Table 2.
NPs | Advantages | Disadvantages |
---|---|---|
Liposomes | Reduced toxicity184 Selective target specificity185 Enhancement of drug activity against pathogens186,187 Improved pharmacokinetics and pharmacodynamics188 |
Low drug entrapment189 Difficulty of sterilization190 Short shelf life due to instability191 Rate of removal from the bloodstream192 |
Polymer Nanoparticles (PNs) | High stability203,204 Various preparation methods205,206 Control and persistence of drug release204,207 Adjustability of chemical and physical properties208 Suitability for hydrophilic and hydrophobic drugs203 |
Difficult scalability213 Inadequate toxicological assessment214 |
Dendrimer Nanoparticles (DNs) | High cell penetration209,210 High structural homogeneity209 High miscibility and solubility211 Controllable synthesis and degradation209,210,212 |
High production cost209 Difficulty of clinical application in basic research215 The need for quality management improvement210 |
Gold Nanoparticles (GNs) | High biocompatibility210 Controllable particle size210 Convenience of synthesis and conjugation of various bioactive agents210 |
Nanoparticle aggregation211 Impossible biodegradation220,221 High cost of large-scale production222 |
Virus Like Particles (VLPs) | Stabilization by disulfide bonds227,228 Produced by cell-free protein synthesis227,229 Small molecule, nucleic acid and protein loading capacity230,231 Functionalization of antibody fragment display for specific cell targeting232,233 |
Low stability227 Phagocytic avoidance234 Extravasate from blood vessel235 |
Cell-Derived Vesicles | Low inherent toxicity246 Low apparent risk of aneuploidy247 Low immune rejection248 |
Promoting metastasis formation in tumor cells249–252 contribution to tumor cell survival253,254 |