Filtration of media in 0.2 micron may remove the contaminants (particles). But the microbial waste/toxin (it wont filtered out) will impede the growth of cells.
Filtration of media in 0.2 micron may remove the contaminants (particles). But the microbial waste/toxin (it wont filtered out) will impede the growth of cells.
Because of contaminated DMEM contains toxin and by product of bacteria and fungi, so, it is preferable not use it. Filtration of the media can not remove toxin and by product.
As a general rule, think about the cost of the contaminated reagent. If it is something cheap, such as media, throw it out as soon as you realise that something is wrong with it. The potential unwanted consequences of using it, especially lost time, are not worth it, not to mention that the cost of the filter is probably not that different to the replacement cost of the media. If it is something rare, unique, expensive or time consuming to replace, then I would consider ways to save it, but always as a last resort.
Just in case you got contamination around 1-2 days, after filtering the media, cells will grow well no problem. For the experiment to observe cell localization, it will not be affected. However, as Thea Anna Monks said we dont know what will happen for long term period. In my opinion, the media can be used but we should throw the cell after several passages.
Thank you for all suggestions. The method for separating media in 50ml tube have been applied by me. For good outcomes, I will just discard the medium. Grateful, the media that I have prepared for 1 week, is still ok and not contaminated.