LL-37 and bisphosphonate co-delivery 3D-scaffold with antimicrobial and antiresorptive activities for bone regeneration

dc.contributor.authorYe P.
dc.contributor.authorYang Y.
dc.contributor.authorQu Y.
dc.contributor.authorYang W.
dc.contributor.authorTan J.
dc.contributor.authorZhang C.
dc.contributor.authorSun D.
dc.contributor.authorZhang J.
dc.contributor.authorZhao W.
dc.contributor.authorGuo S.
dc.contributor.authorSong L.
dc.contributor.authorHou T.
dc.contributor.authorZhang Z.
dc.contributor.authorTang Y.
dc.contributor.authorLimjunyawong N.
dc.contributor.authorXu J.
dc.contributor.authorDong S.
dc.contributor.authorDou C.
dc.contributor.authorLuo F.
dc.contributor.correspondenceYe P.
dc.contributor.otherMahidol University
dc.date.accessioned2024-08-05T18:18:46Z
dc.date.available2024-08-05T18:18:46Z
dc.date.issued2024-10-01
dc.description.abstractThis study introduces a novel 3D scaffold for bone regeneration, composed of silk fibroin, chitosan, nano-hydroxyapatite, LL-37 antimicrobial peptide, and pamidronate. The scaffold addresses a critical need in bone tissue engineering by simultaneously combating bone infections and promoting bone growth. LL-37 was incorporated for its broad-spectrum antimicrobial properties, while pamidronate was included to inhibit bone resorption. The scaffold's porous structure, essential for cell infiltration and nutrient diffusion, was achieved through a freeze-drying process. In vitro assessments using SEM and FTIR confirmed the scaffold's morphology and chemical integrity. Antimicrobial efficacy was tested against pathogens of Staphylococcus aureus (S. aureus) and Pseudomonas aeruginosa (P. aeruginosa). In vivo studies in a murine model of infectious bone defect revealed the scaffold's effectiveness in reducing inflammation and bacterial load, and promoting bone regeneration. RNA sequencing of treated specimens provided insights into the molecular mechanisms underlying these observations, revealing significant gene expression changes related to bone healing and immune response modulation. The results indicate that the scaffold effectively inhibits bacterial growth and supports bone cell functions, making it a promising candidate for treating infectious bone defects. Future studies should focus on optimizing the release of therapeutic agents and evaluating the scaffold's clinical potential.
dc.identifier.citationInternational Journal of Biological Macromolecules Vol.277 (2024)
dc.identifier.doi10.1016/j.ijbiomac.2024.134091
dc.identifier.eissn18790003
dc.identifier.issn01418130
dc.identifier.pmid39059543
dc.identifier.scopus2-s2.0-85200011698
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/100257
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.titleLL-37 and bisphosphonate co-delivery 3D-scaffold with antimicrobial and antiresorptive activities for bone regeneration
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85200011698&origin=inward
oaire.citation.titleInternational Journal of Biological Macromolecules
oaire.citation.volume277
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationThe First Affiliated Hospital of Chongqing Medical University
oairecerif.author.affiliationZunyi Medical University
oairecerif.author.affiliationSouthwestern Hospital Chongqing
oairecerif.author.affiliationArmy Medical University

Files

Collections