Irreversible PDMS bonding using flame activation of adhesives for fabrication of microfluidic and organ-on-chip devices

被引:1
|
作者
Singer, Ryan [1 ,2 ]
Hirota, Jeremy A. [1 ,2 ,3 ,4 ,5 ]
Dabaghi, Mohammadhossein [2 ]
机构
[1] McMaster Univ, Sch Biomed Engn, McMaster Sch Biomed Engn, Engn Technol Bldg,1280 Main St West, Hamilton, ON L8S 4K1, Canada
[2] McMaster Univ, Firestone Inst Resp Hlth, Dept Med, Div Respirol,St Josephs Healthcare Hamilton, 50 Charlton Ave East, Hamilton, ON L8N 4A6, Canada
[3] McMaster Univ, McMaster Immunol Res Ctr, Michael G DeGroote Ctr Learning & Discovery, Hamilton, ON L8S 4K1, Canada
[4] Univ British Columbia, Dept Med, Div Resp Med, Vancouver, BC V6H 3Z6, Canada
[5] Univ Waterloo, Dept Biol, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Adhesives; Bonding; PDMS; Surface activation; Microfluidics; Organ-on-chip;
D O I
10.1016/j.matlet.2023.135221
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Polydimethylsiloxane (PDMS) is widely used for microfluidics fabrication in many disciplines due to its ease of use in soft lithography and its ability to bond liquid-tight seals. A variety of PDMS-PDMS bonding methods exist, but each may have limitations for some applications. For example, chemical bonding via oxygen plasma treatment is reliable but requires expensive equipment and specialized training. Here we present a rapid, low-cost, and accessible method for irreversible PDMS bonding in which flame treatment activates PDMS and Nitto 5302A adhesive surfaces. Using this technique, PDMS microchannels can be fabricated with a bonding integrity of up to 325 kPa burst pressure. This technique is suitable for fabricating organ-on-chip devices that support cell viability and establishment of key cellular features in cell line and primary cell cultures while maintaining bonding integrity.
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页数:5
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