4.8 Article

Biomimetic mineralized hybrid scaffolds with antimicrobial peptides

Journal

BIOACTIVE MATERIALS
Volume 6, Issue 8, Pages 2250-2260

Publisher

KEAI PUBLISHING LTD
DOI: 10.1016/j.bioactmat.2020.12.029

Keywords

Biomimetic mineralization; Antimicrobial; Cationic and amphipathic peptides; Hard tissue cytocompatibility

Funding

  1. National Institute for Dental and Craniofacial Research of the National Institutes of Health [R01DE026117, T90DE0227232]
  2. National Institutes of Health's National Center for Advancing Translational Sciences [UL1TR002494]
  3. Fundamental Research Funds for the Central Universities [2042020kf0191]
  4. National Natural Science Foundation of China [81400506]
  5. Natural Science Foundation of Guangdong Province [2018B030311040]
  6. 3 M Science and Technology Fellowship
  7. NSF through the MRSEC program

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The study developed a scaffold with dual function for promoting tissue growth and preventing bacterial infections. The scaffolds were fabricated through intrafibrillar-mineralization of collagen and coating with antimicrobial peptides, demonstrating both antimicrobial properties and cytocompatibility to human cells. The process of scaffold fabrication is versatile and can be used with other biopolymers for controlling mineral load.
Infection in hard tissue regeneration is a clinically-relevant challenge. Development of scaffolds with dual function for promoting bone/dental tissue growth and preventing bacterial infections is a critical need in the field. Here we fabricated hybrid scaffolds by intrafibrillar-mineralization of collagen using a biomimetic process and subsequently coating the scaffold with an antimicrobial designer peptide with cationic and amphipathic properties. The highly hydrophilic mineralized collagen scaffolds provided an ideal substrate to form a dense and stable coating of the antimicrobial peptides. The amount of hydroxyapatite in the mineralized fibers modulated the rheological behavior of the scaffolds with no influence on the amount of recruited peptides and the resulting increase in hydrophobicity. The developed scaffolds were potent by contact killing of Gram-negative Escherichia coli and Gram-positive Streptococcus gordonii as well as cytocompatible to human bone marrow-derived mesenchymal stromal cells. The process of scaffold fabrication is versatile and can be used to control mineral load and/or intrafibrillar-mineralized scaffolds made of other biopolymers.

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