Patent Application
20170354704
The present invention relates to the field of food processing. Particularly, the invention relates to a biologically-active tomato composition having a reduced amount of lycopene.
Tomato products are widely used in both the food industry and, increasingly, in the preparation of nutraceutical and cosmeceutical compositions. U.S. Pat. No. 5,837,311 describes an industrial process for the preparation of tomato-derived products including inter alia a tomato oleoresin containing high levels of the carotenoid lycopene. This oleoresin product also contains an impressively-large range of additional pharmacologically-active components including other carotenoids such as phytoene, phytofluene and beta-carotene, as well as tocopherols and phytosterols. This oleoresin product has been sold and used extensively and successfully for many years now, and the range of medical conditions that may be prevented and/or treated with it includes, but is not limited to, cancerous conditions (particularly prostate cancer), elevated blood pressure, atherosclerosis, skin conditions and cellular and DNA damage.
While this tomato oleoresin preparation has proven to be highly efficacious in the management of health and the prevention of disease, its striking red color may, in some circumstances, be disadvantageous, for example when its use on the skin as a cosmetic or cosmeceutical agent is contemplated.
It is an object of the present invention to provide a solution to this problem by providing a tomato-derived product having a similar (or improved) range of therapeutic activity to the above-mentioned tomato oleoresin that is known commercially as Lyc-O-Mato®, but which has a much less marked red color, by virtue of its low lycopene content.
Other aims and objectives of the invention will become apparent as the description proceeds.
The present invention is primarily directed to a reduced-lycopene tomato-derived composition, comprising lycopene and one or both of phytoene and phytofluene, wherein the concentration of said lycopene is in the range of 0.3% to 2% (weight/weight), and wherein the weight ratio of said lycopene to one or both of phytoene and phytofluene is in the range of 1:1 to 1:2.5. In addition, said composition further comprises phytosterols.
In one preferred embodiment of the above-disclosed composition the phytosterol concentration is at least 2% (weight/weight).
In one preferred embodiment the above-disclosed composition further comprises vitamin E at a concentration of at least 2% (weight/weight).
In one preferred embodiment of the invention, the concentration of one or both of phytoene and phytofluene at a total concentration of between 0.25% and 3%.
In the context of the present disclosure, the terms “reduced-lycopene” and “low-lycopene” composition, and their like, are used interchangeably, and all of said terms are to be understood to refer to the composition having the carotenoid composition defined in the previous paragraph.
It is to be noted that the composition of the present invention possesses significant biological activity (including, but not limited to, anti-inflammatory activity, despite the fact that the lycopene content of said composition is reduced at least three-fold when compared with a commonly-used tomato oleoresin product of the prior art (Lyc-O-Mato®). This result is entirely unexpected, since many of the therapeutic effects of tomato oleoresins have been attributed to their lycopene content.
In one preferred embodiment, the composition of the present invention has a solvent concentration of less than 50 ppm.
In some embodiments, the composition of the present invention may also comprise one or more additional pharmacologically-active components including, but not limited to, additional carotenoids, vitamin E and polyphenols, such as carnosic acid. Preferred examples of additional carotenoids include phytoene, phytofluene, lutein, zeaxanthin, beta-carotene, astaxanthin. Other carotenoids, however, may also be present in the composition, either in addition to, or instead of, the examples listed above.
In one preferred embodiment of the invention, the reduced-lycopene composition further comprises carnosic acid.
In another preferred embodiment, the reduced-lycopene composition further comprises soluble tomato solids.
In a further preferred embodiment the composition of the present invention further comprises beta-carotene and vitamin E. Preferably, the aforementioned additional components are present in the following concentration ranges: 0.2%-1.0% beta-carotene; 2.0%-4% Vitamin E.
In one preferred embodiment, the above-disclosed composition is prepared from tomatoes.
In another aspect, the present invention provides a process for preparing the above-defined low-lycopene content, tomato-derived composition, wherein said process comprises the steps of:
In one preferred embodiment of the above-disclosed process, the solvent used in step 2 is ethanol.
