Table 2.
Chitosan-based nanocarriers and their mechanism.
Nanocarrier Component | Loaded Drug | Vivo or Vitro | Efficacy Mechanism | Reference |
---|---|---|---|---|
Chitosan nanocarrier | Gemcitabine | In vitro | Oral adsorption | [65] |
Chitosan/poly(ethylene glycol) | Gemcitabine | In vitro and in vivo | Reduce the burden of frequent dosing and higher toxicity | [66] |
Chitosan nanoparticle | Herceptin (HER2)conjugated gemcitabine | In vitro | Eventual uptake and prolonged intracellular retention | [67] |
O-carboxymethyl chitosan | Curcumin | In vitro | Increase drug solubility | [68] |
N-octyl-O-sulfate chitosan micelles | Paclitaxel | In vitro | Solubilization of hydrophobic drugs | [69] |
Glycol chitosan–5βcholanic acid (HGC) | Camptothecin | In vitro and in vivo | Increase drug stability, solubility and retention | [70] |
Hydroxyapatite chitosan nanocomposite | Celecoxib | In vitro and in vivo | Sustained-release patterns | [71] |