Doxorubicin-Loaded Ultrasmall Gold Nanoparticles (1.5 nm) for Brain Tumor Therapy and Assessment of Their Biodistribution.
Benedikt KruseBanendu Sunder DashKathrin KostkaNatalie WolffOleg PrymakKateryna LozaNina GumbiowskiMarc HeggenCristiano Luis Pinto OliveiraJyh-Ping ChenMatthias EpplePublished in: ACS applied bio materials (2024)
Ultrasmall gold nanoparticles (1.5 nm) were covalently conjugated with doxorubicin (AuDox) and AlexaFluor647 (AuAF647) to assess their biodistribution and their efficiency toward brain tumors (glioblastoma). A thorough characterization by transmission electron microscopy, small-angle X-ray scattering, and differential centrifugal sedimentation confirmed their uniform ultrasmall nature which makes them very mobile in the body. Each nanoparticle carried either 13 doxorubicin molecules (AuDox) or 2.7 AlexaFluor-647 molecules (AuAF647). The firm attachment of the ligands to the nanoparticles was demonstrated by their resilience to extensive washing, followed by centrifugation. The particles easily entered mammalian cells (HeLa, T98-G, brain endothelial cells, and human astrocytes) due to their small size. The intravenously delivered fluorescing AuAF647 nanoparticles crossed the blood-brain barrier with ∼23% accumulation in the brain tumor in an orthotopic U87 brain tumor model in nude mice. This was confirmed by elemental analysis (gold; inductively coupled plasma optical emission spectroscopy) in various organs. The doxorubicin-loaded AuDox nanoparticles inhibited brain tumor growth and prolonged animal survival without adverse side effects. Most of the nanoparticles (84%) had been excreted from the animal after 24 h, indicating a high mobility in the body.
Keyphrases
- drug delivery
- gold nanoparticles
- cancer therapy
- endothelial cells
- high resolution
- electron microscopy
- photodynamic therapy
- iron oxide
- white matter
- walled carbon nanotubes
- type diabetes
- signaling pathway
- magnetic resonance imaging
- adipose tissue
- stem cells
- depressive symptoms
- metabolic syndrome
- mass spectrometry
- social support
- induced pluripotent stem cells
- multiple sclerosis
- skeletal muscle
- high speed
- high glucose
- vascular endothelial growth factor
- iron oxide nanoparticles
- subarachnoid hemorrhage
- pi k akt
- brain injury
- adverse drug
- monte carlo
- contrast enhanced