Periodic Reporting for period 1 - PERAMEDIC (Personalised Adaptive Medicine)
Período documentado: 2024-02-01 hasta 2025-01-31
Personalised medicine remains difficult to implement due to challenges in drug manufacturing, regulatory approval, and cost-effectiveness. PERAMEDIC addresses these issues by leveraging advanced 3D printing technology to produce patient-specific medication in a scalable and adaptable manner. This approach ensures that multiple active pharmaceutical ingredients can be incorporated into a single pill, allowing for controlled release tailored to individual medical needs. The project aims to simplify complex medication regimens, improving adherence while reducing the risk of adverse drug interactions.
PERAMEDIC will improve therapeutic efficacy and reduce side effects by delivering optimal dosing and controlled drug release. By enabling small-batch, on-demand manufacturing, it will introduce a new paradigm in pharmaceutical production, making personalised medicine a viable reality. The project’s success will also contribute to healthcare system efficiency by reducing hospital visits and medication-related complications.
A major achievement is the development of a robust adaptive microprinting process, enabling the creation of polypills with multiple compartments. This technique allows precise deposition of pharmaceutical ingredients within controlled-release enclosures, ensuring accurate dosing tailored to patient-specific needs. Studies on pill geometry, microstructure design, and erosion mechanisms are being conducted to achieve drug release profile models. Custom software will be created to accurately predict release patterns with real-world patient data, enabling the prescription of personalised dosage forms.
The precision dosing system and novel dispensing mechanisms are being refined for particle formulation techniques and powder flow properties that will match the challenging requirements of this technology.
While testing of the key system modules will continue, their hardware and operational integration will be the lead activity over the next period. Early-stage regulatory discussions with relevant authorities on compliance requirements guide the development, paving the way for future validation.