IL46461A - Process for the manufacture of tobacco compositions - Google Patents
Process for the manufacture of tobacco compositionsInfo
- Publication number
- IL46461A IL46461A IL46461A IL4646175A IL46461A IL 46461 A IL46461 A IL 46461A IL 46461 A IL46461 A IL 46461A IL 4646175 A IL4646175 A IL 4646175A IL 46461 A IL46461 A IL 46461A
- Authority
- IL
- Israel
- Prior art keywords
- tobacco
- pharmaceutically acceptable
- acceptable salt
- weight
- smoke
- Prior art date
Links
- 235000002637 Nicotiana tabacum Nutrition 0.000 title claims abstract description 71
- 241000208125 Nicotiana Species 0.000 title claims abstract description 70
- 239000000203 mixture Substances 0.000 title claims abstract description 47
- 238000000034 method Methods 0.000 title claims description 29
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 99
- 239000000779 smoke Substances 0.000 claims abstract description 44
- 235000010323 ascorbic acid Nutrition 0.000 claims abstract description 38
- 239000011668 ascorbic acid Substances 0.000 claims abstract description 38
- 229960005070 ascorbic acid Drugs 0.000 claims abstract description 38
- 150000003839 salts Chemical class 0.000 claims abstract description 27
- MGWGWNFMUOTEHG-UHFFFAOYSA-N 4-(3,5-dimethylphenyl)-1,3-thiazol-2-amine Chemical compound CC1=CC(C)=CC(C=2N=C(N)SC=2)=C1 MGWGWNFMUOTEHG-UHFFFAOYSA-N 0.000 claims abstract description 23
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims abstract description 23
- 159000000000 sodium salts Chemical class 0.000 claims abstract description 5
- 239000002253 acid Substances 0.000 claims abstract 3
- 239000000126 substance Substances 0.000 claims description 24
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-araboascorbic acid Natural products OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 claims description 17
- 235000010350 erythorbic acid Nutrition 0.000 claims description 17
- 239000004318 erythorbic acid Substances 0.000 claims description 17
- 229940026239 isoascorbic acid Drugs 0.000 claims description 17
- 101000653791 Bos taurus Protein S100-A12 Proteins 0.000 abstract 1
- 239000011833 salt mixture Substances 0.000 abstract 1
- 235000019504 cigarettes Nutrition 0.000 description 38
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 14
- 235000010378 sodium ascorbate Nutrition 0.000 description 9
- PPASLZSBLFJQEF-RKJRWTFHSA-M sodium ascorbate Substances [Na+].OC[C@@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RKJRWTFHSA-M 0.000 description 9
- 229960005055 sodium ascorbate Drugs 0.000 description 9
- PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 239000011269 tar Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 230000000391 smoking effect Effects 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 150000004005 nitrosamines Chemical class 0.000 description 6
- 230000002588 toxic effect Effects 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 5
- 231100000331 toxic Toxicity 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000002207 metabolite Substances 0.000 description 4
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 229930003268 Vitamin C Natural products 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000000711 cancerogenic effect Effects 0.000 description 3
- 230000000622 irritating effect Effects 0.000 description 3
- UMFJAHHVKNCGLG-UHFFFAOYSA-N n-Nitrosodimethylamine Chemical compound CN(C)N=O UMFJAHHVKNCGLG-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- XKLJHFLUAHKGGU-UHFFFAOYSA-N nitrous amide Chemical compound ON=N XKLJHFLUAHKGGU-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 235000019154 vitamin C Nutrition 0.000 description 3
- 239000011718 vitamin C Substances 0.000 description 3
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 231100000357 carcinogen Toxicity 0.000 description 2
- 239000003183 carcinogenic agent Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 235000019506 cigar Nutrition 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000037406 food intake Effects 0.000 description 2
- 230000009931 harmful effect Effects 0.000 description 2
- 210000004072 lung Anatomy 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229960002715 nicotine Drugs 0.000 description 2
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 235000010352 sodium erythorbate Nutrition 0.000 description 2
- 239000004320 sodium erythorbate Substances 0.000 description 2
- RBWSWDPRDBEWCR-RKJRWTFHSA-N sodium;(2r)-2-[(2r)-3,4-dihydroxy-5-oxo-2h-furan-2-yl]-2-hydroxyethanolate Chemical compound [Na+].[O-]C[C@@H](O)[C@H]1OC(=O)C(O)=C1O RBWSWDPRDBEWCR-RKJRWTFHSA-N 0.000 description 2
