COMPOSITIONS TO ALLEVIATE PRESYSTEMIC METABOLISM OF OPIOIDS
Compositions comprising one or more opioids and one or more inhibitors of uridine diphosphate glucuronosyl transferases (UGTs) are provided. The inhibitors decrease the presystemic metabolism of the one or more opioids, thereby increasing their bioavailability. The inhibitors are compounds that are designated as Generally Regarded as Safe (GRAS) and/or “Everything Added to Food” (EAF) and/or are dietary supplements. Methods of alleviating pain and of treating opiate addiction in a subject by administering the compositions are also provided.
1 . A method of providing one or more opioids to a subject in need thereof so as to enhance systemic bioavailiability of said one or more opioids, comprising the step of
providing said one or more opioids to said subject in combination with one or more inhibitors of one or more uridine diphosphate glucuronosyl transferases (UGTs), wherein said one or more inhibitors of one or more UGTs are classified as Generally Regarded as Safe (GRAS), “Everything Added to Food” (EAF) and/or as a dietary supplement.
2 . The method of claim 1 , wherein said one or more opioids includes buprenorphine.
3 . The method of claim 1 , wherein said one or more opioids includes buprenorphine and naloxone.
4 . The method of claim 1 , wherein said one or more inhibitors of one or more UGTs inhibits at least one of UGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10, UGT2A1, UGT2A2, UGT2A3, UGT2B4, UGT2B7, UGT2B10, UGT2B11, UGT2B15, UGT2B17 and UGT2B28.
5 . The method of claim 1 , further comprising providing said subject with one or both of:
i) one or more inhibitors of at least one cytochrome P450 monooxygenase (CYP) selected from the group consisting of CYP1A1, CYP1A2, CYP2A6, CYP2D6, CYP2C9, CYP2C8, CYP2C18, CYP2C19, CYP3A4, CYP3A5 and CYP3A7; and
ii) one or more inhibitors of at least one sulfotransferase (SULT) selected from the group consisting of SULT1A1, SULT1A2, SULT1A3, SULT1C4 and SULT2B1.
6 . The method of claim 1 , where said one or more inhibitors is selected from the group consisting of propylparaben, ethyl vanillin, eugenol, vanillin, quercetin, resveratrol, isoeugenol, methylparaben, zingerone, piperine, ethyl vanillin propylene, glycol acetal, curcumin, pterostilbene, propylgallate, rasketone, magnolol, guaiacol, a-mangostin, silybin, and pinoresinol.
7 . The method of claim 6 wherein said one or more inhibitors is administered as a combination of inhibitors selected from the group consisting of: isoeugenol and propyl gallate; vanillin and isoeugenol; and vanillin, isoeugenol and propyl gallate.
8 . The method of claim 1 , wherein said step of providing is performed orally or intra-rectally.
9 . A dosage form of one or more opioids, comprising
one or more opioids and
one or more UGT inhibitors that is classified as Generally Regarded as Safe (GRAS), “Everything Added to Food” (EAF) and/or as a dietary supplement.
10 . The dosage form of claim 9 , wherein said one or more opioids includes buprenorphine.
11 . The dosage form of claim 10 , wherein said one or more opioids include buprenorphine and naloxone.
12 . The dosage form of claim 10 , wherein said one or more inhibitors of one or more UGTs inhibits at least one of UGT1A1, UGT1A3, UGT1A4, UGT1A5, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A 10, UGT2A1, UGT2A2, UGT2A3, UGT2B4, UGT2B7, UGT2B10, UGT2B11, UGT2B15, UGT2B17 and UGT2B28.
13 . The dosage form of claim 12 , further comprising one or both of:
i) one or more inhibitors of at least one cytochrome P450 monooxygenase (CYP) selected from the group consisting of CYP1A1, CYP1A2, CYP2A6, CYP2D6, CYP2C9, CYP2C8, CYP2C18, CYP2C19, CYP3A4, CYP3A5 and CYP3A7; and
ii) one or more inhibitors of at least one sulfotransferase (SULT) selected from the group consisting of SULT1A1, SULT1A2, SULT1A3, SULT1C4 and SULT2B1.
