Field of the Invention This invention relates to the treatment of mammalian biological organs, tissues, cells and fluids with one or more of a class of compounds referred to here as glycyrrhizic triterpenoid compounds, exemplary of which are glycyrrhizin, glycyrrhizinic acid or glycyrrhetinic acid glycoside, and analogous triterpenes, e.g. carbenoxolone and cicloxolone and their derivatives, to inactivate viruses, such as cytomegalovirus, bovine diarrhea virus, human immunodeficiency virus.

Background of the Invention This ^' invention relates to the treatment of transplant organs and tissue, e.g. renal, cardiac, cornea, and marrow tissue, and any other tissue intended for transplantation, to inactivate or destroy infective viruses, such as the cytomegalo¬ virus which is- responsible or aggravates serious and sometimes fatal infections, in organ transplant recipients. Cytomegalovirus (CMV) is probably the most ubiquitous of the pathogenic viruses. Virtually all of the people living in the developing countries become infected with CMV early in life, and CMV infects over half the population in the developed countries of the world. CMV may remain essentially inactive in the body following an initial infection and may flare in to an active infection any time, most frequently when the body's immune system is compromised to a greater or lesser degree by disease, radiation or chemotherapy, drug therapy surgical trauma, etc.

CMV is frequently associated with, and may be a causative or contributing factor in, life-threatening disease in individuals with suppressed immune systems, and can be a principal causative factor in pneumonia, neurological disorders, febrile illness, ocular disease and hepatitis. CMV infection is a serious limiting factor in the transplantation of organs, tissues and cells and the transfusion of blood and plasma from one individual to another. The kidney transplant patient runs a high risk of contracting serious, and not infrequently fatal, CMV infection form CMV introduced by the transplant organ. Recipients of whole blood, plasma, bone marrow, cornea, cardiac, and semen run a serious risk of CMV

infectious disease, the risk being multiplied where the immune system of the recipient is suppressed to prevent rejection of the foreign organ or cells, or where immunosuppression is present from natural causes.

CMV is frequently associated with Pneumoncystis carinii and may cause or contribute to encephalitis and colitis and may be associated with Kaposi's sarcoma in AIDS patients. CMV is so ubiquitous in the blood and organs of donors who, frequently, exhibit no symptoms of infection, and its direct and contributory effects in infectious diseases is so pervasive and subtle that a CMV infection is to be presumed if another causative agent cannot be established. There no proven cures or generally effective drugs for the treatment of

CMV infections. Certain drugs, e.g. ganciclovir, has been shown to have limited effectiveness in the treatment of certain CMV infections, e.g. CMV retinitis, but has little effect in the treatment of CMV pneumonia. Live attenuated CMV vaccine has been developed but may not protect against infection by natural CMV and there is a real risk that the attenuated CMV may reactivate during pregnancy and infect the fetus.

While a method of preventing, or even reducing the likelihood, of transmitting CMV via transplant or transfusion organs, tissues, cells or fluids would be of enormous benefit to medical science, the present invention is not limited to treatments to inhibit CMV infection and is applicable to other classes of virus.

CMV is a member of the human herpesvirus (HV) group, which are responsible for much of mankind's discomfort and pain. The herpesviruses represent a very large, clearly defined group of viruses which are responsible for, or involved in, cold sores, shingles, a venereal disease, mononucleosis, eye infections, birth defects and probably several cancers. Three subfamilies are of particularly importance. The alpha subfamily includes HV-1 (herpes virus simplex 1) which causes cold sores, fever blisters, eye and brain infections, HV-2 (herpes virus simplex 2) which cause genital ulceration, and HV-3 (HV varicella zoster) which causes chicken pox, shingles and brain infections. The beta subfamily includes HV-5, the principal member of which is CMV discussed above. The

gamma subfamily includes HV-4 (Epstein-Barr) which cause infectious mononu¬ cleosis and is involved in Burkitt's lymphoma and nasopharyngeal carcinoma. Additional possibly pathogenic herpes viruses no doubt exist, one type of which, HV-6, of unknown pathogenicity has been identified. (Niederman, J.C. et al, The Lancet, Oct. 8, 1988, 817). There is evidence that the methods of this invention are effective in inhibiting the transmission of infections caused by many and perhaps all of the pathogenic herpes viruses.

