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Microspheres of alginate encapsulated minocycline-loaded nanocrystalline carbonated hydroxyapatite: therapeutic potential and effects on bone regeneration

机译:海藻酸盐包裹的米诺环素负载纳米晶碳酸羟基磷灰石微球:治疗潜力和对骨再生的影响。

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摘要

>Background and objective: Tetracycline and its derivatives, combined with calcium phosphates, have been proposed as a delivery system to control inflammatory processes and chronic infections. The objective of this study was to evaluate the microspheres of alginate encapsulated minocycline-loaded nanocrystalline carbonated hydroxyapatite (CHAMINO) as a biomimetic device to carry out target-controlled drug delivery for alveolar bone repair.>Methods: CHAMINO microspheres were implanted in a rat central incisor socket after 7 and 42 days. New bone was formed in both groups between 7 and 42 days of implantation. However, the bone growth was significantly higher for the CHAMINO microspheres.>Results: The minocycline (MINO) loading capacity of the nanocrystaline carbonated hydroxyapatite (CHA) nanoparticles was 25.1±2.2 µg MINO/mg CHA for adsorption over 24 hrs. The alginate microspheres containing minocycline-loaded CHA were biologically active and inhibited the Enterococcus faecalis culture growth for up to seven days of the MINO release. An osteoblastic cell viability assay based on the resazurin reduction was conducted after the cells were exposed to the CHAMINO powder and CHAMINO microspheres. Thus, it was found that the alginate extracts encapsulated the minocycline-loaded CHA microspheres and did not affect the osteoblastic cell viability, while the minocycline-doped CHA powder reduced the cell viability by 90%.>Conclusion: This study concluded that the alginate microspheres encapsulating the minocycline-loaded nanocrystalline carbonated hydroxyapatite exhibited combined antibacterial activity against Enterococcus faecalis with cytocompatibility and osteoconduction properties. The significant improvement in the new bone formation after 42 days of implantation suggests that the CHAMINO microsphere has potential in clinical applications of bone regeneration.
机译:>背景和目的:四环素及其衍生物与磷酸钙结合已被提出作为控制炎症过程和慢性感染的传递系统。这项研究的目的是评估藻酸盐包封的米诺环素负载的纳米晶碳酸羟基磷灰石(CHAMINO)的微球作为仿生装置,以进行目标控制的药物输送以修复牙槽骨。>方法: 7天和42天后,将其植入大鼠中切牙槽中。两组在植入后的7到42天之间形成了新的骨骼。但是,CHAMINO微球的骨生长明显更高。>结果:纳米碳酸盐碳酸羟基磷灰石(CHA)纳米颗粒的米诺环素(MINO)负载量为25.1±2.2 µg MINO / mg CHA,在24小时含有米诺环素负载的CHA的藻酸盐微球具有生物活性,并抑制了粪肠球菌培养物的生长,直至MINO释放达7天。将细胞暴露于CHAMINO粉末和CHAMINO微球后,进行基于刃天青素还原的成骨细胞活力测定。因此,发现藻酸盐提取物包裹了米诺环素负载的CHA微球,并且不影响成骨细胞的活力,而米诺环素掺杂的CHA粉将细胞活力降低了90%。>结论:研究得出的结论是,包裹着米诺环素的纳米碳酸盐碳酸羟基磷灰石包裹的藻酸盐微球对粪便肠球菌具有组合的抗菌活性,具有细胞相容性和骨传导特性。植入42天后,新骨形成的显着改善表明,CHAMINO微球在骨再生的临床应用中具有潜力。

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