Emulsions or microemulsions for use in endoscopic mucosal resectioning and/or endoscopic submucosal dissection

Patent metadata

Field	Value
Publication number	US-2016296659-A1
Application number	US-201415038018-A
Country	US
Kind code	A1
Filing date	Nov 18, 2014
Priority date	Nov 20, 2013
Publication date	Oct 13, 2016
Grant date	—

Abstract

The invention provides a pharmaceutical composition in form of emulsion or microemulsion for use in an endoscopic procedure, said endoscopic procedure preferably comprising the administration of said pharmaceutical composition to a human. The invention herein disclosed provides a method for performing an endoscopic procedure, said method preferably comprising the administration of a pharmaceutical composition in form of emulsion or microemulsion to a human.

First claim

1 . A pharmaceutical composition in form of emulsion or microemulsion, which is in liquid phase up to a temperature of about 40° C. in vitro, comprising:
a) an aqueous phase;
b) an oily phase;
c) at least one surfactant;
d) at least one inverse thermosensitive polymer in an amount below the critical gelation concentration (CGC);
e) optionally at least one physiologically acceptable excipient;
wherein said pharmaceutical composition is for use as aid during endoscopic procedures in which it is injected in a target tissue in order to form a cushion.

2 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said composition is an oil-in-water emulsion or microemulsion.

3 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said composition has a viscosity below about 150 cP (centipoises), preferably below about 100 cP (centipoises), more preferably below about 50 centipoises cP (centipoises), much more preferably below about 20 cP (centipoises).

4 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 3 , wherein said viscosity is measured at about 25° C., at about 30° C. and/or at about 37° C.

5 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said at least one inverse thermosensitive polymer is contained in an amount below about 15% by weight, preferably between about 2% and about 14.5% by weight, more preferably between about 3% and about 12% by weight, much more preferably between about 5% and about 11% by weight, with respect to the weight of the composition.

6 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said at least one inverse thermosensitive polymer is contained in an amount of about 7%, about 8%, about 9% or about 10% by weight, with respect to the weight of the composition.

7 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said at least one inverse thermosensitive polymer is a polyoxyethylene-polyoxypropylene block copolymer, preferably a poloxamer.

8 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 7 , wherein said at least one poloxamer is selected from poloxamer 124, poloxamer 188, poloxamer 237, poloxamer 338, and poloxamer 407.

9 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 8 , wherein said at least one poloxamer is poloxamer 188, poloxamer 407 or a mixture of poloxamer 188 and poloxamer 407.

10 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said poloxamer is poloxamer 407 and it is contained in an amount of about 9% by weight with respect to the weight of the composition.

11 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said poloxamer is poloxamer 188 and it is contained in an amount of about 10% by weight with respect to the weight of the composition.

12 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said poloxamer is a mixture of poloxamer 188 and poloxamer 407, and such a mixture is contained in an amount of about 10% by weight with respect to the weight of the composition.

13 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said oily phase comprises at least one lipophilic compound.

14 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said at least one lipophilic compound is selected from natural oils, such as almond oil, canola oil, castor oil, corn oil, cottonseed oil, olive oil, safflower oil, sesame oil, soybean oil and the like; fatty acid esters, such as isopropyl palmitate, isopropyl myristate, ethyl oleate and the like; fatty alcohols, such as myristic alcohol, oleyl alcohol and the like; fatty acids, such as myristic acid, oleyl acid, palmitic acid and the like, triglycerides, such as long and/or medium-chain triglycerides and the like; diglycerides and monoglycerides.

15 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 12 , wherein said at least one lipophilic compound is medium-chain triglycerides.

16 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 12 , wherein said at least one lipophilic compound is a natural oil, preferably selected from sesame oil, almond oil and soybean oil.

17 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said at least one surfactant is a non-ionic surfactant, an ionic surfactant or a mixture thereof.

18 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 16 , wherein said non-ionic surfactant is selected from polysorbate 80 and PEG-15 hydroxystearate.

19 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 16 , wherein said ionic surfactant is selected from egg lecithin, hydrogenated phosphatidyl choline from egg lecithin, soybean lecithin and hydrogenated soybean lecithin.

20 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , further comprising at least one co-surfactant.

21 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 20 , wherein said at least one co-surfactant is selected from propylene glycol, glycerol and sodium oleate.

22 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 21 , wherein said at least one co-surfactant is a mixture of glycerol and sodium oleate.

23 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , further comprising at least one dye.

24 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 23 , wherein said at least one dye is a vital dye, a non-vital dye, a reactive dye or a mixture thereof.

25 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 23 , wherein said at least one dye is selected from Lugol's solution, methylene blue, toluidine blue, crystal violet, indigo carmine, congo red and phenol red.

26 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 25 , wherein said at least one dye is methylene blue or indigo carmine.

27 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said endoscopic procedure is an endoscopic resection procedure performed during a gastrointestinal endoscopy, preferably a polypectomy, an endoscopic mucosal resection (EMR) and/or an endoscopic submucosal dissection (ESD).

28 . The pharmaceutical composition in form of emulsion or microemulsion for use according to claim 1 , wherein said endoscopic procedure is performed in the esophagous, stomach, small intestine, cecum, colon, sigmoid colon and/or rectum.

29 . The pharmaceutical composition in form

Assignees

• Cosmo Technologies Ltd

Inventors

• Longo Luigi Maria
• Moro Luigi
• Frimonti Enrico
• Repici Alessandro

Classifications

• A61P41/00

  Drugs used in surgical methods, e.g. surgery adjuvants for preventing adhesion or for vitreum substitution · CPC title

• A61L2300/442

  Colorants, dyes · CPC title

• A61K9/1075

  Microemulsions or submicron emulsions; Preconcentrates or solids thereof; Micelles, e.g. made of phospholipids or block copolymers (A61K9/0026 takes precedence) · CPC title

• A61K9/107

  Emulsions {; Emulsion preconcentrates; Micelles (composition of emulsions A61K47/00)} · CPC title

• A61L24/046

  obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds (A61L24/043 takes precedence) · CPC title