14 . The dosage form of claim 9 , where said one or more inhibitors is selected from the group consisting of propylparaben, ethyl vanillin, eugenol, vanillin, quercetin, resveratrol, isoeugenol, methylparaben, zingerone, piperine, ethyl vanillin propylene, glycol acetal, curcumin, pterostilbene, propyl gallate, rasketone, magnolol, guaiacol, a-mangostin, silybin, and pinoresinol.
15 . The dosage form of claim 14 , wherein said one or more inhibitors is administered as a combination of inhibitors selected from the group consisting of: isoeugenol and propyl gallate; vanillin and isoeugenol; and vanillin, isoeugenol and propyl gallate.
16 . The dosage form of claim 9 , wherein said dosage form is formulated for oral, rectal, vaginal or urethral administration.
17 . A method of treating or preventing pain in a subject in need thereof, comprising
administering to said subject a composition comprising
one or more opioids and
one or more UGT inhibitors that is classified as Generally Regarded as Safe (GRAS), “Everything Added to Food” (EAF) and/or as a dietary supplement.
18 . The method of claim 17 , wherein said one or more opioids includes buprenorphine.
19 . The method of claim 17 , wherein said one or more UGT inhibitors is a combination of inhibitors selected from the group consisting of: isoeugenol and propyl gallate; vanillin and isoeugenol; and vanillin, isoeugenol and propyl gallate.
20 . The method of claim 1 , wherein the one or more inhibitors is a combination of at least two inhibitors selected from the group consisting of eugenol, isoeugenol, ethyl vanillin, vanillin, curcumin, silybin A, a-mangostin, resveratrol, propyl gallate, and naringin.
21 . A method of treating or preventing opiate dependency or addiction in a subject in need thereof, comprising
administering to said subject a composition comprising
buprenorphine and naloxone; and
one or more UGT inhibitors that is classified as Generally Regarded as Safe (GRAS), “Everything Added to Food” (EAF) and/or as a dietary supplement.
22 . The method of claim 21 , wherein said one or more UGT inhibitors are selected from the group consisting of eugenol, isoeugenol, ethyl vanillin, vanillin, curcumin, silybin A, a-mangostin, resveratrol, propyl gallate, and naringin.
23 . The method of claim 21 , wherein said one or more UGT inhibitors includes 2, 3, 4, 5, 6, 7, 8, 9 or 10 inhibitors.
24 . The method of claim 21 , wherein said one or more UGT inhibitors is a combination of inhibitors selected from the group consisting of: isoeugenol and propyl gallate; vanillin and isoeugenol; and vanillin, isoeugenol and propyl gallate.
25 . The method of claim 1 , wherein said one or more UGT inhibitors includes a combination of alkylated catechols and other phenolic compounds.
26 . The method of claim 17 , wherein the one or more inhibitors is a combination of at least two inhibitors selected from the group consisting of eugenol, isoeugenol, ethyl vanillin, vanillin, curcumin, silybin A, a-mangostin, resveratrol, propyl gallate, and naringin.
27 . The oral dosage form of claim 9 , wherein the one or more inhibitors is a combination of at least two inhibitors selected from the group consisting of eugenol, isoeugenol, ethyl vanillin, vanillin, curcumin, silybin A, a-mangostin, resveratrol, propyl gallate, and naringin.
28 . The method of claim 17 , wherein said one or more UGT inhibitors includes a combination of alkylated catechols and other phenolic compounds.
29 . The method of claim 21 , wherein said one or more UGT inhibitors includes a combination of alkylated catechols and other phenolic compounds.
30 . The oral dosage form of claim 9 , wherein said one or more UGT inhibitors includes a combination of alkylated catechols and other phenolic compounds.