Table 1.
The list of mitochondria targeting molecules and its targeting mechanism.
Chemical nature | Group | Molecule | Targeting mechanism | Advantage/disadvantage | Ref. |
---|---|---|---|---|---|
Small molecule | TPP+ | Mito-Q; Mito-Vit-E; Mito-TEMPOL; TPP+ functionalized liposomes; Ceria nanoparticle; Silica nanoparticles | Positive charge and lipid solubility | Easy to synthesis/cytotoxicity for drug delivery | 7, 8, 9, 10, 11, 12, 13, 14, 15 |
Small molecule | Pyridinium salt | 5BMF@HSA complex | Positive charge and lipophilic, HSA increasing water solubility | Easy to synthesis, tunable luminescence/cytotoxicity for drug delivery | 16 |
Small molecule | DQA | QDAsomes | Amphipathic | Easy to synthesis, cytotoxicity for drug delivery/low endosomal escape ability and transfection efficiency | 17,18 |
Small molecule | Ru/Ir | Ru/Ir complexes | Positive charge and lipophilic | Cytotoxicity for cancer therapy/multimodal therapy | 19,20 |
Peptide | S-S peptides | SS-02, SS-31 | Positive charge and lipophilic | Hypotoxicity, antioxidant/complex | 21 |
Peptide | MPP | MPP | Positive charge and lipophilic | Hypotoxicity, tunability, desirable pharmacokinetic profiles/complex synthesis | 22,23 |
CPMs | CPM | CPM1, CPM2, CPM3 | Amphipathic | Efficient and universal delivery of cargos/complex synthesis | 24 |
Mito-Porter | Octa arginine | (DF)-Mito-Porter, ASO-Mito-Porer, DOX-Mito-Porter | Lipid compositions promote its fusion with the mitochondrial membrane | Efficient and universal delivery/complex synthesis | 25, 26, 27, 28, 29 |
Gramicidin S | Gramicidin S | XJB-5-131 | High affinity for the membrane | Antioxidant/complex synthesis | 30 |