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EDITORIAL article

Front. Drug Deliv., 26 November 2024
Sec. Technological and Methodological Advances in Drug Delivery
This article is part of the Research Topic 3D Printing in Pharmaceuticals & Medical Applications View all 5 articles

Editorial: 3D printing in pharmaceuticals and medical applications

Italo Rodrigo Calori
Italo Rodrigo Calori1*Dimitrios A. Lamprou
Dimitrios A. Lamprou2*
  • 1Department of Pharmaceutics and Drug Delivery, School of Pharmacy, University of Mississippi, Oxford, MS, United States
  • 2School of Pharmacy, Queen’s University Belfast, Belfast, United Kingdom

In the last years, there is an increased interest in 3D printing (3DP) for applications in drug delivery and tissue engineering, with the potential of the systems to be used also in space explorations for in demand and inhouse manufacturing. 3DP is an innovative and rapidly evolving technology that is revolutionizing the biomedical field, and not only. By enabling the creation of personalized biomedical devices, implants, tissue scaffolds, and drug delivery systems, it meets the growing demand for individualized treatments. 3DP is a layer-by-layer (LbL) deposition process, which allows for precise control over material properties and structures from the macroscopic to the microscopic level. This level of precision overcomes the limitations of traditional manufacturing methods, opening new possibilities for patient-specific solutions that are both effective and cost-efficient. The ability to create advanced, customized devices is transforming medicine, particularly in drug delivery and regenerative therapies.

This Research Topic presents the latest developments in 3DP for biomedical applications, encouraging further innovation and exploration in the field.

Levine et al., investigated how the geometry of laser-sintered tablets containing theophylline affects their properties. Their study focused on key characteristics such as microstructure, volume, disintegration, and dissolution. The authors, tested tablets in three distinct shapes, cylindrical, hollow cylindrical, and frustum, while keeping the surface area constant and varying the cylinder diameters. Advanced characterisation methods, such as Micro-computed tomography (Micro-CT) analysis revealed how these geometric changes influenced tablet properties such as mass uniformity and disintegration, providing valuable insights for drug formulation.

Guimaraes et al., introduced the SpheroMold, a 3D-printed device designed to improve the hanging drop method for spheroid culture. By utilizing stereolithography, they printed a negative mould from photopolymer resin and filled it with Polydimethylsiloxane (PDMS) to create a support for 3D cell culture using the hanging drop method. This device reduced drop coalescence and expanded the culture medium volume, enhancing spheroid formation and improving process efficiency.

In another study, De Vincentiis et al., developed a 3D-printed wearable device for mouse models with spinal cord injury. The authors aimed preparing a non-invasive method and prioritizing animal welfare. The paper provides tests of various formats, including “Fitbit,” “Belt,” “Bib,” and “Cape,” on both healthy and injured mice. The effectiveness of these devices was demonstrated through simulations using the finite element method and magnetic field measurements, showing promising results for spinal injury treatment.

Lastly, Schweiker et al., explored the potential of 3D-printed biodegradable scaffolds for bone regeneration. They combined an alginate core with an outer layer of calcium phosphate cement and employed a modified bioprinter to print the scaffolds. Post-printing treatments such as drying, PBS incubation, and lyophilization were applied to assess the scaffolds’ mechanical strength. Mechanical testing and scanning electron microscopy analysis confirmed the scaffolds’ robustness and potential in tissue engineering and bone regeneration.

In conclusion, these studies highlight the transformative potential of 3DP in various biomedical fields, from drug formulation to tissue engineering. Levine et al.'s investigation of laser-sintered tablets underscores the importance of geometry in drug design. The SpheroMold technology illustrates how 3DP can enhance traditional spheroid culture methods. The wearable device for spinal injury models addresses key concerns such as non-invasive approaches and animal welfare. Finally, Schweiker et al., work on biodegradable scaffolds advances tissue engineering and bone regeneration. These innovations not only enhance scientific understanding but also pave the way for safer, more effective therapies.

The editors, sincerely thank the authors for their valuable contributions, the reviewers for their constructive feedback, and the editorial staff of Frontiers in Drug Delivery for their professional support. We hope this Research Topic will inspire continued research and development in the field of 3DP in the era of biomedical applications and beyond.

Author contributions

IC: Conceptualization, Methodology, Project administration, Writing–original draft. DL: Conceptualization, Methodology, Project administration, Supervision, Writing–review and editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: 3D printing, biomedical applications, drug delivery, tissue engineering, personalized medicine

Citation: Calori IR and Lamprou DA (2024) Editorial: 3D printing in pharmaceuticals and medical applications. Front. Drug Deliv. 4:1527225. doi: 10.3389/fddev.2024.1527225

Received: 13 November 2024; Accepted: 14 November 2024;
Published: 26 November 2024.

Edited and reviewed by:

Gareth Williams, University College London, United Kingdom

Copyright © 2024 Calori and Lamprou. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Italo Rodrigo Calori, aXRhbG9jYWxvcmlAZ21haWwuY29t; Dimitrios A. Lamprou, ZC5sYW1wcm91QHViLmFjLnVr

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.