Evidence map›Paper›PMID 30097806›Full record

ArticleAAPS PharmSciTech2018

Extrusion 3D Printing of Paracetamol Tablets from a Single Formulation with Tunable Release Profiles Through Control of Tablet Geometry.

Shaban A Khaled, Morgan R Alexander, Derek J Irvine, Ricky D Wildman, Martin J Wallace, Sonja Sharpe, Jae Yoo, Clive J Roberts

Open access · hybridAbstract read
In one paragraph

Article in AAPS PharmSciTech, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 147 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

8 authors at 3 institutions in 3 countries.

Shaban A KhaledAdvanced Materials and Healthcare Technologies, School of Pharmacy, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
Morgan R AlexanderAdvanced Materials and Healthcare Technologies, School of Pharmacy, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
Derek J IrvineFaculty of Engineering, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
Ricky D WildmanFaculty of Engineering, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
Martin J WallaceAdvanced Manufacturing Technology, GlaxoSmithKline (Ireland), 12 Riverwalk, Citywest, Business Campus, Dublin, 24, Ireland.
Sonja SharpeAdvanced Manufacturing Technology, GlaxoSmithKline, 709 Swedeland Rd, King of Prussia, Pennsylvania, 19406-0939, USA.
Jae YooAdvanced Manufacturing Technology, GlaxoSmithKline, 709 Swedeland Rd, King of Prussia, Pennsylvania, 19406-0939, USA.
Clive J RobertsAdvanced Materials and Healthcare Technologies, School of Pharmacy, University of Nottingham, University Park, Nottingham, NG7 2RD, UK. clive.roberts@nottingham.ac.uk.
University of Nottingham · GBGlaxoSmithKline (United States) · USGlaxoSmithKline (Ireland) · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An extrusion-based 3D printer was used to fabricate paracetamol tablets with different geometries (mesh, ring and solid) from a single paste-based formulation formed from standard pharmaceutical ingredients. The tablets demonstrate that tunable drug release profiles can be achieved from this single formulation even with high drug loading (> 80% w/w). The tablets were evaluated for drug release using a USP dissolution testing type I apparatus. The tablets showed well-defined release profiles (from immediate to sustained release) controlled by their different geometries. The dissolution results showed dependency of drug release on the surface area/volume (SA/V) ratio and the SA of the different tablets. The tablets with larger SA/V ratios and SA had faster drug release. The 3D printed tablets were also evaluated for physical and mechanical properties including tablet dimension, drug content, weight variation and breaking force and were within acceptable range as defined by the international standards stated in the US Pharmacopoeia. X-ray powder diffraction, differential scanning calorimetry and attenuated total reflectance Fourier transform infrared spectroscopy were used to identify the physical form of the active and to assess possible drug-excipient interactions. These data again showed that the tablets meet USP requirement. These results clearly demonstrate the potential of 3D printing to create unique pharmaceutical manufacturing, and potentially clinical, opportunities. The ability to use a single unmodified formulation to achieve defined release profiles could allow, for example, relatively straightforward personalization of medicines for individuals with different metabolism rates for certain drugs and hence could offer significant development and clinical opportunities.

Indexed as

Drug LiberationPrinting, Three-DimensionalAcetaminophenCalorimetry, Differential ScanningDrug CompoundingExcipientsSpectroscopy, Fourier Transform InfraredTabletsTechnology, PharmaceuticalX-Ray DiffractionAcetaminophenExcipientsTablets3D printinggeometryimmediate releaseparacetamolpersonalised medicinesustained release

Identifiers

PMID30097806
PMCPMC6848047
OpenAlexW2885306056

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.