H2020Individual fellowship2016–2018

DN-CARTILOGEL · Design of double network polycarbonate-based hydrogels by simultaneous reactions: scaffolds for load-bearing soft tissue regeneration

Horizon 2020 — Marie Skłodowska-Curie Actions

Duration
2016-09-12 → 2018-09-11
EU contribution
€183,455
Participants
2
Scheme
MSCA-IF-EF-ST

Lines connect the coordinator with its partners.

Results in brief

Design of double network polycarbonate-based hydrogels by simultaneous reactions: scaffolds for load-bearing soft tissue regeneration

Articular cartilage (AC) is the white flexible load-bearing soft tissue able to withstand the highest loads in physically demanding areas of the body. Once it is damaged, its poor ability for self-repair induces a progressive loss of function that, ultimately, results in severe rheumatic or musculoskeletal degenerative conditions, which are leading causes of morbidity. Among them, osteoarthritis (OA) is already one of the ten most disabling diseases in developed countries. Therefore, OA contributes to functional impairment and loss of independence in the middle-aged and the elderly, and it represents an immense burden to patients, thus having a major impact on European society. Unfortunately, the regeneration of AC is limited by its complex and unique structure and low self-repair capacity. Hence, the preventive repair of damaged AC remains a significant challenge in orthopaedic medicine, and DN-CARTILOGEL aimed at tackling this problem. The overall goal of the project focused on developing a cell-based therapy using polymeric-based hydrogel matrices as biocompatible scaffolds to replace damaged AC or support new functional tissue formation. While commonly used hydrogel fabrication techniques have several practical limitations (i.e. time-consuming, multistep process, lack of control over the reproducibility of the mechanical properties, or high degree of heterogeneity), DN-CARTILOGEL prepared innovative hydrogels based on hydrophilic polymeric materials as versatile biofunctional platforms with improved mechanical strength, toughness and high water content. The ultimate goal covered the development of a straightforward path to design robust hydrogels able to induce the differentiation of adult mesenchymal stem cells (MSCs) into specialized cartilage-producing cells. Indeed, DN-CARTILOGEL project has achieved significant milestones for solving the aforementioned drawbacks and fulfilled the research objectives.

Data: CORDIS, © European Union

Project objective

Polymer materials have outstanding properties with which to be applied for a wide range of applications. In particular, hydrogel materials are widely studied for applications in tissue engineering on account of their high water contents. Despite the advances in these materials, some biomedical targets remain challenging. Articular cartilage (AC) is the white flexible load-bearing soft tissue able to withstand the highest loads in physically demanding areas of the body. Once it is damaged, its poor ability for self-repair may induce a progressive loss of function that, ultimately, results in a severe musculoskeletal degenerative condition. While most commonly used hydrogel fabrication techniques still have practical limitations or do not lead to materials that are sufficiently strong for AC regeneration, the DN-Cartilogel project proposes the preparation of innovative tough, double network hydrogel materials that are based on advanced hydrophilic poly(carbonate)s. The tailored design of polymers with specific side-chain and end group functionalities will lead to hydrogel materials with improved mechanical strength, toughness and high water content. To this end, the project will apply the one-step synthetic methodology based on orthogonal click chemistry that was reported recently by the host group to generate novel and highly tunable materials. The ultimate goal is to develop a straightforward path to design robust DN hydrogels able to induce the differentiation of mesenchymal stem cells into specialized cartilage-producing cells, which directly addresses priorities established by the H2020 Work Programme.

Original text from CORDIS.

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Data: CORDIS, © European Union