Multiscale Porosity in Compressible Cryogenically 3D Printed Gels for Bone Tissue Engineering

被引:63
作者
Gupta, Deepak [1 ]
Singh, Atul Kumar [2 ,3 ]
Dravid, Ashwin [1 ,4 ]
Bellare, Jayesh [1 ,2 ,5 ,6 ]
机构
[1] Indian Inst Technol, Dept Chem Engn, Mumbai 400076, Maharashtra, India
[2] Indian Inst Technol, Ctr Res Nanotechnol & Sci, Mumbai 400076, Maharashtra, India
[3] Indian Inst Technol Delhi, CRF, New Delhi 110016, India
[4] Johns Hopkins Univ, Chem & Biomol Engn, 323 E 33rd St, Baltimore, MD 21218 USA
[5] Indian Inst Technol, Tata Ctr Technol & Design, Mumbai 400076, Maharashtra, India
[6] Indian Inst Technol, WRCB, Mumbai 400076, Maharashtra, India
关键词
cryogenic 3D printing; hydrogel; bone tissue engineering; multiscale porosity; gelatin; carboxymethylchitin; hydroxyapatite; CARBOXYMETHYL-CHITOSAN; MECHANICAL-PROPERTIES; CELL-ADHESION; CROSS-LINKING; SCAFFOLDS; HYDROXYAPATITE; COMPOSITE; COLLAGEN; PROLIFERATION; FABRICATION;
D O I
10.1021/acsami.9b05460
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
Three-dimensional (3D) printing technology has seen several refinements when introduced in the field of medical devices and regenerative medicines. However, it is still a challenge to 3D print gels for building complex constructs as per the desired shape and size. Here, we present a novel method to 3D print gelatin/carboxymethylchitin/hydroxyapatite composite gel constructs of a complex shape. The objective of this study is to fabricate a bioactive gel scaffold with a controlled hierarchical structure. The hierarchy ranges from 3D outer shape to macroporosity to microporosity and rough surface. The fabrication process developed here uses 3D printing in a local cryogenic atmosphere, followed by lyophilization and cross-linking. The gel instantly freezes after extrusion on the cold plate. The cooling action is not limited to the build plate, but the entire gel scaffold is cooled during the 3D printing process. This enables the construction of a stable self-sustaining large-sized 3D complex geometry. Further, lyophilization introduces bulk microporosity into the scaffolds. The outer shape and macroporosity were controlled with the 3D printer, whereas the microporous structure and desirable rough surface morphology were obtained through lyophilization. With cryogenic 3D printing, up to 90% microporosity could be incorporated into the scaffolds. The microporosity and pore size distribution were controlled by changing the cross-linker and total polymer concentration, which resulted in six times increase in surface open pores of size <20 mu m on increasing the cross-linker concentration from 25 to 100 mg/mL. The introduction of bulk microporosity was shown to increase swelling by 1.8 times along with a significant increase in human umbilical cord mesenchymal stem cells and Saos-2 cell attachment (2x), proliferation (2.4x), Saos-2 cell alkaline phosphatase level (2x), and mineralization (3x). The scaffolds are spongy in nature in a wet state, thus making them potential implants for bone cavities with a small opening. The application of these cryogenically 3D printed compressible gel scaffolds with multiscale porosity extends to a small- as well as a large-sized open/partially open patient-specific bone defect.
引用
收藏
页码:20437 / 20452
页数:16
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