Biocompatibility and Reduced Drug Absorption of Sol-Gel-Treated Poly(dimethyl siloxane) for Microfluidic Cell Culture Applications

被引:79
作者
Gomez-Sjoberg, Rafael [1 ]
Leyrat, Anne A. [2 ]
Houseman, Benjamin T. [4 ]
Shokat, Kevan [3 ,5 ,6 ]
Quake, Stephen R. [2 ,3 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Engn, Berkeley, CA 94720 USA
[2] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[3] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
[4] Univ Calif San Francisco, San Francisco Gen Hosp, Dept Anesthesia & Perioperat Care, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
[6] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
LARGE-SCALE INTEGRATION; MICROCHANNELS; POLYMERS; DEVICES;
D O I
10.1021/ac101870s
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
Poly(dimethyl siloxane) (PDMS)-based microfluidic devices are now commonly used for a wide variety of biological experiments, including cell culture assays. However, the porous, hydrophobic polymer matrix of PDMS rapidly absorbs small hydrophobic molecules, including hormones and most small-molecule drugs. This makes it challenging to perform experiments that require such substances in PDMS microfluidic devices. This study presents evidence that a sol-gel treatment of PDMS that fills the polymer matrix with silica nanoparticles is effective at reducing the absorption of drugs into the material while preserving its biocompatibility, transparency, and oxygen permeability. We show that the absorption of two anticancer drugs, camptothecin and a kinase inhibitor, is reduced to such an extent that on-chip microfluidic cell culture experiments can recapitulate the results obtained off-chip.
引用
收藏
页码:8954 / 8960
页数:7
相关论文
共 23 条
[1]
Glass coating for PDMS microfluidic channels by sol-gel methods [J].
Abate, Adam R. ;
Lee, Daeyeon ;
Do, Thao ;
Holtze, Christian ;
Weitz, David A. .
LAB ON A CHIP, 2008, 8 (04) :516-518
[2]
Chemotherapy-Induced Apoptosis in a Transgenic Model of Neuroblastoma Proceeds Through p53 Induction [J].
Chesler, Louis ;
Goldenberg, David ;
Collins, Rodney ;
Grimmer, Matt ;
Kim, Grace E. ;
Tihan, Tarik ;
Nguyen, Kim ;
Yakovenko, Slava ;
Matthay, Katherine K. ;
Weiss, William A. .
NEOPLASIA, 2008, 10 (11) :1268-U93
[3]
Rapid prototyping of microfluidic systems in poly(dimethylsiloxane) [J].
Duffy, DC ;
McDonald, JC ;
Schueller, OJA ;
Whitesides, GM .
ANALYTICAL CHEMISTRY, 1998, 70 (23) :4974-4984
[4]
Versatile, fully automated, microfluidic cell culture system [J].
Gomez-Sjoeberg, Rafael ;
Leyrat, Anne A. ;
Pirone, Dana M. ;
Chen, Christopher S. ;
Quake, Stephen R. .
ANALYTICAL CHEMISTRY, 2007, 79 (22) :8557-8563
[5]
Synthesis and biological evaluation of imidazo[1,2-a]pyridine derivatives as novel PI3 kinase p110α inhibitors [J].
Hayakawa, Masahiko ;
Kaizawa, Hiroyuki ;
Kawaguchi, Ken-ichi ;
Ishikawa, Noriko ;
Koizumi, Tomonobu ;
Ohishi, Takahide ;
Yamano, Mayumi ;
Okada, Minoru ;
Ohta, Mitsuaki ;
Tsukamoto, Shin-ichi ;
Raynaud, Florence I. ;
Waterfield, Michael D. ;
Parker, Peter ;
Workman, Paul .
BIOORGANIC & MEDICINAL CHEMISTRY, 2007, 15 (01) :403-412
[6]
Huang R, 2005, DISCRETE CONT DYN-B, V5, P1005
[7]
Dynamic coating using polyelectrolyte multilayers for chemical control of electroosmotic flow in capillary electrophoresis microchips [J].
Liu, Y ;
Fanguy, JC ;
Bledsoe, JM ;
Henry, CS .
ANALYTICAL CHEMISTRY, 2000, 72 (24) :5939-5944
[8]
Stable permanently hydrophilic protein-resistant thin-film coatings on poly(dimethylsiloxane) substrates by electrostatic self-assembly and chemical cross-linking [J].
Makamba, H ;
Hsieh, YY ;
Sung, WC ;
Chen, SH .
ANALYTICAL CHEMISTRY, 2005, 77 (13) :3971-3978
[9]
Surface modification of poly(dimethylsiloxane) microchannels [J].
Makamba, H ;
Kim, JH ;
Lim, K ;
Park, N ;
Hahn, JH .
ELECTROPHORESIS, 2003, 24 (21) :3607-3619
[10]
Microfluidic large-scale integration: The evolution of design rules for biological automation [J].
Melin, Jessica ;
Quake, Stephen R. .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 2007, 36 :213-231