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WO2011072012A2 - Procédés et compositions améliorés destinés au prélèvement de veines et à l'autogreffe - Google Patents

Procédés et compositions améliorés destinés au prélèvement de veines et à l'autogreffe Download PDF

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Publication number
WO2011072012A2
WO2011072012A2 PCT/US2010/059459 US2010059459W WO2011072012A2 WO 2011072012 A2 WO2011072012 A2 WO 2011072012A2 US 2010059459 W US2010059459 W US 2010059459W WO 2011072012 A2 WO2011072012 A2 WO 2011072012A2
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WO
WIPO (PCT)
Prior art keywords
vein
inhibitor
solution
agent
explant
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
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PCT/US2010/059459
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English (en)
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WO2011072012A3 (fr
Inventor
Colleen Brophy
Padmini Komalavilas
Joyce Cheung-Flynn
Kyle Hocking
Susan Eagle
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Vanderbilt University
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Vanderbilt University
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Filing date
Publication date
Application filed by Vanderbilt University filed Critical Vanderbilt University
Priority to AU2010328203A priority Critical patent/AU2010328203B2/en
Priority to EP10807761.1A priority patent/EP2509609B1/fr
Priority to CA2783236A priority patent/CA2783236C/fr
Priority to CN201080055389.XA priority patent/CN102834102B/zh
Priority to SG2012042677A priority patent/SG182261A1/en
Priority to DK10807761.1T priority patent/DK2509609T3/da
Priority to ES10807761.1T priority patent/ES2524549T3/es
Priority to JP2012543244A priority patent/JP5819846B2/ja
Priority to HK13106474.7A priority patent/HK1178804B/xx
Priority to EP14181978.9A priority patent/EP2848256B1/fr
Publication of WO2011072012A2 publication Critical patent/WO2011072012A2/fr
Publication of WO2011072012A3 publication Critical patent/WO2011072012A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N1/00—Preservation of bodies of humans or animals, or parts thereof
    • A01N1/10—Preservation of living parts
    • A01N1/12—Chemical aspects of preservation
    • A01N1/122—Preservation or perfusion media
    • A01N1/126—Physiologically active agents, e.g. antioxidants or nutrients
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N1/00—Preservation of bodies of humans or animals, or parts thereof
    • A01N1/10—Preservation of living parts
    • A01N1/14—Mechanical aspects of preservation; Apparatus or containers therefor
    • A01N1/142—Apparatus
    • A01N1/143—Apparatus for organ perfusion
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N1/00—Preservation of bodies of humans or animals, or parts thereof
    • A01N1/10—Preservation of living parts
    • A01N1/16—Physical preservation processes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
    • A61K35/44—Vessels; Vascular smooth muscle cells; Endothelial cells; Endothelial progenitor cells
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
    • A61M39/02—Access sites
    • A61M39/06—Haemostasis valves, i.e. gaskets sealing around a needle, catheter or the like, closing on removal thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P41/00—Drugs used in surgical methods, e.g. surgery adjuvants for preventing adhesion or for vitreum substitution
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers

Definitions

  • the invention relates generally to the fields of autologous vein, vein graft, vein preservation, tissue preservation, intimal hyperplasia, vasospasm, pharmaceuticals, devices, and vascular biology.
  • HSV Human greater saphenous vein
  • the branches are ligated and the vein is removed and placed on the "back table" prior to implantation.
  • Most surgeons place the HSV in heparinized saline solution at room temperature.
  • the vein is cannulated at the distal end and manually distended (with a syringe) with heparinized saline. This allows for identification and ligation of side branches that have been missed during harvest. This manual distension leads to injury to the vein.
  • the veins are also marked with a surgical skin marker to optimize orientation during implantation.
  • intimal hyperplasia The leading cause of failure of arterial bypass grafts is intimal hyperplasia (Clowes & Reidy, 1991). Despite the many recent technological advances in vascular interventions, intimal hyperplasia remains an expensive, morbid, and unsolved problem. Intimal hyperplasia is mediated by a sequence of events that include vascular smooth muscle proliferation, migration, phenotypic modulation, and extracellular matrix production (Allaire & Clowes, 1997; Mosse et al., 1985). This process leads to pathologic narrowing of the vessel lumen, graft stenoses, and ultimately graft failure (LoGerfo et al., 1983).
  • a method of treating a vein explant prior to transplant comprising (a) providing a vein explant; (b)stabilizing the vein explants in a buffered solution comprising a P2X 7 receptor antagonist at a pH pH 7.0-7.6 to produce a stabilized vein explant; and (c) preserving functional viability of the stabilized vein explant.
  • the method may further restore functional viability of the vein explant that before step (b) was not viable.
  • Functional viability of smooth muscle is defined here as the ability to contract in response to depolarization or agonists. For endothelium, viability is defined the ability of pre-contracted vessels to relax in response to acetylcholine.
  • the buffered solution may further comprise heparin.
  • the P2X 7 receptor antagonist may be erioglaucine Blue Dye #1 or brilliant blue G, or a combination of these.
  • the buffered solution may comprise phosphate buffered saline, MOPS, Hepes, Pipes, acetate or Plasmalyte.
  • the pH may be 7.35-7.45, or 7.0, 7.1, 7.2, 7.3, 7.4, 7.5 or 7.6.
  • the buffered solution may further comprise magnesium sulfate or Hanks' Balanced Salt Solution.
  • the buffered solution may further comprise one or more of an anti- contractile agent, an anti-oxidant agent, an oligosaccharide, a colloid agent, an antiinflammatory agent, an endothelial function preservative, a metabolic regulator, a hydrogel, an inhibitor of heat shock protein 27 (HSP27), a regulator of HSP20, and/or an inhibitor of MAPKAP kinase 2.
  • an anti- contractile agent an anti-oxidant agent
  • an oligosaccharide a colloid agent
  • an antiinflammatory agent an endothelial function preservative
  • a metabolic regulator a hydrogel
  • HSP27 heat shock protein 27
  • regulator of HSP20 a regulator of HSP20
  • MAPKAP kinase 2 an inhibitor of MAPKAP kinase 2.
  • the anti-contractile agent may be at least one of a phosphodiesterase inhibitor (e.g., papaverine, sildenafil, tadalafil, vardenafil, udenafil, avanafil cilistizol, pentoxifylline, dipyridamole or a combination thereof), a calcium channel blocker (e.g., amlodipine, aranidipine, azelnidipine, barnidipine, cilnidipine, clevidipine, efonidipine, felodipine, lacidipine, lercanidipine, mandipine, nicardipine, nifedipine, nilvadipine, nimodipine, nisoldipine, netrendipine, prandipine or a combination thereof), a nitric oxide donor (e.g., sodium nitroprusside, nitroglycerin or a combination thereof), or a phospho
  • the anti-oxidant agent may be e.g., N-acetylcysteine, allopurinol, glutathione, mannitol, ascorbic acid, a tocopherol, a tocotrienol or a green tea phenol or a combination thereof.
