I prepared microparticles but the problem is that the encapsulation efficiency very low.
My polymer is Ethylcelluose and my compound is soluble in both the aqueous phase and organic phase. I modified the pH of the aqueous phase (PVA) so my compound in this modified pH, and supposed to be not ionized at all as a procedure to decrease aqueous solubility. The drug to polymer ratio is 1:100 which is quite low, but this is my target.