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Pharm/Biotech Resources
Title: Pharmaceutical compositions for promoting the
growth of gram-positive bacilli and increasing the acidity in the vagina
and the use thereof
United States Patent: 6,964,949
Issued: November 15, 2005
Inventors: Zeng; Zhongming (Shenzhen, CN)
Assignee: Shanghai Jiao Da Onlly Co., Ltd. (Shanghai, CN)
Appl. No.: 643003
Filed: August 18, 2003
Abstract
The present invention relates to a pharmaceutical formulation for
stimulating the growth of gram-positive bacilli and increasing the acidity
in the vagina which comprises sucrose and/to maltose, to the use of certain
sucrose and/or maltose, in preparing the pharmaceutical formulation for
stimulating the growth of gram-positive bacilli and increasing the acidity
in the vagina, in particular to a method of stimulating the growth of
gram-positive bacilli and increasing the acidity in the vagina, treating the
reduction of gram-positive bacilli and the lowness of acidity in vagina as
well as the vaginitis and the disturbance of vaginal bacterioflora
accompanying the reduction of gram-positive bacilli, especially bacterial
vaginal disease.
Description of the Invention
FIELD OF THE INVENTION
This invention relates to pharmaceutical compositions containing
saccharides as active ingredients for promoting the growth of Gram-positive
bacilli and increasing the acidity in the vagina, to the use of particular
saccharides in the preparation of compositions for promoting the growth of
Gram-positive bacilli and increasing the acidity in the vagina, and
especially to a method of promoting the growth of Gram-positive bacilli and
increasing the acidity in the vagina, treating decreased levels of
Gram-positive bacilli and decreased levels of acidity in the vagina,
treating vaginitis and disturbances of the vaginal bacterial flora
accompanying the reduction of Gram-positive bacilli, especially bacterial
vaginosis.
BACKGROUND OF THE INVENTION
High acidity in female vagina is one important anti-infective mechanism
of the vagina and is of great significance for vaginal health. Lactobacilli
and other Gram-positive bacilli that can produce and resist acids serve an
important role in maintaining the normal acidity in the vagina by keeping
the vaginal pH value in the range from 4.0 to 4.6. They are the
physiological bacterial flora of vagina, whereas Gram-negative bacilli,
Gram-negative cocci, and Gram-positive cocci are relatively less abundant in
the healthy vagina.
When the Gram-positive bacilli are reduced or disappear in vagina, vaginal
pH value rises and disturbance of vaginal bacterial flora results from
abnormal increases of Gram-negative bacilli, Gram-positive cocci and
Gram-negative cocci, which can cause harm to the human body and lead to a
range of diseases. The most typical condition resulting from altered vaginal
flora is bacterial vaginosis (BV). BV is characterized by the reduction or
even disappearance of Lactobacillus and other Gram-positive bacilli in the
vagina, accompanied by decreased acidity (pH value>4.6) in the vagina, and
abnormal increases of such bacteria as Gram-negative bacilli including
Gardnerella, Bacteroides and motile-curved bacilli; Gram-negative cocci such
as Veillonella; and Gram-positive cocci such as Streptococcus. Such changes
in the bacterial flora can cause vaginal secretions to exhibit an unpleasant
odor, and may be associated with pruritus of vulva, and symptoms. In
addition, BV may also be related to IUGR [1], PTL, PROM [2], abortion, and
obstetric infections such as chorio-amnionitis, puerperal endometritis,
vaginal wall phlegmon after hysterectomy, female upper genital tract
infection (salpingitis), and urinary infection, etc. [3]. A high rate of
morbidity is associated with vaginal bacterial flora disturbance. According
to one report, about 45% or more vaginitis cases result from disturbance of
vaginal bacterial flora [3], and 4-15% of American female students in
universities suffer from bacterial vaginosis [4], which has led to serious
compromise to health and quality of life.