  • the oligosaccharide may be e.g. , lactobionic acid, raffinose, or trehalose or a combination thereof.
  • the colloid agent may be, e.g. , hydroxyethyl starch, dextran, blood or albumin or a combination thereof.
  • the anti-inflammatory agent may be, e.g., a corticosteroid (e.g., dexamethasone, hydrocortisone, cortisone, prednisone, prednisolone, methylprednisolone or a combination thereof), or a nonsteroidal anti-inflammatory (e.g., aspirin, ibuprophen, naproxen salicylic acid or a combination thereof), a MAPKAP kinase 2 inhibitor, anti-TNF- , anti-IL- l- ⁇ , a Cox-2 inhibitor, or a combination thereof
  • a corticosteroid e.g., dexamethasone, hydrocortisone, cortisone, prednisone, prednisolone, methylprednisolone or a combination thereof
  • a nonsteroidal anti-inflammatory e.g., aspirin, ibuprophen, naproxen salicylic acid or a combination thereof
  • the endothelial function preservative may be, e.g., an angiotensin converting enzyme inhibitor (e.g., enalapril, ramipril, quinapril, perindopril, lisinopril, benazepril, monopril or a combination thereof), an angiotensin receptor inhibitor (e.g. losartan), a statin (e.g.
  • atorvastatin cerivastatin, fluvastatin, lovastatin, mevastatin, pitavastatin, pravastatin, rosuvastatin, simvastatin or a combination thereof), metformin, aminoimidazole carboxamide ribonucleotide (AICAR) or an estrogen (e.g., estriol, estradiol, estrone, 17/3-estradiol or a combination thereof).
  • AICAR aminoimidazole carboxamide ribonucleotide
  • an estrogen e.g., estriol, estradiol, estrone, 17/3-estradiol or a combination thereof.
  • the metabolic regulator may be, e.g., glucose, adenosine amylin, calcitonin related gene peptide, insulin, or a combination thereof.
  • the hydrogel may be composed of, for example, a natural polysaccharide such as alginate, dextran, chitosan, and glycosaminoglycan, or a hydrophilic polymer such as polyethylene glycol, methylcellulose, hydroxymethylcellulose, hydroxyethylcellulose, polyhydroxbuterate, or poly(n-isopropylacrylamide).
  • a natural polysaccharide such as alginate, dextran, chitosan, and glycosaminoglycan
  • a hydrophilic polymer such as polyethylene glycol, methylcellulose, hydroxymethylcellulose, hydroxyethylcellulose, polyhydroxbuterate, or poly(n-isopropylacrylamide).
  • the inhibitor of HSP27 may be, for example, an siRNA or miRNA that inhibits HSP27 expression, an anti-miRNA that enhances HSP20 expression, or a combination thereof.
  • the inhibitor of MAPKAP kinase 2 may be, for example, a peptide inhibitor.
  • the explant may be marked with a non-alcohol based marker, such as, without limitation, erioglaucine/Blue Dye #1, indigotine, Allura Red AC, or brilliant blue G.
  • the method may further comprise flushing the lumen of the vein explant such that the internal flushing pressure does not exceed 200 mm Hg, or does not exceed 150 mm Hg.
  • a vein transplant kit comprising (a) a tissue marking pen comprising a P2X 7 receptor antagonist; and (b) a physiologic buffered solution or reagents for making such. Additionally, the kit may further comprise a container suitable for bathing a vein explant. Additionally, the kit may further comprise one or more of heparin, an anti-contractile agent, an anti-oxidant agent, an oligosaccharide, a colloid agent, an antiinflammatory agent, an endothelial function preservative, a metabolic regulator, a hydrogel, an inhibitor of a heat shock protein, magnesium sulfate, and/or an inhibitor of MAPKAP kinase 2.
  • the buffered solution may comprise, for example, phosphate buffered saline, MOPS, Hepes, Pipes, acetate or Plasmalyte.
  • the buffered solution may be at pH 7.0-7.6, or at 7.35- 7.45.
  • the P2X 7 receptor antagonist may comprise, for example, erioglaucine/Blue Dye #1, Allura Red AC, brilliant blue G, or any combination thereof.
  • the kit may further comprise a device for flushing the lumen of a vein explant; said device is designed to prevent flushing pressures inside the vein explant of greater than 200 mm Hg, or greater than 150 mm Hg.
  • the device may comprise a syringe and/or a catheter and a pop-off valve. Additionally, the syringe or catheter may comprise a bullet-shaped tip comprising a lumen for introduction into a proximal end of said vein explant. Additionally, the kit may further comprise a clamp designed to hold said vein explant.
  • a device for flushing the lumen of a vein explant said device is designed to prevent flushing pressures inside the vein explant of greater than 200 mm Hg, or greater than 150 mm Hg.
  • the device may comprise a syringe and/or catheter and a pop-off valve.
  • the syringe or catheter may comprise a bullet-shaped tip comprising a lumen for introduction into a distal end of said vein explant.
  • the device may further comprise a bullet-shaped plug lacking a lumen for introduction into a proximal end of said vein explant.
  • the device may further comprise a clamp designed to hold said vein explant.
  • Still yet another embodiment comprises a buffered solution of pH 7.0-7.6, wherein said buffered solution further comprises heparin and a P2X 7 receptor antagonist.
  • the P2X 7 receptor antagonist may be, for example, erioglaucine/Blue Dye #1 or brilliant blue G, or a combination thereof.
  • the buffered solution may further comprise heparin, along with one or more of erioglaucine/Blue Dye #1, brilliant blue G, or both.
  • the buffered solution may comprise phosphate buffered saline, MOPS, Hepes, Pipes, acetate or Plasmalyte.
  • the pH may be 7.35-7.45, or 7.0, 7.1, 7.2, 7.3, 7.4, 7.5 or 7.6.
  • the buffered solution may further comprise magnesium sulfate or Hanks' Balanced Salt Solution.
  • the buffered solution may further comprises one or more of an anti- contractile agent, an anti-oxidant agent, an oligosaccharide, a colloid agent, an antiinflammatory agent, an endothelial function preservative, a metabolic regulator, a hydrogel, an inhibitor of heat shock protein 27 (HSP27), a regulator of HSP20, an inhibitor of MAPKAP kinase 2, and/or combinations thereof.
