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Related Experiment Video

Updated: Mar 2, 2026

Ceramic Omnidirectional Bioprinting in Cell-Laden Suspensions for the Generation of Bone Analogs
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Bioprinted Osteogenic and Vasculogenic Patterns for Engineering 3D Bone Tissue.

Batzaya Byambaa1,2, Nasim Annabi1,2,3,4, Kan Yue1,2

  • 1Department of Medicine, Biomaterials Innovation Research Center, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02139, USA.

Advanced Healthcare Materials
|May 20, 2017
PubMed
Summary
This summary is machine-generated.

This study presents a bioprinting strategy for creating bone tissue constructs with functional blood vessels. The engineered tissues support cell growth and stability, offering potential for repairing large bone defects.

Keywords:
3D bioprintingangiogenic hydrogelsbone-like tissue constructsvascularized bone tissue

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Area of Science:

  • Biomaterials Engineering
  • Tissue Engineering
  • Regenerative Medicine

Background:

  • Fabricating 3D large-scale bone tissue constructs with functional vasculature is challenging for repairing large bone defects.
  • Existing methods struggle to create complex, perfusable vascular networks within engineered bone.
  • Need for biomimetic matrices that support cell co-culture and promote osteogenesis and angiogenesis.

Purpose of the Study:

  • To develop a direct-writing bioprinting strategy for fabricating microstructured, bone-like tissue constructs with perfusable vascular lumens.
  • To create in vitro matrices for co-culturing endothelial cells and mesenchymal stem cells.
  • To engineer constructs with controlled physical and chemical microniches and gradients.

Main Methods:

  • Utilized extrusion-based direct-writing bioprinting with gelatin methacryloyl (GelMA) hydrogels.
  • Printed a central cylinder of low methacryloyl substituted GelMA (GelMALOW) to form a vascular lumen.
  • Developed cell-laden cylinder elements with silicate nanoplatelets for osteogenesis and synthesized hydrogels with vascular endothelial growth factor for vascularization.

Main Results:

  • The bioprinted constructs supported cell survival and proliferation during 21 days of in vitro maturation.
  • Engineered constructs demonstrated high structural stability throughout the culture period.
  • The method allowed for local control of physical and chemical microniches and gradient establishment.

Conclusions:

  • The developed bioprinting strategy successfully fabricated bone-like tissue constructs with perfusable vasculature.
  • The engineered constructs are suitable for in vitro co-culture and demonstrate potential for bone defect repair.
  • This approach enables precise control over the microenvironment within engineered tissues.