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聚(1,8 - 辛二醇 - 柠檬酸酯)弹性体的本体侵蚀降解机制:体内和体外研究

Bulk Erosion Degradation Mechanism for Poly(1,8-octanediol--citrate) Elastomer: An In Vivo and In Vitro Investigation.

作者信息

Wan Lu, Lu Liangliang, Zhu Tangsong, Liu Zhichang, Du Ruichun, Luo Qiong, Xu Qiang, Zhang Qiuhong, Jia Xudong

机构信息

Key Laboratory of High Performance Polymer Material and Technology of MOE, Department of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, P. R. China.

State Key Laboratory of Pharmaceutical Biotechnology, Department of Biotechnology and Pharmaceutical Sciences, School of Life Sciences, Nanjing University, Nanjing 210023, P R China.

出版信息

Biomacromolecules. 2022 Oct 10;23(10):4268-4281. doi: 10.1021/acs.biomac.2c00737. Epub 2022 Sep 12.

Abstract

As a biodegradable elastomer, poly(1,8-octanediol--citrate) (POC) has been widely applied in tissue engineering and implantable electronics. However, the unclear degradation mechanism has posed a great challenge for the better application and development of POC. To reveal the degradation mechanism, here, we present a systematic investigation into in vivo and in vitro degradation behaviors of POC. Initially, critical factors, including chemical structures, hydrophilic and water-absorbency characteristics, and degradation reaction of POC, are investigated. Then, various degradation-induced changes during in vitro degradation of POC-x (POC with different cross-linking densities) are monitored and discussed. The results show that (1) cross-linking densities exponentially drop with degradation time; (2) mass loss and PBS-absorption ratio grow nonlinearly; (3) the morphology on the cross-section changes from flat to rough at a microscopic level; (4) the cubic samples keep swelling until they collapse into fragments from a macro view; and (5) the mechanical properties experience a sharp drop at the beginning of degradation. Finally, the in vivo degradation behaviors of POC-x are investigated, and the results are similar to those in vitro. The comprehensive assessment suggests that the in vitro and in vivo degradation of POC occurs primarily through bulk erosion. Inflammation responses triggered by the degradation of POC-x are comparable to poly(lactic acid), or even less obvious. In addition, the mechanical evaluation of POC in the simulated application environment is first proposed and conducted in this work for a more appropriate application. The degradation mechanism of POC revealed will greatly promote the further development and application of POC-based materials in the biomedical field.

摘要

作为一种可生物降解的弹性体,聚(1,8 - 辛二醇 - 柠檬酸酯)(POC)已广泛应用于组织工程和可植入电子设备中。然而,其降解机制不明确,这对POC的更好应用和发展构成了巨大挑战。为揭示其降解机制,在此我们对POC的体内外降解行为进行了系统研究。首先,研究了包括化学结构、亲水性和吸水性特征以及POC降解反应等关键因素。然后,监测并讨论了POC - x(具有不同交联密度的POC)在体外降解过程中各种降解诱导的变化。结果表明:(1)交联密度随降解时间呈指数下降;(2)质量损失和PBS吸收率呈非线性增长;(3)微观层面上,横截面形态从平坦变为粗糙;(4)从宏观角度看,立方样品持续膨胀直至坍塌成碎片;(5)降解开始时力学性能急剧下降。最后,研究了POC - x的体内降解行为,结果与体外相似。综合评估表明,POC的体外和体内降解主要通过本体侵蚀发生。POC - x降解引发的炎症反应与聚乳酸相当,甚至不太明显。此外,为了更合适的应用,本文首次提出并进行了模拟应用环境中POC的力学评估。所揭示的POC降解机制将极大地促进基于POC的材料在生物医学领域的进一步发展和应用。

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