TY  - BOOK
A1  - Yoshinobu, Tatsuo
A1  - Schöning, Michael Josef
ED  - Yoshinobu, Tatsuo
ED  - Schöning, Michael Josef
T1  - Light-addressing and chemical imaging technologies for electrochemical sensing
Y1  - 2020
SN  - 978-3-03943-029-1
U6  - http://dx.doi.org/10.3390/books978-3-03943-029-1
N1  - This book is a printed edition of the Special Issue Light-Addressing and Chemical Imaging Technologies for Electrochemical Sensing that was published in Sensors
PB  - MDPI
CY  - Basel
ER  - 
TY  - JOUR
A1  - Yoshinobu, Tatsuo
A1  - Schöning, Michael Josef
T1  - Light-addressable potentiometric sensors (LAPS) for cell monitoring and biosensing
JF  - Current Opinion in Electrochemistry
Y1  - 2021
U6  - http://dx.doi.org/10.1016/j.coelec.2021.100727
SN  - 2451-9103
IS  - In Press, Journal Pre-proof
PB  - Elsevier
CY  - Amsterdam
ER  - 
TY  - JOUR
A1  - Özsoylu, Dua
A1  - Kizildag, Sefa
A1  - Schöning, Michael Josef
A1  - Wagner, Torsten
T1  - Differential chemical imaging of extracellular acidification within microfluidic channels using a plasma-functionalized light-addressable potentiometric sensor (LAPS)
JF  - Physics in Medicine
N2  - Extracellular acidification is a basic indicator for alterations in two vital metabolic pathways: glycolysis and cellular respiration. Measuring these alterations by monitoring extracellular acidification using cell-based biosensors such as LAPS plays an important role in studying these pathways whose disorders are associated with numerous diseases including cancer. However, the surface of the biosensors must be specially tailored to ensure high cell compatibility so that cells can represent more in vivo-like behavior, which is critical to gain more realistic in vitro results from the analyses, e.g., drug discovery experiments. In this work, O2 plasma patterning on the LAPS surface is studied to enhance surface features of the sensor chip, e.g., wettability and biofunctionality. The surface treated with O2 plasma for 30 s exhibits enhanced cytocompatibility for adherent CHO–K1 cells, which promotes cell spreading and proliferation. The plasma-modified LAPS chip is then integrated into a microfluidic system, which provides two identical channels to facilitate differential measurements of the extracellular acidification of CHO–K1 cells. To the best of our knowledge, it is the first time that extracellular acidification within microfluidic channels is quantitatively visualized as differential (bio-)chemical images.
Y1  - 2020
U6  - http://dx.doi.org/10.1016/j.phmed.2020.100030
SN  - 2352-4510
VL  - 10
IS  - 100030
PB  - Elsevier
CY  - Amsterdam
ER  -