TY - JOUR
T1 - 3D-printed microgels supplemented with dentin matrix molecules as a novel biomaterial for direct pulp capping
AU - Cunha, Diana
AU - Souza, Nayara
AU - Moreira, Manuela
AU - Rodrigues, Nara
AU - Silva, Paulo
AU - Franca, Cristiane
AU - Horsophonphong, Sivaporn
AU - Sercia, Ashley
AU - Subbiah, Ramesh
AU - Tahayeri, Anthony
AU - Ferracane, Jack
AU - Yelick, Pamela
AU - Saboia, Vicente
AU - Bertassoni, Luiz
N1 - Funding Information:
This project was supported by funding from the National Institute of Dental and Craniofacial Research (NIDCR) R01DE026170 (to LB) and 3R01DE026170-03S1 (to LB), NIDCR/NIBIB R01DE026731 (to PY), the OHSU-Mahidol University cooperation agreement (to SH), the Oregon Clinical & Translational Research Institute (OCTRI)—Biomedical Innovation Program (BIP), the Michigan-Pittsburgh-Wyss Resource Center – Regenerative Medicine Resource Center (MPW-RM), Conselho Nacional de Desenvolvimento Científico e Tecnológico – CNPq (Proc. Proc. 306464/2016–0 and 423833/2018–9) (to VS).
Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2023/3
Y1 - 2023/3
N2 - Objectives: To develop a 3D-printed, microparticulate hydrogel supplemented with dentin matrix molecules (DMM) as a novel regenerative strategy for dental pulp capping. Materials and methods: Gelatin methacryloyl microgels (7% w/v) mixed with varying concentrations of DMM were printed using a digital light projection 3D printer and lyophilized for 2 days. The release profile of the DMM-loaded microgels was measured using a bicinchoninic acid assay. Next, dental pulp exposure defects were created in maxillary first molars of Wistar rats. The exposures were randomly capped with (1) inert material − negative control, (2) microgels, (3) microgels + DMM 500 µg/ml, (4) microgels + DMM 1000 µg/ml, (5) microgels + platelet-derived growth factor (PDGF 10 ng/ml), or (6) MTA (n = 15/group). After 4 weeks, animals were euthanized, and treated molars were harvested and then processed to evaluate hard tissue deposition, pulp tissue organization, and blood vessel density. Results: All the specimens from groups treated with microgel + 500 µg/ml, microgel + 1000 µg/ml, microgel + PDGF, and MTA showed the formation of organized pulp tissue, tertiary dentin, newly formed tubular and atubular dentin, and new blood vessel formation. Dentin bridge formation was greater and pulp necrosis was less in the microgel + DMM groups compared to MTA. Conclusions: The 3D-printed photocurable microgels doped with DMM exhibited favorable cellular and inflammatory pulp responses, and significantly more tertiary dentin deposition. Clinical relevance: 3D-printed microgel with DMM is a promising biomaterial for dentin and dental pulp regeneration in pulp capping procedures.
AB - Objectives: To develop a 3D-printed, microparticulate hydrogel supplemented with dentin matrix molecules (DMM) as a novel regenerative strategy for dental pulp capping. Materials and methods: Gelatin methacryloyl microgels (7% w/v) mixed with varying concentrations of DMM were printed using a digital light projection 3D printer and lyophilized for 2 days. The release profile of the DMM-loaded microgels was measured using a bicinchoninic acid assay. Next, dental pulp exposure defects were created in maxillary first molars of Wistar rats. The exposures were randomly capped with (1) inert material − negative control, (2) microgels, (3) microgels + DMM 500 µg/ml, (4) microgels + DMM 1000 µg/ml, (5) microgels + platelet-derived growth factor (PDGF 10 ng/ml), or (6) MTA (n = 15/group). After 4 weeks, animals were euthanized, and treated molars were harvested and then processed to evaluate hard tissue deposition, pulp tissue organization, and blood vessel density. Results: All the specimens from groups treated with microgel + 500 µg/ml, microgel + 1000 µg/ml, microgel + PDGF, and MTA showed the formation of organized pulp tissue, tertiary dentin, newly formed tubular and atubular dentin, and new blood vessel formation. Dentin bridge formation was greater and pulp necrosis was less in the microgel + DMM groups compared to MTA. Conclusions: The 3D-printed photocurable microgels doped with DMM exhibited favorable cellular and inflammatory pulp responses, and significantly more tertiary dentin deposition. Clinical relevance: 3D-printed microgel with DMM is a promising biomaterial for dentin and dental pulp regeneration in pulp capping procedures.
KW - 3D printing
KW - Dental pulp capping
KW - Dentin matrix components
KW - Hydrogel
KW - MTA
KW - Tissue engineering
UR - http://www.scopus.com/inward/record.url?scp=85140654264&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85140654264&partnerID=8YFLogxK
U2 - 10.1007/s00784-022-04735-z
DO - 10.1007/s00784-022-04735-z
M3 - Article
C2 - 36287273
AN - SCOPUS:85140654264
SN - 1432-6981
VL - 27
SP - 1215
EP - 1225
JO - Clinical oral investigations
JF - Clinical oral investigations
IS - 3
ER -