In one preferred embodiment of the above-disclosed process, the solvent:tomato product ratio is 4:1.
While any suitable carotenoid-containing product derived from the tomato may be used as the starting material for this process, in one highly preferred embodiment, the tomato product used as the starting material is oleoresin. In another preferred embodiment, the tomato product used as the starting material comprises tomato peels.
The composition disclosed herein has been unexpectedly found, despite its greatly reduced lycopene concentration (in relation to prior art tomato oleoresins) to cause increased production of nitric oxide (NO) in vascular tissues. Furthermore, the present composition has been found to cause significant induction of the endothelial nitric oxide synthase enzyme in vascular endothelium.
The presently-disclosed composition has also been unexpectedly found to cause a significant increase in the activity of the antioxidant responsive element (ARE) system.
The presently-disclosed composition has further been unexpectedly found to cause significant inhibition of the pro-inflammatory NFkB transcription system.
The above-disclosed composition may be used to prepare a medicament for treating many different types of medical conditions. In one preferred embodiment, said medicament is suitable for use in treating disorders of the cardiovascular system, including but not limited to elevated blood pressure.
In another preferred embodiment, the medicament may be used to treat or prevent vascular damage and/or neuropathy in diabetic subjects.
In yet another preferred embodiment, the condition to be treated is characterized by having an inflammatory component. In one particularly preferred embodiment, the medicament is used to treat and/or prevent vascular inflammation.
In a still further preferred embodiment, the medicament of the present invention may be used to prevent the onset of neoplastic conditions.
In some embodiments, said composition further comprises one or more of the additional active components mentioned hereinabove, such as additional carotenoids, polyphenols (such as carnosic acid), vitamin E, phytosterols and soluble tomato solids (e.g. in the form of a clear tomato concentrate (CTC) prepared by concentrating the serum obtained from tomatoes following pulp-serum separation).
In a further aspect, the present invention is directed to the use of the above-defined reduced-lycopene tomato-derived composition in the preparation of a topical medicament. In one preferred embodiment of this aspect, the topical medicament is a cosmetic or cosmeceutical preparation, and may be prepared in the form of a cream, lotion, ointment, gel and so on.
In one preferred embodiment, said cosmetic or cosmeceutical agent is used as sunscreen, wherein the cosmeceutical composition may also additionally comprise conventional sunscreen agents, including but not limited to, PABA, zinc oxide, titanium oxide, cinoxate, Padimate O and Phenylbenzimidazole sulfonic acid.
In another preferred embodiment, the tomato-derived composition of the present invention is used as an anti-aging agent. In some embodiments of the invention, the above-defined tomato composition is used as the sole active agent, in other cases, the cosmetic or cosmeceutical agent comprises an additional active component.
In another preferred embodiment, the present invention is directed to the use of the above-defined reduced-lycopene tomato-derived composition in the preparation of a systemically-administered medicament, including, but not limited to, medicaments for oral delivery and medicaments suitable for parenteral delivery. In addition, the composition of the present invention may be used to prepare a medicament suitable for topical administration.
As disclosed hereinabove, the present invention provides composition comprising a reduced lycopene tomato product, wherein a general scheme of the process for manufacturing said composition is summarized in
Although the active agents, lycopene and phytoene/phytofluene, optionally in combinations with other carotenoids, and/or additional agents, can be administered alone, it is contemplated that these compounds will be administered in a pharmaceutical composition containing the active ingredients together with a pharmaceutically acceptable carrier or excipient.
