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Droplet bioprinting of acellular and cell-laden structures at high-resolutions.
Kunwar, Puskal; Aryal, Ujjwal; Poudel, Arun; Fougnier, Daniel; Geffert, Zachary J; Xie, Rui; Li, Zhen; Soman, Pranav.
Afiliación
  • Kunwar P; Biomedical, and Chemical Engineering Department, Syracuse University, Syracuse, NY 13210, United States of America.
  • Aryal U; BioInspired Institute, Syracuse, NY 13210, United States of America.
  • Poudel A; Biomedical, and Chemical Engineering Department, Syracuse University, Syracuse, NY 13210, United States of America.
  • Fougnier D; BioInspired Institute, Syracuse, NY 13210, United States of America.
  • Geffert ZJ; Biomedical, and Chemical Engineering Department, Syracuse University, Syracuse, NY 13210, United States of America.
  • Xie R; BioInspired Institute, Syracuse, NY 13210, United States of America.
  • Li Z; Biomedical, and Chemical Engineering Department, Syracuse University, Syracuse, NY 13210, United States of America.
  • Soman P; BioInspired Institute, Syracuse, NY 13210, United States of America.
Biofabrication ; 16(3)2024 May 23.
Article en En | MEDLINE | ID: mdl-38749419
ABSTRACT
Advances in digital light projection(DLP) based (bio) printers have made printing of intricate structures at high resolution possible using a wide range of photosensitive bioinks. A typical setup of a DLP bioprinter includes a vat or reservoir filled with liquid bioink, which presents challenges in terms of cost associated with bioink synthesis, high waste, and gravity-induced cell settling, contaminations, or variation in bioink viscosity during the printing process. Here, we report a vat-free, low-volume, waste-free droplet bioprinting method capable of rapidly printing 3D soft structures at high resolution using model bioinks and model cells. A multiphase many-body dissipative particle dynamics model was developed to simulate the dynamic process of droplet-based DLP printing and elucidate the roles of surface wettability and bioink viscosity. Process variables such as light intensity, photo-initiator concentration, and bioink formulations were optimized to print 3D soft structures (∼0.4-3 kPa) with a typical layer thickness of 50µm, an XY resolution of 38 ± 1.5µm and Z resolution of 237 ± 5.4µm. To demonstrate its versatility, droplet bioprinting was used to print a range of acellular 3D structures such as a lattice cube, a Mayan pyramid, a heart-shaped structure, and a microfluidic chip with endothelialized channels. Droplet bioprinting, performed using model C3H/10T1/2 cells, exhibited high viability (90%) and cell spreading. Additionally, microfluidic devices with internal channel networks lined with endothelial cells showed robust monolayer formation while osteoblast-laden constructs showed mineral deposition upon osteogenic induction. Overall, droplet bioprinting could be a low-cost, no-waste, easy-to-use, method to make customized bioprinted constructs for a range of biomedical applications.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bioimpresión / Impresión Tridimensional Límite: Animals / Humans Idioma: En Revista: Biofabrication Asunto de la revista: BIOTECNOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Bioimpresión / Impresión Tridimensional Límite: Animals / Humans Idioma: En Revista: Biofabrication Asunto de la revista: BIOTECNOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido