EP0966203A1 - A process for the production of flavoured sweet products and the products obtained - Google Patents
A process for the production of flavoured sweet products and the products obtainedInfo
- Publication number
- EP0966203A1 EP0966203A1 EP97944825A EP97944825A EP0966203A1 EP 0966203 A1 EP0966203 A1 EP 0966203A1 EP 97944825 A EP97944825 A EP 97944825A EP 97944825 A EP97944825 A EP 97944825A EP 0966203 A1 EP0966203 A1 EP 0966203A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- sugar alcohol
- flavouring agent
- process according
- weight
- flavoured
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G3/00—Sweetmeats; Confectionery; Marzipan; Coated or filled products
- A23G3/34—Sweetmeats, confectionery or marzipan; Processes for the preparation thereof
- A23G3/346—Finished or semi-finished products in the form of powders, paste or liquids
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G2200/00—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF containing organic compounds, e.g. synthetic flavouring agents
- A23G2200/06—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF containing organic compounds, e.g. synthetic flavouring agents containing beet sugar or cane sugar if specifically mentioned or containing other carbohydrates, e.g. starches, gums, alcohol sugar, polysaccharides, dextrin or containing high or low amount of carbohydrate
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G2200/00—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF containing organic compounds, e.g. synthetic flavouring agents
- A23G2200/14—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF containing organic compounds, e.g. synthetic flavouring agents containing fruits, nuts, e.g. almonds, seeds, plants, plant extracts or essential oils
Definitions
- the present invention relates to the production of
- flavoured sweet products and, in particular, to sweet
- sweet products with low calorie content and/or with low
- the problem at the root of the invention is particularly concerned
- sweet products of the type indicated above.
- flavour improvement in the development of flavour is particularly
- flavour related to an organoleptic sensation of flavour
- a first subject of the invention is a process for
- flavoured sweet products including, by:
- one or more crystalline sugar alcohols are provided.
- flavouring agent is previously incorporated in the sugar
- flavouring agent being incorporated in the sugar alcohol
- flavouring agent sufficient to give flavour to the entire mass
- a further subject of the invention is a process for the
- flavouring agent by means of the
- a further subject of the invention is constituted by
- flavoured sweet products including, as the sweetener, a
- a further subject of the invention is a flavoured sugar
- sugar alcohols used in the invention are, in
- hexitols and pentitols and their derivatives such as, in particular, xylitol, sorbitol, lactitol, mannitol,
- maltitol isomaltitol and -I-glucopyrano ⁇ yl-l,6-mannitol, c.-D-gl-
- the sugar alcohols are used preferably in a
- substantially dehydrated form e.g. with a water content not
- the preferred sugar alcohol used in the invention for the incorporation of the flavour is xylitol.
- flavouring agents used in the invention include, but are not limited to,
- pineapple in the form of essences and compounds, such as
- wintergreen methyl salicylate
- flavouring agent is not critical in the flavouring agent
- flavour enhancement achieved by the invention is
- flavour used has aromatic amino acids
- flavouring agent in the sugar alcohol
- gases in particular being nitrogen, argon and carbon
- flavouring agent added to the melt in its
- flavours used In general, quantities of from 0.5 to 10%
- flavouring agent by weight of flavouring agent with respect to the weight
- flavoured crystalline form in which the flavouring agent
- flavoured sugar alcohol thus obtained is used as a
- sweetener and in sweet products .
- alcohol used in the products is preferably between 0.5 and
- the sweet product may also include other conventional sweet product
- sugars such as sucrose, glucose and possibly synthetic
- sweeteners .
