ORGAN ARREST, PROTECTION, PRESERVATION AND RECOVERY
The present invention relates to a composition for controlling viability of a tissue including a potassium channel opener or adenosine receptor agonist, a compound for inducing local anaesthesia and compound for reducing the uptake of water by a cell in the tissue. The present invention also relates to the use of the composition according to the invention for controlling viability of a tissue.
1 . A pharmaceutical composition for controlling viability of an explanted tissue or organ for up to 15 hours comprising a therapeutically effective amount of:
(i) a potassium channel opener or adenosine receptor agonist;
(ii) a local anesthetic; and
(iii) an impermeant;
and a pharmaceutically acceptable carrier, diluent, adjuvant and/or excipient;
wherein the pharmaceutical composition is effective to control viability of an explanted tissue or organ for up to 15 hours.
2 . The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition further comprises at least one compound selected from the group consisting of: a sodium hydrogen exchange inhibitor; an antioxidant; diazoxide; a source of magnesium in a concentration of 0.5 mM to 20 mM; and a source of calcium in a concentration of 0.1 mM to 2.5 mM.
3 . The pharmaceutical composition of claim 2 , wherein the sodium hydrogen exchange inhibitor is selected from the group consisting of: amiloride, EIPA, cariporide, eniporide, triamterene, EMD 84021, EMD 94309, EMD 96785, EMD 85131, HOE 694, BII B-513 and T-162559.
4 . The pharmaceutical composition of claim 1 , wherein the impermeant is sucrose.
5 . The pharmaceutical composition of claim 1 , wherein the concentration of the impermeant is between about 5 and about 500 mM.
6 . The pharmaceutical composition of claim 3 , wherein the antioxidant is selected from the group consisting of: allopurinol, carnosine, histidine, Coenzyme Q-10, n-acetyl-cysteine, superoxide dismutase (SOD), glutathione reductase (GR), glutathione peroxidase (GP) modulators and regulators, catalase and the other metalloenzymes, NADPH and AND(P)H oxidase inhibitors, glutathione, U-74006F, vitamin E, Trolox, tocopherols (gamma and alpha, beta, delta), tocotrienols, ascorbic acid, Vitamin C, Beta-Carotene, selenium, Gamma Linoleic Acid (GLA), alpha-lipoic acid, uric acid (urate), curcumin, bilirubin, proanthocyanidins, epigallocatechin gallate, Lutein, lycopene, bioflavonoids, polyphenols, trolox(R), dimethylthiourea, tempol(R), carotenoids, coenzyme Q, melatonin, flavonoids, polyphenols, aminoindoles, probucol and nitecapone, 21-aminosteroids or lazaroids, sulphydryl-containing compounds (thiazolidine, Ebselen, dithiolethiones), and N-acetylcysteine.
7 . The pharmaceutical composition of claim 1 , wherein the pharmaceutically acceptable carrier is Krebs Henseleit buffer.
8 . The pharmaceutical composition of claim 1 , wherein (i) is adenosine.
9 . The pharmaceutical composition of claim 1 , wherein (ii) is lignocaine.
10 . A method for controlling viability of an explanted tissue or organ for up to 15 hours, comprising the step of contacting the explanted tissue or organ with the pharmaceutical composition of claim 1 .
11 . The method of claim 10 , wherein the pharmaceutical composition is at 10° C. when contacted with the explanted tissue or organ.
12 . The method of claim 10 , further comprising aerating the pharmaceutical composition before and/or during contact with the explanted tissue or organ.
13 . The method of claim 10 , wherein the tissue or organ is a human tissue or organ.
14 . The method of claim 10 , further comprising administering a reperfusion solution along with the pharmaceutical composition.
15 . The method of claim 14 , wherein the reperfusion solution further comprises an energy substrate.
16 . The method of claim 15 , wherein the energy substrate is selected from the group consisting of: pyruvate, glutamate, aspartate, arginine, lactate, glucose, insulin, alpha-keto glutarate, malate, succinate and carnitine.