Title of Invention

TRITERPENE-CONTAINING OLEOGEL FORMING AGENT, TRITERPENE-CONTAINING OLEOGEL AND METHOD FOR PRODUCING A TRITERPENE-CONTAINING OLEOGEL

Abstract An oleogel, comprising: - a nonpolar liquid having a proportion between 80% by weight and 99% by weight, based on the total weight of the gel, - at least one highly dispersed triterpene having an average particle size of less than 50 µm as an oleogel-forming agent between 1% by weight and 20% by weight, based on the total weight of the gel.
Full Text Description
TRITERPENE-CONTAINING OLEOGEL-FORMING AGENT,
TRITERPENE-CONTAINING OLEOGEL AND METHOD FOR PRODUCING
A TRITERPENE-CONTAINING OLEOGEL
The present invention relates to an oleogel-forming agent, an oleogel having this gel-forming
agent and a method for producing an oleogel.
Gels are finely dispersed systems of a liquid and a solid phase in which the solid phase forms a
contiguous three-dimensional structure and the two phases are thoroughly intermingled. A
distinction is made essentially between hydrophilic gels and hydrophobic gels. The latter are also
known as oleogels. Oleogels are based on a nonpolar liquid, e.g., an oil, a wax or a paraffin, to
which a gel-forming agent is added to achieve the desired physical properties.
Such oleogels may fulfill a variety of functions, depending on the composition.
Oleogels are used for topical application, in particular in the pharmaceutical field. In these
pharmaceutical oleogels, a gel-forming agent is present in the gel in addition to the
pharmaceutically active ingredients. Highly dispersed silicon dioxide, available under the brand
name Aerosil®, is a widely used gel-forming agent for pharmaceutical oleogels. Oleogels are
strongly thixotropic, i.e., they liquefy as a result of mechanical action and then solidify again.
Other gels, e.g., gels containing pectin as the gel-forming agent, crosslink under the influence of
an acid, while yet others undergo gelation as a function of temperature, e.g., gelatins.
Oleogels are also used industrially. An example is nonpolar coating agents (dripless paints).
Highly dispersed silicon dioxide may also be used as the gel-forming agent for these
applications. For industrial applications, this mineral gel-forming agent has the disadvantage that
it does not burn without ash formation in thermal utilization of a product treated with such an
oleogel.

The object of the present invention is to provide an oleogel-forming agent which is
pharmaceutically active itself and burns without ash formation, an oleogel having such a gel-
forming agent and a method for producing an oleogel having such a gel-forming agent.
This object is achieved by an oleogel-forming agent having the features of Claim 1. an oleogel
having the features of Claim 11, and a method having the features of Claim 17.
The oleogel-forming agent according to the present invention has at least one highly dispersed
triterpene.
Triterpenes such as betulin, lupeol, betulinic acid, oleanolic acid, and similar compounds are
renewable raw materials that occur in the bark of the birch tree, for example. Betulin, betulinic
acid, lupeol, and oleanolic acid are pentacyclic triterpenes, namely the first three having a lupane
structure and the last having an oleanane structure. The characteristic feature of the lupane group
is a ring having five carbons within the pentacyclic system which has an a-isopentenyl group in
position C19.
A method for producing triterpenes from plant parts, in particular betulin from birch bark, is
described in WO 2001/72315 Al and WO 2004/016336 Al, for example.
The pharmacological properties of triterpenes, in particular betulin, make the triterpene-
containing oleogel-forming agent according to the present invention particularly interesting for
the production of cosmetic and pharmaceutical oleogels.
The antiseptic properties of betulin were demonstrated as early as 1899, so it was used for
sterilizing wound dressings and bandages (J. Wheeler (1899), Pharm. J., Die Darstellung des
Betulin durch Sublimation [Synthesis of betulin by sublimation], 494, Ref. Chem. Centr. 1900 1,
p. 353).
Furthermore, an anti-inflammatory effect similar to that of cortisone as well as a cytostatic effect
have been demonstrated for betulin and betulin derivatives when used on various tumor cell lines
in vitro (M. Carmen Recio et al. (1995), Investigations on the steroidal anti-inflammatory
activity of triterpenoids from Diospyros leucomelas, Planta Med. 61, pp. 9-12; K. Yasukawa et
al. (1991), Sterol and triterpene derivates from plants, Oncogene 48, pp. 72-76).

