3D printed personalized therapies for pediatric patients affected by adrenal insufficiency

Other authors

Institut Català de la Salut

[Rodríguez-Pombo L, Gallego-Fernández C] Departamento de Farmacología, Farmacia y Tecnología Farmacéutica, I+D Farma (GI-1645), Facultad de Farmacia, Instituto de Materiales (iMATUS) and Health Research Institute of Santiago de Compostela (IDIS), Universidade de Santiago de Compostela, Santiago de Compostela, Spain. [Jørgensen AK] Department of Pharmaceutics, UCL School of Pharmacy, University College London, London, UK. [Parramon-Teixidó CJ, Cañete-Ramirez C, Cabañas-Poy MJ] Servei de Farmàcia, Vall d’Hebron Hospital Universitari, Barcelona, Spain

Vall d'Hebron Barcelona Hospital Campus

Publication date

2024-11-19T08:17:13Z

2024-11-19T08:17:13Z

2024-09



Abstract

3D printed medications; Chewable drug; Paediatrics


Medicaments impresos en 3D; Medicaments masticables; Pediatria


Medicamentos impresos en 3D; Medicamentos masticables; Pediatría


Background Adrenal insufficiency is usually diagnosed in children who will need lifelong hydrocortisone therapy. However, medicines for pediatrics, in terms of dosage and acceptability, are currently unavailable. Research design and methods Semi-solid extrusion (SSE) 3D printing (3DP) was utilized for manufacturing of personalized and chewable hydrocortisone formulations (printlets) for an upcoming clinical study in children at Vall d’Hebron University Hospital in Barcelona, Spain. The 3DP process was validated using a specific software for dynamic dose modulation. Results The printlets contained doses ranging from 1 to 6 mg hydrocortisone in three different flavor and color combinations to aid adherence among the pediatric patients. The pharma-ink (mixture of drugs and excipients) was assessed for its rheological behavior to ensure reproducibility of printlets through repeated printing cycles. The printlets showed immediate hydrocortisone release and were stable for 1 month of storage, adequate for prescribing instructions during the clinical trial. Conclusions The results confirm the suitability and safety of the developed printlets for use in the clinical trial. The required technical information from The Spanish Medicines Agency for this clinical trial application was compiled to serve as guidelines for healthcare professionals seeking to apply for and conduct clinical trials on 3DP oral dosage forms.


This paper was funded by the UK Research and Innovation, the Engineering and Physical Sciences Research Council [EP/S023054/1], and the Ministerio de Universidades [FPU20/01245].

Document Type

Article


Published version

Language

English

Publisher

Taylor & Francis

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Attribution 4.0 International

http://creativecommons.org/licenses/by/4.0/

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