Summary
Arthritis, a widespread inflammatory condition, affecting millions globally, necessitates urgent advancements in therapeutic approaches. Predominantly characterized by osteoarthritis (OA), this debilitating condition causes joint pain and stiffness, notably impacting the knee, hand, and hip joints. OA, a chronic degenerative disease, intensifies with age, imposing a significant economic burden on healthcare systems. The insufficiency of current treatments highlights the need for innovative therapies. Tissue engineering and regenerative medicine offer promising avenues, with platelet-rich plasma therapy (PRP) emerging as a forefront contender. PRP harnesses the regenerative potential of growth factors (GFs) to stimulate tissue repair processes, particularly in cartilage and bone cells. However, clinical application faces hurdles, notably the rapid degradation of GFs within the intricate synovial fluid (SF) environment, limiting their therapeutic efficacy and distribution. To overcome these challenges, scientists explore advanced drug delivery systems utilizing nanoparticles (NPs) as carriers. Although promising, passive NPs diffusion through viscous biological barriers, such as joint fluids, remains a significant obstacle. In response, OrthoBots introduces enzyme-powered NPs, termed nanobots, as active carriers of GFs within SF. By utilizing enzymatic propulsion, nanobots aim to enhance GF transport and distribution, facilitating targeted cartilage regeneration. This innovative approach holds transformative potential, potentially revolutionizing arthritis therapy by overcoming current limitations and offering more effective and personalized treatment strategies. Through systematic in vitro studies and in vivo proof-of-concept demonstrations, OrthoBots will pave the way for the next generation of arthritis therapeutics, addressing the unmet clinical needs and improving patient outcomes.
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| Web resources: | https://cordis.europa.eu/project/id/101189423 |
| Start date: | 01-11-2024 |
| End date: | 30-04-2026 |
| Total budget - Public funding: | - 150 000,00 Euro |
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Original description
Arthritis, a widespread inflammatory condition, affecting millions globally, necessitates urgent advancements in therapeutic approaches. Predominantly characterized by osteoarthritis (OA), this debilitating condition causes joint pain and stiffness, notably impacting the knee, hand, and hip joints. OA, a chronic degenerative disease, intensifies with age, imposing a significant economic burden on healthcare systems. The insufficiency of current treatments highlights the need for innovative therapies. Tissue engineering and regenerative medicine offer promising avenues, with platelet-rich plasma therapy (PRP) emerging as a forefront contender. PRP harnesses the regenerative potential of growth factors (GFs) to stimulate tissue repair processes, particularly in cartilage and bone cells. However, clinical application faces hurdles, notably the rapid degradation of GFs within the intricate synovial fluid (SF) environment, limiting their therapeutic efficacy and distribution. To overcome these challenges, scientists explore advanced drug delivery systems utilizing nanoparticles (NPs) as carriers. Although promising, passive NPs diffusion through viscous biological barriers, such as joint fluids, remains a significant obstacle. In response, OrthoBots introduces enzyme-powered NPs, termed nanobots, as active carriers of GFs within SF. By utilizing enzymatic propulsion, nanobots aim to enhance GF transport and distribution, facilitating targeted cartilage regeneration. This innovative approach holds transformative potential, potentially revolutionizing arthritis therapy by overcoming current limitations and offering more effective and personalized treatment strategies. Through systematic in vitro studies and in vivo proof-of-concept demonstrations, OrthoBots will pave the way for the next generation of arthritis therapeutics, addressing the unmet clinical needs and improving patient outcomes.Status
SIGNEDCall topic
ERC-2024-POCUpdate Date
24-11-2024
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