IP Library Granted Patent US 9,844,217
Granted Patent B2
US 9,844,217 · App. 14/321,294 · Granted Dec 19, 2017

Allomone repulsive and kairomone attractive compositions for controlling arachnids

Inventor: Patrick Pageat (Route de Saint-Saturnin, FR)
Assignee: Institut de Recherche en Semiochimie et Ethologie Appliquée
A01N37/06A01N27/00A01N31/02A01N37/02A01N37/04A01N37/12A01N37/14A01N63/02A61K35/55C07C47/02C07C69/02
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,844,217
App. No.
14/321,294
Granted
Dec 19, 2017
Kind
B2
Abstract

Composition of allomones and kairomones derived from the uropygeal gland of ducks and chickens are described, as well as methods to treat Arachnids.

Claims (30)

1. An arachnids repulsive composition comprising about 45.0% to 55.0% (w %/w %) bis(2-ethylhexyl) adipate and/or derivatives thereof and/or spatial isomers thereof, and about 45.0% to 55.0% (w %/w %) 2,2,4-trimethyl 1,3 pentanediol diisobutyrate and/or derivatives thereof and/or spatial isomers thereof.

2. An arachnids repulsive composition consisting of bis(2-ethylhexyl) adipate and/or derivatives thereof and/or spatial isomers thereof, and 2,2,4-trimethyl 1,3 pentanediol diisobutyrate and/or derivatives thereof and/or spatial isomers thereof.

3. The arachnids repulsive composition according to claim 2 , which consists of about 45.0% to 55.0% (w %/w %) bis(2-ethylhexyl) adipate and/or derivatives thereof and/or spatial isomers thereof, and about 45.0% to 55.0% (w %/w %) 2,2,4-trimethyl-1,3 pentanediol diisobutyrate and/or derivatives thereof and/or spatial isomers thereof.

4. The composition according to claim 2 , wherein said derivatives are esters, or salts, alcohols, ketones, ethers, aldehydes, sterols and amides of bis(2-ethylhexyl) adipate and 2,2,4-trimethyl 1,3 pentanediol diisobutyrate.

5. A method of repulsing arachnids said method comprising administering to an animal in need of such treatment a pharmaceutically acceptable amount of a composition according to claim 1 or 2 .

6. A method of treating or preventing chicken mites or Northern fowl mites in hens, chickens and young chicks said method comprising administering to hens, chickens or young chicks in need of such treatment a pharmaceutically effective amount of a composition according to claim 1 or 2 .

7. The method according to claim 5 , wherein said composition comprises about 45.0% to 55.0% (w %/w %) bis(2-ethylhexyl) adipate and about 45.0% to 55.0% (w %/w %) 2,2,4-trimethyl-1,3 pentanediol diisobutyrate and/or derivatives thereof and/or isomers thereof and/or mixtures of bis(2-ethylhexyl) adipate or 2,2,4-trimethyl 1,3 pentanediol diisobutyrate with one or more esters, or salts, alcohols, ketones, ethers, aldehydes, sterols and amides derivatives of bis(2-ethylhexyl) adipate and 2,2,4-trimethyl 1,3 pentanediol diisobutyrate and/or with one or more isomers of bis(2-ethylhexyl) adipate and 2,2,4-trimethyl 1,3 pentanediol diisobutyrate and/or one or more isomers of the derivatives of bis(2-ethylhexyl) adipate and 2,2,4-trimethyl 1,3 pentanediol diisobutyrate.

8. The method according to claim 6 , wherein said composition comprises about 45.0% to 55.0% (w %/w %) bis(2-ethylhexyl) adipate and about 45.0% to 55.0% (w %/w %) 2,2,4-trimethyl-1,3 pentanediol diisobutyrate and/or derivatives thereof and/or isomers thereof and/or mixtures of bis(2-ethylhexyl) adipate or 2,2,4-trimethyl 1,3 pentanediol diisobutyrate with one or more esters, or salts, alcohols, ketones, ethers, aldehydes, sterols and amides derivatives of bis(2-ethylhexyl) adipate and 2,2,4-trimethyl 1,3 pentanediol diisobutyrate and/or with one or more isomers of bis(2-ethylhexyl) adipate and 2,2,4-trimethyl 1,3 pentanediol diisobutyrate and/or one or more isomers of the derivatives of bis(2-ethylhexyl) adipate and 2,2,4-trimethyl 1,3 pentanediol diisobutyrate.