Pharmaceutical compositions for use in accordance with the present invention can be formulated in conventional manner using one or more physiologically acceptable carriers comprising excipients and auxiliaries, which facilitate processing of the active compounds into preparations which can be used pharmaceutically. The active agents are formulated as pharmaceutical compositions and administered to a mammalian subject, such as a human patient in a variety of forms such as liquid, solid, and semisolid. The pharmaceutical compositions can be administered to a subject by any method known to a person skilled in the art, such as orally, topically, parenterally, transmucosally, transdermal, intramuscularly, intravenously, intradermally, subcutaneously, intraperitonealy, intraventricularly, intracranially or intratumorally. For oral administration, the compounds can be formulated by combining the active compounds with pharmaceutically acceptable carriers known in the art. The compositions can be formulated in any solid or liquid dosage form known in the art, including but not limited to, tablet, caplet, capsule, microcapsule, pellet, pill, powder, syrup, gel, slurry, granule, suspension, dispersion, emulsion, liquid, solution, dragee, bead and beadlet. The oral compositions can be formulated as immediate release formulations, or as controlled or sustained release formulations allowing for extended release of the active ingredient(s) over a predetermined time period.
Suitable excipients for solid formulations include but are not limited to fillers such as sugars, including lactose, sucrose, mannitol, or sorbitol; starch based excipients such as maize starch, wheat starch, rice starch, potato starch and the like, gelatin, gum tragacanth, cellulose based excipients as microcrystalline cellulose, carboxymethylcellulose, hydroxymethylcellulose, hydroxyethylcellulose, methylhydroxypropylcellulose, hydroxypropylcellulose and the like. Polymers such as polyvinylpyrrolidone (PVP) and cross-lined PVP can also be used. In addition, the compositions may further comprise binders (e.g. acacia, cornstarch, gelatin, carbomer, ethyl cellulose, guar gum, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, povidone), disintegrating agents (e.g. cornstarch, potato starch, alginic acid, silicon dioxide, croscarmelose sodium, crospovidone, guar gum, sodium starch glycolate), surfactants (e.g. sodium lauryl sulfate), and lubricants (e.g. stearic acid, magnesium stearate, polyethylene glycol, sodium lauryl sulfate).
For liquid formulations, pharmaceutically acceptable carriers may be aqueous or non-aqueous solutions, suspensions, emulsions or oils. Examples of non-aqueous solvents are propylene glycol, polyethylene glycol, and injectable organic esters. Aqueous carriers include water, alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media. Examples of oils include but are not limited to petroleum, animal, vegetable, or synthetic origin, for example, peanut oil, soybean oil, mineral oil, olive oil, sunflower oil, and fish-liver oil.
Preferred oral pharmaceutical compositions include capsules made of gelatin as well as soft, sealed capsules made of gelatin and a plasticizer, such as glycerol or sorbitol. In soft capsules, the active compounds may be dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols. In addition, stabilizers may be added. In certain preferred embodiments the capsules exclude components of animal origin and are acceptable for vegetarians and vegans.
Soft gelatin capsules and methods of preparing them are known in the art. Non-limiting examples can be found in U.S. Pat. Nos. 6,217,902; 6,258,380; 5,916,591, and 4,891,229, all of which are incorporated herein by reference.
Other acceptable excipients and additives known to the person with skill in the art may be included in the compositions of the present invention, for example stabilizers, solubilizers, tonicity enhancing agents, buffer substances, preservatives, thickeners, complexing agents and other excipients, as well as additional therapeutic agents.
A solubilizer can be for example, tyloxapol, fatty acid glycerol polyethylene glycol esters, fatty acid polyethylene glycol esters, polyethylene glycols, glycerol ethers or mixtures of those compounds. A specific example of a solubilizer is a polyoxyethylated castor oil for example, the commercial products Cremophor® or Cremophor® RH40. Another example of a solubilizer is tyloxapol. The concentration used depends especially on the concentration of the active ingredient. The amount added is typically sufficient to solubilize the active ingredient. For example, the concentration of the solubilizer is from 0.1 to 5000 times the concentration of the active ingredient
Examples of buffer substances are acetate, ascorbate, borate, hydrogen carbonate/carbonate, citrate, gluconate, lactate, phosphate, propionate and TRIS (tromethamine) buffers. The amount of buffer substance added is, for example, that necessary to ensure and maintain a physiologically tolerable pH range. The pH range is typically in the range of from 5 to 9, preferably from 5.2 to 8.5.
