Evidence map›Paper›PMID 33807390›Full record

ArticlePharmaceutics2021

Production of Reproducible Filament Batches for the Fabrication of 3D Printed Oral Forms.

Stéphane Roulon, Ian Soulairol, Valérie Lavastre, Nicolas Payre, Maxime Cazes, Laurent Delbreilh, Jean Alié

Abstract read
In one paragraph

Article in Pharmaceutics, 2021. 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
–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

9 citing papers in PubMed.

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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

7 authors.

Stéphane RoulonNormandy University, UNIROUEN Normandie, INSA Rouen, CNRS, Group of Materials Physics, Av. Université, 76801 St Etienne du Rouvray CEDEX, France.ORCID 0000-0003-1051-899X
Ian SoulairolDepartment of Pharmacy, Nimes University Hospital, 30900 Nimes CEDEX 9, France.ORCID 0000-0002-8837-5362
Valérie LavastreSolid State Characterization and 3D Printing Service, Sanofi R&D, 371 rue du Pr. Joseph Blayac, 34080 Montpellier CEDEX 4, France.
Nicolas PayreSolid State Characterization and 3D Printing Service, Sanofi R&D, 371 rue du Pr. Joseph Blayac, 34080 Montpellier CEDEX 4, France.
Maxime CazesSolid State Characterization and 3D Printing Service, Sanofi R&D, 371 rue du Pr. Joseph Blayac, 34080 Montpellier CEDEX 4, France.
Laurent DelbreilhNormandy University, UNIROUEN Normandie, INSA Rouen, CNRS, Group of Materials Physics, Av. Université, 76801 St Etienne du Rouvray CEDEX, France.ORCID 0000-0002-9322-7153
Jean AliéSolid State Characterization and 3D Printing Service, Sanofi R&D, 371 rue du Pr. Joseph Blayac, 34080 Montpellier CEDEX 4, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients need medications at a dosage suited to their physiological characteristics. Three-dimensional printing (3DP) technology by fused-filament fabrication (FFF) is a solution for manufacturing medication on demand. The aim of this work was to identify important parameters for the production of reproducible filament batches used by 3DP for oral formulations. Amiodarone hydrochloride, an antiarrhythmic and insoluble drug, was chosen as a model drug because of dosage adaptation need in children. Polyethylene oxide (PEO) filaments containing amiodarone hydrochloride were produced by hot-melt extrusion (HME). Different formulation storage conditions were investigated. For all formulations, the physical form of the drug following HME and fused-deposition modeling (FDM) 3D-printing processes were assessed using thermal analysis and X-ray powder diffraction (XRPD). Filament mechanical properties, linear mass density and surface roughness, were investigated by, respectively, 3-point bending, weighing, and scanning electron microscopy (SEM). Analysis results showed that the formulation storage condition before HME-modified filament linear mass density and, therefore, the oral forms masses from a batch to another. To obtain constant filament apparent density, it has been shown that a constant and reproducible drying condition is required to produce oral forms with constant mass.

Indexed as

3D printingfilamentfused-filament fabricationhot-melt extrusionimmediate releaseoral formspediatric

Identifiers

PMID33807390
PMCPMC8066748

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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.