- 231100000167 toxic agent Toxicity 0.000 description 2
- 239000003440 toxic substance Substances 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 101100172886 Caenorhabditis elegans sec-6 gene Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 206010047623 Vitamin C deficiency Diseases 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000019522 cellular metabolic process Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- -1 for exam-pie Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000001477 organic nitrogen group Chemical group 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 208000010233 scurvy Diseases 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000007910 systemic administration Methods 0.000 description 1
- 231100000563 toxic property Toxicity 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/24—Treatment of tobacco products or tobacco substitutes by extraction; Tobacco extracts
- A24B15/241—Extraction of specific substances
- A24B15/245—Nitrosamines
-
- A—HUMAN NECESSITIES
- A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
- A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
- A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
- A24B15/18—Treatment of tobacco products or tobacco substitutes
- A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
- A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
- A24B15/32—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances by acyclic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Manufacture Of Tobacco Products (AREA)
Abstract
1484663 Tobacco composition F HOFFMANN-LAROCHE & CO AG 14 Feb 1975 [15 Feb 1974] 6275/75 Heading A2C To reduce the nitrogen dioxide content in tobacco smoke, tobacco is treated with either an equimolar mixture of ascorbic acid and a salt thereof, or an equimolar mixture of erythorbic (isoascorbic) acid and a salt thereof or a mixture of the two. Preferably the tobacco contains between 0.1 and 10% by weight of the acid/salt mixture. The preferred salt is the sodium salt.
[GB1484663A]
Description
Process for the manufacture of a tobacco composition pao nai yn -nxv T^ nn SPARASfflELCfc A»G G. 44452 4226/65 The present invention is concerned ' with novel compositions comprising tobacco and, dispersed therein, a substance selected from the group consisting of an about equimolar mixture of ascorbic acid and a pharmaceutically acceptable salt thereof, an about equimolar mixture of erythorbic acid and a pharmaceutically acceptable salt thereof and mixtures thereof.
The invention further relates to the preparation of the above compositions, as well as to their use in the reduction of the nitrogen dioxide content in tobacco smoke.
The toxic effects of tobacco smoke, which had been .suspect for many years, have now been firmly established by an overwhelming quantity of scientific evidence. Among the various harmful substances which have been shown to be present in tobacco smoke are the various oxides of nitrogen. Of those nitrogen oxides normally present in tobacco smoke, nitrogen dioxide is the most toxic and most irritating. While the views of experts in the field are at a variance, it is estimated that as much as 50 of the nitrogen oxide content of tobacco smoke is nitrogen dioxide. The total nitrogen oxide content of tobacco smoke has been reported to range from about 145 ppm through 1000 ppm.
In addition to the irritating and toxic properties of % shown that nitrogen dioxide and certain other oxides of nitrogen can form nitrosating intermediates, which in turn can react with susceptible organic amines in the unturned tobacco to form nitrosamines . It is reported in the lite-rature that up to 140 ng of N-dimethyl-nitrosamine can be present in the smoke of one cigarette. The nitrosamine content in the smoke from different types of tobacco can vary from practically none up to 140 ng/cigarette . The amount of nitrosamines present in the smoke of a given type of tobacco is influenced by a number of variables such as, for example, the amount of nitrogen-containing fertilizer used in growing the tobacco plants. N-dimethylnitrosamine is a highly toxic substance and is recognized as a potent carcinogen in animal experiments, even at low levels of administration. It is therefore readily apparent that means to effectively reduce the nitrogen dioxide content of tobacco smoke would be of considerable benefit to those individuals who smoke tobacco in some form. Such a means is provided in accordance with the present invention.
