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Conference Paper: Proteomic evaluation of salivary acquired pellicle on restorative material surfaces
Title | Proteomic evaluation of salivary acquired pellicle on restorative material surfaces |
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Authors | |
Issue Date | 2016 |
Publisher | Sage Publications, Inc. The Journal's web site is located at http://jdr.sagepub.com/ |
Citation | The 94th General Session & Exhibition of the IADR, 3rd Meeting of the IADR Asia Pacific Region & 35th Annual Meeting of the IADR Korean Division, Seoul, Korea, 22-25 June 2016. In Journal of Dental Research, 2016, v. 95 Spec. Iss. B, abstract no. 173 How to Cite? |
Abstract | OBJECTIVES: The aim of this study was to analyze salivary protein adsorption behavior onto restorative material surfaces. It was hypothesized that the acquired pellicle formation is material dependent. METHODS: Dental restorative material specimen blocks were prepared of (5×5×1 mm, n=20 each) nano-hybrid resin composite, glass ionomer cements (GIC), resin-modified GIC, GIC containing casein phosphopeptide–amorphous calcium phosphate (CPP-ACP), or human dentine. All specimen surfaces were polished with 1200-grit abrasive paper. The material surface micro morphology and surface roughness (100×100 µm2, n=10) were measured with atomic-force microscopy. After alcohol disinfection, all specimens were incubated in unstimulated, filtered, sterilized saliva for two hours at 37°C. The quantity of adsorbed protein on each material specimen was measured using a bicinchoninic acid assay. Relative acquire pellicle proteomics for each material group was characterized using liquid chromatography – mass spectrometry (LC-MS/MS). Institutional Review Aboard approval was obtained for saliva collection. RESULTS: The surfaces of polished resin-modified GIC, GIC and GIC containing CPP-ACP exhibited a greater micro surface roughness than resin composite or human dentin (P<0.05). The quantity of protein adsorbed varied between materials, with the resin composite (5.74 µg/specimen) and resin-modified GIC (4.67 µg/specimen) adsorbing the most protein (P<0.01), no significant differences were found between dentin (2.74 µg/specimen), GIC containing CPP-ACP (2.15 µg/specimen), and GIC (1.99 µg/specimen). CONCLUSIONS: The data demonstrated that there are noteworthy variations among acquired pellicles protein quantity and in a subtle fashion quality on various material surfaces, which may affect the subsequent biofilm formation on restorative surfaces. |
Description | Oral Session - Biofunctionalization & Biological Effects of Dental Material Surfaces: no. 173 |
Persistent Identifier | http://hdl.handle.net/10722/227499 |
ISSN | 2023 Impact Factor: 5.7 2023 SCImago Journal Rankings: 1.909 |
DC Field | Value | Language |
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dc.contributor.author | Wei, CX | - |
dc.contributor.author | Burrow, M | - |
dc.contributor.author | Botelho, MG | - |
dc.contributor.author | Leung, WK | - |
dc.date.accessioned | 2016-07-18T09:11:04Z | - |
dc.date.available | 2016-07-18T09:11:04Z | - |
dc.date.issued | 2016 | - |
dc.identifier.citation | The 94th General Session & Exhibition of the IADR, 3rd Meeting of the IADR Asia Pacific Region & 35th Annual Meeting of the IADR Korean Division, Seoul, Korea, 22-25 June 2016. In Journal of Dental Research, 2016, v. 95 Spec. Iss. B, abstract no. 173 | - |
dc.identifier.issn | 0022-0345 | - |
dc.identifier.uri | http://hdl.handle.net/10722/227499 | - |
dc.description | Oral Session - Biofunctionalization & Biological Effects of Dental Material Surfaces: no. 173 | - |
dc.description.abstract | OBJECTIVES: The aim of this study was to analyze salivary protein adsorption behavior onto restorative material surfaces. It was hypothesized that the acquired pellicle formation is material dependent. METHODS: Dental restorative material specimen blocks were prepared of (5×5×1 mm, n=20 each) nano-hybrid resin composite, glass ionomer cements (GIC), resin-modified GIC, GIC containing casein phosphopeptide–amorphous calcium phosphate (CPP-ACP), or human dentine. All specimen surfaces were polished with 1200-grit abrasive paper. The material surface micro morphology and surface roughness (100×100 µm2, n=10) were measured with atomic-force microscopy. After alcohol disinfection, all specimens were incubated in unstimulated, filtered, sterilized saliva for two hours at 37°C. The quantity of adsorbed protein on each material specimen was measured using a bicinchoninic acid assay. Relative acquire pellicle proteomics for each material group was characterized using liquid chromatography – mass spectrometry (LC-MS/MS). Institutional Review Aboard approval was obtained for saliva collection. RESULTS: The surfaces of polished resin-modified GIC, GIC and GIC containing CPP-ACP exhibited a greater micro surface roughness than resin composite or human dentin (P<0.05). The quantity of protein adsorbed varied between materials, with the resin composite (5.74 µg/specimen) and resin-modified GIC (4.67 µg/specimen) adsorbing the most protein (P<0.01), no significant differences were found between dentin (2.74 µg/specimen), GIC containing CPP-ACP (2.15 µg/specimen), and GIC (1.99 µg/specimen). CONCLUSIONS: The data demonstrated that there are noteworthy variations among acquired pellicles protein quantity and in a subtle fashion quality on various material surfaces, which may affect the subsequent biofilm formation on restorative surfaces. | - |
dc.language | eng | - |
dc.publisher | Sage Publications, Inc. The Journal's web site is located at http://jdr.sagepub.com/ | - |
dc.relation.ispartof | Journal of Dental Research | - |
dc.rights | Journal of Dental Research. Copyright © Sage Publications, Inc. | - |
dc.title | Proteomic evaluation of salivary acquired pellicle on restorative material surfaces | - |
dc.type | Conference_Paper | - |
dc.identifier.email | Botelho, MG: botelho@hkucc.hku.hk | - |
dc.identifier.email | Leung, WK: ewkleung@hkucc.hku.hk | - |
dc.identifier.authority | Botelho, MG=rp00033 | - |
dc.identifier.authority | Leung, WK=rp00019 | - |
dc.identifier.hkuros | 259742 | - |
dc.identifier.volume | 95 | - |
dc.identifier.issue | Spec. Iss. B | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0022-0345 | - |