WO1994003194A1 - Extract and pharmaceutical composition for treatment of calcium oxalate stone disease and viral infections - Google Patents

Abstract

A compound for the treatment of calcium oxalate kidney stone disease and viral infections caused by enveloped viruses which can be extracted and purified from leaves of the plant Eriobotrya japonica is disclosed. The compound has the following characteristics: inhibits calcium oxalate crystal growth in vitro; inhibits renal calcium oxalate crystal deposition in rats which are fed ethylene glycol, causes rats which are fed ethylene glycol and said compound to excrete less oxalate in their urine as compared to rats which are fed ethylene glycol without said compound; shows little or no loss in activity when exposed to an aqueous solution of pH 1.5 for 14 hours; shows increased activity when exposed to an aqueous solution of pH 12.7 for 15 hours; is polyanionic; is stable when heated in an aqueous solution (at pH of extract) at 98 °C for 3 hours; water-soluble; insoluble in heptane, hexane, chloroform/methanol mix, diethyl ether, and ethanol/aqueous mix; binds to DEAE-A-25 Sephadex at pH 8.6; is eluted from the DEAE-A-25 Sephadex with 2 M Nacl; and prevents cytopathogenicity of enveloped viruses such as herpes simplex virus. The present invention is also directed to a method for the treatment of calcium oxalate stone disease wherein the compound is administered, preferably for a prolonged period of time, to a patient suffering from or prone to calcium oxalate stone disease. The present invention is also directed to a method for the treatment of viral infection.

Description

EXTRACT AND PHARMACEUTICAL COMPOSITION FOR TREATMENT OF CALCIUM OXALATE STONE DISEASE AND VIRAL INFECTIONS

BACKGROUND OF THE INVENTION Technical Field

The present invention relates to the treatment of calcium oxalate stone disease and viral infections.

Description of Background Art

Calcium oxalate is the most common constituent of urinary calculi and relatively large crystals of this salt are frequently found in freshly voided urine from patients with recurrent calcium-containing stones. The rate of crystal growth and aggregation of calcium oxalate will determine whether or not a particle large enough to be trapped at some narrow point in the urinary tract can be formed within the transit time of urine through the urinary system. The chance of a particle being trapped depends partly on the size of the particle. The rate of crystal growth may determine to a large extent the subsequent rate of growth of this nidus into a stone. It is well known that several urinary constituents (e.g., pyrophosphate, glycosaminoglycans, citrate) can inhibit the rate of growth and/or aggregation of seed crystals of calcium oxalate -in vitro.

Considerable research effort has been and is being expended in an attempt to identify or synthesize compounds that act as inhibitors of calcium oxalate crystal growth and which could be used for treatment of patients suffering from recurrent kidney stone disease. Hydrochloro-thiazide, sodium potassium phosphate, and potassium citrate are drugs available for the treatment of calcium oxalate stone disease and reported to reduce its recurrence. These and other drugs available have not been shown to dissolve or remove kidney stones/fragments. The development of drugs more effective in preventing calcium oxalate stone formation and to dissolve kidney stones/fragments is still needed. Since recurrence of stone disease is believed to be largely due to such remnant stone fragments in the kidney, following lithotripsy or other stone removal procedures, their dissolution could dramatically reduce recurrence rates.

Similarly, extensive work is being done to identify compounds that will inhibit the pathogenicity of viruses and prevent and/or treat viral infections. While some anti-viral agents are presently available, there is a great need for additional compounds that would be more active and more specific in preventing or treating various viral infections.

SUMMARY OF THE INVENTION Accordingly, it is an object of the present invention to provide an extract for treatment of calcium oxalate stone disease which is effective in practical use. More specifically, it is an object of the present invention to provide an extract for treatment of calcium oxalate stone disease which exhibits one or more of the following desirable properties (1) it is non-toxic, i.e., safe for human intake, (2) it is absorbed in the gut when taken by oral ingestion, (3) it is excreted by patients in urine, (4) it prevents the formation of and/or dissolves calcium oxalate kidney stones and (5) it does not adversely affect bones of patients treated with the compound.

It is also an object of the present invention to provide an extract which inhibits the cytopathogenic effects of enveloped viruses. The above objects are accomplished by providing a purified extract which possesses one or more of the following properties: inhibits calcium oxalate crystal growth jLn vitro; inhibits renal calcium oxalate crystal deposition in rats which are fed 1% ethylene glycol; causes rats which are fed ethylene glycol and the extract to excrete less oxalate in their urine as compared to rats which are fed ethylene glycol without the extract; retains activity when exposed to an aqueous solution of pH 1.5 for 14 hours; retains or shows increased activity when exposed to an aqueous solution of pH 12.7 for 15 hours; is stable when heated in a neutral aqueous solution at 98 "c for at least 3 hours; is water soluble; is insoluble in heptane, hexane, diethyl ether and chloroform/ methanol mix (1:1); is precipitated out of solution by absolute ethanol, ethanol:aqueous extract (2.5:1 by volume); binds to DEAE-A-25 Sephadex at pH 8.6; is eluted from the DEAE-A- 25 Sephadex with 2M NaCl, which is evidence that it is anionic; binds to calcium oxalate crystals; has an isoelectric point (pi) of 2.7 ± 0.5 (SD) ; and inhibits the cytopathogenic effects of enveloped viruses.

The present invention is also directed to a modified extract which can be formed by treating the extract of the present invention at a basic pH such as a pH of 12 or more to thereby produce a modified extract which has increased inhibitory activity against calcium oxalate crystal growth as compared with the extract which has not been treated with base. Based on in vitro studies, this modified extract appears to have the same properties as the untreated extract except that it has a higher activity as discussed above. The modified extract is preferably used in a purified form. The present invention is also directed to a purified extract fraction which can be prepared by precipitating with ethanol the extract obtained from the cells of the plant Eriobotrva aponica. treating with alkali and chromatographing the supernatant on a Sephadex G-75 column, and collecting the fractions which elute after the fractions containing maximum inhibitory activity against calcium oxalate crystal growth. Said purified extract fraction inhibits the cytopathogenic effects of enveloped viruses, and retains its activity when exposed to an aqueous solution of base.

The purified extract fraction of the present invention which inhibits the cytopathogenic effects of enveloped viruses can be prepared from the extract of the plant Eriobotrva iaponica. by treating the supernatant (obtained following ethanol treatment of the extract and centrifugation) with alkali, then with HC1, followed by ethanol precipitation, and the lyophilized precipitate chromatographed on Sephadex G-75. The active fractions (active against calcium oxalate crystal growth) , which are combined and reprecipitated with ethanol, inhibit the cytopathogenic effects of herpes simplex virus, and retain their activity when exposed to an aqueous solution of base. Compounds that inhibit the cytopathogenicity of one enveloped virus, such as herpes simplex virus, may also be active against other such enveloped viruses (Baba et al, Antimicrobial Agents and Chemotherapy -32., 1742, 1988).

The extract of the present invention can be prepared by a variety of established methods for both extraction and purification. One such method is the one described in the present application. In another approach, for example, the extract of the present invention can be prepared by obtaining the extract from cells of the plant Eriobotrva iaponica. purifying the extract by contacting the extract with an anion exchange material which selectively binds negatively charged materials, and recovering the extract from the anion exchange material .

The present invention is also directed to a pharmaceutical composition suitable for the treatment of calcium oxalate stone disease which contains an effective amount of the above-described extract with or without an appropriate pharmaceutically acceptable carrier therefor, a method for treating calcium oxalate stone disease which comprises administering to a subject an effective amount of the above-described extract or composition.

The present invention is also directed to a pharmaceutical composition suitable for inhibiting the cytopathogenic effects of enveloped viruses such as herpes simplex virus in a patient in need of said inhibition, which composition contains an effective amount of said purified composition or an effective amount of said purified extract fraction, together with a pharmaceutically acceptable carrier therefor. The present invention is also directed to a method for treating enveloped viruses by administering to a patient who has been diagnosed as having said enveloped viruses an effective amount of said purified composition, or of said purified extract fraction, optionally with a pharmaceutically acceptable carrier. More particularly, said patient is a mammal or human which has been diagnosed as having said enveloped virus.

DESCRIPTION OF THE PREFERRED EMBODIMENT

The extract of the present invention is preferably present in a purified form when administered to a patient. When the extract is extracted from plant leaves, it is desirable to separate soluble extract from

(residual) particulate matter by appropriate means

(filtration, centrifugation, or other separation techniques, etc.) . The utility of the extract as a therapeutic agent is enhanced by greater purification. Greater dosages may be necessary for less pure forms of the extract.

The extract of the present invention is preferably substantially free from heavy metals, contaminating plant materials, contaminating microorganisms, oxalic acid or precursors of oxalic acid or any other contaminants which would normally be present in a crude preparation derived from plant material.

