Abstract:
The present invention relates to a method of loading an ionizable drug having a group selected from (Formule I or Formule II) or pharmaceutically acceptable salts thereof into a liposome and the liposomal composition of drug produced therewith.
Abstract:
A method of treating patients suffering from carcinoma of intrahepatic or extra hepatic bile duct or gall bladder which is locally advanced or metastatic, by intravenously administering to the patient, paclitaxel in the form of a nanodispersion. The nanodispersion comprises particles with a mean particle size less than 300 nm and is free of polyoxyethylated castor oil and free of a protein.
Abstract:
The dry powder inhalation composition comprising: (1) salmeterol xinafoate having mean particle size in range of 2.0 μ - 6 μ microns and a tapped density in the range of 0.20 g.com -3 to 0.45 g.com -3 and (2) optionally, one or more other active ingredients and pharmaceutically acceptable carrier.
Abstract:
The present invention provides a stable ready-to-use solution comprising therapeutically effective amounts of glucagon together with pegylated distearoyl-phosphatidylethanolamine.
Abstract:
The present invention relates to a process for the preparation of unilamellar liposomal composition of a polyene antibiotic drug. The present invention further relates to liposomal composition of a polyene antibiotic drug that is stable.
Abstract:
The dry powder inhalation composition comprising (1) salmeterol xinafoate having mean particle size in range of 2.0μ-6μ microns and a tapped density in the range of 0.20 g·cm−3 to 0.45 g·cm−3 and (2) optionally, one or more other active ingredients and pharmaceutically acceptable carrier.