HEIndividual fellowship2023–2025

DrugMOF · Disordered Metal-Organic Frameworks for Drug Delivery

Horizon Europe — Marie Skłodowska-Curie Actions

Duration
2023-09-01 → 2025-08-31
EU contribution
€230,774
Participants
1
Scheme
HORIZON-TMA-MSCA-PF-EF

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Results in brief

Disordered Metal-Organic Frameworks for Drug Delivery

Modern medicine increasingly relies on targeted drug delivery systems to improve therapeutic outcomes while minimizing side effects. Conventional approaches often struggle to balance high drug loading with controlled release, a challenge that is particularly critical in cancer treatment where precise dosing can significantly impact patient safety and efficacy. Metal–organic frameworks (MOFs) have emerged as promising candidates due to their exceptional porosity and tunable chemistry, enabling them to store large amounts of drugs. However, their highly open crystalline structures typically lead to rapid drug release, which can cause harmful reactions and reduce treatment effectiveness. The DrugMOF project attempted to address this gap by exploring disordered MOFs, specifically zeolitic imidazolate frameworks (ZIFs), as drug delivery platforms. Unlike their crystalline counterparts, disordered MOFs exhibited smaller pores and irregular structures that slowed down drug release. The strategy was therefore to first load drugs into crystalline ZIFs for maximum capacity, then transform these materials into amorphous or glassy states through processes such as ball milling or melt-quenching. This order-to-disorder transition combined the benefits of high loading with controlled release, creating biocompatible materials tailored for long-term therapeutic applications. The overall objectives were threefold: (1) Develop and characterize ZIF-based systems capable of transitioning between crystalline and amorphous states while maintaining structural integrity and biocompatibility; (2) Demonstrate controlled drug release from these systems using model compounds, supported by in vitro cytotoxicity studies to ensure safety; and (3) Advance knowledge transfer and researcher training, fostering expertise in interdisciplinary fields spanning materials science, chemistry, and biomedicine. This work aligned with EU priorities on health innovation and advanced materials, contributing to strategic goals of improving patient care and reducing healthcare costs in the long term. By enabling precise, sustained drug delivery, the project addressed pressing societal needs in oncology and chronic disease management. Beyond healthcare, the insights gained strengthened Europe’s leadership in functional materials research, supporting industrial translation and future collaborations.

Data: CORDIS, © European Union

Project objective

Drug delivery systems are often needed for delivering drugs in a targeted organ or tissue at a desired concentration range and without toxic side effects. Metal-organic frameworks (MOFs) have emerged as promising drug delivery systems due to their high loading capacity, but currently this is also their main limitation as it results in too rapid drug release in the human body, causing an excessive response and potentially toxic side effects. Slowing down the drug release rate, while maintaining high loading capacity and biocompatibility, would enable applications within especially cancer therapy.Disordered MOFs (i.e., MOFs without an ordered crystalline structure) have smaller pores and more torturous pathways for drug release. The projects proposed strategy is to load anti-cancer drugs in the crystalline MOF with high surface area and thus high loading capacity and then subsequently subject this material to an order-to-disorder transition, giving rise to slower drug release. This transition can be induced by either mechanical ball milling or thermal melt-quenching. Molecular dynamics and classification-based machine learning will be used to identify which local atomic structures are best correlated with drug release rate in disordered MOFs. Experimental validation will be performed to establish design principles for MOF structures with a tailored drug release profile.The project builds on complementary expertise of the fellow applicant (disordered biomaterials, in vitro studies) and supervisor (MOFs, simulations, machine learning). Combined with the research and training environment offered by the host organization (Aalborg University, Denmark), this will ensure the achievement of this novel project as well as the dissemination and exploitation of the results. The goal is to develop principles for designing disordered MOFs for drug delivery. The fellow applicant will emerge from the project with new skills, and the capability to launch his own research group.

Original text from CORDIS.

Participants

  • AALBORG UNIVERSITET · AalborgCoordinatorDenmark

Links

Data: CORDIS, © European Union