Novel customized age-dependent corneal membranes and interactions with biodegradable nanoparticles loaded with dexibuprofen

Ocular inflammation is one of the most prevalent diseases in ophthalmology and it is currently treated using eye drops of nonsteroidal antiinflammatory drugs such as dexibuprofen (DXI). However, their bioavailability is low and therefore, PLGA nanoparticles constitute a suitable approach to be admin...

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Veröffentlicht in:Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2023-08, Vol.228, p.113394-113394, Article 113394
Hauptverfasser: Esteruelas, Gerard, Ortiz, Alba, Prat, Josefina, Vega, Estefania, Muñoz-Juncosa, Montserrat, López, Maria Luisa Garcia, Ettcheto, Miren, Camins, Antoni, Sánchez-López, Elena, Pujol, Montserrat
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container_title Colloids and surfaces, B, Biointerfaces
container_volume 228
creator Esteruelas, Gerard
Ortiz, Alba
Prat, Josefina
Vega, Estefania
Muñoz-Juncosa, Montserrat
López, Maria Luisa Garcia
Ettcheto, Miren
Camins, Antoni
Sánchez-López, Elena
Pujol, Montserrat
description Ocular inflammation is one of the most prevalent diseases in ophthalmology and it is currently treated using eye drops of nonsteroidal antiinflammatory drugs such as dexibuprofen (DXI). However, their bioavailability is low and therefore, PLGA nanoparticles constitute a suitable approach to be administered as eyedrops. Therefore, DXI has been encapsulated into PLGA nanoparticles (DXI-NPs). Although the eye, and specifically the cornea, suffers from age-related changes in its composition, current medications are not focused on these variations. Therefore, to elucidate the interaction mechanism of DXI-NPs with the cornea in relation with age, two different corneal membrane models have been developed (corresponding to adult and elder population) using lipid monolayers, large and giant unilamellar vesicles. Interactions of both DXI and DXI-NPs were studied with these models by means of Langmuir balance technique, dipole potential, anisotropy and confocal microscopy. In addition, fluorescently labelled nanoparticles were administered to mice in order to corroborate these data obtained in vitro. It was observed that DXI-NPs interact with lipid membranes through an adhesion process, mainly in the rigid regions and afterwards DXI-NPs are internalized by a wrapping process. Furthermore, differences on the dipole potential caused by DXI-NPs in each corneal membrane have been obtained due to the increase of membrane rigidity on the ECMM. Additionally, it can be confirmed that DXI-NPs adhere to Lo phase and also inside the lipid membrane. Finally, in vitro and in vivo results corroborate that DXI-NPs are adhered to the more ordered phase. Finally, differences between interactions of DXI-NPs with the elder and adult corneal tissue were observed. [Display omitted] ●Two customized corneal lipid membrane have been developed and characterized.●DXI NPs interact with lipid-based membranes through an adhesion process.●DXI NPs interact in the rigid areas and are internalized by a wrapping process.●DXI NPs are more retained in adult than elder membranes in vitro and in vivo.
