TY - JOUR
T1 - Highly substituted decoupled gelatin methacrylamide free of hydrolabile methacrylate impurities
T2 - An optimum choice for long-term stability and cytocompatibility
AU - Niu, Xueming
AU - Ferracci, Gaia
AU - Lin, Mian
AU - Rong, Xiaona
AU - Zhu, Mengxiang
AU - Cho, Nam Joon
AU - Lee, Bae Hoon
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2021/1/15
Y1 - 2021/1/15
N2 - Gelatin methacryloyl (GelMA; GM) contains impurities, including hydrolabile photosensitive methacrylate groups or soluble methacrylic acid (MA), which could be potentially detrimental to its in vitro and in vivo applications. To date, the influence of GM photocurable side chains on the cytotoxicity and ambient structural stability has remained to be investigated. Here, we successfully separated highly substituted decoupled gelatin methacrylamide (DGM) from GM via removing methacrylate impurities in order to evaluate its stability, cell viability, and cell toxicity, compared to GM, DGM plus soluble MA, and soluble MA. The photocurable methacrylate groups in GM were hydrolytically labile in neutral solutions, changing into soluble MA over time; on the other hand, the photocurable methacrylamide groups in DGM remained intact under the same conditions. Soluble MA was found to decrease cell viability in a dose dependent manner and caused severe cell toxicity at above 10 mg/mL. DGM plus MA started to impair cell viability at a 25 mg/mL concentration. DGM exhibited excellent cell viability and little cell toxicity across the treated concentrations (0.1–25 mg/mL). DGM without hydrolabile methacrylate and cytotoxic MA impurities could be a better choice for long term stability and good cell compatibility for bioapplications including bioprinting and cell encapsulation.
AB - Gelatin methacryloyl (GelMA; GM) contains impurities, including hydrolabile photosensitive methacrylate groups or soluble methacrylic acid (MA), which could be potentially detrimental to its in vitro and in vivo applications. To date, the influence of GM photocurable side chains on the cytotoxicity and ambient structural stability has remained to be investigated. Here, we successfully separated highly substituted decoupled gelatin methacrylamide (DGM) from GM via removing methacrylate impurities in order to evaluate its stability, cell viability, and cell toxicity, compared to GM, DGM plus soluble MA, and soluble MA. The photocurable methacrylate groups in GM were hydrolytically labile in neutral solutions, changing into soluble MA over time; on the other hand, the photocurable methacrylamide groups in DGM remained intact under the same conditions. Soluble MA was found to decrease cell viability in a dose dependent manner and caused severe cell toxicity at above 10 mg/mL. DGM plus MA started to impair cell viability at a 25 mg/mL concentration. DGM exhibited excellent cell viability and little cell toxicity across the treated concentrations (0.1–25 mg/mL). DGM without hydrolabile methacrylate and cytotoxic MA impurities could be a better choice for long term stability and good cell compatibility for bioapplications including bioprinting and cell encapsulation.
KW - Cytocompatibility
KW - Decoupled gelatin methacrylamide
KW - Methacrylate impurities
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U2 - 10.1016/j.ijbiomac.2020.11.187
DO - 10.1016/j.ijbiomac.2020.11.187
M3 - Article
C2 - 33275977
AN - SCOPUS:85097467634
SN - 0141-8130
VL - 167
SP - 479
EP - 490
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
ER -