摘要
Inspired by the natural synchronization of organic matrix biosynthesis and inorganic mineral deposition in coral reefs, this study introduces a novel synchronous in situ biomineralization method. This strategy aims to overcome the challenges of weak interfacial bonding and complex processing in the fabrication of bacterial cellulose/calcium–phosphorus composites (BC/Ca–P). Calcium gluconate was used as a dual-functional precursor by substituting d -glucose in culture medium to simultaneously supply a carbon source for BC biosynthesis and calcium ions (Ca 2+ ) for mineralization at different substitution ratios (10% for BC-CaG 10 and 100% for BC-CaG 100 ). We achieved concurrent biosynthesis of the BC matrix and deposition of Ca–P phases, leading to a unique inorganic–organic architecture in which Ca–P nanoparticles were uniformly anchored within the BC nanofibrous network and strongly integrated by interfacial interactions. Consequently, the moderate mineralization in BC-CaG 10 significantly enhanced the mechanical strength through a synergistic reinforcement mechanism, reaching 12.03 MPa, representing a 115% increase compared to that of pure BC. Conversely, the high mineral content of BC-CaG 100 facilitated the formation of a bioactive hydroxyapatite (HAP) phase, providing abundant active sites. In preliminary biomedical evaluations, the fabricated composites exhibited favorable biocompatibility. Notably, BC-CaG 100 exhibited efficient hemostatic performance in a rat tail amputation model, reducing hemostasis time by 71% (to 142 s) and blood loss by 97% (to 15 mg). This study presents a facile, scalable, and green approach for preparing novel biomimetic materials with promising potential for biomedical applications, including tissue engineering and wound management.
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