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用气相色谱法在体外和体内测量正畸粘合剂中双酚A的释放量。

Bisphenol A release from orthodontic adhesives measured in vitro and in vivo with gas chromatography.

作者信息

Moreira Marília Rodrigues, Matos Leonardo Gontijo, de Souza Israel Donizeti, Brigante Tamires Amabile Valim, Queiroz Maria Eugênia Costa, Romano Fábio Lourenço, Nelson-Filho Paulo, Matsumoto Mírian Aiko Nakane

机构信息

Department of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.

Department of Pediatric Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.

出版信息

Am J Orthod Dentofacial Orthop. 2017 Mar;151(3):477-483. doi: 10.1016/j.ajodo.2016.07.019.

Abstract

INTRODUCTION

The objectives of this study were to quantify in vitro the Bisphenol A (BPA) release from 5 orthodontic composites and to assess in vivo the BPA level in patients' saliva and urine after bracket bonding with an orthodontic adhesive system.

METHODS

For the in-vitro portion of this study, 5 orthodontic composites were evaluated: Eagle Spectrum (American Orthodontics, Sheboygan, Wis), Enlight (Ormco, Orange, Calif), Light Bond (Reliance Orthodontic Products, Itasca, Ill), Mono Lok II (Rocky Mountain Orthodontics, Denver, Colo), and Transbond XT (3M Unitek, Monrovia, Calif). Simulating intraoral conditions, the specimens were immersed in a water/ethanol solution, and the BPA (ng.g) liberation was measured after 30 minutes, 24 hours, 1 day, 1 week, and 1 month by the gas chromatography system coupled with mass spectrometry. Twenty patients indicated for fixed orthodontic treatment participated in the in-vivo study. Saliva samples were collected before bracket bonding and then 30 minutes, 24 hours, 1 day, 1 week, and 1 month after bonding the brackets. Urine samples were collected before bonding and then at 1 day, 1 week, and 1 month after bonding. The results were analyzed statistically using analysis of variance and Tukey posttest, with a significance level of 5%.

RESULTS

All composites evaluated in vitro released small amounts of BPA. Enlight composite showed the greatest release, at 1 month. Regarding the in-vivo study, the mean BPA level in saliva increased significantly only at 30 minutes after bonding in comparison with measurements recorded before bonding.

CONCLUSIONS

All orthodontic composites released BPA in vitro. Enlight and Light Bond had, respectively, the highest and lowest BPA releases in vitro. The in-vivo experiment showed that bracket bonding with the Transbond XT orthodontic adhesive system resulted in increased BPA levels in saliva and urine. The levels were significant but still lower than the reference dose for daily ingestion.

摘要

引言

本研究的目的是在体外定量测定5种正畸复合材料中双酚A(BPA)的释放量,并在体内评估使用正畸粘接系统粘结托槽后患者唾液和尿液中的BPA水平。

方法

在本研究的体外部分,评估了5种正畸复合材料:Eagle Spectrum(美国正畸公司,威斯康星州希博伊根)、Enlight(奥美科公司,加利福尼亚州奥兰治)、Light Bond(信赖正畸产品公司,伊利诺伊州伊塔斯卡)、Mono Lok II(落基山正畸公司,科罗拉多州丹佛)和Transbond XT(3M Unitek公司,加利福尼亚州蒙罗维亚)。模拟口腔内环境,将标本浸入水/乙醇溶液中,通过气相色谱-质谱联用系统在30分钟、24小时、1天、1周和1个月后测量BPA(ng/g)的释放量。20名接受固定正畸治疗的患者参与了体内研究。在粘结托槽前以及粘结托槽后30分钟、24小时、1天、1周和1个月收集唾液样本。在粘结前以及粘结后1天、1周和1个月收集尿液样本。使用方差分析和Tukey事后检验对结果进行统计学分析,显著性水平为5%。

结果

所有体外评估的复合材料均释放少量BPA。Enlight复合材料在1个月时释放量最大。关于体内研究,与粘结前记录的测量值相比,唾液中BPA的平均水平仅在粘结后30分钟显著增加。

结论

所有正畸复合材料在体外均释放BPA。Enlight和Light Bond在体外的BPA释放量分别最高和最低。体内实验表明,使用Transbond XT正畸粘接系统粘结托槽会导致唾液和尿液中BPA水平升高。这些水平具有显著性,但仍低于每日摄入的参考剂量。

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