Microfluidic Actuation via 3D-Printed Molds toward Multiplex Biosensing of Cell Apoptosis

被引:15
|
作者
Dang, Bac Van [1 ]
Hassanzadeh-Barforoushi, Amin [1 ,2 ]
Syed, Maira Shakeel [1 ]
Yang, Danting [3 ,4 ]
Kim, Sung-Jin [5 ]
Taylor, Robert A. [1 ]
Liu, Guo-Jun [6 ,7 ]
Liu, Guozhen [3 ]
Barber, Tracie [1 ]
机构
[1] Univ New South Wales, Fac Engn, Sch Mech & Mfg Engn, Sydney, NSW 2052, Australia
[2] Kinghorn Canc Ctr, Garvan Inst Med Res, Canc Div, Sydney, NSW 2010, Australia
[3] Univ New South Wales, Fac Engn, Australian Ctr NanoMed, Grad Sch Biomed Engn,ARC Ctr Excellence Nanoscale, Sydney, NSW 2052, Australia
[4] Ningbo Univ, Sch Med, Zhejiang Prov Key Lab Pathol & Physiol Technol, Dept Preventat Med, Ningbo 315211, Zhejiang, Peoples R China
[5] Konkuk Univ, Dept Mech Engn, Seoul 05029, South Korea
[6] Australian Nucl Sci & Technol Org, New Illawarra Rd, Lucas Heights, NSW 2234, Australia
[7] Univ Sydney, Brain & Mind Ctr, Fac Med & Hlth, Discipline Med Imaging & Radiat Sci, 94 Mallett St, Camperdown, NSW 2050, Australia
关键词
microfluidic valve; multiplexed microfluidics; multiplexed biosensing; 3D printing; cell apoptosis; colorimetric assay; MEMBRANE VALVES; PUMPS; FLOW; ACTIVATION;
D O I
10.1021/acssensors.9b01057
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multiplexed analysis of biochemical analytes such as proteins, enzymes, and immune products using a microfluidic device has the potential to cut assay time, reduce sample volume, realize high-throughput, and decrease experimental error without compromising sensitivity. Despite these huge benefits, the need for expensive specialized equipment and the complex photolithography fabrication process for the multiplexed devices have, to date, prevented widespread adoption of microfluidic systems. Here, we present a simple method to fabricate a new microfluidic-based multiplexed biosensing device by taking advantage of 3D-printing. The device is an integration of normally closed (NC) microfluidic valving units which offer superior operational flexibility by using PDMS membrane (E similar to 1-2 MPa) and require minimized energy input (1-5 kPa). To systematically engineer the device, we first report on the geometrical and operational analysis of a single 3D-printed valving unit. Based on the characterization, we introduce a full prototype multiplexed chip comprising several microfluidic valves. The prototype offers-for the first time in a 3D-printed microfluidic device-the capability of on-demand performce of both a sequential and a parallel biochemical assay. As a proof of concept, our device has been used to simultaneously measure the apoptotic activity of 5 different members of the caspase protease enzyme family. In summary, the 3D-printed valving system showcased in this study overcomes traditional bottlenecks of microfabrication, enabling a new class of sophisticated liquid manipulation required in performing multiplexed sensing for biochemical assays.
引用
收藏
页码:2181 / 2189
页数:17
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