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一种新型可持续生物基弹性体纳米复合材料的制备及表征,该复合材料含有聚(癸二酸甘油酯柠檬酸酯)/壳聚糖/羟基磷灰石,有望用于组织工程应用。

Preparation and characterization of a new sustainable bio-based elastomer nanocomposites containing poly(glycerol sebacate citrate)/chitosan/n-hydroxyapatite for promising tissue engineering applications.

机构信息

School of Chemical Engineering, College of Engineering, University of Tehran, Tehran, Iran.

Department of Biomedical Engineering, Islamic Azad University, Tehran, Iran.

出版信息

J Biomater Sci Polym Ed. 2022 Dec;33(18):2385-2405. doi: 10.1080/09205063.2022.2104600. Epub 2022 Jul 28.

DOI:10.1080/09205063.2022.2104600
PMID:35876727
Abstract

Poly (glycerol sebacate citrate) (PGSC) has potential applications in tissue engineering due to its biodegradability and suitable elasticity. However, its applications are restricted owing to its acidity and high degradation rate. In this study, a new bio-nanocomposite based on PGSC has been synthesized by incorporating chitosan (CS) and various concentrations of hydroxyapatite nanoparticles (n-HA). It is assumed that the basicity of a CS and hydroxyl groups of n-HA will reduce the acidity of PGSC and control the rate of degradation. Also, the biocompatibility of n-HA and inherent hydrophilicity of CS can improve cell adhesion and proliferation of PGSC-based scaffolds. FTIR, XRD, FESEM, and EDX tests confirmed the synthesis of these nanocomposites and the interaction between each of the components. The results of the DMTA test also indicated the elastic behavior of the samples embedded with n-HA. The hydrophilicity assay demonstrated that the water contact angle of the scaffolds decreased as the concentration of n-HA augmented, and it reached the value of 44 ± 0.9° for nanocomposite containing 5 wt.% n-HA. The degradation rate of all PGSC nanocomposites was reduced due to the anionic groups of n-HA and CS. TGA assay indicated that the incorporation of n-HA led to the enhancement of scaffolds' thermal stability. Furthermore, the synergistic effect of CS and n-HA on the enhancement of protein adsorption and cell proliferation was confirmed through protein adhesion and MTT assay, respectively. Consequently, the addition of n-HA and CS perform the new bio-nanocomposites scaffolds based on PGSC with sufficient hydrophilicity, flexibility, and thermal stability in tissue engineering applications.

摘要

聚(癸二酸柠檬酸甘油酯)(PGSC)由于其生物降解性和适宜的弹性,在组织工程中有潜在的应用。然而,由于其酸性和高降解率,其应用受到限制。在本研究中,通过将壳聚糖(CS)和不同浓度的羟基磷灰石纳米粒子(n-HA)掺入 PGSC,合成了一种新型的基于 PGSC 的生物纳米复合材料。据推测,CS 的碱性和 n-HA 的羟基基团将降低 PGSC 的酸度并控制降解速率。此外,n-HA 的生物相容性和 CS 的固有亲水性可以提高 PGSC 支架的细胞黏附和增殖。FTIR、XRD、FESEM 和 EDX 测试证实了这些纳米复合材料的合成以及各组分之间的相互作用。DMTA 测试结果还表明了嵌入 n-HA 的样品的弹性行为。亲水性试验表明,随着 n-HA 浓度的增加,支架的水接触角降低,当纳米复合材料中含有 5wt.%n-HA 时,其值达到 44±0.9°。由于 n-HA 和 CS 的阴离子基团,所有 PGSC 纳米复合材料的降解速率均降低。TGA 测试表明,n-HA 的加入导致支架热稳定性增强。此外,通过蛋白质吸附和 MTT 试验分别证实了 CS 和 n-HA 对增强蛋白质吸附和细胞增殖的协同作用。因此,n-HA 和 CS 的添加使基于 PGSC 的新型生物纳米复合材料支架具有足够的亲水性、柔韧性和热稳定性,适用于组织工程应用。

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