Use of pectin or other anionic polymers in the stabilization and controlled release of nicotine in oral sensorial tobacco products or nicotine containing non-tobacco oral sensorial products

Information

  • Patent Grant
  • 11925201
  • Patent Number
    11,925,201
  • Date Filed
    Tuesday, December 22, 2020
    3 years ago
  • Date Issued
    Tuesday, March 12, 2024
    7 months ago
Abstract
The use of pectins and/or polymers to prevent nicotine oxidation in tobacco containing products is disclosed. These polymers may be naturally occurring anionic polymers or synthetic polymers. These pectins and/or polymers prevent nicotine from oxidizing into cotinine, nicotine-cis-N-oxide, nicotine-trans-N-oxide, and/or nicotine-1,1-di-N-oxide. Molluscicides, algaecides, pesticides, and stabilized nicotine compositions comprising nicotine and pectin, anionic polymers, or combinations thereof are disclosed.
Description
BACKGROUND

Nicotine is a well-known and highly characterized naturally occurring alkaloid found in the tobacco plant, Nicotiana tabacum. Under ambient conditions, nicotine is an oily, volatile, hygroscopic liquid that is sensitive to light and air. Due to its volatility, nicotine may evaporate during its processing. Additionally, the nitrogen in the pyrrolidinic ring can undergo protonation in the presence of an acid. Further, any nicotine free base present in an article is susceptible to oxidation through an electrophilic attack.


Thus, the stabilization of nicotine in oral sensorial tobacco products, or nicotine containing non-tobacco oral sensorial products, is desirable.


SUMMARY

The present disclosure is related to the use of pectins and/or polymers to prevent nicotine oxidation in tobacco containing products. In one embodiment, the use of pectins and/or polymers to prevent nicotine oxidation in tobacco containing products, wherein said polymers are naturally occurring anionoic polymers is disclosed. In another embodiment, the use of pectins and/or polymers to prevent nicotine oxidation in tobacco containing products, wherein said polymers are synthetic polymers is disclosed. In another embodiment, the use of pectins and/or polymers to prevent nicotine oxidation in tobacco containing products, wherein nicotine is prevented from oxidizing into cotinine, nicotine-cis-N-oxide, nicotine-trans-N-oxide, and/or nicotine-1,1-di-N-oxide is disclosed. In another embodiment, a method of preventing nicotine oxidation in tobacco containing products comprising mixing the tobacco with pectins and/or polymers is disclosed.


One embodiment is a process for preventing nicotine oxidation in tobacco containing products comprising pectin and/or anionic polymers, which can form salts with protonated forms of nicotine that are typically present below pH levels of around 9 or so, can act like an ion-exchange resin and hold nicotine in close proximity by electrostatic attraction.


Another embodiment is a method for stabilizing nicotine comprising employing pectin and/or an anionic polymer at a pH of around 6 (above pH values of about 4 or so and below pH levels of about 9).


Another embodiment is a method for reducing the formation of oxidation products from nicotine comprising employing pectin and/or an anionic polymer.


Another embodiment is a molluscicide composition comprising nicotine and pectin, an anionic polymer, or a combination thereof, wherein said pectin, an anionic polymer, or a combination thereof stabilizes said nicotine.


Another embodiment is an algaecide composition comprising nicotine, and pectin, an anionic polymer, or a combination thereof, wherein said pectin, an anionic polymer, or a combination thereof stabilizes said nicotine.


Another embodiment is a pesticide composition comprising nicotine, and pectin, an anionic polymer, or a combination thereof, wherein said pectin, an anionic polymer, or a combination thereof stabilizes said nicotine.


Another embodiment is a stabilized nicotine composition comprising nicotine, and pectin, an anionic polymer, or a combination thereof, wherein the pH of said composition is above pH values of about 4 or so and below pH levels of about 9.


A further embodiment is a controlled-release nicotine composition comprising nicotine, and further comprising pectin, an ionic polymer, or a combination thereof.


Another embodiment is a method for controlling the release of nicotine comprising complexing nicotine with a pectin, an anionic polymer, or a combination thereof at a pH of above pH values of about 4 or so and below pH levels of about 9.


A further embodiment is a controlled-release nicotine article comprising pectin, an anionic polymer, or a combination thereof. Further envisioned is a controlled-release nicotine article comprising pectin, an anionic polymer, or a combination thereof, wherein the article is a lit-end cigarette, an electrically heated cigarette, chewing tobacco, snus, dry snuff, moist snuff, tablets, sticks, strips, pouched products, chewable gum, or a wrapper.







