Clinical signs, in vivo confocal

microscopy, and conjunctival impression cytology were performed to assess the safety profile of the different cationic emulsions with BAK or CKC as the cationic agent. This study demonstrated that cationic emulsions using BAK or CKC as the cationic agent were very well tolerated while the tested 0.02% BAK solution was responsible for corneal epithelial cell death related to the proinflammatory and proapoptotic activity of BAK. 4.1.2. Safety of Novasorb Loaded with Active Ingredients The safety profile of the Novasorb used as a vehicle for lipophilic drugs such as cyclosporine (Vekacia/Cyclokat) and latanoprost (Catioprost) was ALK inhibitor evaluated in Inhibitors,research,lifescience,medical animal models [56]. These studies demonstrated that neither Inhibitors,research,lifescience,medical of the two active ingredients (CsA or latanoprost) has an impact on the safety profile of the cationic emulsions as both drug-loaded cationic emulsions were as well tolerated as the cationic emulsion vehicle (Figure 3). For example, in the acute toxicity rabbit model, repeated instillations of Cyclokat/Vekacia Inhibitors,research,lifescience,medical (CsA-containing

0.05 and 0.1% CsA cationic emulsions) were as well tolerated as Restasis (0.05% CsA anionic emulsion), and Catioprost (preservative-free latanoprost 0.005% cationic emulsion) was better tolerated than the 0.02% BAK-preserved Xalatan. Local tolerance studies in the rabbit confirmed that chronic instillations (4–6 times daily over 28 days) with Cyclokat/Vekacia and twice daily for Catioprost were well tolerated by the rabbit eyes. Figure 3 In vivo confocal microscopy score of rabbit ocular surface following repeated instillations with Novasorb cationic emulsion of latanoprost. IVCM images of rabbit ocular surface and conjunctiva associated lymphoid Inhibitors,research,lifescience,medical tissue (CALT) were used to assess the … All the previous in vivo Inhibitors,research,lifescience,medical data were obtained in rabbits with a healthy ocular surface. However, it was of interest to

also assess the effect of Catioprost on damaged corneas to more closely mimic the clinical situation experienced when elderly patients are started on glaucoma therapy. For that purpose, a rat model of debrided cornea was used to assess the effect of Catioprost, its emulsion vehicle, and Xalatan (the commercially available product of latanoprost) on the ocular surface healing process. The in Phosphatidylinositol diacylglycerol-lyase vivo data demonstrated that Xalatan delayed corneal healing, while both Catioprost and its cationic emulsion vehicle (without latanoprost) promoted healing of the ocular surface and restored the function of the injured epithelium, thus confirming the better safety profile of the Novasorb cationic emulsions and confirming that Novasorb could hasten the repair of ocular surface damage. Novasorb was hence shown to be safe, but prior to human testing several other studies were necessary to fulfill the various European and American guidelines.