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银纳米颗粒修饰的细胞外基质移植物:制备及其肌腱重建性能

Silver nanoparticles-decorated extracellular matrix graft: fabrication and tendon reconstruction performance.

作者信息

Chen Sunfang, Cai Dan, Dong Qi, Ma Gaoxiang, Xu Chennan, Bao Xiaogang, Yuan Wei, Wu Bing, Fang Bin

机构信息

Department of Orthopedics, the First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, 310000, China.

Department of Orthopedics, the Central Hospital Affiliated to Shaoxing University, Shaoxing, 312030, China.

出版信息

Biomater Res. 2023 Sep 14;27(1):85. doi: 10.1186/s40824-023-00428-0.

DOI:10.1186/s40824-023-00428-0
PMID:37710328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10503197/
Abstract

BACKGROUND

The reconstruction of tendons with large defects requires grafts with high mechanical strength and is often hindered by complications such as infection and adhesion. Hence, grafts combining the advantages of mechanical resilience and antibacterial/antiadhesion activity are highly sought after.

METHODS

The silver nanoparticles (GA-Ag NPs) synthesized from gallic acid and silver nitrate were attached to a decellularized extracellular matrix (Decellularized Tendon crosslinking GA-AgNPs, DT-Ag). We examined the histological structure, mechanical property, morphology, Zeta potential, cytotoxicity, antibacterial properties, antioxidant and anti-inflammatory properties, and ability of the DT-Ag to treat tendon defects in animals.

RESULTS

Approximately 108.57 ± 0.94 μg GA-Ag NPs loaded per 50 mg DT, the cross-linked part of GA-Ag NPs was 65.47 ± 0.57%, which provided DT-Ag with long-lasting antibacterial activity. Meanwhile, GA endowed DT-Ag with good antioxidant and anti-inflammatory activities. Additionally, The DT-Ag facilitated M2 macrophage polarization, and suppressed fibrin deposition by hindering fibroblast adhesion. Mormore, the main advantages of DT-Ag, namely its long-lasting antibacterial activity (tested using Escherichia coli and Staphylococcus aureus as models) and the ability to prevent tissue adhesion were confirmed in vivo.

CONCLUSION

The fabricated multifunctional tendon graft was highly hydrophilic, biocompatible, and mechanically resilient, and concluded to be well suited for dealing with the main complications of surgical tendon reconstruction and has bright application prospects.

摘要

背景

大缺损肌腱的重建需要具有高机械强度的移植物,且常受感染和粘连等并发症的阻碍。因此,兼具机械弹性和抗菌/抗粘连活性优势的移植物备受青睐。

方法

由没食子酸和硝酸银合成的银纳米颗粒(GA-Ag NPs)附着于脱细胞细胞外基质(脱细胞肌腱交联GA-AgNPs,DT-Ag)。我们研究了DT-Ag的组织结构、力学性能、形态、zeta电位、细胞毒性、抗菌性能、抗氧化和抗炎性能以及在动物体内治疗肌腱缺损的能力。

结果

每50mg DT负载约108.57±0.94μg GA-Ag NPs,GA-Ag NPs的交联部分为65.47±0.57%,这赋予DT-Ag持久的抗菌活性。同时,GA赋予DT-Ag良好的抗氧化和抗炎活性。此外,DT-Ag促进M2巨噬细胞极化,并通过阻碍成纤维细胞粘附抑制纤维蛋白沉积。此外,DT-Ag的主要优势,即其持久的抗菌活性(以大肠杆菌和金黄色葡萄球菌为模型进行测试)和预防组织粘连的能力在体内得到证实。

结论

制备的多功能肌腱移植物具有高度亲水性、生物相容性和机械弹性,结论是非常适合处理手术肌腱重建的主要并发症,具有广阔的应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/b9e7c96eb4e3/40824_2023_428_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/df8246048d9c/40824_2023_428_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/a3ca1e909886/40824_2023_428_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/78d80de1586b/40824_2023_428_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/c31c5dc7e23d/40824_2023_428_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/996426e4a9b3/40824_2023_428_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/16e4d5b6b5fe/40824_2023_428_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/9c207a146451/40824_2023_428_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/b9e7c96eb4e3/40824_2023_428_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/df8246048d9c/40824_2023_428_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/a3ca1e909886/40824_2023_428_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/78d80de1586b/40824_2023_428_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/c31c5dc7e23d/40824_2023_428_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/996426e4a9b3/40824_2023_428_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/16e4d5b6b5fe/40824_2023_428_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/9c207a146451/40824_2023_428_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3828/10503197/b9e7c96eb4e3/40824_2023_428_Fig7_HTML.jpg

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