Evidence map›Paper›PMID 30322058›Full record

ArticlePharmaceutics2018

Characterization of Mechanical Property Distributions on Tablet Surfaces.

Ramon Cabiscol, Jan Henrik Finke, Harald Zetzener, Arno Kwade

Abstract read
In one paragraph

Article in Pharmaceutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Characterization of Pharmaceutical Tablets by X-ray Tomography.Pharmaceuticals (Basel, Switzerland) · 2023
    Review
  9. Tablets Made from Paper-An Industrially Feasible Approach.Pharmaceuticals (Basel, Switzerland) · 2022
    Article
  10. Article
  11. Article
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

4 authors.

Ramon CabiscolInstitute for Particle Technology (iPAT), Technische Universität Braunschweig, 38104 Braunschweig, Germany. r.cabiscol@tu-braunschweig.de.ORCID 0000-0001-7423-772X
Jan Henrik FinkeInstitute for Particle Technology (iPAT), Technische Universität Braunschweig, 38104 Braunschweig, Germany. jan.finke@tu-braunschweig.de.ORCID 0000-0001-6936-9795
Harald ZetzenerInstitute for Particle Technology (iPAT), Technische Universität Braunschweig, 38104 Braunschweig, Germany. h.zetzener@tu-braunschweig.de.
Arno KwadeInstitute for Particle Technology (iPAT), Technische Universität Braunschweig, 38104 Braunschweig, Germany. a.kwade@tu-braunschweig.de.ORCID 0000-0002-6348-7309

Funding

FP7 People: Marie-Curie Actions 607453
6 · The paper itself

Abstract

Powder densification through uniaxial compaction is governed by a number of simultaneous processes taking place on a reduced time as the result of the stress gradients within the packing, as well as the frictional and adhesive forces between the powder and the die walls. As a result of that, a density and stiffness anisotropy is developed across the axial and radial directions. In this study, microindentation has been applied to assess and quantify the variation of the module of elasticity ( E m o d ) throughout the surface of cylindrical tablets. A representative set of deformation behaviors was analyzed by pharmaceutical excipients ranging from soft/plastic behavior (microcrystalline cellulose) over medium (lactose) to hard/brittle behavior (calcium phosphate) for different compaction pressures. The results of the local stiffness distribution over tablet faces depicted a linear and directly proportional tendency between a solid fraction and E m o d for the upper and lower faces, as well as remarkable stiffness anisotropy between the axial and radial directions of compaction. The highest extent of the stiffness anisotropy that was found for ductile grades of microcrystalline cellulose (MCC) in comparison with brittle powders has been attributed to the dual phenomena of overall elastic recovery and Poisson's effect on the relaxation kinetics. As a reinforcement of this analysis, the evolution of the specific surface area elucidated the respective densification mechanism and its implementations toward anisotropy. For ductile excipients, the increase in the contact surface area as well as the reduction and closing of interstitial pores explain the reduction of surface area with increasing compaction pressure. For brittle powders, densification evolves through fragmentation and the subsequent filling of voids.

Indexed as

BETindentationinhomogeneityporositytablets

Identifiers

PMID30322058
PMCPMC6320771

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.