- flavours of the final sweet product may be introduced
- flavoured sugar wholly or only partially by means of the flavoured sugar
- flavoured In the preparation of the sweet product, the flavoured
- sugar alcohol component or mixture of sugar alcohols is
- Heating was carried out by means of the heating jacket up
- the product obtained was used as sweetener component in coated
- Wax (carnauba, beeswax, candle) 0.001-0.1
- flavourings as previously described had already been
- flavourings may have
- coated tablets were prepared with the same
- flavouring agent was added to the flavouring agent
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Seasonings (AREA)
- Confectionery (AREA)
- Medicinal Preparation (AREA)
Abstract
The process for the production of flavoured sweet products including, by way of sweetener, a crystalline sugar alcohol or mixture of sugar alcohols and possibly other sweeteners, is characterised in that the flavouring agent is previously incorporated in the sugar alcohol component used in the sweet product. The flavouring agent is incorporated in the sugar alcohol by a process which includes the steps of: a) heating the sugar alcohol to a temperature above its melting point until it has melted, b) cooling the melt to a temperature below its melting point until it reaches a metastable glassy state, c) adding to the melt in its glassy state under mixing conditions a quantity of the sugar alcohol in crystalline form of from 5 to 120 % by weight with respect to the weight of the molten mass and a quantity of flavouring agent sufficient to give flavour to the entire mass, and d) removing the heat under conditions in which the total mass is mixed in order to cause it to crystallise.
Description
A PROCESS FOR THE PRODUCTION OF FLAVOURED SWEET PRODUCTS AND THE PRODUCTS OBTAINED
The present invention relates to the production of
flavoured sweet products and, in particular, to sweet
products containing, as the sweetener, sugar alcohols
such as hexitols, pentitols and their derivatives and
possibly other sweeteners.
The use of sugar alcohols of the type indicated above is
very widespread today, particularly for the production of
sweet products with low calorie content and/or with low
cariogenic activity.
The problem at the root of the invention is particularly
that of improving the development of flavour in flavoured
sweet products of the type indicated above. The
improvement in the development of flavour is particularly
related to an organoleptic sensation of flavour
enhancement, perceptible by the consumer when the sweet
product is in contact with saliva at the moment of
consumption.
For this purpose, it has been found that the desired
enhancement of the flavour of sweet products may be
achieved by the prior incorporation of the flavouring
agent in the sugar alcohol component, in the specified operative manner.
Thus a first subject of the invention is a process for
the production of flavoured sweet products including, by
way of sweeteners, one or more crystalline sugar alcohols
and possibly other sweeteners, characterised in that the
flavouring agent is previously incorporated in the sugar
alcohol component used in the sweet product, the
flavouring agent being incorporated in the sugar alcohol
by a process which includes the steps of:
a) heating the sugar alcohol to a temperature above its
melting point until it has melted,
b) cooling the melt to a temperature below its melting
point until it reaches a metastable glassy state,
c) adding to the melt in its glassy state under mixing
conditions, a quantity of the sugar alcohol in
crystalline form of from 5 to 120% by weight with respect
to the weight of the molten mass and a quantity of
flavouring agent sufficient to give flavour to the entire
mass , and
d) removing heat under conditions in which the total mass
is mixed in order to cause it to crystallise.
A further subject of the invention is a process for the
preparation of a flavoured sugar alcohol, in solid
crystalline form, characterised in that it includes the
incorporation of the flavouring agent by means of the
operative steps a) , b) , c) and d) indicated above.
A further subject of the invention is constituted by
flavoured sweet products including, as the sweetener, a
sugar alcohol incorporating a flavouring agent, as
obtainable by the operative steps a) , b) , c) and d)
indicated above.
A further subject of the invention is a flavoured sugar
alcohol or mixture of flavoured sugar alcohols obtainable
by a process including the operative steps a) , b) , c) and
d) indicated above.
The sugar alcohols used in the invention are, in
particular, hexitols and pentitols and their derivatives,
such as, in particular, xylitol, sorbitol, lactitol, mannitol,
maltitol, isomaltitol and -I-glucopyranoεyl-l,6-mannitol, c.-D-gl-
ucoj-yranosyl-l,6-sorbitol and their mixtures. In the process of
the invention, the sugar alcohols are used preferably in a
substantially dehydrated form, e.g. with a water content not
exceeding 5% wt. or preferably not exceeding 2% wt.
The definition of sugar alcohol and "their derivates in accordance
with the invention includes comπercial products such as PALATINIT
(registered trade mark) and ISOMALT (registered trade mark). The preferred sugar alcohol used in the invention for the incorporation of the flavour is xylitol.
