Currently, metal hardware is widely used in treating post-traumatic bone injuries. However, this hardware has limitations and can result in poor healing and a lack of mechanical integrity, particularly in fractures occurring in patients with osteoporosis. Bone plates, screws and pins tend to loosen over time, necessitating their removal, which can lead to loss of crucial bone material. Additionally, there is currently no convenient method to stabilise small bone fragments and prevent micromotion in cases involving multiple bone fragments resulting from multiple breaks.
Calcium phosphate cement presents an alternative to metal hardware, but it still has inferior physical and biological properties compared to native tissue. This inferiority is due to its brittle nature and poor tensile and shear properties resulting from randomly organised networks of entangled crystals. The lack of effective commercially available bone bioadhesives is due in part to the complex nature of bone repair, a process which requires mechanical stability in wet conditions, sufficient working time for the surgeon.
OsStic® is an injectable bioadhesive that can be used to treat bone fractures. It is the result of a longstanding research collaboration between Biodesign Europe at Dublin City University and Irish MedTech company PBC Biomed. The recent ‘Breakthrough Device’ designation means the treatment has been ‘recognised as a superior device to medical solutions currently available on the market.’
Biomaterials and bioengineering
The new bioadhesive is a biomaterial, something which has been engineered to interact with biological systems, in this case to heal bone fractures. The bioadhesive uses phosphoserine, a common molecule found in numerous proteins which, when combined with alpha-tricalcium phosphate powder, generates adhesive biomaterial that can stabilise and repair bone fractures.
The underlying research behind this new bioadhesive was recently published in Acta Biomaterialia. The team used specialist data analysis software to investigate the capabilities of the bioadhesive, hitting upon an optimal formulation in terms of key clinical properties that can be manufactured at scale and is cost-effective.
The Biodesign Europe research centre at DCU has been collaborating with PBC Biomed for the last eight years. This research project was made possible by €5.4 million in funding from the Disruptive Technologies fund which the two organisations secured as part of a consortium in 2021. Further funding came from the SFI I-Form research centre. PBC Biomed also has a three year ongoing relationship with DCU Invent, the university’s commercialisation unit. Biomimetic Innovations Ltd, an affiliate of PBC Biomed, made this latest announcement on the 26th January.