The compositions of the present invention may comprise further non-toxic excipients, such as, for example, emulsifiers, wetting agents or fillers, such as, for example, the polyethylene glycols (PEG200, 300, 400 and 600) or Carbowax® (CarbowaxlOOO, 1500, 4000, 6000 and 10000). Other excipients that may be used if desired are listed below but they are not intended to limit in any way the scope of the possible excipients. They can be complexing agents, such as disodium-EDTA or EDTA5 antioxidants, such as ascorbic acid, acetylcysteine, cysteine, sodium hydrogen sulfite, butyl-hydroxyanisole, butyl-hydroxytoluene; stabilizers, such thiourea, thiosorbitol, sodium dioctyl sulfosuccinate or monothioglycerol; or other excipients, such as, for example, lauric acid sorbitol ester, Methanol amine oleate or palmitic acid ester.
The amount of a composition to be administered will, of course, depend on many factors including the subject being treated, the severity of the affliction, the manner of administration, and the judgment of the prescribing physician. However, the dose employed will generally depend on a number of factors, including the age and sex of the patient, and the severity of the disease being treated.
Preferably, the preparations are in unit dosage form, intended for oral administration. In such form, the preparation is subdivided into unit doses containing appropriate quantities of the active components. The unit dosage form can be a packaged preparation, the package containing discrete quantities of preparation, for example, tablets, capsules, and powders in vials or ampoules. The unit dosage form can also be a capsule, cachet, or tablet itself or it can be the appropriate number of any of these in packaged form.
The dosing schedule of the compositions of the present invention can vary according to the particular application and the potency of the active ingredients. Determination of the proper dosage is within the skill of the art. For convenience, a single daily dose is preferred. Alternatively, the total daily dosage may be divided and administered in portions during the day such as twice daily, thrice daily and the like. Biweekly, weekly, bimonthly and monthly administration are also contemplated
The present invention will be further described in the following Examples, which are brought for illustrative purposes only, and do not limit the scope of the invention in any way.
The low-lycopene concentration composition of the present invention was prepared in accordance with the following process steps:
Primary human umbilical vein endothelial cells (HUVECs) were isolated from umbilical cords. The cells were harvested by 0.1% collagenase treatment (Worthington, Lakewood, N.J., USA). HUVECs were grown on 0.2% gelatin pre-coated tissue-culture flasks (Corning, Cole-Parmer, Vernon Hills, Ill., USA) in M-199 medium with 20% BCS and other supplements as described for EA.hy926. EA.hy926 cells were used until passage 37, HUVECs at passage 3-8. U937 monocytes were cultured in RPMI 1640 medium with 10% BCS, L-glutamine and antibiotics as specified earlier. For most experiments the endothelial cells at 70-90% confluence were starved in 5% BCS DMEM/M199 medium for 24 hours and pre-incubated with vehicle or carotenoids solution in 5% BCS DMEM/M199 for 18 to 24 hours, and activated with 10 ng/mL TNF-α (Peprotech, Rocky Hill, N.J., USA) for specified times.
Stock solutions (400 uM) of oleoresin (Lycored Natural Products Ltd., Beer-Sheva, Israel), containing either 6% or 7% lycopene, 0.1% β-carotene, 1% vitamin E and polyphenols, and the low-lycopene composition of the present invention (as obtained according to Preparative Example 1, above) were prepared in fresh tetrahydrofuran (THF) containing 0.025% butylated hydrohytoluene (BHT) (both from Sigma, St. Louis, Mo., USA) as an antioxidant, and were added to the culture medium under N2 stream and reduced lighting.
