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

Patent metadata

Field	Value
Publication number	US-9522216-B2
Application number	US-201615154857-A
Country	US
Kind code	B2
Filing date	May 13, 2016
Priority date	Nov 20, 2013
Publication date	Dec 20, 2016
Grant date	Dec 20, 2016

Abstract

The present invention relates to a pharmaceutical composition in form of emulsion or microemulsion and the use thereof as aid during endoscopic procedures in which it is injected in a target tissue in order to form a cushion. More in details, the invention relates to a method for performing an endoscopic procedure, which comprises injecting said pharmaceutical composition in form of emulsion or microemulsion in a target tissue of a patient, in order to form a cushion, which cushion is then optionally subjected to an endoscopic surgical procedure, such as a resection.

First claim

The invention claimed is:

1. A pharmaceutical composition in the form of an emulsion or a microemulsion comprising:
(a) an aqueous phase;
(b) an oily phase;
(c) at least one surfactant;
(d) at least one of poloxamer 188, poloxamer 407 or a mixture of poloxamer 188 and poloxamer 407; and
(e) at least one physiologically acceptable excipient;
wherein said at least one of poloxamer 188, polyoxamer 407 or a mixture of poloxamer 188 and poloxamer 407 is present in an amount below the critical gelation concentration (CGC), and wherein said composition remains in liquid phase at a temperature between about 5° C. and about 40° C. in vitro.

2. The pharmaceutical composition according to claim 1 , wherein said composition has a viscosity below about 150 cP (centipoises).

3. The pharmaceutical composition according to claim 1 , wherein said at least one of poloxamer 188, poloxamer 407 or a mixture of poloxamer 188 and poloxamer 407 is present in an amount below about 15% by weight, with respect to the weight of the composition.

4. The pharmaceutical composition in form of emulsion or microemulsion according to claim 1 , wherein said at least one of poloxamer 188, polyoxamer 407 or a mixture of poloxamer 188 and poloxamer 407 is present in an amount between about 5% and about 11% by weight, with respect to the weight of the composition.

5. The pharmaceutical composition according to claim 1 , wherein said poloxamer 407 is present in an amount of about 9% by weight with respect to the weight of the composition.

6. The pharmaceutical composition according to claim 1 , wherein said poloxamer 188 is present in an amount of about 10% by weight with respect to the weight of the composition.

7. The pharmaceutical composition according to claim 1 , wherein said mixture of poloxamer 188 and poloxamer 407 is present in an amount of about 10% by weight with respect to the weight of the composition.

8. The pharmaceutical composition according to claim 1 , wherein said oily phase comprises at least one lipophilic compound.

9. The pharmaceutical composition according to claim 8 , wherein said at least one lipophilic compound is selected from medium-chain triglycerides and soybean oil.

10. The pharmaceutical composition according to claim 1 , wherein said at least one surfactant is at least one non-ionic surfactant.

11. The pharmaceutical composition according to claim 10 , wherein said at least one non-ionic surfactant is selected from polysorbate 80 and PEG-15 hydroxystearate.

12. The pharmaceutical composition according to claim 1 , wherein said at least one surfactant is at least one ionic surfactant.

13. The pharmaceutical composition according to claim 12 , wherein said at least one ionic surfactant is selected from egg lecithin, hydrogenated phosphatidyl choline from egg lecithin, soybean lecithin and hydrogenated soybean lecithin.

14. The pharmaceutical composition according to claim 1 , wherein said pharmaceutical composition contains at least one co-surfactant selected from propylene glycol, glycerol and sodium oleate.

15. The pharmaceutical composition according to claim 1 , wherein said pharmaceutical composition further comprises at least one dye.

16. The pharmaceutical composition according to claim 15 , wherein said at least one dye is methylene blue or indigo carmine.

17. The pharmaceutical composition according to claim 1 , wherein
said oily phase comprises at least one lipophilic compound selected from medium-chain triglycerides and soybean oil and
said at least one surfactant is at least one non-ionic surfactant selected from polysorbate 80 and PEG-15 hydroxystearate.

18. The pharmaceutical composition according to claim 17 , wherein said pharmaceutical composition contains at least one co-surfactant selected from propylene glycol, glycerol and sodium oleate.

19. The pharmaceutical composition according to claim 17 , wherein said pharmaceutical composition further comprises at least one dye.

20. The pharmaceutical composition according to claim 19 , wherein said at least one dye is methylene blue or indigo carmine.

21. The pharmaceutical composition according to claim 1 , wherein
said oily phase comprises at least one lipophilic compound selected from medium-chain triglycerides and soybean oil and
said at least one surfactant is at least one ionic surfactant selected from egg lecithin, hydrogenated phosphatidyl choline from egg lecithin, soybean lecithin and hydrogenated soybean lecithin.

22. The pharmaceutical composition according to claim 21 , wherein said pharmaceutical composition contains at least one co-surfactant selected from propylene glycol, glycerol and sodium oleate.

23. The pharmaceutical composition according to claim 21 , wherein said pharmaceutical composition further comprises at least one dye.

24. The pharmaceutical composition according to claim 23 , wherein said at least one dye is methylene blue or indigo carmine.

Assignees

• Cosmo Technologies Ltd

Inventors

• Moro Luigi
• Longo Luigi Maria
• 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

• A61K9/0019 Primary

  Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner (non-active ingredients are additionally classified in A61K47/00) · CPC title

• A61L24/0005

  Ingredients of undetermined constitution or reaction products thereof · CPC title

• A61L2400/06

  Flowable or injectable implant compositions · CPC title

• A61L31/14

  Materials characterised by their function or physical properties {, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials} · CPC title