[0001] The present invention relates to a smokeless tobacco or non-tobacco snuff composition
for oral use comprising at least 1 wt% lactic acid, or a salt thereof, based on the
dry weight of the smokeless tobacco composition, as well as a method for its manufacture
and the use of such composition.
BACKGROUND
[0002] Smokeless tobacco or non-tobacco snuff products for oral use comprise finely divided,
particulate, such as ground, or cut, tobacco or non-tobacco material or a combination
thereof that is not intended for combustion but designed to be placed in the oral
cavity of a user for a period of time.
[0003] There are many various forms of smokeless tobacco or non-tobacco products for oral
use. Such forms include chewing tobacco and tobacco or non-tobacco snuff. Snuff is
available in two forms, as dry snuff for oral or nasal use and moist (or wet) snuff.
There are two types of moist snuff, the American and the Scandinavian type. American-type
moist snuff is available in a loose form or as pre-packed pouches and is typically
used between the lower gum and lip. The use of American-type moist snuff is commonly
called dipping. Snus is the Scandinavian-type of moist snuff which is also available
in loose form or as pre-packed portions in pouches. Snus is typically used between
the upper gum and lip.
[0004] There are a number of properties of the smokeless tobacco or non-tobacco snuff products
for oral use that are very important for the end user. Among them, the organoleptic
properties, such as texture, aroma, taste, form and package of the product, are of
high importance for the consumer.
[0005] There is a merit in offering a range of products with different organoleptic properties
to the consumers. An example of a smokeless tobacco product is described in
WO2006 /065192A1.
SUMMARY OF THE INVENTION
[0006] The present invention relates to a smokeless tobacco or non-tobacco snuff composition
for oral use comprising at least 1 wt% lactic acid or a salt thereof based on the
dry weight of the smokeless tobacco composition. The invention further relates to
a method for manufacturing such composition, the use of such composition and a pouch
containing such composition.
[0007] The present invention is defined in the appended claims.
[0008] Thus, a first aspect of the present invention is a smokeless tobacco or non-tobacco
snuff composition for oral use comprising at least 20 wt% water based on the total
weight of the final composition, wherein the composition further comprises at least
1 wt% lactic acid or a salt thereof based on the dry weight of the final composition.
A second aspect of the present invention is a method for manufacturing of a smokeless
tobacco or non-tobacco snuff composition comprising at least 20 wt% water based on
the total weight of the final composition and at least 1 wt% lactic acid or a salt
thereof based on the dry weight of the final composition, wherein the method comprises:
- a) providing a tobacco or non-tobacco plant material;
- b) processing the material provided in step a) and optionally other ingredients; and
- c) optionally packing the smokeless tobacco or non-tobacco snuff composition, either
in pouches, or as is, in cans, or boxes;
wherein lactic acid or a salt thereof is added at one or more of the following steps:
- i) prior to step b),
- ii) during step b), and/or
- iii) after step b).
[0009] A third aspect of the invention is the use of a smokeless tobacco or non-tobacco
snuff composition according to the first aspect of the invention for making portion
packets comprising said composition.
[0010] A fourth aspect of the present invention is a pouch containing a smokeless tobacco
or non-tobacco snuff composition for oral use according to the first aspect of the
invention.
BRIEF DESCRIPTION OF THE DRAWINGS
[0011]
Figure 1 shows the principle of the manufacturing process according to GothiaTek® standard, as used for the manufacturing of Scandinavian type moist snuff (snus).
Figure 2 shows the bacterial growth in snus compositions comprising different salts
in various amounts, where the compositions have been stored during 3 weeks at 22 °C,
60%RH.
DETAILED DESCRIPTION OF THE INVENTION
[0012] It is intended throughout the present description that the expression "tobacco" stands
for any part, e.g. leaves and stems, of any member of the genus Nicotiana. The tobacco
may be whole, shredded, threshed, cut, ground, cured, aged, fermented, or otherwise,
e.g. granulated or encapsulated. Tobacco may also be in the form of finished products,
including any smokeless tobacco composition that is orally consumed. Such smokeless
tobacco compositions include snuff and chewing tobacco.