HIV antibody screening of corneal and kidney donors has become important because HIV in cornea and kidney from donors who carry the HIV virus but have not exhibited outward symptoms of AIDS may become activated as a result of or incident to the corneal or renal transplant, (see Wilhelmus, K.R. et al, Ophthalmologica (Switzerland) 1987, 195(2) 57; Mal'khanov, V.B. et al, Vopr Virusol 1987, 32(2) 21; Salisbury, J.D. et al, Ophthalmic Surg 1984, 15(5) 406.) Herpetic corneal disease in corneal transplant of herpes virus carrying cornea may have grave consequences, (see Beekhuis, W.H. , Doc Ophthalmol 1983, 55(1-2) 31; Collin, H.B., Arch Ophthalmol 1976, 94(10) 1726.) While it does not appear that cornea from donors dying from- systemic malignancy dispose the donee toward malignancy, great care is required to exclude graft tissues or organs from donors who died of a neurological disease with a suspected viral etiology. (Wagoner, M.D. et al, Ophthalmology 1981, 88(2) 139.) Gandhi, S.S. et al. (Surv Ophthalmol 1981, 25(5) 306) saw evidence of a number of neurologic and other disorders in which a slow virus etiology has been implicated but found no evidence that hepatitis or syphilis were transmitted by corneal transplant; however, Zakov, Z.N. et al, (Am J Ophthalmol 1978, 86(5) 605) concluded from their study that cornea from patients with septecimia, hepatitis, jaundice or any evidence of viral infection were unacceptable. cytomegalovirus (CMV) infections may alter host defense to a variety of pathogens (Miller, S.A., et al, (Infect. Immun 1985, 47(1) 605), it is doubly important to avoid introduction of CMV with a transplanted organ or tissue. It is apparent from the foregoing discussion that a method of killing or inactivating pathogenic viruses in organs, tissues, cell and fluids intended for

transfusion or transplantation would be an enormous advance in medicine. It is to this major national and world wide health care challenge that the present invention is directed.

Licorice is a well-known flavoring agent. In addition to its use as a flavoring agent, licorice has long been a common folk medicine for the treatment of sore throats. While not widely known, various extracts of and preparations derived from licorice, e.g. glycyrrhizin and its derivatives, principally the salts of glycyrrhizic acid, have also been used to a limited degree for many years as an orally administered medication for the treatment of peptic ulcers (Chandler, R. F. , Can. Pharm. J. , V118, No.9, 1985), and oral administration of glycyrrhizin contemporaneously with saponin antiinflamatoiy agents has been reported to inhibit saponin and saponigen hemolysis (Segal, R. et al., Biochem. Pharmacol. 26, 7 1977).

The family of compounds of interest are, chemically, referred to as tri- terpenoids. The specific triterpenoids of interest are, principally, derived as extracts or derivatives of glycyrrhiza and are referred to here as GTPD com¬ pounds. GTPDs have been evaluated extensively in vitro, and have been administered orally, intramuscularly and intravenously. No significant toxicity from limited, short term administration of glycyrrhizin has been reported. Adverse reactions have been reported in certain instances of prolonged oral ingestion and a slight relapse after rapid discontinuation of intravenous administra¬ tion of Stronger Neo-Minaphagen C (SNMC) solution, glycyrrhizin (0.2%), cys- teine(0.1%) and glycine (2%) was attributed to the steroid ring in glycyrrhizin (Fujϊsawa K. et al., Asian Med. J. (Japan), 23,10 1980). Dosages of SNMC as high as 60 ml/day (— 12 mg/dy of glycyrrhizin) have been reported (Iwamura

K., Therapiewoche (W. Germany) 30,34 1980).

Inactivation of viruses, in vitro, under certain conditions, has been reported (see, e.g., Pompei R., Exprientia (Switzerland) 36/3 1980). Such anti-viral activity as GTPD compounds sometimes exhibit has been attributed to reverse transcriptase-inhibitory activity (Nakashima, H. et al., Jpn. J. Cancer. Res. 78,8

1987) and to enhancement of interferon-gamma production (Shinada, M. et al. ,

Proc. Soc. Exp. Biol. 181,2 1986), but the exact mechanism of the anti-viral function has not been confirmed.

Dargan, D. J., and Subak-Sharpe, J. H., ( J. Gen. Virol., 1985-1986) reported antiviral action of carbenoxolone and cicloxolone on herpes simplex virus. Their dose-response experiments showed cicloxolone sodium or carben¬ oxolone sodium interfered with the HSV replication cycle and reduced the infectious virus yield by 10,000- to 100,000-fold, cicloxolone being the more potent anti-herpes agent, but no consistent effect on HSV DNA synthesis was identified. Some inhibition of cellular DNA synthesis was observed, but this was relatively slight.

