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Hypoxia-targeted drug delivery

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dc.contributor.authorSharma, Amit-
dc.contributor.authorArambula, Jonathan F.-
dc.contributor.authorKoo, Seyoung-
dc.contributor.authorKumar, Rajesh-
dc.contributor.authorSingh, Hardev-
dc.contributor.authorSessler, Jonathan L.-
dc.contributor.authorKim, Jong Seung-
dc.date.accessioned2021-09-01T19:14:01Z-
dc.date.available2021-09-01T19:14:01Z-
dc.date.created2021-06-19-
dc.date.issued2019-02-04-
dc.identifier.issn0306-0012-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/67675-
dc.description.abstractHypoxia is a state of low oxygen tension found in numerous solid tumours. It is typically associated with abnormal vasculature, which results in a reduced supply of oxygen and nutrients, as well as impaired delivery of drugs. The hypoxic nature of tumours often leads to the development of localized heterogeneous environments characterized by variable oxygen concentrations, relatively low pH, and increased levels of reactive oxygen species (ROS). The hypoxic heterogeneity promotes tumour invasiveness, metastasis, angiogenesis, and an increase in multidrug-resistant proteins. These factors decrease the therapeutic efficacy of anticancer drugs and can provide a barrier to advancing drug leads beyond the early stages of preclinical development. This review highlights various hypoxia-targeted and activated design strategies for the formulation of drugs or prodrugs and their mechanism of action for tumour diagnosis and treatment.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectSELECTIVE ANTITUMOR AGENTS-
dc.subjectCELL LUNG-CANCER-
dc.subjectHUMAN TUMOR-CELLS-
dc.subjectPHASE-III TRIAL-
dc.subjectDT-DIAPHORASE ACTIVITY-
dc.subjectMONO-N-OXIDES-
dc.subjectO-6-ALKYLGUANINE-DNA ALKYLTRANSFERASE AGT-
dc.subjectNADPH CYTOCHROME-P450 REDUCTASE-
dc.subjectBIOREDUCTIVE PRODRUG PR-104A-
dc.subjectMUSTARD QUATERNARY-SALTS-
dc.titleHypoxia-targeted drug delivery-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jong Seung-
dc.identifier.doi10.1039/c8cs00304a-
dc.identifier.scopusid2-s2.0-85060630431-
dc.identifier.wosid000457793900008-
dc.identifier.bibliographicCitationCHEMICAL SOCIETY REVIEWS, v.48, no.3, pp.771 - 813-
dc.relation.isPartOfCHEMICAL SOCIETY REVIEWS-
dc.citation.titleCHEMICAL SOCIETY REVIEWS-
dc.citation.volume48-
dc.citation.number3-
dc.citation.startPage771-
dc.citation.endPage813-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusSELECTIVE ANTITUMOR AGENTS-
dc.subject.keywordPlusCELL LUNG-CANCER-
dc.subject.keywordPlusHUMAN TUMOR-CELLS-
dc.subject.keywordPlusPHASE-III TRIAL-
dc.subject.keywordPlusDT-DIAPHORASE ACTIVITY-
dc.subject.keywordPlusMONO-N-OXIDES-
dc.subject.keywordPlusO-6-ALKYLGUANINE-DNA ALKYLTRANSFERASE AGT-
dc.subject.keywordPlusNADPH CYTOCHROME-P450 REDUCTASE-
dc.subject.keywordPlusBIOREDUCTIVE PRODRUG PR-104A-
dc.subject.keywordPlusMUSTARD QUATERNARY-SALTS-
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