  • an anti- contractile agent an anti-oxidant agent
  • an oligosaccharide a colloid agent
  • an antiinflammatory agent an endothelial function preservative
  • a metabolic regulator a hydrogel
  • HSP27 heat shock protein 27
  • HSP20 a regulator of HSP20
  • MAPKAP kinase 2 an inhibitor of MAPKAP kinase 2
  • the anti-contractile agent may be a phosphodiesterase inhibitor (e.g., papaverine, sildenafil, tadalafil, vardenafil, udenafil, avanafil cilistizol, pentoxifylline, dipyridamole or a combination thereof), a calcium channel blocker (e.g.
  • a nitric oxide donor sodium nitroprusside, nitroglycerin or a combination thereof
  • a cyclic nucleotide analogue e.g. dibutyryl cAMP, dibutyryl cGMP or a combination thereof.
  • the anti-oxidant agent may be, e.g. , N-acetylcysteine, allopurinol, glutathione, mannitol, ascorbic acid, a tocopherol, a tocotrienol or a green tea phenol, or a combination thereof.
  • the oligosaccharide may be e.g., lactobionic acid, raffinose, trehalose, or a combination thereof.
  • the colloid agent may be, e.g., hydroxyethyl starch, dextran, blood or albumin or a combination thereof.
  • the anti-inflammatory agent may be, e.g., a corticosteroid (e.g. dexamethasone, hydrocortisone, cortisone, prednisone, prednisolone, methylprednisolone or a combination thereof), a nonsteroidal anti-inflammatory (e.g. aspirin, ibuprophen, naproxen salicylic acid or a combination thereof), a MAPKAP kinase 2 inhibitor, anti-TNF-a, anti-IL-1- ⁇ , a Cox-2 inhibitor or a combination thereof.
  • a corticosteroid e.g. dexamethasone, hydrocortisone, cortisone, prednisone, prednisolone, methylprednisolone or a combination thereof
  • a nonsteroidal anti-inflammatory e.g. aspirin, ibuprophen, naproxen salicylic acid or a combination thereof
  • MAPKAP kinase 2 inhibitor
  • the endothelial function preservative may be an angiotensin converting enzyme inhibitor (e.g., enalapril, ramipril, quinapril, perindopril, lisinopril, benazepril, monopril or a combination thereof), an angiotensin receptor inhibitor (e.g. , losartan), a statin (e.g.
  • atorvastatin cerivastatin, fluvastatin, lovastatin, mevastatin, pitavastatin, pravastatin, rosuvastatin, simvastatin or a combination thereof), metformin, an estrogen (e.g., estriol, estradiol, estrone, 17 3-estradiol or a combination thereof) or a combination thereof.
  • an estrogen e.g., estriol, estradiol, estrone, 17 3-estradiol or a combination thereof
  • the metabolic regulator may be e.g., glucose, adenosine amylin, calcitonin related gene peptide, insulin or a combination thereof.
  • the hydrogel may be composed of a natural polysaccharide such as alginate, dextran, chitosan, and glycosaminoglycan, or a hydrophilic polymer such as polyethylene glycol, methylcellulose, hydroxymethylcellulose, hydroxyethylcellulose, polyhydroxbuterate, or poly(n-isopropylacrylamide).
  • the inhibitor of HSP27 may be, for example, an siRNA or miRNA that inhibits HSP27 expression, an anti-miRNA that enhances HSP20 expression or a combination thereof.
  • the inhibitor of MAPKAP kinase 2 may be, e.g., a peptide inhibitor.
  • compositions of the present invention have broad uses including use in healthcare by providing sterile medical devices and surface sterilization and decontamination.
  • FIG. 1 shows the variable smooth muscle functional viability in human saphenous vein.
  • FIGS. 2A-B show that the current surgical harvest techniques lead to decreased smooth muscle functional viability.
  • FIG. 3 demonstrates that the current surgical harvest techniques lead to reduced endothelial functional viability.
  • FIGS. 4A-B show that the current surgical harvest techniques reduce endothelial- independent relaxation of human saphenous vein.
  • FIG. 5 demonstrates that human saphenous vein grafts with blue markings displayed reduced smooth muscle functional viability.
  • FIG. 6 demonstrates that surgical skin marking reduced smooth muscle viability of human saphenous vein.
  • FIG. 7 shows surgical skin marking pens reduce the viability of pig saphenous vein.
  • FIG. 8 shows functional response (contractile response to KC1) correlates with cell viability in human saphenous veins.
  • FIGS. 9A-B demonstrate that erioglaucine restores functional viability after stretch injury in porcine saphenous vein.
  • FIG. 10 shows that Allura Red did not restore stretch-induced injury in porcine saphenous veins.
  • FIG. 11 demonstrates that erioglaucine restores smooth muscle viability in human saphenous vein.
  • FIGS. 12A-C show that erioglaucine blocks BzATP-induced contraction in saphenous vein.
  • FIG. 13 demonstrates that the erioglaucine reduces intimal thickness in human saphenous vein in an organ culture model.
  • FIG. 14 shows erioglaucine reduces intimal layer thickening in distended porcine saphenous vein.
  • FIG. 15 demonstrates that manipulation during surgical preparation impair endothelial dependent relaxation in human saphenous vein.
  • FIG. 16 shows that a pressure release (pop-off) valve limits pressure in human saphenous vein during manual distention.
  • FIG. 17 shows that manual distension with a pressure release valve prevents loss of endothelial function in porcine saphenous vein.
  • FIG. 18A-B show that preincubation with papaverine inhibits histamine and KCl induced contractions in porcine coronary artery.
  • FIG. 19A-B show that preincubation with papaverine inhibits norepinephrine induced contractions in human saphenous vein.
  • FIG. 20 shows the vein harvest device kit.
  • the present invention provides new methods and reagents with which to harvest, treat, preserve and transplant autologous conduits and inhibit mtimal hyperplasia.
  • the pH of the solution used to store autologous vein conduits prior to implantation which includes heparinized saline, is highly acidic (pH 6.2). This acidic pH has been shown to reduce the functionality of the conduit.
  • the use of surgical skin markers comprising isopropyl alcohol, to mark the autologous conduits also reduces the functionality of the conduit.
  • Erioglaucine otherwise known as FD&C blue dye #1, is not toxic to the vein and restores functional integrity after injury.
  • the present invention provides a buffered solution, pH 7.0-7.6, in which to place the vein after harvest.
  • the buffer is phosphate buffered saline; however, MOPS, Hepes, Pipes, and acetate are alternative formulations.
  • Magnesium sulfate (5 mM) can also be added to the solution to stabilize membranes.