Csonka, G. W. and Tyrrell, D. A. (Br. J. Vener. Dis. 1984, 60 (3) pl78) undertook a double blind clinical study to compare the efficacy of carbenoxolone and cicloxolone creams with placebo in initial and recurrent herpes genitalis and reported significant differences in the time to disappearance of pain and the healing of lesions using cicloxolone, but carbenoxolone showed insignificant beneficial effect.

GTPDs have also been evaluated therapeutically as anti-viral agents in the chemotherapy of acquired immune deficiency syndrome (AIDS) (Ito, M., Yamamoto, N., Yakaguaku Zasshi (Japan) 188,2 1988), treatment of Epstein- Barr virus (EBV) infections (Van Benschoten, M. M., Am. J. Acupunct, 16,1 1988), and in the treatment of chronic hepatitis (Fujisawa, K. et al., Asian Med. J. (Japan), 23,10 1980).

The anti-viral activity of GTPDs varies so unpredictably as to preclude any generalized statements as to whether such compounds have general anti-viral effect or even as to whether such compounds will generally have anti-viral value as to any given virus. While GTPD drugs do, in some environments and under some conditions, exhibit some activity against some viruses, no anti-viral therapy based on GTPDs or in vitro anti-viral application of GTPDs has been generally accepted. The AIDS-causing viruses, HIV-I and HIV-II, are the first retroviruses identified as pathogenic in man. While HIV are more fragile than most infectious viruses and are susceptible to destruction by most virus-inactivating methods, such

^' as heating, use of detergent compounds, etc., these methods also damage cells.

In addition, any substance added to blood will, unless removed, remain in the medium, and must, therefore, be non-toxic when the medium is used.

The addition of detergents to various blood fractions has been described. My European Patent Specification 0 050 061, published December 11, 1985, in which the term "detergent" is equated with the term "amphophil" to encompass cationic, anionic and nonionic detergents, describes the addition of various detergents to plasma protein products and suggests the addition thereof to other blood derivative products to inactivate virus and for other purposes, followed by the removal of the detergent from the product. High concentrations of detergents, from 0.25 to 10%, were required the process described in the European patent specification.

Bosslet and Hilfenhause, European Patent Specification 0 278 487, discloses that high concentrations of selected detergents inactivate certain envelope viruses.

Neurath and Horowitz, e.g. U.S. Patents 4,540,573, 4,481,189, and

4,591,505, indicate, however, that detergent alone is not effective as an antiviral agent in blood plasma and related products. In spite of these teachings, however, it seems safe to conclude that at least some classes of detergents in high con- centrations in some types of blood derivatives do have some inactivating effect.

The extent and efficacy oi such procedures seems open to considerable doubt, however.

The major constituent of plasma is albumin whose primary role is that of osmotic regulation; it is responsible for 75-80 % of the osmotic pressure of plasma. Albumin also serves important roles in the transport of small molecules such as drugs.

An important feature which segregates albumin from other colloids as well as crystalloids is its unique ability to bind reversibly with both anions and cations; hence, albumin can transport a number of substances including fatty acids, hormones, enzymes, dyes, trace metals, and drugs. Substances which are toxic in the unbound or free state are generally not toxic when bound to albumin. This

binding property also enables albumin to regulate the extracellular concentration of numerous endogenous as well as exogenously administered substances.

Albumin in general has three types of binding sites (one for acidic, one for basic, and one for neutral compounds), and it plays a critical role in the binding and transport of lipid and lipid-soluble material. Albumin binds with and transports many administered drugs. Because of the phenomenon of mutual displacement of similar type substances, adverse drug interactions may occur. This phenomenon may have important ramifications during disease states such as sepsis, burn injury, and circulatory shock due to a number of etiologies, especially in conjunction with treatment with drugs which may be toxic at high concentra¬ tions.

Human serum albumin is believed to be a scavenger of oxygen-free radicals, an important phenomenon which also extends to scavenging of radicals required for lipid peroxidation. Albumin is a potent scavenger of oxygen radicals. Concentrations of human serum albumin below those present in normal human plasma completely inhibit the inactivation of α,'-antiproteina ^' se (α_,-pro einase inhibitor [α,-PI], α,- antitrypsin) by hypochlorous acid.

