Toward smart design of retinal drug carriers: a novel bovine retinal explant model to study the barrier role of the vitreoretinal interface

Retinal gene delivery via intravitreal injection is hampered by various physiological barriers present in the eye of which the vitreoretinal (VR) interface represents the most serious hurdle. In this study, we present a retinal explant model especially designed to study the role of this interface as...

Full description

Bibliographic Details
Main Authors: Karen Peynshaert, Joke Devoldere, Valérie Forster, Serge Picaud, Christian Vanhove, Stefaan C. De Smedt, Katrien Remaut
Format: Article
Language:English
Published: Taylor & Francis Group 2017-01-01
Series:Drug Delivery
Subjects:
Online Access:http://dx.doi.org/10.1080/10717544.2017.1375578
id doaj-f88c2ea9df46469e9518a08a7dfd7990
record_format Article
spelling doaj-f88c2ea9df46469e9518a08a7dfd79902020-11-25T02:53:11ZengTaylor & Francis GroupDrug Delivery1071-75441521-04642017-01-012411384139410.1080/10717544.2017.13755781375578Toward smart design of retinal drug carriers: a novel bovine retinal explant model to study the barrier role of the vitreoretinal interfaceKaren Peynshaert0Joke Devoldere1Valérie Forster2Serge Picaud3Christian Vanhove4Stefaan C. De Smedt5Katrien Remaut6Ghent UniversityGhent UniversityINSERM, Université Paris 6INSERM, Université Paris 6Ghent UniversityGhent UniversityGhent UniversityRetinal gene delivery via intravitreal injection is hampered by various physiological barriers present in the eye of which the vitreoretinal (VR) interface represents the most serious hurdle. In this study, we present a retinal explant model especially designed to study the role of this interface as a barrier for the penetration of vectors into the retina. In contrast to all existing explant models, the developed model is bovine-derived and more importantly, keeps the vitreous attached to the retina at all times to guarantee an intact VR interface. After ex vivo intravitreal injection into the living retinal explant, the route of fluorescent carriers across the VR interface can be tracked. By applying two different imaging methods on this model, we discovered that the transfer through the VR barrier is size-dependent since 40 nm polystyrene particles are more easily taken up in the retina than 100 and 200 nm sized particles. In addition, we found that removing the vitreous, as commonly done for culture of conventional explants, leads to an overestimation of particle uptake, and conclude that the ultimate barrier to overcome for retinal uptake is undoubtedly the inner limiting membrane. Damaging this matrix resulted in a massive increase in particle transfer into the retina. In conclusion, we have developed a highly relevant ex vivo model that maximally mimics the human in vivo physiology which can be applied as a representative test set-up to assess the potential of promising drug delivery carriers to cross the VR interface.http://dx.doi.org/10.1080/10717544.2017.1375578vitreoretinal interfaceretinal gene deliveryinner limiting membranevitreousretinal explantex vivolarge animalnanoparticle
collection DOAJ
language English
format Article
sources DOAJ
author Karen Peynshaert
Joke Devoldere
Valérie Forster
Serge Picaud
Christian Vanhove
Stefaan C. De Smedt
Katrien Remaut
spellingShingle Karen Peynshaert
Joke Devoldere
Valérie Forster
Serge Picaud
Christian Vanhove
Stefaan C. De Smedt
Katrien Remaut
Toward smart design of retinal drug carriers: a novel bovine retinal explant model to study the barrier role of the vitreoretinal interface
Drug Delivery
vitreoretinal interface
retinal gene delivery
inner limiting membrane
vitreous
retinal explant
ex vivo
large animal
nanoparticle
author_facet Karen Peynshaert
Joke Devoldere
Valérie Forster
Serge Picaud
Christian Vanhove
Stefaan C. De Smedt
Katrien Remaut
author_sort Karen Peynshaert
title Toward smart design of retinal drug carriers: a novel bovine retinal explant model to study the barrier role of the vitreoretinal interface
title_short Toward smart design of retinal drug carriers: a novel bovine retinal explant model to study the barrier role of the vitreoretinal interface
title_full Toward smart design of retinal drug carriers: a novel bovine retinal explant model to study the barrier role of the vitreoretinal interface
title_fullStr Toward smart design of retinal drug carriers: a novel bovine retinal explant model to study the barrier role of the vitreoretinal interface
title_full_unstemmed Toward smart design of retinal drug carriers: a novel bovine retinal explant model to study the barrier role of the vitreoretinal interface
title_sort toward smart design of retinal drug carriers: a novel bovine retinal explant model to study the barrier role of the vitreoretinal interface
publisher Taylor & Francis Group
series Drug Delivery
issn 1071-7544
1521-0464
publishDate 2017-01-01
description Retinal gene delivery via intravitreal injection is hampered by various physiological barriers present in the eye of which the vitreoretinal (VR) interface represents the most serious hurdle. In this study, we present a retinal explant model especially designed to study the role of this interface as a barrier for the penetration of vectors into the retina. In contrast to all existing explant models, the developed model is bovine-derived and more importantly, keeps the vitreous attached to the retina at all times to guarantee an intact VR interface. After ex vivo intravitreal injection into the living retinal explant, the route of fluorescent carriers across the VR interface can be tracked. By applying two different imaging methods on this model, we discovered that the transfer through the VR barrier is size-dependent since 40 nm polystyrene particles are more easily taken up in the retina than 100 and 200 nm sized particles. In addition, we found that removing the vitreous, as commonly done for culture of conventional explants, leads to an overestimation of particle uptake, and conclude that the ultimate barrier to overcome for retinal uptake is undoubtedly the inner limiting membrane. Damaging this matrix resulted in a massive increase in particle transfer into the retina. In conclusion, we have developed a highly relevant ex vivo model that maximally mimics the human in vivo physiology which can be applied as a representative test set-up to assess the potential of promising drug delivery carriers to cross the VR interface.
topic vitreoretinal interface
retinal gene delivery
inner limiting membrane
vitreous
retinal explant
ex vivo
large animal
nanoparticle
url http://dx.doi.org/10.1080/10717544.2017.1375578
work_keys_str_mv AT karenpeynshaert towardsmartdesignofretinaldrugcarriersanovelbovineretinalexplantmodeltostudythebarrierroleofthevitreoretinalinterface
AT jokedevoldere towardsmartdesignofretinaldrugcarriersanovelbovineretinalexplantmodeltostudythebarrierroleofthevitreoretinalinterface
AT valerieforster towardsmartdesignofretinaldrugcarriersanovelbovineretinalexplantmodeltostudythebarrierroleofthevitreoretinalinterface
AT sergepicaud towardsmartdesignofretinaldrugcarriersanovelbovineretinalexplantmodeltostudythebarrierroleofthevitreoretinalinterface
AT christianvanhove towardsmartdesignofretinaldrugcarriersanovelbovineretinalexplantmodeltostudythebarrierroleofthevitreoretinalinterface
AT stefaancdesmedt towardsmartdesignofretinaldrugcarriersanovelbovineretinalexplantmodeltostudythebarrierroleofthevitreoretinalinterface
AT katrienremaut towardsmartdesignofretinaldrugcarriersanovelbovineretinalexplantmodeltostudythebarrierroleofthevitreoretinalinterface
_version_ 1724726276602724352