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Antioxidant Iron Oxide Nanoparticles: Their Biocompatibility and Bioactive Properties

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dc.contributor.author김한상-
dc.date.accessioned2024-01-03T00:52:01Z-
dc.date.available2024-01-03T00:52:01Z-
dc.date.issued2023-11-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/197395-
dc.description.abstractA 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.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherMDPI-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntioxidants* / pharmacology-
dc.subject.MESHFerric Compounds / chemistry-
dc.subject.MESHFerric Compounds / pharmacology-
dc.subject.MESHHumans-
dc.subject.MESHHydrogen Peroxide / pharmacology-
dc.subject.MESHMagnetic Iron Oxide Nanoparticles-
dc.subject.MESHNanoparticles* / chemistry-
dc.subject.MESHOxidative Stress-
dc.subject.MESHReactive Oxygen Species-
dc.titleAntioxidant Iron Oxide Nanoparticles: Their Biocompatibility and Bioactive Properties-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorJaewook Lee-
dc.contributor.googleauthorJi-Heon Lee-
dc.contributor.googleauthorSeung-Yeul Lee-
dc.contributor.googleauthorSin A Park-
dc.contributor.googleauthorJae Hoon Kim-
dc.contributor.googleauthorDajeong Hwang-
dc.contributor.googleauthorKyung A Kim-
dc.contributor.googleauthorHan Sang Kim-
dc.identifier.doi10.3390/ijms242115901-
dc.contributor.localIdA01098-
dc.relation.journalcodeJ01133-
dc.identifier.eissn1422-0067-
dc.identifier.pmid37958885-
dc.subject.keywordantioxidant effect-
dc.subject.keywordantioxidant iron oxide-
dc.subject.keywordbiocompatibility-
dc.subject.keywordcell protective effect-
dc.subject.keywordgallic acid-
dc.subject.keywordiron oxide-
dc.subject.keywordnanomaterials-
dc.contributor.alternativeNameKim, Han Sang-
dc.contributor.affiliatedAuthor김한상-
dc.citation.volume24-
dc.citation.number21-
dc.citation.startPage15901-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, Vol.24(21) : 15901, 2023-11-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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