NO is a key signaling molecule in many biological processes and tissues. In the case of vascular tissues, the endothelium uses nitric oxide to signal the surrounding smooth muscle to relax, thus resulting in vasodilation and increased blood flow. NO further plays a role in vascular function by inhibiting vascular smooth muscle growth, platelet aggregation, and leukocyte adhesion to the endothelium. In many cases of human disease that are characterized by the presence of cardiovascular lesions (such as atherosclerosis, diabetes, or hypertension), impaired NO pathway function may often be found.
In the present study, a cultured human coronary endothelial cell model was used to assess the effect of the low-lycopene (2%) concentration composition of the present invention on the induction of NO. This was achieved both by the direct measurement of NO production by the cultured cells, and by assay of the activity of the endothelial cell NO synthase enzyme, peNOS. The results achieved with the composition of the present invention were compared with results obtained with the use of a high-lycopene tomato-derived composition, 7% Lyc-O-Mato (manufactured and supplied by LycoRed Ltd., Be'er Sheva, Israel).
The low-lycopene (2%) composition of the present invention (prepared as described hereinabove and the various control solutions (medium, THF and 7% Lyc-O-Mato) were added to confluent cultured human coronary endothelial cells (plated in 2 ml endothelial cell basal medium per 60 mm dish) for 24 hours, following which the supernatant culture fluid was collected.
Nitrite and nitrate (NOx), stable oxidized products of nitric oxide, were measured in the culture medium collected 24 h following the exposure to carotenoids using Greiss reagent, using the method described in Miranda K M, Espey M G and Wink D A, 2001 (Nitric Oxide 5: 62-71; “A rapid, simple spectrophotometric method for simultaneous detection of nitrate and nitrite”).
Experiments were performed at room temperature or at 37° C. in a warm room, as noted.
peNOS Analysis
Expression of the endothelial NO synthase enzyme, peNOS was assessed using Western blot analysis, as well known in the art. In brief, the protein content of an endothelial cell lysate was quantified using a BCA protein assay kit (Pierce, Rockford, Ill., USA. Equal quantities of cell proteins were separated by 7.5% SDS-PAGE and blotted to nitrocellulose membrane. After blocking and incubation with the primary peNOS antibody, the relative changes in the proteins content were quantified using densitometry in a reflectance mode.
As shown in
It may be concluded from these results that the low-lycopene concentration composition of the present invention is capable of significantly increasing the induction of NO in vascular endothelial cells, and that this effect is at least in part caused by increased expression of NO synthase enzyme in said cells. In view of these results, it may be concluded that the composition of the present system has activity of relevance that may be utilized in the treatment and prevention of various types of cardiovascular disease.
Antioxidant responsive elements (AREs) are identified in gene promoters and mediate a transcriptional induction of a battery of genes which comprise a chemoprotective response system. Said system is essential for resistance against a broad set of carcinogens. In addition, the activation of cytoprotective ARE-regulated genes can suppress inflammatory responses, whereas decreased expression of these genes results in autoimmune disease and enhanced inflammatory responses to oxidant insults. Therefore this ARE model is used as well in order to determine the anti-inflammatory effects of the tested compositions.
The aim of the present study was to assess the activity of a reduced-lycopene (0.7% w/w) modified oleoresin composition of the present invention, in the ARE system. The results obtained using this composition were compared with those obtained using LycoMato (containing 6% or 7% lycopene), present in equal molar concentrations of lycopene
A cell culture model, using both mammary (T47D) and prostate (LnCAP) cancer cells, was used to assess the activity of a low lycopene composition of the present invention, prepared as disclosed hereinabove, on the ARE system. Said low lycopene composition comprised 0.7% lycopene, 1.7% phytoene/phytofluene, 2.4% phytosterols and 2.5% vitamin E. Two commercially-available high-lycopene compositions (LycoMato 6% and LycoMato 7%; manufactured by LycoRed Ltd., Be'er Sheva, Israel) were also tested, for the purpose of comparison.
