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Resorption of the calcium phosphate layer on S53P4 bioactive glass by osteoclasts

机译:破骨细胞对S53P4生物活性玻璃上磷酸钙层的吸收

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摘要

Clinically, S53P4 bioactive glass (BAG) has shown very promising results in bone infection treatment, but it is also known to degrade very slowly in vivo. To evaluate which mechanisms (cellular or dissolution) can play a role in the degradation of S53P4 BAG and S53P4 BAG putty, in vitro degradation experiments at different pH (7.4 and 4.6) were performed. Micro computed tomography showed a rapid dissolution of the synthetic binder in the putty formulation, within 12 h is simulated body fluid (pH = 7.4), leaving behind only loose granules. Therefore the degradation of the loose granules was investigated further. Significant weight loss was observed and ion chromatography showed that Ca2+, Na+ and PO43− ions were released from S54P4 BAG granules in the two fluids. It was observed that the weight loss and ion release were increased when the pH of the fluid was decreased to 4.6. Osteoclasts are known to create such a low pH when resorbing bone and therefore their capacity to degrade S53P4 surfaces were studied as well. Scanning electron microscopy and energy-dispersive X-ray spectroscopy confirmed that osteoclasts were able to create resorption pits in the calcium phosphate layer on S53P4 BAG surfaces. The silica of the BAG, located underneath the calcium phosphate, seemed to hinder further osteclastic resorption of the material. To our knowledge we were the first to observe actively resorbing osteoclasts on S53P4 bioactive glass surfaces, in vitro. Future research is needed to define the specific role osteoclasts play in the degradation of BAG in vivo.
机译:在临床上,S53P4生物活性玻璃(BAG)在骨骼感染治疗中显示出非常有希望的结果,但众所周知它在体内的降解速度非常慢。为了评估哪些机制(细胞或溶解)可在S53P4 BAG和S53P4 BAG油灰的降解中发挥作用,在不同pH(7.4和4.6)下进行了体外降解实验。显微计算机断层扫描显示合成粘合剂在油灰配方中迅速溶解,在12?h内被模拟的体液(pH == 7.4),仅留下疏松的颗粒。因此,对松散颗粒的降解进行了进一步研究。观察到显着的重量减轻,离子色谱法表明,S54P4 BAG颗粒中的Ca 2 + ,Na + 和PO4 3 − 离子被释放出。两种液体。观察到,当流体的pH降低至4.6时,重量损失和离子释放增加。已知破骨细胞在吸收骨骼时会产生如此低的pH值,因此也研究了其降解S53P4表面的能力。扫描电子显微镜和能量色散X射线光谱证实,破骨细胞能够在S53P4 BAG表面的磷酸钙层中产生吸收凹坑。 BAG的二氧化硅位于磷酸钙下方,似乎阻碍了该材料的进一步骨弹性吸收。据我们所知,我们是第一个在体外观察到在S53P4生物活性玻璃表面上主动吸收破骨细胞的方法。需要进一步的研究来确定破骨细胞在体内BAG降解中所起的特定作用。

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