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Title: Effervescent formulation containing plant extract
United States Patent: 6,190,697
Inventors: Gergely; Gerhard (Gartengasse 8, A-1053 Vienna,
AT); Gergely; Irmgard (Vienna, AT); Gergely; Thomas (Vienna, AT); Gergely;
Stefan (Vienna, AT)
Assignee: Gergely; Gerhard (AT)
Appl. No.: 178639
Filed: October 26, 1998
Foreign Application Priority Data: Oct 27, 1997[EP]
(97118648)
Abstract
The effervescent formulation elation in the form of granules or of a
tablet contains, in addition to the effervescent base, at least one
water-soluble or at least suspendable plant extract whose particles are
coated with at least one oily, fatty or waxy substance. At least one
emulsifier and/or at least one antifoam may be present in the coating
and/or as a further component of the mixture, in particular applied as a
further component of the mixture to a pharmaceutically permissible filler
as carrier. The individual phases are prepared by a procedure in which the
plant extract or the filler is heated--preferably in a granulator, in
particular in a vacuum granulator--and wet or mixed with a melt or
solution of the oily, fatty or waxy substance or at least one emulsifier
and/or at least one antifoam and then dried--preferably in a vacuum--and
sieved to the desired particle size.
Description of the Invention
The invention relates to an effervescent formulation
according to the preamble of claim 1. Plant extracts have long been a
popular dosage form for prophylaxis and therapy; they are becoming more
important, not least owing to the increasing elucidation of the action
mechanism and of the structure of the active ingredients. Where higher
doses are necessary, instant tea has to date been the most important
dosage form but has some disadvantages, namely on the one hand the inexact
dosage as a result of dissolving a teaspoon or tablespoon of the instant
tea in water, It being scarcely possible exactly to maintain the
fill-weight; on the other hand, the instant teas containing plant extracts
and usually present in powder or granular form are very hygroscopic and
agglomerate in a container after the latter has been opened a few times.
In order to avoid these disadvantages and to provide an attractive dosage
form, the administration of the plant extracts in the form of an
effervescent tablet was developed. However, it has been found that in
particular the very water-soluble plant extracts, which are generally
present in a finely pulverulent form spray-dried from aqueous and/or
alcoholic solution, slow down the dissolution of the effervescent tablet
to an extreme extent. These include, inter alia, ivy and sabale dry
extracts, solidago, plantago, nettle root, nettle leaf, birch leaf, cynara
and thyme extracts, extracts of hypericum, harpagophytum, gingko and
ruscus (Extractum Rusci aculeati). The dissolution is slowed down because,
on admission of water, these very soluble plant extracts very rapidly form
highly concentrated, tacky, slimy solutions which prevent the further
admission of water to the interior of the tablet, thus hindering rapid
dissolution. Moreover, effervescent particles which are intended to
promote disintegration and dissolution of the tablet are also coated with
the solution and their reaction with the water is thus suppressed. In
addition, most plant extracts contain saponin and consequently exhibit
extreme foaming behavior in the effervescent tablet. The dissolution is
thus further slowed down because frothy, highly concentrated solutions
form between the effervescent particles.
Thus, for example when a dose of 400 mg of solidago extract is added to
effervescent granules which are then compressed to form tablets,
dissolution times of 15 to 20 minutes result on dissolution in water. Even
smaller amounts, for example 65 mg of an ivy dry extract in an
effervescent tablet, exhibit dissolution times of 5 to 7 minutes or more
on dissolution in water at 17oC. This no longer meets the
requirements of pharmacopoeias, according to which the dissolution time of
effervescent tablets in water at 20oC. should be less than 5
minutes.
By means of conventional measures, such as, for example, by the addition
of antifoams, such as, for example, simethicone or dimethicone, or by the
application of the antifoam to the dry plant extract itself it was
possible to achieve only a slight improvement by reducing the foaming
and--associated with this--also only a slight reduction in the dissolution
time of the effervescent tablet.
Granulation of the plant extracts with the object of increasing the size
of the particles and reducing their number within the effervescent tablet
in order thus to prevent the formation of a concentrated solution around
the plant extract particles and effervescent particles during dissolution
of the tablet in water also did not achieve the object since precisely
these granulated particles then agglomerated to an extreme extent and
exhibited undesired and by no means rapid dissolution properties.
