The cryorolled sample shows a high dissolution rate.

What always matters in dissolution rate is the Stirring Speed.

The intrinsic dissolution rate is defined by the United States Pharmacopeia.

The typical unit for dissolution rate is mol/s.

For example, slow dissolution rates can prolong the duration of action or avoid initial high plasma levels.

The most stable crystalline polymorph has the lowest dissolution rate.

For this reason, different forms of the same medication can have the same active ingredients but different dissolution rates.

Simulations suggest that photoelectron generation from the gold substrate may affect dissolution rates.

Amorphous form have higher dissolution rate compared to any other form.