doi_str_mv 10.1016/j.colsurfb.2023.113394
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However, their bioavailability is low and therefore, PLGA nanoparticles constitute a suitable approach to be administered as eyedrops. Therefore, DXI has been encapsulated into PLGA nanoparticles (DXI-NPs). Although the eye, and specifically the cornea, suffers from age-related changes in its composition, current medications are not focused on these variations. Therefore, to elucidate the interaction mechanism of DXI-NPs with the cornea in relation with age, two different corneal membrane models have been developed (corresponding to adult and elder population) using lipid monolayers, large and giant unilamellar vesicles. Interactions of both DXI and DXI-NPs were studied with these models by means of Langmuir balance technique, dipole potential, anisotropy and confocal microscopy. In addition, fluorescently labelled nanoparticles were administered to mice in order to corroborate these data obtained in vitro. It was observed that DXI-NPs interact with lipid membranes through an adhesion process, mainly in the rigid regions and afterwards DXI-NPs are internalized by a wrapping process. Furthermore, differences on the dipole potential caused by DXI-NPs in each corneal membrane have been obtained due to the increase of membrane rigidity on the ECMM. Additionally, it can be confirmed that DXI-NPs adhere to Lo phase and also inside the lipid membrane. Finally, in vitro and in vivo results corroborate that DXI-NPs are adhered to the more ordered phase. Finally, differences between interactions of DXI-NPs with the elder and adult corneal tissue were observed. [Display omitted] ●Two customized corneal lipid membrane have been developed and characterized.●DXI NPs interact with lipid-based membranes through an adhesion process.●DXI NPs interact in the rigid areas and are internalized by a wrapping process.●DXI NPs are more retained in adult than elder membranes in vitro and in vivo.</description><identifier>ISSN: 0927-7765</identifier><identifier>EISSN: 1873-4367</identifier><identifier>DOI: 10.1016/j.colsurfb.2023.113394</identifier><identifier>PMID: 37301018</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>adhesion ; adults ; Animals ; anisotropy ; bioavailability ; biodegradability ; Biodegradable nanoparticles ; confocal microscopy ; Cornea ; Corneal membrane models ; Dexibuprofen ; Ibuprofen - pharmacology ; inflammation ; Langmuir monolayers ; Lipids ; Liposomes ; Mice ; Nanoparticles ; ophthalmology</subject><ispartof>Colloids and surfaces, B, Biointerfaces, 2023-08, Vol.228, p.113394-113394, Article 113394</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2023 The Authors. 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However, their bioavailability is low and therefore, PLGA nanoparticles constitute a suitable approach to be administered as eyedrops. Therefore, DXI has been encapsulated into PLGA nanoparticles (DXI-NPs). Although the eye, and specifically the cornea, suffers from age-related changes in its composition, current medications are not focused on these variations. Therefore, to elucidate the interaction mechanism of DXI-NPs with the cornea in relation with age, two different corneal membrane models have been developed (corresponding to adult and elder population) using lipid monolayers, large and giant unilamellar vesicles. Interactions of both DXI and DXI-NPs were studied with these models by means of Langmuir balance technique, dipole potential, anisotropy and confocal microscopy. In addition, fluorescently labelled nanoparticles were administered to mice in order to corroborate these data obtained in vitro. It was observed that DXI-NPs interact with lipid membranes through an adhesion process, mainly in the rigid regions and afterwards DXI-NPs are internalized by a wrapping process. Furthermore, differences on the dipole potential caused by DXI-NPs in each corneal membrane have been obtained due to the increase of membrane rigidity on the ECMM. Additionally, it can be confirmed that DXI-NPs adhere to Lo phase and also inside the lipid membrane. Finally, in vitro and in vivo results corroborate that DXI-NPs are adhered to the more ordered phase. Finally, differences between interactions of DXI-NPs with the elder and adult corneal tissue were observed. [Display omitted] ●Two customized corneal lipid membrane have been developed and characterized.●DXI NPs interact with lipid-based membranes through an adhesion process.●DXI NPs interact in the rigid areas and are internalized by a wrapping process.●DXI NPs are more retained in adult than elder membranes in vitro and in vivo.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>37301018</pmid><doi>10.1016/j.colsurfb.2023.113394</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-4301-7297</orcidid><orcidid>https://orcid.org/0000-0003-1889-8763</orcidid><orcidid>https://orcid.org/0000-0001-9675-1789</orcidid><orcidid>https://orcid.org/0000-0002-1229-5956</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects adhesion
adults
Animals
anisotropy
bioavailability
biodegradability
Biodegradable nanoparticles
confocal microscopy
Cornea
Corneal membrane models
Dexibuprofen
Ibuprofen - pharmacology
inflammation
Langmuir monolayers
Lipids
Liposomes
Mice
Nanoparticles
ophthalmology
title Novel customized age-dependent corneal membranes and interactions with biodegradable nanoparticles loaded with dexibuprofen
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