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α-羟基酸作为牙本质预处理剂对生长因子释放的影响:一项体外研究。

Effect of Alpha Hydroxy Acids as Dentin Conditioning Agents on Growth Factor Release: An In Vitro Study.

作者信息

Tulasi Lakshmi, Dhanasekaran Sihivahanan, Venkatesh Vijay

机构信息

Conservative Dentistry and Endodontics, Sri Ramaswamy Memorial (SRM) Kattankulathur Dental College, Chennai, IND.

出版信息

Cureus. 2024 Sep 18;16(9):e69646. doi: 10.7759/cureus.69646. eCollection 2024 Sep.

Abstract

AIM

The study aimed to evaluate the effects of alpha hydroxy acids and chelating agents on dentin conditioning for the release of growth factors.

METHODS

The agents used for dentin conditioning included 17% ethylenediaminetetraacetic acid (EDTA), 10% glycolic acid (GA), 10% citric acid (CA), and 5% maleic acid (MA). Forty horizontally sectioned (SV1) human dentine slices were conditioned for 5 and 10 minutes so that the growth factor liberation reached quantifiable levels. Transforming growth factor beta-1 (TGF-β1) release and surface exposure were quantified by enzyme-linked immunosorbent assay (ELISA). Growth factor measurement required immediately removing the solutions from each of the 48-well plates (with consistent dentine surface area and weight) and freezing at -20°C so that ELISA measured the growth factors.

RESULTS

After 5-min conditioning of dentine slices, CA was the most effective agent for growth factor release into the aqueous environment as measured by ELISA (post hoc Tukey's test p<0.05). Furthermore, dentine slices subjected to GA treatment for the same duration of time showed noticeably lower surface levels of TGF-β1 in comparison to the other agents employed.

CONCLUSIONS

Based on the findings of this in vitro study, a desirable biological growth factor-mediated effect may be gained when conditioning dentin with milder acidic or chelating agents such as CA, MA, and EDTA.

摘要

目的

本研究旨在评估α-羟基酸和螯合剂对牙本质预处理以释放生长因子的效果。

方法

用于牙本质预处理的试剂包括17%乙二胺四乙酸(EDTA)、10%乙醇酸(GA)、10%柠檬酸(CA)和5%马来酸(MA)。将40片水平切片的(SV1)人牙本质薄片分别预处理5分钟和10分钟,以使生长因子释放达到可量化水平。通过酶联免疫吸附测定(ELISA)对转化生长因子β-1(TGF-β1)的释放和表面暴露情况进行定量。生长因子测量要求立即从每个48孔板(具有一致的牙本质表面积和重量)中取出溶液,并在-20°C下冷冻,以便ELISA测量生长因子。

结果

通过ELISA测定,牙本质薄片预处理5分钟后,CA是使生长因子释放到水性环境中最有效的试剂(事后Tukey检验p<0.05)。此外,与其他试剂相比,GA处理相同时间的牙本质薄片显示TGF-β1的表面水平明显较低。

结论

基于这项体外研究的结果,在用较温和的酸性或螯合剂如CA、MA和EDTA预处理牙本质时,可能会获得理想的生物生长因子介导效应。

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