After purification, the extract should have a purity level of at least 50,000, preferably at least 150,000 and more preferably at least 175,000 Units of activity per gram of solid matter. The extract prepared to date has a purity level of between about 50,000 and about 250,000, preferably between about 150,000 and about 250,000, and most preferably between about 175,000 and about 200,000 Units of activity per gram of solid matter, i.e., matter remaining after evaporation of all liquids. As used in this application, the term "units" is defined as follows. One unit of inhibitory activity is defined as the quantity of extract that causes 50% inhibition of calcium oxalate crystal growth in the assay system described. Zero inhibition is where the amount of radioactivity lost from solution, during the assay, is equivalent to or more than that lost from the Reference sample. One hundred percent inhibition is where there is no loss of radioactivity from solution during the crystal growth assay. To Calculate % inhibition of any sample:

1. Determine dpm (disintegrations per minute) lost from reference sample (Reference Sample has 0.15 M NaCl in place of sample) = Total dpm added/100 μl - dpm/100 μl in solution at end of the assay

2. Determine as in (1) dpm lost from the analytical sample

3. Calculate difference between dpm lost (reference sample) and dpm lost (Analytical Sample) 4. Calculate (difference obtained in setp (3))/(dmp lost (reference sample)) X 100 to determine % inhibition 5. Calculate units of inhibitory activity in analytical sample as % inhibition ÷ 50

Example:

Calculation of % inhibition and inhibitory activity of extract #60, Table 1. = 5,818 dpm

= 1,520 dpm

= 4,298 dpm

= 73.9% inhibition

= 1.48 Units of

inhibitory activity/10 μl of Extract #60

The following abbreviations, wherever they are used in this application, shall have the meanings ascribed thereto unless some other meaning is clearly required by the context in which such term is used: AA (Atomic Absorption) , BUN (Blood Urea Nitrogen) , Ci (Curie) , dpm (disintegrations per minute) , EDTA (ethylenediamine- tetraacetic acid) , EG (ethylene glycol) , EGTA (ethylene glycol-bis (beta-aminoethyl ether)-N,N,N' ,N' ,- tetraacetic acid), g (gravity), gr (gram(s)), h (hour(s)), HSV (herpes simplex virus) , kg (Kilogra (s) ) , M (molar), mg (milligram(s) ) , ml (milliliter(s) ) , N (normality) , NS (not significant) , P-P (pyrophosphate) , and rpm (revolutions per minute) , U (units) , V (volume) , W (weight) , pi (isoelectric point) .

The extract of the present invention can be used for the treatment and/or prevention of calcium oxalate stone disease by administering an effective amount of the extract to a subject. For laboratory experiments, laboratory mammals such as rats, mice, monkeys, as well as other mammals can be used. However, the ultimately desired use is to treat human patients who suffer from calcium oxalate stone disease. The extract of the present invention can also be used to inhibit the cytopathogenic effects of enveloped viruses, such as HSV, in mammals, more particularly in humans.

Although at present isolation of the extract from the leaves of Eriobotrva iaponica plants is the most practical method for obtaining the extract, the present invention also contemplates obtaining the extract from other sources such as other plants which may contain recoverable amounts of the extract. It is also possible that the extract could be obtained by culturing plant cells, such as Eriobotrva iaponica cells, in vitro and extracting the active ingredients from the cells or recovering the active ingredients from the cell culture medium. The present invention also contemplates the use of synthetic extracts having the above-described characteristics. Presumably, such synthetic compounds could be synthesized after the chemical structure of the compound of the present invention has been elucidated.

As used herein, the term "extract" means the active ingredients isolated from leaves or other parts of Eriobotrva iaponica or other natural sources including but not limited to all varieties, species, hybrids or genera of the plant regardless of the exact structure of the active ingredients, form or method of preparation or method of isolation. The term "extract" is also intended to encompass salts, complexes and/or derivatives of the extract which possess the above- described biological characteristics or therapeutic indication. The term "extract" is also intended to cover synthetically or biologically produced active ingredients with the same or similar characteristics yielding the same or similar biological effects. It is contemplated that the extract will be formulated into a pharmaceutical composition comprising an effective amount of the extract with or without a pharmaceutically acceptable carrier. The pharmaceutically acceptable carrier may be any carrier which is non-toxic, i.e., safe for human intake, and which is compatible with the extract and the desired route of administration.

Pharmaceutically acceptable carriers are materials useful for the purpose of administering the extract, which are preferably non-toxic, i.e., safe for human intake, and may be solid, liquid or gaseous material, which are otherwise inert and medically acceptable and are compatible with the active ingredient. The pharmaceutically acceptable carrier may be a carrier of a type which has been or would be approved by the Food and Drug Administration for administration to human subjects. The pharmaceutical composition may also contain other active ingredients. For oral administration, fine powders or granules may contain diluting, dispersing and/or surface active agents, and may be presented in a draught, in water or in a syrup; in capsules in the dry state or in a non- aqueous solution or suspension, wherein suspending agents may be included; in tablets, wherein binders and lubricants may be included; or in a solution or suspension in water or other liquid or a syrup. Where desirable or necessary, flavoring, preserving, suspending, thickening or emulsifying agents may be included. Tablets and granules are preferred and these may be coated.

For buccal administration the compositions may take the form of tablets, gum, syrups as well as other liquid forms, lozenges formulated in a conventional manner. The extract of the invention may also be formulated for injection and may be presented in unit dose forms in ampules or in multi-dose containers with or without an added preservative. The compositions may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain for ulatory agents such as suspending, stabilizing and/or dispersing agents. Alternatively, the active ingredient may be in powder form for constitution with a suitable vehicle, e.g., sterile physiological saline, before use.

Therapeutic or Pharmaceutical Compositions for the prevention/treatment of Renal Stone Disease In a particular embodiment of the invention, the therapeutic or pharmaceutical composition comprises the extract in an effective unit dosage form. As used herein, the term "effective unit dosage" or "effective unit dose" means a predetermined amount of the extract sufficient to be effective for dissolution of calcium oxalate kidney stones in vivo or effective to prevent or reduce the degree of formation of kidney stones -in vivo. Pharmaceutically acceptable carriers are materials useful for the purpose of administering the extract, which are preferably non-toxic, i.e., safe for human intake, and may be solid, liquid or gaseous material, which are otherwise inert and medically acceptable and are compatible with the active ingredient. The pharmaceutically acceptable carrier may be a carrier of a type which has been or would be approved by the Food and Drug Administration for administration to human subjects which have experienced calcium oxalate kidney stones. The pharmaceutical compositions may contain other active ingredients such as magnesium. Vitamin B₆ or potassium citrate. The pharmaceutical composition may also contain other active ingredients which are effective against calcium oxalate kidney stone disease.

The pharmaceutical compositions may be administered orally or parenterally, including by injection, subcutaneously or used as a suppository or pessary. The only limitation on the route of administration is that the extract should reach the kidneys in an amount effective to treat kidney stone disease. It is also possible that it may be desirable for the extract to reach the urinary tract or bladder of the patient being treated. The compositions may contain 5,000 to 30,000, more preferably 10,000 to 20,000 Units of the extract per unit dosage. Typically, the extract will be present in an amount of 0.1 to 90 percent by weight of the pharmaceutical composition, preferably 0.5 to 50 percent by weight of the pharmaceutical composition.

At the present time, oral administration is preferred since the extract appears to be absorbed through the gut and transported to and excreted by the kidneys. For oral administration, the daily dosage as employed for adult human treatment may range from about 5,000 to 30,000 Units, preferably about 10,000 to 20,000 Units, which may be administered in 1 to 5 daily doses, for example, depending on the route of administration and the condition of the patient. When the composition comprises dosage units, each dosage unit may contain about 1,000 to 20,000 Units of active ingredient, preferably about 5,000 to 10,000 Units. Dosages for human therapy will be established by standard techniques through the experience gained in clinical trials. Initial estimates are based on the following assumptions.

In order to prevent renal stone formation in rats (300 gr weight) during ethylene glycol ingestion, a daily dose of 487 Units (unpurified extract) was administered. To treat a 70 kg man with recurrent calcium oxalate stone disease, the following calculated dose units, based on rat studies, may be appropriate. Rats were given 1623 Units/kg weight/day. In extrapolating from Units/kg in the rat to Units/kg in man for drug concentrations, a correction factor of 1/7 has been applied (Gσldin, A. et al, Quantitative and qualitative prediction of toxicity from animals to humans. In: Tagnon HJ, Stagnet MJ (eds.), Controversies in Cancer, New York: Masson Publishing USA, Inc., pp. 83-104 (1978)), resulting in 232 Units/kg/day for man (1623 x 1/7) . Using this treatment dose, a man of 70 kg should receive 16,240 Units of inhibitor/day. When the purified extract (inhibitor) contains 183,871 Units/gr, then a daily dose of 88 mg would provide the appropriate quantity of inhibitor. The extract preferably will be administered to a patient as soon as a diagnosis of stone disease has been made and more preferably after a determination that a patient suffers from recurrent kidney stones containing calcium oxalate. The treatment preferably will continue on a daily basis for at least five days, more preferably at least two weeks and even more preferably for at least one month. The extract may be administered at least three times a week for at least three months to prevent or reduce recurrence of stone disease. It is also possible that if recurrence of calcium oxalate kidney stones is or has been a significant problem for a particular patient, treatment may continue indefinitely, e.g., it may continue for the rest of a patient's life. It is anticipated that if the extract of the present invention is administered to patients for prolonged periods of time, the recurrence of kidney stones can be prevented or minimized.

It is also possible that other forms of treatment can be used in conjunction with administration of the extract of the present invention, i.e., ultrasound treatment to break up the stones can be utilized on a patient who has been treated with the extract of the present invention.

