Pharmacodynamics
Nystatin is a channel-forming ionophore, meaning that it exerts its therapeutic effect via the formation of a membrane-spanning pore in the plasma membrane of the fungus. Formation of this pore results in a change in membrane permeability that allows leakage of intracellular contents and subsequent disruption of the electrochemical gradient, which are necessary for proper cell function. The selectivity for fungal cells over mammalian cells is due to the greater binding affinity of nystatin for ergosterol, a molecule found only in fungal cells.
Pharmacokinetics
Systemic absorption of nystatin is minimal after oral administration, and no detectable plasma concentrations are achieved after topical or vaginal administration. Nystatin is not absorbed into the systemic circulation; therefore, there are no data on the pharmacokinetic properties of this drug.