在不同临床方案中使用CPP-ACP和CPP-ACFP评估白斑病变的矿物质增益:概念验证研究

Carol Tran, L. Walsh
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摘要

酪蛋白磷酸肽无定形磷酸钙(CPP-ACP)纳米颗粒的局部应用可以促进亚表面再矿化。为了评估釉质白斑病变的变化,采用交叉研究设计,对5名受试者(均为健康年轻人)进行了原位概念验证研究。将定制的正畸托槽固定在上颌第二前臼齿和第一磨牙的颊面上。每个托槽都有一个凹陷,凹陷处有一块标准的100μm深白斑病变(WSL)的珐琅质。使用反向散射电子成像(BSE)和电子探针微量分析(EPMA)评估病变横截面中矿物的变化。以下产品每天使用两次,持续两周:GC牙刷™ (CPP-ACP),Tooth Mousse Plus™ (CPP-ACFP)、CPP-ACFP矿物增强型(CPP-ACFP-Enh)或含有900ppm氟化物的CPP-ACFP的车辆糊状物。为了确保致盲,所有产品都有相同的口味和包装。对于每个受试者,产品按随机顺序使用,产品之间有冲洗期。与基线情况相比,所有产品的白斑病变都发生了有利的变化。对牙釉质样品横截面的分析显示,矿物质水平有所改善,如从牙釉质表面到病变的BSE灰度级所示。如使用EPMA所见,伴随着钙和磷水平的提高。地下矿物增益产品的排名从最好到最差依次为:CPP-ACFP=CPP-ACFP-Enh>CPP-ACP>含氟车辆。该临床模型中发生了快速再矿化,这是由于多种因素的综合作用:牙釉质板位于暴露于腮腺唾液的牙齿表面,定期刷洗表面以去除牙菌斑生物膜,并且每天两次局部使用产品的依从性很高。这种模型系统可用于筛选新产品配方对釉质WSL的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of Mineral Gain in White Spot Lesions Using CPP-ACP and CPP-ACFP in Different Clinical Protocols: A Proof of Concept Study
Subsurface remineralization can be promoted by the topical application of nanoparticles of casein phosphopeptide-amorphous calcium phosphate (CPP-ACP). To assess changes in enamel white spot lesions, an in situ proof-of-concept investigation was performed using 5 subjects (all of whom were healthy young adults) with a cross-over study design. Custom orthodontic brackets were attached to the buccal surfaces of the maxillary second premolar and first molar teeth. Each bracket had a recess that held a slab of enamel with a standardized 100 μm deep white spot lesion (WSL). Changes in mineral were evaluated in lesion cross sections using backscatter electron imaging (BSE) and electron probe microanalysis (EPMA). The following products were applied twice daily for 2 weeks: GC Tooth Mousse™ (CPP-ACP), Tooth Mousse Plus™ (CPP-ACFP), CPP-ACFP Mineral Enhanced (CPP-ACFP Enh), or the vehicle paste of CPP-ACFP containing 900 ppm fluoride. To ensure blinding, all products had identical flavours and packaging. For each subject, the products were used in a random sequence, with washout periods between products. Compared to the baseline situation, favourable changes in white spot lesions occurred with all products. Analysis of enamel samples in cross section showed improvements in mineral levels, as seen in BSE grey scale levels from the enamel surface through the lesion. These were accompanied by enhanced calcium and phosphorus levels as seen using EPMA. The ranking of products for subsurface mineral gain, from best to worst, was: CPP-ACFP = CPP-ACFP Enh > CPP-ACP > vehicle with fluoride. Rapid remineralization occurred in this clinical model, which is due to a combination of factors: the enamel slabs were located on tooth surfaces exposed to parotid saliva, the surfaces were brushed regularly to remove dental plaque biofilm, and compliance with twice daily topical use of products was high. Such model systems may be useful for screening new product formulations for their effect on enamel WSL.
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