Binding to a slightly soluble substance also did not lead to a short
dissolution time since the extracts at the surface of the slightly soluble
substance likewise formed highly concentrated solutions and thus rendered
this measure ineffective.
Although granulation with slightly soluble substances once again resulted
in the effervescent tablet with plant extracts dissolving somewhat more
rapidly, the granulated particles could not dissolve completely and formed
a residue.
The object of the invention was therefore to provide a galenical
formulation for freely soluble plant extracts in the form of an
effervescent tablet, which formulation has a dissolution time of less than
4 minutes and significantly reduced foam formation.
Surprisingly, the achievement of this object and the overcoming of the
above-mentioned problems were possible for the first time by the measures
described in the defining clause of claim 1. Particular embodiments and
further developments of the concept of the invention are described in the
defining clauses of the dependent claims.
The invention comprises treating the plant extract with at least one
fatty, oily or waxy substance, in particular producing a thin coating film
of this substance or these substances on the plant extract particles,
preferably emulsifiers also being added to this hydrophobic extract phase
with fatty, oily or waxy substances. The fatty, oily or waxy substances
can be applied to the plant extract particles either in the molten state
or in solution in a solvent in which the emulsifiers too are soluble. The
plant extracts treated in this manner can then--optionally with further
addition of the emulsifier--be mixed with effervescent granules and the
mixture compressed to give tablets. Effervescent tablets containing plant
extracts which dissolve in water at 17oC. within 11/2 to 4
minutes are obtained.
As a result of the treatment with the above-mentioned substances, the
plant extracts become sufficiently hydrophobic to prevent conversion of
the effervescent tablet into a paste on dissolution of water, so that the
effectiveness of the effervescent particles on admission of water is
displayed as desired and rapid dissolution of the tablet is thus
permitted. As a result of the contact with water, the effervescent
particles display their effervescent activity and the plant extract
particles are ejected from the tablet owing to the hydrophobic structure
and because of the effervescent effect and dissolve only thereafter. It
has proven advantageous to add suitable emulsifiers to the phase
containing the fatty, oily or waxy substances, in order to achieve
appropriate suspension properties for these substances on dissolution of
the effervescent tablet in water.
In particular, the following substances can be used as fatty, oily or waxy
substances which are suitable for the surface treatment of the plant
extract particles: esters of medium-chain, vegetable fatty acids, such as,
for example, caprylic and capric acid, with glycerol and propylene glycol,
preferably Miglyol.RTM. neutral oils.
Furthermore, all edible, animal and vegetable fats may be used as fat
components. These are in particular triglycerides which essentially
consist of mixtures of glyceryl esters of higher fatty acids, in
particular of vegetable or animal origin, having a chain length of about
10 to 22 C atoms. These include, for example, microcrystalline
triglycerides and glyceryl esters of saturated, linear and unbranched
fatty acids, e.g. glyceryl trimyristate, glyceryl tripalmitate,
trimyristin, etc. Further suitable fat components are, for example,
coconut oil, hydrogenated coconut oil, hydrogenated castor oils,
tocopheryl acetate, esters of higher fatty acids, such as, for example,
isopropyl palmitate, polyethylene glycol, such as, for example,
Carbowax.RTM., it being possible to use Carbowax.RTM. 400 or Carbowax.RTM.
6000, depending on the plant extract.
The fat, oily or waxy substances are used in an amount of 0.5 to 25 parts
by weight, preferably 0.8-19 parts by weight, based on 100 parts by weight
of the freely soluble plant extract, these substances being at least
partly contained in the plant extract phase but possibly also additionally
being added as a separate fat phase to the effervescent granules. The
emulsifiers are on the one hand applied together with the fatty, oily or
waxy substances directly to the plant extract and optionally on the other
hand added in the form of a phase, the emulsifier being applied with
suitable solvents to a carrier, the solvent being evaporated off and this
emulsifier phase being mixed with the effervescent tablet.
A variety of emulsifiers may be used, depending on the fatty, oily or waxy
substances employed. Phospholipids, such as lecithin, Metarin and Epikuron,
furthermore polysorbates (sorbitan monolaurate, etc.) and ethoxylated
glycerol fatty acid esters (e.g. Tagat.RTM.), sugar esters, glycerol
polyethylene glycol oxystearate (Cremophor RH 40), Macrogol glycerol
ricinoleate or sodium stearoyllactate are recommended. It is also possible
to use wetting agents, such as sodium dioctylsulfosuccinate or sodium
laurylsulphate. One or more emulsifiers can be incorporated into the plant
extract phase and/or also added in a further emulsifier phase to the final
mixture for the ready-to-press granules. The amount of emulsifier is
between 0.2 and 10, preferably 0.3-8, parts by weight, based on 100 parts
by weight of the freely soluble plant extract to be used, some
emulsifiers, owing to their oily property, also enhancing the
effectiveness of the fatty substances and some lipids also having an
emulsifier character, such as propylene glycol stearate and glyceryl
oleate, laurate and stearate.