An antiviral action of betulin against herpes simplex viruses is described in US 5,750,578.
US 2002/0119935 Al describes the action of triterpenes on bacterial infections and
US 2002/0128210 Al describes the action of triterpenes on fungal infections.
The average particle size of the at least one triterpene in the oleogel-forming agent is preferably
less than 50 µm. The average particle size is particularly preferably less than 10 µm or even less
than 100 nm to achieve excellent gel-forming properties. In this context we speak of a fine
dispersivity if the particle size is between 100 nm and 10 µm and colloidal dispersivity if the
particle size is between 1 nm and 100 nm.
The amount of secondary agglomerates of the at least one triterpene in the oleogel-forming agent
preferably is less than 20% by weight. Ideally there is a homogeneous particle size distribution,
i.e., a normal distribution of the frequency of individual particle sizes. The presence of secondary
agglomerates may have a negative effect on the gel-forming properties of a powder, as suggested
by the article by Knop, Reimann: "Kolloidale Kieselsauren als Gelbildner" [Colloidal silicas as
gel-forming agents], GOVI Verlag [GOVI Publishers], 2001.
The specific surface area of this triterpene may also have effects on the properties of the at least
one highly dispersed triterpene as an oleogel-forming agent. Experiments have shown that gel-
forming properties are improved with an increase in specific surface area. This specific surface
area of the at least one triterpene is in one embodiment between 1 m2/g and 500 m2/g and is
preferably between 10 m2/g and 100 m2/g and particularly preferably between 20 m2/g and 50
m2/g.
In addition to triterpenes such as betulin, betulinic acid, lupeol or allobetulin, the oleogel-
forming agent in the form of a micronized triterpene-containing powder may also contain a small
amount of other substances, e.g., those substances that are also present naturally in a certain
amount in triterpene-containing plant parts, e.g., birch bark from which triterpenes may be
extracted. The triterpene content in the oleogel-forming agent according to the present invention
is preferably more than 80% by weight, particularly preferably more than 90% by weight, based
on the weight of the oleogel-forming agent. The betulin content is advantageously more than
80% by weight, based on the triterpene content.

The triterpene-containing oleogel-forming agent according to the present invention may also be
used for industrial applications, e.g., in nonpolar coating agents. It has the advantage for such
applications that it burns without ash formation in thermal utilization - unlike mineral gel-
forming agents.
The oleogel according to the present invention contains:
- a nonpolar liquid in a proportion between 80% by weight and 99% by weight, based on the
total weight of the gel and
- the above mentioned triterpene-containing oleogel-forming agent as the gel-forming agent in a
proportion between 1% by weight and 20% by weight, preferably between 3% by weight and
15% by weight, particularly preferably between 6% by weight and 12% by weight, based on the
total weight of the gel.
The advantage of this semisolid preparation in the form of an oleogel lies in the simplicity of its
formulation, whereby the triterpene functions simultaneously as a pharmaceutically active
substance and as a gel-forming agent, so that no additional gel-forming agents need to be used.
The oleogel is therefore particularly suitable for allergy-prone skin.
Using the triterpene-containing highly dispersed, preferably finely dispersed or colloidally
dispersed powder mentioned above as the oleogel-forming agent having a triterpene content in
the concentration range as indicated and having the stated average particle size, it is possible to
produce a gel which does not contain any other ingredients in addition to the at least one
pharmaceutically active triterpene which is present in powder form and the nonpolar liquid.
Triterpenes have a solubility of less than 0.5% in nonpolar liquids, so the triterpenes are present
primarily in the form of undissolved solid particles in the gel.
However, there is of course also the possibility of adding other pharmaceutically active
substances to the oleogel in addition to the triterpene present in the gel-forming agent.
The advantages of an oleogel with a triterpene-containing oleogel-forming agent are varied,
depending on the area of use.

