Evidence map›Paper›PMID 36380170›Full record

ArticlePharmaceutical research2023

Development of a Workflow to Engineer Tailored Microparticles Via Inkjet Printing.

Christina Winter, Manuel Zettl, Jérôme Mantanus, Eftychios Hadjittofis, Gerd Leitinger, Dagmar Kolb, Wen-Kai Hsiao, Martin Spoerk, Amrit Paudel, Eva Roblegg and 1 more

Abstract read
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In one paragraph

Article in Pharmaceutical research, 2023. 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
0.7field-weighted citation impact, top 36% 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

0 citing papers in PubMed, 8 citations in OpenAlex.

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

11 authors at 5 institutions in 2 countries.

Christina WinterResearch Center Pharmaceutical Engineering GmbH, Inffeldgasse 13/II, 8010, Graz, Austria.
Manuel ZettlResearch Center Pharmaceutical Engineering GmbH, Inffeldgasse 13/II, 8010, Graz, Austria.
Jérôme MantanusUCB S.A., Allée de la Recherche, 60, 1070, Brussels, Belgium.
Eftychios HadjittofisUCB S.A., Allée de la Recherche, 60, 1070, Brussels, Belgium.
Gerd LeitingerDivision of Cell Biology, Histology and Embryology, Gottfried Schatz Research Center, Medical University of Graz, Neue Stiftingtalstrasse 6/II, 8010, Graz, Austria.
Dagmar KolbCore Facility Ultrastructure Analysis, Center for Medical Research, Gottfried Schatz Research Center, Medical University of Graz, Neue Stiftingtalstrasse 6/II, 8010, Graz, Austria.
Wen-Kai HsiaoResearch Center Pharmaceutical Engineering GmbH, Inffeldgasse 13/II, 8010, Graz, Austria.
Martin SpoerkResearch Center Pharmaceutical Engineering GmbH, Inffeldgasse 13/II, 8010, Graz, Austria.
Amrit PaudelResearch Center Pharmaceutical Engineering GmbH, Inffeldgasse 13/II, 8010, Graz, Austria.
Eva RobleggResearch Center Pharmaceutical Engineering GmbH, Inffeldgasse 13/II, 8010, Graz, Austria.
Joana T PintoResearch Center Pharmaceutical Engineering GmbH, Inffeldgasse 13/II, 8010, Graz, Austria. joana.pinto@rcpe.at.ORCID http://orcid.org/0000-0003-2599-4569
Research Center Pharmaceutical Engineering (Austria) · ATMedical University of Graz · ATUCB Pharma (Belgium) · BEGraz University of Technology · ATUniversity of Graz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeNew drug development and delivery approaches result in an ever-increasing demand for tailored microparticles with defined sizes and structures. Inkjet printing technologies could be promising new processes to engineer particles with defined characteristics, as they are created to precisely deliver liquid droplets with high uniformity.

methodsD-mannitol was used as a model compound alone or co-processed with the pore former agent ammonium bicarbonate, and the polymer polyethylene glycol 200. Firstly, a drop shape analyzer was used to characterize and understand ink/substrate interactions, evaporation, and solidification kinetics. Consequently, the process was transferred to a laboratory-scale inkjet printer and the resulting particles collected, characterized and compared to others obtained via an industrial standard technique.

resultsThe droplet shape analysis allowed to understand how 3D structures are formed and helped define the formulation and process parameters for inkjet printing. By adjusting the drop number and process waveform, spherical particles with a mean size of approximately 100 µm were obtained. The addition of pore former and polymer allowed to tailor the crystallization kinetics, resulting in particles with a different surface (i.e., spike-like surface) and bulk (e.g. porous and non-porous) structure.

conclusionThe workflow described enabled the production of 3D structures via inkjet printing, demonstrating that this technique can be a promising approach to engineer microparticles.

Indexed as

PolymersWorkflowPolymersD-mannitolexcipientinkjet printingmicroparticlesparticle engineeringspray drying

Identifiers

PMID36380170
OpenAlexW4309159254

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.