  • Plasma-Lyte 56 Injection Multiple Electrolytes .Injection
  • Type 1 USP a sterile, nonpyrogenic, hypotonic solution in a single dose container for intravenous administration.
  • Each 100 mL contains 234 mg of Sodium Chloride, USP (NaCl); 128 mg of Potassium Acetate, USP (C 2 H 3 K0 2 ); and 32 mg of Magnesium Acetate Tetrahydrate (Mg(C 2 H 3 0 2 )2 » 4H 2 0). It contains no antimicrobial agents.
  • the pH is adjusted with hydrochloric acid.
  • the harvest solution can be prepared as a highly viscous solution such as that described in Seal & Panitch (20Q3).
  • Seal & Panitch (20Q3) Seal & Panitch
  • the biopolymer mixtures recovered quickly following thermal denaturation and mechanical insult.
  • the solutions of the present invention may contain additional additives to address various protective aspects of the invention.
  • the solutions of the present invention may include heparin (1-10 U/ml) to prevent thrombus formation.
  • Heparin is a highly sulfated glycosaminoglycan that is widely used as an injectable anticoagulant, and has the highest negative charge density of any known biological molecule. It can also be used to form an inner anticoagulant surface on various experimental and medical devices such as test tubes and renal dialysis machines.
  • Pharmaceutical grade heparin is derived from mucosal tissues of slaughtered meat animals such as porcine (pig) intestine or bovine (cow) lung.
  • Heparin Although used principally in medicine for anticoagulation, the true physiological role of heparin in the body remains unclear, because blood anti-coagulation is achieved mostly by endothelial cell-derived heparan sulfate proteoglycans. Heparin is usually stored within the secretory granules of mast cells and released only into the vasculature at sites of tissue injury. It has been proposed that, rather than anticoagulation, the main purpose of heparin is in a defensive mechanism at sites of tissue injury against invading bacteria and other foreign materials. In addition, it is preserved across a number of widely different species, including some invertebrates that do not have a similar blood coagulation system.
  • Native heparin is a polymer with a molecular weight ranging from 3 kDa to 50 kDa, although the average molecular weight of most commercial heparin preparations is in the range of 12 kDa to 15 kDa.
  • Heparin is a member of the glycosaminoglycan family of carbohydrates (defined as an organic compound which has the empirical formula Cm(H20)n; that is, consists only of carbon, hydrogen and oxygen, with a hydrogemoxygen atom ratio of 2: 1).
  • Glycosaminoglycans (GAGs) or mucopolysaccharides are long unbranched polysaccharides consisting of a repeating disaccharide unit.
  • the repeating unit consists of a hexose (six-carbon sugar) or a hexuronic acid, linked to a hexosamine (six-carbon sugar containing nitrogen).
  • Heparin (which includes the closely-related molecule heparan sulfate) consists of a variably-sulfated repeating disaccharide unit. The main disaccharide units that occur in heparin are shown below. The most common disaccharide unit is composed of a 2-O-sulfated iduronic acid and 6-O-sulfated, N-sulfated glucosamine, IdoA(2S)-GlcNS(6S).
  • the rare disaccharides containing a 3-O-sulfated glucosamine (GlcNS(3S,6S)) or a free amine group (GlcNH 3 + ).
  • GlcNS(3S,6S) the rare disaccharides containing a 3-O-sulfated glucosamine
  • GlcNH 3 + free amine group
  • the ester and amide sulfate groups are deprotonated and attract positively-charged counterions to form a heparin salt. It is in this form that heparin is usually administered as an anticoagulant.
  • the harvest solution can be a hydrogel that coats the vessel to minimize volume while keeping the vessel moist.
  • the hydrogel can contain a therapeutic to help maintain vasorelaxation.
  • Hydrogels include those synthesized from hydrophilic polymers that are crosslinked through covalent bods such as poly (ethylene glycol), polyacrylamide, polyfumerate, poly(N-siopropyl acrylamide), etc., or any gel like material crosslinking through physical interactions including hydrophobic and ionic. Gels include polyurethanes, agarose and alginates.
  • the present invention includes papaverine (1 mM) to inhibit contraction and spasm of the vein.
  • Alternative anti-spasmodic agents are nicardipine, sodium nitroprusside, nitroglycerine (0.5-1.0 mM), or dibutyryl cAMP (2 mM).
  • the present invention includes antioxidants to prevent oxidative damage to the vein.
  • N-acetylcysteine (10 mM), allopurinol (1 mM), glutathione (3 mM), mannitol (30-60 mM), or green tea phenols (0.5-1.0 mg/ml) are particular antioxidants of interest.
  • the present invention provides oligosaccharides in the harvest solution to prevent desiccation of the graft.
  • Lactobionic acid 100 mM
  • raffmose (30 mM)
  • trehalose (30 mM) are particular oligosaccharides.
  • Lactobionic acid is a disaccharide that provides osmotic support and prevents cell swelling.
  • Raffmose is a trisaccharide that provides hypertonicity.
  • Trehalose is a disaccharide with water retention properties.
  • the present invention provides starch in the harvest solution to support colloid osmotic pressure.
  • Hydroxyethyl starch (30-50 mM), dextran (40 g/1), blood, or albumin, are particularly contemplated colloid agents.
  • the present invention includes anti-inflammatory agents.
  • Steroids such as dexamethasone (5-10 mg/1) or salicylic acid are examples of antiinflammatory agents.
  • drugs will be included to prevent endothelial dysfunction. Angiotensin converting enzyme inhibitors, statins, metformin, AICAR and estrogens are examples of such drugs.
  • the present invention includes metabolic regulators.
  • Glucose 200 mM
  • adenosine 5 mM
  • insulin 100 U/ml
  • the present invention includes a novel peptide inhibitor of MAPKAP kinase 2 (and related peptides) to reduce inflammation, enhance relaxation of the smooth muscle, and prevent spasm.
  • MAPKAP kinase 2 and related peptides
  • the present invention includes siRNA or miRNA to decrease the expression of HSP27 to prevent intimal hyperplasia.
  • the sense strand siRNA sequences are 1) GACCAAGGAUGGCGUGGUGUU (SEQ ID NO: 1) and 2) AUACACGCUGCCCCCCGGUUU (SEQ ID NO: 2).
  • the sense strand miRNA sequences are 1) miR-580 or miR-1300, AACUCUUACUACUUAGUAAUCC (SEQ ID NO: 3) and 2) miR-552, UUGUCCACUGACCAAUCUGUU (SEQ ID NO: 4).
