Nanostructured Pluronic hydrogels as bioinks for 3D bioprinting

被引:280
作者
Mueller, Michael [1 ]
Becher, Jana [2 ]
Schnabelrauch, Matthias [2 ]
Zenobi-Wong, Marcy [1 ]
机构
[1] ETH, Cartilage Engn Regenerat Lab, CH-8093 Zurich, Switzerland
[2] INNOVENT eV Jena, Biomat Dept, D-07745 Jena, Germany
关键词
bioprinting; tissue engineering; thermoresponsive polymer; Pluronic; nanostructuring; CHONDROGENIC DIFFERENTIATION; HYALURONIC-ACID; STEM-CELLS; TISSUE; CARTILAGE; CHONDROCYTES; ALGINATE; CULTURE; CONSTRUCTS; COPOLYMERS;
D O I
10.1088/1758-5090/7/3/035006
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Bioprinting is an emerging technology in the field of tissue engineering as it allows the precise positioning of biologically relevant materials in 3D, which more resembles the native tissue in our body than current homogenous, bulk approaches. There is however a lack of materials to be used with this technology and materials such as the block copolymer Pluronic have good printing properties but do not allow long-term cell culture. Here we present an approach called nanostructuring to increase the biocompatibility of Pluronic gels at printable concentrations. By mixing acrylated with unmodified Pluronic F127 it was possible to maintain the excellent printing properties of Pluronic and to create stable gels via UV crosslinking. By subsequent elution of the unmodified Pluronic from the crosslinked network we were able to increase the cell viability of encapsulated chondrocytes at day 14 from 62% for a pure acrylated Pluronic hydrogel to 86% for a nanostructured hydrogel. The mixed Pluronic gels also showed good printability when cells where included in the bioink. The nanostructured gels were, with a compressive modulus of 1.42 kPa, mechanically weak, but we were able to increase the mechanical properties by the addition of methacrylated hyaluronic acid. Our nanostructuring approach enables Pluronic hydrogels to have the desired set of properties in all stages of the bioprinting process.
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页数:17
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共 60 条
[1]   A bioresponsive hydrogel tuned to chondrogenesis of human mesenchymal stem cells [J].
Bahney, Chelsea S. ;
Hsu, Chih-Wei ;
Yoo, Jung U. ;
West, Jennifer L. ;
Johnstone, Brian .
FASEB JOURNAL, 2011, 25 (05) :1486-1496
[2]   Biopolymer-Based Hydrogels for Cartilage Tissue Engineering [J].
Balakrishnan, Biji ;
Banerjee, R. .
CHEMICAL REVIEWS, 2011, 111 (08) :4453-4474
[3]   Optimal structure requirements for pluronic block copolymers in modifying P-glycoprotein drug efflux transporter activity in bovine brain microvessel endothelial cells [J].
Batrakova, EV ;
Li, S ;
Alakhov, VY ;
Miller, DW ;
Kabanov, AV .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 304 (02) :845-854
[4]   The 3D printing of gelatin methacrylamide cell-laden tissue-engineered constructs with high cell viability [J].
Billiet, Thomas ;
Gevaert, Elien ;
De Schryver, Thomas ;
Cornelissen, Maria ;
Dubruel, Peter .
BIOMATERIALS, 2014, 35 (01) :49-62
[5]  
Bohner M, 2002, J BIOMAT SCI-POLYM E, V13, P733
[6]   Crosslinking density influences chondrocyte metabolism in dynamically loaded photocrosslinked poly(ethylene glycol) hydrogels [J].
Bryant, SJ ;
Chowdhury, TT ;
Lee, DA ;
Bader, DL ;
Anseth, KS .
ANNALS OF BIOMEDICAL ENGINEERING, 2004, 32 (03) :407-417
[7]   Encapsulating Chondrocytes in degrading PEG hydrogels with high modulus: Engineering gel structural changes to facilitate cartilaginous tissue production [J].
Bryant, SJ ;
Bender, RJ ;
Durand, KL ;
Anseth, KS .
BIOTECHNOLOGY AND BIOENGINEERING, 2004, 86 (07) :747-755
[8]   Hydrogel properties influence ECM production by chondrocytes photoencapsulated in poly(ethylene glycol) hydrogels [J].
Bryant, SJ ;
Anseth, KS .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 59 (01) :63-72
[9]  
Cao YL, 1998, J BIOMAT SCI-POLYM E, V9, P475
[10]   Technology insight: Adult stem cells in cartilage regeneration and tissue engineering [J].
Chen, Faye H. ;
Rousche, Kathleen T. ;
Tuan, Rocky S. .
NATURE CLINICAL PRACTICE RHEUMATOLOGY, 2006, 2 (07) :373-382