Pegylated compounds for age-related macular degeneration
View Patent ↗A special photosensitizer formulation and Photodynamic Therapy method for treating choroidal neovascularization (CNV) associated with age-related macular degeneration (AMD) is provided. CNV is a major cause for vision loss in elderly patients. A special drug delivery formulation is used to encapsulate the hydrophobic photosensitizer, preferably a pegylated liposome. This improves the solubility and therapeutic index of the photosensitizers. In one preferred embodiment, a pegylated photoactive agent remains confined in the intravascular compartment of neovasculature for a longer duration. Thus efficient elimination of neovascular proliferation and minimal damage to extravascular tissue and normal vessels is ensured. In this method, a hydrophobic photosensitizer, that is able to photochemically destroy neovessels, is injected into the patient. CNV irradiation with a non-thermal laser follows after a predefined time interval. The excited photosensitizer photocoagulates newly formed blood vessels thereby improving the vision and preventing further loss of vision.
1. A chemical formulation for the delivery of a hydrophobic drug to a choroidal neovascular region, comprising:
a carrier for solubilizing a hydrophobic drug; and
a therapeutically effective amount of hydrophobic photosensitize; wherein said carrier is a liposomal bilayer comprising synthetic phospholipids that are a mixture of dipalmitoyl phosphatidyl choline (DPPC), dipalmitoyl phosphatidyl glycerol (DPPG), and pegylated distearoyl phosphatidyl ethanol amine (PEG-DSPE) present in a weight ratio of DPPC:DPPG:PEG-DSPE of 9:1:1 and said drug is present in said liposomal bilayer; and wherein said hydrophobic photosensitizer is temoporfin.
2. A method for effecting closure of choroidal neovasculature related to age related macular degeneration (AMD) in patients using photodynamic therapy (PDT) comprising the steps of:
administering a therapeutically effective amount of pegylated liposome comprising synthetic phospholipids that are a mixture of dipalmitoyl phosphatidyl choline (DPPC), dipalmitoyl phosphatidyl glycerol (DPPG), and pegylated distearoyl phosphatidyl ethanol amine (PEG-DSPE) present in a weight ratio of DPPC:DPPG:PEG-DSPE of 9:1:1 and, which has a predetermined amount of a hydrophobic photosensitizer in its bilayer;
allowing sufficient time to release and localize said photosensitizer in chorodial neovasculature; and
irradiating the photosensitizer with non-thermal laser radiation, so as to occlude the choroidal neovasculature; and wherein said photosensitizer is temoporfin administered at a drug dosage ranging between about 0.25 to 1.0 mg/kg body weight.
3. The method according to claim 2 , wherein said photosensitizer is administered intravenously.
4. The method according to claim 2 , wherein said photosensitizer remains confined within the choroidal neovasculature for at least 700 sec.
5. The method according to claim 2 , wherein said non-thermal laser irradiation is applied at a power density between about 12.5 J/cm 2 to 100 J/cm 2 .