Cyclosporine A (CsA) loaded solid lipid nanoparticles (SLNs) for topical ophthalmic applications were prepared by high shear homogenization and ultrasound method using Compritol 888 ATO, Poloxamer 188 and Tween 80, to investigate the cellular uptake of rabbit corneal epithelial cells (RCE) and to evaluate the cytotoxicity. The size of the optimized formulation was 225.9±5.5nm with a polydispersity index of 0.253±0.05. The zeta potential and entrapment efficiency was detected as −16.9±0.7mV and 95.6%, respectively. The CsA release was found to be enzyme (lipase/co-lipase complex) dependent. SLNs were sterilized at 110 and 121 ◦C. The cytotoxicity was evaluated in vitro by means of RCE cells and was higher at 121 ◦C sterilization temperature, probably due to a supposed leakage of Tween 80 following lipid recrystallization. The permeation and penetration of CsA across/into the corneal cells were evaluated using in vitro and ex vivo experiments. The cellularuptakewas investigated by replacing CsA with the fluorescent dye Rhodamine B. The penetration enhancement properties were supported by confocal laser scanning microscopy analysis. The internalization of SLNs in cornea and in RCE cell lines was confirmed, pointing out the possibility of CsA targeting to the cornea.
Cyclosporine A loaded SLNs: Evaluation of cellular uptake and corneal cytotoxicity
SANDRI, GIUSEPPINA;BONFERONI, MARIA CRISTINA;ROSSI, SILVIA STEFANIA;FERRARI, FRANCA;CARAMELLA, CARLA MARCELLA
2008-01-01
Abstract
Cyclosporine A (CsA) loaded solid lipid nanoparticles (SLNs) for topical ophthalmic applications were prepared by high shear homogenization and ultrasound method using Compritol 888 ATO, Poloxamer 188 and Tween 80, to investigate the cellular uptake of rabbit corneal epithelial cells (RCE) and to evaluate the cytotoxicity. The size of the optimized formulation was 225.9±5.5nm with a polydispersity index of 0.253±0.05. The zeta potential and entrapment efficiency was detected as −16.9±0.7mV and 95.6%, respectively. The CsA release was found to be enzyme (lipase/co-lipase complex) dependent. SLNs were sterilized at 110 and 121 ◦C. The cytotoxicity was evaluated in vitro by means of RCE cells and was higher at 121 ◦C sterilization temperature, probably due to a supposed leakage of Tween 80 following lipid recrystallization. The permeation and penetration of CsA across/into the corneal cells were evaluated using in vitro and ex vivo experiments. The cellularuptakewas investigated by replacing CsA with the fluorescent dye Rhodamine B. The penetration enhancement properties were supported by confocal laser scanning microscopy analysis. The internalization of SLNs in cornea and in RCE cell lines was confirmed, pointing out the possibility of CsA targeting to the cornea.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
