Abstract |
Methazolamide ( MTA) is an antiglaucoma drug; however, there are many side effects of its systemic administration with insufficient ocular therapeutic concentrations. The aim of this study was to formulate MTA-loaded solid lipid nanoparticles (SLNs) and evaluate the potential of SLNs as a new therapeutic system for glaucoma. SLNs were prepared by a modified emulsion- solvent evaporation method and their physicochemical characteristics were evaluated. The pharmacodynamics was investigated by determining the percentage decrease in intraocular pressure. The ocular irritation was studied by Draize test. Despite a burst release of SLNs, the pharmacodynamic experiment indicated that MTA-SLNs had higher therapeutic efficacy, later occurrence of maximum action, and more prolonged effect than drug solution and commercial product. Formulation of MTA-SLNs would be a potential delivery carrier for ocular delivery, with the advantages of a more intensive treatment for glaucoma, lower in doses and better patient compliance compared to the conventional eye drops.
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Authors | Rui Li, Sunmin Jiang, Dongfei Liu, Xinyun Bi, Fengzhen Wang, Qing Zhang, Qunwei Xu |
Journal | Journal of microencapsulation
(J Microencapsul)
Vol. 28
Issue 2
Pg. 134-41
( 2011)
ISSN: 1464-5246 [Electronic] England |
PMID | 21142697
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Carbonic Anhydrase Inhibitors
- Lipids
- Methazolamide
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Topics |
- Animals
- Carbonic Anhydrase Inhibitors
(chemistry, pharmacokinetics, pharmacology)
- Drug Delivery Systems
- Female
- Glaucoma
(drug therapy)
- Humans
- Lipids
(chemistry, pharmacokinetics, pharmacology)
- Male
- Methazolamide
(chemistry, pharmacokinetics, pharmacology)
- Nanoparticles
(chemistry)
- Rabbits
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