It is known that albumin binds to glycyrrhizic triterpenoids. Carben- oxolone is a potent ulcer-healing drug which is extensively bound to plasma proteins and therefore has the potential for displacement interaction. Carben¬ oxolone has been shown to be bound to human serum albumin in vitro at a different class of binding site to many other drugs and does not potentiate the pharmacological activity of warfarin, tolbutamide, chlorpropamide or phenytoin in the rat. Thornton PC; Papouchado M; Reed PI Scand J Gastroenterol Suppl

1980, 65 p35-9

The binding of glycyrrhizin to human serum and human serum albumin (HSA) was examined by an ultrafiltration technique. Specific and nonspecific bindings were observed in both human serum and HSA. The association constants (K) for the specific bindings were very similar: 1.31 x 10 ⁵ M ^'1 in human serum and 3.87 x 105 M ^'1 in HSA. Glycyrrhizin binds to only the albumin fraction. It

was concluded that the glycyrrhizin-binding sites in human serum exist mainly on albumin and glycyrrhizin binds to specific and nonspecific binding sites at lower and higher concentrations than approximately 2 mM, respectively. Ishida S; Sa ya Y; Ichikawa T; Kinoshita M; Awazu S , Chem Pharm Bull (Tokyo) 37 (1). 1989. 226-228.

Comparison by equilibrium dialysis of plasma protein binding sites for carbenoxolone in people under 40 yr of age and in people over 65 yr of age showed that the number of binding sites was reduced in the elderly and that this fall was associated with a reduction in plasma albumin levels. Hayes M J; Spraclding M; Langman M, Gut 18 (12) 1977 1054-1058.

Albumin has been used as an emulsion stabilizer oil-and-water emulsion injectable medical preparations, e.g. fluorbiprofen, Mizushima et al, U.S. Patent 4,613,505, Sept. 23, 1966; as a binding molecule for tryptophan, Pollack, U.S. Patent No. 4,650,789, Mar. 17, 1987; with chemical modification as complexing agents for cholesterol derivatives, Arakawa, U.S. Patent No. 4,442,037, Apr. 10, 1984; as conjugates with enzyme chemically linked to an antibody, Poznansky, U.S. Patent No. 4,749,570, June 7, 1988; and as chemically coupled conjugates of leukotrienes, Young, et al, U.S. Patent No. 4,767,745, Aug. 30, 1988.

See UNIQUE FEATURES OF ALBUMIN: A BRIEF REVIEW, Thomas E. Emerson, Jr., Ph.D., Critical Care Medicine, Vol. 17, No. 7 (1989), for a recent review of the characteristics of albumin.

The major hazard in producing fractions from large pools of plasma is the transmission of virus, the most serious, being hepatitis. This is a danger both for the recipient of the fractions and for the workers in fractionation plants. It has been shown that fractionation workers, particularly those engaged in the preparation of plasma pools, are at high risk of developing hepatitis B.

Another hazard of plasma fractionation is the partial denaturation of some fractions such as ISG, caused by the fractionation methods. These denatured proteins may have toxic effects or may be immunogenic in the recipients. Among these undesirable side effects is the significant degree of loss of biological competence and the loss or blockage of many binding sites on albumin are lost by

the inherent denaturation resulting from this pasteurization or heating process. According to present technology, the disadvantages of denaturation are more than compensated for by the increased stability and potency of concentrated fractions, but there remains a great need for a fully bio-competent albumin.

Summary of the Invention It has now been discovered that glycyrrhizin, carbenoxolone and cicloxolone and the analogues thereof inactivate CMV, and other viruses, in transplant organs and are known to be well-tolerated physiologically. Viral inactivation, as used here, means rendering the virus non-infective, i.e. the virus does not induce disease in a patient. In most instances traditional methods of quantifying virus population growth and reduction, e.g. log kill (See Fraenkel-Conrat, H., Kimball, P.C., and Levy, J.A. VIROLOGY, Second Edition, Prentice Hall, Englewood Cliffs, N.J., 1988, and Jakoby, W. H. and Pastan, I. H. (Eds), CELL CULTURE, (Volume LVIII of "Methods in Enzymology", Academic Press, Inc. , New York, Chapter 11) are good indicators of viral inactivation. ^' However, viral inactivation is accomplished by GTPD- Albumin beyond the log kill measurement since any remaining virus are incapable of infecting a patient and are incapable of replicating. This invention relates to methods for treating transplant organs with glycyrrhizic triterpenoid compounds, e.g. glycyrrhizic acid, its analogues such as carbenoxolone and cicloxolone, analogues thereof and the salts, esters and other derivatives thereof.

This invention is also embodied in transplant organs in which the fluid constituent consists essential of a solution of glycyrrhizic triterpenoid compounds, the transplant being substantially free of active CMV.

This invention is embodied in the process of treating organs from a donor comprising infusing the transplant organ with an effective amount of a glycyrrhizic triterpenoid compound consisting essentially of glycyrrhizin, carbenoxolone, cicloxolone analogues and derivatives thereof, or mixtures thereof, for inactivating CMV and other viruses.

