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. 2019 Jul 8;7:e7271. doi: 10.7717/peerj.7271

Table 2. Comparison of various printed cartilage scaffolds in several in vitro and in vivo studies.

Authors Materials Strategies Evidence Model of study Periods Effects
Cao, Ho & Teoh (2003) PCL (NaOH treated) FDM In vitro hOB(iliac crest) hChondrocytes (rib cartilage) 50 days Osteogenic and chondrogenic cells can grow, proliferate, distribute, and produce extracellu-lar matrix in these PCL scaffolds.
Smith et al. (2007) PCL SLS In vivo Yucatan minipig mandibles 3 months Cartilaginous tissue regeneration along the articulating surface with exuberant osseous tissue formation.
Yen et al. (2009) PLGA (type II collagen) FDM In vitro Chondrocytes (condyles of Yorkshire pigs) 4 weeks Scaffolds swell slightly. The cartilaginous tissue formation was observed around but not yet in the interior of the constructs.
Yen et al. (2009) PLGA (lyophilized for 48 h) LFDM In vitro Chondrocytes (condyles of Yorkshire pigs) 4 weeks Decrease swelling significantly. Mechanical strength is closer to native articular cartilage. Proliferate well and secret abundant ECM.
Soman et al. (2012) ZPR PEG SLA In vitro hMSCs 1 week Zero Poisson‘s ratio (ZPR) material PEG has been printed to generate 3D printed scaffolds. The hMSCs adhere and proliferate well.
Grogan et al. (2013) GelMA SLA In vitro Ex vivo human avascular zone meniscus cells; Human meniscus ex vivo repair model 6 weeks Micropatterned GelMA scaffolds are non-toxic, produce organized cellular alignment, and promote meniscus-like tissue formation.
Mannoor et al. (2013) Alginate, silicon, (AgNP infused) syringe extrusion In vitro Chondrocytes (articular cartilage of calves) 10 weeks The ears are cultured in vitro for 10 weeks. Audio signals are received by the bionic ears.
Lee et al. (2013) PCL, hyaluronic acid, gelatin SLS In vitro Chondrocytes (New Zealand white rabbit) 4 weeks This study successfully forms a soft/hard bi-phase scaffold, which offers a better environment for producing more proteins.
Xu et al. (2013) PCL, FN, Collagen Inkjet, Electrospun In vitro In vivo Rabbit elastic chondrocytes; Immunodeficient mice subcutaneous model 8 weeks The hybrid electrospinning/inkjet printing technique simplifies production of complex tissues.
Schuller-Ravoo et al. (2013) PTMC SLA In vitro Bovine chondrocytes 6 weeks The compression moduli of the constructed cartilage increases 50% to approximately 100 kPa.
Gao et al. (2014) PEG Inkjet, UV In vitro human chondrocytes 4 weeks Printed neocartilage demonstrated excellent glycosaminoglycan (GAG) and collagen II production with consistented gene expression.
Pati et al. (2015) dECM, PCL Extrusion, FDM In vitro hASCs hTMSCs 2 weeks Tissue-specific dECM bioinks achieve high cell viability and functionality.
Chen et al. (2014) PCL (coating with collagne) SLS In vivo Subdermally dorsal model of female nude mice 8 week Collagen as a surface modification material is superior to gelatin in supporting cells growth and stimulating ECM protein secretion.
Chang et al. (2014) PCL FDM In vivo Rabbit half-pipe-shaped tracheal defect. Rabbit MSCs 8 weeks The 3DP scaffold with fibrin/MSCs served as a resorbable, chondro-productive, and proper cartilage regeneration strategy.
Zhang et al. (2014) PEG/ β-TCP SLA & hydrogel In vivo Rabbit trochlea critical size osteochondral defects. 52 weeks The repaired subchondral bone formed from 16 to 52 weeks in a “flow like” manner from surrounding bone to the defect center gradually.
Yao et al. (2015) PCL/HA FDM in vitro in vivo Bone marrow clots and BMSC from 30 female New Zealand white rabbits (5-6 months old). 60 Female nude mice (6-7 weeks old). 4 weeks Combination with MC is a highly efficient, reliable, and simple method that improves the biological performance of 3D PCL/HA scaffold.
Zopf et al. (2015) PCL SLA In vitro In vivo Yorkshire pigs Supraperichondrial soft tissue flaps 2 months The histological evidence present that anatomically PCL based ear and nose resulted in the growth and maintenance of cartilage-like tissue.