The extract could be used to treat the great majority of patients suffering from recurrent stone disease, since over 75% of all renal stones contain calcium oxalate. For example, the extract may be useful to prevent formation of stones by preventing or inhibiting nucleation, growth and/or aggregation of crystals. It could also be used to treat these patients following extracorporeal Shockwave lithotripsy to help ensure passage in the urine of shattered stone particles and renal crystal deposits. The extract may also be effective in treating patients with primary hyperoxaluria (a genetic disease resulting in massive over-production of oxalic acid) many of whom suffer total loss of renal function in the early years of life. The extract has potential use in dissolving recurrent renal stones in patients with a history of calcium oxalate stone disease. This could result in less frequent use of the lithotripter and other techniques now used to remove kidney stones. The extract may have use in treating patients post renal transplantation in order to prevent calcium oxalate deposition in the renal graft since many of these patients have substantial body stores of calcium oxalate following long-term dialysis. Finally, it is possible that the extract could be used to treat patients suffering from systemic oxalosis, i.e., deposition of calcium oxalate crystals in many tissues of the body. The stones being treated (or the formation of which is to be prevented) may be present in the kidney, bladder and/or urinary tract.

Therapeutic or Pharmaceutical Compositions for the Topical or Endogenous Treatment of Viral Infections

The extract or extract fractions that are active in preventing the cytopathogenic effects of the virus could be used to treat enveloped viral infections in human subjects in the following ways. i) A unit of blood withdrawn from a patient with the viral infection could be incubated in vitro with a concentration of the compounds shown to be effective against the virus. After an incubation period, determinable for each virus using methods known in the art, the blood could be transfused back to the patient. Repeated treatments in this manner could reduce the potential for viral associated disease. ii) Since the untreated extract has been administered orally to rats with no apparent side effects it could also be ingested by human subjects and may reduce the potential for viral associated disease. iii) It is conceivable that the compounds that are active against the virus could be administered intravenously to patients with viral infection after these compounds have been further purified. The compounds may be more effective when administered I.V. than orally since it is unlikely that 100% of the active compounds would be absorbed from the gastrointestinal tract. iv) It is also conceivable that the purified compounds active against the virus could be administered into the spinal fluid and may prevent the potential for viral associated disease in patients with viral infection.

Based on our in vitro data, a concentration of 46 to 230 μgr of the purified fraction (Sample 6, Example 20) per gram of cream or ointment should be effective for topical application in preventing the cytopathogenicity of the herpes simplex virus.

Based on our in vitro data, a concentration of 125 to 625 μgr of the unpurified extract (Sample l, Example 20) per gram of cream or ointment should be effective for topical application in preventing the cytopathogenicity of the herpes simplex virus.

Based on our in vitro data, Table 18, and on the n vitro results of Baba et al (Antimicrobial Agents and Chemotherapy 22., 1742, 1988) . it would appear that the extract preparations (Sample 6, Example 20) are at least as potent as heparin, pentosan polysulfate (PPS) and other glycosaminoglycans in inhibiting the cytopathogenicity of HSV and other enveloped viruses. Intravenous doses of PPS and multisulfated dermatin (MSD) of 40 and lOOmg respectively have been safely administered to human subjects (Danielson et al, in, Inhibitors of Crystallization in Renal Lithiasis and their Clinical Application. Eds. A. Martelli, P. Buli and B. Marchesini, Acta Medica, Bologna 1987, p. 193) . Oral doses of PPS, 500mg/day (Norman et al, Clin Sci 68, 369, 1985) and D-glucosamine, 750mg/day, (Strohmaier et al, in, Inhibitors of Crystallization in Renal Lithiasis and their Clinical Application, Eds. A. Martelli, P. Buli and B. Marchesini, Acta Medica, Bologna 1987, p. 205) have been administered daily to human subjects without significant adverse effects. Rats were administered oral extract preparations of 130 to 1300 mg/kg/day with no apparent side effects (unpublished data) . From the above results we suggest that I.V. dosages of 0.2 to 1.5 mg/kg and oral doses of 2.0 to 15.0 mg/kg/day would appear appropriate to inhibit the cytopathogenicity of the enveloped viruses without being toxic to the tissues.

It is contemplated that the extract will be formulated into a pharmaceutical composition comprising an effective amount of the extract with or without a pharmaceutically acceptable carrier (as previously described in this section) . EXAMPLES

The Examples that follow describe extraction of Eriobotrva iaponica plant leaves and the effect of the extract on: i) inhibition of calcium oxalate crystal growth in vitro, ii) inhibition of stone formation and crystal deposition in vivo in a rat model, iii) dissolution of renal stones in vivo in a rat model; and iv) inhibition of the cytopathogenic effects of herpes simplex virus.

EXAMPLE 1

Eriobotrva iaponica plant leaves are removed from a tree and are stored at -20^*C the day they are removed from the tree or extracted the same day. Before extraction, fresh or frozen leaves are gently hand- washed in water at 35^*C to remove surface dirt. Aliquots of the leaves are then homogenized in distilled water with a food mincer for two to four minutes at room temperature. The entire homogenate (containing 150 g of leaves) is combined in a conical Pyrex flask and made up to 1300 ml with further addition of distilled water. The homogenate is brought to a boil and allowed to simmer for 4.5 + 1.5 h. The temperature of the solution during the extraction is 90-105^*C. The extract is allowed to cool and the solution poured through a funnel containing a stainless steel wire mesh which retains the leaf particles. A precipitate which settles at the bottom of the flask is discarded and only the clear supernatant retained. The volume of the extract is brought to 1300 ml by addition of water to compensate for losses by evaporation during extraction. The extract is stored in the form of a frozen liquid at -20^*C or lower. Various batches of the extract in the form of a frozen solution have been designated N-l, N-2, N-3, #- 60, etc. These extracts were prepared at different times from different Eriobotrva iaponica plants. Instead of bringing the volume to 1300 ml, the extract can be lyophilized to prepare a powder.

EXAMPLE 2

To determine the effect of the extract on calcium oxalate crystal growth, a modification of the method of Ligabue et al, Clin. Chim. Acta, .98., 39 (1979) was used. The principle of the assay is based on the loss of oxalate, over time, from a metastable solution of calcium oxalate following addition of calcium oxalate crystals. The loss of oxalate from solution represents crystal growth of calcium oxalate. The inhibitory effect of a extract is determined by adding the extract to the metastable solution and comparing the rate of crystal growth to that in its absence.

The inhibitory activity of the extract as well as the inhibitory activity of citrate and pyrophosphate, two compounds known to inhibit calcium oxalate crystal growth under conditions described above, was determined.

The metastable solution used in this experiment contained the following: NaCl 0.15 M

CaCl₂ 1.0 mM

Na₂C₂0. (sodium oxalate) 0.2 mM Na cacodylate 5.0 mM

The solution, 200 ml, was brought to 37^*C and filtered through a millipore filter (0.45 μm) . To the filtrate, C-oxalate (3.4 m Ci/mmol) was added to give approximately 10,000 disintegrations per minute (dpm)/100μl [100 μl of ¹C-oxalate (50 μ Ci/ml)/100 ml filtrate]. The pH of the solution was adjusted to 6.0. A 100 mM solution of citrate and a 1.25 mM solution of pyrophosphate were prepared on the day of the assay. Aliquots, 50 μl and 10 μl, respectively, of these solutions were analyzed for inhibitory activity. Aliquots, 10 μl, of two extract preparations, which had been stored at -20^*C, were analyzed.

A stock suspension of seed crystals, 200 g of calcium oxalate monohydrate crystals in 200 ml of 0.15 M NaCl, was prepared and incubated with magnetic stirring for a minimum of 48 hours (h) at 37^*C before using. Test tubes were set up containing 5 ml of the metastable - ^uC-oxalate .solution at 37"C. Aliquots of samples for analysis, 5-50 μl, were added to appropriate tubes, followed by 200 μl of seed crystal suspension. Tubes were capped and continuously mixed during incubation, for 90 minutes at 37^*C. Tubes were then centrifuged (5 min, 1500 rpm) and aliquots (100 μl) removed from the supernatant for radioactive counting in 5 ml of Biofluor and counted on a Packard liquid scintillation counter. All samples were run in duplicate, while triplicate analysis of the reference tubes (0.15 M NaCl in place of inhibitor) and "total tubes" (no crystals added) was run. The results of this study are shown in Table 1. Results are expressed as percentage loss of ^uC-oxalate from solution.

Table 1

The Effect of Two Extract Preparations, Pyrophosphate (P_P) , and Citrate on Calcium Oxalate Crystal Growth In Vitro. SAMPLE dpm REMAINING % LOSS (GROWTH)

*Total dpm 11,252 ~

♦Reference (0.15 M NaCl)

(50 μl) 5,434 51.7

Extract #N-1, (10 μl) 8,403 25.3

#60, (10 μl) 9,732 13.5

P_P (1.25 mM) , 10 μl 8,619 23.4

Citrate (100 mM) ,

50 μl 8,829 21.5 *Mean of triplicate determinations. All other samples were assayed in duplicate.

The reference sample showed 51.7% loss of C- oxalate from solution. Both pyrophosphate and citrate showed considerable inhibitory activity of crystal growth at the concentrations studied. Both extract samples caused considerable inhibition, with extract #60 showing the highest inhibitory activity. This experiment demonstrates that the plant extracts cause significant inhibition of calcium oxalate crystal growth -in vitro when compared to compounds with known inhibitory activity, i.e., citrate and pyrophosphate.

EXAMPLE 3

Having confirmed that the plant extract inhibited calcium oxalate crystal growth -in vitro, an experiment in rats was carried out. The purpose of this experiment was to determine if the extract inhibited kidney stone formation -in vivo in an animal model of calcium oxalate stone disease.