This invention is also embodied in a process using a composition of matter consisting essentially of a glycyrrhizic triterpenoid compound consisting essentially of glycyrrhizin, carbenoxolone, cicloxolone analogues and derivatives thereof, or mixtures thereof in a concentration of from about 0.05 w/% to about 10 w/%, preferably in the range of from about 0.5 to 3 percent, which is effective to inactivate CMV and/or other viruses to infuse transplant organs and maintaining the organ for a sufficient time, typically from 15 minutes to an hour after complete infusion is accomplished, to substantially inactivate CMV and other susceptible viruses which may be present in the transplant organ. Description of the Preferred Embodiment

The preferred method of carrying out the invention comprises providing an aqueous solution which contains a concentration of the glycyrrhizic triterpenoid compound, e.g. glycyrrhizin, carbenoxolone or cicloxolone to comprise from about 0.0001 weight/percent to about 10 weight percent of the solution, the concentration being sufficient to inactivate CMV and/or other viruses in transplant organs when the organ is infused with the solution. The infusion is carried out for* a sufficient period of time to assure that substantial all of the fluid in the organ has been displaced with the glycyrrhizic triterpenoid compound solution. The time will, of course, depend upon the nature and size of the organ. While the invention is not limited to the use of the use of glycrrhizic compounds in any particular solution, it is desirable to include such compounds in solutions prepared for organ infusion, such as, for example, Collins Solution which contains potassium and phosphate in concentrations similar to normal cell fluids. Collins Solution may be modified, if desired, as Collins C _z solution, which includes dextrose and magnesium sulfate, or as Euro-Collins Solution, which contains dextrose, or in any other desired way. Any physiologically acceptable solution may, of course, be used, and reagents for particular purposes may also be included in the infusion solution.

It has been established that an exemplary glycyrrhizic triterpenoid compound, carbenoxolone and cicloxolone, as will as glycyrrhizic acid, and derivatives thereof, typically in the form of salts, in a concentration range of from

about 0.0001 to 10 wt/% effectively inactivates CMV by at least one log (one logarithmic factor). Solutions of glycyrrhizic triterpenoid compounds in the range of from about 0.5 to about 2 or 3 percent are presently considered optimal as to concentration. Perfusion data using kidney tissue as the exemplary implant tissue established the feasibility of 100% perfusion resulting in the removal of virus- containing natural liquids and inactivation of CMV virus in the organ.

Complete organs, e.g. kidneys, corneas, etc., and tissue, either as a body or comminuted, may be treated according to this invention. Such tissues, whether or not complete organs, are prepared, according to this invention, to result in solid tissue, in whatever form the tissue is desired, bathed or saturated in or substantial¬ ly entirely wetted by an infusion or perfusion solution which comprises one or more glycyrrhizic triterpenoid compounds, and may include enhancing materials such as detergent, glycerol, EDTA or albumin. The tissue may be implanted containing such solution or washed free of the infusion or transfusion solution before transplantation.

The risks of CMV, and other virus, infection resulting from implanting an untreated organ are very great. In a very high percentage of such cases, serious CMV infection results, which, not infrequently, is fatal. Some apprecia¬ tion of the importance of eliminating pathogenic viruses, the most common of which is CMV, from organs before implanting the organ into a patient is gained when one realizes that from one in ten to one in three donee's will succumb to infection. Such procedures are acceptable only because there is no acceptable alternative.

The present invention inactivates CMV the most common, and one of the more serious, of the pathogenic viruses found in transplant organs. The invention also inactivates HIV, the AIDS causing virus, which are far less common than CMV but, when received by a patient in a weakened state, as is nearly always the case, is nearly always fatal. Hepatitis viruses will, it is believed, be inactivated, but conclusive data proving inactivation of HBV are not yet available. The anti-coagulant characteristics of the glycyrrhizic triterpenoid compounds of this invention are an added benefit by reducing the likelihood of

thrombus formation in the implant organ and resulting emboli in the cardiovascu¬ lar system.

Data indicate that carbenoxolone, over a comparatively short period of time, about an hour or less, is bound by proteins and/or lipids and/or lipoproteins. Such data provide the basis for a nearly ideal method of treatment of solutions and organs for transfusion or implantation is now possible. According to this nearly ideal method, carbenoxolone is added to a fluid, such as blood, blood plasma, tissue culture medium or nutrient, or the like, which contains or to which protein, lipid, or lipoprotein is added, either contemporaneously or subsequently. The virus in the fluid are inactivated immediately, before the carbenoxolone is completely bound, and, thereafter, the carbenoxolone is completely bound. If the protein, etc. , is added, the addition can be effected after inactivation of the virus. When the fluid, e.g. blood or plasma, is transfused or the organ transplanted into the donee-patient, the fluid or organ is free of carbenoxolone. While car- benoxolone is well-tolerated, the ideal would be to avoid the introduction of any foreign substance not necessary to the in vivo functioning of the fluid or implant organ. This ideal is attainable using the principles of this invention.