A novel semisolid preparation is thus made available for the cosmetic pharmaceutical field. It is
good in particular on dry skin and on the lips in comparison with preparations containing water.
Topical use of the oleogel according to the present invention is advantageous in particular for
people at risk of allergies because no other gel-forming agents are necessary. On the other hand,
the oleogel may also be used as an additive-free pharmaceutical base into which other lipophilic
and, using water, also hydrophilic active ingredients or excipients may be easily incorporated.
A thixotropic composition having a nonmineral oleogel-forming agent which therefore burns
without ash formation is made available for the industrial field. For example, nonpolar coating
agents (dripless paints) having an increased thixotropy thanks to the oleogel-forming agent
according to the present invention constitute one area of application. The gel-forming agent also
has the antiseptic properties and light-stabilizing effects known for triterpenes.
The proportion of nonpolar liquid in the oleogel is preferably between 88% by weight and 94%
by weight and the amount of triterpene-containing powder is preferably between 6% by weight
and 12% by weight.
Any nonpolar liquids such as vegetable, animal or synthetic oils, waxes, and paraffins are
suitable as the nonpolar liquid for the oleogel. The nonpolar liquid is, for example, a vegetable
oil such as sunflower oil, olive oil, avocado oil, almond oil, or a mixture of these oils.
The oleogel according to the present invention has a viscosity that has only a slight dependence
on temperature, but it has a strong thixotropic behavior so that the gel is simple to store and use.
The oleogel-forming agent in the form of the highly dispersed, preferably finely dispersed or
colloidally dispersed triterpene powder may also be used as a thickener if it is used in the liquid
to be thickened in a concentration below the gelation limit, i.e., the concentration that would be
necessary to form an oleogel from the liquid and the triterpene.
There is the possibility of adding the highly dispersed triterpene to the nonpolar liquid in a
concentration that is below the gelation limit, i.e., below the concentration required for gelation.
The result is an oleosol, i.e., a viscous preparation, in which the highly dispersed, preferably
finely dispersed, or colloidally dispersed triterpene acts as a thickener.

The present invention is explained in greater detail below on the basis of an exemplary
embodiment with reference to the attached figure.
The top part of the figure is a histogram illustrating the homogeneous particle size distribution of
a sample of a highly dispersed oleogel-forming agent according to the present invention. The
measured values on which the curve is based are shown in the form of a table in the bottom part
of the figure. A value for the frequency distribution in the right-hand part of the table is based on
an interval of two particle sizes which are shown in the left part of the table with an offset in the
upper and lower directions for the respective frequency value. The table thus indicates, for
example, that the amount of particles having a size between 0.209 µm and 0.240 µm in the
sample investigated is 0.14%.
The particle sizes of the sample are between 0.2 µm and 60.2 µm with the maximum size
distribution being between 2.5 µm and 5 µm.
The distribution of particle sizes for the sample investigated is almost homogeneous, i.e., the
frequency of the distribution increases steadily for diameters less than the maximum, which is
approximately 3.5 urn, and decreases steadily for diameters greater than the maximµm. The
frequency increases again somewhat only for particles between approximately 34 µm and 45 µm in size. This increase might be attributable to secondary agglomerates, i.e., accumulations of
particles formed only after the actual crystallization or formed by agglomeration of two or more
crystals that initially crystallize independently of one another.
According to gas chromatographic analysis, this powder contains 85% by weight betulin, 5% by
weight betulinic acid, 3% oleanolic acid, 0.7% by weight lupeol, and 6.3% by weight other
triterpene derivatives.
Using this highly dispersed powder as a gel-forming agent, an oleogel was produced by mixing
the powder with 9% by weight sunflower oil, based on the total weight of the oleogel. The result
was a stable semisolid gel with a very strong thixotropic behavior.