When ethylene glycol is ingested by animals or man, 1 to 2 % of the compound is converted to oxalic acid, resulting in dramatic increases in urinary oxalate excretion and deposition of calcium oxalate crystals and stone formation in both kidneys. When 1% ethylene glycol solution was given to rats in the drinking water, the animals developed kidney stones within a period of 21-28 days, (Hodgkinson, A., Oxalic acid in Biology and Medicine. Academic Press, London 1977, p. 251-253). This animal model has proved valuable for many in vivo studies of calcium oxalate stone disease and was used in this experiment. Male Wistar rats were used in this study. The animals were treated as outlined in Table 2.

Table 2

Treatment protocol of rats used to study the effect of the plant extract on prevention and dissolution of calcium oxalate renal stones.

DAY III* IV V VI

r

HEMATURIA FOR 1 DAY

104 EX EX

*Data from control Rats I and II omitted for brevity.

EG = ETHYLENE GLYCOL Ex = EXTRACT

Controls, I and II, were given deionized water (i.e., no treatment) , III and IV were given 1% (W/V) ethylene glycol (EG) in the drinking water, V and VI were given 1% (W/V) ethylene glycol plus 5% extract, by volume, in the drinking water. All rats received a normal rat chow diet and were housed in individual metabolic cages. All six rats were X-rayed for the presence of renal stones prior to beginning treatment and at intervals thereafter as outlined in Table 3. The results of the X-rays are shown in Table 3.

Table 3

Renal stone formation in rats given ethylene glycol (Rats III and IV) or ethylene glycol plus extract (Rats V and VI)

N = NORMAL = NO STONE

Data for control Rats I and II omitted for brevity.

Animals were fasted for 24 h before each X-ray since the high calcium content of the diet makes interpretation of the X-ray very difficult. Twenty-four hour urine collections were made in a container with 1.0 ml of 7.0 N HCl, added. The control rats I and II (data not shown) were normal throughout the experiment .

Urinary oxalate was determined as described by Costello, J. et al, J. Lab. Clin. Med. , JT7, 903 (1976) . The presence or absence of renal stones was confirmed by a radiologist utilizing X-ray analysis.

Rats I and II (no treatment) did not form renal stones. Rats III and IV formed renal stones by day 57 and 14, respectively, while rats V and VI formed stones by day 104 and 57, respectively. The size of the stones formed by rats III and IV was visibly larger than those formed by rats V and VI.

Rat IV had a very large stone by day 37. On day 42 this animal was taken off EG treatment and given 5% extract in the drinking water. This resulted in severe hematuria (blood in the urine) for 5 consecutive days which is indicative of passage of calcium oxalate crystals in the urine. On X-ray, day 57, the stone appeared to be breaking up, however, the rat died from anesthesia that day. Examination of the kidneys revealed a large number of stones in one kidney. No further analysis on the stone(s) was carried out.

Rat VI had a small renal stone by day 57. On day 69 the extract and EG were discontinued and the animal was given deionized water. On day 89 the rat was given 5% extract which continued until day 140. When both kidneys were removed, dissected and examined for renal stones, no stones could be found.

The results of rat VI are summarized in Table 4.

Table 4

The effect of the plant extract on dissolution of a calcium oxalate renal stone in Rat VI.

As can be seen on Table 4, this rat excreted very large quantities of oxalate in the urine over the initial period of extract ingestion (days 96-99) . Rats on a normal diet excrete 0.5 to 0.7 mg of oxalate per 24 h urine. Post-mortem, both kidneys were normal in size and there was no sign of stones in either kidney. Hematuria was observed on day 96 following 5% extract treatment which was restarted on day 89.

This experiment (two rats per group) supports the view that 5% extract has an inhibitory effect on renal stone formation when rats are fed 1% EG compared to animals given 1% EG without extract (rats III and IV) . When the presence of renal stones was confirmed, the EG discontinued and the animals (rats IV and VI) treated with extract, there is evidence, especially for rat VI, that the renal stone was disintegrated and passed in the urine as calcium oxalate.

EXAMPLE 4

In the experiment described in Example 3, an inhibitory effect of the extract on renal stone formation as well as causing stone dissolution was observed. The purpose of this experiment was to investigate this inhibitory activity in greater detail in a large group of control and experimental animals. The experimental conditions of fluid intake (i.e., EG intake), weight gain, renal stone formation and calcium oxalate deposition were carefully monitored. Renal function and urinary oxalate excretion were also determined.

The same animal model as described in Example 3 was used. Male Wistar rats were used with 12 animals in each group. Animals were fed ad libitum rat chow diet. Urinary oxalate determination was as described by Costello, J. et al, J. Lab. Clin. Med., 87, 903 (1976).

Animals were housed in individual metabolic cages and allowed 10 days to become acclimated. During this period a 24 h urine was collected and blood withdrawn for determination of urinary oxalate and creatinine clearance values. Twenty-four male Wistar rats were randomly divided into two groups of 12. One group (controls) was given 1% (W/V) ethylene glycol (EG) in the drinking water for 41 days, while the experimental group received 1% (W/V) EG and 10% (V/V) extract in the drinking water for a similar period. Plasma creatinine, BUN, urinary oxalate, creatinine and animal weights were determined prior to beginning treatment. Fluid intake of the animals was carefully recorded daily. Weekly 24 h urinary collections were made for oxalate determination and the urine collected in 3 ml, 3.5 Ν HC1. BUN and creatinine clearance were also determined at the end of the study. Blood samples were withdrawn by retro-orbital bleeding. After completion of the study the animals were weighed, sacrificed and the kidneys removed for subsequent calcium oxalate analysis.

Kidneys were dissected and visible gross stones removed and weighed. Calcium oxalate crystal deposition refers to deposits that were not visible to the naked eye and consequently had to undergo acid extraction as described hereinbelow. Kidneys were then minced with a scalpel, transferred to screw-top Nalgene centrifuge tubes, lyophilized for 16 h and the dry powder crushed with a spatula. The weight of the wet tissue and lyophilized powder were recorded. Lyophilized kidneys were defatted with four washes of a 1:1 ether: petroleum ether mixture, 2 ml/wash. Washings 1-3 were allowed to settle for 5 min and the organic solvent removed and discarded. Following the final wash, the samples were centrifuged (15 min, 7000 g) to allow maximum removal of the solvent. The tissue was dispersed in each tube and allowed to dry in the fume hood for about 2.5 h before being lyophilized for 1 h. To extract the calcium oxalate, 6 ml (0.5 N) HC1 was added to each tube containing lyophilized defatted kidney tissue. The tubes were capped and continuously mixed for 16 h at room temperature, centrifuged (20 min, 7000 g) and the supernatant removed and retained. A second extraction was carried out using 4 ml (0.5 N) HCl, treated as above and the supernatant combined with the first acid extract in a 50 ml pyrex tube. The volume of the combined supernatants was determined and aliquots retained for calcium determination.

¹⁴C-oxalate, 100 μl (0.5 μCi/ml) was added to each kidney extract, aliquots (100 μl) removed for counting and the extract titrated to pH 5.0 with NaOH (10 N) . Oxalate was precipitated from solution by addition of saturated calcium sulfate and ethanol, 0.33 and 2.25 ml, respectively,/ml acid extract, mixed and allowed to stand at room temperature for 3 h. Tubes were centrifuged (15 min, 1500 rpm) , the supernatant removed and discarded and the precipitate lyophilized. The dry precipitate was analyzed as previously described for urinary oxalate, Costello, J. et al, J. Lab. Clin. Med., 82, 903 (1976). Calcium content of the kidney extract was determined by atomic absorption using a Perkin Elmer AA Model 2380. Plasma and urinary creatinine were determined using an Abbot A-Gent creatinine test kit on an Abbot Biochromatic Analyzer 100. Blood urea nitrogen (BUN) was determined using an Abbot A-Gent BUN test kit on the same analyzer. Results were analyzed using Students t test and p values reported are for a two tail test.

The results are summarized in Table 5. The results are mean + SD.

Table 5

Urinary oxalate excretion, kidney calcium, oxalate, and stone formation, renal function, fluid intake, and weight of rats given ethylene glycol (Controls) or ethylene glycol plus 10% extract (Extract Rats) for 41 days.

Control Rats on

Rats Extract P Value

Urinary oxalate, Prior to treatment

(mg/24 h) 0.656 0.574 N.S.

Urinary oxalate during treatment

(mg/24 h) 7.854+3.817 4.928±3.023 < 0.001 Kidney calcium

(mg/rat) 2.03±2.806 0.237+0.117 < 0.05

Kidney oxalate

(mg/rat) 4.59±5.627 0.227±0.189 < 0.02 mg of stones formed/group 11.4 4.1 N.S.

Number of stones formed/group 54 21 N.S.

♦Total kidney calcium oxalate (mg/rat) 7.570+8.882 0.805+1.098 < 0.02 Rat weight before study (gr/rat) 201.6+30.9 193.5±26.4 N.S.

Rat weight at end of study (gr/rat) 337.8±30.6 327.3±41.3 N.S.

Fluid intake/ rat, during

Study (ml/24 h) 41.8+4.9 38.9±8.5 N.S.

Creatinine clearance before study (ml/min) 0.86+0.48 0.93+0.29 N.S.

Creatinine clearance at end of study

(ml/min) 1.15±0.42 1.70±0.23 < 0.001

All the above values are mean + SD. There were 12 rats in each group. *The sum of kidney stones (mg) and calcium oxalate deposits, mg/rat.

