Particle size |
The diameter of nanocarriers should be preferably within the range of 10–150 nm, which is beneficial to accumulate drugs in cancer cell by EPR effect. |
[145] |
Surface charge |
The nanocarriers with positive or slight negative charges can be easily internalized into cells. |
[145,146]
|
Targetability |
The nanocarriers surface-functionalized with peptides, proteins or antibodies displayed superior targetability to delivering nanoparticles into tumor tissue. |
[142] |
Biodegradability |
The nanocarriers should have complete degradation in the host tissues but without leaving any toxic byproducts. |
[141] |
Biocompatibility |
The nanocarriers and its metabolites in vivo should not induce any negative response, thereby reducing the incidence of side effects. |
[147] |
Biostability |
Nanocarriers should have superior physical and chemical stability for long time circulation in vivo as to maximize its biological functions as delivery vehicles. |
[148] |
Preparation procedure |
The nanocarriers should be extracted or synthesized by using safe techniques and convenient procedures. |
[147,149]
|
Drug release manner |
The nanocarriers with controlled release manner have better uptake capacity and less toxic side effects. |
[150,151]
|