氟暴露下牙种植体释放的钛颗粒与巨噬细胞相互作用

Brazilian dental journal Pub Date : 2025-04-14 eCollection Date: 2025-01-01 DOI:10.1590/0103-644020256187
Waad Kheder, Soumya Sheela, A R Samsudin, Sausan Al Kawas, Nadia Khalifa, Ali Qabbani
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引用次数: 0

摘要

研究了氟和pH值对喷砂和酸蚀制备的疏水微孔Ti6Al4V牙种植体中钛颗粒释放的影响;并将颗粒大小与巨噬细胞的摄取和炎症细胞因子的表达联系起来。将15个种植体浸泡在5种不同氟浓度和pH值的测试溶液中。3个对照植入物在扫描电镜下被扫描,15个测试植入物在测试溶液中浸泡后也被扫描。对浸液中钛颗粒/离子的大小范围和数量进行了分析。研究了巨噬细胞对钛颗粒的摄取及暴露于钛颗粒后Il-1 β和IL-8的表达。高氟化物和酸度的测试溶液释放出微型钛颗粒(4551.7±114.5 nm和2783±101.13 nm);而在低氟、中性pH和碱性环境下,钛颗粒的释放量分别为431.2±80.6 nm、448.3±112 nm和484.5±85.3 nm。巨噬细胞对纳米颗粒的摄取增加,但不改变其膜完整性。二氧化钛颗粒暴露后M0巨噬细胞IL-1β和IL-8表达的增加可能有助于我们理解免疫细胞群体特异性分子事件,引起钛颗粒对种植体周围炎症的反应。氟化物和pH值影响钛颗粒从种植体表面的释放。激活的炎症介质是成骨细胞-破骨细胞活性失衡和种植体骨整合失败的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Titanium Particles Released from Dental Implants Under Fluoride Exposure Interact with Macrophages.

This study is designed to investigate the influence of fluoride and pH value on the release of titanium particles from Ti6Al4V dental implants with hydrophobic microrough surface produced by sandblasting and acid-etching techniques; and correlate particle size to their uptake by macrophages and expression of inflammatory cytokines. Fifteen dental implants were immersed in five test solutions with different fluoride concentrations and pH values. Three control implants were scanned using a scanning electron microscope and fifteen test implants were also scanned after their immersion in the test solutions. The immersion solutions were analyzed for titanium particles/ions size-range and amount. The uptake of titanium particles by macrophages and expression of Il-1 β and IL-8 following their exposure to titanium particles were investigated. Test solutions with high fluoride and acidity resulted in the release of micro-size titanium particles (4551.7 ± 114.5 nm and 2783 ± 101.13 nm); while those with low fluoride, neutral pH, and alkaline environment resulted in the release of nano-size titanium particles (431.2 ± 80.6 nm, 448.3 ± 112 nm, and 484.5 ± 85.3 nm respectively). There was an increase in the uptake of nanoparticles by macrophages without altering their membrane integrity. The increase in expression of IL-1β and IL-8 by M0 macrophages after exposure to titanium dioxide particles may facilitate our understanding of immune cell population-specific molecular events deriving the peri-implant inflammation in response to titanium particles. Fluoride and pH values influence the release of titanium particles from the implant's surface. The activated inflammatory mediators are key to imbalance in osteoblast-osteoclast activity and failure of implant osseointegration.

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