[0013] "Non-tobacco snuff" as used herein is used for a snuff composition that does not
comprise tobacco but resembles a tobacco snuff composition in that it has similar
texture, color, taste, flavor andmouthfeel. Non-tobacco snuff compositions are usually
based on non-tobacco plant fibers. Examples of non-tobacco plant materials are oat
fibers, apple fibers, sugar beet fibers, potato fibers, corn fibers, buckwheat fibers,
cocoa fibers, and cellulose fibers. Smokeless non-tobacco snuff products for oral
use are used in the same manner as the corresponding smokeless tobacco products for
oral use.
[0014] Snuff is available in two forms, as dry nasal snuff for sniffing, and moist (or wet)
snuff, such as snus, for use in the oral cavity by placing between the lip and gum.
[0015] Dry snuff for nasal use have a low water content, typically less than 10 wt%, and
is commonly made from fire-cured fermented tobacco. The tobacco is ground into a powder
and optionally other ingredients are added.
[0016] American-type moist snuff for oral use is commonly produced through a fermentation
process of moisturized ground or cut tobacco. The water content is typically greater
than 40 wt%. American-type moist snuff is available in a loose form or as pre-packed
pouches and is most commonly used between the lower gum and lip but could also be
used as snus between the upper gum and lip.
[0017] "Snus" as used herein denotes the Scandinavian type of moist snuff for oral use,
which is produced in a heat-treatment process instead of by fermentation. The tobacco
or non-tobacco snuff product may be provided in particulate form, as a loose powder,
or portion packed in a pouch. The final water content is typically greater than 40
wt%, but semi-dry products having less than 40 wt% water content, such as a water
content from about 20 wt%, are also available. Snus is typically used between the
upper gum and lip.
[0018] "Oral" and "oral use" is in all contexts used herein as a description for use in
the oral cavity, i.e. chewing purposes, or buccally placement, such as between the
lip and gum.
[0019] As used herein, the expression "water content" means the total water content in a
smokeless tobacco or non-tobacco snuff composition including natural water contained
in the materials used in the composition, as well as added pure water, as measured
by using a standardized method for water analysis, such as, Karl Fischer titration
or gas chromatography (GC). The water content is given herein as percent by weight
(wt%).
[0020] Smokeless tobacco or non-tobacco snuff products for oral use may have a water content
ranging from around 10 wt% for very dry products and up to about 65 wt% based on the
total weight of the final composition, usually from 20 to 60 wt%, or from 30 to 60
wt%. The water holding capacity of the tobacco or non-tobacco snuff compositions affects
the moist feeling of the product. A composition having a high water holding capacity
can feel more dry than a composition with a lower water holding capacity, although
both compositions have the same water content. Some consumers prefer products that
are more dry while others prefer more moist products.
[0021] "Water activity" (a
w) is defined as the vapour pressure above a sample divided by the vapour pressure
of pure water at the same temperature. The water activity is related to the water
content of a sample in a non-linear relationship. Water activity values are obtained
by either a capacitance or a dew point hygrometer. The water activity, as used herein,
is measured with a Decagon AquaLab series 3 instrument that employs a cold mirror/dew
point technique and is calibrated with certified standard solutions.
[0022] The term "dry weight", as used herein, incorporates the common usage of the term
and, in the context of the smokeless tobacco or non-tobacco snuff products disclosed
herein, means the weight of a smokeless tobacco or non-tobacco snuff product after
substantially all of the water or any other liquid has been removed.
[0023] The smokeless tobacco or non-tobacco snuff composition for oral use according to
the present invention comprises at least 20 wt%, at least 25 wt%, at least 30 wt%,
at least 35 wt%, at least 40 wt%, at least 50 wt% water, or at least 55 wt% water,
based on the total weight of the final composition, and at least 1 wt% lactic acid
or a salt thereof based on the dry weight of the final composition.
[0024] The composition according to the present invention may comprise not more than 70
wt% water, or not more than 65 wt%, or not more than 60 wt% water, based on the total
weight of the final composition.
[0026] Sodium chloride, NaCl, is an additive used in moist smokeless tobacco or non-tobacco
snuff compositions for oral use as a preservative for preventing microbial growth,
such as growth of bacteria, in general by decreasing the water activity. The use of
sodium chloride may render the composition a salty taste.
[0027] The natural occurrence of NaCl in tobacco, such as in tobacco lamina and stem, is
below 1 wt%, typically below 0.5 wt% based on the dry weight of the tobacco.