9. The method according to claim 5 , wherein said administering comprises oral administration.

10. The method according to claim 6 , wherein said administering comprises oral administration.

11. The method according to claim 7 , wherein said administering comprises oral administration.

12. The method according to claim 5 , wherein said administering comprises a topical administration.

13. The method according to claim 6 , wherein said administering comprises a topical administration.

14. The method according to claim 7 , wherein said administering comprises a topical administration.

15. A solution comprising the arachnids repulsive composition of claim 1 .

16. A method of repulsing arachnids said method comprising administering to a human in need of such treatment a pharmaceutically acceptable amount of a composition according to claim 1 or 2 .

17. The method according to claim 5 , wherein said arachnid is a Dermanyssus gallinae , a tick or an Ornithonyssus sylviarum.

18. The method according to claim 16 , wherein said arachnid is a Dermanyssus gallinae , a tick or an Ornithonyssus sylviarum.

19. The composition according to claim 1 , wherein said derivatives are esters, or salts, alcohols, ketones, ethers, aldehydes, sterols and amides of bis(2-ethylhexyll) adipate and 2,2,4-trimethyl 1,3 pentanediol diisobutyrate.

20. A solution comprising the arachnids repulsive composition of claim 2 .

21. The solution according to claim 15 , wherein said solution comprises a nonaqueous solvent selected from the group consisting of alcohol, diethyl ether, chloroform, ethanol, benzene, propyl alcohol, isopropanol, 2-propanol and acetone polysorbate 80.

22. The solution according to claim 20 , wherein said solution comprises a nonaqueous solvent selected from the group consisting of alcohol, diethyl ether, chloroform, ethanol, benzene, propyl alcohol, isopropanol, 2-propanol and acetone polysorbate 80.

23. The solution according to claim 15 , wherein said solution comprises a solvent of water, or vegetal or animal oil.

24. The solution according to claim 20 , wherein said solution comprises a solvent of water, or vegetal or animal oil.

25. The composition according to claim 1 , comprising about 45.0% to 55.0% (w %/w %) bis(2-ethylhexyl) adipate and/or derivatives thereof, and about 45.0% to 55.0% (w %/w %) 2,2,4-trimethyl 1,3 pentanediol diisobutyrate and/or derivatives thereof, wherein said derivatives are esters, or salts, alcohols, ketones, ethers, aldehydes, sterols and amides of bis(2-ethylhexyl) adipate and 2,2,4-trimethyl 1,3 pentanediol diisobutyrate.

26. The composition according to claim 1 , comprising about 45.0% to 55.0% (w %/w %) bis(2-ethylhexyl) adipate and about 45.0% to 55.0% (w %/w %) 2,2,4-trimethyl 1,3 pentanediol diisobutyrate.

27. The composition according to claim 2 , wherein said derivatives are esters, or salts, alcohols, ketones, ethers, aldehydes, sterols and amides of bis(2-ethylhexyl) adipate and 2,2,4-trimethyl 1,3 pentanediol diisobutyrate.

28. The composition according to claim 2 , or consisting of bis(2-ethylhexyl) adipate and 2,2,4-trimethyl 1,3 pentanediol diisobutyrate.

29. The composition according to claim 27 , which consists of about 45.0% to 55.0% (w %/w %) bis(2-ethylhexyl) adipate and/or derivatives thereof, and about 45.0% to 55.0% (w %/w %) 2,2,4-trimethyl-1,3 pentanediol diisobutyrate and/or derivatives thereof.

30. The composition according to claim 28 , which consists of about 45.0% to 55.0% (w %/w %) bis(2-ethylhexyl) adipate and about 45.0% to 55.0% (w %/w %) 2,2,4-trimethyl-1,3 pentanediol diisobutyrate.

Assignments (2)
CHANGE OF NAME Recorded Oct 18, 2017
From: FIDELINE
To: INSTITUT DE RECHERCHE EN SEMIOCHIMIE ET ETHOLOGIE APPLIQUÉE
Reel/Frame 044221/0448 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 5, 2014
From: PAGEAT, PATRICK
To: FIDELINE
Reel/Frame 033468/0612 →
Priority Claims (1)
EP 02291534 · Jun 19, 2002 · regional
Continuity (4)
Continuation 11003530 · Dec 6, 2004
Continuation PCTEP0307143 · Jun 19, 2003
Provisional Application 60390059 · Jun 19, 2002
Related Publication 20140316000A1 · Oct 23, 2014