The effect of smoking on the ascorbic acid content of the human body, as well as the benefit heavy smokers might possibly derive from ingestion of large amounts of ascorbic acid, have been the subject of a number of reports in the literature. Thus, for example, the substantial depletion of vitamin C in the body, caused by smoking, is known and some experts recommed the ingestion of large amounts of of what is termed "smoker's scurvy". This depletion of vitamin C in the body of heavy smokers has been substantiated by numerous others working in the field. These workers also have recommended that heavy smokers consume an abundance of vitamin C to prevent development of These findings and recommendations are directed to the alleviation of one of the harmful effects of heavy smoking in the body, but do not effect the prevention of the formation of nitrosamines or oxides of nitrogen and their presen- ce in the inhaled tobacco smoke.
French Patent No. 932,560 discloses a device such as cigarette paper, straw-like structure, holder, mouthpiece or similar article with which the smoke comes in contact as it is being inhaled. The device, which may or may not be burned with tobacco, is of a fibrous nature and is either impregnated or covered with a "metabolite" which is stated as being a subBtance which can interact with normal cell metabolism such as, for example, vitamins including ascorbic acid, enzymes, co-enzymes and the like. French Patent No. 932,561 discloses treatment of tobacco with such "metabolites". The stated object in having such substances impregnated in or coated on such a device or the tobacco, is that these metabolites are thereby mixed with the smoke in appreciable quantities thereby causing them to be inhaled with the smoke. The patents state that the presence of one or more of these metabolites in appreciable quantities in the smoke increases the tolerance of the user to "the toxic products (nicotine)" contained in or coated on the device or the tobacco, are stated as being progressively volatilized by the heat of combustion and are mixed with and consumed with the smoke.
British Patent No. 1,204,018 describes the use of inter alia ascorbic acid in filters and other portions of smoking devices to increase the ascorbic acid content of tobacco smoke and thus to increase the physiological availability of ascorbic acid into the lung.
The stated object of the device disclosed and i claimed in these references is to increase the tolerance of the smoker to the toxic products (nicotine) in the smoke. The teachings of these references, therefore, parallel those concerning the systemic administration of ascorbic acid to offset the deleterious effects of smoking, in that all are concerned with attempting to minimize such effects after the smoke has been inhaled.
It has been found in accordance with the present inve- tion that the amounts of at least one toxic substance, i.e. nitrogen dioxide, which is normally consumed with tobacco smoke can be sharply reduced before the smoke is inhaled.
The present invention is based on the discovery that the nitrogen dioxide content of tobacco smoke is markedly reduced as it is being drawn through uncombusted tobacco having dispersed therein an effective amount of a substance selected from the group consisting of an about equimolar mixture of ascorbic acid and a pharmaceutically acceptable salt thereof, an about equimolar mixture of erythorbic acid and a pharmaceutically acceptable salt thereof and mixtures thereof. Further, where tobacco is treated with these substances in accordance with the invention, the reduction 46461/2 in nitrogen dioxide content of the smoke in turn causes a reduction in the formation of nitrosamines which can be inhaled with the smoke. The formation of nitrosamines has been shown to occur as a result of reaction of nitrogen dioxide in the smoke with susceptible organic amines in the un-combusted tobacco. Thus the effects achieved according to the invention are most important, as nitrogen dioxide is the moat toxic and irritating of the nitrogen oxides normally preeent in the smoke and at least one nitrosamine, i.e.
N-dimethylnitrosamine, is a recognized carcinogen.
The compositions of the present invention can be prepared according to methods known per se, e.g. by dispersing throughout the tobacco an effectiveamount of a substance selected from the group consisting of an about equimolar mixture of ascorbic acid and a pharmaceutically acceptable salt thereof, an about equimolar mixture of erythorbic acid and a pharmaceutically acceptable salt thereof and mixtures thereof .
The amount of such substances to be utilized in accor-dance with the invention will vary over a wide range depending on such criteria as the "tar" content of the tobacco and, more particularly, on the organic nitrogen content thereof. Generally, treatment of tobacco with any amount of the substances named herein will cause some reduction in the nitrogen dioxide content of the smoke. As a practical matter, it has been found that an effective amount of such substances, utilized to treat tobacco in the practice of the invention, constitutes from about 0.1% by weight to about 10% by weight of the tobacco on a dry basis. In a more preferred embodiment, tobacco is treated with from about 1% by weight to about 4% by weight, on a dry basis, of one or more members of the group of substances mentioned above. As the average cigarette contains approximately one gram of tobacco, the above preferred percent range represents from about 10 mg to about 40 mg of the substances of the invention per cigarette.
