Functionalized Collagen/Elastin-like Polypeptide Hydrogels for Craniofacial Bone Regeneration.
Pallabi PalMichelle A TucciLir-Wan FanRatna BollavarapuJonathan W LeeSusana M Salazar MarochoAmol V JanorkarPublished in: Advanced healthcare materials (2022)
Critical-sized cranial bone defects fail to re-ossify and require the surgical intervention of cranioplasty. To achieve superior bone healing in such cases, a hydrogel consisting of an interpenetrating network of collagen and elastin-like polypeptide to encapsulate bone morphogenetic protein-2 (BMP-2), doxycycline, and 45S5 Bioglass is developed. This hydrogel has an appropriate elastic modulus of 39 ± 2.2 kPa to allow proper handling during implantation. The hydrogel promotes human adipose-derived stem attachment, proliferation, and differentiation toward the osteogenic lineage, including the deposition of hydroxyapatite particles embedded within a collagenous fibrillar structure after 21 days of in vitro culture. After eight weeks of implantation of the acellular hydrogel in a critical-sized rat cranial defect model, only a small quantity of various pro-inflammatory (< 20 pg mg -1 ) and anti-inflammatory (< 10 pg mg -1 ) factors in the adjacent cranial tissue is noticed, indicating the overall biocompatibility of the hydrogel. Scanning electron microscopy evidenced the presence of new fibrous extracellular matrix and mineral aggregates at the defect site, with calcium/phosphorus ratio of 0.5 and 2.0 by eight and twelve weeks, respectively. Microcomputed tomography (Micro-CT) and histological analyses showed formation of mature mineralized tissue that bridged with the surrounding bone. Taken together, the acellular composite hydrogel shows great promise for superior bone healing after cranioplasty.
Keyphrases
- bone regeneration
- tissue engineering
- wound healing
- drug delivery
- hyaluronic acid
- electron microscopy
- extracellular matrix
- bone mineral density
- mesenchymal stem cells
- randomized controlled trial
- bone marrow
- computed tomography
- anti inflammatory
- soft tissue
- endothelial cells
- postmenopausal women
- risk assessment
- oxidative stress
- signaling pathway
- gestational age
- machine learning
- drug release
- quantum dots
- positron emission tomography
- sewage sludge
- breast reconstruction
- artificial intelligence