전누리 교수
Noo Li Jeon
서울대학교 · 공학
연구실 소개
전누리 교수의 연구실은 마이크로유체 기반의 생체 모방 시스템을 핵심으로 하여, 세포의 생존과 기능을 정밀하게 조절하는 새로운 생물의학 기술을 개발하고 있습니다. 특히 3차원 생체 환경을 재현하는 마이크로유체 장치를 통해 혈관 네트워크, 뇌혈류장벽, 신경줄기세포의 분화 조건 최적화 등 다양한 생체 모델을 구축하고 있으며, 이는 조직공학과 암 생물학 연구에 중요한 기여를 하고 있습니다. 연구는 세포의 미세환경 제어를 통해 생체 내에서의 세포 행동을 정밀하게 재현하는 데 초점을 맞추고 있습니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15This paper describes a simple, versatile method of generating gradients in composition in solution or on surfaces using microfluidic systems. This method is based on controlled diffusive mixing of species in solutions that are flowing laminarly, at low Reynolds number, inside a network of microchannels. We demonstrate the use of this procedure to generate (1) gradients in the compositions of solutions, measured directly by colorimetric assays and (2) gradients in topography of the surfaces produ
This paper describes the generation of gradients having complex shapes in solution using microfluidic networks. Flowing multiple streams of fluid each carrying different concentrations of substances laminarly and side-by-side generated step concentration gradients perpendicular to the direction of the flow. Appropriately designed networks of microchannels for controlled diffusive mixing of substances generated a range of shapes for the gradients, including linear, parabolic, and periodic. The la
Three-dimensional microfluidic systems were fabricated and used to pattern proteins and mammalian cells on a planar substrate. The three-dimensional topology of the microfluidic network in the stamp makes this technique a versatile one with which to pattern multiple types of proteins and cells in complex, discontinuous structures on a surface. The channel structure, formed by the stamp when it is in contact with the surface of the substrate, limits migration and growth of cells in the channels.
This paper describes a simple plasma-based dry etching method that enables patterned cell culture inside microfluidic devices by allowing patterning, fluidic bonding and sterilization steps to be carried out in a single step. This plasma-based dry etching method was used to pattern cell-adhesive and non-adhesive areas on the glass and polystyrene substrates. The patterned substrate was used for selective attachment and growth of human umbilical vein endothelial cells, MDA-MB-231 human breast can
A novel three dimensional blood brain barrier (BBB) platform was developed by independently supplying different types of media to separate cell types within a single device. One channel (vascular channel, VC) is connected to the inner lumen of the vascular network while the other supplies media to the neural cells (neural channel, NC). Compared to co-cultures supplied with only one type of medium (or 1:1 mixture), best barrier properties and viability were obtained with culturing HUVECs with end
The field of microfluidics-based three-dimensional (3D) cell culture system is rapidly progressing from academic proof-of-concept studies to valid solutions to real-world problems. Polydimethylsiloxane (PDMS)-based platform has been widely adopted as in vitro platforms for mimicking tumor microenvironment. However, PDMS has not been welcomed as a standardized commercial application for preclinical screening due to inherent material limitations that make it difficult to scale-up production. Here,
Many chemical and biological processes are dependent on molecular gradients. We describe a new microfluidic approach that can be used to produce spatiotemporal gradients across two-dimensional surfaces and three-dimensional gels under flow-free conditions. Free diffusion between dynamically replenished flow channels acting as a sink and source is utilized to give rise to stable steady-state gradient profiles. The gradient profile is dictated by the engineered design of the device's gradient-gene
Adoptive cell transfer against solid tumors faces challenges to overcome tumor microenvironment (TME), which plays as a physical barrier and provides immuno-suppressive conditions. Classical cytotoxicity assays are widely used to measure killing ability of the engineered cytotoxic lymphocytes as therapeutics, but the results cannot represent the performance in clinical application due to the absence of the TME. This paper describes a 3D cytotoxicity assay using an injection molded plastic array
We introduce a novel microfluidic device to co-culture a blood vessel network and cell tissues in an in vivo-like niche. Our "open-top" microfluidic device is composed of microchannels with micropores in the ceiling, which provides direct fluid access from reservoir to microchannel. Fluid connections through micropores afford novel advantages, including: i) the long-term culture of large-scale microvessel network, ii) access of different fluids to inner and exterior sides of the microvessel, and
Rapid micropatterning of polymers on rigid and flexible substrates can be achieved by the method—vacuum-assisted micromolding in capillaries (MIMIC)—introduced here. The Figure shows an oblique-view SEM image of a single hexagonal cell of a pattern produced by vacuum-assisted MIMIC. The use of vacuum reduced the time taken to fill the pattern with UV-curable polyurethane from ∼30 min to ∼15 s.
High-purity platinum and palladium thin films can be deposited selectively by combining microcontact printing (μCP) and metal−organic chemical vapor deposition (MOCVD). Printed patterns of octadecyltrichlorosilane thin films are used to direct the selective deposition of the metallic thin films from bis(hexafluoroacetylacetonato)platinum(II), Pt(hfac)2, and bis(hexafluoroacetylacetonato)palladium(II), Pd(hfac)2, in the presence of hydrogen. This process has been used successfully to fabricate Pt
A novel hybrid construct was developed by combining aligned fibers (AFs) and random fibers (RFs) to form a scaffolding system. Homogeneous fiber-based structures were fabricated by electrospinning, which produced both random and aligned fiber mats depending on the collection method. The upper part of the scaffold contained an AF layer, which possessed a well-organized configuration that provided uniaxial topographic guidance. For mechanical stability and support, the lower part of the scaffold w
We describe a non-lithographic monolayer based patterning process for depositing copper thin film microstructures by chemical vapor deposition (CVD). The technique combines the microcontact printing of octadecyltrichlorosilane (OTS) monolayers, nonselective copper CVD, and mild (abrasive-free) mechanical polishing to fabricate thin film microstructures on both planar and nonplanar substrates. This technique has been used successfully to deposit copper features with sizes ranging from 5 to 250 μm
We present a novel approach for assembling 3D tissue by layer-by-layer stacking of cell sheets formed on aligned nanofiber mesh. A rigid frame was used to repeatedly collect aligned electrospun PCL (polycaprolactone) nanofiber to form a mesh structure with average distance between fibers 6.4 µm. When human umbilical vein endothelial cells (HUVECs), human foreskin dermal fibroblasts, and skeletal muscle cells (C2C12) were cultured on the nanofiber mesh, they formed confluent monolayers and could
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