Abstract

Adequate bone tissue regeneration has been challenging to achieve at critical-sized bone defects caused by disease. Bone tissue engineering using a combination of scaffolds and bioactive factors provides new hope for the treatment of this extreme condition. Icaritin, a herb-derived chemical, has shown its ability to enhance bone formation both in vitro and in vivo, and it has been found that sub-micron surface structure instructs bone formation in calcium phosphate ceramics (CaPs). Here, we evaluated the possibility of using a submicron surface structured CaP ceramic as the carrier of icaritin for bone tissue regeneration in critical-sized bone defects. Icaritin, an herb-derived chemical, was loaded into a submicron surface structured porous calcium phosphate ceramic (Ø12.8 × 3 mm) to get samples with 0, 10, 50, 250, and 1,250 µg icaritin per CaP disc (M0, M10, M50, M250, M1250 groups, respectively). In vitro evaluation with the certain dosages correlated to those released from the samples showed a dose-dependent enhancement of osteogenic differentiation and mineralization of human bone marrow stromal cells with the presence of osteogenic factors in the culture medium, indicating icaritin is an osteopromotive factor. After intramuscular implantation of the samples in dogs for 8 weeks, a dose-dependent of bone formation was seen with enhanced bone formation at the dosage of 50 and 250 µg. To evaluate the in vivo osteogenic potentials of icaritin-containing CaP ceramic scaffolds in the orthopedic site, a 12.8 mm calvarial defect model in rabbits was established. Micro-computed tomography (micro-CT) and histology results at weeks 4, 8 and 12 post-surgery showed more newly formed bone in M250 group, with correspondingly more new vessel ingrowth. The results presented herein suggested that being osteopromotive, icaritin could enhance bone formation initiated by sub-microstructured CaP ceramics and the CaP ceramics scaffold incorporating icaritin is a promising biomaterial for the treatment of critical-sized defect.

Highlights

  • The orthopedic critical-sized defect due to traumatic injuries or tumor resection is still a significant challenge

  • Considering the possible bone-enhancing function of icaritin as previously shown, we introduced icaritin into submicron surface structured tricalcium phosphate ceramic and characterized the resulting materials concerning for their physicochemical properties and icaritin release

  • Following the in vitro evaluation of icaritin released with Human Bone Marrow Stromal cells (hBMSC), we investigated the bone-forming ability of the materials after intramuscular implantation in a canine model

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Summary

Introduction

The orthopedic critical-sized defect due to traumatic injuries or tumor resection is still a significant challenge. Allowing bone formation on their surface and form chemical bonding to the new bone, calcium phosphate (CaP) ceramics have been widely used as bone graft substitutes (Hench and Wilson, 1984; Damien and Parsons, 1991; Bohner et al, 2012). Compared with autogenous bone, the capacity of CaP ceramics for repairing critical-sized defects still seems to be insufficient. Surface modification may improve the bone regeneration ability of CaP ceramics. Calcium phosphate ceramics enhanced bone regeneration in non-critically sized bone defects (Habibovic et al, 2004; Yuan et al, 2006) and could repair criticalsized defects (Yuan et al, 2010) and enhance bone formation in the spinal environment (van Dijk et al, 2018)

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