Investigation of ethanol infiltration into demineralized dentin collagen fibrils using molecular dynamics simulations

Sang Eun Jee, Jienfeng Zhou, Jianquo Tan, Lorenzo Breschi, Franklin R. Tay, Geneviève Grégoire, David H. Pashley, Seung Soon Jang

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

The purpose of this study is to investigate the interaction of neat ethanol with bound and non-bound water in completely demineralized dentin that is fully hydrated, using molecular dynamics (MD) simulation method. The key to creating ideal resin-dentin bonds is the removal of residual free water layers and its replacement by ethanol solvent in which resin monomers are soluble, using the ethanol wet-bonding technique. The test null hypotheses were that ethanol cannot remove any collagen-bound water, and that ethanol cannot infiltrate into the spacing between collagen triple helix due to narrow interlayer spacing. Collagen fibrillar structures of overlap and gap regions were constructed by aligning the collagen triple helix of infinite length in hexagonal packing. Three layers of the water molecules were specified as the layers of 0.15-0.22 nm, 0.22-0.43 nm and 0.43-0.63 nm from collagen atoms by investigating the water distribution surrounding collagen molecules. Our simulation results show that ethanol molecules infiltrated into the intermolecular spacing in the gap region, which increased due to the lateral shrinkage of the collagen structures in contact with ethanol solution, while there was no ethanol infiltration observed in the overlap region. Infiltrated ethanol molecules in the gap region removed residual water molecules via modifying mostly the third water layer (50% decrease), which would be considered as a loosely-bound water layer. The first and second hydration layers, which would be considered as tightly bound water layers, were not removed by the ethanol molecules, thus maintaining the helical structures of the collagen molecules.

Original languageEnglish (US)
Pages (from-to)175-185
Number of pages11
JournalActa biomaterialia
Volume36
DOIs
StatePublished - May 1 2016

Fingerprint

Dentin
Molecular Dynamics Simulation
Infiltration
Collagen
Molecular dynamics
Ethanol
Computer simulation
Water
Molecules
Resins
Fibrillar Collagens
Hydration
Contacts (fluid mechanics)
Monomers
Atoms

Keywords

  • Bound water
  • Collagen
  • Dentin matrix
  • Ethanol
  • Gap regions
  • Molecular dynamics simulation

ASJC Scopus subject areas

  • Biotechnology
  • Biomaterials
  • Biochemistry
  • Biomedical Engineering
  • Molecular Biology

Cite this

Investigation of ethanol infiltration into demineralized dentin collagen fibrils using molecular dynamics simulations. / Jee, Sang Eun; Zhou, Jienfeng; Tan, Jianquo; Breschi, Lorenzo; Tay, Franklin R.; Grégoire, Geneviève; Pashley, David H.; Jang, Seung Soon.

In: Acta biomaterialia, Vol. 36, 01.05.2016, p. 175-185.

Research output: Contribution to journalArticle

Jee, Sang Eun ; Zhou, Jienfeng ; Tan, Jianquo ; Breschi, Lorenzo ; Tay, Franklin R. ; Grégoire, Geneviève ; Pashley, David H. ; Jang, Seung Soon. / Investigation of ethanol infiltration into demineralized dentin collagen fibrils using molecular dynamics simulations. In: Acta biomaterialia. 2016 ; Vol. 36. pp. 175-185.
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abstract = "The purpose of this study is to investigate the interaction of neat ethanol with bound and non-bound water in completely demineralized dentin that is fully hydrated, using molecular dynamics (MD) simulation method. The key to creating ideal resin-dentin bonds is the removal of residual free water layers and its replacement by ethanol solvent in which resin monomers are soluble, using the ethanol wet-bonding technique. The test null hypotheses were that ethanol cannot remove any collagen-bound water, and that ethanol cannot infiltrate into the spacing between collagen triple helix due to narrow interlayer spacing. Collagen fibrillar structures of overlap and gap regions were constructed by aligning the collagen triple helix of infinite length in hexagonal packing. Three layers of the water molecules were specified as the layers of 0.15-0.22 nm, 0.22-0.43 nm and 0.43-0.63 nm from collagen atoms by investigating the water distribution surrounding collagen molecules. Our simulation results show that ethanol molecules infiltrated into the intermolecular spacing in the gap region, which increased due to the lateral shrinkage of the collagen structures in contact with ethanol solution, while there was no ethanol infiltration observed in the overlap region. Infiltrated ethanol molecules in the gap region removed residual water molecules via modifying mostly the third water layer (50{\%} decrease), which would be considered as a loosely-bound water layer. The first and second hydration layers, which would be considered as tightly bound water layers, were not removed by the ethanol molecules, thus maintaining the helical structures of the collagen molecules.",
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