Due to its small size, it can be injected into the vitreous directly using a 25-gauge transconjunctival injector system, eliminating the need for an invasive procedure [59, 60]. With glaucoma currently classified as a neurodegenerative

disorder, Neurotech’s (NT-501) a nonbiodegradable implant has recently gained consideration for the delivery of protein therapeutics for up to a year to preserve vision cells. The implant encapsulates genetically engineered human retinal pigment epithelium (RPE) cells that secrete CNTF. The device is administered in the vitreous through a small incision in the sclera Inhibitors,research,lifescience,medical and secured at the implantation site by suturing through the titanium loop [61]. The semipermeable membrane allows the entry of Smad inhibitor nutrients and oxygen to the cells encapsulated within the implant. Similarly, the permeability of the membrane also allows the CNTF secreted by the human RPE cells to diffuse Inhibitors,research,lifescience,medical to the target site. Since the cells are sealed within the device, it prevents any possible foreign body reactions. Neurotech’s device was initially designed for potential treatment of retinitis pigmentosa (RP) and age-related macular degeneration (AMD). A phase 1 clinical trial in ten participants with RP demonstrated that this device was safe and well tolerated during the 6

months implantation period [62]. Inhibitors,research,lifescience,medical Also a phase 2 clinical study in 51 patients with advanced AMD slowed visual loss in 96.3% of treated patients at 12 months compared to the 75% of patients in control group [61, 63]. Following the successful use of this implant in other ocular neurodegenerative conditions, NT-501 could be the first device in delivering Inhibitors,research,lifescience,medical neurotrophic factor in human glaucomatous conditions [42]. 2.2.3. Injectable Formulations Particulate drug delivery systems or Inhibitors,research,lifescience,medical injectable formulations such as microspheres, liposomes, and nanospheres/nanoparticles are other attractive alternatives used for extended drug release. The

delivery platform involves entrapment of the drug within the nanocarrier matrix for subsequent intraocular delivery [64, 65]. Upon administration to the target site of the eye, the bioactive Digestive enzyme agent is released in a controlled manner by diffusion through the matrix or degradation of the polymer matrix. Also, the nanomicrocarriers once injected could act as a reservoir system for drug release for prolonged time period [66, 67]. Bertram et al. evaluated the release of timolol maleate from biodegradable microspheres composed of PLGA and PLA in vitro. Upon administration by subconjunctival injection, it was reported that drug release was sustained for more than 3 months, a time scale that could overcome the fundamental problem with patient adherence to treatment [34]. Since subconjunctival injection is less invasive than intravitreal injection, this study also demonstrated a potential route for prolonged drug delivery through penetration across the sclera.