Preventing bacterial colonization
on scaffolds while supporting
tissue formation is highly desirable in tissue engineering as bacterial
infection remains a clinically significant risk to any implanted biomaterials.
Elemental selenium (Se0) nanoparticles have emerged as
a promising antimicrobial biomaterial without tissue cell toxicity,
yet it remains unknown if their biological properties are from soluble
Se ions or from direct cell–nanoparticle interactions. To answer
this question, in this study, we developed a layered coating consisting
of a Se nanoparticle layer underneath a micrometer-thick, biomimetic
calcium phosphate (CaP) layer. We showed, for the first time, that
the release of soluble HSe– ions from the Se nanoparticles
strongly inhibited planktonic growth and biofilm formation of key
bacteria, Staphylococcus aureus. The
Se-CaP coating was found to support higher bone formation than the
CaP-only coating in critical-size calvarial defects in rats; this
finding could be directly attributed to the released soluble Se ions
as the CaP layers in both groups had no detectable differences in
the porous morphology, chemistry, and release of Ca or P. The Se-CaP
coating was highly versatile and applicable to various surface chemistries
as it formed through simple precipitation from aqueous solutions at
room temperature and therefore could be promising in bone regeneration
scaffolds or orthopedic implant applications.