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Self-sealing hyaluronic acid-coated 30-gauge intravitreal injection needles for preventing vitreous and drug reflux through needle passage

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dc.contributor.authorEom, Youngsub-
dc.contributor.authorKim, Soomi-
dc.contributor.authorHuh, Jungah-
dc.contributor.authorKoh, Mi Young-
dc.contributor.authorHwang, Jin Young-
dc.contributor.authorKang, Boram-
dc.contributor.authorLi, Xiangzhe-
dc.contributor.authorLee, Moon Sue-
dc.contributor.authorLee, Haeshin-
dc.contributor.authorKim, Hyo Myung-
dc.contributor.authorSong, Jong Suk-
dc.date.accessioned2022-02-25T07:40:27Z-
dc.date.available2022-02-25T07:40:27Z-
dc.date.created2022-02-07-
dc.date.issued2021-08-20-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/136834-
dc.description.abstractSelf-sealing hyaluronic acid (HA)-coated self-sealing 30-gauge needles exhibiting instant leakage prevention of intravitreal humor and injected drug were developed in this study. Ninety New Zealand rabbits were used in this study. We assessed dye regurgitation in intravitreal ICG dye injections using HA-coated needles (HA needle group) and conventional needles (control group). Vitreous humor levels of anti-vascular endothelial growth factor (VEGF) were compared between groups one, three, and seven days after intravitreal bevacizumab (0.016 mL) injections. Expression levels of inflammatory cytokines in the aqueous humor and vitreous humor, including prostaglandin E-2 (PGE(2)), interferon-gamma, tumor necrosis factor-alpha, interleukin (IL)-1 beta, IL-4, IL-6, IL-17, and IL-8, were compared between HA needle, control, and normal (in which intravitreal injection was not performed) groups following 12 intravitreal injections over a period of one week. In the HA needle group, HA remained at the injection site and blocked the hole after intravitreal injection. Dye regurgitation occurred significantly less frequently in the HA needle group (16.7%) than the control group (55.6%) after intravitreal ICG dye injection. Meanwhile, vitreous anti-VEGF levels were markedly higher in the HA needle group than the control group one and three days after intravitreal bevacizumab injections. After 12 intravitreal injections, expression levels of aqueous and vitreous IL-8 significantly increased in the control group compared to the HA needle and normal groups. Conversely, there were no significant differences in the expression of the other seven cytokines among the three groups. Intravitreal injections using HA-coated self-sealing 30-gauge needles can block the outflow of vitreous humor and drugs through the needle passage.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherNATURE PORTFOLIO-
dc.subjectOCULAR BIOCOMPATIBILITY-
dc.subjectMACULAR DEGENERATION-
dc.subjectENDOPHTHALMITIS-
dc.subjectPHARMACOKINETICS-
dc.subjectBEVACIZUMAB-
dc.subjectRANIBIZUMAB-
dc.subjectASSOCIATION-
dc.subjectBEVACKUMAB-
dc.subjectHYDROGELS-
dc.subjectSURFACE-
dc.titleSelf-sealing hyaluronic acid-coated 30-gauge intravitreal injection needles for preventing vitreous and drug reflux through needle passage-
dc.typeArticle-
dc.contributor.affiliatedAuthorEom, Youngsub-
dc.contributor.affiliatedAuthorSong, Jong Suk-
dc.identifier.doi10.1038/s41598-021-96561-8-
dc.identifier.scopusid2-s2.0-85113268109-
dc.identifier.wosid000687326500067-
dc.identifier.bibliographicCitationSCIENTIFIC REPORTS, v.11, no.1-
dc.relation.isPartOfSCIENTIFIC REPORTS-
dc.citation.titleSCIENTIFIC REPORTS-
dc.citation.volume11-
dc.citation.number1-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusASSOCIATION-
dc.subject.keywordPlusBEVACIZUMAB-
dc.subject.keywordPlusBEVACKUMAB-
dc.subject.keywordPlusENDOPHTHALMITIS-
dc.subject.keywordPlusHYDROGELS-
dc.subject.keywordPlusMACULAR DEGENERATION-
dc.subject.keywordPlusOCULAR BIOCOMPATIBILITY-
dc.subject.keywordPlusPHARMACOKINETICS-
dc.subject.keywordPlusRANIBIZUMAB-
dc.subject.keywordPlusSURFACE-
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