Assessment of normal human breast cells (MCF10A cells)–Surface interactions on porous poly-di-methyl-siloxane (PDMS) structures for potential biomedical applications

S. C. Eluu, A. O. Oko, C. O. Esimone, K. Eluu, U.U. Onyekwere, S. Uzor, E. Ekuma, C.S. Okoye, E.G. Ofobuike, N.R. Obaji
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Abstract

Biocompatibility stands out as a crucial and fundamental requirement before approval of biomaterials for medical use. The study aimed to evaluate the interaction between normal human breast cells (MCF10A cells) and porous poly-di-methyl-siloxane (PDMS) structures for potential biomedical applications. Preparation and characterization of the PDMS substrate were carried out, followed by the assessment of cell proliferation and fluorescence imaging using an Alamar blue assay and fluorescence microscopy, respectively. The results revealed that initially (at 4 hours post-incubation), there was no notable difference in cell proliferation among the various groups (non-porous PDMS, PDMS_0-150, PDMS_150-250, and PDMS_250500). However, at 48 and 96 hours, a significant increase in cell proliferation was observed in the PDMS_250–500 μm group compared to other groups (P<0.05). Furthermore, the results of the fluorescence microscopy corroborated a substantial enhancement in cell growth and attachment as the porosity of the PDMS substrate increased. However, cells seeded on non-porous PDMS surfaces exhibited a significant decline (P<0.05) in cell growth in both the Alamar blue assay and fluorescence imaging. These findings hold great promise for the creation of surfaces and materials that are specifically designed to influence biological reactions and show potential for a range of biomedical uses.
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评估多孔聚二甲基硅氧烷(PDMS)结构上的正常人乳腺细胞(MCF10A 细胞)与表面的相互作用,促进潜在的生物医学应用
生物相容性是生物材料获准用于医疗用途前的一项关键和基本要求。本研究旨在评估正常人乳腺细胞(MCF10A 细胞)与多孔聚二甲基硅氧烷(PDMS)结构之间的相互作用,以确定其潜在的生物医学应用。研究人员首先制备了 PDMS 基底并对其进行了表征,然后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。结果显示,最初(培养后 4 小时),各组(无孔 PDMS、PDMS_0-150、PDMS_150-250 和 PDMS_250-500)的细胞增殖没有明显差异。然而,在 48 小时和 96 小时时,与其他组相比,PDMS_250-500 μm 组的细胞增殖明显增加(P<0.05)。此外,荧光显微镜的结果也证实,随着 PDMS 基底孔隙率的增加,细胞的生长和附着也大大增强。然而,在无孔的 PDMS 表面上播种的细胞,在阿拉玛蓝检测和荧光成像中的细胞生长速度都明显下降(P<0.05)。这些发现为创造专门用于影响生物反应的表面和材料带来了巨大的希望,并显示出一系列生物医学用途的潜力。
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