There are few options for treatment of reduced Gram-positive bacilli
colonization, decreased vaginal acidity, and related disturbances of vaginal
bacterial flora, vaginitis, and bacterial vaginosis. Therapeutic options
currently include:
1) Antibacterial drugs which are used to suppress the growth of
Gram-negative bacilli and other abnormal bacteria. These most commonly
include clindamycin and metronidazole [5-6]. These drugs suppress the
bacteria that are abnormally increased in the vagina but may also affect the
Gram-positive bacilli. After administration of these drugs, the
Gram-positive bacilli (lactobacilli) can not be restored very well, and it
is very difficult to lower the pH value in the vagina to normal level.
2) Lactic acid-containing pharmaceutical compositions. Vaginal secretions
from patients suffering from bacterial vaginosis have elevated pH values.
Swedish researchers used lactic acid gel for the improvement and recovery of
the low-acidity conditions in vagina, and reported that this treatment can
restore the Gram-positive bacilli (lactobacilli) in the vaginas of some of
the patients [7]. But the study also showed that the lactic acid
pharmaceutical preparation is less effective than the antibacterial drugs
[8].
3) Lactobacillus preparations. Most of the Gram-positive bacilli in vagina
are lactobacillus. If there is disturbance of vaginal bacterial flora, the
lactobacilli will be reduced or disappear, and Gram-negative bacilli,
Gram-negative, and Gram-positive cocci, will increase. The Gram-positive
bacilli in the vagina of some patients can be restored by directly adding
lactobacilli in the vagina [9]. However, stable colonization is generally
not achieved. Moreover, it is difficult to maintain viability of the
lactobacillus preparations during storage, with viable counts in such
preparations decreasing during storage, compromising their useful shelf life
[10].
The international Patent Application WO94/02148 discloses a pharmaceutical
composition for treating vulvitis and vulvovaginitis, and indicates that
such compositions can promote restoration of vaginal epithelium tissues
while alleviating the symptoms. Its preferred composition comprises 7 to 8
active substances. Some preferred compositions may contain 3.0-15.0% (by
weight/volume) lactose or glucose. As mentioned in page 5 lines 8-10 of the
published specification, the lactose or glucose contained in these
compositions is used as carbon source. But this application does not mention
that saccharides can be used solely as the effective component for treating
vulvitis and vulvovaginitis, and nor does it disclose explicitly or
implicitly that the disclosed compositions can stimulate the growth of
Gram-positive bacilli in vagina. Furthermore, it does not indicate that any
other kinds of sugar can be used as active components of a composition for
treating related vaginal diseases. Besides, as mentioned in page 5 lines
17-18 of the specification, this application emphasizes that it is important
for the pH value of the compositions be between 2 and 3.5.
The U.S. Pat. No. 3,860,707 teaches a method for treating trichomonal
vaginitis and monilial vaginitis. This method comprises administering
lactulose into the vagina. This patent also indicates that lactulose can be
administered after being mixed with some carriers such as glucose, lactose
and galactose, wherein lactulose is required to have a concentration as high
as 50%, and the mixture also contains 5% lactose, 8% galactose as carriers,
as mentioned in column 1 lines 51-55 and column 5 lines 1-5 of the patent
specification. The quantity of lactulose is 4-10 grams administered with
each dose, which is taken once or twice daily, as shown in Column 4 Lines
63-66 of the specification. But this patent does not describe the treatment
effectiveness on bacterial vaginosis or other vaginal diseases different
from monilial vaginitis, nor does it suggest that the lactulose of low or
medium concentration (2.5-17%) and small dosage (daily total amount 0.24-2.1
grams) would be able to stimulate the growth of Gram-positive bacillus and
increase the acidity of the vagina. Furthermore, it fails to indicate
whether any saccharide other than lactulose has treatment effects.
European Patent Application EP-A-0257007 discloses a pharmaceutical
composition containing lactic acid and buffering substances and substrate to
support growth of lactobacillus, which can be used to improve
micro-environment in vagina and suppress the growth of harmful bacteria in
the vagina, so as to facilitate the growth of lactobacilli. This patent
application discloses that glycogen or lactose can be used as the said
substrate. But as mentioned in Column 6 Line 10-14 of the specification, the
main ingredient of this composition is lactic acid. The lactic acid and the
glycogen and/or lactose are incorporated in a ratio by weight of from 20:1
down to 500:1, and the content of glycogen and/or lactose is only 0.1-0.166%
(W/V). It also stresses that the pH value of the pharmaceutical composition
should be adjusted to 3.5 to 4.0, which is very important. The in vitro
experimental results disclosed in this application show that this
composition can effectively and selectively kill pathogenic bacteria, and
lactobacilli can survive in this composition for a longer time than the
pathogenic microorganisms. But no test in vitro or vivo shows that this
composition can stimulate the growth of lactobacilli or produce acids. Nor
does this application mention the treatment effect of glycogen or lactose or
any other saccharides when they are used separately as active ingredients.
