I'm doing primary tumor spheroids to a drug screening. We're having success to make the spheroids but I'm not having succes to dissociate the spheroids to evaluate the cell viability (using trypan blue to count).

I tryed to use trypsin 5 and 10 min (37ºC) and Accutase 10 min (R.T.) and the spheroids not dissociated completely. Could you help me?

p.s.: Spheroids were plated with 5000 cells, so they are ver small to dissociate mecanically.

Thank you!

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