| Literature DB >> 33586366 |
Nanditha Anandakrishnan1, Hang Ye2, Zipeng Guo2, Zhaowei Chen1, Kyle I Mentkowski1,3, Jennifer K Lang1,3,4, Nika Rajabian5, Stelios T Andreadis1,5, Zhen Ma6, Joseph A Spernyak7, Jonathan F Lovell1, Depeng Wang1, Jun Xia1, Chi Zhou2, Ruogang Zhao1.
Abstract
Large size cell-laden hydrogel models hold great promise for tissue repair and organ transplantation, but their fabrication using 3D bioprinting is limited by the slow printing speed that can affect the part quality and the biological activity of the encapsulated cells. Here a fast hydrogel stereolithography printing (FLOAT) method is presented that allows the creation of a centimeter-sized, multiscale solid hydrogel model within minutes. Through precisely controlling the photopolymerization condition, low suction force-driven, high-velocity flow of the hydrogel prepolymer is established that supports the continuous replenishment of the prepolymer solution below the curing part and the nonstop part growth. The rapid printing of centimeter-sized hydrogel models using FLOAT is shown to significantly reduce the part deformation and cellular injury caused by the prolonged exposure to the environmental stresses in conventional 3D printing methods. Embedded vessel networks fabricated through multiscale printing allows media perfusion needed to maintain the high cellular viability and metabolic functions in the deep core of the large-sized models. The endothelialization of this vessel network allows the establishment of barrier functions. Together, these studies demonstrate a rapid 3D hydrogel printing method and represent a first step toward the fabrication of large-sized engineered tissue models.Entities:
Keywords: 3D bioprinting; continuous printing; endothelialization; hydrogels; stereolithography
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Year: 2021 PMID: 33586366 PMCID: PMC8212355 DOI: 10.1002/adhm.202002103
Source DB: PubMed Journal: Adv Healthc Mater ISSN: 2192-2640 Impact factor: 9.933