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检测在不同材料上原位形成的薄膜上暴露的唾液α-淀粉酶和溶菌酶。

Detection of salivary alpha-amylase and lysozyme exposed on the pellicle formed in situ on different materials.

作者信息

Hannig Christian, Huber Karin, Lambrichts Ivo, Gräser Jan, D'Haen Jan, Hannig Matthias

机构信息

Department of Operative Dentistry and Periodontology, University of Freiburg, Hugstetter Street 55, D-79106 Freiburg, Germany.

出版信息

J Biomed Mater Res A. 2007 Oct;83(1):98-103. doi: 10.1002/jbm.a.31313.

Abstract

Amylase and lysozyme are components of the salivary pellicle, exposing considerable enzymatic activity in the immobilized state. The purpose of the present study was to elucidate the influence of different solid substrata on the amount and distribution of amylase and lysozyme exposed on the surface of the salivary pellicle formed in situ. Slabs of titanium, feldspar ceramic, and bovine enamel were fixed on the buccal sites of individual splints worn by three subjects for 3 or 30 min, respectively, to allow pellicle formation. Subsequently, slabs were removed from the splints and rinsed with running water. Detection of amylase and lysozyme was performed by FEI-SEM after gold-immunolabeling of the enzymes. Both enzymes were found to be distributed randomly at the pellicle surface. Irrespective of formation time and substratum, significantly more labeled lysozyme molecules (5.23 +/- 4.5 microm(-2)) were detected compared with amylase (3.4 +/- 2.9 microm(-2)). Neither the substratum nor the pellicle formation time had significant impact on the amount of the respective enzyme that could be detected. This study for the first time provides evidence, that amylase and lysozyme are exposed at the surface of the salivary pellicle formed in situ on titanium and ceramics. Both enzymes are distributed randomly on the surface of the pellicle, irrespective of the underlying substratum.

摘要

淀粉酶和溶菌酶是唾液薄膜的组成成分,在固定状态下具有相当可观的酶活性。本研究的目的是阐明不同固体基质对原位形成的唾液薄膜表面所暴露的淀粉酶和溶菌酶的数量及分布的影响。将钛板、长石陶瓷板和牛牙釉质板分别固定在三名受试者佩戴的单个夹板的颊侧部位3分钟或30分钟,以使薄膜形成。随后,将板从夹板上取下并用流水冲洗。在对酶进行金免疫标记后,通过场发射扫描电子显微镜(FEI-SEM)检测淀粉酶和溶菌酶。发现这两种酶在薄膜表面随机分布。无论形成时间和基质如何,与淀粉酶(3.4±2.9μm⁻²)相比,检测到的标记溶菌酶分子显著更多(5.23±4.5μm⁻²)。基质和薄膜形成时间对可检测到的相应酶的量均无显著影响。本研究首次提供了证据,表明淀粉酶和溶菌酶暴露于原位在钛和陶瓷上形成的唾液薄膜表面。无论底层基质如何,这两种酶均随机分布在薄膜表面。

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