1. Development of in situ thermosensitive drug vehicles for glaucoma therapy
- Author
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Ging-Ho Hsiue, Ru-Wen Chang, Shih-Huang Lee, and Chau-Hui Wang
- Subjects
Drug ,Intraocular pressure ,Hot Temperature ,Materials science ,Epinephrine ,media_common.quotation_subject ,Acrylic Resins ,Biophysics ,Glaucoma ,Bioengineering ,Methacrylate ,2-Hydroxyethyl Methacrylate ,Cornea ,Diffusion ,Biomaterials ,In vivo ,medicine ,Animals ,Cells, Cultured ,Intraocular Pressure ,Polyhydroxyethyl Methacrylate ,media_common ,medicine.disease ,Controlled release ,Microspheres ,eye diseases ,medicine.anatomical_structure ,Mechanics of Materials ,Delayed-Action Preparations ,Ceramics and Composites ,Female ,Rabbits ,Ophthalmic Solutions ,Pharmaceutical Vehicles ,Biomedical engineering - Abstract
The goal of this research was to design thermosensitive drug vehicles for glaucoma therapy. Thermosensitive ophthalmic drop was prepared by mixing linear poly(N-isopropylacrylamide-g-2-hydroxyethyl methacrylate) (PNIPAAm-g-PHEMA), PNIPAAm-g-PHEMA gel particles and antiglaucoma drug. This produced polymeric eyedrop containing the drug epinephrine was a clear solution at room temperature which became a soft film after contacting the surface of cornea. The drug entrapped within the tangled polymer chains was therefore released progressively after topical application. Evaluation of the drug release responded as a function of crosslinking density and PHEMA macromer contents. The in vivo studies indicated that the intraocular pressure (IOP)-lowering effect for a polymeric eyedrop lasted for 26 h, which is significantly better than the effect of traditional eyedrop (8 h). Hence our investigations successfully prove that the thermosensitive polymeric eyedrop with ability of controlled drug release exhibits a greater potential for glaucoma therapy.
- Published
- 2003