Trabecular-bone mimicking osteoconductive collagen scaffolds: an optimized 3D printing approach using freeform reversible embedding of suspended hydrogels

被引:0
|
作者
Kontakis, Michael G. [1 ]
Moulin, Marie [2 ]
Andersson, Brittmarie [1 ]
Norein, Norein [3 ]
Samanta, Ayan [3 ]
Stelzl, Christina [2 ]
Engberg, Adam [2 ]
Diez-Escudero, Anna [1 ]
Kreuger, Johan [2 ]
Hailer, Nils P. [1 ]
机构
[1] Uppsala Univ, Dept Surg Sci Orthopaed, Ortholab, SE-75185 Uppsala, Sweden
[2] Uppsala Univ, Dept Med Cell Biol, Sci Life Lab, SE-75123 Uppsala, Sweden
[3] Uppsala Univ, Dept Chem, Angstrom Lab Macromol Chem, SE-75121 Uppsala, Sweden
关键词
FRESH; Bioprinting; Additive manufacturing; Tissue engineering; Collagen; LONG-TERM; COMPOSITE;
D O I
10.1186/s41205-025-00255-0
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
BackgroundTechnological constraints limit 3D printing of collagen structures with complex trabecular shapes. However, the Freeform Reversible Embedding of Suspended Hydrogels (FRESH) method may allow for precise 3D printing of porous collagen scaffolds that carry the potential for repairing critical size bone defects.MethodsCollagen type I scaffolds mimicking trabecular bone were fabricated through FRESH 3D printing and compared either with 2D collagen coatings or with 3D-printed polyethylene glycol diacrylate (PEGDA) scaffolds. The porosity of the printed scaffolds was visualized by confocal microscopy, the surface geometry of the scaffolds was investigated by scanning electron microscopy (SEM), and their mechanical properties were assessed with a rheometer. The osteoconductive properties of the different scaffolds were evaluated for up to four weeks by seeding and propagation of primary human osteoblasts (hOBs) or SaOS-2 cells. Intracellular alkaline phosphatase (ALP) and lactate dehydrogenase (LDH) activities were measured, and cells colonizing scaffolds were stained for osteocalcin (OCN).ResultsThe FRESH technique enables printing of constructs at the millimetre scale using highly concentrated collagen, and the creation of stable trabecular structures that can support the growth osteogenic cells. FRESH-printed collagen scaffolds displayed an intricate and fibrous 3D network, as visualized by SEM, whereas the PEGDA scaffolds had a smooth surface. Amplitude sweep analyses revealed that the collagen scaffolds exhibited predominantly elastic behaviour, as indicated by higher storage modulus values relative to loss modulus values, while the degradation rate of collagen scaffolds was greater than PEGDA. The osteoconductive properties of collagen scaffolds were similar to those of PEGDA scaffolds but superior to 2D collagen, as verified by cell culture followed by analysis of ALP/LDH activity and OCN immunostaining.ConclusionsOur findings suggest that FRESH-printed collagen scaffolds exhibit favourable mechanical, degradation and osteoconductive properties, potentially outperforming synthetic polymers such as PEGDA in bone tissue engineering applications.
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页数:13
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