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电化学 ELISA 和分光光度 ELISA 检测牙骨质涎磷蛋白在牙根吸收中的比较。

Comparison between electrochemical ELISA and spectrophotometric ELISA for the detection of dentine sialophosphoprotein for root resorption.

机构信息

Associate chief physician, Department of Orthodontics, School of Dentistry, Capital Medical University, Beijing, China.

Professor, Department of Orthodontics, School of Dentistry, Capital Medical University, Beijing, China.

出版信息

Am J Orthod Dentofacial Orthop. 2014 Jan;145(1):36-40. doi: 10.1016/j.ajodo.2013.09.008.

Abstract

INTRODUCTION

Root resorption is an undesirable sequela of orthodontic treatment. It is necessary to establish sensitive methods for identification of teeth at risk for resorption. The x-ray is the traditional method to diagnose root resorption, which is often at a late stage. Some researchers used enzyme-linked immunosorbent immunoassay (ELISA) combined with spectrophotometry to study some biochemical markers of root resorption. However, spectrophotometric detection often has a poor detection limit. Electrochemical detection has inherent advantages over spectrophotometric detection, which is especially suitable for small biologic samples.

METHODS

We used ELISA combined with electrochemistry and ELISA combined with spectrophotometry to measure the biochemical marker dentine sialophosphoprotein in gingival crevicular fluid of orthodontic patients (treated for 8-12 months).

RESULTS

Standard dentine sialophosphoprotein was used to calculate the linear regression equation. No significant difference was found between the electrochemical outcome and the spectrophotometric outcome. But the electrochemical results extended the lower end of detection from 5 pg per milliliter (by spectrophotometry) to 0.5 pg per milliliter.

CONCLUSIONS

These results showed that ELISA combined with electrochemistry is a reliable and sensitive method to detect dentine sialophosphoprotein in gingival crevicular fluid.

摘要

简介

牙根吸收是正畸治疗的一种不良后果。有必要建立敏感的方法来识别有吸收风险的牙齿。射线照相是诊断牙根吸收的传统方法,但通常处于晚期。一些研究人员使用酶联免疫吸附试验(ELISA)结合分光光度法来研究牙根吸收的一些生化标志物。然而,分光光度法检测往往检测限较差。电化学检测比分光光度法检测具有固有优势,特别适用于小生物样本。

方法

我们使用 ELISA 结合电化学和 ELISA 结合分光光度法来测量正畸患者(治疗 8-12 个月)龈沟液中的生化标志物牙本质涎磷蛋白。

结果

使用标准牙本质涎磷蛋白计算线性回归方程。电化学结果与分光光度结果没有显著差异。但电化学结果将检测下限从每毫升 5 皮克(分光光度法)扩展到每毫升 0.5 皮克。

结论

这些结果表明,ELISA 结合电化学是检测龈沟液中牙本质涎磷蛋白的一种可靠和敏感的方法。

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