TY - JOUR
T1 - Bionic Mineralized 3D-Printed Scaffolds with Enhanced In Situ Mineralization for Cranial Bone Regeneration
AU - Wang, Ling
AU - Li, Dongxuan
AU - Huang, Yawen
AU - Mao, Ruiqi
AU - Zhang, Boqing
AU - Luo, Fengxiong
AU - Gu, Peiyang
AU - Song, Ping
AU - Ge, Xiang
AU - Lu, Jian
AU - Yang, Xusheng
AU - Fan, Yujiang
AU - Zhang, Xingdong
AU - Wang, Kefeng
N1 - Funding Information:
This work was supported by the National Key Research and Development Program of China, China (2021YFB3802105, 2021YFB3802100, and 2021YFB3802101), Natural Science Foundation of Sichuan Province, China (2022NSFSC0290), Chengdu Municipal Science and Technology Program, China (2021‐YF08‐00107‐GX), National Natural Science Foundation of China, China (Grant No. 52075371), the Natural Science Foundation of Tianjin, China (Tianjin Applied Basic Research Multi‐Input Foundation, No. 21JCQNJC01360) and The Hong Kong Polytechnic University Gants (1‐CD4K and 1‐W196). The authors would like to thank Guolong Meng, Lingzhu Yu, Jiao Lu, and Ruiqi Dong (National Engineering Research Center for Biomaterials, Sichuan University) for helping in characterizing SEM, CLSM, and DMA.
Publisher Copyright:
© 2023 Wiley-VCH GmbH.
PY - 2024/1/15
Y1 - 2024/1/15
N2 - In situ mineralization is a promising strategy to mimic the physicochemical properties of biominerals and is widely applied in the field of bone repair. Given the high requirement for substance exchange in cranial bone regeneration, in situ mineralized organic–inorganic hybrid materials exhibit advantages. However, the integration of remarkable mineral content, mechanical properties, and osteogenic properties also remains a major challenge. Herein, enhanced in situ mineralization through combining the enzymatic and anion-boosted mineralization is applied to promote the mineralization efficiency, mineral content, and mechanical properties. Based on the results of computational calculations and in vitro mineralization experiments, the mechanism of mineralization enhancement is investigated from the perspectives of nucleation sites and the saturation of in situ mineralization. Anionic polyaspartic acid (pAsp) can increase the saturation of in situ mineralization; enzymatic mineralization shows high efficiency, with minerals of low crystallinity. The changes in the properties of the minerals effectively enhance the biological properties of 3D-printed scaffolds, as confirmed by cell proliferation/differentiation experiments in vitro and in cranial bone regeneration in vivo. This strategy provides a new thinking for the preparation of bionic mineralized scaffolds for cranial bone repair, and can greatly promote the efficiency of bone regeneration.
AB - In situ mineralization is a promising strategy to mimic the physicochemical properties of biominerals and is widely applied in the field of bone repair. Given the high requirement for substance exchange in cranial bone regeneration, in situ mineralized organic–inorganic hybrid materials exhibit advantages. However, the integration of remarkable mineral content, mechanical properties, and osteogenic properties also remains a major challenge. Herein, enhanced in situ mineralization through combining the enzymatic and anion-boosted mineralization is applied to promote the mineralization efficiency, mineral content, and mechanical properties. Based on the results of computational calculations and in vitro mineralization experiments, the mechanism of mineralization enhancement is investigated from the perspectives of nucleation sites and the saturation of in situ mineralization. Anionic polyaspartic acid (pAsp) can increase the saturation of in situ mineralization; enzymatic mineralization shows high efficiency, with minerals of low crystallinity. The changes in the properties of the minerals effectively enhance the biological properties of 3D-printed scaffolds, as confirmed by cell proliferation/differentiation experiments in vitro and in cranial bone regeneration in vivo. This strategy provides a new thinking for the preparation of bionic mineralized scaffolds for cranial bone repair, and can greatly promote the efficiency of bone regeneration.
KW - 3D printing
KW - cranial bone regeneration
KW - enzymatic mineralization
KW - hybrid mineralized scaffolds
KW - in situ mineralization
UR - http://www.scopus.com/inward/record.url?scp=85174166776&partnerID=8YFLogxK
U2 - 10.1002/adfm.202309042
DO - 10.1002/adfm.202309042
M3 - Journal article
AN - SCOPUS:85174166776
SN - 1616-301X
VL - 34
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 3
M1 - 2309042
ER -