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Biocompatible alginate/nano bioactive glass ceramic composite scaffolds for periodontal tissue regeneration.用于牙周组织再生的生物相容性海藻酸盐/纳米生物活性玻璃陶瓷复合支架
Carbohydr Polym. 2012 Jan 4;87(1):274-283. doi: 10.1016/j.carbpol.2011.07.058. Epub 2011 Aug 3.
2
Enhanced mechanical, biomineralization, and cellular response of nanocomposite hydrogels by bioactive glass and halloysite nanotubes for bone tissue regeneration.生物活性玻璃和埃洛石纳米管增强纳米复合水凝胶的力学性能、生物矿化及细胞反应用于骨组织再生
Mater Sci Eng C Mater Biol Appl. 2021 Sep;128:112236. doi: 10.1016/j.msec.2021.112236. Epub 2021 Jun 18.
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A Review of Bioactive Glass/Natural Polymer Composites: State of the Art.生物活性玻璃/天然聚合物复合材料综述:现状
Materials (Basel). 2020 Dec 6;13(23):5560. doi: 10.3390/ma13235560.
4
Biofabrication of 3D printed hydroxyapatite composite scaffolds for bone regeneration.3D 打印羟基磷灰石复合支架的生物制造用于骨再生。
Biomed Mater. 2021 Mar 8;16(4). doi: 10.1088/1748-605X/abcf03.
5
Bioglass incorporated methacrylated collagen bioactive ink for 3D printing of bone tissue.生物玻璃复合甲基丙烯酸化胶原蛋白生物活性墨水用于骨组织的3D打印。
Biomed Mater. 2021 Feb 26;16(3). doi: 10.1088/1748-605X/abc744.
6
Composite Fiber Networks Based on Polycaprolactone and Bioactive Glass-Ceramics for Tissue Engineering Applications.基于聚己内酯和生物活性玻璃陶瓷的复合纤维网络在组织工程中的应用
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Polymer-Bioactive Glass Composite Filaments for 3D Scaffold Manufacturing by Fused Deposition Modeling: Fabrication and Characterization.用于熔融沉积建模3D支架制造的聚合物-生物活性玻璃复合长丝:制备与表征
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Fabrication and characterization of dextran/nanocrystalline β-tricalcium phosphate nanocomposite hydrogel scaffolds.葡聚糖/纳米晶β-磷酸三钙纳米复合水凝胶支架的制备与表征。
Int J Biol Macromol. 2020 Apr 1;148:434-448. doi: 10.1016/j.ijbiomac.2020.01.112. Epub 2020 Jan 15.
9
Synthesis of plate-like β-tricalcium phosphate nanoparticles and their efficiency in remineralization of incipient enamel caries.片状β-磷酸三钙纳米颗粒的合成及其对早期釉质龋再矿化的效果
Prog Biomater. 2019 Dec;8(4):261-276. doi: 10.1007/s40204-019-00126-y. Epub 2019 Dec 7.
10
Bone tissue regeneration: biology, strategies and interface studies.骨组织再生:生物学、策略与界面研究
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用于骨再生的葡聚糖纳米复合水凝胶的生物学及生物活性评估

Biological and bioactivity assessment of dextran nanocomposite hydrogel for bone regeneration.

作者信息

Nikpour Parisa, Salimi-Kenari Hamed, Rabiee Sayed Mahmood

机构信息

Department of Chemical Engineering, Faculty of Engineering and Technology, University of Mazandaran, P.O. Box 416, Babolsar, Iran.

Department of Materials Engineering, Faculty of Mechanical Engineering, Babol Noshirvani University of Technology, Babol, Iran.

出版信息

Prog Biomater. 2021 Dec;10(4):271-280. doi: 10.1007/s40204-021-00171-6. Epub 2021 Nov 1.

DOI:10.1007/s40204-021-00171-6
PMID:34724183
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8633275/
Abstract

Insufficient biological and bioactive properties of dextran hydrogels limit their applications as promising scaffolds for tissue engineering. We developed nanocomposite dextran hydrogels comprised of bioactive glass (nBGC: 64% SiO2, 31% CaO, 5% PO) nanoparticles with an average particle size of 77 nm using a chemical crosslinking of dextran chains to form 3D hydrogel networks. In the current study; bioactivity of the obtained nanocomposite hydrogels was evaluated through the formation of apatite crystal structures after the incubation in simulated body fluid (SBF) at various submersion periods and nBGC content. The scanning electron microscopy (SEM) micrographs represented an enhanced hydroxyapatite formation on the cross section of nanocomposite comprising of nBGC content from 2 to 8 (% by wt). Biomineralization results of Dex-8 (% by wt) composite during 7, 14 and 28 days immersion indicated the apatite layer formation and the growth of apatite crystal size on the surface and cross section of the nanocomposite. Moreover, MTT assessments indicated that human osteosarcoma cells (SaOS-2) were able to adhere and spread within the dextran hydrogels reinforced with the bioactive glass nanoparticles. With regard to enhanced bioactivity and biocompatibility, the developed dextran-nBGC hydrogel could be considered as a suitable candidate for bone tissue engineering application.

摘要

葡聚糖水凝胶的生物及生物活性特性不足,限制了其作为组织工程理想支架的应用。我们通过葡聚糖链的化学交联形成三维水凝胶网络,开发了由平均粒径为77纳米的生物活性玻璃(nBGC:64%二氧化硅、31%氧化钙、5%五氧化二磷)纳米颗粒组成的纳米复合葡聚糖水凝胶。在本研究中,通过在不同浸泡时间和nBGC含量的模拟体液(SBF)中孵育后磷灰石晶体结构的形成,评估所得纳米复合水凝胶的生物活性。扫描电子显微镜(SEM)显微照片显示,在nBGC含量为2%至8%(重量百分比)的纳米复合材料横截面上,羟基磷灰石形成增强。Dex-8(重量百分比)复合材料在浸泡7天、14天和28天后的生物矿化结果表明,在纳米复合材料的表面和横截面上形成了磷灰石层,且磷灰石晶体尺寸增大。此外,MTT评估表明,人骨肉瘤细胞(SaOS-2)能够在生物活性玻璃纳米颗粒增强的葡聚糖水凝胶内粘附和铺展。鉴于其增强的生物活性和生物相容性,所开发的葡聚糖-nBGC水凝胶可被视为骨组织工程应用的合适候选材料。