  • the anti-miR-320 sequence is: UCGCCCUCUCAACCCAGCUUUU Expression of the siRNA and miRNA is plasmid based or synthetic. Delivery of the DNA or synthetic oligo-duplexes can be performed via reversible permeabilization or pressurization (Monahan et al., 2009).
  • P2X receptors are a family of ligand-gated ion channels that bind extracellular ATP.
  • the P2X 7 receptor is responsible for the ATP-dependent lysis of macrophages and is also found on human saphenous vein smooth muscle (Cario-Toumaniantz et al., 1998). Activation of the P2X 7 receptor can form membrane pores permeable to large molecules in human saphenous vein (Cario-Toumaniantz et al., 1998).
  • P2X 7 receptor antagonists have been described in the literature. For example, Alcaraz et al. (2003) describe the synthesis and pharmacological evaluation of a series of potent P2X 7 receptor antagonists. The compounds inhibit BzATP -mediated pore formation in THP-1 cells. The distribution of the P2X 7 receptor in inflammatory cells, most notably the macrophage, mast cell and lymphocyte, suggests that P2X 7 antagonists have a significant role to play in the treatment of inflammatory disease. Carroll et al. (2009) review distinct chemical series of potent and highly selective P2X 7 receptor antagonists.
  • P2X 7 receptor antagonists 7,709,469, 6,812,226, 7,741,493 7,718,693 and 7,326,792.
  • P2X 7 receptor antagonists 2010/0292295, 2010/0292224, 2010/0286390, 2010/0210705, 2010/0168171, 2010/0160389, 2010/0160388, 2010/0160387, 2010/0160384, 2010/0160373, 2010/0144829, 2010/0144727, 2010/0105068, 2010/0075968, 2010/0056595, 2010/0036101, 2009/0264501, 2009/0215727, 2009/0197928, 2009/0149524, 2009/0005330, 2008/0132550, 2008/0009541, 2007/0122849, 2007/0082930, 2005/0054013, 2005/0026916 and 2002/0
  • an aspect of the invention includes a marker that contains a nontoxic dye to mark the vein.
  • FD&C Blue #1 an artificial food dye approved by the FDA (E #133)
  • E #133 also has not only been shown to be non-toxic, but protective of harvest techniques that are injurious to saphenous veins and is a P2X 7 receptor antagonist.
  • Brilliant blue G an analog erioglaucine, also is contemplated as a P2X 7 receptor antagonist.
  • Indigo tine (El 32) is another dark blue artificial dye approved by the FDA.
  • Fast Green (El 43) is another bluish green artificial dye approved by the FDA.
  • Natural dyes such as curcurmin or betanin are other alternatives. Curcumin is the principal curcuminoid of the spice tumeric and has antioxidant and anti-inflammatory properties. As a food additive, its E number is E100. Betanin is a red glycosidic food dye obtained from beets and is a natural food dye. Other possible dyes include genestein blue, evans blue, india ink, Allura Red AC, Tartazine, and Erythrosine.
  • the present invention includes a "pop off valve to prevent over distension of the vein during side branch ligation.
  • Qosina pressure relief T valve (part # D002501) is one example.
  • the present invention includes a "bullet tipped” needle that is used to secure the vein and a device to prevent stretch of the vein.
  • the present invention may also be embodimed in a kit for use in conjunction with surgical vein transplant procedures.
  • the immunodetection kits will comprise, in suitable container means, various containers, devices and/or reagents, along with appropriate instructions for use.
  • the kit will comprise harvest solutions, or reagents for making such.
  • the solutions or reagents would be provided in sterile form, optionally with sterile containers for mixing and storing harvest solutions.
  • the kit may also advantageously comprise a chamber for bathing/storing transplant tissue following explant and prior to transplant.
  • Various other supplemental additives described above may also be included.
  • kits may be the inclusion of a surgical marking pen comprising a non-toxin dye/marker, as described above.
  • the pen may be "preloaded" with the marker/dye, or may be provided empty, with the marker/dye in solution or in reagent form to be loaded into the pen by the user.
  • a syringe, catheter, and/or tubing equipped or including a pop-off valve as described above Also included may be a device for holding a vein in place, such as a clamp, optionally provided with a stand or base, permitting "hands-free" positioning of the graft for further treatment.
  • the container aspect of the kit will generally include means for holding at least one vial, test tube, flask, bottle, packet, syringe, catheter or other container in a secure and protected fashion, for example, in close confinement for commercial sale.
  • Such means may include injection or blow-molded plastic containers into which the desired containers, devices or reagents are retained.
  • the veins were stored in a saline solution until the end of the surgical procedure at which time they were placed in cold transplant harvest buffer (100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM raffinose, 5 mM adenosine, 3 mM glutathione, 1 mM allopurinol, 50 g/L hydroxyethyl starch, pH 7.4) and stored at 4°C.
  • cold transplant harvest buffer 100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM raffinose, 5 mM aden
  • Rings 1.0 mm in width were cut from segments of saphenous vein dissected free of fat and connective tissue, stripped of the endothelium and were suspended in a muscle bath containing a bicarbonate buffer (120 mM NaCl, 4.7 mM KCl, 1.0 mM MgS0 4 , 1.0 mM NaH 2 P0 4 , 10 mM glucose, 1.5 mM CaCl 2 , and 25 mM Na 2 HC0 3 , pH 7.4), gassed with 95% 0 2 / 5% C0 2 at 37°C.
  • a bicarbonate buffer 120 mM NaCl, 4.7 mM KCl, 1.0 mM MgS0 4 , 1.0 mM NaH 2 P0 4 , 10 mM glucose, 1.5 mM CaCl 2 , and 25 mM Na 2 HC0 3 , pH 7.4
  • the rings were manually stretched to 4 g of tension, and was maintained at a resting tension of lg was obtained and equilibtrated for ⁇ 2 hr.
  • Force measurements were obtained using a Radnoti Glass Technology (Monrovia, CA) force transducer (159901 A) interfaced with a Powerlab data acquisition system and Chart software (AD Instruments, Colorado Springs, CO).
  • the rings were contracted with 110 mM KCl (with equimolar replacement of NaCl in bicarbonate buffer), and the force generated was measured.
  • Segments of human saphenous vein were collected prior to preparation of the vein for transplantation into the arterial circulation (unmanipulated, UM) and after surgical preparation (after manipulation, AM). Preparation involves manual distension of the vein, marking with a surgical skin marker, and placing the vein in heparinized saline.
  • the contractile response to 110 mM KC1 (FIG. 2 A) or phenylephrine (10 "6 M, FIG. 2B) was determined and force generated was converted to stress (10 N/m ).