LNCaP, human prostate cancer cells were purchased from American Type Culture Collection (Manassas, Va., USA) and grown in RPMI 1640 medium containing sodium pyruvate (0.11 mg/ml) and DHT (10-9 M). To each medium, penicillin (100 units/nil), streptomycin (0.1 mg/ml), nystatin (12.5 μg/ml), Hepes (10 mM), and 10% FCS were added.
T47D, a human mammary cancer cell line, was kindly provided by Dr. Iafa Keydar (Tel Aviv University, Israel). T47D cells were grown in DMEM containing insulin (0.6 μg/ml or 6 μg/ml).
T47D cells were transfected using jet PEI reagent (Polyplus Transfection, Illkrich, France) in 24-well plates (100,000 cells per well). Cells were rinsed once with the appropriate culture medium without serum, followed by the addition of 0.45 ml of medium containing 3% DCC-FCS and 50 μl of a mixture containing DNA and jetPEI reagent at a charge ratio of 1:5. The total amount of DNA was 0.25 μg containing 0.2 μg reporter and 0.05 μg Renilla luciferase. The cells were then incubated for 4-6 h at 37° C. in 95% air/5% CO2. Medium was replaced with one supplemented with 3% DCC-FCS plus the test compounds, and cells were incubated for another 16 h.
LNCaP cells were transfected using the jetPEI reagent. Cells (70,000) were seeded in 1 ml medium without phenol red containing 3% DCCFCS. On the next day, 500 μl of medium was removed and 50 μl of a mixture containing DNA and jetPEI reagent at a charge ratio of 1:10 was added. The total amount of DNA was 0.2 μg containing 0.16 μg reporter and 0.04 μg Renilla luciferase vectors. Cells were incubated for 4-6 h followed by addition of the test compounds for 24 h.
Cell extracts were prepared for luciferase reporter assay (Dual Luciferase Reporter Assay (DLR™) System, Promega) according to the manufacturer's instructions. The Dual-Luciferase Reporter Assay System provides an efficient means of performing dual-reporter assays. In the DLR™ Assay, the activities of firefly (Photinus pyralis) and Renilla (Renilla reniformis, also known as sea pansy) luciferases are measured sequentially from a single sample. The firefly luciferase reporter is measured first by adding Luciferase Assay Reagent II (LAR II) to generate a stabilized luminescent signal. After quantifying the firefly luminescence, this reaction is quenched, and the Renilla luciferase reaction is simultaneously initiated by adding Stop & Glo® Reagent to the same tube. The Stop & Glo® Reagent also produces a stabilized signal from the Renilla luciferase, which decays slowly over the course of the measurement.
As demonstrated in
As shown in
It may be concluded from these results that the low-lycopene concentration composition of the present invention is a highly active inducer of ARE activity. Said composition therefore has the potential for influencing important cellular machinery that are of great importance in both the prevention of cancer and the reduction of inflammation.
Expression of inflammatory cytokines as well enzyme protein expression can be regulated by the activation of the transcription factor nuclear factor-kappa B (NFκB), which is critically involved in several aspects of the pathogenesis chronic inflammatory diseases. NFκB is activated as a consequence of phosphorylation, ubiquitination, and subsequent proteolytic degradation of the IκB protein through activation of IκB kinase (IKK). The liberated NFκB translocates into nuclei and binds to motifs in the promoters of pro-inflammatory genes such as inducible nitric oxide synthase (iNOS) and of cyclooxygenase 2 (COX2) TNF-α, and IL-1β, leading to the induction of their mRNA expression. Many of the anti-inflammatory drugs previously developed have been shown to suppress the expression of these genes by inhibiting the NFκB activation pathway. Thus, an NFκB inhibitor may be useful as a potential therapeutic drug in clinical applications for regulating the inflammation associated human diseases.
The aim of this study was to investigate whether the low-lycopene composition of the present invention can inhibit the NFkB transcription system in T47D mammary cancer cells.
The results of this study are shown in
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IL2015/051129 | 11/23/2015 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62083909 | Nov 2014 | US |
