增强生物医学应用:用磁铁矿纳米颗粒(MNPs)改性多孔聚二甲基硅氧烷(PDMS)结构,改善与正常人乳腺细胞(MCF10A 细胞)的相互作用

S. C. Eluu, A. O. Oko, K. Eluu, U.U. Onyekwere, E. Ekuma, C.S. Okoye, O.A. Omoniyi, N.R. Obaji, S. Uzor
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摘要

细胞与生物材料相互作用的现象是粘附细胞粘附到生物材料表面并产生相应细胞活性的原因。本研究旨在通过用 MNPs 对多孔 PDMS 结构进行改性,提高其生物相容性和多功能性,使其能与正常人乳腺细胞 MCF10A 细胞系安全地相互作用。制备 MNP 改性多孔 PDMS 基底的方法是将硅树脂弹性体基底与固化剂按特定比例(通常为 10:1)混合,然后用 MNP 进行改性并形成不同尺寸的孔。随后利用傅立叶变换红外光谱对基底进行表征。此外,还分别使用阿拉玛蓝检测法和荧光显微镜对细胞增殖和荧光成像进行了评估。研究结果表明,与 PDMS + MNP_0-150、PDMS + MNP_150-250 和 PDMS + MNP_250-500 相比,PDMS + MNP(无孔)与 PDMS + MNP_0-150、PDMS + MNP_150-250 和 PDMS + MNP_250-500 在 4 小时后的阿拉玛蓝减少百分比上没有显著差异。此外,除 PDMS+MNP_150-250 组与 PDMS+MNP_250-500 组相比无显著差异(P>0.05)外,其他各组在 48 小时和 96 小时均有显著差异(P>0.05)。结果进一步显示,与所有其他组相比,荧光成像结果显示,96 小时后,PDMS+MNP(无孔)表面的细胞附着和增殖非常少。而其他组则随着时间的推移显示出明显的细胞附着和增殖。这些结果表明了多孔性在影响细胞相互作用方面的重要性,并突出了多孔性在生物材料上细胞增殖中的作用。
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Enhancing biomedical applications: Modifying porous poly-di-methyl-siloxane (PDMS) structures with magnetite nanoparticles (MNPs) to improve interaction with normal human breast cells (MCF10A cells)
The phenomenon of cell-biomaterial interaction is responsible for adherent cells' adhesion to the biomaterial surface and the corresponding cell activities. The study aimed to enhance biocompatibility and versatility by modification of porous PDMS structures with MNPs for their safe interaction with normal human breast cells, MCF10A cell line. Preparation of the MNP-modified porous PDMS substrate was carried out by mixing a silicone elastomer base with a curing agent at a specific ratio, typically in a 10:1, followed by modification with MNP and the creation of pores of different dimensions. The substrate was subsequently characterized with Fourier-transform infrared spectroscopy. Furthermore, the assessment of cell proliferation and fluorescence imaging was done using the Alamar blue assay and fluorescence microscopy, respectively. The result of the study showed that PDMS + MNP (non-porous) did not significantly differ in percentage Alamar blue reduction at 4 hours when compared to PDMS + MNP_0-150, PDMS + MNP_150-250, and PDMS + MNP_250-500. Additionally, all the groups differed significantly (P>0.05) from one another at 48 and 96 h, except the PDMS+MNP_150-250 group compared to the PDMS+MNP_250-500 group, which did not exhibit any significant differences (P>0.05). The result further showed that when compared to all other groups, the fluorescence imaging result revealed that, after 96 h, there was very little cell attachment and proliferation on the surface of PDMS+MNP (non-porous). Other groups demonstrated discernable cell adhesion and proliferation over time. These outcomes demonstrate the significance of porosity in influencing cellular interactions and highlight its role in cell proliferation on biomaterial.
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