It is recognized that the tar and impurity content of tobacco smoke is materially increased as the cigarette, cigar, etc. is consumed. Therefore, it is to be understood that treatment of tobacco in accordance with the present invention may not have an appreciable effect on the last two or threee inhalations of smoke. Thus, in order to achieve the full effect of the method of the invention, smoking of a cigarette, cigar, etc. containing treated tobacco should be discontinued while a reasonable amount remains unburned. It has been demonstrated by taste tests on human volunteers that the amount of the substances to be dispersed in the tobacco has no detectable adverse effect on the taste of the smoke.
It is hypothesized that the substances utilized to treat tobacco in accordance with the present invention, react with nitrogen dioxide to form nitric oxide and water. This so-called "trapping" of the nitrogen dioxide, in addition to the lungs, acts to competitively inhibit the formation of carcinogenic nitrosamines by reaction of nitrogen dioxide with amines in the unburned tobacco. In one series of tests, it has been demonstrated that smoke from cigarettes prepared from com-positions in accordance with the present invention and comprising a mixture of about 12 mg of equal parts ascorbic acid and sodium ascorbate per cigarette, contains about one-third of the nitrogen dioxide content of untreated controls utilizing a slow puff test and about one-half the nitrogen dioxide con-tent of controls using a fast puff test. It has also been demonstrated, using cigarettes containing approximately 25 mg of an equimolar mixture of ascorbic acid and sodium ascorbate per cigarette, that essentially none of said substances is taken into the body with the smoke.
The method of incorporating the substances of the present invention into the tobacco is not critical to the invention. Any method commonly recognized in the tobacco arts for incorporating additives into tobacco, which results in a substantially uniform dispersion of the additive, may be utilized, so long as the conditions are not such as would adversely affect the active compounds used in the practice of this invention, i.e., excessive heat and prolonged exposure to moisture. The stability characteristics of ascorbic and erythorbic acid and their salts, as well as methods of preventing or retarding degradation thereof, are well known in the art of food and pharmaceutical formulating. It is - tion to tobacco by blending therewith, in the dry state or by applying them as a solution or suspension in a suitable solvent such as water, ethanol, a po-L hydric alcohol or the like.
In accordance with the present invention, ascorbic acid, erythorbic acid and their pharmaceutical salts may be utilized in approximately equimolar proportions, but equimolar proportions are preferred. By pharmaceutically acceptable salts is meant those salts of ascorbic acid and erythorbic acid with pharmaceutically acceptable inorganic bases such as, for exam-pie, the sodium salt, the potassium salt, the calcium salt and the like.
The following examples are given to further illustrate the invention.
Example 1 Tobacco removed from commercially prepared cigarettes was treated in the following manner. An aqueous solution containing 75 mg/ml of an equimolar mixture of ascorbic acid and sodium ascorbate was sprayed onto the tobacco. The amount of said solution applied was approximately 157° by weight based on the dry weight of the tobacco. The tobacco was then dried utilizing a stream of nitrogen gas until the weight gain of the treated tobacco was equal to the amount of the ascorbic acid/ sodium ascorbate mixture deposited, i.e. all the applied water had been removed. The tobacco thus-treated was then weighed to give the same proportionate fill as that previously recorded for the commercial cigarettes and formed into ' cigarettes .
Cigarettes prepared in this manner were approximately 7 cm in length and contained 0.83 grams of tobacco per cigarette.
A total of 15 grams of an equimolar mixture of ascorbic acid and sodium ascorbate was pulverized to a fine powder utilizing a mortar and pestle . A sufficient quantity of this mixture was added to the tobacco taken from commercially prepa-red cigarettes to represent 3·75 by weight thereof. The ascorbic acid mixture was added in small portions while rotating the mixing vessel thereby assuring homogeneous distribution. Cigarettes were prepared from this tobacco. removed from commercial cigarettes which had been sprayed with distilled water and dried utilizing nitrogen gas until the initial weight of the tobacco was achieved.