  • Manipulation during vein preparation led to decreased contractile response to KC1 and phenylephrine (FIGS. 2A-B). Each point represents a different patient and an aggregate of the response of at least three separate rings from each patient.
  • Typical manipulation during surgical preparation reduced endothelial-independent relaxation of human saphenous vein (FIGS. 4A-B).
  • Representative force tracings of the UM and AM segments collected from the same patient in response to PE and SNP (FIG. 4A).
  • UM veins displayed an 86.62 +/- 5.986% relaxation
  • AM veins displayed a 4.292 +/- 1.397% relaxation (FIG. 4B).
  • the rings were stripped of the endothelium and were suspended in a muscle bath containing a bicarbonate buffer (120 mM NaCl, 4.7 mM KC1, 1.0 mM MgS0 4 , 1.0 mM NaH 2 P0 4 , 10 mM glucose, 1.5 mM CaCl 2 , and 25 mM Na 2 HC0 3 , pH 7.4), gassed with 95% 0 2 / 5% C0 2 at 37°C.
  • the rings were manually stretched to 4 g of tension, and were maintained at a resting tension of lg and equilibtrated for ⁇ 2 hr.
  • the rings that did not have markings had an average stress of 0.110 ⁇ 0.014 10 5 N/m 2
  • the rings that were marked with the surgical skin marker had an average stress of 0.003 ⁇ 0.00110 5 N/m 2
  • rings marked with 50% isopropyl alcohol had an average stress of 0.005 ⁇ 0.003 10 5 N/m 2
  • rings marked with methylene blue had an average stress of 0.014 ⁇ 0.01 10 5 N/m 2 .
  • Freshly isolated porcine saphenous veins were used to test the effect of different marking methods.
  • the veins were collected and placed in cold transplant harvest buffer [100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM raffinose, 5 mM adenosine, 3 mM glutathione, 1 mM allopurinol, 50g/L hydroxyethyl starch, pH 7.4].
  • the vessels were stored in transplant harvest buffer at 4°C and tested within 24 hours of harvest and. To test the viability, rings 1.0 mm in width were cut from segments of saphenous vein and dissected free of fat and connective tissue.
  • the veins were stored in a saline solution until the end of the surgical procedure at which time they were placed in cold transplant harvest buffer (100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM raffmose, 5 mM adenosine, 3 mM glutathione, 1 mM allopurinol, 50 g/L hydroxyethyl starch, pH 7.4).
  • the vessels were stored in transplant harvest buffer at 4°C and tested within 24 hours of harvest.
  • each vein was subject to physiologic experiment and live cell assay using 3-(4,5-Dimethyl-2-thiazolyl)-2,5-diphenyl- 2H-tetrazolium bromide (MTT).
  • MTT 3-(4,5-Dimethyl-2-thiazolyl)-2,5-diphenyl- 2H-tetrazolium bromide
  • rings 1.0 mm in width were cut from segments of saphenous vein dissected free of fat and connective tissue, some were stripped of the endothelium and suspended in a muscle bath containing a bicarbonate buffer (120 mM NaCl, 4.7 mM KC1, 1.0 mM MgS0 4 , 1.0 mM NaH 2 P0 4 , 10 mM glucose, 1.5 mM CaCl 2 , and 25 mM Na 2 HC0 3 , pH 7.4), gassed with 95% 0 2 /5% C0 2 at 37°C.
  • a bicarbonate buffer 120 mM NaCl
  • the rings were manually stretched to 4 g of tension, and was maintained at a resting tension of lg was obtained and equilibtrated for ⁇ 2 hr. Force measurements were obtained using a Radnoti Glass Technology (Monrovia, CA) force transducer (159901 A) interfaced with a Powerlab data acquisition system and Chart software (AD Instruments, Colorado Springs, CO). The rings were contracted with 110 mM KC1 (with equimolar replacement of NaCl in bicarbonate buffer), and the force generated was measured. Any tissue failing to contract with KC1 was considered non- viable. Force was converted to stress 10 5 N/m 2 for each ring and was averaged for each vein.
  • Freshly isolated porcine saphenous vein was collected in cold transplant harvest buffer (100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM raffmose, 5 mM adenosine, 3 mM glutathione, 1 mM allopurinol, 50 g/L hydroxyethyl starch, pH 7.4).
  • the vessels were tested within 24 hours of harvest and storage in transplant harvest buffer at 4°C.
  • the rings were suspended in a muscle bath containing a bicarbonate buffer (120 mM NaCl, 4.7 mM KC1, 1.0 mM MgS0 4 , 1.0 niM NaH 2 P0 4 , 10 mM glucose, 1.5 mM CaCl 2 , and 25 mM Na 2 HC0 3 , pH 7.4), bubbled with 95% 0 2 /5% C0 2 at 37°C.
  • the rings were manually stretched to 4 g of tension, and maintained at a resting tension of lg and equilibtrated for ⁇ 2 hr.
  • the control rings had an average stress of 0.47 ⁇ 0.034 N/m 2
  • the rings that were marked with the erioglaucine dye had an average stress of 0.566 ⁇ 0.064 N/m
  • rings stretched had an average stress of 0.367 ⁇ 0.042 N/m 2
  • the stretched rings with erioglaucine dye had an average stress of 0.713 ⁇ 0.111 N/m 2
  • the stress for the stretched vein was significantly (*p ⁇ 0.05) different from the control unstretched veins and the stretched vein with erioglaucine dye was significantly (#p ⁇ 0.05) different when compared to stretched without erioglaucine dye (FIG. 9).
  • NS Allura Red
  • the vessels were tested within 24 hrs of harvest storage in transplant harvest buffer at 4°C.
  • rings 1.0 mm in width were cut from segments of saphenous vein dissected free of fat and connective tissue, treated with either a solution of erioglaucine (FCF, 2.6 mM, in 5% propylene glycol and water) or vehicle and incubated for 30 min at room temperature.
  • FCF erioglaucine
  • the tissues were then stripped of the endothelium and suspended in a muscle bath containing a bicarbonate buffer, gassed with 95% 0 2 /5% C0 2 at 37°C.
  • the rings were manually stretched to 4 g of tension, and was maintained at a resting tension of lg was obtained and equilibrated for ⁇ 2 hr.
  • the vehicle rings had an average stress of 0.015 ⁇ 0.012 N/m
  • the erioglaucine-treated rings had an average stress of 0.103 ⁇ 0.021 N/m (FIG. 11B).
  • the two groups were significantly different (p ⁇ 0.05).
