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Neutron-Activatable Holmium-Containing Mesoporous Silica Nanoparticles as a Potential Radionuclide Therapeutic Agent for Ovarian Cancer

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dc.contributor.authorDi Pasqua, Anthony J.-
dc.contributor.authorYuan, Hong-
dc.contributor.authorChung, Younjee-
dc.contributor.authorKim, Jin-Ki-
dc.contributor.authorHuckle, James E.-
dc.contributor.authorLi, Chenxi-
dc.contributor.authorSadgrove, Matthew-
dc.contributor.authorThanh Huyen Tran-
dc.contributor.authorJay, Michael-
dc.contributor.authorLu, Xiuling-
dc.date.accessioned2021-06-23T04:22:51Z-
dc.date.available2021-06-23T04:22:51Z-
dc.date.issued2013-01-
dc.identifier.issn0161-5505-
dc.identifier.issn1535-5667-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/29239-
dc.description.abstractMesoporous silica nanoparticles (MSNs) were explored as a carrier material for the stable isotope Ho-165 and, after neutron capture, its subsequent therapeutic radionuclide, Ho-166 (half-life, 26.8 h), for use in radionuclide therapy of ovarian cancer metastasis. Methods: Ho-165-MSNs were prepared using Ho-166-acetylacetonate and MCM-41 silica particles, and stability was determined after irradiation in a nuclear reactor (reactor power, 1 MW; thermal neutron flux of approximately 5.5 x 10(12) neutrons/cm(2).s). SPECT/CT and tissue biodistribution studies were performed after intraperitoneal administration of Ho-166-MSNs to SKOV-3 ovarian tumor-bearing mice. Radiotherapeutic efficacy was studied by using PET/CT with F-18-FDG to determine tumor volume and by monitoring survival. Results: The holmium-MSNs were able to withstand long irradiation times in a nuclear reactor and did not release Ho-166 after significant dilution. SPECT/CT images and tissue distribution results revealed that Ho-166-MSNs accumulated predominantly in tumors (32.8% +/- 8.1% injected dose/g after 24 h; 81% +/- 7.5% injected dose/g after 1 wk) after intraperitoneal administration. PET/CT images showed reduced F-18-FDG uptake in tumors, which correlated with a marked increase in survival after treatment with approximately 4 MBq of Ho-166-MSNs. Conclusion: The retention of holmium in nanoparticles during irradiation and in vivo after intraperitoneal administration as well as their efficacy in extending survival in tumor-bearing mice underscores their potential as a radiotherapeutic agent for ovarian cancer metastasis.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherSOC NUCLEAR MEDICINE INC-
dc.titleNeutron-Activatable Holmium-Containing Mesoporous Silica Nanoparticles as a Potential Radionuclide Therapeutic Agent for Ovarian Cancer-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.2967/jnumed.112.106609-
dc.identifier.scopusid2-s2.0-84872050514-
dc.identifier.wosid000313606800038-
dc.identifier.bibliographicCitationJOURNAL OF NUCLEAR MEDICINE, v.54, no.1, pp 111 - 116-
dc.citation.titleJOURNAL OF NUCLEAR MEDICINE-
dc.citation.volume54-
dc.citation.number1-
dc.citation.startPage111-
dc.citation.endPage116-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaRadiology, Nuclear Medicine & Medical Imaging-
dc.relation.journalWebOfScienceCategoryRadiology, Nuclear Medicine & Medical Imaging-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusHEPATOCELLULAR-CARCINOMA-
dc.subject.keywordPlusRADIATION-THERAPY-
dc.subject.keywordPlusMICROSPHERES-
dc.subject.keywordPlusBIOCOMPATIBILITY-
dc.subject.keywordPlusRADIOTHERAPY-
dc.subject.keywordAuthorholmium-
dc.subject.keywordAuthormesoporous silica nanoparticle-
dc.subject.keywordAuthorovarian cancer-
dc.subject.keywordAuthorradiotherapeutics-
dc.subject.keywordAuthordrug delivery-
dc.identifier.urlhttps://jnm.snmjournals.org/content/54/1/111-
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