A combination of a GTPD compound and albumin, referred to here as GTPD-Albumin, significantly enhances the effectiveness of the GTPD when added, in lieu of or in addition to GTPD alone, at any stage, directly or indirectly, to the infusion or perfusion solution. An amount of the GTPD compound, e.g. glycyrrhizin, glycyrrhetinic acid, carbenoxolone or cicloxolone in combination with albumin, the combination being referred to as GTPD-Albumin, is added sufficient to inactivate CMV and/or other viruses in the organ treated with infusion or perfusion solution such that the GTPD comprises from about 0.001 weight/percent (w/%) to about 10 w/%, generally in the range of about 0.05 to about 3 w/%, of infusion or perfusion solution.

Albumin from any source which is safe for intravenous use may be used to form GTPD-Albumin for use in this invention. Conventional caprylate stabilized, heat treated albumin may be used, for example. GTPD-Albumin is prepared simply by mixing GTPD into an albumin solution and allowing the

solution to equilibrate a sufficient period of time, a few minutes being sufficient, to assure homogeneity and the formation of GTPD-Albumin. It is convenient to form a saturated solution of GTPD-Albumin, allow it to stand overnight and, if necessary, to filter the solution to assure that any excess GTPD or any precipitate is removed, and then to dilute the GTPD-Albumin solution as desired, or use it full-strength as an additive to infusion or perfusion solution. Prolonged standing or storage, e.g. several days to a few weeks, is not detrimental. The GTPD- Albumin is then mixed with the infusion or perfusion solution. After infusion or perfusion, the organ is maintained at a suitable temperature long enough, as discussed above, to inactivate the virus which may be in the organ. For example, GTPD-Albumin may be prepared the day preceding or a few hours before preparing the organ perfusion or infusion solution or adding the GTPD to the organ perfusion or infusion solution. The GTPD-Albumin - organ perfusion or infusion solution and the organ thus treated is, preferably, maintained at about 37°C. plus or minus about 8°C. for an hour or more and the virus-inactivated organ is then implanted and handled in any conventional manner.

Particularly striking result ^' s are accomplished using albumin which has not been stabilized in the traditional way, e.g. with caprylate, and has not been heated. According to the prior art, such an albumin product would be regarded as unsafe because of the potential presence of pathogenic virus. If, however, the stabilization step and the heating step are replaced by the addition of GTPD to the albumin, the virus are inactivated and the albumin is biologically competent. GTPD-Albumin formed in this manner has higher biological activity than GTPD- Albumin prepared from conventional albumin. In a test using a VSV/BVD sensitive cell line performed when the cells were in log phase, the samples were inoculated with 10' pfu of vesicular stomatitis virus (VSV), incubated overnight and serially diluted in MEM with 10% FBS (fetal bovine serum), and then inoculated with VSV. The 0.10% GTPD (carbenoxolone) alone and 0.10% GTPD (carbenoxolone) in 5% solutions of various albumins were introduced at dilutions of from 1: 10 ² to 1: 10 ⁹ . The cells were examined daily for five days for virus caused CPE. following table summarizes the comparative results.

LOG KILL OF VSV BY TPD

Log Kill Albumin Used Five Days

None 4.6

Baxter Buminate ^® (USP Lot 2746M011 AA) 1.3

Miles Human Albumin Fatty Acid Free (Lot 82-324) 1.6

Hyland IS 9988 Human Albumin 2.0

Non-Stabilized, solvent detergent albumin ⁾ 5.6+ ^ω Human serum albumin prepared by Cohn Fractionation, Solvent-

Detergent precipitation and alcohol ultrafiltration, not heated and no stabilizer, e.g. caprylate or tryptophan added.

It should be noted that at extreme dilutions of GTPD, binding to albumin may actually reduce antiviral activity; however, higher concentrations of GTPD can be used and the viral inactivation is not decreased even with the least biologically competent albumin and enhancement is generally observed.

Non-stabilized, non-heated albumin is, however, vastly superior to "conventional", i.e. stabilized and pasteurized, albumin, presumably because of a greatly increased ability to form GTPD-Albumin as a result of greater biological competence. Even at extreme dilution, an approximately 6 log kill was found. ^• At lower dilutions (higher concentrations of GTPD) the kill was apparently complete, probably 7 to 9 logs.

