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以方钠石(NaCaSiO)相为主的纳米结构 45S5 生物活性玻璃:探索其结构和生物学性能。

Devitrite (NaCaSiO) phase dominated nanostructured 45S5 bioactive glass: exploring its structural and biological properties.

机构信息

National Centre for Nanoscience and Nanotechnology, University of Madras, Guindy Campus, Chennai 600 025, India.

Centre for Functional and Surface-Functionalized Glass, Alexander Dubček University of Trenčín, 911 50 Trenčín, Slovakia.

出版信息

Biomed Mater. 2024 Feb 16;19(2). doi: 10.1088/1748-605X/ad2708.

Abstract

This research study is primarily centred around calcination temperature and time influence on phase formation in bioactive glasses (BGs). In the present study, BG with a nominal composition of 45S5 was synthesized through the sol-gel process. The developed BGs then underwent heat treatment for various sintering durations and temperatures. X-ray diffraction (XRD) patterns of the BGs reveals that the sintering process led to the crystallization of both devitrite (NaCaSiO) and combeite (NaCaSiO) phases. The field emission scanning electron microscopy study divulges morphological alterations, from sheet-like to rod-like structures to eventually transforming into spherical and sheet-like structures. The surface area and Type-IV mesoporous porosity were validated through Brunauer Emmett Teller analysis, highlighting a notable increase in pore volume and mechanical strength at a lower sintering temperature.apatite formation was carried out in Hank's balance salt in order to evaluate the bioactivity of the glass. After 7 d of immersion in simulated body fluid (SBF), XRD patterns and scanning electron microscopy micrographs results showed that formation of hydroxyapatite layer on the surface of the BGs. The BG compatibility with erythrocytes (red blood cells) was also studied, and the results revealed that there was only a low 2% lysis, showing good hemocompatibility. The drug loading and release behaviour of the BGs was studied in theanalysis. The findings showed a high drug encapsulation effectiveness of up to 90% and continuous drug release from the BGs for 24 h. The materials biocompatibility was unambiguously confirmed by cytocompatibility and proliferation studies. This study provides compelling evidence for the exceptional efficacy and promise of the distinct 45S5 BGs in advancing the field of regenerative medicine.

摘要

这项研究主要集中在煅烧温度和时间对生物活性玻璃(BGs)相形成的影响。在本研究中,通过溶胶-凝胶法合成了名义组成 45S5 的 BG。然后,将所开发的 BG 进行不同烧结时间和温度的热处理。BG 的 X 射线衍射(XRD)图谱表明,烧结过程导致无定形(NaCaSiO)和硅钙石(NaCaSiO)相的结晶。场发射扫描电子显微镜研究揭示了形态的变化,从片状到棒状结构,最终转化为球形和片状结构。通过 Brunauer Emmett Teller 分析验证了比表面积和 IV 型中孔孔隙率,突出了在较低烧结温度下孔体积和机械强度的显著增加。在汉克平衡盐中进行了磷灰石形成实验,以评估玻璃的生物活性。在模拟体液(SBF)中浸泡 7 天后,XRD 图谱和扫描电子显微镜照片结果表明,BG 表面形成了羟基磷灰石层。还研究了 BG 与红细胞(红细胞)的相容性,结果表明溶血率仅为 2%,表现出良好的血液相容性。对 BG 的药物负载和释放行为进行了研究。研究结果表明,药物包封效率高达 90%,并且 BG 能够在 24 小时内持续释放药物。细胞相容性和增殖研究明确证实了材料的生物相容性。这项研究为独特的 45S5 BG 在推进再生医学领域的卓越疗效和前景提供了有力证据。

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