**The p values, Table 5, reported are for a two tail test, and are derived by comparing each column in the control group with the corresponding column in the extract-treated

Table 8

Weekly Urinary Oxalate excretion in male Wistar rats on 1% Ethylene Glycol in drinking water for 41 days (mg/24 h)

Table 9

Weekly Urinary Oxalate excretion in male Wistar rats on 1% Ethylene Glycol and 10% extract in drinking water for 41 da s (mg/24 h)

Table 10

Comparison of Total Kidney Calcium Oxalate Deposits

(Renal Stones Plus Calcium Oxalate Crystal Deposition)

In Control Rats (1% Ethylene Glycol) and Extract-Treated

Rats (1% Ethylene Glycol Plus 10% Extract)

**τ NS 0.02 0.02

♦Total kidney calcium oxalate (column 4) is the sum of renal stones (column 2) and calcium oxalate deposits (column 3) in mg per rat. There was a substantial increase in urinary oxalate excretion of both groups during EG ingestion, however, control rats excreted significantly more oxalate (p <.001) than rats on extract, Table 5 (also Tables 7 and 8) . These results suggest the extract may inhibit oxalate synthesis from EG in this animal model. The number and weight of renal stones found in the control rats were greater than in the experimental group but neither reached significance, Table 5. Kidney calcium in the control rats was almost 9 times that found in the extract treated rats (p <0.05), while the oxalate content was 20 times higher in the control rats, (p <0.02) Table 5. These results demonstrate substantial inhibition of renal calcium oxalate crystal deposition in the extract treated group. If the weight (in mg) of renal stones found in each animal (and presumed here to be calcium oxalate, although not analyzed) is combined with the weight of calcium oxalate deposits, the total calcium oxalate deposition (i.e., weight in mg of renal stones plus acid extracted calcium oxalate deposits) in the control group is significantly more than that in the experimental group p <0.02, Table 5.

Recent -in vivo observations (Kok, D.J. et al. Crystal agglomeration is a major element in calcium oxalate urinary stone formation. Kidney Int., 37, 51, 1990) while identifying crystal growth as an important part in the process of stone formation, suggest that crystal agglomeration is the decisive element in the formation of large crystal particles and therefore in the process of renal stone formation. Since the extract significantly inhibits crystal deposition/stone formation in rats fed 1% EG, it is reasonable to suggest that it inhibits not only crystal growth, as shown by -in vitro studies, but also inhibits crystal agglomeration (formation of crystal clumps) in vivo. The BUN value of the control rats was significantly higher (p <0.05, data not shown) than the extract group while their renal function, as determined by creatinine clearance, 1.15 ml/min was significantly less than the extract treated rats. Table 5. These findings demonstrate that the extract prevented loss of renal function probably as a result of decreased renal calcium oxalate crystal deposition in this group. By comparison, the control rats showed significant loss of renal function.

The water intake and weight of the rats are shown in Table 5, and no significant difference in either parameter was observed. The significant difference in calcium oxalate deposition and renal function between the two groups. Table 5 and discussed above, cannot therefore be accounted for by differences in intake of EG.

In Tables 6 and 7 the individual calcium and oxalate content of both kidneys from each rat are provided, while in Tables 8 and 9 the weekly urinary oxalate values of each animal over five consecutive weeks as well as weekly mean values for each group of animals are shown.

The results can be summarized as follows:

1. Extract treated rats excreted significantly less oxalate in the urine, suggesting inhibition of oxalate synthesis from EG.

2. Kidney calcium and oxalate were significantly lower in the extract group demonstrating inhibition of calcium oxalate deposition by the extract.

3. Kidney function was significantly greater in the extract group at the completion of the study, again supporting the view that the extract inhibits calcium oxalate crystal deposition and loss of renal function.

4. Number and weight of renal stones was greater in the control group but did not reach significance. 5. However, when the weight of renal stones (presumed to be calcium oxalate) in each rat is combined with the weight of calcium oxalate crystal deposits, control rats have significantly more total calcium oxalate deposited in their kidneys than the extract group.

6. It is suggested from these findings that the extract prevents calcium oxalate crystal formation -in vivo.

7. Fluid intake and therefore EG intake was similar in both groups.

8. Weight gain was similar in both groups over the period of the study.

In the above experimental renal stone animal model the extract showed potent inhibitory activity in preventing calcium oxalate crystal deposition and loss of renal function. The significant decrease in urinary oxalate excretion in the presence of extract ingestion suggests inhibition of oxalate synthesis from EG.

EXAMPLE 5

The purpose of this investigation was to determine the effect, if any, of extract ingestion on EG absorption from the gut (gastrointestinal tract) . It was important to determine any change in absorption of EG due to extract ingestion, in order to establish more clearly the site of action of the extract on renal calcium oxalate stone formation. Male Wistar rats were housed and fed as described in

Example 3. Tracer ¹⁴C-EG (4.7 mCi/mmol) in an amount of 1.6 μCi/rat/day was added to the drinking water to monitor absorption of EG. The urinary ¹⁴C values and fecal loss of ¹⁴C label as an indication of gastrointestinal absorption were determined.

Twenty-four hour fecal collection was mixed with HCl (25%), 1.0 ml/0.1 gr feces, allowed to extract for 3h at room temperature, and then centrifuged (15 min, 1500 rpm) . The supernatant was decanted, volume determined and 0.5 ml aliquots taken for scintillation counting in Biofluor scintillation fluid on a Packard liquid scintillation counter. The dpm were determined by quench correction.

¹⁴C present in urine was similarly determined by counting 0.5 ml of a 24-h urine collection. The daily intake of ¹⁴C-EG was determined by monitoring the water intake and counting an aliquot of the drinking water as described above for urine.

Twelve male Wistar rats were acclimated in individual metabolic cages for one week. Animals were then randomized into two groups, 6 rats/group, control and experimental. Control animals received 1% (W/V) EG and ¹C-EG (1.6 μCi/rat/day) in the drinking water, while the experimental group received 1% (W/V) EG and ¹⁴C-EG, as in controls, and 10% extract (by volume) . Both groups were studied over 5 consecutive days. Daily 24-h urine and fecal collections were made throughout the study and the intake of drinking solution accurately recorded per 24-h period.

The fecal and urinary u C excretion values are shown in Table 11.

Table 11

Urinary and fecal excretion of ¹⁴C in control rats and rats on extract (10% by vol) following oral ingestion or ¹⁴C- ethylene glycol.

DAY

Results are expressed as a percentage of the 14,C-EG intake (% dpm) and mean + SD shown for each group. Fecal ¹⁴C-excretion for days 3 and 4 are not shown as these samples were lost. Urinary ¹⁴C-excretion was similar in both groups, except for day 2 when the extract-treated rats showed a significantly greater excretion, p < 0.01. However, when compared over the 5-day period, there was no significant difference between the groups. Fecal ¹⁴C was higher in the extract group on day 1, and similar on days 4 and 5, but was only a small percentage of the total ¹⁴C ingested on each day. The results show that 10% extract solution does not significantly alter the absorption of 1% EG.

From the above, it can be concluded that the inhibitory effect of the extract on renal calcium oxalate deposition demonstrated in the previous study does not result from altered EG absorption. The findings support the view that the extract prevents calcium oxalate deposition by acting at a renal site.

EXAMPLE 6

Treatment of Plant Extract with Heptane. Hexane. and Chloroform Methanol

An aqueous solution of an extract was treated separately with equal volumes of hexane and heptane, vortexed vigorously for 1.5 min, centrifuged at 1,000 rpm for 10 minutes, and the lower aqueous phase removed for assay. Two ml of extract was also treated with 4 ml of a mixture of chloroform/methanol (1:1 V/V), vortexed and centrifuged as above, and the upper aqueous-methanol phase retained for assay. All samples were assayed in duplicate and compared to the untreated extract. Five μl of all samples were assayed except the chloroform/methanol- treated sample in which 10 μl was used to correct for a 1:2 dilution by the methanol. Table 12 EFFECTS OF ORGANIC SOLVENTS ON EXTRACT ACTIVITY Sample % Inhibition of

Crystal Growth Untreated extract 44.20

Hexane-treated 50.53

Heptane-treated 46.22

Chloroform/Methanol-treated 42.63

. These data, Table 12, show that there is no significant loss of activity when the extract is treated with hexane, heptane or chloroform/methanol, demonstrating that all the activity remains in the aqueous phase and is not soluble in these organic solvents.

EXAMPLE 7 Solubility of Inhibitor Activity in Diethyl Ether

Four ml of aqueous extract, N-3, was treated with 40 ml of ether and mixed by vigorous stirring for 20 min and the aqueous phase removed by a separating funnel. The aqueous phase was further mixed with 10 ml of ether for 5 min and again separated. The ether phase from both extractions was combined, allowed to evaporate, lyophilized and redissolved in 0.5 ml of distilled water. The treated extract (aqueous phase) showed no loss in activity while the ether extract contained no more than 2% of the total inhibitory activity.

