IP Library › Granted Patent US 10,226,455
Granted Patent B2
US 10,226,455 · App. 15/240,270 · Granted Mar 12, 2019

Compositions and methods for drug sensitization of parasites

Inventors: James C. Sacchettini (College Station, TX); Matthew W. Miller (College Station, TX); Deeann Wallis (College Station, TX); Nian E. Zhou (College Station, TX); Theresa W. Fossum (College Station, TX)
Assignee: The Texas A&M University System
A61K31/454A61K31/427A61K31/435A61K31/5377A61K31/7048A61K45/06A61K47/542A61K47/545Y02A50/411Y02A50/414Y02A50/419Y02A50/421Y02A50/423Y02A50/491
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Quick Facts
Patent No.
US 10,226,455
App. No.
15/240,270
Granted
Mar 12, 2019
Kind
B2
Abstract

Compositions and methods for inhibiting and/or sensitizing or re-sensitizing a parasite to an antiparasitic drug are provided. The compositions can comprise a rifamycin derivative or a pharmaceutically acceptable salt, hydrate, or prodrug thereof in an amount and formulation sufficient to inhibit or induce drug-sensitization in a parasite. The methods can comprise administering a rifamycin derivative or a pharmaceutically acceptable salt, hydrate, or prodrug thereof to a parasite in an amount and formulation sufficient to inhibit or induce drug-sensitization in the parasite.

Claims (20)

1. A method of sensitizing a parasite to an antiparasitic drug comprising administering a composition having the following formula:

wherein R comprises one of the following structures:

to the parasite that expresses a P-glycoprotein pump in an amount and for a time sufficient to sensitize the parasite to the antiparasitic drug by inhibiting the P-glycoprotein pump in the parasite and thereby reducing efflux of the antiparasitic drug from the parasite, wherein the antiparasitic drug is a macrocyclic lactone or a quinoline.

2. The method of claim 1 , further comprising administering the composition to the parasite before administering the antiparasitic drug.

3. The method of claim 1 , further comprising administering the composition to the parasite concurrently with the antiparasitic drug.

4. The method of claim 1 , further comprising administering the composition to the parasite after administering the antiparasitic drug.

5. The method of claim 1 , further comprising administering the composition to the parasite a second or greater time.

6. The method of claim 1 , wherein administering the composition to the parasite in an amount and for a time sufficient to sensitize the parasite to the antiparasitic drug comprises rendering the parasite susceptible to the antiparasitic drug at a lower dose than in the absence of the composition.

7. The method of claim 1 , wherein administering the composition to the parasite in an amount and for a time sufficient to sensitize the parasite to the antiparasitic drug comprises rendering the parasite susceptible to the antiparasitic drug that the parasite would not be susceptible to in the absence of the composition.

8. The method of claim 1 , wherein administering the composition to the parasite in an amount and for a time sufficient to sensitize the parasite to the antiparasitic drug comprises rendering the parasite susceptible to death or a decrease in growth due to the antiparasitic drug.

9. The method of claim 1 , wherein the parasite is a species of the genus Plasmodium or a species of the genus Haemonchus.

10. The method of claim 1 , wherein the parasite is Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale , or Plasmodium malariea.

11. The method of claim 1 , wherein the composition is 4-deoxy-3,4[2-spiro-[1-(t-butyloxycarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4[2-spiro-[1-ethyloxycarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4 [2-spiro-[1-(n-propyloxycarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4[2-spiro-[1-(isobutyloxycarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4[2-spiro-[1-(benzyloxycarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4[2-spiro-[1-(ethylaminocarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4[2-spiro-[1-(isopropyloxycarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4[2-spiro-[1-(phenylaminocarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4[2-spiro-[1-(acetyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4[2-spiro-[1-(beRTIoyl)-piperdin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4[2-spiro-[1-(3,3-dimethylbutanoyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4[2-spiro[1-(isobutylaminocarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4[2-spiro-[1-(isopropylaminocarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, 4-deoxy-3,4[2-spiro-[1-((1-methylpropyl) aminocarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S, or 4-deoxy-3,4[2-spiro-[1-(t-butylaminocarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S,.

12. The method of claim 1 , wherein the composition is 4-deoxy-3,4[2-spiro-[1-(isobutyloxycarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S.

13. The method of claim 1 , wherein the parasite is Haemonchus contortus.

14. The method of claim 1 , wherein the antiparasitic drug is ivermectin.

15. The method of claim 1 , wherein the antiparasitic drug is iodoquinol.

16. The method of claim 1 , wherein the antiparasitic drug is chloroquine, primaquine, mefloquine, quinine, or quinidine.

17. The method of claim 1 , wherein the antiparasitic drug is praziquantel, or oxyminquine.

18. The method of claim 1 , wherein the composition is 11-deoxy-11-amino-4-deoxy-3,4[2-spiro-[1-(isobutyloxycarbonyl)-piperidin-4-yl]]-(1H)-imidazo-(2,5-dihydro)rifamycin S.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 27, 2017
From: SACCHETTINI, JAMES C.; MILLER, MATTHEW W.; WALLIS, DEEANN; ZHOU, NIAN E.; FOSSUM, THERESA W.
To: THE TEXAS A&M UNIVERSITY SYSTEM
Reel/Frame 044225/0392 →
Continuity (3)
Continuation PCTUS2015016631 · Feb 19, 2015
Provisional Application 61941879 · Feb 19, 2014
Related Publication 20160354358A1 · Dec 8, 2016
Cited By (1)
US 12,544,336