The oleogel produced in this way is suitable for treatment of a wide variety of skin diseases in
humans and animals. Examples include actinic keratoses and basalioma in humans and mastitis
in mammals.
The powder containing at least one triterpene and being active as an oleogel-forming agent may
be obtained from plant parts by any traditional extraction methods. If the powder obtained by
such extraction methods does not have the dispersibility, average particle size, and homogeneous
particle size distribution required for the gel-forming properties, then the powder may be
subjected to various procedures to arrive at the desired particle size, homogeneity, and
dispersibility. Various methods for this, some of which are explained briefly below, are known to
those skilled in the art who are trained in this field.
If the particle size in the powder is too high, impact or gravitation methods are suitable for
reducing the size of the particles.
In addition, there is the possibility of dissolving the powder in a suitable solvent, e.g.,
tetrahydrofuran (THF) and subsequent recrystallization. This crystallization may be
accomplished by spray drying or by cooling a saturated solvent, for example. The particle size
may be adjusted via the crystallization conditions. In spray drying, for example, the
crystallization conditions depend on the diameter of the nozzle through which the triterpene-
solvent mixture is sprayed and on the temperature and pressure in the chamber into which the
mixture is sprayed. In crystallization by cooling a saturated solution, the crystallization
conditions depend on the temperature gradient over time during cooling and on the triterpene
concentration in the solution.
It has been found that particularly small triterpene particles having a large specific surface area
may be obtained by adding cold solvent to a saturated triterpene-solvent-mixture. This admixture
of cold solvent results in cooling of the solution, causing the triterpenes to crystallize out. At the
same time, the added cold solvent decreases the triterpene concentration in the solvent, with the
result that small crystals tend to be formed, which is advantageous from the standpoint of the
gel-forming properties.

Finally, there is also the possibility of sizing an existing powder to obtain a powder having the
desired size distribution.

We Claim:
1. An oleogel, comprising:
- a nonpolar liquid having a proportion between 80% by weight and 99% by
weight, based on the total weight of the gel,
at least one highly dispersed triterpene having an average particle size of less than
50 µm as an oleogel-forming agent between 1% by weight and 20% by weight,
based on the total weight of the gel.
2. The oleogel as claimed in claim 1, wherein the average particle size of the at least one
triterpene is less than 10 µm.
3. The oleogel as claimed in claim 1 or 2, wherein the proportion of secondary agglomerates
of the at least one triterpene is less than 20% by weight.

4. The oleogel as claimed in any one of claims 1 through 3, wherein the at least one
triterpene has a homogeneous particle size distribution.
5. The oleogel as claimed in any one of claims 1 through 4, wherein the specific surface
area of the at least one triterpene is between 1 m2/g and 500 m2/g.
6. The oleogel as claimed in claim 5, wherein the specific surface area of the at least one
triterpene is between 10 m /g and 100 m /g.
7. The oleogel as claimed in claim 6, wherein the specific surface area of the at least one
triterpene is between 20 m2/g and 50 m2/g.
8. The oleogel as claimed in any one of claims 1 through 7, wherein the proportion of the at
least highly dispersed triterpene is more than 80% by weight.
9. The oleogel as claimed in claim 8, wherein the proportion of the at least on highly
dispersed triterpene is more than 90% by weight.
10. The oleogel as claimed in any one of claims 1 through 9, wherein the at least one
triterpene has a proportion of more than 80% by weight betulin.

