Log K o/w outside of 1-3 = Partition Coefficient Emulsions Partitioning Suspensions Dissolution Semisolids Suspended Dissolution Dissolved Partition Solids Powders Dissolution Granules Dissolution Tablets Immediate Release ~ Dissolution (Undergoes quick disintegration, deaggregation and dissolution) *IR coatings DO NOT affect 4Ds Chewable, Sublingual, Dissolution (Fast disintegration) Effervescent Rapid Dissolving Diffusion & Partition Coefficient (liquefies in mouth) (FAST disintegration Tablets (RDT) and dissolution) Modified Release (MR) Enteric-coated/General Disintegration (enteric coating), then 4 Ds *See below Buccal & Vaginal Dissolution Coefficient (NO DISINTEGRATION & slow dissolution) Capsules HGC Solid dosage forms Dissolution *rupture dissolution of (powders, granules, *generally ⬆ oral gelatin capsule in GIT tablets) bioavailability than not a RLS because ER depends on rate control (refer to below ) a tablet occurs rapidly Suspension Solid Particle Dissolution *Depends on inside formualation Solution (nonaqueous) Diffusion Coefficient or Partition Coefficient SGC Depends on dosage form inside; refer to HGC above Modified Release Delayed Release (DR) Coating must dissolve for the drug to undergo the 4D processes and so the removal of the coating is rate limited. (Dissolution or disintegration?) Repeat Action Tablets First layer is IR and the solution is rate limiting (dissolution) and for the (RA/Repetabs) second layer the removal of the coating is rate limiting (?) Targeted Release ??? Extended Release (ER) Dissolution Coated Systems Dissolution Controlled Soluble Matrix Systems Dissolution Diffusion Resevoir/semi-permeable Diffusion Controlled membrane system Insoluble Matrix Systems Diffusion Ion Exchange Displacement of the drug on the insoluble polymer matrix Controlled reservoir by endogenous electrolytes Osmosis Push pull layer of the polymer in the tablet that is pulling Controlled the water into the tablet and pushing the drug out