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Dive into the research topics where Gary P. Cook is active.

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Featured researches published by Gary P. Cook.


Investigative Ophthalmology & Visual Science | 2008

Simultaneous but not prior inhibition of VEGF165 enhances the efficacy of photodynamic therapy in multiple models of ocular neovascularization

Meihua Ju; Carolina Mailhos; John S. Bradley; T. Dowie; Mary A. Ganley; Gary P. Cook; Perry Calias; Norbert Lange; Anthony P. Adamis; David T. Shima; Gregory S. Robinson

PURPOSE To investigate the effect of the combined treatment of photodynamic therapy and specific VEGF165 inhibition with pegaptanib sodium (Macugen; Eyetech Pharmaceuticals, Lexington, MA) on ocular neovascularization. METHODS Photodynamic therapys (PDTs) effects on the integrity of pegaptanib sodium were analyzed by HPLC, a VEGF165-binding assay, and a VEGF165-induced tissue factor gene expression assay. The effects of mono- or combined treatment on vessel growth and regression were determined in a murine corneal neovascularization model. The effects of combined treatment on vessel growth were also determined in a murine choroidal neovascularization model. RESULTS PDT did not affect the chemical composition of pegaptanib sodium nor the efficacy of pegaptanib sodium in the inhibition of VEGF165 binding to Flt-1 and VEGF165-induced gene expression. In an animal model of effects on existing ocular neovascular lesions (corneal neovascularization), PDT monotherapy yielded an initial regression of these vessels, but there followed a rapid regrowth. In contrast, pegaptanib sodium monotherapy yielded little regression but potently abrogated further vessel growth. The combination of pegaptanib sodium and PDT resulted in the regression of the neovascular lesions, as observed with PDT alone, but also prevented significant vessel regrowth, leading to a significantly greater reduction in lesion size than did each monotherapy. In addition, there was a significantly greater effect of the combination of pegaptanib sodium and PDT on lesion size in choroidal neovascularization than with each monotherapy. Pretreatment with pegaptanib sodium appeared to decrease the efficacy of PDT-induced vessel regression in corneal neovascularization, and as such the enhanced efficacy over monotherapy when the agents were delivered simultaneously was not observed. CONCLUSIONS Although the combined simultaneous treatment of ocular neovascularization with PDT and pegaptanib sodium may provide a more effective approach for the regression and overall treatment of CNV associated with AMD, the order of addition of these treatments may play a role in achieving optimal efficacy.


Archive | 2005

Enhanced biologically active conjugates

Pericles Calias; Gary P. Cook; David T. Shima; Anthony P. Adamis; Yin-Shan Ng; Gregory S. Robinson; David I. Turner; Mary A. Ganley


Archive | 2006

Controlled release microparticles

Kathleen M. Campbell; Pericles Calias; Gary P. Cook; Mary A. Ganley


Archive | 2006

Cyclitol linker polymer conjugate

David I. Turner; Perry Calias; Gary P. Cook; David T. Shima


Archive | 2005

Nucleic acid aptamers conjugated to high molecular weight steric groups

Pericles Calias; Gary P. Cook; David T. Shima; Anthony P. Adamis; Yin-Shan Ng; Gregory S. Robinson; David I. Turner; Mary A. Ganley


Archive | 2005

Facilitation of iontophoresis using charged moieties

Pericles Calias; Gary P. Cook; David T. Shima; David I. Turner; Mary A. Ganley


Archive | 2013

Delivery of corticosteroids through iontophoresis

Mike Jaffe; Gary P. Cook; Perry Calias; Michael A. Patane


Archive | 2009

Enhanced delivery of a therapeutic to ocular tissues through iontophoresis

Mike Jaffe; Gary P. Cook; Perry Calias; Mike Patane


Investigative Ophthalmology & Visual Science | 2006

Pegaptanib in Combination With Verteporfin–Based PDT Increases Regression of Murine Ocular Neovascularization

Meihua Ju; Carolina Mailhos; Mary A. Ganley; T. Dowie; Gary P. Cook; Perry Calias; A.P. Adams; Norbert Lange; Gregory S. Robinson; David T. Shima


Archive | 2009

Apport amélioré d'une substance thérapeutique à des tissus oculaires par iontophorèse

Mike Jaffe; Gary P. Cook; Perry Calias; Mike Patane

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David T. Shima

University College London

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Yin-Shan Ng

UCL Institute of Ophthalmology

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