Example 2 Cigarettes were prepared in accordance with the method of example 1, utilizing a sufficient amount of an aqueous solution of an equimolar mixture of ascorbic acid and sodium as-corbate so that each cigarette contained a total of 25 mg. The cigarettes of the mixture were smoked in an apparatus similar to that described by Millar et al., Cancer Research, Vol. 28, pages 968-971 (1968). The collected tars from treated and untreated control cigarettes were individually analyzed for ascorbic acid content . The analytical procedure utilized was that outlined by Roe et al. "Methods of vitamin assay" third edition, pages 318 ff., Interscience (1966). The results of this analysis are given in the following table.
Table I ^ig. Ascorbic Acid in Sample tars from 20 cigarettes Untreated cigarettes 20 Untreated cigarettes + 100 >ug. added for analysis purposes 117 Treated cigarettes 27 The results of the foregoing analysis indicate that a- maximum of 1 part in 10,000 of the ascorbic acid content of the tobacco was carried over into the tar fraction of the smoke . The value of 27 micrograms per 20 cigarettes lies near the limit of detection for ascorbic acid under the analytical conditions utilized. It is therefore a reasonable assumption that more sensitive methods of testing may reveal that the value of ascorbic acid in the tar may be even lower than shown in the above table. The results given in the above Table can be inter- preted as indicating that essentially no ascorbic acid is transferred from the treated tobacco to the tar during the smoking process.
Example 3 Whatman No. 1 filter paper was cut into discs having a diameter of 13 mm. These discs were treated with an aqueous ' solution of equimolar concentrations of ascorbic acid and sodium ascorbate in accordance with the procedure of Example 1, so that the concentration thereof in each disc was 0.6 mg of the combination. Discs treated with distilled water served as controls. Such discs were individually mounted in an adapter 3 3 which was fitted onto a 5 cnr gas tight syringe. A 2 cm sample of a gaseous mixture containing 10 parts per million nitrogen dioxide was passed twice through each paper disc.
The nitrogen dioxide content of this Bample was analyzed by the method of Greiss-Saltzman, "Methods of Air Sampling and Analysis" American Public Health Assoc., page 333f (1972).
The results of this experiment show that the nitrogen dioxide content of the sample passed through the untreated controlled disc was approximately equal to that passed through the syringe with no disc at all and that the content of the sample passed through the treated disc was, on the average, approximately 10 of the original content of the sample .
Example 4 Cigarettes treated with 12 mg/cigarette of equimolar mixtures of ascorbic acid/sodium ascorbate and erythorbic acid/ sodium erythorbate , in accordance with the aqueous solution method of Example l,were smoked in the following manner. A 50 ml syringe was utilized to draw smoke from a cigarette attached to an adaptor. The smoke was immediately deposited in a collection vessel containing Greiss-Saltzmann reagent. The smoke of treated and untreated (control) cigarettes was then analyzed for nitrogen dioxide content. A standardized fast draw and slow draw technique was utilized to smoke the cigarettes. The definitions of these techniques are set forth in Table I.
TABLE I Parameter Past Draw Slow Draw Puff volume 35 cur 35 cm5 Puff duration 2 sec 6 sec Puff frequency l/min l/min Average butt length 23 mm 23 mm The results of the tests are set forth in Table II, wherein the amount of nitrogen dioxide in the smoke is given as a percent of control.
TABIE II Slow Draw Fast Draw Ascorbic Acid & Sodium Ascorbate 38 58 Erythorbic Acid & Sodium Erythorbate 35 52 Example 5 Cigarettes prepared in accordance with Example 1 utilizing a sufficient amount of a powder mixture of equimolar amounts of ascorbic acid and sodium ascorbate so that each cigarette contained 35 mg of the mixture were smoked on an apparatus described by Millar et al. in Cancer Research, Vol. 28, pages 968-971, May, 1968. The tars from treated cigarettes and controls were analyzed for N-nitrosamine content according to the method of Rhoades et al. described in the Journal of the National Cancer Institute, "Vol. 48, pages 1841-1843 and 1845-1847 (1972). The results of this test show that the content of dimethyl-N-nitrosamine of the cigarette smoke in controls was reduced by approximately 70 in the treated cigarettes.
Claims (16)
1. Process for the manufacture of compositions based on tobacco, characterised in that a substance selected from the group consisting of an about equimolar mixture of ascorbic acid and a pharmaceuticall acceptable salt thereof, an about equimolar mixture of erythorbic acid and a pharmaceutically acceptable salt thereof and mixtures thereof is dispersed throughout the tobacco.
