Evidence map›Paper›PMID 41341004›Full record

Article3D printing and additive manufacturing2025

Biopolymer Hydroxypropyl Methylcellulose-Based Filaments Prepared by Hot-Melt Extrusion Suitable for Fused Deposition Modeling 3D Printing of Personalized Capsules.

Jana Macháčková, Alena Komersová, Marie Nevyhoštěná, Roman Svoboda, Martin Bartoš, Kevin Matzick

Abstract read
In one paragraph

Article in 3D printing and additive manufacturing, 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

6 authors.

Jana MacháčkováDepartment of Physical Chemistry, Faculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.ORCID https://orcid.org/0000-0001-8561-1828
Alena KomersováDepartment of Physical Chemistry, Faculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.
Marie NevyhoštěnáDepartment of Physical Chemistry, Faculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.
Roman SvobodaDepartment of Physical Chemistry, Faculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.
Martin BartošDepartment of Analytical Chemistry, Faculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.
Kevin MatzickDepartment of Physical Chemistry, Faculty of Chemical Technology, University of Pardubice, Pardubice, Czech Republic.ORCID https://orcid.org/0000-0001-9444-7521

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Materials based on the hydroxypropyl methylcellulose mixed with different biopolymers (BioP; 5 w% of chitosan, sodium alginate, apple pectin, or citrus pectin) were processed by hot-melt extrusion and 3D printing to produce capsules intended for controlled drug release. Microscopic analyses confirmed significant impact of BioP on the processing temperatures and quality of the 3D printing. The capsules' chemical composition had a more significant impact on the dissolution profiles in acidic and neutral media, which are a robust function of the intermolecular bonds and swelling characteristics of the particular BioP (as indicated by the combined results of Raman spectroscopy, differential scanning calorimetry [DSC], and thermogravimetry). The capsules of all tested compositions retained the model drug for 120 min in pH 1.2, i.e., fulfilled the condition of targeting the small intestine. The presence of the particular BioP was found to be particularly beneficial in the development of personalized capsules for oral administration. The addition of both pectins led to a relatively fast pH-independent release of the model drug and has the potential applications in the targeting of the duodenum or jejunum. The capsules containing alginate and chitosan exhibited later initial release in pH 1.2, guaranteeing an unaltered passage through the stomach environment.

Indexed as

3D printingbiopolymerscapsulesfused deposition modelinghot-melt extrusion

Identifiers

PMID41341004
PMCPMC12670669

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.