Refine
Year of publication
- 2020 (240) (remove)
Institute
- Fachbereich Medizintechnik und Technomathematik (59)
- Fachbereich Wirtschaftswissenschaften (35)
- Fachbereich Energietechnik (34)
- Fachbereich Luft- und Raumfahrttechnik (33)
- IfB - Institut für Bioengineering (33)
- Fachbereich Elektrotechnik und Informationstechnik (29)
- ECSM European Center for Sustainable Mobility (18)
- Fachbereich Maschinenbau und Mechatronik (17)
- Fachbereich Bauingenieurwesen (14)
- Fachbereich Chemie und Biotechnologie (13)
Language
- English (170)
- German (68)
- Multiple languages (1)
- Dutch (1)
Document Type
- Article (132)
- Conference Proceeding (55)
- Part of a Book (18)
- Book (9)
- Review (7)
- Other (4)
- Doctoral Thesis (3)
- Patent (3)
- Administrative publication (3)
- Conference Poster (2)
- Conference: Meeting Abstract (1)
- Contribution to a Periodical (1)
- Part of a Periodical (1)
- Report (1)
Keywords
- Amtliche Mitteilung (3)
- MINLP (3)
- Additive manufacturing (2)
- Adjacent buildings (2)
- Experimental validation (2)
- Historical centres (2)
- INODIS (2)
- SIJ (2)
- Shake table test (2)
- Solar-Institut Jülich (2)
Is part of the Bibliography
- no (240)
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.