The flavouring agents used in the invention include, but
are not limited to, peppermint, spearmint, cinnamon,
lemon, orange, citron, grapefruit, strawberry, cherry and
pineapple in the form of essences and compounds, such as
wintergreen (methyl salicylate) . The chemical nature of
the flavouring agent is not critical in the
incorporation process of the invention.
The flavour enhancement achieved by the invention is
particularly evident when the flavour used has aromatic
components which give a fresh sensation; thus mint
flavours are particularly preferred. The process of
incorporating the flavouring agent in the sugar alcohol
is preferably carried out in an autoclave under light
pressure with inert gas; excess pressures of from 0.5 to
2 bars in an inert gas atmosphere are preferred, the
gases in particular being nitrogen, argon and carbon
dioxide. The use of an excess pressure of inert gas is
advantageous in that it limits the loss of flavour.
However, the process could be carried out at atmospheric
pressure in an ambient environment .
The quantity of flavouring agent added to the melt in its
glassy state, in the operative step c) , may vary within
wide limits according to the flavouring capacity of the
flavours used. In general, quantities of from 0.5 to 10%
by weight of flavouring agent with respect to the weight
of the molten mass and, more preferably, from 1.5 to 2%
by weight are used.
The process of incorporating the flavour in the sugar
alcohol results in the production of a sugar alcohol in
flavoured crystalline form in which the flavouring agent
is presumably co-crystallised in the crystal lattice of
the sugar alcohol.
The flavoured sugar alcohol thus obtained is used as a
sweetener and in sweet products . The sweet products
include, in particular, pastils and tablets (coated and
uncoated) , chewing gum and bubble gum, soft caramels,
toffees and chocolates. The quantity of flavoured sugar
alcohol used in the products is preferably between 0.5 and
20% by weight, preferably 1 to 5% by weight, of the
overall weight of the sweet product.
The sweet product may also include other conventional
sugars such as sucrose, glucose and possibly synthetic
sweeteners .
The flavours of the final sweet product may be introduced
wholly or only partially by means of the flavoured sugar
alcohol component as described above .
In the preparation of the sweet product, the flavoured
sugar alcohol component or mixture of sugar alcohols is
preferably introduced as the final ingredient in the
final stage in the production of the finished product, or
of any intermediate products, in order to prevent the
component from coming into contact with moisture or from
being exposed to high temperatures which could alter the
physical structure of the component itself.
Example
50 kg of xylitol in powdered crystalline form were
introduced into a 200 1 autoclave provided with a heat-
exchange jacket and scraping stirrer. The autoclave was
pressurised with nitrogen to 1.5 bar.
Heating was carried out by means of the heating jacket up
to a temperature of 110°C until the xylitol had melted, the molten mass being stirred slowly. The melt was then
cooled to 80-82°C until it had reached its metastable
glassy state. 50 kg of crystalline xylitol containing peppermint flavouring in quantities of 1 to 5% by weight
of the weight of the molten mass (in this particular case
2% by weight) were then added under slow stirring.
Slow stirring was continued while the heat of fusion of
the xylitol which diffused through the molten mass was
removed in order to cause the mass to crystallise. The
product was discharged from the autoclave at the ambient
temperature of 25°C.
The product obtained was used as sweetener component in coated
tablets having the following composition expressed in
percentage terms:
Ingredients % wt.
Sucrose 80-95
Maltodextrin 2-10
Polyalcohols (xylitol, mannitol,
lactitol, altitol) 2-6
Arabic Gum 1-5
Rice starch 0.5-5
organic acids (tartaric, citric,
malic) 0.2-4
Wax (carnauba, beeswax, candle) 0.001-0.1
Natural and artificial flavourings 0.05-3
In order to produce the tablets, a granular composition
was first formed by the mixing together of the sucrose,
maltodextrin, arabic gum and polyalcohols in which
flavourings as previously described had already been
incorporated .