It has also been found that the deactivation of anti-viral power of GTPD by lipoproteins and/or fatty acids is eliminated or greatly reduced by adding the GTPD as GTPD-Albumin. It is important, therefore, that the GTPD-Albumin be formed using delipidated albumin, to obtain maximum effect with minimum concentration. If, for example, it were desired to use the infusion or perfusion solution in connection with an organ rich in lipids and lipoproteins, it may be of beneficial, using the albumin enhancement, to prepare GTPD-Albumin before addition and add the GTPD as GTPD-Albumin.

The ability of albumin to (a) bind GTPD and (b) not reduce and generally to enhance the viral inactivation power of GTPD. These results mean that GTPD can be carried into the system via albumin without losing its viral inhibition power, can be used at much higher concentrations than would otherwise be possible.

As reported in the prior art, it is known that GTPD will bind to albumin. The nature of the binding, which results in GTPD-Albumin, is not fully understood. GTPD bound to albumin would be expected to be less active chemically and biologically. Quite surprisingly, however, it was found that the viral inactivation characteristics of GTPD bound to albumin were not only not decreased but were, in some instances at least, enhanced.

In all embodiments, the invention exhibits a number of surprising results. The spotty results reported in efforts to determine if, and to what extent, GTPD compounds are indeed virucidal agents led the art to believe, as has been reported, that "the likelihood of developing a blood additive that would kill HIV and HBV and have no effect on laboratory examination of blood seems small." (Peter C. Fuchs, M.L.O., Oct. 1988, 13). In addition, notwithstanding the prior art in which anti-viral activity, to the extent it exists, of GTPD compounds is uncertain, unpredictable and, as yet, unexplained, and the widely accepted proposition that no infusion or perfusion solution additive could be found which would inactivate blood-borne viruses without adversely effecting the infusion or perfusion solution. The present invention embodies a processes and infusion or perfusion solution compositions in which these desired but hitherto unattainable results are accomplished. ^" Carbenoxolone, alone, at a concentration of 0.01 wt/% was compared with carbenoxolone was compared with 0.01 carbenoxolone containing, respectively, 0.00025, 0.005 and 0.01 wt % of glycerol, and, in another test, with 0.0005, 0.001 and 0.002 wt% detergent, TRITON X-100 ^® . The test used a VSV/BVD sensitive cell line (EBtr = embryonic bovine tracheal fibroblast). The test was performed when the cells were in log phase to optimize virus-caused CPE. The samples were inoculated with 10 ⁹ pfu of VSV and incubated. The

samples were then serially diluted with MEM with 10% FBS to reach a 9-fold dilution of the virus. The serial dilutions were inoculated in quadruplicate wells (24 well plate of Ebtr cells) and inoculated at 37°C. VSV il was increased by the addition of glycerol or the detergent, except that extremely dilute solutions of glycerol did not give a significant enhancement of virus inactivation.

Thus, it has been established that an exemplary glycyrrhizic triterpenoid compound, carbenoxolone, glycyrrhizin and cicloxolone, as well as glycyrrhizic acid and derivatives thereof, typically in the form of salts, in a concentration range of from about 0.001 to 0.005 to 10 wt % when combined with one or more enhancers, e.g. glycerol, detergent, EDTA or albumin, in the range of from 0.001 to 0.0001 to 5 wt %, preferably under about 0.001 to 0.01 wt/%, greatly accelerates the inactivation of virus and increases the ultimate inactivation, typically by at least 1 log and as high as 3 logs.

Solutions of glycyrrhizic triterpenoid compounds in the range of from about 0.1 to about 2 or 3 wt/% are presently considered optimal as to concentra¬ tion, lower concentrations of glycyrrhizic triterpenoid compounds being possible when combined with detergent.

The full scope of types of detergents which may be used in this invention has not been fully determined. The essential requirements are that the detergent have a high detergency action and not interfere with the laboratory tests, at the level of addition involved.

The preferred detergents are classed as nonionic detergents, examples of which include: polyoxyethylene-based detergents such as TWEEN ^® and octyl phenoxy polyethoxy ethanol-based detergents such as TriTON X-100 ^® , which are preferred, and detergents based upon polyethylene glycol and condensation polymers of ethylene oxide and propylene glycol. These are, of course, merely examples of some of the more common classes of detergents suitable for use in this invention and other classes of nonionic detergents may be used.

Ionic detergents such as, for example, sodium lauryl sulfonates, may also be used, but it may be necessary to make adjustments in the laboratory procedures or results to compensate for the addition of components of the detergent.

