TOPICAL PHARMACEUTICAL COMPOSITION COMPRISING NANONIZED SILVER SULFADIAZINE AND CHLORHEXIDINE GLUCONATE
The invention relates to an improved topical pharmaceutical composition for burn treatment and microbial infections on human beings or animals. The pharmaceutical composition comprises 0.1% w/w to 1% w/w of an antimicrobial drug, i.e., silver sulfadiazine and 0.2% w/w antiseptic, i.e., chlorhexidine gluconate; wherein silver sulfadiazine is in nanonized form.
1 . A topical pharmaceutical composition comprising 0.1% w/w to 1% w/w silver sulfadiazine, 0.2% w/w chlorhexidine gluconate, and one or more pharmaceutically acceptable excipients; wherein the silver sulfadiazine has a Z-average molar mass between 150 nm to 500 nm.
2 . The topical pharmaceutical composition according to claim 1 , wherein the pharmaceutically acceptable excipients comprise one or more of thickening agents, emulsifying agents, fragrance/perfumes, preservatives, chelating agents, pH modifiers, and antioxidants.
3 . The topical pharmaceutical composition according to claim 2 , wherein the thickening agents comprises one or more of soft paraffin, aluminum stearate, cetostearyl alcohol, propylene glycol, polyethylene glycols, povidone, wool-fat, hydrogenated lanolin and beeswax.
4 . The topical pharmaceutical composition according to claim 2 , wherein the emulsifying agent comprises one or more of cetomacrogol, non-ethoxylated glyceryl monostearate, carbopols, cetearyl alcohol, sodium stearoyl lactylate and lecithin.
5 . The topical pharmaceutical composition according to claim 2 , wherein the preservative comprises one or more of methylparaben, propylparaben, benzyl alcohol, benzoic acid, sodium benzoate, chlorocresol, sorbic acid and its salt, and phenylethyl alcohol.
6 . The topical pharmaceutical composition according to claim 2 , wherein the chelating agent comprises one or more of dimercaprol, ethylene diamine tetra acetic acid (EDTA), ethylene glycol tetra acetic acid, deferoxamine and alfa lipoic acid.
7 . The topical pharmaceutical composition according to claim 2 , wherein the pH modifier comprises one or more of citric acid, sodium citrate; acetic acid, sodium acetate; phosphoric acid, disodium orthophosphate; borax and sodium hydroxide.
8 . The topical pharmaceutical composition according to claim 2 , wherein the antioxidant comprises one or more of hydrogen peroxide, sodium metabisulfite, butylated hydroxytoluene, butylated hydroxyanisole, propyl gallate, ethyl gallate, methyl gallate, ascorbic acid, or tocopherol.
9 . The topical pharmaceutical composition according to claim 8 , wherein the antioxidant comprises a combination of hydrogen peroxide, sodium metabisulfite, and butylated hydroxytoluene.
10 . The topical pharmaceutical composition according to claim 1 , wherein the composition is a cream, lotion, ointment or gel.
11 . A process for the preparation of a topical pharmaceutical composition of claim 2 , wherein the process comprises the steps of:
a) dispersing the silver sulfadiazine and the thickening agent(s) in water;
b) charging the dispersion of step a) in a Dynomill and unloading the slurry when silver sulfadiazine attains a Z-average particle size between 150 nm to 500 nm;
c) emulsifying suitable oil and aqueous phases containing excipients;
d) adding chlorhexidine gluconate and the slurry containing nanonized silver sulfadiazine to the emulsion of step c); and
e) adjusting the pH with one or more pH modifiers and finally adjusting the weight using purified water and mixing.
12 . (canceled)
13 . The topical pharmaceutical composition according to claim 1 , whereby said topical pharmaceutical composition exhibits a microbial log reduction of Pseudomonas aeruginosa count in a mouse superficial skin model with thermal injury that is greater than or equal to that achieved by Silverex®.