4.8 Article

3D printing of mechanically functional meniscal tissue equivalents using high concentration extracellular matrix inks

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MATERIALS TODAY BIO
卷 20, 期 -, 页码 -

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DOI: 10.1016/j.mtbio.2023.100624

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Decellularization; ECM; Meniscus; Ink; 3D printing; Collagen alignment

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Decellularized extracellular matrix (dECM) is a promising biomaterial for tissue engineering and regenerative medicine. This study successfully produced highly concentrated dECM inks with improved mechanical properties through different solubilization and decellularization methods. The 3D printing of these dECM inks at higher pH levels enabled the fabrication of anatomically defined meniscal implants with compressive mechanical properties similar to native tissue. These findings demonstrate the potential of 3D printing of highly concentrated dECM inks for meniscal tissue regeneration and have applications in tissue engineering and surgical planning.
Decellularized extracellular matrix (dECM) has emerged as a promising biomaterial in the fields of tissue engineering and regenerative medicine due to its ability to provide specific biochemical and biophysical cues supportive of the regeneration of diverse tissue types. Such biomaterials have also been used to produce tissuespecific inks and bioinks for 3D printing applications. However, a major limitation associated with the use of such dECM materials is their poor mechanical properties, which limits their use in load-bearing applications such as meniscus regeneration. In this study, native porcine menisci were solubilized and decellularized using different methods to produce highly concentrated dECM inks of differing biochemical content and printability. All dECM inks displayed shear thinning and thixotropic properties, with increased viscosity and improved printability observed at higher pH levels, enabling the 3D printing of anatomically defined meniscal implants. With additional crosslinking of the dECM inks following thermal gelation at pH 11, it was possible to fabricate highly elastic meniscal tissue equivalents with compressive mechanical properties similar to the native tissue. These improved mechanical properties at higher pH correlated with the development of a denser network of smaller diameter collagen fibers. These constructs also displayed repeatable loading and unloading curves when subjected to longterm cyclic compression tests. Moreover, the printing of dECM inks at the appropriate pH promoted a preferential alignment of the collagen fibers. Altogether, these findings demonstrate the potential of 3D printing of highly concentrated meniscus dECM inks to produce mechanically functional and biocompatible implants for meniscal tissue regeneration. This approach could be applied to a wide variety of different biological tissues, enabling the 3D printing of tissue mimics with diverse applications from tissue engineering to surgical planning.

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