Evaluating Osteogenic Cell Differentiation Efficacy in the Presence of Polylactide Samples With Varied Compositions for Bone Grafting: In Vitro Study.

Jaime L Lozada, Ekaterina A Zernitckaia, Andrei I Yaremenko, Anastasiia P Reutova
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Abstract

In oral implantology, surgeons often confront the need to improve alveolar bone quality and volume before implantation in patients with bone defects. Whereas guided bone regeneration with titanium meshes is a clinical gold standard for bone augmentation, mesh removal pre-implantation presents a drawback. This study explores biodegradable scaffolds as an alternative. The research investigates the impact of various compositions of customized bone-grafting scaffolds on proliferation and osteogenic differentiation processes in vitro. Plates (10 × 10 × 0.5 mm) were fabricated from polylactide (PLA), PLA with 15% hydroxyapatite nanoparticles (PLA/HA), and polylactide with glycolic acid copolymers (PLGA 60:40 and 85:15). Gingival fibroblasts assessed the influence of experimental samples on proliferation and osteogenic differentiation in a low-glucose medium. Osteogenic differentiation was induced, and alizarin red staining measured extracellular matrix calcification via spectrophotometry. Active proliferation of gingival fibroblasts occurred along scaffold edges during cultivation. Although cells proliferated with experimental samples, rates were lower than control cells. PLA/HA showed higher alizarin red staining intensity, indicating enhanced matrix calcification. Experimental samples (PLA, PLA/HA, PLGA 85:15, PLGA 60:40) supported cell proliferation at lower rates than control. PLA/HA demonstrated increased matrix calcification. Biodegradable membranes were nontoxic, suggesting potential for bone augmentation.

评估用于骨移植的不同成分聚乳酸样本的成骨细胞分化功效:体外研究。
在口腔种植学中,外科医生经常面临在骨缺损患者种植前改善牙槽骨质量和体积的需要。虽然使用钛网进行引导骨再生(GBR)是骨增量的临床 "黄金标准",但种植前去除钛网会带来缺陷。这项研究探索了生物可降解支架作为替代方案。研究调查了各种成分的定制骨移植支架对体外增殖和成骨分化过程的影响。平板(10 x 10 x 0.5 毫米)由聚乳酸(PLA)、聚乳酸与 15%羟基磷灰石纳米颗粒(PLA/HA)以及聚乳酸与乙醇酸共聚物(PLGA 60:40 和 85:15)制成。牙龈成纤维细胞在低糖培养基中评估了实验样品对增殖和成骨分化的影响。诱导成骨分化,茜素红染色通过分光光度法测量细胞外基质钙化。在培养过程中,牙龈成纤维细胞沿着支架边缘活跃增殖。虽然实验样本的细胞也在增殖,但增殖率低于对照细胞。聚乳酸/羟乙基纤维素显示出更高的茜素红染色强度,表明基质钙化增强。实验样品(PLA、PLA/HA、PLGA 85:15、PLGA 60:40)的细胞增殖率低于对照组。PLA/HA显示基质钙化增加。生物降解膜无毒,具有增强骨质的潜力。
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