  • Human saphenous vein segments were collected after harvest before surgical manipulation from patients undergoing coronary artery bypass or peripheral vascular bypass surgery and stored in PlasmaLyte. The vessels were tested within 2 hours of harvest. Freshly isolated porcine saphenous vein was collected in cold transplant harvest buffer (100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 , 30 mM Raffinose, 5 mM Adenosine, 3 mM Glutathione, 1 mM Allopurinol, 50 g/L Hydroxyethyl starch, pH 7.4). The vessels were tested within 24 hours of harvest. Rings 1.0 mm in width were cut from porcine saphenous veins (FIG.
  • FIG. 12C Representative force tracing of human saphenous vein contracted with BzATP after pretreatment with vehicle (control) or 50 ⁇ erioglaucine (FCF pretreatment) are depicted in FIG. 12C.
  • Segments of human saphenous vein were collected prior to preparation of the vein for transplantation into the arterial circulation (unmanipulated, UM) and after surgical preparation (after manipulation, AM) from the same patients in PlasmaLyte and were used within 2 hr of harvest.
  • the segment was cut into ⁇ 1 mm rings and one ring from each group was fixed in formalin (Pre-culture).
  • the other rings were cultured in RPMI medium supplemented with 1% L-glutamine, 1% penicillin/streptomycin and 30% fetal bovine serum at 5% C0 2 and 37°C in the absence (Control) or presence of 50 ⁇ erioglaucine (FCF) for 14 days.
  • Fresh porcine saphenous vein was harvested by a no touch method under sterile conditions and stored in cold transplant harvest buffer (100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM Raffmose, 5 mM Adenosine, 3 mM Glutathione, 1 mM Allopurinol, 50 g/L Hydroxyethyl starch, pH 7.4). The vessels were used within 24 hr of harvest.
  • cold transplant harvest buffer 100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM Raffmose, 5 mM Adenosine, 3 mM Glutathione, 1 mM Allopurinol, 50 g/L Hydroxyethyl starch, pH 7.4
  • FCF ⁇ erioglaucine
  • BBG brilliant blue G
  • Red Allura Red
  • Rings cut from the UM segments were incubated in University of Wisconsin Solution (UW), heparinized saline (HS), heparinized PlasmaLyte (HP) or heparinized PlasmaLyte containing 30 mM trehalose (HPT) for 2 hrs at room temperature. Rings were cut from the veins, suspended in a muscle bath and equilibrated in bicarbonate buffer. The rings were precontracted with 10 "6 M phenylephrine and then treated with 5 x 10 "7 M carbachol to determine endothelial dependent relaxation. Rings from the LIMA had greater endothelial dependent relaxation than saphenous vein (FIG. 15).
  • the veins were stored in a saline solution until the end of the surgical procedure at which time they were placed in cold transplant harvest buffer (100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM raffinose, 5 mM adenosine, 3 mM glutathione, 1 mM allopurinol, 50 g/L hydroxyethyl starch, pH 7.4).
  • cold transplant harvest buffer 100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM raffinose, 5 mM adenosine, 3 mM gluta
  • the vessels were tested within 24 hours of harvest and storage in transplant harvest buffer at 4°C.
  • a pop off valve was connected to a syringe at one end and to a cannulated saphenous vein at the other.
  • the distal end of the saphenous vein was also cannulated and connected to a pressure transducer. Pressure was monitored while the vein was distended with a hand held syringe with and without the pressure release valve. The pressure monitor would not measure pressures above 300 mmHg. This created three groups and they were the following: pop-off pressure (Popoff), max pressure with pop-off valve (Max with valve), and max pressure without pop-off valve (Max without valve).
  • the veins that had a pop-off valve had a mean pressure of 129 ⁇ 1.265 mm Hg and maximum pressure of 141.8 ⁇ 1.985 mm Hg, while the veins with out the pop off valve had a maximum pressure of 300 ⁇ 0.00 mm Hg (FIG. 16).
  • the average and maximum pressure in the veins with the pop-off valve were significantly different from the veins without the pop-off valve (p ⁇ 0.05).
  • Porcine coronary arteries were freshly isolated from euthanized pigs and placed directly into cold transplant harvest buffer (100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM Raffmose, 5 mM Adenosine, 3 mM Glutathione, 1 mM Allopurinol, 50 g/L Hydroxyethyl starch, pH 7.4). Coronary arteries were dissected free of fat and adventitial tissues and the endothelium was removed.
  • cold transplant harvest buffer 100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM Raffmose, 5 mM Adenosine, 3 mM Glutathione, 1 mM Allopurinol, 50 g/L Hydroxyethyl starch, pH 7.4
  • Transverse rings (1.0 mm thickness) were cut and suspended in muscle bath, via silk 3-0 linked to force transducers (Kent Scientific, CT) interfaced with a Data Translation A-D board (Data Translation, MA). Data was acquired with the Power Lab software program. Porcine coronary artery rings were suspended in a muscle bath and equilibrated in Krebs Ringer bicarbonate buffer for 2 h. The rings were stretched and the length progressively adjusted until maximal tension was obtained.
  • PAP mM papaverine
  • FIG. 18 A Representative force tracings of rings treated with 5 ⁇ histamine (Hist), 110 mM KCl (KCl), 1 mM papaverine (PAP), 1 mM papaverine for 10 min followed by 5 ⁇ histamine (Pap+Hist) or 1 mM papaverine for 10 min followed by 110 mM KCl (Pap+KCl) were depicted in FIG. 18 A. Decrease in stress was converted to a percentage of the maximal initial KCl contraction which was set as 100%. Papaverine treatment reduced basal tension in the rings (-15.0 ⁇ 3.135%) (FIG. 18B).
  • the veins were stored in a saline solution until the end of the surgical procedure at which time they were placed in cold transplant harvest buffer (100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM raffmose, 5 mM adenosine, 3 mM glutathione, 1 mM allopurinol, 50 g/L hydroxyethyl starch, pH 7.4).
  • cold transplant harvest buffer 100 mM potassium lactobionate, 25 mM KH 2 P0 4 , 5 mM MgS0 4 , 30 mM raffmose, 5 mM adenosine, 3 mM glutathione
  • the vessels were tested within 24 hrs of harvest and storage in transplant harvest buffer at 4°C. Veins were cleaned off fat and adventitial tissues and the endothelium was removed. Transverse rings (1.0 mm thickness) were cut and suspended in muscle bath, via silk 3-0 linked to force transducers (Kent Scientific, CT) interfaced with Powerlab data acquisition system and Chart software (AD Instruments, Colorado Springs, CO). Human saphenous vein rings were suspended in a muscle bath and equilibrated in Krebs Ringer bicarbonate buffer for 2 hr. The rings were stretched and the length progressively adjusted until maximal tension was obtained.
