File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Transdentinal cytotoxicity and macrophage phenotype of a novel quaternary ammonium silane cavity disinfectant

TitleTransdentinal cytotoxicity and macrophage phenotype of a novel quaternary ammonium silane cavity disinfectant
Authors
KeywordsALP
Cell viability
Dentine
Fibroblasts
M1/M2
Issue Date2019
PublisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/dental
Citation
Dental Materials, 2019, v. 35 n. 2, p. 206-216 How to Cite?
AbstractObjective: To evaluate the transdentinal cytotoxicity and macrophage phenotype response to a novel quaternary ammonium silane (QAS) cavity disinfectant. Methods: NIH 3T3 mouse fibroblasts were cultured in Dulbecco's Modified Eagle's Medium and incubated for 3 days. The cells (3 × 104) were seeded on the pulpal side of dentine discs and the occlusal side of the discs were treated with different cavity disinfectants: Group 1: de-ionized water (control); Group 2: 2% chlorhexidine (CHX); Group 3: 2% QAS; Group 4: 5% QAS, and Group 5: 10% QAS. Cell morphology of NIH 3T3 cells was examined using scanning electron microscopy (SEM) and cell viability was assessed using Trypan blue assay. The eluates were collected and applied on cells seeded in 24-well plates. The total protein production, alkaline phosphatase activity and deposition of mineralized nodules were evaluated after 7 and 14 days. Immunofluorescence staining was performed on the samples with primary antibodies of CD68+, CD80+, and CD163+ assessing the macrophage M1/M2 phenotypes. The macrophages were imaged using a confocal scanning light microscope with an excitation wavelength of 488 nm. Results: No significant difference in cell viability (p < 0.0001), total protein production (p < 0.01) and mineralized nodule production (p < 0.05) was found between 2% QAS and the control, which was significantly higher than 2% CHX, 5% and 10% QAS after 14 days. Alkaline phosphatase production of 2% QAS was significantly lower than the control (p < 0.001), but higher than 2% CHX at 14 days. The M1/M2 macrophage ratio was also significantly lower in the 2% and 10% QAS groups (p < 0.05) compared to the control and 2% CHX groups. Significance: The 2% QAS cavity disinfectant does not have cytotoxic effects on 3T3 NIH mouse fibroblast cells and the predominance of the anti-inflammatory phenotype after its application may stimulate healing and tissue repair. © 2018 The Academy of Dental Materials
Persistent Identifierhttp://hdl.handle.net/10722/274805
ISSN
2021 Impact Factor: 5.687
2020 SCImago Journal Rankings: 1.770
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorDaood, U-
dc.contributor.authorYiu, CKY-
dc.date.accessioned2019-09-10T02:29:09Z-
dc.date.available2019-09-10T02:29:09Z-
dc.date.issued2019-
dc.identifier.citationDental Materials, 2019, v. 35 n. 2, p. 206-216-
dc.identifier.issn0109-5641-
dc.identifier.urihttp://hdl.handle.net/10722/274805-
dc.description.abstractObjective: To evaluate the transdentinal cytotoxicity and macrophage phenotype response to a novel quaternary ammonium silane (QAS) cavity disinfectant. Methods: NIH 3T3 mouse fibroblasts were cultured in Dulbecco's Modified Eagle's Medium and incubated for 3 days. The cells (3 × 104) were seeded on the pulpal side of dentine discs and the occlusal side of the discs were treated with different cavity disinfectants: Group 1: de-ionized water (control); Group 2: 2% chlorhexidine (CHX); Group 3: 2% QAS; Group 4: 5% QAS, and Group 5: 10% QAS. Cell morphology of NIH 3T3 cells was examined using scanning electron microscopy (SEM) and cell viability was assessed using Trypan blue assay. The eluates were collected and applied on cells seeded in 24-well plates. The total protein production, alkaline phosphatase activity and deposition of mineralized nodules were evaluated after 7 and 14 days. Immunofluorescence staining was performed on the samples with primary antibodies of CD68+, CD80+, and CD163+ assessing the macrophage M1/M2 phenotypes. The macrophages were imaged using a confocal scanning light microscope with an excitation wavelength of 488 nm. Results: No significant difference in cell viability (p < 0.0001), total protein production (p < 0.01) and mineralized nodule production (p < 0.05) was found between 2% QAS and the control, which was significantly higher than 2% CHX, 5% and 10% QAS after 14 days. Alkaline phosphatase production of 2% QAS was significantly lower than the control (p < 0.001), but higher than 2% CHX at 14 days. The M1/M2 macrophage ratio was also significantly lower in the 2% and 10% QAS groups (p < 0.05) compared to the control and 2% CHX groups. Significance: The 2% QAS cavity disinfectant does not have cytotoxic effects on 3T3 NIH mouse fibroblast cells and the predominance of the anti-inflammatory phenotype after its application may stimulate healing and tissue repair. © 2018 The Academy of Dental Materials-
dc.languageeng-
dc.publisherElsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/dental-
dc.relation.ispartofDental Materials-
dc.subjectALP-
dc.subjectCell viability-
dc.subjectDentine-
dc.subjectFibroblasts-
dc.subjectM1/M2-
dc.titleTransdentinal cytotoxicity and macrophage phenotype of a novel quaternary ammonium silane cavity disinfectant-
dc.typeArticle-
dc.identifier.emailYiu, CKY: ckyyiu@hkucc.hku.hk-
dc.identifier.authorityYiu, CKY=rp00018-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.dental.2018.11.018-
dc.identifier.pmid30509480-
dc.identifier.scopuseid_2-s2.0-85057486288-
dc.identifier.hkuros303625-
dc.identifier.volume35-
dc.identifier.issue2-
dc.identifier.spage206-
dc.identifier.epage216-
dc.identifier.isiWOS:000456070900005-
dc.publisher.placeUnited States-
dc.identifier.issnl0109-5641-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats