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. 2019 Oct 17;11(10):540. doi: 10.3390/pharmaceutics11100540

Table 1.

Liposomal formulations designed for nose-to-brain delivery of hydrophilic drugs.

Composition Particle Size Zeta Potential Drug
(MW)
Target Disease In Vivo Dosing Position Dosing Volume Ref.
DOPC:CHOL:SA 149 nm +30 mV GDNF
(15,100)
Parkinson’s Disease SD rat supine 25 μL [64,65]
DOPC:CHOL:SA 299 nm +19 mV ovalbumin
(43,000)
SD rat supine 25 μL [66]
HSPC:CHOL 128 nm −15 mV bFGF
(16,500)
ischemic stroke SD rat supine ~30 μL [67]
EPC:CHOL:DSPE-PEG 112 nm +3 mV H102 peptide
(1,289)
AD SD rat 40 μL [68]
soyPC:DHAHAB 142 nm +6 mV 2-PAM (173) Organoph-osphorous poisoning Wistar rat [69]
EPC:CHOL 166 nm +11 mV rivastigmine tartrate
(400)
AD SD rat supine ~80 μL [70]
EPC:CHOL 40 nm −48 mV ferric ammonium citrate (262) iron deficiency SD rat supine 45 μL [71]
soyPC:CHOL
(30:0.2)
112 nm +49 mV galanthamine hydrobromide (368) AD SD rat prone 40 μL [72]

1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC); cholesterol (CHOL); N-(Carbonyl-methoxypolyethyleneglycol 2000)-1, 2-distearoyl-sn-glycero-3-phosphoethanolamine (DSPE-PEG); egg-phosphatidylcholine (EPC); stearylamine (SA); glial-derived neutotrophic factor (GDNF); dihexadecylmethylhydroxyethylammonium bromide (DHAHAB); hydrogenated soy phosphatidylcholine (HSPC); basic fibroblast growh factor (bFGF); pyridine-2-aldoxime methochloride (2-PAM).