Passive |
CD47 surface decoration |
SIRPα |
Increased exosome circulation time |
Mouse embryonic fibroblasts (MEFs) |
mRNA |
[130] |
Surface PEGylation |
N/A |
Reduced exosome clearance Enhanced tumor penetration |
4T1 murine breast cancer cells |
N/A |
[131] |
iRGD peptide fusion with Lamp2b |
N/A |
Inhibited tumor growth without overt toxicity |
Mouse immature dendritic cells |
Doxorubicin |
[132] |
Active |
IL3-Lamp2b expressing exosome production |
IL3 receptors |
Increased intratumoral accumulation |
HEK293T cells |
Imatinib, BCR-ABL siRNA |
[133] |
Exosome azide integration, DBCO-PEG4-biotin avidin conjugation |
Biotin receptors, glycan biosynthesis process |
Higher uptake levels |
B16F10 cells |
Streptavidin-HRP |
[134] |
Neuraminidase |
Terminal sialic acid residues from glycoproteins |
Rapid accumulation of EVs in the liver |
MLP29 cells |
N/A |
[135] |
3-(diethylamino) propyl-amine (DEAP) |
N/A |
pH sensitive uptake |
RAW 264.7 cells |
N/A |
[136] |
αCD3 and αHER2 antibodies’ surface expression |
CD3, HER2 receptors |
Increased T cell activation |
Expi293 cells |
N/A |
[137] |
anti-SSTR2 mAb |
Somatostatin receptor 2 (SSTR2) |
High toxicity of cancer cells |
HEK 293 cells |
Romidepsin |
[138] |
DSPE-PEG biotin and avidin conjugation |
Biotin receptors |
Increased stability and encapsulation efficiency |
HUVECs |
N/A |
[139] |
Diacyllipid–aptamer(sgc8) PEG conjugation |
PTK7 |
Increased cellular uptake |
ImDC cells |
Doxorubicin |
[140] |