Dual-Functional Implant Based on Gellan-Xanthan Hydrogel with Diopside, BMP-2 and Lysostaphin for Bone Defect Repair and Control of Staphylococcal Infection.
Anna S KaryaginaAlexander V GrishinAlina G KudinovaInna N BulyginaElizaveta V KoudanPolina A OrlovaVera P DatsenkoAnna V ZhulinaTatyana M GruninaMaria S PoponovaMikhail S KrivozubovMaria S GromovaNatalia V StrukovaMaria S GeneralovaKirill E NikitinIgor V ShchetininLev O LuchnikovSvetlana V ZaitsevaMaria A KirsanovaEugene S StatnikFedor S SenatovVladimir G LuninAlexander V GromovPublished in: Macromolecular bioscience (2024)
A new dual-functional implant based on gellan-xanthan hydrogel with calcium-magnesium silicate ceramic diopside and recombinant lysostaphin and bone morphogenetic protein 2 (BMP-2)-ray is developed. In this composite, BMP-2 is immobilized on microparticles of diopside while lysostaphin is mixed directly into the hydrogel, providing sustained release of BMP-2 to allow gradual bone formation and rapid release of lysostaphin to eliminate infection immediately after implantation. Introduction of diopside of up to 3% (w/v) has a negligible effect on the mechanical properties of the hydrogel but provides a high sorption capacity for BMP-2. The hydrogels show good biocompatibility and antibacterial activity. Lysostaphin released from the implants over a 3 h period efficiently kills planktonic cells and completely destroys 24 h pre-formed biofilms of Staphylococcus aureus. Furthermore, in vivo experiments in a mouse model of critically-sized cranial defects infected with S. aureus show a complete lack of osteogenesis when implants contain only BMP-2, whereas, in the presence of lysostaphin, complete closure of the defect with newly formed mineralized bone tissue is observed. Thus, the new implantable gellan-xanthan hydrogel with diopside and recombinant lysostaphin and BMP-2 shows both osteogenic and antibacterial properties and represents a promising material for the treatment and/or prevention of osteomyelitis after bone trauma.
Keyphrases
- bone regeneration
- mesenchymal stem cells
- drug delivery
- hyaluronic acid
- soft tissue
- tissue engineering
- staphylococcus aureus
- wound healing
- mouse model
- bone mineral density
- bone marrow
- drug release
- risk assessment
- induced apoptosis
- cell free
- heavy metals
- oxidative stress
- silver nanoparticles
- postmenopausal women
- endoplasmic reticulum stress
- quantum dots
- mass spectrometry
- sewage sludge