TABLE 3.
Advances in the uses of nanoparticles in glioma therapy and diagnosis.
Use | Experimental setting and nanoparticle type |
Nanocarrier: Drug bioavailability/therapeutic efficacy enhancer
|
Preclinical:
|
Standalone therapy | Preclinical
|
Drug sensitizer | Temozolomide: direct attenuation on EGFR and MET signaling, through delivered miRNAs (Meng et al., 2020) |
Imaging technologies enhancer | Fluorescence: USPION (Denora et al., 2019) |
Magnetic hyperthermia |
Clinical
|
Preclinical
|
|
Sonodynamic therapy | Preclinical
|
Radiotherapy enhancer | Charged particles |
|
|
Photon therapy (X-rays)
|
|
Photodynamic therapy enhancer | Preclinical
|
Immunotherapy enhancer | Functionalization with anti-PDL1 (Ruan et al., 2019; Zhang et al., 2019) |
SPION, superparamagnetic iron oxide nanoparticles; USPION, ultrasmall SPION; PLGA, poly-lactide-co-glycolic acid; PEG, polyethylene glycol; RGD, arginyl-glycyl-aspartic tripeptide; TPLN, FONP, fluorescent organic nanoparticles; pSiNPs, porous silicon nanoparticles; terpolymer-lipid nanoparticles; MP, permalloy magnetic particles; FA-AuNC, folic acid gold nanoclusters; AuNP, gold nanoparticles, AgNP, silver nanoparticles; AGuIX, gadolinium-based nanoparticle; 5-ALA, 5-aminolevulinic acid; AuNS, gold nanospheres; ICG, indocyanine green; HSPA5, heat shock protein A5r4t. *Theranostic NP: Possesses diagnostic and therapeutic functions. aImprove CT/MRI imaging and also works as radiosensitizer by AuNS properties and loading an HSPA inhibitor.