Example 8

Treatment of Extract with Ethanol

When 2.5 ml of ethanol (200 proof) was added to 1.0 ml of extract N-3 an immediate precipitate formed. The sample was centrifuged, supernatant removed, and the precipitate redissolved in 3.5 ml of distilled water. The resuspended precipitate contained over 85% of the inhibitory activity of N-3. Example 9

Typical Purification of Inhibitor of Crystal Growth from

Plant Extract

A frozen liquid plant extract was prepared from the leaves in a similar fashion to that described in Example 1, and was then stored at -2θ'c. The frozen liquid extract was thawed out in hot water, 5 ml removed, mixed with 5 ml of hexane, vortexed for about 2 minutes, centrifuged for 10 minutes at 1,000 rpm, and the lower phase, approximately 4.6 ml, removed and lyophilized. The dry powder (about 40 mg) was dissolved in 2.0 ml of Tris-HCl, 0.02 M, pH 7.38, and chromatographed on a G-75 sephadex column (dimensions 1 x 44 cm) which was equilibrated with the same Tris-HCl buffer. The sample was eluted from the column at a flow rate of 40 ml/h, and 144, 1.0 ml fractions collected and assayed for activity. The active peak (fractions containing most inhibitory activity of calcium oxalate crystal growth) was eluted in fractions, 13-32, which were combined, dialyzed against distilled water through a membrane with a molecular weight cut off of 12,000-14,000 daltons, and then lyophilized. The powder was redissolved in 4.5 ml of distilled water, and further purified by isoelectric focusing on a BioRad Rotofor (conditions: 1% ampholytes, 653 volts, 19 mA, 12 watts for 70 minutes). Fractions 1-3, which had most of the activity, were combined, dialyzed as above, and lyophilized. The lyophilized compound was a white powder. The activity of this purified powder was 183,871 U/gr compared to 17,400 U/gr for the unpurified extract. In future studies, the above purification will be somewhat modified in preparing larger quantities of purified inhibitor. Following elution of the active peak fractions from G-75 Sephadex and dialysis, the samples will be chromatographed on a DEAE Sephadex-A25 (2.5 x 20 cm) column, and eluted with a linear NaCl gradient, 0-2.0 M. This step should concentrate the sample and result in further purification. Following this ion exchange step, the activity will be precipitated with ethanol, redissolved in distilled water and run on isoelectric focusing as described in Example 12 below, again treated with ethanol as above, and lyophilized. The purity of the compound will be further examined by running on an appropriate HPLC column.

EXAMPLE 10

Effect of PH adjustment on inhibitory activity of extract

N-l: Effect of acidic pH:

A 5 ml aliquot of extract N-l, pH 5.33, was titrated to pH 1.48 with IN HCl, left to stand at 4^*C for 14 h, and then titrated to pH 5.36 (close to original pH) with IN NaOH. The acid-treated sample showed no loss in activity compared to the control untreated extract.

Table 13 Effect of PH Adjustment on Inhibitory Activity of Extract

% Inhibitory Extract Sample Activity ♦ N-l (untreated)♦♦ 37.32

N-l (pH adjusted) 37.47

♦Inhibitory activity against calcium oxalate crystal growth.

♦♦Value corrected for dilution effect of N-l with acid/alkali.

EXAMPLE 11

Effect of alkaline pH:

Aliquots of extracts, N-l, N-2, and #-60, were titrated to pH 12.60 or slightly higher with 2.5 N NaOH, left to stand for a minimum of 15 h at 4^*C, and then titrated to within 0.1 of original pH with 3.5 N HCl. All samples were assayed for activity along with untreated controls. All three extracts showed a substantial increase in activity against calcium oxalate crystal growth as shown below. Table 14. Table 14

♦These values. Example 11, were corrected for dilution effect resulting from acid/alkali addition to the treated extract.

A similar increase in activity was obtained when N-l, pH

12.7, was put in a boiling water bath for 1 h and the pH then adjusted to near original value (data not shown) . When purified N-l (hexane-treated 1:1, chromatographed on G-75 Sephadex, active fractions combined, dialyzed, and lyophilized) was treated in a similar way, activity increased from 22.6% to 49.4%. Since the large increase in activity is not reversed on titration back to the original pH, and occurs to both the unpurified and purified extracts, it suggests a permanent modification to the inhibitor or other active ingredient(s) present in the extract. The increase may be a consequence of a chemical or structural alteration to the inhibitory active ingredient(s) or the conversion of an inactive ingredient ("pre-inhibitor") to an active ingredient (inhibitor) .

EXAMPLE 12

Stability of purified extract and modified extract (pH adjusted) : N-2 which had been adjusted to pH 12.6 for 16 h and then readjusted to original pH (i.e., modified N-2) was put in a boiling bath for 3 h. A separate aliquot of N-2 was adjusted to pH 1.5 for 16.5 h. Both treatments of N-2 caused little or no loss in activity. Purified N-l (Sephadex G 100/120, dialyzed and lyophilized) showed no loss in activity when kept at pH 12.7 for 16.5 h, pH 1.5 for 16.5 h, and when boiled for 3 h (data for these experiments not shown) . The results confirm that these different preparations of the extract show no loss in activity when treated with acid, alkali, or heat. (The increase in activity following alkali treatment is discussed in Example 11.) .

Example 13

Isoelectric point (pi) determination of plant extract inhibitor of calcium oxalate crystal growth: Extract samples were run on a BioRad isoelectric focusing cell that allows collection of the different "pH fractions" in separate test tubes at the end of the run.

Isoelectric point (pi) of extract inhibitor:

The following samples were focused on the Rotofor cell(Bio-Rad free solution isoelectric focusing apparatus) , purified N-l (Sephadex G-100/120, dialyzed, lyophilized), N-3, purified N-l (dialyzed, EDTA/EGTA treated, run on G-75, peak fractions focused), modified N- 1 (pH 12.7 for 16 hr, titrated to original pH) . All samples were focused following two pre-focusing steps (a) and (b) :

(a) 3 M urea containing 0.75% ampholytes was focused for 60-75 min.

(b) Following step (a) , 5-7 ml was removed from position one and replaced with 5 ml of 0.2 M phosphoric acid and the cell focused again. Following steps (a) and (b) about 5 ml was removed from position 10, the appropriate sample to be focused was added to position 10, and the cell focused again. After this third and final run, all 20 fractions were harvested, and both the pH and activity were determined. Similar pi values were obtained for all samples, giving a mean pi value of 3.07.

It has been observed by Gelse a et al, Journal of

Chromatography, 171:171-181 (1979), that the apparent pi (pi app) in the presence of 3M urea, used in the present studies described above, is greater than the pi by 0.3 of a pH unit (i.e., pi app - pi = 0.3). Consequently, a correction of 0.3 to the value derived above would give a pi of approximately 2.7 + 0.5 (SD) .

EXAMPLE 14

Binding of an inhibitor of crystal growth from extract N-2 to calcium oxalate crystals.

Calcium oxalate crystals were generated in the presence of 50 ml of extract N-2 by the simultaneous dropwise addition of 25 ml of 0.2 M solutions of CaCl₂ and potassium oxalate over 1 h at 45-50^*C. Stirring was continued for a further 2h and the suspension centrifuged at 2,500 rpm for 10 min, supernatant removed (96 ml), and the precipitate washed with 15 ml distilled H₂0, centrifuged as above and the supernatant removed.

To the crystal pellet was added 30 ml of 0.9% NaCl in 3.5 N HCl and mixed; few crystals dissolved. Four grams of KC1 was then added to the crystal suspension and shaken for approximately 2h, and the suspension dialyzed against 2 1 of 1 M KC1 for 17 h at 22^*C through a dialysis membrane with a molecular weight cut off of 12,000-14,000 daltons. The suspension was recovered and centrifuged, 1500 rpm for 15 min, and the supernatant, 32 ml, removed and retained. The supernatant was further dialyzed against 51 distilled H₂0 at pH 2.0 for 67 h, against 5 1 H₂0 for 24 h, and, finally, against 4 1 H₂0 for 25 h. The dialyzed solution, 29.5 ml, was lyophilized to give 12.7 mg of white powder. Analysis of the recovered powder confirmed it had considerable inhibitory activity (57,834 U/g) and that the inhibitor was strongly adsorbed onto calcium oxalate crystals.

EXAMPLE 15

Binding of calcium and magnesium by the extract:

N-l extract was dialyzed in Spectra Por 6 dialysis tubing (MW cut off 10,0000) against deionized water over 6 days with several changes of deionized water. Little or no inhibitory activity was lost. Aliquots of N-l, post dialysis, were separately mixed with EDTA lOOmM, EGTA 3mM, and EDTA lOOmM + EGTA 3mM, final concentrations. Samples were then redialyzed through Spectra Por 2 against deionized water. The results below, Table 15, show that calcium and magnesium bind to the extract fraction containing the inhibitory activity. Magnesium is more readily removed following treatment with EDTA than is calcium. All the calcium could not be removed. EGTA was less effective than EDTA in removing calcium (data not shown) . These results confirm that calcium is bound to the extract fraction containing the inhibitory activity along with magnesium but calcium is more firmly bound.

Table 15 Effect of Dialysis, and treatment with EDTA and EGTA on Calcium and Magnesium Concentrations of N-l

Calcium Magnesium (mg/lOOml)

Original extract N-l 8.78 7.74

After exhaustive dialysis against deionized water 1.03 0.73

Mixed with lOOmM EDTA and then dialyzed 0.049 0.008

Mixed with 3mM EGTA + lOOmM EDTA and then dialyzed 0.084 0.010

EXAMPLE 16

Confirmation of a Polyanion: The presence of polyanions in extract N-3 was determined with Alcian Blue 8 GX(Sigma) as described by Fellstrom et al (European J. Clinical Investigation 16_f 292, 1986). Heparin was used as a standard. The inhibitory activity was precipitated from N-3 with 2.5 volumes of ethanol (as described in Example 8) and the lyophilized precipitate redissolved in distilled water and assayed for polyanions. The assay confirmed the presence of a considerable quantity of polyanions (>45%) in the fraction of N-3 precipitated with ethanol. This fraction also contained over 85% of the inhibitory activity of N-3 suggesting that the inhibitory ingredient is a polyanion (data not shown) .

