TY - JOUR
T1 - An all-glass microfluidic network with integrated amorphous silicon photosensors for on-chip monitoring of enzymatic biochemical assay
AU - Costantini, Francesca
AU - Tiggelaar, Roald M.
AU - Salvio, Riccardo
AU - Nardecchia, Marco
AU - Schlautmann, Stefan
AU - Manetti, Cesare
AU - Gardeniers, Han J.G.E.
AU - de Cesare, Giampiero
AU - Caputo, Domenico
AU - Nascetti, Augusto
PY - 2017
Y1 - 2017
N2 - A lab-on-chip system, integrating an all-glass microfluidics and on-chip optical detection, was developed and tested. The microfluidic network is etched in a glass substrate, which is then sealed with a glass cover by direct bonding. Thin film amorphous silicon photosensors have been fabricated on the sealed microfluidic substrate preventing the contamination of the micro-channels. The microfluidic network is then made accessible by opening inlets and outlets just prior to the use, ensuring the sterility of the device. The entire fabrication process relies on conventional photolithographic microfabrication techniques and is suitable for low-cost mass production of the device. The lab-on-chip system has been tested by implementing a chemiluminescent biochemical reaction. The inner channel walls of the microfluidic network are chemically functionalized with a layer of polymer brushes and horseradish peroxidase is immobilized into the coated channel. The results demonstrate the successful on-chip detection of hydrogen peroxide down to 18 μM by using luminol and 4-iodophenol as enhancer agent.
AB - A lab-on-chip system, integrating an all-glass microfluidics and on-chip optical detection, was developed and tested. The microfluidic network is etched in a glass substrate, which is then sealed with a glass cover by direct bonding. Thin film amorphous silicon photosensors have been fabricated on the sealed microfluidic substrate preventing the contamination of the micro-channels. The microfluidic network is then made accessible by opening inlets and outlets just prior to the use, ensuring the sterility of the device. The entire fabrication process relies on conventional photolithographic microfabrication techniques and is suitable for low-cost mass production of the device. The lab-on-chip system has been tested by implementing a chemiluminescent biochemical reaction. The inner channel walls of the microfluidic network are chemically functionalized with a layer of polymer brushes and horseradish peroxidase is immobilized into the coated channel. The results demonstrate the successful on-chip detection of hydrogen peroxide down to 18 μM by using luminol and 4-iodophenol as enhancer agent.
KW - Amorphous silicon photosensors
KW - Chemiluminescent based assay
KW - Lab-on-chip
KW - Microfluidic channel
KW - Surface functionalization
UR - http://www.scopus.com/inward/record.url?scp=85037642042&partnerID=8YFLogxK
U2 - 10.3390/bios7040058
DO - 10.3390/bios7040058
M3 - Article
AN - SCOPUS:85037642042
SN - 2079-6374
VL - 7
JO - Biosensors
JF - Biosensors
IS - 4
M1 - 58
ER -