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May 28, 2026Small0 citations

Near‐Infrared Responsive Property and Nanozyme Effect‐Mediated 3D‐Printed Gradient Bioactive Scaffold for Intelligent Immunomodulation in Regeneration of Large Segmental Bone Defects

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KWK WangYQYuxiang QinKCKong Chuiping

Key Points

  • This research aims to develop an advanced scaffold that enhances bone regeneration by actively modulating immune responses.
  • Fabricated a NIR-responsive 3D-printed gradient scaffold using digital light processing and secondary sintering.
  • Incorporated MnFePBA nanozymes to mitigate oxidative stress and regulate macrophage polarization.
  • Conducted in vitro and in vivo studies to evaluate scaffold performance in bone regeneration.
  • The scaffold significantly reduced oxidative stress and improved the immune microenvironment for bone healing.
  • MnFePBA nanozymes promoted M1 to M2 macrophage polarization, enhancing regenerative potential.
  • Scaffold use resulted in marked improvements in bone repair compared to conventional methods.

Abstract

ABSTRACT Regeneration of large segmental bone defects remains a formidable challenge, mainly due to the lack of a supportive microenvironment for the host's intrinsic repair cascade. Although 3D‐printed porous calcium phosphate ceramics have osteoconductive properties, their inability to actively regulate key immune processes and compromised mechanical strength caused by porosity greatly limit therapeutic efficacy. Herein, an “osteoimmunology”‐informed design of a near‐infrared (NIR)‐responsive 3D‐printed gradient scaffold is proposed for intelligent bone regeneration by temporally modulating macrophage phenotypic polarization. Fabricated via digital light processing (DLP) printing combined with secondary sintering, this scaffold has a core–shell‐like gradient structure (dense interior, porous exterior), achieving a balanced combination of mechanical robustness and bioactivity. Manganese iron Prussian blue analogue (MnFePBA) nanozymes were incorporated onto the scaffold surface. Under NIR irradiation, MnFePBA not only scavenges excessive reactive oxygen species (ROS) but also triggers controlled release of Mn 2 + , synergistically driving macrophages to polarize from proinflammatory M1 to proregenerative M2 phenotype. In vitro and in vivo studies confirm that the scaffold alleviates post‐implantation oxidative stress, fosters a favorable immune microenvironment, and significantly enhances bone repair, establishing a new paradigm for developing next‐generation smart bone grafts via active immunomodulation.

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Cite This Study

Wang et al. (2026) studied this question.

synapsesocial.com/papers/6a17dcbb3fad632b0f9d9630https://doi.org/10.1002/smll.202514837
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