Abstract

Scaffolds used to receive stem cells are a promising perspective of tissue regeneration research, and one of the most effective solutions to rebuild organs. In the near future will be possible to reconstruct a natural tooth using stems cells, but to avoid an immune-defensive response, sterilize the scaffold is not only desired, but also essential to be successful. A study confirmed stem cells extracted from rat’s natural teeth, and implanted into the alveolar bone, could differentiate themselves in dental cells, but the scaffold’s chemistry, geometry, density, morphology, adherence, biocompatibility and mechanical properties remained an issue. This study intended to produce a completely sterilized dental scaffold with preserved extracellular matrix. Fifty-one samples were collected, kept in formaldehyde, submitted to partial demineralization and decellularization processes and sterilized using four different methods: dry heating; autoclave; ethylene-oxide and gamma-radiation. They were characterized through optical images, micro-hardness, XRD, EDS, XRF, SEM, histology and sterility test. The results evidenced the four sterilization methods were fully effective with preservation of ECM molecular arrangements, variation on chemical composition (proportion of Ca/P) was compatible with Ca/P proportional variation between enamel and dentine regions. Gamma irradiation and ethylene oxide presents excellent results, but their viability are compromised by the costs and technology’s accessibility (requires very expensive equipment and/or consumables). Excepted gamma irradiation, all the sterilization methods more than sterilizing also reduced the remaining pulp. Autoclave presents easy equipment accessibility, lower cost consumables, higher reduction of remaining pulp and complete sterilization, reason why was considered the most promising technique.

Highlights

  • Scaffolds used to receive stem cells are a promising perspective of tissue regeneration research, and one of the most effective solutions to rebuild organs

  • The control group presented micro-hardness slightly below indicated by Garcia-Garcia[41] (45.69, varying from 38 to 53HVN), GD5 presented the expected hardness (69.53, varying from 50 to 67HVN), GD2 (69.53 HVN), GD3 (70.61 HVN) and GD1 (77.55 HVN) these results, associated to statistical validation indicates the sterilization method interfere directly on the micro-hardness of teeth, it is important to confirm if this hardness increase can interfere on cell adhesion or not

  • The results suggest the influence of temperature and pressure variation on reduction of remaining pulp

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Summary

Introduction

Scaffolds used to receive stem cells are a promising perspective of tissue regeneration research, and one of the most effective solutions to rebuild organs. Ceramic scaffolds exhibit excellent biocompatibility, due to similarity with hydroxyapatite (HA), the applications are limited by the brittleness and difficulty to sharp, in addition new bone formed in a porous HA cannot sustain the mechanical loading needed for remodeling or the compressive forces on chewing (near 700 N)[10]. These difficulties in terms of structure, functionality and mechanical properties, when producing scaffolds from single phase biomaterial, encouraged research with composite materials, as ceramic-polymer or metal-ceramic based s­ caffolds[11–13]. Additional care need to be taken with sterilization, to avoid infection and r­ ejection[19–21]

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