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• W2056795722 abstract "Systemic administration of cyclosporine A (CsA) is commonly used in the treatment of local ophthalmic conditions involving cytokines, such as corneal graft rejection, autoimmune uveitis and dry eye syndrome. Local administration is expected to avoid the various side effects associated with systemic delivery. However, the currently available systems using oils to deliver CsA topically are poorly tolerated and provide a low bioavailability. These difficulties may be overcome through formulations aimed at improving CsA water solubility (e.g. cyclodextrins), or those designed to facilitate tissue drug penetration using penetration enhancers. The use of colloidal carriers (micelles, emulsions, liposomes and nanoparticles) as well as the approach using hydrosoluble prodrugs of CsA have shown promising results. Solid devices such as shields and particles of collagen have been investigated to enhance retention time on the eye surface. Some of these topical formulations have shown efficacy in the treatment of extraocular diseases but were inefficient at reaching intraocular targets. Microspheres, implants and liposomes have been developed to be directly administered subconjunctivally or intravitreally in order to enhance CsA concentration in the vitreous. Although progress has been made, there is still room for improvement in CsA ocular application, as none of these formulations is ideal." @default.
• W2056795722 created "2016-06-24" @default.
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• W2056795722 date "2003-11-01" @default.
• W2056795722 modified "2023-10-18" @default.
• W2056795722 title "Cyclosporine A delivery to the eye: A pharmaceutical challenge" @default.
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• W2056795722 doi "https://doi.org/10.1016/s0939-6411(03)00138-3" @default.
• W2056795722 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/14602172" @default.
• W2056795722 hasPublicationYear "2003" @default.
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