Kick-off meeting spring semester 2022

From mn.fysikk.laglivlab
Revision as of 16:47, 27 January 2022 by Dagkd@uio.no (talk | contribs) (CO2 measurement)

Jump to: navigation, search

Present: Kristina, Erik, Claudia, Tiril, Thomas and Dag

Plan for spring 2022

Current state of project

  • We have some microfluidic chip designs we can use although none are perfect (see examples below)
  • Protocol for fibronectin coating is established
  • Filling with cells works and cells do adhere.
  • Problems with air bubbles.
  • Finite lifetime of cells. Probably because they lack oxygen and correct CO2 level.

Goal for semester

Make a device that fulfills the following

  • Controls CO2 level
    • CO2 input can be quickly changed
    • CO2 concentration is measured
    • feedback from measurement to CO2 input
  • Cells adhere
  • Cells stay alive and divide until they are confluent
  • Splitting: partial cell release by trypsination and increased flow rate
  • Cells continue to adhere and divide after splitting
  • Possibly perform an additional experimentlike
    • migration assay by entering SDF-1/CXCL12 into a side channel
    • Ca2+ activation by flow, PBS and other changes

Write a scientific paper. Possible journals:

  • Micromachines (MDPI)
  • Sensors (MDPI)
  • Frontiers in Bioengineering and Biotechnology
  • Biomicrofluidics
  • Microfluidics and Nanofluidics


Specific sub-projects

CO2 measurement

In order to integrate a reliable CO2-measurement without too much development we will use the Zimmer & Peacock ISE OEM, pH sensor and software.

CO2 input change

Choice of method

  • Control of CO2 in media source
  • Control of CO2 in side channel
    • Choose membrane to side channel
      • PDMS
      • Gel

Robust microfluidic protocols

Bubble-free operation

Defining safe flow levels for cells

Switching of different fluids

Gel barrier filling

Network with gradient generator
Network with gas flow channels separated from cell area with gel channels.