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Ipriflavone-Loaded Mesoporous Nanospheres with Potential Applications for Periodontal Treatment

机译:具有型牙周治疗潜在应用的Ipriflavone负载的介孔纳米球

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摘要

The incorporation and effects of hollow mesoporous nanospheres in the system SiO2–CaO (nanoMBGs) containing ipriflavone (IP), a synthetic isoflavone that prevents osteoporosis, were evaluated. Due to their superior porosity and capability to host drugs, these nanoparticles are designed as a potential alternative to conventional bioactive glasses for the treatment of periodontal defects. To identify the endocytic mechanisms by which these nanospheres are incorporated within the MC3T3-E1 cells, five inhibitors (cytochalasin B, cytochalasin D, chlorpromazine, genistein and wortmannin) were used before the addition of these nanoparticles labeled with fluorescein isothiocyanate (FITC–nanoMBGs). The results indicate that nanoMBGs enter the pre-osteoblasts mainly through clathrin-dependent mechanisms and in a lower proportion by macropinocytosis. The present study evidences the active incorporation of nanoMBG–IPs by MC3T3-E1 osteoprogenitor cells that stimulate their differentiation into mature osteoblast phenotype with increased alkaline phosphatase activity. The final aim of this study is to demonstrate the biocompatibility and osteogenic behavior of IP-loaded bioactive nanoparticles to be used for periodontal augmentation purposes and to shed light on internalization mechanisms that determine the incorporation of these nanoparticles into the cells.
机译:评估了含有Ipriflavone(IP)的系统SiO2-CaO(Nanombgs)中的中空介孔纳米球的掺入和作用,得到了防止骨质疏松症的合成异黄酮。由于它们的优异孔隙度和宿主药物的能力,这些纳米颗粒被设计为常规生物活性玻璃的潜在替代物,用于治疗牙周缺陷。为了鉴定这些纳米球在MC3T3-E1细胞内掺入的内吞机制,在添加这些纳米粒子(FitC-Nanombgs)中添加这些纳米颗粒之前使用了五种抑制剂(细胞酵母B,细胞蛋白B,细胞蛋白B,细胞蛋白酶D,Chlorpromazine,Genistein和Wortmannin) 。结果表明,纳米环主要通过Clathrin依赖性机制进入预成骨细胞,并以大型细胞增生率低的比例较低。本研究证明了MC3T3-E1骨催化剂细胞的活性掺入,其刺激其分化为成熟成骨细胞表型,随着碱性磷酸酶活性增加。本研究的最终目的是证明IP负载的生物活性纳米颗粒的生物相容性和成骨行为用于牙周增强目的,并在内化机制上脱光,从而确定将这些纳米颗粒掺入细胞中。

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