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. 2020 Dec 7;8:558375. doi: 10.3389/fbioe.2020.558375

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
  • Usually loaded with drugs such as doxorubicin or biological agents such as siRNA (Yu et al., 2017)

  • Usually functionalized with ligands of common GBM membrane proteins

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.