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Development of an aspiration-based open microfluidic platform using micropillars to recreate the lung cellular microenvironment : 미세 구조체와 aspiration 기반 세포 패터닝 기술을 통한 폐포 조직 환경 모사 개방형 구조 미세유체 플 랫폼의 개발

DC Field Value Language
dc.contributor.advisor전누리-
dc.contributor.author트리 토 이브 응우옌-
dc.date.accessioned2022-06-08T06:39:20Z-
dc.date.available2022-06-08T06:39:20Z-
dc.date.issued2022-
dc.identifier.other000000170726-
dc.identifier.urihttps://hdl.handle.net/10371/181169-
dc.identifier.urihttps://dcollection.snu.ac.kr/common/orgView/000000170726ko_KR
dc.description학위논문(석사) -- 서울대학교대학원 : 공과대학 기계공학과, 2022.2. 전누리.-
dc.description.abstractEngineering a thin air-liquid interface membrane is important to model in vitro the complex lung alveoli structure. To date, only few in vitro microfluidic platforms have been able to reproduce the in vivo size of alveoli while making it fast, easy to pattern and with a high yield. Moreover, no current platforms are including lung fibroblasts in the model. Here, we introduce a 3D printed open microfluidic and technique to create a thin hydrogel membrane close to the alveoli dimensions around a 100µm and usable for cell culture. 3D printed organ-on-chips allow the same biological performance and biodegradability in comparison to the usual PDMS chips while providing a high-throughput and no small molecule absorption. Utilizing the strong surface tension between hydrogel and closely spaced micropillars, after the suction of the liquid, provides a solution to pattern the desired thin hydrogel membrane. These platforms using specific patterning techniques can be used for a wide range of applications as an air-liquid interface model for powder inhalation tests or pharmaceutical drugs screening for instance.-
dc.description.tableofcontentsAbstract iii
List of Tables 1
List of Figures 2
Chapter 1. Introduction 3
1.1. Study Background 3
1.2. Purpose of Research 5
Chapter 2. Materials and methods 7
2.1. Device fabrication 7
2.2. Cell preparation 8
2.3. Preparation and loading of the alveoli cell configuration 8
2.4. Immunostaining 10
2.5. Imaging 10
2.6. Numerical simulation 11
2.7. Statistical analysis 11
Chapter 3. Results and discussion 12
3.1. Capillary pinning liquid patterning process 13
3.1 Surface treatment 13
3.1.2. Numerical simulation 16
3.1.3. Theoretical analysis of the capillary pinning 17
3.2. Patterning for cells co culture in a 3D microenvironment 27
3.3. An open microfluidic platform to recreate the in vivo environment 30
Chapter 4. Conclusion 34
Bibliography 37
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dc.format.extentv, 41-
dc.language.isoeng-
dc.publisher서울대학교 대학원-
dc.subjectLung-on-chips, Open microfluidic platform, capillary pinning, microfluidic patterning technique-
dc.subject.ddc621-
dc.titleDevelopment of an aspiration-based open microfluidic platform using micropillars to recreate the lung cellular microenvironment-
dc.title.alternative미세 구조체와 aspiration 기반 세포 패터닝 기술을 통한 폐포 조직 환경 모사 개방형 구조 미세유체 플 랫폼의 개발-
dc.typeThesis-
dc.typeDissertation-
dc.contributor.AlternativeAuthorNGUYEN Tri Tho Yves-
dc.contributor.department공과대학 기계공학과-
dc.description.degree석사-
dc.date.awarded2022-02-
dc.identifier.uciI804:11032-000000170726-
dc.identifier.holdings000000000047▲000000000054▲000000170726▲-
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