GB21 12285A discloses a lotion composition for cleaning the vagina. It is a
buffering liquid comprising acetic acid or lactic acid plus sodium acetate
with a pH value of 5.71 to 6.2 as shown in the examples. It also contains
nutrients to support the growth of lactobacillus [1-2% (W/V) glucose and
unsaturated fatty acid]. It also generally mentions inclusion of mono-
and/or disaccharides. The main therapeutic mechanism of this composition is
that the buffering lotion comprising acetic acid or lactic acid plus sodium
acetate can selectively suppress pathogens and not suppress lactobacilli. As
shown in claims 2 and 3 and the in vitro test data of this application, this
lotion can effectively suppress many kinds of pathogens, and lactobacilli
survive in this composition for a longer time. No data from test in vitro or
vivo indicates that this lotion has an activity of promoting the growth of
lactobacilli and producing acid, nor does it indicate the treatment effect
of glucose or any other sugar when used separately as active ingredients.
This application teaches that lactobacilli regulate pH value in vagina to
about 5.8, as shown in Page 1 Lines 20-23 of the specification, which is
strongly contradicted by most knowledgeable investigators.
The above-mentioned pharmaceutical compositions disclosed in patent
applications EP-A-0257007 and GB2112285A which contain lactic acid, acetic
acid and other selective inhibitors as main active ingredients have strong
suppressive action on pathogens but no explicit suppressive action on
lactobacilli, although they may indirectly facilitate the growth of vaginal
lactobacilli. These compositions themselves, however, cannot directly
promote significant growth of lactobacilli, and only regulate vaginal
acidity for a short time. Therefore, it remains very difficult to restore
the physiological conditions dominated by the Gram-positive bacillus-flora
and to restore the vaginal acidity to its normal value.
The object of the present invention is to provide a composition for
promoting the growth of Gram-positive bacilli and the production of acids,
and thus increase the acidity in the vagina. Another object of the present
invention is to provide a method by using such composition for reversing the
reduction of Gram-positive bacilli, lack of vaginal acidity and treating
related vaginal diseases.
In order to seek a composition which is effective in promoting the growth of
Gram-positive bacilli, producing acid, and enhancing the acidity in the
vagina, the inventor has conducted an extensive study, performed tests by
using various pharmaceutical compositions known in the prior art, and has
not found any compositions promoting the growth of Gram-positive bacilli
among the existing compositions. After repeated tests and intensive study,
the inventor has found very surprisingly that sucrose and maltose both have
a strong effect in promoting the growth of Gram-positive bacilli and
producing acids if they are presented in a concentration and at a pH value
in specific ranges. Combined in vitro culturing experiments show that the
two saccharides can stimulate the growth of Gram-positive bacilli,
increasing their numbers significantly. To our surprise, although pH values
above 4.6 in vagina are considered un-physiologic, and most of
state-of-the-art technologies stress that the pharmaceutical compositions
used in vagina must have a pH value equal to 4.0 or below, the inventor has
discovered that, if they have pH value between 4.1 and 7.2, and especially
above pH 5.0, sucrose and maltose can stimulate the growth of Gram-positive
bacilli of women vagina and the production of acid, and are able to decrease
the pH value in vagina to less than 4.6. However, if they have pH values of
4.0 or less, they do not exert significant growth-promoting effects on
Gram-positive bacilli nor upon acid production and the pH of the vagina can
rarely be reduced to below 4.6. Based on the above discoveries and further
study, the inventor has completed the present invention.
