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dc.contributor.authorTian, Chutongen
dc.contributor.authorZheng, Shunzheen
dc.contributor.authorLiu, Xinyingen
dc.contributor.authorKamei, Ken-ichiroen
dc.contributor.alternative亀井, 謙一郎ja
dc.date.accessioned2022-12-01T00:38:25Z-
dc.date.available2022-12-01T00:38:25Z-
dc.date.issued2022-07-20-
dc.identifier.urihttp://hdl.handle.net/2433/277563-
dc.description.abstractDespite explosive growth in the development of nano-drug delivery systems (NDDS) targeting tumors in the last few decades, clinical translation rates are low owing to the lack of efficient models for evaluating and predicting responses. Microfluidics-based tumor-on-a-chip (TOC) systems provide a promising approach to address these challenges. The integrated engineered platforms can recapitulate complex in vivo tumor features at a microscale level, such as the tumor microenvironment, three-dimensional tissue structure, and dynamic culture conditions, thus improving the correlation between results derived from preclinical and clinical trials in evaluating anticancer nanomedicines. The specific focus of this review is to describe recent advances in TOCs for the evaluation of nanomedicine, categorized into six sections based on the drug delivery process: circulation behavior after infusion, endothelial and matrix barriers, tumor uptake, therapeutic efficacy, safety, and resistance. We also discuss current issues and future directions for an end-use perspective of TOCs.en
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.publisherBMCen
dc.rights© The Author(s) 2022.en
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.subjectTumor-on-a-Chipen
dc.subjectMicrofluidic deviceen
dc.subjectNanomedicinesen
dc.subjectDrug delivery processen
dc.subjectPreclinical predictionen
dc.titleTumor-on-a-chip model for advancement of anti-cancer nano drug delivery systemen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleJournal of Nanobiotechnologyen
dc.identifier.volume20-
dc.relation.doi10.1186/s12951-022-01552-0-
dc.textversionpublisher-
dc.identifier.artnum338-
dc.identifier.pmid35858898-
dcterms.accessRightsopen access-
datacite.awardNumber21H01728-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-21H01728/-
dc.identifier.eissn1477-3155-
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitle非アルコール性脂肪性肝疾患を再現する小腸-肝臓・オン・チップja
出現コレクション:学術雑誌掲載論文等

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