Antioxidant Iron Oxide Nanoparticles: Their Biocompatibility and Bioactive Properties

被引:7
作者
Lee, Jaewook [1 ]
Lee, Ji-Heon [2 ]
Lee, Seung-Yeul [3 ]
Park, Sin A. [3 ]
Kim, Jae Hoon [3 ]
Hwang, Dajeong [4 ]
Kim, Kyung A. [5 ]
Kim, Han Sang [5 ,6 ]
机构
[1] Dongguk Univ, Res Inst Biomol Chem, Seoul 04620, South Korea
[2] Korea Natl Univ Transportat, Nat Key Technol Inst Univ, 4D Convergence Technol Inst, Jungpyeong 27909, South Korea
[3] Genomictree Inc, 44-6 10 Ro Techno, Daejeon 34027, South Korea
[4] Chungnam Natl Univ, Dept Chem Engn & Appl Chem, Daejeon 34134, South Korea
[5] Yonsei Canc Ctr, Seoul 30722, South Korea
[6] Yonsei Univ, Grad Sch Med Sci, Div Med Oncol, Coll Med,Dept Internal Med,Brain Korea Project 21, Seoul 03722, South Korea
基金
新加坡国家研究基金会;
关键词
iron oxide; antioxidant iron oxide; gallic acid; biocompatibility; antioxidant effect; nanomaterials; cell protective effect; DRUG-DELIVERY SYSTEMS; GALLIC ACID; TETRASPANIN CD9;
D O I
10.3390/ijms242115901
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A lot of nanomaterials have been applied to various nano-biotechnological fields, such as contrast agents, drug or gene delivery systems, cosmetics, and so on. Despite the expanding usage of nanomaterials, concerns persist regarding their potential toxicity. To address this issue, many scientists have tried to develop biocompatible nanomaterials containing phytochemicals as a promising solution. In this study, we synthesized biocompatible nanomaterials by using gallic acid (GA), which is a phytochemical, and coating it onto the surface of iron oxide nanoparticles (IONPs). Importantly, the GA-modified iron oxide nanoparticles (GA-IONPs) were successfully prepared through environmentally friendly methods, avoiding the use of harmful reagents and extreme conditions. The presence of GA on the surface of IONPs improved their stability and bioactive properties. In addition, cell viability assays proved that GA-IONPs possessed excellent biocompatibility in human dermal papilla cells (HDPCs). Additionally, GA-IONPs showed antioxidant activity, which reduced intracellular reactive oxygen species (ROS) levels in an oxidative stress model induced by hydrogen peroxide (H2O2). To investigate the impact of GA-IONPs on exosome secretions from oxidative stress-induced cells, we analyzed the number and characteristics of exosomes in the culture media of HDPCs after H2O2 stimulation or GA-IONP treatment. Our analysis revealed that both the number and proportions of tetraspanins (CD9, CD81, and CD63) in exosomes were similar in the control group and the GA-IONP-treated groups. In contrast, exosome secretion was increased, and the proportion of tetraspanin was changed in the H2O2-treated group compared to the control group. It demonstrated that treatment with GA-IONPs effectively attenuated exosome secretion induced by H2O2-induced oxidative stress. Therefore, this GA-IONP exhibited outstanding promise for applications in the field of nanobiotechnology.
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页数:12
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