Curcumin delivery using tetrahedral framework nucleic acids enhances bone regeneration in osteoporotic rats

姜黄素 再生(生物学) 核酸 骨质疏松症 间充质干细胞 运行x2 化学 抗氧化剂 小干扰RNA 药物输送 间质细胞 碱性磷酸酶 骨细胞 骨组织 药理学 生物化学 癌症研究 成骨细胞 细胞生物学 医学 生物医学工程 内科学 生物 核糖核酸 体外 基因 有机化学
作者
Long Bai,Maogeng Feng,Qiumei Li,Yuxuan Zhao,Geru Zhang,Zhengwen Cai,Jingang Xiao,Yunfeng Lin
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:472: 144978-144978 被引量:16
标识
DOI:10.1016/j.cej.2023.144978
摘要

Osteoporosis is an age-related disorder characterized by progressive bone loss and impaired bone regeneration following surgery. The key to the treatment of osteoporosis is the ability to promote bone differentiation of bone marrow mesenchymal stem cells (BMSCs). Curcumin (Cur) is a class of flavonoids with antioxidant and anti-apoptotic ability to promote osteogenesis in osteoporosis. However, Cur has deficiencies such as low cell entry efficiency, easy degradation and hydrophobicity, and new drug delivery strategies are urgently needed to improve the application prospects of Cur. Tetrahedral framework nucleic acids (tFNAs) are a class of anti-inflammatory and antioxidant nanomedicines with spatial structure, as well as small molecule drug delivery systems with good biosafety. tFNAs can bind herbal monomers and small molecule peptides through electrostatic interaction and grooves to promote drug utilization. Meanwhile, tFNAs can connect miRNAs and siRNAs through specially designed sticky ends to regulate the biological functions and activities of cells. In this study, we synthesized tFNAs/Cur complexes, a novel nucleic acid drug system for promoting osteoporotic bone regeneration, to deliver Cur into BMSCs and to exert antioxidant and anti-apoptotic effects. tFNAs/Cur complexes reverse TNF-α-promoted osteogenic inhibition, and facilitate the expression of alkaline phosphatase (Alp), runt-related transcription factor 2 (Runx2), and osterix (Osx). The effect of tFNAs/Cur on the repair of tibial defects in rats with postmenopausal osteoporosis was studied. The experimental group exhibited a higher bone-formation capacity than the control group after 14 and 21 days. In conclusion, tFNAs improve Cur utilization, promote bone repair, and are promising osteoporosis-treatment interventions.
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