Three-dimensional bioprinting is an innovative technique in tissue engineering, to create layer-by-layer structures, required for mimicking body tissues. However, synthetic bioinks do not generally possess high printability and biocompatibility at the same time. So, there is an urgent need for naturally derived bioinks that can exhibit such optimized properties. We used furfuryl-gelatin as a novel, visible-light crosslinkable bioink for fabricating cell-laden structures with high viability. Hyaluronic acid was added as a viscosity enhancer and either Rose Bengal or Riboflavin was used as a visible-light crosslinker. Crosslinking was done by exposing the printed structure for 2.5 min to visible light and confirmed using Fourier transform infrared spectroscopy and rheometry. Scanning electron microscopy revealed a highly porous networked structure. Three different cell types were successfully bioprinted within these constructs. Mouse mesenchymal stem cells printed within monolayer and bilayer sheets showed viability, network formation and proliferation (∼5.33 times) within 72 h of culture. C2C12 and STO cells were used to print a double layered structure, which showed evidence of the viability of both cells and heterocellular clusters within the construct. This furfuryl-gelatin based bioink can be used for tissue engineering of complex tissues and help in understanding how cellular crosstalk happens in vivo during normal or diseased pathology. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2018.

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We elucidate here process-structure-property relationships in implantable biomaterials processed by rapid prototyping approaches that are based on the principle of additive manufacturing. The conventional methods of fabrication of biomedical devices including freeze casting and sintering are limited because of difficulties in adaptation at the host site and mismatch in micro/ macrostructure, mechanical and physical properties with the host tissue. Moreover, additive manufacturing has the advantage of fabricating patient-specific designs, which can be obtained from the computed tomography scan of the defect site. The discussion here comprises two partsthe first part briefly describes the evolution and underlying reasons that have led to 3D printing of scaffolds for tissue regeneration. The second part focuses on biocompatibility and mechanical properties of 3D scaffolds, fabricated by different approaches. The article concludes with a discussion on functionally graded scaffolds and vascularisation of 3D porous scaffolds that are envisaged to meet the requirements of the biomedical industry. In general, the mechanical properties of 3D printed scaffolds are governed by pore architecture, pore volume and percentage porosity. To ensure long-term endurance and the ability to withstand abrupt impact, it is important that the fabricated materials have a good combination of strength and energy absorption capability. While scaffolds with high interconnected porosity are preferred for tissue regeneration, such structures lack adequate mechanical strength and energy absorption capability. These mutually opposing requirements of high porosity and mechanical strength in conjunction with high energy absorption have hindered the application of 3D scaffolds as biomedical devices. In this regard, functionally graded 3D structures with high strength and energy absorption are potentially attractive for biomedical devices.

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