[0028] The amount of NaCl needed to achieve an antimicrobial effect depends on the water
content of the smokeless tobacco or non-tobacco snuff composition.
[0029] Smokeless tobacco or non-tobacco snuff compositions comprising less than 20 wt% water
based on the total weight of the final composition may not need any addition of NaCl
in order to prevent microbial growth. However, commercially available smokeless tobacco
or non-tobacco snuff compositions for oral use that comprises more than 20 wt% water,
based on the total weight of the final composition, typically comprise at least 4
wt% NaCl, based on the dry weight of the final composition while compositions comprising
more than 50 wt% water based on the total weight of the final composition typically
comprise more than 8 wt% NaCl based on the dry weight of the final composition. These
amounts of NaCl are usually needed to achieve an antimicrobial effect. However, a
composition comprising such amount of NaCl may be perceived too salty by many consumers.
[0030] By reducing the content of NaCl in a smokeless tobacco or non-tobacco snuff composition
for oral use it may obtain a less salty taste, but it would also be expected that
the water activity (a
w) would increase, and also the probability for microbial growth, compared with a corresponding
composition having the same water content but a greater content of NaCl. When the
a
w is above 0.90 for a smokeless tobacco or non-tobacco snuff composition for oral use,
such as in compositions with a relatively high water content, for example comprising
at least 30 wt% water based on the total weight of the final composition, such as
Swedish snus, the risk for microbial growth in the product increases. An a
w of 0.92 would normally result in strong microbial growth.
[0031] Compositions according to the present invention show negligible or a very limited
microbial growth even though these compositions may have an increased water activity,
such as an a
w of 0.92.
[0032] An advantage with lactic acid or a salt thereof is that it has a neutral taste in
addition to its ability to limit the microbial growth in a composition according to
the present invention.
[0033] The amount of lactic acid or a salt thereof that is needed in a smokeless tobacco
or non-tobacco snuff composition for oral use to provide a desired water activity
and to achieve an antimicrobial effect depends on the water content of the composition
and, if NaCl is added, the amount of NaCl.
[0034] The smokeless tobacco or non-tobacco snuff composition for oral use according to
the present invention comprises at least 1 wt% lactic acid or a salt thereof, at least
2 wt%, at least 3 wt%, at least 4 wt%, at least 5 wt%, at least 6 wt%, at least 7
wt%, at least 10 wt%, at least 12 wt%, at least 15 wt%, or at least 20 wt%, based
on the dry weight of the final composition. The natural occurrence of lactic acid
or a salt thereof in smokeless tobacco or non-tobacco snuff composition for oral use
is typically below 1 wt%, or even below 0.5 wt%.
[0035] The composition according to the present invention may comprise not more than 30
wt% lactic acid or a salt thereof, not more than 25 wt%, or not more than 20 wt%,
based on the dry weight of the final composition.
[0036] Salts of lactic acid that are suitable in the composition according to the present
invention may be lactate salts of an alkali metal, such as sodium lactate or potassium
lactate, and more specifically sodium lactate.
[0037] An advantage with a smokeless tobacco or non-tobacco snuff composition for oral use
according to the present invention is that by adding lactic acid or a salt thereof,
the amount NaCl in a composition may be lowered without risk for increased microbial
growth. Compositions according to the present invention may therefore be provided
with a less salty taste compared to corresponding compositions without lactic acid
or a salt thereof, while the microbial growth is maintained at the same level.
[0038] A smokeless tobacco or non-tobacco snuff composition according to the present invention
may comprise less than 8 wt% NaCl, less than 4 wt% NaCl, or less than 1 wt% NaCl,
based on the dry weight of the final composition.
[0039] With the use of lactic acid or a salt thereof in a smokeless tobacco or non-tobacco
snuff composition according to the present invention it is possible to achieve an
antimicrobial effect even without any addition of NaCl.
[0040] The greater the amount of water and the lower the amount of NaCl in a tobacco or
non-tobacco snuff composition for oral use, the greater amount of lactic acid may
be required to avoid microbial growth.