2. Process according to claim 1, characterized in that the ascorbic acid and a pharmaceutically acceptable salt thereof and the erythorbic acid and a pharmaceutically acceptable salt thereof, respectively, are used in equimolar proportions.
3. Process according to claim 1 or 2, characterised in that the sodium salt is used as pharmaceutically acceptable salt of ascorbic and erythorbic acid.
4. Process according to claim 1, 2 or 3> characterised in that the substance is used in an amount of from about 0,1 by weight to about 10$ by weight of the tobacco.
5. Process according to claim 4, characterised in that the substance is used in an amount of from about 1% by weight to about o by weight of the tobacco. 46461/2
6. Process for the manufacture of compositions as hereinbefore particularly described, especially with reference to the foregoing examples.
7. Compositions comprising tobacco and, dispersed therein, a substance selected from the group consisting of an about equimolar mixture of ascorbic acid and a pharmaceutically acceptable Bait thereof, an about equMolar mixture of ery-thorbic acid and a pharmaceutically acceptable salt thereof and mixtures thereof.
8. Compositions according to claim 7, comprising the ascobirc acid and a pharmaceutically acceptable salt thereof and the erythorbic acid and a pharmaceutically acceptable salt thereof, respectively, in equimolar proportions.
9. Compositions according to claim 7 or 8, wherein the sodium salt is present as pharmaceutically acceptable salt of aBcorbic and erythorbic acid.
10. Compositions according to claim 7, 8 or 9, wherein the substance is present in an amount of from about 0,1 by weight to about 10$ by weight of the tobacco.
11. Compositions acoording to claim 10, wherein the substance is present in an amount of from about 1% by weight to about 4$ by weight of the tobacco.
12. A method for the reduction of nitrogen dioxide content in tobacco smoke, which comprises passing said smoke through uncombusted tobacco having dispersed therein an effective amount of a substance selected from the group consisting of an about equimolar mixture of ascorbic acid and a pharmaceutically acceptable salt thereof, an about equimolar mixture of erythorbic acid and a pharmaceutically acceptable salt thereof and mixtures thereof.
13. . A method according to claim 12, wherein the smoke is passes through tobacco having dispersed therein the ascorbic acid and a pharmaceutically acceptable salt thereof and the erythorbic acid and a pharmaceutically acceptable salt thereof, respectively, in equimolar proportions.
14. . A method according to claim 12 or 13, wherein the sodium salt is used as pharmaceutically acceptable salt of ascorbic and erythorbic acid.
15. · A method according to claim 12, 13 or 14, wherein the tobacco contains from about 0,l° by weight to about 10% by weight of the substance.
16. A method according to claim 15, wherein the tobacco contains from about 1% by weight to about 4% by weight of the substance .
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US44299074A | 1974-02-15 | 1974-02-15 |
Publications (2)
Publication Number | Publication Date |
---|---|
IL46461A0 IL46461A0 (en) | 1975-04-25 |
IL46461A true IL46461A (en) | 1977-11-30 |
Family
ID=23758994
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL46461A IL46461A (en) | 1974-02-15 | 1975-01-20 | Process for the manufacture of tobacco compositions |
Country Status (14)
Country | Link |
---|---|
JP (1) | JPS50111295A (en) |
AT (1) | AT340297B (en) |
BE (1) | BE825514A (en) |
CH (1) | CH600804A5 (en) |
DE (1) | DE2506100A1 (en) |
DK (1) | DK53875A (en) |
FR (1) | FR2260960B1 (en) |
