6533b7d3fe1ef96bd1261408
RESEARCH PRODUCT
Bone Scaffolds Based on Degradable Vaterite/PEG‐Composite Microgels
Alena KuzminaRomina SchröderElena StengelinSebastian SeiffertWolfgang TremelLaura BeschMartha F. KoziolRonald E. UngerGuillermo Beltramosubject
BiocompatibilityDispersityBiomedical EngineeringPharmaceutical Science02 engineering and technology010402 general chemistryBone tissue01 natural sciencesBone and BonesCalcium CarbonateBiomaterialschemistry.chemical_compoundOsteogenesisVateritePEG ratiomedicineddc:610chemistry.chemical_classificationMicrogelsOsteoblastPolymer021001 nanoscience & nanotechnology0104 chemical sciencesmedicine.anatomical_structurechemistryChemical engineering0210 nano-technologyGelsEthylene glycoldescription
Vaterite, a metastable modification of calcium carbonate, embedded in a flexible microgel packaging with adjustable mechanical properties, functionality, and biocompatibility, provides a powerful scaffolding for bone tissue regeneration, as it is easily convertible to bone-like hydroxyapatite (HA). In this study, the synthesis and physical analysis of a packaging material to encapsulate vaterite particles and osteoblast cells into monodisperse, sub-millimeter-sized microgels, is described whereby a systematic approach is used to tailor the microgel properties. The size and shape of the microgels is controlled via droplet-based microfluidics. Key requirements for the polymer system, such as absence of cytotoxicity as well as biocompatibility and biodegradability, are accomplished with functionalized poly(ethylene glycol) (PEG), which reacts in a cytocompatible thiol-ene Michael addition. On a mesoscopic level, the microgel stiffness and gelation times are adjusted to obtain high cellular viabilities. The co-encapsulation of living cells provides i) an in vitro platform for the study of cellular metabolic processes which can be applied to bone formation and ii) an in vitro foundation for novel tissue-regenerative therapies. Finally, the degradability of the microgels at physiological conditions caused by hydrolysis-sensitive ester groups in the polymer network is examined.
year | journal | country | edition | language |
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2019-12-18 |