期刊
COLLOIDS AND SURFACES B-BIOINTERFACES
卷 136, 期 -, 页码 935-943出版社
ELSEVIER
DOI: 10.1016/j.colsurfb.2015.10.026
关键词
Carprofen; PLGA; Nanoparticles; Factorial design; Freeze-drying; Eye surgery
资金
- Spanish Ministry of Science and Innovation [MAT2011-26994, MAT2014-59134R]
This work aimed the design and development of poly(lactic-co-glycolic) acid (PLGA) nanoparticles (NPs) for the ocular delivery of Carprofen (CP) by a central rotatable composite design 2(3)+ star. NPs showed adequate size for ocular administration (189.50 +/- 1.67 nm), low polydispersity (0.01 +/- 0.01), negative charge surface (-22.80 +/- 0.66 mV) and optimal entrapment efficiency (74.70 +/- 0.95%). Physicochemical analysis confirmed that CP was dispersed inside the NPs. The drug release followed a first order kinetic model providing greater sustained CP release after lyophilization. Ex vivo permeation analysis through isolated rabbit cornea revealed that a sufficient amount of CP was retained in the tissue avoiding excessive permeation and thus, potential systemic levels. Ex vivo ocular tolerance results showed no signs of ocular irritancy, which was also confirmed by in vivo Draize test. In vivo ocular anti-inflammatory efficacy test confirmed an optimal efficacy of NPs and its potential application in eye surgery. (C) 2015 Elsevier B.V. All rights reserved.
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