  • Vein harvest device is shown in FIG. 20.
  • the distal end of the vein (the vein is reversed because of valves in the vein) is cannulated with a bullet tipped plastic catheter which has a lumen for irrigation and secured to the catheter with a spring loaded clamp.
  • the catheter is clipped into the base.
  • An additional bullet tipped catheter with no lumen is attached to the proximal end of the vein clipped into the opposite end of the base.
  • the device is ratcheted open until the vein is at the same length as in vivo.
  • a syringe with extension tubing and an in line pressure release valve is attached to the distal end of the vein.
  • the vein can now be distended and side branches ligated.
  • the greater saphenous vein will be surgically harvested using standard surgical technique.
  • the distal end of the vein will be cannulated with a bullet tipped vein cannula and secured with either a clamp or a silk tie.
  • the pressure release valve will be attached to the cannula with a 10 or 20 cc syringe attached to the other end of the valve.
  • extension tubing will be placed between the syringe and the valve.
  • the vein will be distended with the vein harvest solution and tributaries identified and ligated with either silk ties or clips.
  • the vein will be marked with the marker in the kit along one long surface to maintain orientation of the vein. In some cases, the vein may be marked prior to removal from the patient.
  • the vein will then be placed in the harvest solution until implanted into the arterial circulation.
  • the dye from the pen will contain a P2X 7 receptor antagonist, and the harvest solution will not contain a P2X 7 receptor antagonist.
  • the dye from the pen will not contain a P2X 7 receptor antagonist, but the solution will.
  • both the pen dye and the solution will contain a P2X 7 receptor antagonist.
  • compositions and/or methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the compositions and methods of this invention have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be applied to the compositions and/or methods and in the steps or in the sequence of steps of the method described herein without departing from the concept, spirit and scope of the invention. More specifically, it will be apparent that certain agents which are both chemically and physiologically related may be substituted for the agents described herein while the same or similar results would be achieved. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the invention as defined by the appended claims.
  • Clowes AW Reidy MA (1991) Prevention of stenosis after vascular reconstruction: pharmacologic control of intimal hyperplasia-a review. J Vase Surg 13: 885-891. Allaire E, Clowes AW (1997) Endothelial cell injury in cardiovascular surgery: the intimal hyperplastic response. Ann Thorac Surg 63: 582-591.
  • Patent Publication 2009/0005330 U.S. Patent Publication 2008/0132550 U.S. Patent Publication 2008/0009541 U.S. Patent Publication 2007/0122849 U.S. Patent Publication 2007/0082930 U.S. Patent Publication 2005/0054013 U.S. Patent Publication 2005/0026916 U.S. Patent Publication 2002/0182646

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Abstract

La principale cause d'échec d'une greffe est le développement a posteriori d'une hyperplasie intimale, représentant une réponse à une blessure qui est considérée comme comprenant une prolifération des muscles lisses, une migration, une modulation phénotypique, et un dépôt de matrice extracellulaire (ECM). Les techniques chirurgicales typiquement utilisées pour le prélèvement des veines, à savoir l'étirement des veines, les placer dans des solutions à pH faible, et l'utilisation de marqueurs cutanés chirurgicaux toxiques, sont présentées ici comme provoquant une blessure. L'invention concerne ainsi des marqueurs chirurgicaux non toxiques qui protègent également contre la perte de la viabilité fonctionnelle induite par l'étirement, ainsi que d'autres additifs. L'invention concerne également des dispositifs et des compositions destinés à réduire le stress physique ou à protéger contre les effets découlant de ceux-ci.
PCT/US2010/059459 2009-12-08 2010-12-08 Procédés et compositions améliorés destinés au prélèvement de veines et à l'autogreffe Ceased WO2011072012A2 (fr)

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AU2010328203A AU2010328203B2 (en) 2009-12-08 2010-12-08 Improved methods and compositions for vein harvest and autografting
EP10807761.1A EP2509609B1 (fr) 2009-12-08 2010-12-08 Procédés et compositions améliorés destinés au prélèvement de veines et à l'autogreffe
CA2783236A CA2783236C (fr) 2009-12-08 2010-12-08 Procedes et compositions ameliores destines au prelevement de veines et a l'autogreffe
CN201080055389.XA CN102834102B (zh) 2009-12-08 2010-12-08 用于静脉采集和自体移植的改进的方法和组合物
SG2012042677A SG182261A1 (en) 2009-12-08 2010-12-08 Improved methods and compositions for vein harvest and autografting
DK10807761.1T DK2509609T3 (da) 2009-12-08 2010-12-08 Forbedrede fremgangsmåder og sammensætninger for venehøst og autotransplantation
ES10807761.1T ES2524549T3 (es) 2009-12-08 2010-12-08 Procedimientos y composiciones para la extracción de venas y autotransplante
JP2012543244A JP5819846B2 (ja) 2009-12-08 2010-12-08 静脈摘出および自家移植のための改善された方法および組成物
HK13106474.7A HK1178804B (en) 2009-12-08 2010-12-08 Improved methods and compositions for vein harvest and autografting
EP14181978.9A EP2848256B1 (fr) 2009-12-08 2010-12-08 Méthodes et compositions améliorées pour la récolte de veine et autogreffage

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US9700549B2 (en) 2013-10-03 2017-07-11 David Wise Compositions and methods for treating pelvic pain and other conditions
US9756850B2 (en) 1997-09-23 2017-09-12 The Department Of Veteran Affairs Compositions, methods and devices for maintaining an organ
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US10531654B2 (en) 2020-01-14
CN102834102A (zh) 2012-12-19
CN102834102B (zh) 2015-01-14
EP2848256A3 (fr) 2015-09-30
US20140220547A1 (en) 2014-08-07
JP5819846B2 (ja) 2015-11-24
EP2848256B1 (fr) 2018-11-14
WO2011072012A3 (fr) 2011-09-09
CA2783236A1 (fr) 2011-06-16
US20110190572A1 (en) 2011-08-04
EP2509609B1 (fr) 2014-10-01
ES2524549T3 (es) 2014-12-10
US8691556B2 (en) 2014-04-08
CA2783236C (fr) 2020-03-10
EP2509609A2 (fr) 2012-10-17
ES2710522T3 (es) 2019-04-25
US10149470B2 (en) 2018-12-11
AU2010328203B2 (en) 2014-05-15
CN104623665A (zh) 2015-05-20
CN104623665B (zh) 2018-01-12
DK2509609T3 (da) 2014-11-10
US20170071192A1 (en) 2017-03-16
SG182261A1 (en) 2012-08-30
DK2848256T3 (en) 2019-03-04

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