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dc.contributor.authorGe, Xueping
dc.contributor.authorYe, Qiang
dc.contributor.authorSong, Linyong
dc.contributor.authorSpencer, Paulette
dc.contributor.authorLaurence, Jennifer S.
dc.date.accessioned2017-08-30T18:30:59Z
dc.date.available2017-08-30T18:30:59Z
dc.date.issued2015-10
dc.identifier.citationGe, X., Ye, Q., Song, L., Spencer, P., & Laurence, J. S. (2015). Effect of crosslinking density of polymers and chemical structure of amine-containing monomers on the neutralization capacity of dentin adhesives. Dental Materials : Official Publication of the Academy of Dental Materials, 31(10), 1245–1253. http://doi.org/10.1016/j.dental.2015.08.153en_US
dc.identifier.urihttp://hdl.handle.net/1808/24881
dc.description.abstractObjectives

Neutralization of the acidic micro-environment at the tooth/material interface is expected to provide enhanced durability for dental composite restorations. The objective of this study is to explore the effect of amine-containing monomer formulations and the crosslinking density of the resultant polymers on the neutralization capacity.

Materials and methods

The co-monomer system was varied systematically to obtain different proportions of Bisphenol A glycerolate dimethacrylate (BisGMA) and 2-hydroxyethyl methacrylate (HEMA), while maintaining a constant amount of amine-containing methacrylate monomer. A series of amine-containing monomers covering a range of pKa values were examined. Crosslinking density of formed copolymers was controlled by adjusting the weight content of the dimethacrylate monomer BisGMA. Lactic acid (LA) was used as a probe to analyze the effectiveness of the basic polymers to neutralize acid. The neutralization capacity of each amine-containing crosslinked copolymer was characterized by measuring pH as a function of time when the specimens were soaked in 1-mM LA solution, and the results were compared to the control formulations composed solely of BisGMA and HEMA. Polymer surfaces were examined using the methyl orange (MO) assay to quantify the amount of accessible amine groups. Results

For each amine-containing crosslinked co-polymer, the neutralization capacity is enhanced by decreasing crosslinking density (e.g., by reducing BisGMA concentration in the formulation). In addition, more amine groups were accessible when crosslinking density was decreased. For different amine-containing polymers with the same BisGMA concentration, the neutralization capacity is higher when the amino monomers with higher pKa values were used in the formulations. Significance

This is the first time that the neutralization capacity based on crosslinked dental polymers has been studied. The information is important for future development of durable dentin adhesives.
en_US
dc.publisherElsevieren_US
dc.rights© 2015. This article is made available under a CC BY-ND 3.0 creative commons license.en_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/en_US
dc.subjectAmine monomeren_US
dc.subjectCrosslinking densityen_US
dc.subjectDentin adhesiveen_US
dc.subjectNeutralizationen_US
dc.subjectpKaen_US
dc.titleEffect of crosslinking density of polymers and chemical structure of amine-containing monomers on the neutralization capacity of dentin adhesivesen_US
dc.typeArticleen_US
kusw.kuauthorGe, Xueping
kusw.kuauthorYe, Qiang
kusw.kuauthorSong, Linyong
kusw.kuauthorSpencer, Paulette
kusw.kuauthorLaurence, Jennifer S.
kusw.kudepartmentBioengineering Research Centeren_US
kusw.kudepartmentMechanical Engineeringen_US
kusw.kudepartmentPharmaceutical Chemistryen_US
dc.identifier.doi10.1016/j.dental.2015.08.153en_US
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC5515479en_US
dc.rights.accessrightsopenAccess


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© 2015. This article is made available under a CC BY-ND 3.0 creative commons license.
Except where otherwise noted, this item's license is described as: © 2015. This article is made available under a CC BY-ND 3.0 creative commons license.