Revision as of 13:25, 9 July 2022 (view source) Krisheye@uio.no (talk | contribs) (Starting to change the front page and adding some details) (Tag: Visual edit) ← Older edit		Revision as of 13:27, 9 July 2022 (view source) Krisheye@uio.no (talk | contribs) m (Tag: Visual edit) Newer edit →
Line 1:		Line 1:
		+	Click here for [[Lab and Planning Notes|Lab and Planning Notes]]
		+
	= Microfluid monitoring incubator =		= Microfluid monitoring incubator =
Line 18:		Line 20:
	We have used some time to create new wafers with a new design, which we successfully used in our experiments.		We have used some time to create new wafers with a new design, which we successfully used in our experiments.
−	When trying to integrate the Zimmer & Peacock pH sensor we did not receive the results we were hoping for. The issue of integrating the sensor together with the medium flow is still under planning stage.	+	When trying to integrate the Zimmer & Peacock pH sensor we did not receive the results we were hoping for. The issue of integrating the sensor together with the medium flow is still under planning stage.
−
−	=== Notes ===
−
−	To test the gradient generator we use methylene blue that has a diffusion coefficient of (6.74 ± 1.32) × 10−10 m2/s (https://doi.org/10.1134/S0030400X19060213). The gradient generator worked well, but it has to be repeated at controlled flow rates to find max flow rate
−
−	==== Cell adhesion ====
−	Cells did not adhere directly on the glass bottom surface. Next, we tried filling the channels with collagen, but only a few cells adhered. According to doi:10.3390/bios10110182 collagen is found to be the best surface treatment for adhering cells in microfluidic circuits. We should therefore check the protocol and try again. According to doi:10.1016/j.colsurfb.2016.11.011 (3-Aminopropyl)triethoxysilane (APTES) can be used as a linker of collagen to PDMS, maybe it works for glass as well?
−
−	==== Possible continuations ====
−	[[Vascularization|Vascularization]]
−
−	== [[Lab and Planning Notes|Lab and Planning Notes]] ==

---

Revision as of 13:27, 9 July 2022

Click here for Lab and Planning Notes

Microfluid monitoring incubator

Check out this introduction to Cell biology: Microfluidic Concepts and methodologies

Description

Here's a presentation of the concept

Introduction

The rage of the 2020s are organs-on-a-chip [1]. These are systems that have to be specifically engineered for each type of organ. Growing and maintaining cell cultures, however is a more generic activity of cell biology. They are kept in expensive incubators and several times a week they have to be looked after and the growth media replaced. When there are too many cells, most of them are killed and some are re-applied in a new flask/petri dish. All this can be done inside a lab on a chip[4]. In addition, the incubator functions of controlling temperature, CO2 and O2 pressure can be reduced to small modules in a standalone cell culture system that is small enough to be moved from lab to lab and between research microscopes at different imaging facilities. Adding electrodes to the system will allow electrochemical or bioimpedance monitoring of the cell coverage, a feature that will be publishable in a scientific journal.

The system is perhaps not the most exciting project to start with, but it contains all the basic technology needed for more advanced organ-on-a-chip systems: temperature, gas and fluid control, hydrogel membranes, monitoring of cell state, etc. It will be a platform that LagLivLab students can build on and modify for years.

[1] B. Zhang, A. Korolj, B.F.L. Lai, M. Radisic, Advances in organ-on-a-chip engineering, Nat. Rev. Mater. 3 (2018) 257–278. doi:10.1038/s41578-018-0034-7. [4] F. Bunge, S. van den Driesche, M.J. Vellekoop, Microfluidic platform for the long-term on-chip cultivation of mammalian cells for Lab-on-a-Chip applications, Sensors (Switzerland). 17 (2017) 1–15. doi:10.3390/s17071603.

Progression Spring Semester 2022

This semester we have worked hard in order to achieve control over CO2 concentration inside the incubator in order to prolong the life of the cells. We have received Zimmer & Peacock ISE OEM, pH sensor and software which we needed to integrate into our experiment in order to measure the pH concentration.

We have used some time to create new wafers with a new design, which we successfully used in our experiments.

When trying to integrate the Zimmer & Peacock pH sensor we did not receive the results we were hoping for. The issue of integrating the sensor together with the medium flow is still under planning stage.