Casein phosphopeptide-amorphous calcium phosphate and glass ionomer show distinct effects in the remineralization of proximal artificial caries lesion in situ
This study aimed to compare the ability of casein-phosphopeptide amorphous-calcium-phosphate (CPP-ACP) and glass-ionomer (GI) in remineralizing proximal artificial caries lesions (ACLs). Molar enamel-slabs were divided into: original-lesion control, intra-oral controls, and experimental (CPP-ACP or...
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Published in | Dental Materials Journal Vol. 32; no. 4; pp. 648 - 653 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Japan
The Japanese Society for Dental Materials and Devices
2013
Japanese Society for Dental Materials and Devices |
Subjects | |
Online Access | Get full text |
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Summary: | This study aimed to compare the ability of casein-phosphopeptide amorphous-calcium-phosphate (CPP-ACP) and glass-ionomer (GI) in remineralizing proximal artificial caries lesions (ACLs). Molar enamel-slabs were divided into: original-lesion control, intra-oral controls, and experimental (CPP-ACP or GI) groups. Specimens received ACLs and were bonded on subject maxillary first molars. After 4-weeks, mineral density (MD) was analyzed by μCT. Compared to control, CPP-ACP increased MD at 0–38/68–84 microns and the GI group had an increase at 0–68 microns, with a greater increase in MD compared to the CPP-ACP group from 0–53 microns. The mean percent remineralization (%R) showed differences between the GI, CPP-ACP groups and their paired controls. GI tended to increase remineralization more than CPP-ACP. In conclusion, CPP-ACP and GI demonstrated distinct remineralizing ability. GI induced greater remineralization in the superficial lesion, while CPP-ACP remineralized the lesion body. Their effects on percent remineralization and reducing lesion depth of proximal ACLs were similar. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Undefined-3 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0287-4547 1881-1361 1881-1361 |
DOI: | 10.4012/dmj.2012-253 |