EXAMPLE 17

Chemical Composition of Extract Inhibitor: Aliquots of N-3 and purified N-l (Sephadex G100/120, dialysis and lyophilization) were analyzed for the presence of (a) carbohydrate, (b) protein, and (c) ribonucleic acid. Anthrone test for carbohydrate (qualitative) : Aliquots of N-3 and purified N-l (Sephadex G100/120, dialyzed, lyophilized) were assayed for carbohydrate. To 2 ml of Anthrone reagent (0.2%, W/V, Anthrone in concentrated sulfuric acid) in a test tube, 200 ul of sample was added. Both N-3 and purified N-l formed a green color which is positive for carbohydrate. Bio-Rad (Comassie Blue) protein assay: Aliquots of N-3, precipitate of N-3 (precipitated with ethanol and NaCl and redissolved in distilled water) , and purified N-l (G100/120, dialyzed, lyophilized) , were assayed for protein. Bovine serum albumin was used as a standard. There was no protein detectable in any of the samples, N- 3, precipitate of N-3, or purified N-l.

Pronase test for presence of protein in extract inhibitor: Aliquots of N-3 and purified N-l, as above, were incubated with Pronase (a non-specific protease from Streptomyces griseus) for 24 h as described by Koide et al. (Invest Urol 18., 382, 1981) with appropriate controls. Results show a loss of 20% of the inhibitory activity from purified N-l preparation, but no loss from N-3 extract. These contradictory results suggest that the inhibitory ingredient may contain a protein/peptide component. Ribonuclease assay for presence of ribonucleic acid:

If the inhibitor is composed of ribonucleic acid, treatment with the enzyme, ribonuclease, should destroy its activity. Aliquots of N-3 and purified N-l, as above, were incubated with ribonuclease for 24 h as described by Koide et al. (Invest Urol 18., 382, 1981). Controls containing N-3 and N-l without ribonuclease, as well as, ribonuclease only in buffer were also run. Results show no loss of inhibitory activity after ribonuclease treatment and suggest the inhibitory ingredient(s) not to be ribonucleic acid.

Assay for the presence of uronic acids in extract inhibitor: Aliquots of N-3 and precipitate of N-3 (precipitated with ethanol and NaCl and redissolved in distilled water) were assayed for uronic acid content as described by Blumenkrantz and Asboe-Hansen (Anal Biochem 54. 484, 1973). Glucuronic acid was used as a standard. Results show that N-3 contains 2.6 + 0.1 (SD) mg(uronic acid)/ml and the ethanol precipitate of N-3, 4.3 + 0.2 (SD) mg(uronic acid)/ml or 4.3 + 0.2 mg(uronic acid)/15 mg (i.e., 29% is uronic acid). Since the ethanol precipitate also contains >85% of the inhibitory activity of N-3 (see Example 8) the results suggest the inhibitor contains a high percentage of uronic acid. Based on these results there is a high probability that the inhibitor is a glycosaminoglycan type substance.

A summary of the above results suggests the extract inhibitor does not contain ribonucleic acid but contains carbohydrate, and may be a glycosaminoglycan. The protein analyses suggest it is not a protein, but does not exclude the possibility that it may contain a protein/peptide component.

Example 18

The effect of treating extract N-3 at different pH values:

Extract N-3 was titrated to pH 12.5, allowed to stand at this pH for 2 min and then back-titrated as close as possible to the original pH of 5.2, and the activity then determined.

Separate samples of N-3 were titrated to the different pH values shown in Table 16 below, left to stand for 1 h and then back-titrated as close as possible to the original pH, and the activity was then determined.

Table 16 Effect of pH over 1 h on activity of extract N-3 pH Treatment for 1 h % increase in activity pH 8.2 no change

9.2 3.6

10.5 34.2

11.2 76.4

12.48 (for 2 min) 107.2 The results, Table 16, demonstrate that the higher the pH of the extract the more rapid the increase in activity (against calcium oxalate crystal growth) .

Example 19 The isolation of different GAG compounds from extract N-3 following treatment with ethanol before and after modification with alkali:

(a) To 13 ml of extract N-3 was added 32.8 ml of absolute ethanol, mixed vigorously and allowed stand for 2.17 h at room temperature. The sample was centrifuged, 2500 rpm for 10 min, and the supernatant, 45 ml, retained. Treatment of this supernatant is described in section (b) below. Analysis of N-3 and the supernatant for activity (following lyophilization and resuspension in distilled H₂0 to the original volume of N-3) demonstrated that 97.4% of the activity was precipitated with ethanol (data not shown) . The precipitate was dissolved in 2.5 ml of distilled water, lyophilized to dryness (93.03 mg) and stored at -20 °C for 3 days. The precipitate was then dissolved in 5 ml of 0.02 M Tris/0.15 M NaCl, pH 7.3, mixed with 5.0 ml of hexane for 2 min and centrifuged for 10 min. The lower aqueous layer, 4.81 ml, was removed. Half of this sample, 2.3 ml, was chromatographed on a G-75 Sephadex column (1.5 X 72.4 cm) which had previously been equilibrated with the Tris buffer used above. This buffer was used to elute the sample. Fractions of 1.77 ml were collected at a flow rate of 0.214 ml/min and the elution profile monitored at 200 nm. The activity of the fractions against calcium oxalate crystal growth was determined. The peak activity eluted at a volume of 60.02 ml. The other half of the hexane treated ethanol precipitate of N-3 described above was chromatographed on the same Sephadex column (previously equilibrated with elution buffer) under similar conditions. A similar elution profile at 200 nm was obtained for both samples. The active fractions from both G-75 runs were combined to give a volume of 138 ml. This was concentrated to 10.3 ml on a rotary evaporator, the activity was then precipitated with 25 ml of ethanol and centrifuged as above. The precipitate was lyophilized to give 267.4 mg, then redissolved in 10 ml distilled H₂0, reprecipitated with ethanol as above and the precipitate lyophilized to give 68.6 mg. This procedure was repeated a third time and 51.3 mg obtained. This sample was dissolved in 1.0 ml distilled water and assayed for uronic acid by the method of Blumenkrantz and Asbol-Hansen (Anal. Biochem. 54. 48, 1973). The results are shown in Table 17 below.

(b) The supernatant obtained following treatment of N-3 with ethanol in (a) above was studied here. The supernatant, 45 ml, was lyophilized to give 32.31 mg and dissolved in 12.86 ml of distilled water. This latter volume was used in order to reconstitute this fraction of N-3 to the same concentration as present in the untreated N-3 extract. This solution was titrated to pH 12.72 with 5 N NaOH, left at room temperature for 17 hours, and then back-titrated to pH 5.17 with 3.5 N HCl. Analysis of the supernatant before and after alkali treatment showed that alkali treatment resulted in a 10.9 fold increase in activity (data not shown) . To the solution was added 40 ml of ethanol, mixed vigorously, left at 22 "C for 21.5 h, centrifuged at 2,500 rpm for 10 min and the supernatant removed and retained. The precipitate was lyophilized to give 16.7 mg. This sample was dissolved in 1.0 ml of distilled H₂0 and chromatographed on the same G-75 Sephadex column (1.5 X 72.4 cm) as used in (a) above. The column had been washed and equilibrated with the same elution buffer (0.02 M Tris/0.15 M NaCl, pH 7.28). Fractions, 2.01 ml, were collected at a flow rate of 0.297 ml/min. On assay the peak activity was found at an elution volume of 104.52 ml. The active fractions were combined to give 57.4 ml and concentrated on a rotary evaporator to 6.97 ml. To this sample was added 17.5 ml of ethanol, mixed well and left for 21 h at 22 °C. The precipitate was removed by centrifugation, lyophilized, redissolved in distilled water and again precipitated with ethanol to give a lyophilized sample of 11.3 mg. This sample was assayed for uronic acid as previously described. The results are shown in the below Table 17.

(c) Extract N-3, 13 ml, was titrated to pH 12.71 with NaOH, allowed to stand for 15.5 h at room temperature, and back-titrated to pH 5.14 with HCl. This modified N-3 was then treated in a similar manner as outlined in (a) above, the ethanol precipitate being chromatographed on the same G-75 Sephadex column, the activity of the fractions determined and the active fractions combined to give 144.6 ml. The peak activity eluted at a volume of 65.92 ml. The combined fractions (144.6 ml) were concentrated to 6.1 ml on a rotary evaporator and the activity precipitated with ethanol three times to remove buffer salts and other impurities as done in (a) above. The final lyophilized precipitate contained 50.5 mg. This sample was assayed for uronic acid. The results are shown in Table 17 below. Table 17

defers to samples isolated following treatments of extract N-3 outlined in (a) , (b) and (c) above.

In brief:

(a) Is activity isolated from unmodified N-3 and purified on G-75.

(b) Is activity isolated from the alkali-treated supernatant of (a) and purified on G-75.

(c) Is activity isolated from alkali-treated N-3 and purified on G-75.

²Samples were diluted to these concentrations before being assayed; 5 μl of each sample was assayed.

Is the elution volume from Sephadex G-75 column at which the peak activity was obtained.

Is activity against calcium oxalate crystal growth in units/mg.

Conclusions from the above studies.

The results show that the increased activity which results from alkali treatment of N-3 is derived mostly from compound (s) that are different from those providing the activity in untreated N-3. This is supported by the following data:

As much as 97.4% of the activity in untreated N-3 is precipitated with ethanol, sample (a) above, however, the increased activity is only precipitated following alkali treatment and subsequent ethanol treatment, samples (b) and (c) above.

