Novel formulations of pharmacological agents, methods for the preparation thereof and methods for the use thereof
In accordance with the present invention, there are provided compositions and methods useful for the in vivo delivery of substantially water insoluble pharmacologically active agents (such as the anticancer drug paclitaxel) in which the pharmacologically active agent is delivered in the form of suspended particles coated with protein (which acts as a stabilizing agent). In particular, protein and pharmacologically active agent in a biocompatible dispersing medium are subjected to high shear, in the absence of any conventional surfactants, and also in the absence of any polymeric core material for the particles. The procedure yields particles with a diameter of less than about 1 micron. The use of specific composition and preparation conditions (e.g., addition of a polar solvent to the organic phase), and careful selection of the proper organic phase and phase fraction, enables the reproducible production of unusually small nanoparticles of less than 200 nm diameter, which can be sterile-filtered. The particulate system produced according to the invention can be converted into a redispersible dry powder comprising nanoparticles of water-insoluble drug coated with a protein, and free protein to which molecules of the pharmacological agent are bound. This results in a unique delivery system, in which part of the pharmacologically active agent is readily bioavailable (in the form of molecules bound to the protein), and part of the agent is present within particles without any polymeric matrix therein.
1 - 65 . (canceled)
66 . A composition comprising: (a) particles that are less than about 2 microns comprising a pharmacologically active agent, and (b) a stabilizing peptide or polypeptide.
67 . The composition according to claim 66 , wherein the particles have an average particle size of less than about 1 micron.
68 . The composition according to claim 67 , wherein the particles have an average particle size of less than about 200 nm.
69 . The composition according to claim 66 , wherein the particles are coated with the peptide or polypeptide.
70 . The composition according to claim 66 , wherein the peptide or polypeptide is water soluble.
71 . The composition according to claim 66 , wherein the peptide or polypeptide is a synthetic polypeptide.
72 . The composition according to claim 66 , wherein the synthetic polypeptide is a synthetic polyamino acid.
73 . The composition according to claim 66 , wherein the pharmacologically active agent is amorphous.
74 . The composition according to claim 66 , wherein the pharmacologically active agent is crystalline.
75 . The composition according to claim 66 , wherein the pharmacologically active agent is substantially water insoluble.
76 . The composition according to claim 75 , wherein the pharmacologically active agent is paclitaxel.
77 . A method of treating a subject in need comprising administering a composition according to claim 66 .
78 . The composition according to claim 67 , wherein the particles are coated with the peptide or polypeptide.
79 . The composition according to claim 67 , wherein the peptide or polypeptide is water soluble.
80 . The composition according to claim 67 , wherein the peptide or polypeptide is a synthetic polypeptide.
81 . The composition according to claim 67 , wherein the synthetic polypeptide is a synthetic polyamino acid.
82 . The composition according to claim 67 , wherein the pharmacologically active agent is amorphous.
83 . The composition according to claim 67 , wherein the pharmacologically active agent is crystalline.
84 . The composition according to claim 67 , wherein the pharmacologically active agent is substantially water insoluble.
85 . The composition according to claim 84 , wherein the pharmacologically active agent is paclitaxel.
86 . A method of treating a subject in need comprising administering a composition according to claim 67 .
87 . The composition according to claim 69 , wherein the peptide or the polypeptide is water soluble, and wherein the peptide or polypeptide is albumin.
88 . The composition according to claim 78 , wherein the peptide or the polypeptide is water soluble, and wherein the peptide or polypeptide is albumin.