Evidence map›Paper›PMID 38472727›Full record

ArticleDrug delivery and translational research2025

Imiquimod nanocrystal-loaded dissolving microneedles prepared by DLP printing.

Eliška Petrová, Stanislav Chvíla, František Štěpánek, Jarmila Zbytovská, Dimitrios A Lamprou

Open access · hybridAbstract read
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Article in Drug delivery and translational research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
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

9 citing papers in PubMed, 13 citations in OpenAlex.

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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

5 authors at 2 institutions in 2 countries.

Eliška PetrováSchool of Pharmacy, Queen's University Belfast, 97 Lisburn Road, BT9 7BL, Belfast, UK.ORCID 0000-0003-0691-8667
Stanislav ChvílaFaculty of Chemical Technology, Department of Organic Technology, University of Chemistry and Technology Prague, Technická 5, 166 28, Prague, Czech Republic.ORCID 0000-0003-2953-1756
František ŠtěpánekFaculty of Chemical Technology, Department of Organic Technology, University of Chemistry and Technology Prague, Technická 5, 166 28, Prague, Czech Republic.ORCID 0000-0001-9288-4568
Jarmila ZbytovskáDepartment of Organic Technology, University of Chemistry and Technology Prague, Faculty of Chemical Technology, Technická 5, 166 28, Prague 6, Czech Republic. jarmila.zbytovska@vscht.cz.ORCID 0000-0003-1541-8488
Dimitrios A LamprouSchool of Pharmacy, Queen's University Belfast, 97 Lisburn Road, BT9 7BL, Belfast, UK. d.lamprou@qub.ac.uk.ORCID 0000-0002-8740-1661
University of Chemistry and Technology, Prague · CZQueen's University Belfast · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The utilization of 3D printing- digital light processing (DLP) technique, for the direct fabrication of microneedles encounters the problem of drug solubility in printing resin, especially if it is predominantly composed of water. The possible solution how to ensure ideal belonging of drug and water-based printing resin is its pre-formulation in nanosuspension such as nanocrystals. This study investigates the feasibility of this approach on a resin containing nanocrystals of imiquimod (IMQ), an active used in (pre)cancerous skin conditions, well known for its problematic solubility and bioavailability. The resin blend of polyethylene glycol diacrylate and N-vinylpyrrolidone, and lithium phenyl-2,4,6-trimethylbenzoylphosphinate as a photoinitiator, was used, mixed with IMQ nanocrystals in water. The final microneedle-patches had 36 cylindrical microneedles arranged in a square grid, measuring approximately 600 μm in height and 500 μm in diameter. They contained 5wt% IMQ, which is equivalent to a commercially available cream. The homogeneity of IMQ distribution in the matrix was higher for nanocrystals compared to usual crystalline form. The release of IMQ from the patches was determined ex vivo in natural skin and revealed a 48% increase in efficacy for nanocrystal formulations compared to the crystalline form of IMQ.

Indexed as

ImiquimodNanoparticlesNeedlesPrinting, Three-DimensionalSolubilityAdministration, CutaneousAnimalsDrug Delivery SystemsDrug LiberationMicroinjectionsPolyethylene GlycolsPovidoneSkinSkin AbsorptionImiquimodpoly(ethylene glycol)diacrylatePolyethylene GlycolsPovidone3D printingDermal deliveryImiquimodMicroneedlesNanocrystals

Identifiers

PMID38472727
PMCPMC11614970
OpenAlexW4394763327

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.