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 inDental Materials Journal Vol. 32; no. 4; pp. 648 - 653
Main Authors CHANMITKUL, Wanvipa, THEPYOU, Rathapong, THANATVARAKORN, Ornnicha, TAGAMI, Junji, TRAIRATVORAKUL, Chutima, HAMBA, Hidenori, CHOB-ISARA, Wanwalai
Format Journal Article
LanguageEnglish
Published Japan The Japanese Society for Dental Materials and Devices 2013
Japanese Society for Dental Materials and Devices
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ISSN0287-4547
1881-1361
1881-1361
DOI10.4012/dmj.2012-253

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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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ISSN:0287-4547
1881-1361
1881-1361
DOI:10.4012/dmj.2012-253