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. 2022 Jun 10;14(6):1228. doi: 10.3390/pharmaceutics14061228

Table 2.

Multiply TLRa in combination with nanoparticles.

Nanoparticles Sub Classses TLRa Immunoadjuvants Administration Route Tumor Model References
phospholipid micelles loaded with zinc-doped iron oxide magnetic nanoparticles (MNPs) TLR3, TLR7 Poly(I:C), R837 ovalbumin subcutaneous B16-F10 [114]
liposomes TLR3, TLR9 Poly(I:C), CpG-ODN ovalbumin intraperitoneal EL4 [115]
PCL−PEG-PCL & DOTAP(IMNPs) & DSPE-PEG-mannose (MAN-IMNPS)lipid-polymer hybrid
nanoparticles
TLR4, TLR7/8 MPLA, R837 ovalbumin, anti-PD-1 subcutaneous E.G7-OVA [43]
mannose-functionalized lipid-hybrid polymersomes (MAN-IMO-PS) TLR4, TLR7/8 MPLA, R837 ovalbumin intramuscular E.G7-OVA [117]
the lipids shell POPC/DMPG, PLGA of PEGylated-coated nanoparticles (NPs) TLR4, TLR9 MPLA, CpG α-galactosylceramide
(GalCer), melanoma antigens
subcutaneous B16-F10 [118]
mesoporous silicon vector (MSV) microparticles TLR4, TLR9 MPLA, CpG tyrosinase related protein 2 (TRP2) peptide intravenous B16 [119]
sHDL nanodiscs(ND) TLR4, TLR9 MPLA, CpG ovalbumin, E7 peptide antigen subcutaneous B16F10-OVA, TC-1 [120]
PLGA/PEI NPs TLR9 + TLR4 or TLR7/8 CpG ODN, MPLA or R848 N/A subcutaneous J774 [116]
BanNVs TLR7/8, TLR9 R848, CpG-ODNs Adpgk, aPD-1 subcutaneous MC38 [121]