@article {202371,
	title = {Galactosylated Chitosan Coated Liposomes of Ledipasvir for Liver Targeting: Chemical Synthesis, Statistical Optimization, In-vitro and In-vivo evaluation},
	volume = {110},
	year = {2021},
	note = {n/a},
	month = {2021},
	pages = {1148 - 1159},
	abstract = {<p>Ledipasvir is a novel antiviral agent used in the treatment of hepatitis C. We aim in our study to increase its delivery to hepatocytes and prolong its retention within liver. Several formulae of ledipasvir loaded liposomes were prepared and the best formula regarding particle size, zeta potential, polydispersity index and entrapment efficiency was selected. On the other hand, galactosylated chitosan was synthesized in a chemical reaction. Then the best liposomes formula was coated with the galactosylated chitosan. Having galactose residues on their surface, the coated liposomes can bind to the asialoglycoprotein receptors on the targeted hepatocytes enhancing ledipasvir uptake into them. The galactosylated chitosan coated liposomes had particle size of 218.2~nm~{\textpm}~7.21, zeta potential of 27.15~mV~{\textpm}~1.76, polydispersity index of 0.278~{\textpm}~0.055 and entrapment efficiency \% of 54.63\%~{\textpm}~0.05 respectively. The pharmacokinetic study revealed a significant increase in the liver peak concentration (Cmax) and the area under liver concentration versus time curve AUC(0{\textendash}72~h) and significant prolongation in the liver terminal half life (t{\textonehalf}) and mean residence time (MRT) in comparison to the oral dispersion of ledipasvir with values of 11,400~ng/g, 88,855~ng*h/g, 32.00~h and 18.11~h respectively.</p>
},
	keywords = {liposomes, pharmacokinetics, Targeted drug delivery},
	isbn = {0022-3549},
	url = {https://www.sciencedirect.com/science/article/pii/S0022354920305864},
	author = {Fatouh, Ahmed M. and Ahmed H. Elshafeey and Ahmed Abd Elbary}
}