11. The oleogel as claimed in any one of claims 1 through 10, wherein the proportion of
oleogel-forming agent is between 3% by weight and 15% by weight.
12. The oleogel as claimed in claim 11, wherein the proportion of the nonpolar liquid is
between 88% by weight and 94% by weight and the proportion of the oleogel-forming
agent is between 6% by weight and 12% by weight.
13. The oleogel as claimed in any one of claims 1 through 12, wherein the nonpolar liquid is
a vegetable, animal, mineral, or synthetic oil.
14. The oleogel as claimed in claim 13, wherein the oil is one of the following vegetable oils
or a mixture of the following vegetable oils: sunflower oil, olive oil, avocado oil, almond
oil.
15. The oleogel as claimed in any one of claims 1 through 12, wherein the nonpolar liquid is
a wax or a paraffin.
16. A method for producing an oleogel comprising mixing the following ingredients:

- a nonpolar liquid in a proportion between 80% by weight and 99% by weight,
based on the total weight of the gel,
- at least one highly dispersed triterpene having an average particle size of less than
50 µm as the oleogel-forming agent in a proportion between 1% by weight and
20% by weight, based on the total weight of the gel.

17. The method as claimed in claim 16, wherein the average particle size of the at least one
triterpene is less than 10 µm.
18. The method as claimed in claim 16 or 17, wherein the proportion of secondary
agglomerates of the at least one triterpene is less than 20% by weight.
19. The method as claimed in any one of claims 16 through 18, wherein the at least one
triterpene has a homogeneous particle size distribution.
20. The method as claimed in any one of claims 16 through 19, wherein the specific surface
area of the at least one triterpene is between 1 m2/g and 500 m2/g.
21. The method as claimed in claim 20, wherein the specific surface area of the at least one
triterpene is between 10 m2/g and 500 m2/g.

22. The method as claimed in claim 21, wherein the specific surface area of the at least one
triterpene is between 20 m /g and 50 m /g.
23. The method as claimed in any one of claims 16 through 22, wherein the proportion of the
at least highly dispersed triterpene is more than 80% by weight.
24. The method as claimed in claim 23, wherein the proportion of the at least one highly
dispersed triterpene is more than 90% by weight.
25. The method as claimed in any one of claims 16 through 24, wherein at least one
triterpene has a proportion of more than 80% by weight betulin
26. The method as claimed in any one of claims 16 through 25, wherein the proportion of
oleogel-forming agent is between 3% by weight and 15% by weight.
27. The method as claimed in claim 26, wherein the proportion of nonpolar liquid is between
88% by weight and 94% by weight and the proportion of oleogel-forming agent is
between 6% by weight and 12% by weight.

28. The method as claimed in any one of claims 16 through 27, wherein the nonpolar liquid
is a vegetable, animal or synthetic oil.
29. The method as claimed in claim 28, wherein the oil is one of the following vegetable oils
or a mixture of the following vegetable oils: sunflower oil, olive oil, avocado oil, almond
oil.
30. The method as claimed in any one of claims 16 through 27, wherein the nonpolar liquid
is a wax or a paraffin.


ABSTRACT

Title:
TRITERPENE-CONTAINING OLEOGEL. FORMING AGENT, TRITERPENE-
CONTAINING OLEOGEL AND METHOD FOR PRODUCING A TRITERPENE-
CONTAINING OLEOGEL.
An oleogel, comprising:
- a nonpolar liquid having a proportion between 80% by weight and 99% by
weight, based on the total weight of the gel,
- at least one highly dispersed triterpene having an average particle size of less than
50 µm as an oleogel-forming agent between 1% by weight and 20% by weight,
based on the total weight of the gel.

Documents:

