Table 2.
Intranasal administration of bioactive agents via in situ gels.
| Bioactive Agents | Formulation Composition | Neurological Disorder | Efficacy | References | 
|---|---|---|---|---|
| Levodopa | Pluronic F127, chitosan | Parkinson’s syndrome | Delayed mucociliary clearance | [56] | 
| Amantadine | Pluronic F127, carboxymethylcellulose | Parkinson’s syndrome | No cellular toxicity to human nasal epithelial cells | [57,58] | 
| Ropinirole | Chitosan, hydroxyl propyl methyl cellulose | Parkinson’s syndrome | Enhanced brain uptake of drug in vivo | [59] | 
| Rasagiline mesylate | Poloxamer 407, poloxamer 188, carbopol 934 P and chitosan | Parkinson’s syndrome | 6-fold higher drug bioavailability | [60] | 
| Ropinirole | Pluronic F-127 and hydroxy methyl propyl cellulose | Parkinson’s syndrome | Five-fold brain uptake of the drug | [61] | 
| Sumatriptan | Gellan gum | Migraine | High drug concentration in plasma and brain tissues | [62] | 
| Huperzine A | Gellan gum | Alzheimer’s | Increased drug distributions in the rat brain tissues: the cerebrum and hippocampus | [63] | 
| Curcumin | Pluronic F127, Poloxamer | Alzheimer’s | Improved drug-targeting efficiencies in the cerebrum, cerebellum, hippocampus and olfactory bulb | [64] | 
| Geniposide | Poloxamers (P407, P188) and hydroxypropyl methylcellulose | Alzheimer’s | In vitro release profile of the drug was zero-order, and the ex vivo release mechanism was the Weibull model | [65] | 
| Rivastigmine | Poloxamer 407®, poly(lactic-co-glycolic acid) nanoparticles | Alzheimer’s | Enhanced drug permeability and sustained drug release profile; the cellular uptake of the drug from the formulation was time dependent | [66] | 
| Rivastigmine tartrate | Pluronic F127, HPMC Chitosan, Carbopol 934 and sodium carboxymethyl cellulose | Alzheimer’s | Good distribution to the brain (0.54% ID/g) when compared to intravenous administration | [67] | 
| Doxepin | Chitosan and glycerophosphate, poly(ethylene) glycol | Depression | In vivo studies in Swiss albino mice showed a good increase in activity count and a decrease in immobility time | [68] | 
| Agomelatine | Pluronic F127, Carbopol, chitosan, sodium carboxymethylcellulose, sodium alginate, and hydroxypropyl methylcellulose | Depression | Significantly enhanced brain uptake in vivo | [69] | 
| Fluoxetine hydrochloride | Gellan gum and HPMC (hydroxypropyl methylcellulose) | Depression | Reduced immobility, increased climbing and swimming behavior | [70] | 
| Tramadol hydrochloride | Chitosan, Pluronic, HPMC | Depression | Increased locomotor activity and body weight of the rat model in vivo | [71] | 
| Nortriptyline hydrochloride | Poloxamer 188 and HPMC | Depression | Enhanced drug release profile | [72] | 
| Venlafaxine | Sodium alginate | Depression | Brain uptake was 742.5 ng/mL, tmax 60 min; improved swimming and climbing and reduced immobility in vivo | [73] | 
| Paliperidone | Carbopol 934 and hydroxypropyl methyl cellulose | Schizophrenia | High rate of drug permeation via sheep nasal mucosa | [74] |