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Prof. Dr. Martin F. Wilks

Department of Pharmaceutical Sciences
Profiles & Affiliations

Projects & Collaborations

8 found
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ToxOligo2 - Toxicological properties of oligomers present in food contact materials

Research Project  | 6 Project Members

ToxOligo addresses an important knowledge gap by evaluating toxicological properties of oligomers released from polymers as food contact materials (FCM). The formation and presence of oligomers is inevitable in such FCM. Despite known migration into food, these substances are toxicologically poorly characterized, preventing adequate risk assessment. The ongoing project phase allowed essential new insights into available information on oligomers from all polymeric FCM. A pilot study on PET helped to design an optimized strategy and workflow to address this task. Information on physicochemical, ADME and toxicological properties was collected using computational methods. In a second project phase, a collection of oligomers from all other materials will be made based on the obtained information. The focus will be on bioactivity assessment of these substances. Hazard profiles will be established using various in vitro assays to assess general toxicity, cellular stress pathways, macrophage activation and endocrine effects. These studies aim at assessing the level of concern of such substances and providing recommendations for prioritization of future toxicological testing.

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ToxOligo - Toxicological properties of oligomers present in food contact materials

Research Project  | 6 Project Members

ToxOligo addresses an important knowledge gap by characterizing toxicological properties of oligomers released from food contact materials (FCM) such as plastics, adhesives, printing inks and coatings. Despite known high levels in FCM, these substances are toxicologically poorly investigated, preventing adequate risk assessment. A systematic review of the literature and expert interviews will provide insight on available knowledge of types of structures involved, exposure estimates and toxicological information. Physico-chemical and ADME properties, reactivity of building blocks, stability of oligomers, genotoxicity, endocrine disrupting potentials, and chronic and developmental toxicity will be predicted by in silico methods. Hazard profiles will be established for relevant selected oligomers using in vitro assays on general cytotoxicity, cellular stress pathways, neuronal cell toxicity, macrophage activation, and endocrine regulation. Selected FCM extracts will be considered to identify potentially hazardous materials. Levels of concern will be estimated, information gaps identified, and recommendations for follow-on toxicological analyses and an evaluation concept for safety assessment of oligomers will be proposed.

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NanoREG II - Development and Implementation of Grouping and Safe-by-Design approaches within regulatory frameworks

Research Project  | 2 Project Members

One of the greatest challenges facing regulators in the ever changing landscape of novel nano-materials is how to design and implement a regulatory process which is robust enough to deal with a rapidly diversifying system of manufactured nanomaterials (MNM) over time. The challenge is to build a regulatory system which is flexible enough to be able to deal with new targets and requirements in the future, and this can be helped by the development and introduction of Safe by Design (SbD) principles. The NANoREG II project, built around the challenge of coupling SbD to the regulatory process, will demonstrate and establish new principles and ideas based on data from value chain implementation studies to establish SbD as a fundamental pillar in the validation of a novel MNM. Grouping concepts that will be developed by NanoREG II can be regarded as a major innovation, and in the form of guidance documents will support industries and regulatory agencies as well as supporting commercial launch of new NM.