GB (1) | GB1484663A (en) |
HU (1) | HU170011B (en) |
IL (1) | IL46461A (en) |
NL (1) | NL7501600A (en) |
PH (1) | PH12188A (en) |
SE (1) | SE7501578L (en) |
ZA (1) | ZA75351B (en) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3200305C2 (en) * | 1982-01-08 | 1983-11-17 | B.A.T. Cigaretten-Fabriken Gmbh, 2000 Hamburg | Process for improving the filling capacity of tobacco, in particular tobacco leaf cut |
HU192213B (en) * | 1985-04-29 | 1987-05-28 | Pecsi Dohanygyar | Method for producing smoke filter neutralizing the materials injurious the health being in tobacco smoke particularly aldehydes |
USRE38123E1 (en) | 1996-06-28 | 2003-05-27 | Regent Court Technologies, Llc. | Tobacco products having reduced nitrosamine content |
US6311695B1 (en) | 1996-06-28 | 2001-11-06 | Regent Court Technologies | Method of treating tobacco to reduce nitrosamine content, and products produced thereby |
US6135121A (en) | 1996-06-28 | 2000-10-24 | Regent Court Technologies | Tobacco products having reduced nitrosamine content |
US6202649B1 (en) | 1996-12-02 | 2001-03-20 | Regent Court Technologies | Method of treating tobacco to reduce nitrosamine content, and products produced thereby |
US6805134B2 (en) | 1999-04-26 | 2004-10-19 | R. J. Reynolds Tobacco Company | Tobacco processing |
US8151804B2 (en) | 2008-12-23 | 2012-04-10 | Williams Jonnie R | Tobacco curing method |
DK2818058T3 (en) | 2012-02-24 | 2019-02-18 | Japan Tobacco Inc | PROCEDURE FOR MANUFACTURING BUBBLE MATERIALS AND BUBBLE MATERIALS |
WO2014141201A2 (en) * | 2013-03-15 | 2014-09-18 | Fall Safall | Method of reducing tobacco-specific nitrosamines |
JP7292035B2 (en) | 2015-06-26 | 2023-06-16 | アルトリア クライアント サーヴィシーズ リミテッド ライアビリティ カンパニー | Compositions and methods for producing alkaloid level-modified tobacco plants and products |
EA201892755A1 (en) * | 2016-05-27 | 2019-05-31 | Джапан Тобакко Инк. | TObacco FILLING FOR HEATING CURRENT PRODUCT OF NON-Flammable |
WO2022049703A1 (en) * | 2020-09-03 | 2022-03-10 | 日本たばこ産業株式会社 | Tobacco filling material, non-combustion heating-type flavor inhaler, and method for producing tobacco filling material |
-
1975
- 1975-01-17 ZA ZA00750351A patent/ZA75351B/en unknown
- 1975-01-20 IL IL46461A patent/IL46461A/en unknown
- 1975-02-07 CH CH154875A patent/CH600804A5/xx not_active IP Right Cessation
- 1975-02-10 PH PH16794A patent/PH12188A/en unknown
- 1975-02-11 NL NL7501600A patent/NL7501600A/en not_active Application Discontinuation
- 1975-02-12 JP JP50016972A patent/JPS50111295A/ja active Pending
- 1975-02-12 SE SE7501578A patent/SE7501578L/xx unknown
- 1975-02-13 FR FR7504495A patent/FR2260960B1/fr not_active Expired
- 1975-02-13 DE DE19752506100 patent/DE2506100A1/en active Pending
- 1975-02-14 DK DK53875*#A patent/DK53875A/da unknown
- 1975-02-14 GB GB6275/75A patent/GB1484663A/en not_active Expired
- 1975-02-14 AT AT112275A patent/AT340297B/en not_active IP Right Cessation
- 1975-02-14 HU HUHO1769A patent/HU170011B/hu unknown
- 1975-02-14 BE BE153339A patent/BE825514A/en unknown
Also Published As
Publication number | Publication date |
---|---|
DK53875A (en) | 1975-10-06 |
FR2260960B1 (en) | 1978-02-03 |
DE2506100A1 (en) | 1975-08-21 |
BE825514A (en) | 1975-08-14 |
ATA112275A (en) | 1977-03-15 |
AT340297B (en) | 1977-12-12 |
HU170011B (en) | 1977-03-28 |
SE7501578L (en) | 1975-08-18 |
AU7759675A (en) | 1976-07-29 |
PH12188A (en) | 1978-11-21 |
CH600804A5 (en) | 1978-06-30 |
NL7501600A (en) | 1975-08-19 |
FR2260960A1 (en) | 1975-09-12 |
GB1484663A (en) | 1977-09-01 |
IL46461A0 (en) | 1975-04-25 |
ZA75351B (en) | 1976-01-28 |
JPS50111295A (en) | 1975-09-01 |
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