Surface modification of poly(dimethylsiloxane) (PDMS) microchannels with DNA capture-probes for potential use in microfluidic DNA analysis systems

被引:1
|
作者
Khodakov, Dmitriy A. [1 ]
Thredgold, Leigh D. [1 ]
Lenehan, Claire E.
Andersson, Gunther A. [1 ]
Kobus, Hilton
Ellis, Amanda V. [1 ]
机构
[1] Flinders Univ S Australia, Flinders Ctr NanoScale Sci & Technol, Sturt Rd, Adelaide, SA 5042, Australia
来源
关键词
Poly(dimethylsiloxane) (PDMS); oligonucleotides; microfluidic devices; surface modification; silanization; microchannels; DEVICES; TECHNOLOGY; CHIP; IMMOBILIZATION; HYBRIDIZATION; FABRICATION; MICROCHIP; CELLS;
D O I
10.1117/12.903208
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Poly(dimethylsiloxane) (PDMS) is an elastomeric material used for microfluidic devices and is especially suited to medical and forensic applications. This is due to its relatively low cost, ease of fabrication, excellent optical transmission characteristics and its ability to support electroosmotic flow, required during electrophoretic separations. These aspects combined with its large range of surface modification chemistries, make PDMS an attractive substrate in microfluidic devices for, in particular, DNA separation. Here, we report the successful wet chemical surface modification of PDMS microchannels using a simple three step method to produce an isothiocyanate-terminated surface. Initially, PDMS was oxygen plasma treated to produce a silanol-terminated surface, this was then reacted with 3-aminopropyltriethoxysilane with subsequent reaction of the now amine-terminated surface with p-phenylenediisothiocyanate. Water contact angle measurements both before and after modification showed a reduction in hydrophobicity from 101 degrees for native PDMS to 94 degrees for the isothiocyante-terminated PDMS. The isothiocyanate-terminated surface was then coupled with an amine-terminated single-stranded DNA (ssDNA) oligonucleotide capture probe via a thiourea linkage. Confirmation of capture probe attachment was observed using fluorescent microscopy after hybridization of the capture probes with fluorescently labeled complimentary ssDNA oligonucleotides.
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页数:9
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