From: Peptide–nanoparticle conjugates: a next generation of diagnostic and therapeutic platforms?
Imaging | Peptide | Nanoparticle (NP) | Animal studies | Results | Refs. | |||
---|---|---|---|---|---|---|---|---|
Modality | Probe | Name | Target or role | Type | Size | |||
NIR | FITC | DEVD peptide sequence | Cleave caspase-3 | Biotinylated NP, Acetyl-Asp-Glu-Val-Asp-Cys(StBu)-Lys(Biotin)-CBT | 100–300 nm | N/A | Twofold enhanced (fluorescent intensity, vs. SA-FITC) | [80] |
Zn2+ coordinated cyclic peptide NP (f-PNP) | RGD | Targets αvβ3 Integrin | Fluorescent cyclic peptide NP (f-PNP, self-assembled) | 28 nm | Xenografted EC mouse model | Highly photostable and narrow emission spectrum | ||
Small-molecule NIR-II organic dye | RM26 peptide | Targets gastrin-releasing peptide receptor | DSPE-mPEG NP | 60 nm | U87MG (glioblastoma) tumor bearing mouse model | Highly sensitive and specific to GRPR | [83] | |
CT | AuNP | RGD | Targets αvβ3 integrin | Dendrimer-entrapped gold nanoparticles (Au DENPs) | 4.0 nm (Au core) | N/A | Enhanced X-ray attenuation compared to Omnipaque | [84] |
AuNP + IR780 (Fluor) | Angiopep-2 | Targets glioma | DTX-loaded PLGA@Au NP | 180 nm | U87MG (glioblastoma) tumor bearing mice | 4 h (Whitening effect AT the target site) | [85] | |
AuNP + Cy5.5 (Fluor) | Fibrin-targeting peptide and Thrombin-activatable fluorescent peptide | Targets fibrin and Cleave thrombin | Glycol-chitosan-coated AuNP (GC-AuNP) and SiO2@AuNP | 127 nm (Pep-GC-AuNP) and 39.8 nm (Pep-SiO2@AuNP) | C57Bl/6 mouse model | Remained at the target site for up to 3 weeks | ||
PET | 18F | CK and CLPFFD peptides | Targets β-amyloid fiber | AuNP | 12 nm (hybrids) | Sprague–Dawley rat model | NPs were trapped by reticuloendothelial system (RES) | |
64Cu | RGD | Targets αvβ3 integrin | Au-tripods | 10–15 nm | U87MG (glioblastoma) tumor bearing mice | Threefold enhanced (PAI contrast, vs. blocking group) | [91] | |
125I 76Br | RGD | Targets αvβ3 integrin | PEO dendrimer | 12 nm | Unilateral hindlimb ischemia-induced mice | 50-fold enhanced (affinity, vs. free peptide) > twofold enhanced (ischemic to nonischemic hindlimb ratio, vs. nontargeted NP) | [92] | |
MRI | Iron oxide | RGD | Targets αvβ3 integrin | Iron oxide NP | < 10 nm (NP) 8.4 nm (Hybrid) | U87MG (glioblastoma) tumor bearing mice | 42% (tumor MR signal intensity reduction, 15% for free peptide) | [94] |
Iron oxide | RGD | Targets αvβ3 integrin | Superparamagnetic polymeric micelles (SPPM): SPIO NPs inside the core of a PEG-PLA co-polymer micelle | 9.9 nm (SPIO) 50–75 nm (SPPM) | A549 (lung), MDA-MB-231 (breast), U87MG (Glioblastoma) tumor bearing mice | 10−12 mol/L (detection limit) | ||
Iron oxide | CREKA | Targets fibrin | Amino dextran-coated SPIO | 50 nm | Mouse model | NPs accumulates in tumor vessel → self-amplifying tumor homing | [97] | |
Multi-modal | Hollow Au nanosphere (HAuNS, CT) 64Cu (PET) | RGD | Targets αvβ3 integrin | HAuNS | 44.7 nm | VX2 tumor-bearing rabbit model | 0.20% (tumor uptake, vs. 0.099% for non-RGD NP) | [98] |
Cy5 (Fluor) Gd (MRI) | Activatable cell penetrating peptides (ACPPs) | Targets active MMP-2 and -9 | G5 PAMAM dendrimer | 4.6 nm | HT-1080 (fibrosarcoma) tumor-harboring mice | 4- to 15-fold enhanced (NP uptake, vs. unconjugated peptides) | [99] |