The granular composition was then pressed to a desired
shape in suitable tableting machines to obtain the
cores. These latter were then coated with a sugar and
starch solution in a bowl in which the cores were rotated
and sprayed with small quantities of sugar solution to
which further quantities of flavourings may have
been added in known manner. Thus the final tablets were
obtained.
Comparative example
By way of control, coated tablets were prepared with the
same formulation as that described in the above example
but in which the flavouring agent was added to the
composition in the conventional manner.
Tests carried out by a panel of 100 tasters showed that
the tasters had a general preference for the product
obtained by the invention with respect to the following
parameters :
- general preference,
- sensation of greater freshness,
- improved mint flavour, and
- enhancement of flavour.
The results of these tests are given in the single figure
which shows a histogram, in which the overall evaluation vote of the tasters for the tablets of the invention and
for those made in the conventional manner respectively
are given on the abscissa and the numbers of tasters who expressed a particular vote are given on the ordinate .
Claims
1. A process for the production of flavoured sweet
products including, by way of sweetener, a crystalline
sugar alcohol or mixture of sugar alcohols and possibly
other sweeteners, characterised in that the flavouring
agent is previously incorporated in the sugar alcohol
component used in the sweet product, the flavouring agent being incorporated in the sugar alcohol by a process
which includes the steps of :
a) heating the sugar alcohol to a temperature above its
melting point until it has melted,
b) cooling the melt to a temperature below its melting
point until it reaches a metastable glassy state.
c) adding to the melt in its glassy state under mixing
conditions, a quantity of the sugar alcohol in
crystalline form of from 5 to 120% by weight with respect
to the weight of the molten mass and a quantity of
flavouring agent sufficient to give flavour to the entire mass, and
d) removing heat under conditions in which the total mass
is mixed in order to cause it to crystallise.
2. A process according to Claim 1, characterised in that the sugar alcohol is selected from the group
consisting of xylitol, sorbitol, lactitol, mannitol,
maltitol, isomaltitol and glucopyranosyl derivatives of
mannitol and sorbitol.
3. A process according to Claim 1 or Claim 2, in which
the flavouring is incorporated in the crystalline sugar
under a pressure of from 0.5 to 2 bar in an inert gas
atmosphere .
4. A process according to any one of Claims 1 to 3 ,
characterised in that the flavouring agent is an essence
or a compound selected from the group consisting of
spearmint, peppermint, cinnamon, lemon, orange, citron,
grapefruit, cherry, strawberry, pineapple and methyl
salicylate .
5. A process according to any one of Claims 1 to 4 , in
which the flavouring agent is added in stage c) in
quantities of from 0.5 to 10% by weight of the molten
mass .
6. A process for the preparation of a flavoured crystalline sugar alcohol, characterised in that it
includes the steps of:
a) heating the sugar alcohol to a temperature above its
melting point until it has melted,
b) cooling the melt to a temperature below its melting
point until it reaches a metastable glassy state,
c) adding to the melt in its glassy state under mixing
conditions a quantity of the sugar alcohol in crystalline
form of from 5 to 120% by weight with reference to the
weight of the molten mass and a quantity of flavouring
agent sufficient to give flavour to the entire mass, and
d) removing heat under conditions in which the total mass
is mixed to cause it to crystallise.
7. A process according to Claim 6, characterised in
that the sugar alcohol is selected from the group
consisting of xylitol, sorbitol, lactitol, mannitol,
maltitol, isomaltitol, glucopyranosyl mannitol,
glucopyranosyl sorbitol and their mixtures.
8. A process according to Claim 6 and Claim 7, in which
the flavouring agent is selected from the group
consisting of compounds or essences of spearmint, peppermint, cinnamon, lemon, orange, citron, grapefruit,
cherry, strawberry, pineapple.
9. A process according to any one of Claims 6 to 8 ,
characterised in that the flavouring agent is added in
stage c) in quantities of from 0.5 to 10% by weight with
reference to the weight of the molten mass.
10. A process according to any one of Claims 6 to 9,
characterised in that the flavouring agent is added under
pressure in inert gas .
