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通过添加植物疗法药物和介孔生物活性玻璃纳米颗粒(MBGNs)来增强用于生物制造的基于海藻酸钠二醛-明胶(ADA-GEL)的水凝胶。

Enhancing alginate dialdehyde-gelatin (ADA-GEL) based hydrogels for biofabrication by addition of phytotherapeutics and mesoporous bioactive glass nanoparticles (MBGNs).

作者信息

Bider Faina, Gunnella Chiara, Reh Jana T, Clejanu Corina-Elena, Kuth Sonja, Beltrán Ana M, Boccaccini Aldo R

机构信息

Institute of Biomaterials, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany.

Department of Electronics, Information and Bioengineering, Politecnico di Milano, Milano, Italy.

出版信息

J Biomater Appl. 2025 Jan;39(6):524-556. doi: 10.1177/08853282241280768. Epub 2024 Sep 21.

DOI:10.1177/08853282241280768
PMID:39305217
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11707976/
Abstract

This study explores the 3D printing of alginate dialdehyde-gelatin (ADA-GEL) inks incorporating phytotherapeutic agents, such as ferulic acid (FA), and silicate mesoporous bioactive glass nanoparticles (MBGNs) at two different concentrations. 3D scaffolds with bioactive properties suitable for bone tissue engineering (TE) were obtained. The degradation and swelling behaviour of films and 3D printed scaffolds indicated an accelerated trend with increasing MBGN content, while FA appeared to stabilize the samples. Determination of the degree of crosslinking validated the increased stability of hydrogels due to the addition of FA and 0.1% (w/v) MBGNs. The incorporation of MBGNs not only improved the effective moduli and conferred bioactive properties through the formation of hydroxyapatite (HAp) on the surface of ADA-GEL-based samples but also enhanced VEGF-A expression of MC3T3-E1 cells. The beneficial impact of FA and low concentrations of MBGNs in ADA-GEL-based inks for 3D (bio)printing applications was corroborated through various printing experiments, resulting in higher printing resolution, as also confirmed by rheological measurements. Cytocompatibility investigations revealed enhanced MC3T3-E1 cell activity and viability. Furthermore, the presence of mineral phases, as confirmed by an in vitro biomineralization assay, and increased ALP activity after 21 days, attributed to the addition of FA and MBGNs, were demonstrated. Considering the acquired structural and biological properties, along with efficient drug delivery capability, enhanced biological activity, and improved 3D printability, the newly developed inks exhibit promising potential for biofabrication and bone TE.

摘要

本研究探索了藻酸盐二醛 - 明胶(ADA - GEL)油墨的3D打印,该油墨含有阿魏酸(FA)等植物治疗剂以及两种不同浓度的硅酸盐介孔生物活性玻璃纳米颗粒(MBGNs)。获得了具有适合骨组织工程(TE)的生物活性特性的3D支架。薄膜和3D打印支架的降解和溶胀行为表明,随着MBGN含量的增加呈加速趋势,而FA似乎使样品稳定。交联度的测定证实了由于添加FA和0.1%(w/v)MBGNs,水凝胶的稳定性增加。MBGNs的掺入不仅提高了有效模量,并通过在基于ADA - GEL的样品表面形成羟基磷灰石(HAp)赋予生物活性特性,还增强了MC3T3 - E1细胞的VEGF - A表达。通过各种打印实验证实了FA和低浓度MBGNs对基于ADA - GEL的油墨用于3D(生物)打印应用的有益影响,流变学测量也证实了这导致更高的打印分辨率。细胞相容性研究显示MC3T3 - E1细胞活性和活力增强。此外,体外生物矿化测定证实了矿物相的存在,并且由于添加了FA和MBGNs,在21天后碱性磷酸酶(ALP)活性增加。考虑到所获得的结构和生物学特性,以及有效的药物递送能力、增强的生物活性和改进的3D可打印性,新开发的油墨在生物制造和骨TE方面显示出有前景的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/c15ac197411b/10.1177_08853282241280768-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/ce4d81401b1d/10.1177_08853282241280768-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/678174a67137/10.1177_08853282241280768-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/2194beefe3e6/10.1177_08853282241280768-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/d6f4e04c034c/10.1177_08853282241280768-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/61d7e44ef462/10.1177_08853282241280768-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/33b4a35dedbb/10.1177_08853282241280768-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/b413248b76a4/10.1177_08853282241280768-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/f14e728b6411/10.1177_08853282241280768-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/10f3705888cf/10.1177_08853282241280768-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/c15ac197411b/10.1177_08853282241280768-fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/ce4d81401b1d/10.1177_08853282241280768-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/678174a67137/10.1177_08853282241280768-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/2194beefe3e6/10.1177_08853282241280768-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/d6f4e04c034c/10.1177_08853282241280768-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/61d7e44ef462/10.1177_08853282241280768-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/33b4a35dedbb/10.1177_08853282241280768-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/b413248b76a4/10.1177_08853282241280768-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/f14e728b6411/10.1177_08853282241280768-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/10f3705888cf/10.1177_08853282241280768-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e3d/11707976/c15ac197411b/10.1177_08853282241280768-fig10.jpg

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本文引用的文献

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