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Proceedings of the International Conference on Digital Manufacturing –
                                         Volume 1

               collagen synthesis, alkaline phosphatase  (ALP)  activity, and
               osteogenic gene expression  (Liu,  Dan,  Lu &  Pan, 2018).
               Therefore, in  future scaffold designs, careful consideration of
               geometry could help modulate local pH environments, balancing
               scaffold degradation with optimal bone regeneration responses.


                  However, excessive pH drops  or  accumulation of acidic
               byproducts may impair  osteogenic differentiation or  trigger
               inflammatory responses (Zhang et al., 2025). This highlights the
               importance of balancing scaffold degradation kinetics with
               cellular compatibility. Scaffold geometries should be designed to
               avoid enclosed regions where degradation byproducts
               accumulate, or otherwise be combined with buffering agents such
               as calcium phosphates to regulate pH (Zhang et al., 2025).

                  In   summary,    incorporating  geometry-driven  design
               considerations  into scaffold fabrication allows for enhanced
               control over not only mechanical strength and degradation rate,
               but also the local biological environment. These insights support
               a tailored approach in scaffold design for bone repair, particularly
               in critical-size defects, where geometric  optimisation  can  be a
               strategic tool to promote effective healing outcomes.


               CONCLUSION

               This study  examined  the degradation  behaviour  of 3D-printed
               PLA samples with different geometries in SBF over 28 days. The
               results  confirmed  the slow hydrolytic degradation of PLA and
               demonstrated that sample geometry influences both degradation
               rate and local pH variation. Higher surface-area-to-volume ratios
               accelerated mass loss, while confined geometries induced greater
               local pH shifts. These findings emphasise that scaffold geometry
               can be strategically designed to modulate degradation behaviour
               and the biochemical environment, providing valuable insights for
               future bone scaffold development. Future work should focus on
               long-term degradation studies under dynamic and physiological
               conditions, the  incorporation of bioactive materials to enhance




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