dc.contributor.author |
Ninawe, PR |
en |
dc.contributor.author |
Hatziavramidis, D |
en |
dc.contributor.author |
Parulekar, SJ |
en |
dc.date.accessioned |
2014-03-01T01:33:07Z |
|
dc.date.available |
2014-03-01T01:33:07Z |
|
dc.date.issued |
2010 |
en |
dc.identifier.issn |
0009-2509 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/20326 |
|
dc.subject |
Anti-VEGF agent |
en |
dc.subject |
Drug macromolecule |
en |
dc.subject |
Ocular drug delivery |
en |
dc.subject |
Sclera permeability |
en |
dc.subject |
Sustained delivery |
en |
dc.subject |
Thermally responsive gel |
en |
dc.subject.classification |
Engineering, Chemical |
en |
dc.subject.other |
Anti-VEGF agent |
en |
dc.subject.other |
Ocular drug delivery |
en |
dc.subject.other |
Sclera permeability |
en |
dc.subject.other |
Sustained delivery |
en |
dc.subject.other |
Thermally responsive |
en |
dc.subject.other |
Acrylic monomers |
en |
dc.subject.other |
Amides |
en |
dc.subject.other |
Drug delivery |
en |
dc.subject.other |
Macromolecules |
en |
dc.subject.other |
Phase transitions |
en |
dc.subject.other |
Gels |
en |
dc.title |
Delivery of drug macromolecules from thermally responsive gel implants to the posterior eye |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1016/j.ces.2010.06.014 |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1016/j.ces.2010.06.014 |
en |
heal.language |
English |
en |
heal.publicationDate |
2010 |
en |
heal.abstract |
Therapeutic modalities for posterior-eye diseases involve mostly interventions through the anterior eye, which are difficult for physicians and patients alike. Currently, sustained drug delivery to the posterior eye is gaining importance. A study for sustained delivery of an anti-VEGF agent to the posterior eye from an implant, made of poly(N-isopropylacrylamide) (NIPAM) and placed episclerally, is presented. The thermally sensitive gel is modelled as a poroelastic material with a phase transition characterized by a lower critical solution temperature (LCST). The study utilizes compartments for various eye tissues, with individual compartments considered to be completely mixed and drug transport between compartments occurring by one-dimensional diffusion. (C) 2010 Elsevier Ltd. All rights reserved. |
en |
heal.publisher |
PERGAMON-ELSEVIER SCIENCE LTD |
en |
heal.journalName |
Chemical Engineering Science |
en |
dc.identifier.doi |
10.1016/j.ces.2010.06.014 |
en |
dc.identifier.isi |
ISI:000280660400010 |
en |
dc.identifier.volume |
65 |
en |
dc.identifier.issue |
18 |
en |
dc.identifier.spage |
5170 |
en |
dc.identifier.epage |
5177 |
en |