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Frontiers of Materials Science

ISSN 2095-025X

ISSN 2095-0268(Online)

CN 11-5985/TB

Postal Subscription Code 80-974

2018 Impact Factor: 1.701

Front. Mater. Sci.    2015, Vol. 9 Issue (3) : 293-302    https://doi.org/10.1007/s11706-015-0298-4
RESEARCH ARTICLE
Remineralization of initial enamel caries in vitro using a novel peptide based on amelogenin
Danxue LI,Xueping LV,Huanxin TU,Xuedong ZHOU,Haiyang YU,Linglin ZHANG()
State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China
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Abstract

Dental caries is the most common oral disease with high incidence, widely spread and can seriously affect the health of oral cavity and the whole body. Current caries prevention measures such as fluoride treatment, antimicrobial agents, and traditional Chinese herbal, have limitations to some extent. Here we design and synthesize a novel peptide based on the amelogenin, and assess its ability to promote the remineralization of initial enamel caries lesions. We used enamel blocks to form initial lesions, and then subjected to 12-day pH cycling in the presence of peptide, NaF and HEPES buffer. Enamel treated with peptide or NaF had shallower, narrower lesions, thicker remineralized surfaces and less mineral loss than enamel treated with HEPES. This peptide can promote the remineralization of initial enamel caries and inhibit the progress of caries. It is a promising anti-caries agent with various research prospects and practical application value.

Keywords dental caries      peptide      remineralization     
Corresponding Author(s): Linglin ZHANG   
Online First Date: 28 May 2015    Issue Date: 23 July 2015
 Cite this article:   
Danxue LI,Xueping LV,Huanxin TU, et al. Remineralization of initial enamel caries in vitro using a novel peptide based on amelogenin[J]. Front. Mater. Sci., 2015, 9(3): 293-302.
 URL:  
https://academic.hep.com.cn/foms/EN/10.1007/s11706-015-0298-4
https://academic.hep.com.cn/foms/EN/Y2015/V9/I3/293
Time Experimental or control solution
8.00 a.m.-8.05 a.m. treatment solution
8.05 a.m.-9.00 a.m. remineralization solution
9.00 a.m.-9.05 a.m. treatment solution
9.05 a.m.-11.00 a.m. remineralization solution
11.00 a.m.-1.00 p.m. demineralization solution
1.00 p.m.-3.00 p.m. remineralization solution
3.00 p.m.-3.05 p.m. treatment solution
3.05 p.m.-4.00 p.m. remineralization solution
4.00 p.m.-4.05 p.m. treatment solution
4.05 p.m.-8.00 a.m. remineralization solution
Tab.1  The pH-cycling model in the experiment
Fig.1  X-ray photoelectron spectroscopy of peptide adsorbed to demineralized enamel: the demineralized enamel treated with peptide (a); the demineralized enamel treated with buffer only (b).
Fig.2  CD spectrum of the peptide.
Fig.3  SEM images of enamels before and after pH cycling: (a) demineralized; (b) NaF; (c) peptide; (d) HEPES.
Fig.4  PLM images of enamel sections from all treatment groups before and after pH cycling: (a) peptide; (b) NaF; (c) HEPES.
Fig.5  TRM images of all treatment groups after pH-cycling: (a) peptide; (b) NaF; (c) HEPES.
Group Mineral loss /(vol.%·μm) Lesion depth /μm
Before After Before After
NaF 2965±670 a 2162±683 a* 112±39 c 86±43 c*
peptide 2523±547 a 2201±469 a* 135±25 c 108±12 d*
HEPES 2561±310 a 2725±283 b* 100±38 c 127±17 e*
Tab.2  Mineral loss, lesion depth of all groups before and after pH-cycling (mean±SD, N = 10)
The depth to the surface /μm Mineral content
NaF Peptide HEPES
20 65.7±5.7 a 64.3±5.4 a 63.7±3.3 a
40 64.0±6.2 a 62.4±4.5 a 61.9±3.8 a
60 70.5±6.3 a 68.6±2.0 b 65.9±3.6 b
80 76.4±6.0 a 74.9±3.1 b 71.4±3.8 c
100 80.5±4.9 a 80.2±2.6 b 76.1±4.0 c
120 82.4±3.9 a 81.9±1.7 b 79.0±3.3 c
140 84.4±2.8 a 85.1±1.7 a 81.6±1.7 b
160 85.6±2.2 a 85.1±1.8 b 84.0±1.5 b
180 86.0±2.0 a 86.0±1.6 b 84.4±1.8 c
200 86.3±1.6 a 85.6±1.4 b 86.0±1.2 b
Tab.3  Mineral content of all groups at several selected depths (mean±SD, N = 10)
AFMatomic force microscopy
ANOVAanalysis of variance
CDcircular dichroism
EMPenamel matrix protein
HEPES2-[4-(2-hydroxyethyl)-1-piperazinyl]ethanesulfonic acid
KHNKnoop hardness number
MREmean residue ellipticity
PLMpolarized light microscopy
SEMscanning electron microscopy
SMHsurface microhardness
TMRtransverse microradiography
UVultraviolet
WHOWorld Health Organization
XRDX-ray diffraction
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