Controlled delivery of procyanidin through magnesium oxide nanoparticles (MgO NPs) to improve the activity and mineralization of osteoblasts under oxidative stress in vitro
- PMID: 38815600
- DOI: 10.1088/1748-605X/ad5260
Controlled delivery of procyanidin through magnesium oxide nanoparticles (MgO NPs) to improve the activity and mineralization of osteoblasts under oxidative stress in vitro
Abstract
Excessive reactive oxygen species (ROS) in the microenvironment of osteoporosis (OP) not only accelerate the bone absorption, but also affect the osteogenic and mineralized effect of osteoblasts. Procyanidins (PC) have been reported to have anti-oxidation effects, but low bioavailability. This study aimed to explore the effect of magnesium oxide nanoparticles (MgO-PC NPs)-loaded PC on the osteogenesis and mineralization of osteoblasts that stimulated by H2O2. PC was loaded onto MgO NPs and characterized by transmission electron microscopy, energy dispersive spectroscopy, dynamic light scattering, and Fourier transform infrared spectroscopy. After primary screening by cytotoxicity assay, MgO-PC NPs containing 20 μM of PC were chosen for further studies. In H2O2-stimulated osteoblasts, dichlorodihydrofluorescein diacetate probe, Cell Counting Kit-8, quantitative real-time polymerase chain reaction, alkaline phosphatase staining/activity and Alizarin red staining were used to detect the ROS production, cell viability and osteogenic and mineralized markers of osteoblasts. PC was loaded onto MgO NPs to successfully receive MgO-PC NPs with a diameter of about 144 nm and negative potential. PC can sustain release from MgO-PC NPs for at least 16 d. The controlled release of PC from MgO-PC NPs can effectively eliminate ROS and thereby promoted the cell activity. Most importantly, the osteogenesis and mineralization of osteoblasts under oxidative stress were also significantly reversed by MgO-PC NPS. Thus, these findings indicate that MgO-PC NPs may be developed as a potential therapeutic strategy for OP.
Keywords: magnesium oxide nanoparticles; mineralization; osteoblasts; oxidative stress; procyanidin.
© 2024 IOP Publishing Ltd.
Similar articles
-
Magnesium oxide nanoparticles alleviate arsenic toxicity, reduce oxidative stress and arsenic accumulation in rice (Oryza sativa L.).Environ Sci Pollut Res Int. 2023 Nov;30(55):117932-117951. doi: 10.1007/s11356-023-30411-0. Epub 2023 Oct 24. Environ Sci Pollut Res Int. 2023. PMID: 37872343
-
Cytoprotective effect of Fufang Lurong Jiangu capsule against hydrogen peroxide-induced oxidative stress in bone marrow stromal cell-derived osteoblasts through the Nrf2/HO-1 signaling pathway.Biomed Pharmacother. 2020 Jan;121:109676. doi: 10.1016/j.biopha.2019.109676. Epub 2019 Nov 25. Biomed Pharmacother. 2020. PMID: 31810119
-
The Effect of Sulforaphane on the Activity and Mineralization of Osteoblasts under Oxidative Stress.Pharmacology. 2019;104(3-4):147-156. doi: 10.1159/000500846. Epub 2019 Jul 30. Pharmacology. 2019. PMID: 31362292
-
Effects of silica-gentamicin nanohybrids on osteogenic differentiation of human osteoblast-like SaOS-2 cells.Int J Nanomedicine. 2018 Feb 9;13:877-893. doi: 10.2147/IJN.S147849. eCollection 2018. Int J Nanomedicine. 2018. PMID: 29445277 Free PMC article.
-
Blockage of both the extrinsic and intrinsic pathways of diazinon-induced apoptosis in PaTu cells by magnesium oxide and selenium nanoparticles.Int J Nanomedicine. 2016 Nov 22;11:6239-6250. doi: 10.2147/IJN.S119680. eCollection 2016. Int J Nanomedicine. 2016. PMID: 27920530 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous