In vivo imaging of β-galactosidase stimulated activity in hepatocellular carcinoma using ligand-targeted fluorescent probe

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dc.contributor.authorE J Kim-
dc.contributor.authorR Kumar-
dc.contributor.authorA Sharma-
dc.contributor.authorB Yoon-
dc.contributor.authorHyun Min Kim-
dc.contributor.authorHyunseung Lee-
dc.contributor.authorKwan Soo Hong-
dc.contributor.authorJ S Kim-
dc.date.accessioned2017-08-29-
dc.date.available2017-08-29-
dc.date.issued2017-
dc.identifier.issn0142-9612-
dc.identifier.uri10.1016/j.biomaterials.2017.01.009ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/17019-
dc.description.abstractDevelopment of targeted, selective, and noninvasive fluorescent probes for in vivo visualization of tumor-associated overexpressed enzymes are highly anticipated for cancer diagnosis and therapy. Herein, we developed a noninvasive fluorescent probe (DCDHF-βgal) for the sensitive detection, and in vivo visualization of β-galactosidase in hepatocyte HepG2 cells and its xenograft model. As a model system for in vivo targeted imaging, DCDHF-βgal possessing galactose unit selectively target hepatocyte and monitor the β-galactosidase activity with deep tissue penetration, and low background interference. DCDHF-βgal was activated by intracellular β-galactosidases as the driving force for the release of NIR fluorophore, thereby exhibiting ratiometric optical response. Initial fluorescence emission measured at 615nm was changed to fluorescence at 665nm upon activation of DCDHF-βgal with β-galactosidase. Ratiometric fluorescence detection of β-galactosidase was also observed in hepatocellular carcinoma cells and tumor xenograft. The noninvasive in vivo optical imaging facilitated by targeted and enzyme-activated imaging agent would be useful in various biomedical and diagnostic applications.-
dc.publisherElsevier-
dc.titleIn vivo imaging of β-galactosidase stimulated activity in hepatocellular carcinoma using ligand-targeted fluorescent probe-
dc.title.alternativeIn vivo imaging of β-galactosidase stimulated activity in hepatocellular carcinoma using ligand-targeted fluorescent probe-
dc.typeArticle-
dc.citation.titleBiomaterials-
dc.citation.number0-
dc.citation.endPage90-
dc.citation.startPage83-
dc.citation.volume122-
dc.contributor.affiliatedAuthorHyun Min Kim-
dc.contributor.affiliatedAuthorHyunseung Lee-
dc.contributor.affiliatedAuthorKwan Soo Hong-
dc.contributor.alternativeName김은중-
dc.contributor.alternativeNameKumar-
dc.contributor.alternativeNameSharma-
dc.contributor.alternativeName윤병권-
dc.contributor.alternativeName김현민-
dc.contributor.alternativeName이현승-
dc.contributor.alternativeName홍관수-
dc.contributor.alternativeName김종승-
dc.identifier.bibliographicCitationBiomaterials, vol. 122, pp. 83-90-
dc.identifier.doi10.1016/j.biomaterials.2017.01.009-
dc.subject.keywordFluorescent probe-
dc.subject.keywordHepatocellular-
dc.subject.keywordIn vivo imaging-
dc.subject.keywordRatiometric-
dc.subject.keywordβ-galactosidase-
dc.subject.localFluorescent probes-
dc.subject.localfluorescent probe-
dc.subject.localFluorescent probe-
dc.subject.localfluorescent probes-
dc.subject.localHepatocellular-
dc.subject.localhepatocellular-
dc.subject.localin vivo imaging-
dc.subject.localIn vivo imaging-
dc.subject.localRatiometric-
dc.subject.localβ-galactosidase-
dc.subject.localbeta galactosidase-
dc.subject.localß-Galactosidase-
dc.subject.localβ-Galactosidase-
dc.description.journalClassY-
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