A multifunctional composite hydrogel promotes treatment of bisphosphonate-related osteonecrosis of the jaws

骨钙素 运行x2 化学 碱性磷酸酶 双膦酸盐 体内 体外 骨桥蛋白 癌症研究 生物化学 成骨细胞 医学 生物 骨质疏松症 内科学 生物技术
作者
Qianming Du,Na Li,Ziwei Jing,Lianping Xue,Haojie Fu,Jiyun Liu,Qingquan Jia,Zhi Sun,Wei He,Xiaojian Zhang
出处
期刊:Applied Materials Today [Elsevier BV]
卷期号:32: 101787-101787 被引量:3
标识
DOI:10.1016/j.apmt.2023.101787
摘要

The growing use of bisphosphonates (BPs) is a great challenge to the treatment of bisphosphonate-related osteonecrosis of the jaws (BRONJ), however effective treatment methods are currently lacking. Here, modified citraconic amide-functionalized chitosan (CAS) was selected to encapsulate the zeolite imidazolate framework 8 (ZIF-8) loaded with gold nanoparticles (Au NPs) to prepare Au@ZIF-8/CAS. Characterizations confirmed the successful synthesis of Au@ZIF-8/CAS. Mass spectrometry-based metabolomics detected the effects of Au@ZIF-8/CAS on significant metabolic pathways of macrophages in the presence of zoledronic acid (ZA). Twenty-three candidate key metabolites were identified, mainly focusing on the phenylalanine/tyrosine/tryptophan biosynthetic metabolic pathway in the amino acid metabolic pathway. In vitro experiments further confirmed that Au@ZIF-8/CAS could promote the polarization of macrophages from M1 pro-inflammatory phenotype to M2 anti-inflammatory phenotype, so as to produce a good immune microenvironment. In the co-culture system, Au@ZIF-8/CAS could also promote the expression of alkaline phosphatase (ALP), Osteocalcin (OCN), and Runt-related transcription factor 2 (Runx2), and synergistically increased the osteogenic differentiation ability of MC3T3-E1 cells through immunomodulatory effects and direct osteogenic stimulation. Furthermore, the antibacterial properties of Au@ZIF-8/CAS were also investigated. In vivo experiments further verified the potential role of Au@ZIF-8/CAS in treatment of BRONJ. These results will provide new directions and ideas for the treatment of inflammatory diseases.

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