4.7 Article

A micro-extrusion 3D printing platform for fabrication of orodispersible printlets for pediatric use

Journal

INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 605, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ijpharm.2021.120854

Keywords

Semi-solid micro-extrusion 3D printing; Pediatric drug delivery; Quality by design (QbD); 3D printer parametrization; Hydrochlorothiazide orodispersible tablet; Process Analytical Technology (PAT)

Funding

  1. Gobierno de Canarias (Spain) [ProID2017010094]
  2. FEDER [TESIS2020010087]
  3. European Social Fund (ESF)

Ask authors/readers for more resources

3D printing pharmaceuticals can offer personalized medicines, particularly beneficial for treating pediatric patients. This study successfully optimized printing parameters and surface materials to produce high-quality orodispersible printlets of hydrochlorothiazide that meet European Pharmacopoeia requirements.
3D printed pharmaceuticals offers the potential to manufacture personalized medicines for patients. Such technology is of particular benefit to pediatric populations from the offer of increased patient compliance and dose flexibility. With a bench-to-patient approach, this study established and optimized the critical parameters of the semi-solid micro-extrusion 3D printing process to guarantee the quality attributes of the final dosage form. Pediatrics orodispersible printlets of hydrochlorothiazide were manufactured through the modification of printing parameters, as well as printing surfaces materials. The printlets were characterized and the dimensions were measured using a digital caliper and computer vision algorithm. This study identified that the printing surface material and the first printing layer are critical parameters for high-resolution printlets. Following the optimization of 3D printing parameters, high quality orodispersible printlets loaded with hydrochlorothiazide - specifically tailored for pediatric patient's dosage forms - were obtained (4.62 mm x 1.90 mm). Mass and content uniformity assays demonstrated that the printlets satisfied the requirements for orodispersible printlets set by the European Pharmacopoeia. As such, in order to transition from laboratory research towards the treatment of patients, distinguishing accurate 3D printing parameters is necessary for the manufacture of medicines with key quality attributes that follow Pharmacopoeia requirements.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available