Two bisphosphonic
acid-functionalized cross-linkers (one novel)
with different spacer chain characteristics were synthesized and incorporated
into hydrogels by copolymerization with 2-hydroxyethyl methacrylate
at different ratios to control the hydrogels’ swelling, mechanical
properties, and ability to support mineralization for biomedical applications.
The cross-linkers were synthesized by reaction of 2-isocyanatoethyl
methacrylate and bisphosphonated diamines followed by selective dealkylation
of the bisphosphonate ester groups. The hydrogels provide in vitro
growth of carbonated apatite, morphology affected by the cross-linker
structure. The hydrogels exhibit a high Young’s modulus
E
(up to 400 kPa) and can sustain up to 10.2 ± 0.1
MPa compressive stresses.
E
and hence the cross-link
density significantly increases upon mineralization reflecting the
formation of many bisphosphonate BP–Ca
2+
bonds acting
as additional cross-links. Cyclic mechanical tests reveal self-recoverability
of hydrogels because of reversible nature of BP–Ca
2+
bonds. The results suggest that these cross-linkers can add calcium-binding
abilities to hydrogels synthesized from any monomer and improve their
mechanical, swelling, and mineralization properties and hence are
potentially useful materials for biomedical applications.