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dc.contributor.authorPark, Dong Jin-
dc.contributor.authorMin, Kyung Hyun-
dc.contributor.authorLee, Hong Jae-
dc.contributor.authorKim, Kwangmeyung-
dc.contributor.authorKwon, Ick Chan-
dc.contributor.authorJeong, Seo Young-
dc.contributor.authorLee, Sang Cheon-
dc.date.accessioned2024-01-20T05:01:49Z-
dc.date.available2024-01-20T05:01:49Z-
dc.date.created2022-01-25-
dc.date.issued2016-02-
dc.identifier.issn2050-7518-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/124420-
dc.description.abstractIn this work, we have developed photosensitizer-loaded bubble-generating calcium carbonate (CaCO3)-mineralized nanoparticles that have potential for ultrasound imaging (US)-guided photodynamic therapy (PDT) of tumors. A photosensitizer, chlorin e6 (Ce6)-loaded CaCO3-mineralized nanoparticles (Ce6-BMNs), was prepared using an anionic block copolymer-templated in situ mineralization method. Ce6-BMNs were composed of the Ce6-loaded CaCO3 core and the hydrated poly(ethylene glycol) (PEG) shell. Ce6-BMNs exhibited excellent stability under serum conditions. Ce6-BMNs showed enhanced echogenic US signals at tumoral acid pH by generating carbon dioxide (CO2) bubbles. Ce6-BMNs effectively inhibited Ce6 release at physiological pH (7.4). At a tumoral acidic pH (6.4), Ce6 release was accelerated with CO2 bubble generation due to the dissolution of the CaCO3 mineral core. Upon irradiation of Ce6-BMN-treated MCF-7 breast cancer cells, the cell viability dramatically decreased with increasing Ce6 concentration. The phototoxicity of the Ce6-BMNs was much higher than that of free Ce6. On the basis of tumoral pH-responsive CO2 bubble-generation and simultaneous Ce6 release at the target tumor site, these CaCO3 mineralized nanoparticles can be considered as promising theranostic nanoparticles for US imaging-guided PDT in the field of tumor therapy.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titlePhotosensitizer-loaded bubble-generating mineralized nanoparticles for ultrasound imaging and photodynamic therapy-
dc.typeArticle-
dc.identifier.doi10.1039/c5tb02338f-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF MATERIALS CHEMISTRY B, v.4, no.7, pp.1219 - 1227-
dc.citation.titleJOURNAL OF MATERIALS CHEMISTRY B-
dc.citation.volume4-
dc.citation.number7-
dc.citation.startPage1219-
dc.citation.endPage1227-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000370427400003-
dc.identifier.scopusid2-s2.0-84957998604-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.relation.journalResearchAreaMaterials Science-
dc.type.docTypeArticle-
dc.subject.keywordPlusMICROBUBBLE CONTRAST AGENTS-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusTUMOR ANGIOGENESIS-
dc.subject.keywordPlusCONTROLLED-RELEASE-
dc.subject.keywordPlusMESOPOROUS SILICA-
dc.subject.keywordPlusTHERANOSTIC AGENT-
dc.subject.keywordPlusCANCER-TREATMENT-
dc.subject.keywordPlusHYALURONIC-ACID-
dc.subject.keywordPlusBLOCK-COPOLYMER-
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