Enhanced parmacokinetic profile of hydrophobic substances
OwnerThomas C Pinkertoninventor
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Abstract
A method for systemic administration of a hydrophobic substance to a mammal is disclosed. The method involves delivering the hydrophobic substance to the dermis of the mammal whereby improved systemic absorption is obtained compared to absorption produced upon delivering the substance subcutaneously by bolus administration.
Claims135
A method for systemic administration of a hydrophobic substance to a mammal, the method comprising delivering the substance to the dermis of the mammal, wherein improved systemic absorption is produced as compared to absorption produced upon delivering the substance subcutaneously by bolus injection.
A method for administration of a hydrophobic substance to a mammal, the method comprising selectively delivering the substance to the dermis of the mammal to obtain systemic absorption of the substance from the dermis.
37 The method of claim 36, wherein the improved pharmacokinetic parameter comprises increased bioavailability of the substance.
A method for administration of a hydrophobic substance to a mammal, the method comprising selectively delivering the substance to the dermis of the mammal wherein systemic absorption of the substance from the dermis is obtained.
71 The method of claim 70 wherein the at least one hollow needle comprises an array of microneedles.
The method of claim 71 wherein the substance is delivered by infusion pump, piezoelectric pump, electromotive pump, electromagnetic pump, Belleville spring, iontophoresis, or sonophoresis.
A method for administration of a hydrophobic substance to a mammal, the method comprising selectively delivering the substance to the dermis of the mammal to achieve a substantially higher bioavailability and/or a substantially higher Cmax and/or a substantially shorter Tmax and/or a substantially shorter Tmax, and/or a substantially greater Ka as compared to that produced upon bolus subcutaneous administration of the substance at an identical dose.
A method for administration of a hydrophobic substance to a mammal, the method comprising selectively delivering the substance to the dermis of the mammal wherein a substantially higher bioavailability and/or a substantially higher Cmax and/or a substantially shorter Tmax and/or a substantially shorter Tlag, and/or a substantially greater Ka is produced as compared to that produced upon bolus subcutaneous administration of the substance at an identical dose.
Dependencies are inferred from the claim text.