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Table 2 NPs targeting macrophages

From: Nanobiotechnology approaches for cardiovascular diseases: site-specific targeting of drugs and nanoparticles for atherothrombosis

Targeting approach

Delivered drugs

Models

Effect

Refs.

Amphiphilic macromolecule (AM)

 

In vitro SMCs

Prevented LDL internalization in SMCs and reduced MSR1 and CD36 expression

[108]

AM (1 cM)

Ferulic acid

In vitro human monocyte– derived macrophages

Reduced uptake of oxLDL and ROS level

[103]

Scorpion-like AM

Lithocholic acid

In vitro human monocyte– derived macrophages

Lowered oxLDL uptake by macrophages

[107]

PLA-PEG NP

Rosiglitazone (RSG)

In vitro RAW264.7 macrophages

Significantly inhibited IL-10 expression

[121]

rHDL NP

Statin

ApoE−/− on HFD (mice)

Accumulated in macrophages and decreased inflammation and lower inflammatory factors

[96, 100]

AM

GW3965

HFD (rats)

Lowered intimal levels of accumulated cholesterol, inhibited macrophage retention

[105]

Sugar-based AM (M12PEG) against MSR1 & CD36 SR

 

ApoE−/− mice on Harlan Teklad diet

Reduced artery occlusion, inhibited uptake of oxLDL, downregulated expression of SRs

[106]

Mannose-functionalized NPs

LXR ligand

LDLR−/− on HFD (mice)

Reduction of lesion area in atherosclerotic plaques

[138]

Hyaluronan NPs

 

ApoE−/− on HFD (mice)

Lowered number of immune cells in plaques

[111]

LOX-1 siRNA

ApoE−/− on HFD (mice)

Reduced plaque area and lipid content

[113]

Simvastatin

ApoE−/− on HFD (mice)

Significantly reduced plaque size

[114]

Cationic peptide containing pH-sensing residues (p5RHH)

JNK2 siRNA

ApoE−/− on HFD (mice)

Decreased thrombotic risk, restored endothelial barrier integrity, reduced plaque necrosis, and depleted plaque-macrophage content

[115]