TY - JOUR
T1 - Chitosan-based nanoparticles for rosmarinic acid ocular delivery-In vitro tests
AU - Silva, Sara Baptista da
AU - Ferreira, Domingos
AU - Pintado, Manuela
AU - Sarmento, Bruno
N1 - Funding Information:
This work was also financed by European Regional Development Fund (ERDF) through the Programa Operacional Factores de Competitividade—COMPETE, by Portuguese funds through FCT—Fundação para a Ciência e a Tecnologia in the framework of the project PEst-OE/EQB/LA0016/2013, and co-financed by North Portugal Regional Operational Programme (ON.2–O Novo Norte) in the framework of project SAESCTN-PIIC&DT/2011, under the National Strategic Reference Framework (NSRF).
Funding Information:
Funding for author Sara B. Silva was via a PhD fellowship, administered by Fundação para a Ciência e a Tecnologia ( SFRH/BD/61423/2009 ). This work was supported by National Funds from FCT—Fundação para a Ciência e a Tecnologia through project PEst-OE/EQB/LA0016/2013.
Publisher Copyright:
© 2015 Elsevier B.V.
PY - 2016/3/1
Y1 - 2016/3/1
N2 - In this study, chitosan nanoparticles were used to encapsulate antioxidant rosmarinic acid, Salvia officinalis (sage) and Satureja montana (savory) extracts as rosmarinic acid natural vehicles. The nanoparticles were prepared by ionic gelation using chitosan and sodium tripolyphosphate (TPP) in a mass ratio of 7:1, at pH 5.8. Particle size distribution analysis and transmission electron microscopy (TEM) confirmed the size ranging from 200 to 300nm, while surface charge of nanoparticles ranged from 20 to 30mV. Nanoparticles demonstrate to be safe without relevant cytotoxicity against retina pigment epithelium (ARPE-19) and human cornea cell line (HCE-T). The permeability study in HCE monolayer cell line showed an apparent permeability coefficient Papp of 3.41±0.99×10-5 and 3.24±0.79×10-5cm/s for rosmarinic acid loaded chitosan nanoparticles and free in solution, respectively. In ARPE-19 monolayer cell line the Papp was 3.39±0.18×10-5 and 3.60±0.05×10-5cm/s for rosmarinic acid loaded chitosan nanoparticles and free in solution, respectively. Considering the mucin interaction method, nanoparticles indicate mucoadhesive proprieties suggesting an increased retention time over the ocular mucosa after instillation. These nanoparticles may be promising drug delivery systems for ocular application in oxidative eye conditions.
AB - In this study, chitosan nanoparticles were used to encapsulate antioxidant rosmarinic acid, Salvia officinalis (sage) and Satureja montana (savory) extracts as rosmarinic acid natural vehicles. The nanoparticles were prepared by ionic gelation using chitosan and sodium tripolyphosphate (TPP) in a mass ratio of 7:1, at pH 5.8. Particle size distribution analysis and transmission electron microscopy (TEM) confirmed the size ranging from 200 to 300nm, while surface charge of nanoparticles ranged from 20 to 30mV. Nanoparticles demonstrate to be safe without relevant cytotoxicity against retina pigment epithelium (ARPE-19) and human cornea cell line (HCE-T). The permeability study in HCE monolayer cell line showed an apparent permeability coefficient Papp of 3.41±0.99×10-5 and 3.24±0.79×10-5cm/s for rosmarinic acid loaded chitosan nanoparticles and free in solution, respectively. In ARPE-19 monolayer cell line the Papp was 3.39±0.18×10-5 and 3.60±0.05×10-5cm/s for rosmarinic acid loaded chitosan nanoparticles and free in solution, respectively. Considering the mucin interaction method, nanoparticles indicate mucoadhesive proprieties suggesting an increased retention time over the ocular mucosa after instillation. These nanoparticles may be promising drug delivery systems for ocular application in oxidative eye conditions.
KW - Cell models
KW - Chitosan
KW - Nanoparticles
KW - Rosmarinic acid
UR - http://www.scopus.com/inward/record.url?scp=84950272691&partnerID=8YFLogxK
U2 - 10.1016/j.ijbiomac.2015.11.070
DO - 10.1016/j.ijbiomac.2015.11.070
M3 - Article
C2 - 26645149
AN - SCOPUS:84950272691
SN - 0141-8130
VL - 84
SP - 112
EP - 120
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
ER -