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Controllable in-situ hydrogels membrane formation using microfluidics

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dc.contributor.authorChoi, Eunpyo-
dc.contributor.authorJun, Indong-
dc.contributor.authorPark, Kyung Min-
dc.contributor.authorPark, Ki Dong-
dc.contributor.authorShin, Heungsoo-
dc.contributor.authorPark, Jungyul-
dc.date.accessioned2022-07-16T19:17:18Z-
dc.date.available2022-07-16T19:17:18Z-
dc.date.created2021-05-11-
dc.date.issued2011-09-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/167719-
dc.description.abstractThis paper reports a novel method for the in-situ hydrogel membrane fabrication in a simple PDMS channel. We used two separate solutions of 0.0625 wt% of H2O2 in PBS with the 5.2 wt% of the Tetronic-succinic anhydride-tyramine (Tet-SA-TA), and 0.0625 mg/ml of horseradish peroxidase (HRP) in PBS with the same concentration of Tet-SA-TA. These two solutions were introduced into the typical microfluidic channel and the mixing of these solutions spontaneously formed the in-situ crosslinked hydrogels membrane in the microfluidic channel. The width of the membrane can be controlled quantitatively by adjusting gelation time and the velocity of microfluidics. Moreover, by using the formed inner-channel membrane, the permeation of chemical molecules through the membrane was observed and its quantitative value was analyzed with multiphysics modeling. The parallel hydrogel membranes were also formed using a time-dependent procedure, and, in addition, this separated channel by the hydrogel membranes was applied for the generation of stable concentration gradients into the microchannel. These results can be used to realize the complicated diffusive 3D structure, such as biomimetic blood vessels.-
dc.language영어-
dc.language.isoen-
dc.publisherIEEE-
dc.titleControllable in-situ hydrogels membrane formation using microfluidics-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Heungsoo-
dc.identifier.doi10.1109/NEMS.2011.6017387-
dc.identifier.scopusid2-s2.0-80053305908-
dc.identifier.bibliographicCitationNEMS 2011 - 6th IEEE International Conference on Nano/Micro Engineered and Molecular Systems, pp.441 - 444-
dc.relation.isPartOfNEMS 2011 - 6th IEEE International Conference on Nano/Micro Engineered and Molecular Systems-
dc.citation.titleNEMS 2011 - 6th IEEE International Conference on Nano/Micro Engineered and Molecular Systems-
dc.citation.startPage441-
dc.citation.endPage444-
dc.type.rimsART-
dc.type.docTypeConference Paper-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlus3D Structure-
dc.subject.keywordPlusBiomimetic blood vessels-
dc.subject.keywordPlusChemical molecules-
dc.subject.keywordPlusConcentration gradients-
dc.subject.keywordPlusCross-linked hydrogels-
dc.subject.keywordPlusGelation time-
dc.subject.keywordPlusHorseradish peroxidase-
dc.subject.keywordPlusHydrogel membrane-
dc.subject.keywordPlusIn-situ-
dc.subject.keywordPlusIn-situ formations-
dc.subject.keywordPlusMembrane formation-
dc.subject.keywordPlusMicrofluidic channel-
dc.subject.keywordPlusMulti-physics modeling-
dc.subject.keywordPlusQuantitative values-
dc.subject.keywordPlusSeparated channels-
dc.subject.keywordPlusTime-dependent-
dc.subject.keywordPlusBiomimetics-
dc.subject.keywordPlusBlood vessels-
dc.subject.keywordPlusChemical analysis-
dc.subject.keywordPlusCoagulation-
dc.subject.keywordPlusCrosslinking-
dc.subject.keywordPlusFluidic devices-
dc.subject.keywordPlusGelation-
dc.subject.keywordPlusHydrophobicity-
dc.subject.keywordPlusMembranes-
dc.subject.keywordPlusMicrochannels-
dc.subject.keywordPlusMicrofluidics-
dc.subject.keywordPlusSeparation-
dc.subject.keywordPlusHydrogels-
dc.subject.keywordAuthorConcentration gradients-
dc.subject.keywordAuthorHydrogel membrane-
dc.subject.keywordAuthorIn-situ formation-
dc.subject.keywordAuthorMicrofluidics-
dc.identifier.urlhttps://ieeexplore.ieee.org/document/6017387-
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