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Citation: Kollmuss, Maximilian and Edelhoff, Daniel and Schwendicke, Falk and Wuersching, Sabina Noreen: In vitro cytotoxic and inflammatory response of gingival fibroblasts and oral mucosal keratinocytes to 3D printed oral devices. 30. April 2024. Open Data LMU. 10.5282/ubm/data.480

In vitro cytotoxic and inflammatory response of gingival fibroblasts and oral mucosal keratinocytes to 3D printed oral devices
In vitro cytotoxic and inflammatory response of gingival fibroblasts and oral mucosal keratinocytes to 3D printed oral devices

The purpose of this study was to examine the biocompatibility of 3D printed materials used for additive manufacturing of rigid and flexible oral devices. Oral splints were produced and finished from six printable resins (pairs of rigid/flexible materials: KeySplint Hard [KR], KeySplint Soft [KF], V-Print Splint [VR], V-Print Splint Comfort [VF], NextDent Ortho Rigid [NR], NextDent Ortho Flex [NF]), and two types of PMMA blocks for subtractive manufacturing (Tizian Blank PMMA [TR], Tizian Flex Splint Comfort [TF]) as controls. The specimens were eluted in a cell culture medium for 7d. Human gingival fibroblasts (hGF-1) and human oral mucosal keratinocytes (hOK) were exposed to the eluates for 24 h. Cell viability, glutathione levels, apoptosis, necrosis, the cellular inflammatory response (IL-6 and PGE2 secretion), and cell morphology were assessed. All eluates led to a slight reduction of hGF-1 viability and intracellular glutathione levels. The strongest cytotoxic response of hGF-1 was observed with KF, NF, and NR eluates (p < 0.05 compared to unexposed cells). Viability, caspase-3/7 activity, necrosis levels, and IL-6/PGE2 secretion of hOK were barely affected by the materials. All materials showed an overall acceptable biocompatibility. hOK appeared to be more resilient to noxious agents than hGF-1 in vitro. There is insufficient evidence to generalize that flexible materials are more cytotoxic than rigid materials. From a biological point of view, 3D printing seems to be a viable alternative to milling for producing oral devices.

3D-printing, oral splints, cytotoxicity
Kollmuss, Maximilian
Edelhoff, Daniel
Schwendicke, Falk
Wuersching, Sabina Noreen
2024

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DOI: 10.5282/ubm/data.480

This dataset is available unter the terms of the following Creative Commons LicenseCC BY 4.0

Abstract

The purpose of this study was to examine the biocompatibility of 3D printed materials used for additive manufacturing of rigid and flexible oral devices. Oral splints were produced and finished from six printable resins (pairs of rigid/flexible materials: KeySplint Hard [KR], KeySplint Soft [KF], V-Print Splint [VR], V-Print Splint Comfort [VF], NextDent Ortho Rigid [NR], NextDent Ortho Flex [NF]), and two types of PMMA blocks for subtractive manufacturing (Tizian Blank PMMA [TR], Tizian Flex Splint Comfort [TF]) as controls. The specimens were eluted in a cell culture medium for 7d. Human gingival fibroblasts (hGF-1) and human oral mucosal keratinocytes (hOK) were exposed to the eluates for 24 h. Cell viability, glutathione levels, apoptosis, necrosis, the cellular inflammatory response (IL-6 and PGE2 secretion), and cell morphology were assessed. All eluates led to a slight reduction of hGF-1 viability and intracellular glutathione levels. The strongest cytotoxic response of hGF-1 was observed with KF, NF, and NR eluates (p < 0.05 compared to unexposed cells). Viability, caspase-3/7 activity, necrosis levels, and IL-6/PGE2 secretion of hOK were barely affected by the materials. All materials showed an overall acceptable biocompatibility. hOK appeared to be more resilient to noxious agents than hGF-1 in vitro. There is insufficient evidence to generalize that flexible materials are more cytotoxic than rigid materials. From a biological point of view, 3D printing seems to be a viable alternative to milling for producing oral devices.

Uncontrolled Keywords

3D-printing, oral splints, cytotoxicity

References

Polymers 2024, 16(10), 1336; https://doi.org/10.3390/polym16101336

Item Type:Data
Contact Person:Kollmuss, Maximilian
E-Mail of Contact:maximilian.kollmuss at med.uni-muenchen.de
Subjects:Medicine
Dewey Decimal Classification:600 Technology, Medicine
600 Technology, Medicine > 610 Medical sciences and medicine
ID Code:480
Deposited By: PD Dr. Maximilian Kollmuß
Deposited On:13. May 2024 10:58
Last Modified:13. May 2024 10:58

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