Abstract

This study aimed to improve the mechanical, drug loading/release and bioactive characteristics of hydroxyapatite (HAP). The covalent functionalization of PAMAM dendrimer with MWCNT (d-MWCNT), and in situ synthesis of strontium substituted HAP (SrHAP) on d-MWCNT yielded a composite, d-MWCNT-SrHAP. The composite was characterized by FT-IR, XRD, HR-SEM, AFM, EDS, TGA and zeta potential. It was hydrophilic (water contact angle 25.25 ± 4.21°), porous (89.63 ± 2.4%), bioresorbable, mechanically strong (0.415 ± 0.04 GPa) and protein adsorbing. The d-MWCNT-SrHAP exhibited a 30-fold increase in curcumin loading and a 1.7-fold delay in burst release compared to SrHAP. Further, in vitro studies using human osteoblast-like MG-63 cells demonstrated that the curcumin-loaded composite, d-MWCNT-SrHAP-C, encouraged osteoblast survival, proliferation, differentiation and matrix mineralization. The desirable physico-chemical properties and in vitro bioactivity of the d-MWCNT-SrHAP-C composite strongly suggest its potential application as a drug delivery system in hard tissue engineering.

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