Evaluation of drug blood-brain-barrier permeability using a microfluidic chip

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dc.contributor.authorJ Y Yang-
dc.contributor.authorD S Shin-
dc.contributor.authorMoonkyu Jeong-
dc.contributor.authorS S Kim-
dc.contributor.authorH N Jeong-
dc.contributor.authorB H Lee-
dc.contributor.authorK S Hwang-
dc.contributor.authorY Son-
dc.contributor.authorHyeon Cheol Jeong-
dc.contributor.authorC H Choi-
dc.contributor.authorKyeong-Ryoon Lee-
dc.contributor.authorM A Bae-
dc.date.accessioned2024-05-27T16:32:52Z-
dc.date.available2024-05-27T16:32:52Z-
dc.date.issued2024-
dc.identifier.issn1999-4923-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/35130-
dc.description.abstractThe blood-brain-barrier (BBB) is made up of blood vessels whose permeability enables the passage of some compounds. A predictive model of BBB permeability is important in the early stages of drug development. The predicted BBB permeabilities of drugs have been confirmed using a variety of in vitro methods to reduce the quantities of drug candidates needed in preclinical and clinical trials. Most prior studies have relied on animal or cell-culture models, which do not fully recapitulate the human BBB. The development of microfluidic models of human-derived BBB cells could address this issue. We analyzed a model for predicting BBB permeability using the Emulate BBB-on-a-chip machine. Ten compounds were evaluated, and their permeabilities were estimated. Our study demonstrated that the permeability trends of ten compounds in our microfluidic-based system resembled those observed in previous animal and cell-based experiments. Furthermore, we established a general correlation between the partition coefficient (?? ) and the apparent permeability (???? ). In conclusion, we introduced a new paradigm for predicting BBB permeability using microfluidic-based systems.-
dc.publisherMDPI-
dc.titleEvaluation of drug blood-brain-barrier permeability using a microfluidic chip-
dc.title.alternativeEvaluation of drug blood-brain-barrier permeability using a microfluidic chip-
dc.typeArticle-
dc.citation.titlePharmaceutics-
dc.citation.number5-
dc.citation.endPage574-
dc.citation.startPage574-
dc.citation.volume16-
dc.contributor.affiliatedAuthorMoonkyu Jeong-
dc.contributor.affiliatedAuthorHyeon Cheol Jeong-
dc.contributor.affiliatedAuthorKyeong-Ryoon Lee-
dc.contributor.alternativeName양정윤-
dc.contributor.alternativeName신대섭-
dc.contributor.alternativeName정문규-
dc.contributor.alternativeName김성순-
dc.contributor.alternativeName정하늘-
dc.contributor.alternativeName이병회-
dc.contributor.alternativeName황규석-
dc.contributor.alternativeName손유지-
dc.contributor.alternativeName정현철-
dc.contributor.alternativeName최치훈-
dc.contributor.alternativeName이경륜-
dc.contributor.alternativeName배명애-
dc.identifier.bibliographicCitationPharmaceutics, vol. 16, no. 5, pp. 574-574-
dc.identifier.doi10.3390/pharmaceutics16050574-
dc.subject.keywordBBB-
dc.subject.keywordMicrofluidic chip-
dc.subject.keywordPhysiologically based pharmacokinetic modeling-
dc.subject.localMicrofluidic chip-
dc.subject.localPhysiologically based pharmacokinetic modeling-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Laboratory Animal Resource & Research Center > 1. Journal Articles
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