0 592

Cited 0 times in

In vivo near-infrared imaging and phototherapy of tumors using a cathepsin B-activated fluorescent probe

DC Field Value Language
dc.contributor.author남기택-
dc.contributor.author유성숙-
dc.date.accessioned2017-11-02T08:12:01Z-
dc.date.available2017-11-02T08:12:01Z-
dc.date.issued2017-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/154190-
dc.description.abstractThe development of multifunctional reagents for simultaneous specific near-infrared (NIR) imaging and phototherapy of tumors is of great significance. This work describes the design of a cathepsin B-activated fluorescent probe (CyA-P-CyB) and its applications as an NIR imaging probe for tumor cells and as a phototherapy reagent for tumors. In vitro experiments demonstrated that CyA-P-CyB was activated via the cleavage of a peptide linker by cathepsin B in tumor cells to produce fluorescence in the NIR region based on a FRET mechanism. MTT assays showed that the phototoxicity of CyA-P-CyB toward cells depended on the activity of cathepsin B, and the probe exhibited specific phototoxicity toward tumor cells. CyA-P-CyB was also successfully applied to the in vivo imaging and phototherapy of tumors. Histological analysis indicated that CyA-P-CyB had no cytotoxic effects on seven mouse tissues (lung, liver, heart, kidney, pancreas, spleen and brain) after the CyA-P-CyB treatment and laser irradiation.-
dc.description.statementOfResponsibilityrestriction-
dc.publisherElsevier Science-
dc.relation.isPartOfBIOMATERIALS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnimals-
dc.subject.MESHCathepsin B-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHFluorescent Dyes/chemical synthesis-
dc.subject.MESHHumans-
dc.subject.MESHInfrared Rays-
dc.subject.MESHMale-
dc.subject.MESHMice-
dc.subject.MESHMice, Inbred BALB C-
dc.subject.MESHMice, Nude-
dc.subject.MESHMicroscopy, Fluorescence/methods*-
dc.subject.MESHNeoplasms, Experimental/drug therapy*-
dc.subject.MESHNeoplasms, Experimental/metabolism-
dc.subject.MESHNeoplasms, Experimental/pathology*-
dc.subject.MESHOligopeptides/chemistry-
dc.subject.MESHOligopeptides/pharmacokinetics*-
dc.subject.MESHPhotochemotherapy/methods*-
dc.subject.MESHPhotosensitizing Agents/administration & dosage-
dc.subject.MESHTheranostic Nanomedicine/methods*-
dc.subject.MESHTreatment Outcome-
dc.titleIn vivo near-infrared imaging and phototherapy of tumors using a cathepsin B-activated fluorescent probe-
dc.typeArticle-
dc.publisher.locationNetherlands-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Life Science-
dc.contributor.googleauthorXiaoqiang Chen-
dc.contributor.googleauthorDayoung Lee-
dc.contributor.googleauthorSungsook Yu-
dc.contributor.googleauthorGyoungmi Kim-
dc.contributor.googleauthorSongyi Lee-
dc.contributor.googleauthorYejin Cho-
dc.contributor.googleauthorHaengdueng Jeong-
dc.contributor.googleauthorKi Taek Nam-
dc.contributor.googleauthorJuyoung Yoon-
dc.identifier.doi10.1016/j.biomaterials.2017.01.020.-
dc.contributor.localIdA02473-
dc.contributor.localIdA01243-
dc.relation.journalcodeJ00312-
dc.identifier.eissn1878-5905-
dc.identifier.pmid28113107-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0142961217300285-
dc.subject.keywordEnzyme-activated fluorescence-
dc.subject.keywordMultiple functional probe-
dc.subject.keywordNIR bioimaging-
dc.subject.keywordSpecific phototherapy-
dc.contributor.alternativeNameNam, Ki Taek-
dc.contributor.alternativeNameYu, Sungsook-
dc.contributor.affiliatedAuthorYu, Sungsook-
dc.contributor.affiliatedAuthorNam, Ki Taek-
dc.citation.titleBiomaterials-
dc.citation.volume122-
dc.citation.startPage130-
dc.citation.endPage140-
dc.identifier.bibliographicCitationBIOMATERIALS, Vol.122 : 130-140, 2017-
dc.date.modified2017-11-01-
dc.identifier.rimsid42155-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.