Carriers
|
no carriers/self-delivery |
Well-defined nanoparticles |
Formulation
|
Molecular self-assembly |
Physical encapsulation |
Drug loading capacity
|
100% prodrug loading |
Vary from system to system, typically less than 5% |
Physiochemical properties
|
Defined by the prodrug molecular design |
Defined by the nanoparticle carrier |
Release mechanism
|
Linker cleavage through enzymes, hydrolysis or other metabolism pathways |
Nanoparticle breakdown and drug diffusion |
Excretion
|
Drug metabolism |
Nanoparticle breakdown and chemical degradation |