At the moment I'm struggling with the documentation of my labs cell culture work, and would be happy to hear some suggestions.

I've established an excel table that I though is easy to use and straight forward, calculates some parameters automatically (Population Doubling Time (PDT), cumulative population doubling). Intention was that each passage is one row in the table. This would be ideal if we would have a defined optimal seeding cell density range for the cell lines and with every passage we only prepare one (or multiple) flasks with the same seeding density.

However, when technicians are preparing multiple flasks with various seeding cell density within one passage step, then the whole table is not useful anymore: there is only 1 next row in the table (as the automatic calculations are using the seeded and the harvested cell numbers), but multiple new cultures that needs to be followed separately, as - depending on how the cells feel themselves - these flask may have different outcomes (viability, VCD, PDT, next passage date).

I have done various paper-based cell culture documentation earlier, none of them were able to track properly such dichotomy when multiple flasks were prepared with different parameters (seeding cell density or different volume) at the same time.

Anyone has experienced the same? Any idea what would be the best solution (besides obviously optimize cell culture conditions and than stick to them later on)?

More Daniel Szili's questions See All
Similar questions and discussions