[0041] Lactic acid and salts thereof have been reported to decrease microbiological growth
at a low pH, such as pH 7.25 or lower (
De Wit, J. C., et al. 1990, Food Microbiol., 7:113-120; and
Shelef, L. A. 1994, J. Food Prof., 57:445-450). Further reports show that the antimicrobial effect tends to increase with lower
pH (
Houtsma, 1996, Ph.D. thesis, Agricultural University Wageningen). In an acidic environment lactic acid is undissociated, and can diffuse into the
microbial cell wherein it subsequently has an antimicrobial effect.
[0042] The pH of smokeless tobacco or non-tobacco snuff compositions for oral use is typically
higher than pH 7.5, typically higher than pH 8. Therefore it was not expected that
a composition according to the present invention would show a negligible microbial
growth, as is shown in Table 1 and Figure 2.
[0043] The smokeless tobacco or non-tobacco snuff composition for oral use according to
the present invention may have a pH of at least 7.5, or at least 8. The pH may not
be higher than 9.8, or preferably not higher than 9.5. The composition preferably
has a pH in the range from 7.5 to 9.8, or in the range from 8 to 9.5.
[0044] Another advantage with the use of lactic acid or a salt thereof in the smokeless
tobacco or non-tobacco snuff composition of the present invention is that they might
be used in effective amounts without being subject to regulatory restrictions. Other
preservatives, such as salts of sorbic and propionic acids, may be subject to regulatory
requirements in certain jurisdictions and may not provide any antimicrobial effect
even when used at their maximal allowed concentration according to said regulation
requirements. With a composition according to the present invention the amount of
preservatives, such as sorbates, e.g. potassium sorbate; propionates, e.g. sodium
propionate; or benzoic acid or salts thereof may be completely avoided or reduced
without increasing the risk for microbial growth. Thus, the smokeless tobacco or non-tobacco
snuff compositions for oral use according to the present invention may comprise no
preservatives selected from the group consisting of sorbates, propionates, and benzoic
acid or salts thereof.
[0045] A further advantage of using of lactic acid or a salt thereof in the smokeless tobacco
or non-tobacco snuff composition of the present invention is that it alters the consistency
of the composition so that it becomes more cohesive than a composition with the same
water content but without lactic acid or a salt thereof. Thus, the water content of
the composition according to the present invention can be reduced while preserving
the same consistency as perceived by the consumer. A reduced water content has the
further advantage that it also may contribute to a reduced microbial growth since
the water activity will be decreased.
[0046] A more cohesive texture of smokeless tobacco or non-tobacco snuff compositions for
oral use with a reduced water content may also be an advantage during manufacture,
such that it is possible to pack in pouches at a lower water content than would normally
be possible. A process for making pouches of a smokeless tobacco or a non-tobacco
snuff composition for oral use is described in
US Patent No. 6,135,120.
[0047] Further, because of the increased cohesive texture when lactic acid or a salt thereof
is added to a smokeless tobacco or non-tobacco snuff composition for oral use according
to the present invention it is easier to form the composition into a portion packet
or a pinch, compared with a corresponding composition for oral use with the same water
content but without the addition of lactic acid or a salt thereof.
[0048] The composition for oral use according to the present invention is preferably a smokeless
tobacco composition, such as snus.
[0049] The smokeless tobacco or non-tobacco snuff composition for oral use according to
the present invention may be provided in form of pouches, or as is in particular form
in cans or boxes.
[0051] The smokeless tobacco or non-tobacco snuff composition according to the present invention
may be manufactured according to the GothiaTek
® standard.
[0052] A second aspect of the present invention is a method for manufacturing of a smokeless
tobacco or non-tobacco snuff composition for oral use according to the first aspect
of the invention, wherein the method comprises:
- a) providing a tobacco material or non-tobacco plant fibre material;
- b) processing the material provided in step a) and optionally other ingredients; and
- c) optionally packing the smokeless tobacco or non-tobacco snuff composition, either
in pouches, or as is, in cans, or boxes;
wherein lactic acid or a salt thereof is added at one or more of the following steps:
- i) prior to step b),
- ii) during step b), and/or
- iii) after step b).
[0053] The processing of the material in step b) may comprise a heat treatment, such as
a pasteurization process.
[0054] In the method according to the present invention the lactic acid or a salt thereof
may be added prior to step b), during step b), or after step b).
