There is a problem in my research. When I mixed tannic acid with proteins in ddH2O, the complexation would form stable nanoparticles. After that, I added PLL (a kind of polycations) into the system, it seems good. But obvious aggregates formed after dilution with PBS buffer.
Besides, I found that the mixture of PLL and Tannic acid without proteins was good in ddH2O. However, the mixture in PBS buffer would aggregate and the solution turned cloudy.
I am wondering why the system is unstable in PBS buffer?
I am looking forward to your reply!