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3D Bioprinting of Multi-Material Decellularized Liver Matrix Hydrogel at Physiological Temperatures

Khati, Vamakshi (författare)
KTH,Nanobioteknologi,Science for Life Laboratory, SciLifeLab
Ramachandraiah, Harisha (författare)
Biopr AB, S-17165 Solna, Sweden.
Pati, Falguni (författare)
Indian Inst Technol Hyderabad, Dept Biomed Engn, Kandi 502285, India.
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Svahn Andersson, Helene (författare)
KTH,Nanobioteknologi,Science for Life Laboratory, SciLifeLab
Gaudenzi, Giulia (författare)
Karolinska Institutet,KTH,Nanobioteknologi,Science for Life Laboratory, SciLifeLab,Department of Global Public Health, Karolinska Institute, 17165 Solna, Sweden
Russom, Aman, Prof. 1976- (författare)
KTH,Nanobioteknologi,Science for Life Laboratory, SciLifeLab,AIMES—Center for the Advancement of Integrated Medical and Engineering Sciences, Karolinska Institute and KTH Royal Institute of Technology, 11428 Stockholm, Sweden
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 (creator_code:org_t)
2022-07-13
2022
Engelska.
Ingår i: Biosensors. - : MDPI AG. - 2079-6374. ; 12:7
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Bioprinting is an acclaimed technique that allows the scaling of 3D architectures in an organized pattern but suffers from a scarcity of appropriate bioinks. Decellularized extracellular matrix (dECM) from xenogeneic species has garnered support as a biomaterial to promote tissue-specific regeneration and repair. The prospect of developing dECM-based 3D artificial tissue is impeded by its inherent low mechanical properties. In recent years, 3D bioprinting of dECM-based bioinks modified with additional scaffolds has advanced the development of load-bearing constructs. However, previous attempts using dECM were limited to low-temperature bioprinting, which is not favorable for a longer print duration with cells. Here, we report the development of a multi-material decellularized liver matrix (dLM) bioink reinforced with gelatin and polyethylene glycol to improve rheology, extrudability, and mechanical stability. This shear-thinning bioink facilitated extrusion-based bioprinting at 37 degrees C with HepG2 cells into a 3D grid structure with a further enhancement for long-term applications by enzymatic crosslinking with mushroom tyrosinase. The heavily crosslinked structure showed a 16-fold increase in viscosity (2.73 Pa s(-1)) and a 32-fold increase in storage modulus from the non-crosslinked dLM while retaining high cell viability (85-93%) and liver-specific functions. Our results show that the cytocompatible crosslinking of dLM bioink at physiological temperatures has promising applications for extended 3D-printing procedures.

Ämnesord

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

Nyckelord

decellularized liver matrix bioink
bioprinting at physiological temperatures
cytocompatible crosslinking
robust bioink
viscoelasticity

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