2. Following chromatography on G-75, samples (a) and (b) showed different elution patterns. The modified compound(s) , (b) , eluted at a later time than the unmodified compound(s) , sample (a) , strongly suggesting that the modified compounds are smaller (see Table 17 above) .

3. The uronic acid content of both samples (a) and (b) are dramatically different (see Table 17 above) .

4. The activity of the modified compound(s) , U/mg, is almost five times that of the untreated compound(s) (see Table 17 above) .

5. The activity and uronic acid content of sample (c) (which contains both the unmodified and modified activities) is intermediate between samples (a) and (b) , (see Table 17 above) .

6. Earlier studies (see Example 11) have shown that alkali treatment causes a two fold increase in activity of the compounds purified from untreated

N-l. However, a 10.9 fold increase in activity was found in sample (b) above following alkali treatment.

Example 20 Effect of extracts and isolates of the plant on inhibition of herpes simplex virus cytopathogenic effects:

METHODS AND MATERIALS

Stock Virus. A stock strain of herpes simplex virus type I (HSV-1) was maintained at -70 "C. The serotype of the virus was verified by immunofluorescence. The virus was passaged in primary rabbit kidney cell monolayer cultures four times before use. The infectivity titer of the virus stock was 10^"4-⁵ to 10^"4-0 50% tissue culture infectious doses per 0.1 ml. The working suspension of virus was sterile filtered through a 0.45μ Millipore filter unit into a sterile tube.

Plant extract preparations analyzed.

1. Extracts 14 and 15 combined.

2. A purified fraction, containing the activity against calcium oxalate crystal growth, was isolated from extract N-l (N-l, after being treated with hexane was chromatographed on a G-75 Sephadex column. The active fractions were combined, dialyzed and lyophilized) . 3. The purified fraction in (2) above was treated at pH 12.7 and then back titrated to pH 5.3 and lyophilized.

4. Fractions 27 to 48 were combined following elutions of extract N-l from Sephadex G-75 (maximum activity against calcium oxalate crystal growth was eluted in fractions 10 to 25) .

5. Fractions 49 to 72 were combined following elution of extract N-l from Sephadex G-75 (maximum activity against calcium oxalate crystal growth was eluted in fractions 10 to 25) .

6. Sample (b) above (Example 19).

Assay to determine viral neutralization bv plant extract. The plant extract was solubilized in minimal essential medium and sterile filtered. Samples 2 to 5, inclusive, were in solution. These samples were also sterile filtered before being analyzed. Two-fold dilutions of the sterile plant extracts were then prepared in Eagle-minimal essential medium with 2% calf serum. Four tubes of primary kidney cell monolayers were used for each mixture of plant extract concentration and working virus suspension tested. For each set of four tubes, the working virus suspension was added to the plant extract to give a final dilution of 1:11 of the virus suspension. All the tubes containing the virus, plant extract and cell inoculum were capped and incubated at 37 °C. For virus control, four tubes of primary rabbit kidney cells were inoculated with a similar volume of the working suspension of virus. All the tubes were examined daily for five days and again after 7 days for the. presence of cytopathogenic effects associated with HSV. Confirmation as to the specificity of HSV cytopathogenic effects was accomplished with immunofluorescence using monoclonal antisera specific for HSV-1.

RESULTS

The results shown in Table 18 below demonstrate that untreated extract 14 and 15 prevented cytopathogenic effects of HSV at a concentration of 0.125 mg/ml. The extract was equally effective at higher concentrations (data not shown) . Samples 2 and 3 isolated and purified from untreated N-l were not effective in inhibiting the cytopathogenic effects of the virus while samples 4 and 6 were. In these studies confirmation by immunofluorescence indicated that HSV-1 was only present in the monolayers presenting visible cytopathogenic effects.

The results, Table 18, demonstrate that the compounds that prevent the cytopathogenic effects of the virus are present in (i) the untreated extract (extract 14 and 15, (ii) in a fraction of the extract eluted from Sephadex G-75, fractions 27-48, (maximum activity against calcium oxalate being eluted in fractions 10-25) , and (iii) in a fraction of the extract with activity mostly due to alkali treatment (Sample 6) .

Compounds present in the untreated extract (Sample 1, Example 20) and in the purified fraction (Sample 6, Example 20) are active in suppressing the cytopathogenic effects of HSV in vitro. Based on this latter activity and certain of their biochemical characteristics (particularly their anionic properties and being glycosaminoglycans) these preparations of the extract appear to be capable of suppressing the cytopathogenicity of other enveloped viruses. This extrapolation is supported by Baba et al (Antimicrobial Agents and Chemotherapy -32., 1742, 1988).

Further purification of the active fractions is being pursued in order to increase the sensitivity and further define the active compound(s) . In addition, studies will be carried out to confirm that these compounds prevent the cytopathogenic effects of other viruses.

Table 18

Effect of Plant Extract Preparations on Inhibition of Herpes Simplex Virus Cytopathogenic Effects

Sample ^aFinal Extract Stock Viral Effective Time Cytopathogenic Effects, Number Concentration Dilution of inhibition Viral Control mg/ml h h O 1 0.125 0 2 3

4 0.925

---

0.046

"These are the lowest concentrations that were effective in preventing the cytopathogenic effects of the virus. At higher concentrations of these compound(s) similar inhibition was observed (data not shown) .

'Time of incubation at which no cytopathogenic effects were observed.

The invention being thus described, it will be obvious that the same may be varied in many ways. Such variations are not to be regarded as a departure from the spirit and scope of the invention, and all such modifications and uses as would be obvious to one skilled in the art are intended to be included within the scope of the claims herein.

SUBSTITUTESHEET

Claims

WHAT IS CLAIMED IS: 1. A pharmaceutical composition comprising an amount of a purified composition effective for inhibiting the cytopathogenic effects of enveloped viruses, said purified composition having the following properties: inhibits calcium oxalate crystal growth in vitro; inhibits renal calcium oxalate crystal deposition in rats which are fed 1% ethylene glycol; is anionic and binds to anion exchange resin DEAE-A25 at pH 8.6; is soluble in water; is stable when heated in an aqueous solution (at pH of extract) of 98°C for at least three hours; retains activity when exposed to an aqueous solution of pH 1.5 for 14 hours; retains or shows increased activity when exposed to an aqueous solution of pH 12.7 for 15 hours; has a purity level of at least 50,000 Units of activity (against calcium oxalate crystal growth) per gram of solid matter; and inhibits the cytopathogenic effects of enveloped viruses; and a pharmaceutically acceptable carrier.

2. The purified composition of claim 1 in an amount effective for inhibiting the cytopathogenic effects of herpes simplex virus.

3. A purified extract fraction obtained from cells of the plant Eriobotrva iaponica, said extract fraction having the following properties: (1) inhibits the cytopathogenic effects of an enveloped virus; (2) elutes from Sephadex G-75 following elution of an extract fraction having maximum activity against calcium oxalate crystal growth; (3) is precipitated with ethanol from an aqueous solution of the extract after treatment with alkali; (4) is precipitated with ethanol from an alkali treated supernatant, which has been processed by: (i) lyophilizing the supernatant; (ii) resuspending the lyophilisate in water to the original concentration; (iii) treating the resultant aqueous solution with alkali; (iv) and titrating the alkali treated solution to the original extract pH with HCl; (5) retains activity against said enveloped virus when exposed to an aqueous solution at pH 12.72 for 17 hours.

4. The purified extract fraction of claim 3, wherein said enveloped virus is herpes simplex virus.

5. A pharmaceutical composition comprising the purified extract fraction of claim 3 in an amount effective for inhibiting the cytopathogenic effects of an enveloped virus, and a pharmaceutically acceptable carrier.

6. • A pharmaceutical composition comprising the purified extract fraction of claim 3 in an amount effective for inhibiting the cytopathogenic effects of herpes simplex virus, and a pharmaceutically acceptable carrier.

7. A method for inhibiting the cytopathogenic effects of an enveloped virus comprising administering to a patient who has been diagnosed as having said enveloped virus an effective amount of the composition of claim 1.

8. The method of claim 7, wherein said enveloped virus is herpes simplex virus.

9. A method for inhibiting the cytopathogenic effects of an enveloped virus comprising administering to a patient who has been diagnosed as having said enveloped virus an effective amount of the purified extract fraction of claim 3.

10. The method of claim 9, wherein said enveloped virus is herpes simplex virus.

11. The method of claim 7, wherein said composition is administered by following the steps of (1) withdrawing a sample of blood from a patient with said enveloped virus infection; (2) incubating said sample of blood with said composition; and (3) transferring said incubated blood back into said patient.

12. The method of claim 9, wherein said purified extract fraction is administered by following the steps of (1) withdrawing a sample of blood from a patient with said enveloped virus infection; (2) incubating said sample of blood with said composition; and (3) transferring said incubated blood back into said patient.

13. The method of claim 11, wherein said steps (1) to (3) are repeated at least once.

14. The method of claim 12, wherein said steps (1) to (3) are repeated at least once.

15. The method of claim 7, wherein said composition is administered orally.

16. The method of claim 9, wherein said purified extract fraction is administered orally.

17. The method of claim 7, wherein said composition is administered intravenously.

18. The method of claim 9, wherein said purified extract fraction is administered intravenously.

19. The method of claim 7, wherein said composition is administered into the spinal fluid.

20. The method of claim 9, wherein said purified extract fraction is administered into the spinal fluid.

21. The method of claim 7, wherein said composition is administered topically.

22. The method of claim 9, wherein said purified extract fraction is administered topically.