[0055] Prior to the processing of the tobacco material or non-tobacco plant fiber material
in step b) water and possibly additional additives may be added. During the processing
of the tobacco material or non-tobacco plant fiber material in step b) water, flavors,
sodium carbonate and possibly additional additives may be added.
EXAMPLES
Example 1
[0056] 3000 g snus was produced in accordance with a modified version of the GothiaTek
® standard. The method was modified by omitting the addition of sodium chloride before
heat treatment. A mixture of ground tobacco and water was heat-treated at a temperature
of 100°C for 2 hours and thereafter at a declining temperature of from 100°C to 70°C
for 8 hours, reaching a water content of about 42 wt% of the total weight of the final
composition. After the heat-treatment, the mixture was chilled to about 20°C and sodium
carbonate was added to adjust the mixture to an alkaline pH of about 8.3 and water
was added to adjust the water content to about 50 wt% based on the total weight of
the final composition. The resulting base snus had a water content of 51.2 wt% and
a pH value of 8.33. A bacteria culture, with bacillus bacteria, known to be able to
reproduce in snus environment, was added to the snus base. This resulted in a bacterial
count in the snus base of about log 4.5 CFU/g snus.
[0057] From this snus a 250 g reference sample (NaCl 9%) was produced by addition of a water
solution with sodium chloride to produce snus with a water content of about 57 wt%
based on the total weight of the final composition and containing 9 wt% NaCl based
on the dry weight of the formulation. This corresponds to a concentration of NaCl
and a water content commonly used in Swedish type snus. Further, from the same base
snus, a second reference sample (Ref 0 %) of 250 g was prepared by addition of water
to obtain a snus with about 57 % water content, but containing no added NaCl. Further,
from the same base snus, three 250 g snus samples were prepared by addition of water
solutions with sodium lactate (NaL) to produce snus with a water content of about
57 wt% based on the total weight of the final composition and containing 7, 12 and
16 wt% sodium lactate based on the dry weight of the formulation. The samples are
called NaL 7%, NaL 12% and NaL 16%, respectively.
[0058] All samples were analyzed regarding pH, water content, water activity (a
w) and bacterial count before they were packed and stored. The pH and water activity
for each sample are presented in Table 1. The samples were then packed into sealed
plastic bags and transferred to a controlled climate (22°C, 60% RH) where they were
stored for 3 weeks. After 1, 2 and 3 weeks of storage the samples were analyzed for
pH and bacterial count. The pH for all samples remained above 7.7. The bacterial count
results, shown in Fig. 2, clearly show a bacteriostatic effect of addition of sodium
lactate in snus in all three samples. In general, Swedish snus products require a
water activity of no more than 0.90 to ensure that no bacterial growth takes place.
Samples NaL 7% and NaL 12% have a water activity of 0.92, as presented in Table 1,
which would suggest strong bacterial growth, but unexpectedly these samples exhibit
a static bacterial count as presented in Figure 2. This indicates an antibacterial
effect beyond the a
w lowering effect.
Table 1
| Sample |
Added Salt |
Added amount of salt (wt%) |
pH |
Water activity (aw) |
| Ref 0% (reference) |
No addition |
0 |
8.32 |
0.93 |
| Ref 9% NaCl (reference) |
NaCl |
9 |
8.33 |
0.9 |
| NaL 7% |
NaL |
7 |
8.27 |
0.92 |
| NaL 12% |
NaL |
12 |
8.23 |
0.92 |
| NaL 16% |
NaL |
16 |
8.22 |
0.9 |
1. A smokeless tobacco or non-tobacco snuff composition for oral use comprising at least
20 wt% water based on the total weight of the final composition, wherein the composition
comprises at least 1 wt% lactic acid or a salt thereof based on the dry weight of
the final composition.
2. The composition according to claim 1, wherein the composition comprises at least 30
wt% water based on the total weight of the final composition.
3. The composition according to claim 1 or 2, wherein the composition comprises less
than 4 wt% NaCl based on the dry weight of the final composition.
4. The composition according to any one of claims 1 to 3, wherein the composition comprises
less than 1 wt% NaCl based on the dry weight of the final composition.
5. The composition according to any one of claims 1 to 4, wherein the composition comprises
at least 6 wt% lactic acid or a salt thereof based on the dry weight of the final
composition.