11. A sugar alcohol composition including a flavouring
agent, obtainable by means of the process according to
any one of Claims 6 to 10.
12. A flavoured sweet product, including a sugar alcohol
component as obtainable by the process according to any
one of Claims 6 to 10.
13. A sweet product according to Claim 12, particularly
a coated tablet, including flavoured xylitol, as obtained
by a process according to any one of Claims 6 to 11.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH221696 | 1996-09-11 | ||
CH02216/96A CH690704A5 (en) | 1996-09-11 | 1996-09-11 | Process for the production of flavored sweet products and products thus obtained. |
PCT/EP1997/004798 WO1998010662A1 (en) | 1996-09-11 | 1997-09-04 | A process for the production of flavoured sweet products and the products obtained |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0966203A1 true EP0966203A1 (en) | 1999-12-29 |
Family
ID=4228574
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP97944825A Ceased EP0966203A1 (en) | 1996-09-11 | 1997-09-04 | A process for the production of flavoured sweet products and the products obtained |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP0966203A1 (en) |
AU (1) | AU713774B2 (en) |
CA (1) | CA2264531A1 (en) |
CH (1) | CH690704A5 (en) |
CZ (1) | CZ85199A3 (en) |
HU (1) | HUP9904506A3 (en) |
NO (1) | NO991171L (en) |
PL (1) | PL332073A1 (en) |
SK (1) | SK29899A3 (en) |
WO (1) | WO1998010662A1 (en) |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE759609A (en) * | 1969-12-16 | 1971-04-30 | Towa Kasei Kogyo Cy Ltd | PROCESS FOR PREPARING CRYSTALLINE SORBITOL IN GRANULAR FORM AND A NEW PRODUCT THUS OBTAINED |
FR2202867B1 (en) * | 1972-10-13 | 1978-02-10 | Roquette Freres | |
US4659582A (en) * | 1983-11-17 | 1987-04-21 | Nabisco Brands, Inc. | Compressible soft confection |
US5370881A (en) * | 1987-04-20 | 1994-12-06 | Fuisz Technologies Ltd. | Water-soluble delivery systems for hydrophobic liquids |
US5158789A (en) * | 1991-08-09 | 1992-10-27 | Ici Americas Inc. | Melt cocrystallized sorbitol/xylitol compositions |
-
1996
- 1996-09-11 CH CH02216/96A patent/CH690704A5/en not_active IP Right Cessation
-
1997
- 1997-09-04 SK SK298-99A patent/SK29899A3/en unknown
- 1997-09-04 CA CA002264531A patent/CA2264531A1/en not_active Abandoned
- 1997-09-04 EP EP97944825A patent/EP0966203A1/en not_active Ceased
- 1997-09-04 CZ CZ99851A patent/CZ85199A3/en unknown
- 1997-09-04 HU HU9904506A patent/HUP9904506A3/en unknown
- 1997-09-04 PL PL97332073A patent/PL332073A1/en unknown
- 1997-09-04 WO PCT/EP1997/004798 patent/WO1998010662A1/en not_active Application Discontinuation
- 1997-09-04 AU AU46204/97A patent/AU713774B2/en not_active Ceased
-
1999
- 1999-03-10 NO NO991171A patent/NO991171L/en not_active Application Discontinuation
Non-Patent Citations (1)
Title |
---|
See references of WO9810662A1 * |
Also Published As
Publication number | Publication date |
---|---|
NO991171D0 (en) | 1999-03-10 |
AU4620497A (en) | 1998-04-02 |
CA2264531A1 (en) | 1998-03-19 |
HUP9904506A3 (en) | 2000-06-28 |
PL332073A1 (en) | 1999-08-30 |
WO1998010662A1 (en) | 1998-03-19 |
NO991171L (en) | 1999-03-10 |
CZ85199A3 (en) | 1999-08-11 |
AU713774B2 (en) | 1999-12-09 |
SK29899A3 (en) | 1999-09-10 |
CH690704A5 (en) | 2000-12-29 |
HUP9904506A2 (en) | 2000-05-28 |
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