DETAILED DESCRIPTION

Nicotine, or 3-[(2S)-1-methylpyrrolidin-2-yl]pyridine, is a tertiary amine with the following structure:




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Nicotine constitutes approximately 0.6-3.0% of the dry weight of tobacco. Nicotine has numerous commercial uses including as a fumigant, an insecticide, and in smoking articles such as cigarettes, cigars, and in pipes and smokeless tobacco products such as chewing tobacco, snuff, pouches and gum. It is well known that nicotine oxidation is catalyzed by light and that nicotine is more stable in its protonated form. In nicotine chewing gum products (pharmaceutical products designed for smoking cessation therapy) the nicotine can be bound to the weak cation-exchanger polyacrilex to prevent oxidation.


It is desirable to prevent the oxidation of the nicotine in smoking articles and smokeless tobacco products. A common method to reduce the processing and stability issues associated with the nicotine compound involves the preparation of a complex of nicotine and an ion exchange resin. Nicotine ion exchange complexes are described in U.S. Pat. Nos. 5,935,604 and 6,607,752 and U.S. Pat. App. Pub. Nos. 2009/0092573 and 2010/0130562.


Ion exchange resins are characterized by their capacity to exchange ions. The ion exchange capacity is measured as the number of equivalents of an ion that can be exchanged and can be expressed with reference to the mass of the polymer or its volume. Ion exchange resins are known in the art and can be manufactured in forms such as spherical and non-spherical particles with size in the range of 0.001 mm to 2 mm.


Pectins are natural polymers related to carbohydrates, except that C-6 contains a fully oxidized carboxylic acid (or corresponding methyl ester or carboxamide) group instead of a hydroxymethyl group. The principal subunit is known as galacturonic acid, which can be copolymerized with L-rhamnose. Other sugars are featured as side-chain substituents. The carboxylic acid form, more particularly the carboxylate anionic form present at pH values above about 4 or so, forms “salts” with protonated forms of nicotine that are typically present below pH levels of around 9 or so.


Provided herein is the use of pectins combined with nicotine or nicotine-containing tobacco extracts to create reconstituted tobaccos or other nicotine-containing materials that can be used in an oral sensorial (including chewable) product. Chewable products include chewing tobacco, snus, dry snuff, moist snuff, tablets, sticks, strips, pouched products, chewable gum, spongy material, or combination of these.


An embodiment is the use of pectins and/or polymers to prevent nicotine oxidation in tobacco containing products. These polymers may be naturally occurring anionic polymers or synthetic polymers. Described herein is a use wherein nicotine is prevented from oxidizing into cotinine, nicotine-cis-N-oxide, nicotine-trans-N-oxide, and/or nicotine-1,1-di-N-oxide.


Also described is the use of pectin to allow greater recovery of nicotine from tobacco-processing streams involved in reconstituted-leaf production for lit-end cigarettes and electrically heated cigarettes. If the more soluble versions of anionic pectins are used and ingested, they will continue to bind nicotine.


If the pectin used has low water-solubility, the pectin, within the appropriate pH range, can act like an “ion-exchange resin,” and hold nicotine in close proximity by electrostatic attraction that is characteristic of ionized salts. Natural tobacco pectins attract nicotine at pH levels of around 6, which can prolong the release of nicotine when such tobaccos are chewed or otherwise exposed to saliva in the mouth.


Pectin may be extracted from tobacco, but also commercially available pectin isolated from sources such as apple pomace, citrus peels, sugarbeet waste from sugar manufacturing, sunflower heads discarded from seed harvesting, mango waste, and other commercially available pectins may be used.


Physical properties of several types of pectin suitable for use herein are provided in Table 1.