6. The composition according to any one of claims 1 to 5, wherein the composition comprises
at least 10 wt% lactic acid or a salt thereof based on the dry weight of the final
composition.
7. The composition according to any one of claims 1 to 6, wherein the lactic acid or
a salt thereof is sodium lactate.
8. The composition according to any one of claims 1 to 7, wherein the composition has
a pH of at least 7.5 and less than 9.8.
9. The composition according to any one of claims 1 to 8, wherein the composition is
a smokeless tobacco composition for oral use.
10. The composition according to claim 9, wherein the composition is snus.
11. The composition according to any one of claims 1 to 10, wherein the composition comprises
no preservatives selected from the group consisting of sorbates, propionates, and
benzoic acid or salts thereof.
12. A method for manufacturing of a smokeless tobacco or non-tobacco snuff composition
for oral use according to any one of claims 1 to 11, wherein the method comprises:
a) providing a tobacco or non-tobacco plant material;
b) processing the material provided in step a) and optionally other ingredients; and
c) optionally packing the smokeless tobacco or non-tobacco snuff composition, either
in pouches, or as is, in cans, or boxes;
wherein lactic acid or a salt thereof is added at one or more of the following steps:
i) prior to step b),
ii) during step b), and/or
iii) after step b).
13. Use of a smokeless tobacco or non-tobacco snuff composition according to any one of
claims 1-11 for making portion packets comprising said composition.
14. A pouch containing a smokeless tobacco or non-tobacco snuff composition according
to any one of claims 1-11.
1. Rauchlose Tabak- oder Nicht-Tabak-Schnupf-Zusammensetzung zur oralen Verwendung, umfassend
mindestens 20 Gew.-% Wasser, basierend auf dem Gesamtgewicht der fertigen Zusammensetzung,
wobei die Zusammensetzung mindestens 1 Gew.-% Milchsäure oder ein Salz davon, basierend
auf dem Trockengewicht der fertigen Zusammensetzung, umfasst.
2. Zusammensetzung nach Anspruch 1, wobei die Zusammensetzung mindestens 30 Gew.-% Wasser,
basierend auf dem Gesamtgewicht der fertigen Zusammensetzung, umfasst.
3. Zusammensetzung nach Anspruch 1 oder 2, wobei die Zusammensetzung weniger als 4 Gew.-%
NaCl, basierend auf dem Trockengewicht der fertigen Zusammensetzung, umfasst.
4. Zusammensetzung nach einem der Ansprüche 1 bis 3, wobei die Zusammensetzung weniger
als 1 Gew.-% NaCl, basierend auf dem Trockengewicht der fertigen Zusammensetzung,
umfasst.
5. Zusammensetzung nach einem der Ansprüche 1 bis 4, wobei die Zusammensetzung mindestens
6 Gew.-% Milchsäure oder ein Salz davon, basierend auf dem Trockengewicht der fertigen
Zusammensetzung, umfasst.
6. Zusammensetzung nach einem der Ansprüche 1 bis 5, wobei die Zusammensetzung mindestens
10 Gew.-% Milchsäure oder ein Salz davon, basierend auf dem Trockengewicht der fertigen
Zusammensetzung, umfasst.
7. Zusammensetzung nach einem der Ansprüche 1 bis 6, wobei die Milchsäure oder ein Salz
davon Natriumlactat ist.
8. Zusammensetzung nach einem der Ansprüche 1 bis 7, wobei die Zusammensetzung einen
pH von mindestens 7,5 und weniger als 9,8 aufweist.
9. Zusammensetzung nach einem der Ansprüche 1 bis 8, wobei die Zusammensetzung eine rauchlose
Tabak-Zusammensetzung zur oralen Verwendung ist.
10. Zusammensetzung nach Anspruch 9, wobei die Zusammensetzung Snus ist.
11. Zusammensetzung nach einem der Ansprüche 1 bis 10, wobei die Zusammensetzung keine
Konservierungsmittel, ausgewählt aus der Gruppe, bestehend aus Sorbaten, Propionaten
und Benzoesäure oder Salzen davon, umfasst.
