Table 2.
List of the advantage and disadvantage for nanomaterials.
Nanomaterials | Advantages | Disadvantages |
---|---|---|
Liposome | High efficiency, low toxicity, long-term efficacy, ability to deliver both hydrophilic and lipophilic compounds [262] | Rapid systemic elimination, rapid metabolic degradation of phospholipids. Stability problems associated with long-term storage. Inability to provide sustained drug release. They are only moderately efficient for the encapsulation of lipophilic compounds [[263], [264], [265], [266], [267], [268]] |
Polymeric nanoparticles | the ability to modify drug release; increase the stability of volatile drug; incorporate into other activities related to drug delivery [269] | high cost; the preparation process is complex and the reproducibility is low |
Metal nanoparticles | MRI and magnetic targeting performance; free radical scavenging | Potential toxicity associated with complex ingredients [270] |
Carbon nanotubes | High penetration power and surface area; more than one molecule can be conjugated to their surface | Low biodegradability and dispersivity, possible induced oxidative stress and Lung disease [170,171] |
Graphene | Polyaromatic structure and higher surface area | The lack of standardization; Difficult to biodegrade; Damage to the lungs [215,271] |
Black phosphorus | Biodegradable; selectively capture Cu2+64 | High cost; difficult to control shape and size |
Hydrogels | Similar to the flexibility of natural tissue; PH or temperature sensitive; Biocompatible and biodegradable [272] | Thermosensitive hydrogel may cause excessive or insufficient drug release due to temperature stimulation [273]. |
Dendrimers | Easy surface modification; ability to interact with charged functional groups [274]. | The specific toxicology, biocompatibility and in vivo distribution of various dendrimers need further in-depth study [274]. |