03888-kolnp-2006 abstract.pdf

03888-kolnp-2006 claims.pdf

03888-kolnp-2006 correspondence others.pdf

03888-kolnp-2006 description(complete).pdf

03888-kolnp-2006 drawings.pdf

03888-kolnp-2006 form-1.pdf

03888-kolnp-2006 form-2.pdf

03888-kolnp-2006 form-3.pdf

03888-kolnp-2006 form-5.pdf

03888-kolnp-2006 international publication.pdf

03888-kolnp-2006 international search authority report.pdf

03888-kolnp-2006 pct others.pdf

03888-kolnp-2006 priority document.pdf

03888-kolnp-2006-correspondence others-1.1.pdf

03888-kolnp-2006-correspondence-1.2.pdf

03888-kolnp-2006-correspondence-1.3.pdf

03888-kolnp-2006-form-26.pdf

03888-kolnp-2006-others document.pdf

03888-kolnp-2006-priority document-1.1.pdf

3888-KOLNP-2006-(14-02-2012)-ABSTRACT.pdf

3888-KOLNP-2006-(14-02-2012)-AMANDED CLAIMS.pdf

3888-KOLNP-2006-(14-02-2012)-CORRESPONDENCE.pdf

3888-KOLNP-2006-(14-02-2012)-DESCRIPTION (COMPLETE).pdf

3888-KOLNP-2006-(14-02-2012)-DRAWINGS.pdf

3888-KOLNP-2006-(14-02-2012)-FORM-1.pdf

3888-KOLNP-2006-(14-02-2012)-FORM-2.pdf

3888-KOLNP-2006-(14-02-2012)-FORM-3.pdf

3888-KOLNP-2006-(14-02-2012)-OTHERS.pdf

3888-KOLNP-2006-(14-02-2012)-PETITION UNDER RULE 137.pdf

3888-KOLNP-2006-ABSTRACT.pdf

3888-KOLNP-2006-CLAIMS.pdf

3888-KOLNP-2006-CORRESPONDENCE 3.1.pdf

3888-KOLNP-2006-CORRESPONDENCE 3.2.pdf

3888-KOLNP-2006-CORRESPONDENCE-3.pdf

3888-KOLNP-2006-DESCRIPTION (COMPLETE).pdf

3888-KOLNP-2006-DRAWINGS.pdf

3888-KOLNP-2006-EXAMINATION REPORT.pdf

3888-KOLNP-2006-FORM 1.pdf

3888-KOLNP-2006-FORM 13 1.1.pdf

3888-KOLNP-2006-FORM 13 1.2.pdf

3888-KOLNP-2006-FORM 13.pdf

3888-KOLNP-2006-FORM 18 1.1.pdf

3888-kolnp-2006-form 18.pdf

3888-KOLNP-2006-FORM 2.pdf

3888-KOLNP-2006-FORM 26 1.1.pdf

3888-KOLNP-2006-FORM 26.pdf

3888-KOLNP-2006-FORM 3 1.1.pdf

3888-KOLNP-2006-FORM 3.pdf

3888-KOLNP-2006-FORM 5 1.1.pdf

3888-KOLNP-2006-FORM 5.pdf

3888-KOLNP-2006-GRANTED-ABSTRACT.pdf

3888-KOLNP-2006-GRANTED-CLAIMS.pdf

3888-KOLNP-2006-GRANTED-DESCRIPTION (COMPLETE).pdf

3888-KOLNP-2006-GRANTED-DRAWINGS.pdf

3888-KOLNP-2006-GRANTED-FORM 1.pdf

3888-KOLNP-2006-GRANTED-FORM 2.pdf

3888-KOLNP-2006-GRANTED-SPECIFICATION.pdf

3888-KOLNP-2006-OTHERS 1.1.pdf

3888-KOLNP-2006-OTHERS.pdf

3888-KOLNP-2006-REPLY TO EXAMINATION REPORT 1.1.pdf

3888-KOLNP-2006-REPLY TO EXAMINATION REPORT.pdf

3888-KOLNP-2006-SPECIFICATION.pdf


Patent Number 256193
Indian Patent Application Number 3888/KOLNP/2006
PG Journal Number 20/2013
Publication Date 17-May-2013
Grant Date 15-May-2013
Date of Filing 22-Dec-2006
Name of Patentee BIRKEN GMBH
Applicant Address STREIFLINGSWEG 11 75223 NIEFERN-OSCHELBRONN
Inventors:
# Inventor's Name Inventor's Address
1 SCHEFFLER,ARMIN FORSTSTRASSE 7 75229 NIEFERN-OSCHELBRONN
PCT International Classification Number A61K 9/06
PCT International Application Number PCT/EP2005/006710
PCT International Filing date 2005-06-21
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 102004030044.5 2004-06-22 Germany