Table 1.
Delivery system | Classification | Advantages | Disadvantages |
---|---|---|---|
Viral vectors |
Adenovirus Adeno-associated virus, lentivirus Retrovirus Herpes simplex viruses |
High transduction efficiency High tolerance Standardized transduction procedures Long-term and stable gene expression |
Limited loading space High immunogenicity Risk of insertional mutagenesis, Potential carcinogenicity |
Lipid-based nanoparticles |
Liposomes Lipid nanoparticles Solid lipid nanoparticles Nanostructured lipid carriers |
Good biocompatibility Easy preparation Large drug encapsulation space |
Toxicity and immunogenicity Limited stability |
Polymer nanoparticles |
Chitosan nanoparticles PLGA nanoparticles, Dendrimers |
Good biocompatibility and biodegradability Ability to target specific cells Easy functionalization Controlled drug release |
Toxicity Non-degradability for some chitosan nanoparticles |
Inorganic nanoparticles |
Metal nanoparticles Iron-based nanoparticles Bimetallic nanoparticles Carbon-based nanostructures Selenium nanoparticles Silica nanoparticles Quantum dots |
Easy surface modification High loading capacity and fast release rates Noninvasive imaging |
Potential toxicity Non-degradability |
Extracellular vesicles and exosomes |
Exosomes Microvesicles Apoptotic bodies |
Good biocompatibility and biodegradability High permeability Low immunogenicity Long half-life High delivery efficiency |
Uncontrollable genomic or protein components Potential toxicity High cost |
Nucleic acid conjugates |
GalNAc molecular conjugation Aptamer |
Low immunogenicity Ability to target specific cells Long-term and gene expression |
Low stability Potential toxicity Limited targets |