recognized for their potential as therapeutic agents for the treatment of a variety of pathologies, such as genetic diseases, viral infections, and cancer. However, the safe delivery of these negatively charged macromolecules to their intended sites of action remains a major challenge. Purpose: This study aimed to design and characterize cationic particles for use as nonviral vectors for nucleic acid delivery; another primary objective was to evaluate the biocompatibility between the particles and DNA. Methods: The particles were synthesized via a polyaddition process between isophorone diisocyanate and a mixture of polyethylene glycol and polycaprolactone diol. The structural characteristics were assayed using a variety of techniques, including measurements of pH, refractive index, and Zetasizer, drug release and penetration through an artificial membrane, SEM, FTIR and Raman spectroscopy, thermal analyses, cell viability, and in vivo evaluation of skin parameters. Results: The findings revealed that nearly neutral-pH particles were successfully synthesized, displaying a broad size distribution ranging from 400-900 nm, a prolonged release profile, and an encapsulation efficacy of 72.5%. Thermal analyses demonstrated that the samples remained stable at temperatures up to 200 °C, and the results of the spectroscopy, cell assay, and evaluations on mouse skin suggest that the obtained particles are safe for use as DNA carriers. Conclusion: Cationic polyurethane carriers present a potential alternative to the more established polyethylenimine. However, additional studies are necessary to fully assess the therapeutic effectiveness of these formulations.

Indexed as

DNADrug CarriersPolyurethanesAnimalsCationsCell SurvivalDrug LiberationMiceParticle SizePolyestersPolyethylene GlycolsCationsDNADrug CarrierspolycaprolactonePolyestersPolyethylene GlycolsPolyurethanescell culturesFT-IRmice skinRamanthermal analysisZetasizer

Identifiers

PMID40657043
PMCPMC12255259

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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.