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  4. Use microfluidic chips to study the effects of ultraviolet lights on human fibroblasts
 
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Use microfluidic chips to study the effects of ultraviolet lights on human fibroblasts

Journal
Microfluidics and Nanofluidics
Journal Volume
21
Journal Volume
21
Journal Issue
4
Journal Issue
4
ISSN
16134982
Date Issued
2017-04-01
Author(s)
Huang, Chien-Hsun
Hou, Hsien-San
KAI-YIN LO  
Cheng, Ji-Yen
Sun, Yung-Shin
DOI
10.1007/s10404-017-1922-7
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/446178
https://www.scopus.com/pages/publications/85017427670?origin=resultslist
URL
https://www2.scopus.com/inward/record.uri?eid=2-s2.0-85017427670&doi=10.1007%2fs10404-017-1922-7&partnerID=40&md5=a3a09da92b7d7c3089f34b9c5b1494fc
Abstract
The ultraviolet (UV) radiation from sunlight exposure is highly related to skin damages such as photoaging and skin cancers. UVA radiation can cause altered expression of extracellular matrix proteins, and UVB is believed to be an apoptosis induction factor. In the past, many experiments have been conducted in vitro to investigate how UV lights are responsible for cell damages. However, most of these studies were done under static conditions such as culture dishes, which were quite different from the in vivo dynamic circulatory system. Also, in these studies, only one UV dose was applied at one time, limiting the experimental throughput. To best mimic the physiological condition as well as to increase the throughput, a microfluidic chip was designed and fabricated to create five different UV doses in one single experimental run. This biocompatible chip is used for seeding and culturing cells, together with observing cell morphology in a circulating condition. By using the “Christmas tree” structure, five different concentrations of blue dye solutions were generated within a microfluidic chip. And by illuminating this chip with the UV light, five different UV doses could be attained on cells cultured within this chip. The effects of UVB dose on NIH/3T3 fibroblasts, mainly in terms of morphology and fluorescence-based cell damage rate, were studied.
Subjects
Cell damage
Cell morphology
Microfluidic chips
NIH/3T3 cells
Ultraviolet light
SDGs

[SDGs]SDG3

Publisher
Springer Verlag
Type
journal article

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