2007
DOI: 10.1016/s0181-5512(07)79290-2
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Dispositifs de délivrance de principes actifs pour des applications ophtalmologiques

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Cited by 7 publications
(2 citation statements)
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“…After local injection administration, sustained-release preparations can directly release drug at the therapeutic position and slowly enter into the bloodstream, thereby extending treatment time, enhancing treatment effects, and reducing systemic toxicity. Thus, this technology has the potential to reduce administration time, increase patient medication adherence and reduce therapeutic expenses 28,29. Several injectable sustained-release preparations have been developed, including for analgesic and endomyocardial applications, the steroid amcinonide, polypeptides, vaccines and gene-targeting drugs 30,31…”
Section: Discussionmentioning
confidence: 99%
“…After local injection administration, sustained-release preparations can directly release drug at the therapeutic position and slowly enter into the bloodstream, thereby extending treatment time, enhancing treatment effects, and reducing systemic toxicity. Thus, this technology has the potential to reduce administration time, increase patient medication adherence and reduce therapeutic expenses 28,29. Several injectable sustained-release preparations have been developed, including for analgesic and endomyocardial applications, the steroid amcinonide, polypeptides, vaccines and gene-targeting drugs 30,31…”
Section: Discussionmentioning
confidence: 99%
“…In addition, the liposomal membrane is flexible and supports deformation stress. The property makes them suitable for administering intraocular injections for treating posterior segment ocular diseases [45]. Positively charged liposomes disintegrate completely upon contact with negatively charged mucin membrane [46].…”
Section: Ophthalmic Nanoformulationsmentioning
confidence: 99%