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借助烷氧基硅烷可纺性制备的用于骨再生的柔性高强度生物活性玻璃纤维膜

Flexible and high-strength bioactive glass fiber membrane for bone regeneration with the aid of alkoxysilane sol spinnability.

作者信息

Mao Junjie, Sun Junyuan, Wang Lu, Liu Xinyu, Bi Jianqiang

机构信息

Liquid-Solid Structural Evolution & Processing of Materials (Ministry of Education), School of Materials Science and Engineering, Shandong University, Jinan, Shandong, 250061, PR China.

Department of Orthopaedics, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, PR China.

出版信息

Mater Today Bio. 2024 Sep 4;28:101224. doi: 10.1016/j.mtbio.2024.101224. eCollection 2024 Oct.

DOI:10.1016/j.mtbio.2024.101224
PMID:39290465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11407074/
Abstract

In this research, the spinnability of bioactive glass (BG) precursor solution was supplied by alkoxysilane sol with appropriate molar ratio of HO/silicon (R) to prepare bioactive glass fiber membrane (BFM) using electrospinning (ES) technique. Alkoxysilane could form a linear or chain-like colloidal aggregation in hydrolysis-polycondensation with R = 2 or so, thereby exhibiting good spinnability. Therefore, the role of polymer binders could be largely replaced. Due to the significant decrease of polymer binder, the defects within the fibers are largely reduced and degree of fiber densification was improved after calcination, leading to BFM drastically enhanced strength and flexibility. The effect of R and calcination temperature on mechanical performance were investigated in detail. The tensile strength could reach the highest value 2.31 MPa with R = 2 and calcination at 700 °C. In addition, under this preparation condition, the BFM also possessed good flexibility with bending rigidity 37.7 mN. Furthermore, the great performance of promoting cell proliferation and osteogenesis could be observed from cellular experiment. The BFM calcined at 750 °C exhibited the best promoting osteogenic differentiation ability. The rat skull defect model revealed BFM could perform well in osteogenesis .

摘要

在本研究中,通过具有适当的羟基/硅摩尔比(R)的烷氧基硅烷溶胶来提供生物活性玻璃(BG)前驱体溶液的可纺性,以利用静电纺丝(ES)技术制备生物活性玻璃纤维膜(BFM)。当R约为2时,烷氧基硅烷在水解缩聚过程中可形成线性或链状胶体聚集体,从而表现出良好的可纺性。因此,聚合物粘合剂的作用在很大程度上可以被取代。由于聚合物粘合剂的显著减少,纤维内部的缺陷大幅减少,并且煅烧后纤维致密化程度提高,导致BFM的强度和柔韧性大幅增强。详细研究了R和煅烧温度对力学性能的影响。当R = 2且在700℃煅烧时,拉伸强度可达到最高值2.31MPa。此外,在该制备条件下,BFM还具有良好的柔韧性,弯曲刚度为37.7mN。此外,从细胞实验中可以观察到BFM具有促进细胞增殖和成骨的优异性能。在750℃煅烧的BFM表现出最佳的促进成骨分化能力。大鼠颅骨缺损模型表明BFM在骨生成方面表现良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/66752a40e741/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/24d377e59d98/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/88c55d33c97f/sc1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/33a3ecd9d603/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/c023df918fe0/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/db06d19d3c29/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/4f7d6a5d1323/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/3110458f9fd1/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/ab3927a24599/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/66752a40e741/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/24d377e59d98/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/88c55d33c97f/sc1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/33a3ecd9d603/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/c023df918fe0/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/db06d19d3c29/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/4f7d6a5d1323/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/3110458f9fd1/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/ab3927a24599/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a75/11407074/66752a40e741/gr7.jpg

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