Nanocarrier Type | Toxicity Endpoint | Dose–Response | Time Course | Mechanism of Toxicity | Mitigation Strategies | References |
---|---|---|---|---|---|---|
Liposomes | Hepatotoxicity | Dose-dependent | Acute | Reactive oxygen species-induced apoptosis | Use of antioxidants; reduction of drug dose | [13] |
Polymeric nanoparticles | Nephrotoxicity | Nonlinear | Sub-acute | Accumulation in renal tubules and glomeruli | Use of PEGylation; adjustment of molecular weight | |
Carbon nanotubes | Pulmonary toxicity | Dose-dependent | Chronic | Inflammation, oxidative stress, fibrosis, and granuloma formation | Surface modification; reduction of length and aspect ratio | |
Gold nanoparticles | Cytotoxicity | Dose-dependent | Sub-chronic | Uptake and accumulation in mitochondria, inducing oxidative stress and apoptosis | Surface coating; use of size-limited particles | [121] |
Iron oxide nanoparticles | Hemotoxicity | Dose-dependent | Acute | ROS-induced apoptosis; complement activation | Surface coating; chelation of iron ions | [121] |
Dendrimers | Neurotoxicity | Dose-dependent | Sub-acute | BBB disruption, microglial activation, oxidative stress | Modification of dendrimer size and surface charge; use of biodegradable dendrimers | [99] |