Evidence map›Paper›PMID 42791497›Full record

ArticleMacromolecular bioscience2026

Personalized 3D-Printed Affinisol-Based Pharmaceutical Delivery Systems: The Case Study for Alternative Sulfonamides for Alzheimer's Disease.

Marie Nevyhoštěná, Alena Komersová, Roman Svoboda, Vladimír Pejchal, Adéla Pospíšilová, Jan Muselík, Aleksandra Łapa, Paulina Koczurkiewicz-Adamczyk

Abstract read
In one paragraph

Article in Macromolecular bioscience, 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

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.

Marie NevyhoštěnáFaculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.ORCID https://orcid.org/0009-0006-9004-5430
Alena KomersováFaculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.ORCID https://orcid.org/0000-0002-4510-4124
Roman SvobodaFaculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.ORCID https://orcid.org/0000-0002-1253-366X
Vladimír PejchalFaculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.
Adéla PospíšilováFaculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.ORCID https://orcid.org/0009-0008-2792-0268
Jan MuselíkFaculty of Pharmacy, Masaryk University, Brno, Czech Republic.ORCID https://orcid.org/0000-0002-4289-3885
Aleksandra ŁapaFaculty of Pharmacy, Jagiellonian University Medical College, Kraków, Poland.ORCID https://orcid.org/0009-0007-6870-5567
Paulina Koczurkiewicz-AdamczykFaculty of Pharmacy, Jagiellonian University Medical College, Kraków, Poland.

Funding

Internal Grant Agency of the University of Pardubice SGS_2026_006
6 · The paper itself

Abstract

The use of hot melt extrusion combined with fused deposition modeling 3D printing was explored to enhance the solubility and bioavailability of poorly water-soluble compounds intended for Alzheimer's disease (AD) therapy. AD, a neurodegenerative disorder with no definitive treatment, affects millions worldwide, underscoring the urgent need for effective and personalized therapeutic strategies. Four sulfonamide-derived compounds, identified as potential AD therapeutics, were synthesized and successfully incorporated (loads between 10 and 50 wt.%) into customized, 3D-printed oral dosage forms. These 3D-printed tablets were evaluated for properties such as hardness, thermo-analytical characterization, dissolution, cytotoxicity, and stability. Notably, successful amorphization of the incorporated APIs was observed in most 3D-printed tablets, which may be critical for improving solubility. In vitro dissolution testing revealed multiple favorable release profiles, with several formulations demonstrating sustained or enhanced drug release suitable for the therapeutic requirements of AD. When compared to the dissolution data of the corresponding conventional matrix tablets, the present 3D-printed tablets offered superior or comparable dissolution characteristics, demonstrating the potential of personalized medicine and remote digital control for optimizing patient-specific treatments.

Indexed as

Alzheimer DiseaseDrug Delivery SystemsPrecision MedicinePrinting, Three-DimensionalSulfonamidesDrug LiberationHumansSolubilityTabletsSulfonamidesTabletsAlzheimer's diseasedissolution testingFDM 3D printinghot melt extrusionpersonalized medicine

Identifiers

PMID42791497
PMCPMC13615160

What OpenQuestion holds

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Registered trials

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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.