In order, if required, to impart better flowability to the extracts
treated with fatty, oily or waxy substances, it is possible to add a fine
filler which adheres to the fatty surface and thus prevents the
agglomeration of the active ingredient phase. All conventional
pharmaceutical tablet fillers suitable for this purpose, such as sugar
alcohols, mannitol, sorbitol and furthermore maltodextrin, pulverized
sucrose, pulverized lactose, fructose, glucose, etc. These fillers can be
introduced directly into the plant extract phase (cf. Example 1), or the
plant extract phase is homogeneously mixed with a filler after the
preparation and then mixed with the effervescent granules containing the
remaining ingredients, flavors, etc.
For example, mannitol or sorbitol takes up a part of the oily, fatty or
waxy substance and also the emulsifier and prevents the agglomeration of
the coated particles of the plant extract phase. Incidentally, the fillers
mentioned are also suitable as carriers for the emulsifier or emulsifiers,
for the antifoam or antifoams and for any additional amounts of oily,
fatty or waxy substance, particularly when the absorptivity of the plant
extract particles for these substances on the surface is not sufficient
for achieving the optimum effect.
The preparation of the plant extract phase can be carried out as follows:
the freely soluble plant extracts are preheated to 45 to 60oC.;
a solution or melt of the fatty, oily or waxy substances--preferably with
one or more emulsifiers--is applied. This solution is uniformly
distributed while stirring, and the solvent is then evaporated, preferably
by means of a vacuum Before drying, it is also possible to add a filler.
To reduce foam formation, it is necessary in most cases, but not
essential, to add an antifoam, which on the one hand can be introduced
into the fat/emulsifier phase but on the other hand may also be added as a
separate phase to a mixture of the effervescent granules and the plant
extract phase, the antifoam being applied to a neutral excipient or
filler. For the preparation of the antifoam phase, the antifoam is applied
to a filler by means of a solvent or of an aqueous suspension; the solvent
is evaporated off, and this phase is added to the tablet.
The amount of antifoam used, based on 100 parts by weight of plant
extract, may be between 0 and 10 parts by weight, i.e. in the case of
freely soluble plant extracts having a low saponin content the use of an
antifoam is not required in specific cases.
However, it is also possible to add the oily, fatty or waxy substance and
any intended emulsifiers and/or antifoams to the solution intended for the
preparation of the plant extract for spray-drying.
All conventional effervescent components may be used for the preparation
of the effervescent base or of the effervescent granules, the acid
component preferably consisting of citric acid, tartaric acid, malic acid
or of the salts thereof, such as, for example, monosodium citrate or
monosodium tartrate. The base fraction of the effervescent base
expediently consists of CO2 -eliminating alkali metal
bicarbonates or carbonates, such as sodium and/or potassium bicarbonate or
carbonate, and partly, but not exclusively, of alkaline earth metal
carbonates, such as calcium carbonate and/or magnesium carbonate.
In particular, sweeteners, such as sugar, sodium cyclamate, saccharin
sodium, aspartame and acesulfame, and flavors or other galenical fillers,
such as sugar alcohols, e.g. mannitol and sorbitol, and also maltodextrin,
optionally sucrose, fructose, lactose, etc., may be used as additives and
excipients.
The effervescent plant extract formulation prepared according to the
invention is distinguished by rapid dissolution in water (dissolution time
at 17oC., 11/2 to 4 minutes) and by substantially improved
foaming behavior, i.e. only slight foaming.
Claim 1 of 23 Claims
What is claimed is:
1. An effervescent formulation in the form of granules or of a tablet,
containing at least one water-soluble or at least suspendable dry plant
extract and an effervescent base comprising at least one solid, edible,
organic acid and at least one alkali metal and/or alkaline earth metal
carbonate or bicarbonate, wherein the dry plant extract particles are
coated with at least one oily, fatty or waxy substance.
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