A comparison of results using GTPD compounds alone by adding from approximately 0.0001 to 5 wt/%, preferably 0.001 to 1.0 and to 0.0001 to 0.1 wt/% detergent to accomplish virus inactivation, two results were striking. First, inactivation adequate for most purposes, e.g. 2-4 log kills, could be obtained in a fraction of the time previously required. Secondly, the ultimate inactivation was increased by a minimum of 1 log in most cases and typically up to 3 logs, or more, in some instances.

The result was particularly surprising in view of the general lore of the art that low levels of detergent have little or inadequate anti-viral effects. Quite clearly, there is more here than a mere additive effect, since the GTPD effect plus a negligible or zero effect would have been predicted. It is speculated that in some way the detergent renders the cell membrane more accessible to GTPD, which is believed to attach to the membrane but which as no detergency of consequence. This is, however, only a speculation, and there is no hard evidence to support an elucidation of the mechanism of action.

The speed of action and ultimate inactivation achievable using GTPD alone or with detergent is also significantly increased by maintaining the infusion or perfusion solution at approximately body temperature, 27°C. or higher, up to 40-

45°C, preferably, or up to 60°C. if desired to accelerate inactivation or for other reasons.

It may not be necessary to remove the very small, trace amounts of non- toxic detergent which is sufficient for the present invention. This feature, alone, is of very significant economic and practical importance.

Solutions of glycyrrhizic triterpenoid compounds in the range of from about 0.01 to about 2 or 3 wt/% are presently considered optimal as to concen¬ tration, lower concentrations of glycyrrhizic triterpenoid compounds being possible when combined with glycerol.

A comparison of results using GTPD compounds alone and GTPD modified by adding from approximately 0.0001 to 5 wt/%, preferably 0.001 to 0.1 wt%, glycerol, to accomplish virus inactivation was striking. First, inactivation adequate for most purposes, e.g. 2-4 log kills, could be obtained in

a fraction of the time previously required. Secondly , the ultimate inactivation was increased by a minimum of 1 log in most cases and typically up to 3 logs, or more, in some instances.

The result was particularly surprising in view of the general lore of the art that low levels of glycerol have little or inadequate anti-viral effects. Quite clearly, there is more here than a mere additive effect, since the GTPD effect plus a negligible or zero effect would have been predicted. It is speculated that in some way the glycerol renders the cell membrane more accessible to GTPD, which is believed to attach to the membrane but which as no detergency of consequence. This is, however, only a speculation and there is no hard evidence to support an elucidation of the mechanism of action.

Solutions of glycyrrhizic triterpenoid compounds in the range of from about 0.01 to about 2 or 3 wt % are presently considered optimal as to concen¬ tration, lower concentrations of glycyrrhizic triterpenoid compounds being possible when combined with EDTA.

A comparison of results using GTPD compounds alone, by adding from approximately O.OOl to 5 wt/%, preferably 0.001 to 1 wt/% EDTA to accomplish virus inactivation was striking. First, inactivation adequate for most purposes, e.g. 2-4 log kills, could be obtained in a fraction of the time previously required. Secondly, the ultimate inactivation was increased by a minimum of 1 log in most cases and typically up to 3 logs, or more, in some instances.

Quite clearly, there is more here than a mere additive effect. It is speculated that in some way the EDTA renders the cell membrane more accessible to GTPD, which is believed to attach to the membrane but which as no detergency of consequence. This is, however, only a speculation and there is no hard evidence to support an elucidation of the mechanism of action.

The GTPD compounds can be mixed with other active compounds with synergistic results in inactivation of virus. Such synergistic and potentially synergistic compounds include the anti-viral drug AZT, which is known to act synergistically with the GTPD compounds, dextrans, butyl hydroxy toluene, fatty

acids such as oleic acid, chelating agents such as EDTA, and compounds of transition and heavy metals.

The GTPD compounds can be mixed with other active compounds with synergistic results in inactivation of virus. Such synergistic and potentially synergistic compounds include the anti-viral drug AZT, which is known to act synergistically with the GTPD compounds, dextrans, butyl hydroxy toluene, fatty acids such as oleic acid, chelating agents such as EDTA, and compounds of transition and heavy metals.

In the case of whole blood, plasma or other fluid collection in a bag, vacuum tube, vial or other container, a highly desirable and preferred method and apparatus are utilized. The GTPD compound, in dry form, is in or associated with the container and is dissolved and added to the fluid either immediately before collection or soon afterward. Since some forms of the GTPD compounds decompose in solution, a fresh source of the GTPD compounds is provided by the method just described.

Industrial Application . . .

This invention has direct application in the organ bank industry and in the practice of medicine.