3D-Printed Antibacterial Scaffolds for the Regeneration of Alveolar Bone in Severe Periodontitis.
Konstantinos TheodoridisAthanasios S ArampatzisGeorgia LiasiLazaros TsalikisPanagiotis BarmpalexisDimitrios ChristofilosAndreana N AssimopoulouPublished in: International journal of molecular sciences (2023)
Current clinical treatment of periodontitis alleviates periodontal symptoms and helps to keep the disease under control for extended periods. Despite this, a significant destruction of the tooth's underlying bone tissue often takes place progressively. Herein, we present a two-way therapeutic approach for local delivery of antibacterial agents and bone tissue regeneration, incorporating ~1% w / w tetracycline hydrochloride (TCH) into a 3D-printed scaffold composed of poly(ε-caprolactone) (PCL). Samples were assessed for their morphological, physicochemical, pharmacokinetic, and antibacterial properties. Furthermore, osteoprecursor cells (MC3T3-E1) were employed to evaluate the osteoinductive potential of the drug-loaded scaffolds. Cell proliferation, viability, and differentiation were determined on all cell-seeded scaffolds. At the end of the culture, PCL-TCH scaffolds promoted abundant collagen organic matrix, demonstrating augmented alkaline phosphatase (ALP) activity and areas of accumulated mineralised bone tissue, despite their belayed cell proliferation. Based on the observed effectiveness of the PCL-TCH scaffolds to inhibit Staphylococcus aureus , these constructs could serve as an alternative bioactive implant that supports bacterial inhibition and favours a 3D microenvironment for bone tissue regeneration in severe periodontitis.
Keyphrases
- tissue engineering
- bone mineral density
- cell proliferation
- stem cells
- soft tissue
- wound healing
- staphylococcus aureus
- bone loss
- postmenopausal women
- drug delivery
- induced apoptosis
- escherichia coli
- silver nanoparticles
- physical activity
- body composition
- oxidative stress
- anti inflammatory
- mesenchymal stem cells
- risk assessment
- biofilm formation
- cancer therapy
- bone marrow
- cell death
- adverse drug
- electronic health record
- cell cycle arrest
- endoplasmic reticulum stress
- virtual reality