TABLE 1







PHYSICAL PROPERTY DATA FOR PECTINS















Intrinsic








viscosity
Huggins
Solvent


Pectin
Description
(dl/g)
coefficient
conditions
pH
MW
















Sigma
6% ester,
5.8556
0.0643
Good
3.389
613,740


apple
low ester


draining


pectin
pectin


Genu
Amidated
4.9261
0.8462
Poor
2.984
479,760


Pectin
low ester


solvent


Type
pectin, 17%


conditions


X-916-02
amidation,



34% ester,



no sugar


Genu
Around
3.6156
0.827
Poor, non-
3.052
376,300


Pectin
40% ester


draining


Type LM
pectin, no


18-CG-Z
sugar


Tobacco
Very low
1.881
0.4154
Very
2.983
259,530


pectin
ester


good


(unwashed)
pectin


draining


Tobacco
Very low
1.3514
0.02749
Very
4.420
237,270


pectin
ester


good


(dialyzed)
pectin


draining









Other naturally occurring anionic polymers, or synthetic anionic polymers that have achieved GRAS status for use in foods or cosmetics, may also be used. Such polymers include carboxymethylcellulose, other carboxylated carbohydrate-derived polymers such as alginate or alginic acid, sulfated carbohydrate polymers such as carrageenan, fucoidans, heparan sulfate or heparin, and phosphorylated polymers such as deoxyribonucleic acid (DNA) or ribonucleic acid (RNA). All of these exhibit ion-exchange characteristics with respect to nicotine, within an appropriate pH range. The sulfated or phosphorylated polymers have a lower effective pH range than the carboxylate-containing polymers, due to their inherently lower pKa values, subject to chemical stability impairments that may occur under excessively acidic conditions.


Another embodiment is the use of pectins combined with nicotine or nicotine-containing tobacco extracts to create nicotine releasing wrappers of oral sensorial (including chewable) products.


The examples explained below are given by way of illustration only and should not be interpreted as constituting any limitation of the subject of the present invention.


EXAMPLES
Example 1

Nicotine and pectin compositions may be formed by mixing nicotine (about 1%-about 30%) with pectin or anionic polymer combinations (about 70%-about 99%).


While the foregoing describes in detail the use of pectin or other anionic polymers in the stabilization of nicotine in oral sensorial tobacco products or nicotine containing non-tobacco oral sensorial products with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications equivalents to the use of pectin or other anionic polymers in the stabilization of nicotine in oral sensorial tobacco products or nicotine containing non-tobacco oral sensorial products may be employed, which do not materially depart from the spirit and scope. Accordingly, all such changes, modifications, and equivalents that fall within the spirit and scope as defined by the appended claims are intended to be encompassed thereby.


All publications cited herein are incorporated by reference in their entireties for all purposes.

Claims
  • 1. A nicotine composition comprising: a complex consisting essentially of nicotine and one or more pectins, the complex including the nicotine in an amount ranging from 1 weight percent to 30 weight percent and the one or more pectins in an amount ranging from 70 weight percent to 90 weight percent, the one or more pectins including unwashed tobacco pectin.
  • 2. The nicotine composition of claim 1, wherein a pH of the complex is in a range of 4 to 9.
  • 3. The nicotine composition of claim 2, wherein the pH is 6.
  • 4. The nicotine composition of claim 1, wherein the one or more pectins further comprise apple-derived pectin, citrus-derived pectin, sugar beet-derived pectin, sunflower-derived pectin, mango-derived pectin, or any combination thereof.
  • 5. The nicotine composition of claim 1, wherein the nicotine is tobacco-extracted nicotine.
  • 6. An oral sensorial product comprising: a nicotine composition including a complex consisting essentially of nicotine and one or more pectins, the complex including the nicotine in an amount ranging from 1 weight percent to 30 weight percent and the one or more pectins in an amount ranging from 70 weight percent to 90 weight percent, the one or more pectins includingunwashed tobacco pectin, the oral sensorial product being in a form of chewing tobacco, snus, dry snuff, moist snuff, tablets, sticks, strips, pouched products, chewable gum, spongy material, or any combination thereof.
  • 7. A nicotine composition comprising: a complex consisting essentially of nicotine and one or more pectins, the complex including the nicotine in an amount ranging from 1 weight percent to 30 weight percent and the one or more pectins in an amount ranging from 70 weight percent to 90 weight percent, the one or more pectins includingdialyzed tobacco pectin.
  • 8. The nicotine composition of claim 7, wherein a pH of the complex is in a range of 4 to 9.
  • 9. The nicotine composition of claim 8, wherein the pH is 6.
  • 10. The nicotine composition of claim 7, wherein the one or more pectins further comprise apple-derived pectin, citrus-derived pectin, sugar beet-derived pectin, sunflower-derived pectin, mango-derived pectin, or any combination thereof.
  • 11. The nicotine composition of claim 7, wherein the nicotine is tobacco-extracted nicotine.
  • 12. An oral sensorial product comprising: a nicotine composition including, a complex consisting essentially of nicotine and one or more pectins, the complex including the nicotine in an amount ranging from 1 weight percent to 30 weight percent and the one or more pectins in an amount ranging from 70 weight percent to 90 weight percent, the one or more pectins includingdialyzed tobacco pectin, the oral sensorial product being in a form of chewing tobacco, snus, dry snuff, moist snuff, tablets, sticks, strips, pouched products, chewable gum, spongy material, or any combination thereof.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation application of U.S. patent application Ser. No. 16/194,787, filed on Nov. 19, 2018, which is a continuation application of U.S. patent application No. 14/206,515, filed on Mar. 12, 2014, now U.S. Pat. No. 10,130,120, issued on Nov. 20, 2018, which claims priority to U.S. Provisional Patent Application Ser. No. 61/799,428, filed on Mar. 15, 2013, the entire contents of each of which are incorporated herein by reference thereto.

