‘Effects of novel root repair materials on attachment and morphological behaviour of periodontal ligament fibroblasts: Scanning electron microscopy observation’

Microscopy Research and Technique - Tập 79 Số 12 - Trang 1214-1221 - 2016
Makbule Bilge Akbulut1, Pembegül Uyar Arpacı2, Ayçe Ünverdi Eldeniz3
1Department of Endodontics, Faculty of Dentistry, Necmettin Erbakan University, Konya, Turkey
2Department of Biotechnology, Faculty of Science, Selcuk University, Konya, Turkey
3Department of Endodontics, Faculty of Dentistry, Selcuk University, Konya, Turkey.

Tóm tắt

AbstractThe aim of this study was to evaluate the adhesion of periodontal ligament fibroblasts (PDLs) on newly proposed root repair materials [Biodentine, MM‐MTA, polymethylmethacrylate (PMMA) bone cement, and SDR], in comparison with contemporary root repair materials [IRM, Dyract compomer, ProRoot MTA (PMTA), and Vitrebond]. Five discs from each material were fabricated in sterile Teflon molds, and the specimens were aged and prewetted in cell culture media for 96 hours. Three material discs were used for scanning electron microscopy (SEM) for the assessment of the attachment, density, and morphological changes in the PDLs, while two samples were used for energy dispersive x‐ray spectroscopy (SEM‐EDX) to determine the elemental composition of the materials. Human PDLs were plated onto the materials at a density of 10,000/well, and incubated for 3 days. The SEM micrographs were taken at different magnifications (500× and 5000×). In the SEM, the cells were attached and well spread‐out on the surfaces of the Biodentine, PMTA, and Dyract compomer, while varied cell densities and morphological alterations were observed in the Vitrebond, IRM, MM‐MTA, SDR, and PMMA bone cement groups. The SEM‐EDX analysis revealed a maximum calcium percentage in the PMTA specimens, as well a maximum silicon percentage in the Dyract compomer specimens. This in vitro study demonstrated that the Biodentine and Dyract compomer supported PDL cell adhesion and spreading. The PMTA presented a favorable scaffold for better attachment of the PDL cell aggregates. Therefore, the calcium and silicon content of a material may enhance the PDL cell attachment.

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Tài liệu tham khảo

10.1097/01.don.0000145429.04231.e2

10.1016/j.joen.2008.08.001

10.1097/01.don.0000137650.61607.25

10.1097/00004770-200401000-00004

10.1097/00004770-200311000-00014

10.1111/iej.12261

10.1016/j.joen.2010.02.018

10.1097/00004770-200401000-00005

10.1111/j.1365-2591.2008.01506.x

10.1111/j.1365-2591.2008.01483.x

10.1111/j.1365-2591.2012.02027.x

10.1111/j.1365-2591.2004.00859.x

10.1016/j.joen.2013.09.036

10.1016/j.joen.2013.11.006

10.1016/0267-6605(91)90078-T

10.1097/01.don.0000145428.26880.e5

10.1016/j.dental.2010.06.002

10.1016/j.joen.2007.09.001

10.1177/00220345980770121001

10.1002/jbm.a.20075

10.1002/jbm.a.31005

10.1067/moe.2003.231

10.1016/j.biomaterials.2006.11.041

10.1097/00004770-200204000-00008

10.1111/iej.12373

10.1002/(SICI)1097-4636(19971205)37:3<432::AID-JBM14>3.0.CO;2-D

10.1111/j.1365-2842.2006.01622.x

10.1111/iej.12208

10.1038/ijos.2014.5

10.1016/j.dental.2008.02.020

Leirskar J., 1977, Toxicity of some dental cements in a cell culture system, Scandinavian Journal of Dental Research, 85, 471

10.1016/j.jdent.2013.12.011

10.1016/j.joen.2011.02.029

10.1590/1678-775720130523

10.1016/S0099-2399(98)80180-5

10.1002/(SICI)1097-4636(199611)32:3<341::AID-JBM6>3.0.CO;2-S

10.1016/S0099-2399(98)80084-8

10.1016/j.biomaterials.2003.10.006

Rodriguez I. A., 2013, An in vitro biocompatibility study of conventional and resin‐modified glass ionomer cements, The Journal of Adhesive Dentistry, 15, 541

10.1902/jop.1999.70.10.1144

10.1016/j.dental.2008.03.024

10.1163/156856200743706

10.1016/S0099-2399(98)80171-4

10.1016/S0109-5641(85)80005-1

10.1016/j.jbiomech.2004.03.002

Weine F. S.(2004).Endodontic Therapy. 6th ed. St Louis: Mosby. Initiating endodontic treatment; pp. 104–163.

10.1016/j.joen.2012.04.018

10.1016/j.joen.2012.11.026

10.1097/00004770-200007000-00006

10.1016/S0099-2399(99)80267-2