Pharmaceutical formulation and a method of making same
The methods of the present invention and the formulations made from those methods, allow the stable integration of multiple actives within a single formulation. The solubilisation of an active in a suitable solvent and the subsequent adsorption onto a sorbing medium provide effective protection for the active from any adverse conditions within the liquid in which the active-loaded sorbing medium is dispersed. As a result the liquid can be formulated to suit the requirements of the actives that may include therein. As a result the actives may be stably integrated within the formulation.
1 ) A method of manufacturing a pharmaceutical formulation comprising the steps:
a) Dissolving an active in a solvent;
b) Sorbing the solvent containing active composition on to a sorbing medium; and then
c) Dispersing the sorbing medium loaded with the solvent composition in a liquid.
2 ) A method as claimed in claim 1 , wherein the active is a lipophilic active.
3 ) A method as claimed in claim 2 , wherein the lipophilic active is selected from the group including the avermectins and the milbemycins.
4 ) A method as claimed in claim 1 , wherein the liquid is an aqueous vehicle.
5 ) A method as claimed in claim 1 , wherein the solvent is selected from oils and organic solvents.
6 ) A method as claimed in claim 5 , wherein the solvent is selected from medium chain mono-/di-glycerides (Capmul MCM) in the range of 0.1-10% preferably between 2-4%.
7 ) A method as claimed in claim 1 , wherein the liquid optionally includes one or more medicaments selected from the group including vitamins, minerals, anthelmintics or antigens.
8 ) A method as claimed in claim 7 , wherein the minerals are selected from selenium salts, cobalt salts, copper salts, zinc salts, iodine salts and their chelates.
9 ) A method as claimed in claim 8 wherein the minerals are selected from sodium selenate and cobalt EDTA.
10 ) A method as claimed in claim 7 wherein the anthelmintics are selected from the group including thiazole derivatives such as a levamisole salt and benzimidazole derivates such as albendazole, oxfendazole, fenbendazole, mebendazole and acylated quinoline such as praziquantel, and benzenesulphonamide such as a clorsulon and closantel.
11 ) A method as claimed in claim 1 wherein the sorbing medium is selected from magnesium aluminometasilicate, cellulose, microcrystalline cellulose, diatomaceous earth, montmorillonite, betonite, titanium dioxide, amorphous silicon dioxide, colloidal silicon dioxide (Aerosil), calcium carbonate, talc (SiO2+MgO), attapulgite (silicon), aluminium and iron oxides clay), kaolin (aluminium silicate) preferably Aerosil more preferably Aerosil R972.
12 ) A method as claimed in claim 1 , wherein the liquid optionally comprises further excipients including but not limited to preservatives, suspending agents, buffering agents, antifoaming agents and the like.
13 ) A pharmaceutical formulation capable of dilution and capable of being administered to an animal, said formulation comprising:
a) an active dissolved in a suitable solvent to form a solution and sorbed on to a sorbing medium; and
b) optionally including a liquid diluent.
14 ) A formulation as claimed in claim 13 , wherein the active is a lipophilic active.
15 ) A formulation as claimed in claim 14 , wherein the active is selected from the group including the avermectins and the milbemycins.
16 ) A formulation as claimed in claim 15 , wherein the solvent is selected from oils and organic solvents.
17 ) A formulation as claimed in claim 16 , wherein the solvent is medium chain mono-/di-glycerides (Capmul MCM).
18 ) A formulation as claimed in claim 13 , wherein the liquid diluent comprises an aqueous vehicle.
19 ) A formulation as claimed in claim 13 , wherein the aqueous vehicle optionally includes one or more additional medicaments selected from the group including vitamins, minerals, anthelmintics or antigens.
20 ) A formulation as claimed in claim 19 , wherein the medicament is either soluble and/or dispersible in the liquid.
21 ) A formulation as claimed in claim 19 wherein the minerals are selected from wherein the minerals are selected from selenium salts, cobalt salts, copper salts, zinc salts, iodine salts and their chelates.
22 ) A formulation as claimed in claim 19 wherein the minerals are selected from sodium selenate and cobalt EDTA.
23 ) A formulation as claimed in claim 19 wherein the anthelmintics are selected from the group including thiazole derivatives such as a levamisole salt and benzimidazole derivates such as albendazole, oxfendazole, fenbendazole, mebendazole and acylated quinoline such as praziquantel, and benzenesulphonamide such as a clorsulon and closantel.
24 ) A formulation as claimed in claim 13 , which additionally includes preservatives, suspending agents, buffering agents, antifoaming agents and the like.
25 ) A method of medical treatment comprising administering a formulation as described in claim 13 to an animal.