“…The high in vivo/vitro inertness of PTN is conditioned by the negligible anodic dissolution of the dynamically loaded PTN sample in simulated body fluids [6,7,8,9,25,28]. In the early in vivo terms, the anodic passivity of the PTN scaffold is beneficial for the attachment, cytocompatibility, and proliferation of seeded precursor cells as it sustains the formation of manifold tissular variants, reported in References [45,46,47,48,49]. Afterwards, a newly formed interface (e.g., bone regenerate) owes its vitality to the two factors as follows: (i) Continuing superficial anodic passivity of the PTN scaffold and (ii) minimum viscoelastic discrepancy between the surrounding bone tissue and the PTN matrix.…”