US Referenced Citations (32)
Number Name Date Kind
3746012 Deszyck Jul 1973 A
3861400 Perkins et al. Jan 1975 A
4142535 Perkins et al. Mar 1979 A
4674519 Keritsis et al. Jun 1987 A
5525351 Dam Jun 1996 A
5567462 Ehrlich Oct 1996 A
5935604 Illum Aug 1999 A
6110495 Dam Aug 2000 A
6432440 Watts et al. Aug 2002 B1
6607752 Bellamy et al. Aug 2003 B2
8042552 Xue et al. Oct 2011 B2
8733369 Rees et al. May 2014 B2
10881134 Mishra Jan 2021 B2
20040194793 Lindell Oct 2004 A1
20060147498 Jonsson et al. Jul 2006 A1
20060275344 Mody et al. Dec 2006 A1
20080286340 Andersson et al. Nov 2008 A1
20090092573 Andersen Apr 2009 A1
20090293895 Axelsson et al. Dec 2009 A1
20100086981 LaTouf Apr 2010 A1
20100130562 Hite et al. May 2010 A1
20100247582 Sorensen et al. Sep 2010 A1
20100247586 Hugerth et al. Sep 2010 A1
20100303969 Sengupta et al. Dec 2010 A1
20110071184 Bunick Mar 2011 A1
20110083681 Sengupta et al. Apr 2011 A1
20120048285 Mishra et al. Mar 2012 A1
20120052021 Kobal et al. Mar 2012 A1
20120128734 Hubinette et al. May 2012 A1
20120247492 Kobal et al. Oct 2012 A1
20130125904 Chen et al. May 2013 A1
20130192620 Tucker et al. Aug 2013 A1
Foreign Referenced Citations (2)
Number Date Country
1495941 Dec 1977 GB
WO-2010104464 Sep 2010 WO
Non-Patent Literature Citations (5)
Entry
Definition of “complex”, IUPAC. Compendium of Chemical Terminology, 2nd ed. (the “Gold Book”), 1997, [online], [retrieved on Jun. 24, 2014], Retrieved from the Internet: <URL: http://goldbook.iupac.org (2006-)>. (Year: 1997).
Polysacharrides (Sugars, Gums) Used in Cosmetics, MakingCosmetics Inc., no date, [online], retrieved from the Internet, [retrieved Apr. 4, 2015],<URL:http://www.makingcosmetics.com/articles/20-polysaccharides-sugars- -gums-in-cosmetics.pdf>.
Definition of complex, Chemistry Dictionary, no date, [online], retrieved from the Internet, [retrieved Apr. 4, 2015], <URL:http://www.chemicool.com/definition/complex.html>.
Definition of “complex”, IUPAC Gold Book, 1994, [online], retrieved from the Internet, retrieved Jun. 24, 2014], <URL:http://goldbook.iupac.org/C01203.html>.
International Search Report dated Jun. 26, 2014, for International Patent Publication No. PCT/US2014/025931.
Related Publications (1)
Number Date Country
20210106044 A1 Apr 2021 US
Provisional Applications (1)
Number Date Country
61799428 Mar 2013 US
Continuations (2)
Number Date Country
Parent 16194787 Nov 2018 US
Child 17130542 US
Parent 14206515 Mar 2014 US
Child 16194787 US