12. Verfahren zur Herstellung einer rauchlosen Tabak- oder Nicht-Tabak-Schnupf-Zusammensetzung
zur oralen Verwendung nach einem der Ansprüche 1 bis 11, wobei das Verfahren umfasst:
a) Bereitstellen eines Tabak- oder Nicht-Tabak-Pflanzenmaterials;
b) Verarbeiten des in Schritt a) bereitgestellten Materials und gegebenenfalls anderer
Bestandteile; und
c) gegebenenfalls Verpacken der rauchlosen Tabak- oder Nicht-Tabak-Schnupf-Zusammensetzung,
entweder in Säckchen oder, wie vorliegend, in Dosen oder Schachteln;
wobei Milchsäure oder ein Salz davon bei einem oder mehreren der nachstehenden Schritte
zugegeben wird:
i) vor Schritt b),
ii) während Schritt b), und/oder
iii) nach Schritt b).
13. Verwendung einer rauchlosen Tabak- oder Nicht-Tabak-Schnupf-Zusammensetzung nach einem
der Ansprüche 1-11 zur Herstellung von die Zusammensetzung umfassenden Portionspäckchen.
14. Säckchen, enthaltend eine rauchlose Tabak- oder Nicht-Tabak-Schnupf-Zusammensetzung
nach einem der Ansprüche 1-11.
1. Composition de tabac sans fumée ou de tabac à priser sans tabac pour une utilisation
orale comprenant au moins 20 % en poids d'eau sur la base du poids total de la composition
finale, dans laquelle la composition comprend au moins 1 % en poids d'acide lactique
ou d'un sel de celui-ci sur la base du poids sec de la composition finale.
2. Composition selon la revendication 1, dans laquelle la composition comprend au moins
30 % en poids d'eau sur la base du poids total de la composition finale.
3. Composition selon la revendication 1 ou 2, dans laquelle la composition comprend moins
de 4 % en poids de NaCl sur la base du poids sec de la composition finale.
4. Composition selon l'une quelconque des revendications 1 à 3, dans laquelle la composition
comprend moins de 1 % en poids de NaCl sur la base du poids sec de la composition
finale.
5. Composition selon l'une quelconque des revendications 1 à 4, dans laquelle la composition
comprend au moins 6 % en poids d'acide lactique ou d'un sel de celui-ci sur la base
du poids sec de la composition finale.
6. Composition selon l'une quelconque des revendications 1 à 5, dans laquelle la composition
comprend au moins 10 % en poids d'acide lactique ou d'un sel de celui-ci sur la base
du poids sec de la composition finale.
7. Composition selon l'une quelconque des revendications 1 à 6, dans laquelle l'acide
lactique ou un sel de celui-ci est le lactate de sodium.
8. Composition selon l'une quelconque des revendications 1 à 7, dans laquelle la composition
a un pH d'au moins 7,5 et inférieur à 9,8.
9. Composition selon l'une quelconque des revendications 1 à 8, dans laquelle la composition
est une composition de tabac sans fumée pour une utilisation orale.
10. Composition selon la revendication 9, dans laquelle la composition est du snus.
11. Composition selon l'une quelconque des revendications 1 à 10, dans laquelle la composition
ne comprend pas de conservateurs sélectionnés dans le groupe constitué de sorbates,
de propionates et d'acide benzoïque ou de sels de celui-ci.
12. Procédé de fabrication d'une composition de tabac sans fumée ou de tabac à priser
sans tabac pour une utilisation orale selon l'une quelconque des revendications 1
à 11, dans lequel le procédé comprend :
a) fournir un matériel végétal de tabac ou sans tabac ;
b) traiter le matériel fourni dans l'étape a) et éventuellement d'autres ingrédients
; et
c) éventuellement emballer la composition de tabac sans fumée ou de tabac à priser
sans tabac, soit dans des poches, soit en l'état, dans des cannettes, ou des boîtes
;
dans lequel de l'acide lactique ou un sel de celui-ci est ajouté à une ou plusieurs
des étapes suivantes :
i) avant l'étape b),
ii) au cours de l'étape b), et/ou
iii) après l'étape b).
13. Utilisation d'une composition de tabac sans fumée ou de tabac à priser sans tabac
selon l'une quelconque des revendications 1 à 11 pour faire des paquets de portions
comprenant ladite composition.
14. Poche contenant une composition de tabac sans fumée ou de tabac à priser sans tabac
selon l'une quelconque des revendications 1 à 11.