SUMMARY OF THE INVENTION
The present invention provides a water-based pharmaceutical composition
for promoting the growth of Gram-positive bacilli and increasing the acidity
in the vagina comprising, based on the volume of the composition, 2.5% to
17% (W/V) of sucrose and/or maltose and optionally one or more saccharides
selected from the group consisted of glucose, fructose, galactose, mannose,
lactose, lactulose, mycose, cellobiose, melibiose, melitose, malto-oligosaccharide,
iso-malto-oligosaccharide and oligo-fructose, dextrim, starch and glycogen,
at pH-value of 4.1-7.2 adjusted with pharmaceutically acceptable acid or
alkali, optionally a pharmaceutically acceptable viscous base, and
optionally an effective amount of anti-fungal and/or an anti-bacterial
agents.
The invention also provides a use of sucrose and/or maltose as active
ingredient in the preparation of pharmaceutical compositions for promoting
the growth of Gram-positive bacilli and increasing the acidity in the
vagina.
The invention also relates to a method for promoting the growth of
Gram-positive bacilli and increasing the acidity in the vagina, comprising
administering to the subject in need of such treatment a therapeutically
effective amount of the pharmaceutical composition according to the present
invention.
The present application further relates to a composition for treating a
patient suffering from vaginitis, a disturbance of the vaginal bacterial
flora or bacterial vaginosis, wherein said vaginitis, disturbance of the
vaginal bacterial flora or bacterial vaginosis are accompanied with a
reduction of the number of Gram-positive bacilli, said composition
comprising:
 | (a) Sucrose and/or maltose in a concentration of from about 2.5% to
about 17% w/v based on the total volume of the composition, |
 | (b) An anti-fungal drug in a concentration of from about 0.0001% to
about 5% w/v based on the total volume of the composition, and |
 | (c) A sufficient amount of a pharmaceutically acceptable acid or
alkali, which results in a pH of the composition from about 4.1 to about
7.2. |
The above-mentioned pharmaceutical composition, use and method of treatment
according to the invention are useful for the reversal of the reduced
numbers of vaginal Gram-positive bacilli, decreased vaginal acidity, as well
as for treating vaginitis and the disturbance of vaginal bacterial flora
accompanied with the reduction in numbers of Gram-positive bacilli,
especially bacterial vaginosis.
DETAILED DESCRIPTION OF THE INVENTION As mentioned above, this invention relates to water-based pharmaceutical
compositions with pH values between 4.1 and 7.2 intended to promote the
growth of Gram-positive bacilli and enhance vaginal acidity, and which
contains 2.5-17% (WIV) of one or more of such saccharides as defined above.
The compositions according to the present invention may contain one or a
mixture of two or several of such saccharides as defined above. Any hexose
used in the invention is of D-type. Starch used in the invention may be
amylose or amylopectin. The preferred saccharides are those having low price
and abundant sources.
According to this invention, the pharmaceutical composition contains a total
content of 2.5-17% (W/V) of saccharides, especially 2.5-16% (W/V),
preferably 8-14% (W/V), more preferably 10-13% (W/V), and most preferably
10-12% (W/V). However, the content of the disaccharides other than sucrose
and maltose mixed with sucrose and/or maltose must not exceed [(17—content
of sucrose and/or maltose) % (W/V)]. The maximum content of hexoses mixed
with sucrose and/or maltose should be less than [0.42×(17—disaccharides
content) % (W/V)].
The weight/volume content (W/V) mentioned in the context of this application
refers to the grams of the specified component in 100 milliliters of the
composition.
The compositions formulated according to the preferred contents of
saccharides are useful for treating the patients with any vaginal illness
states, especially with severe illness (with pH value of vaginal secretion
greater than 5.0, and when the vaginal Gram smear proves that there are few
or no Gram-positive bacilli). The compositions with a content of saccharides
below 8% (W/V) are applicable to the patients suffering from mild diseases
(with a vaginal pH value of greater than 4.6, and the vaginal Gram smear
proves that there are Gram-positive bacilli, but in which the Gram positive
bacilli are fewer in number than the Gram-negative bacilli, Gram-negative
cocci, or Gram-positive cocci).
The pH value of the pharmaceutical compositions of this invention is between
4.1 and 7.2, with the optimum pH value between 4.5 and 6.5. The pH value of
these compositions can be adjusted by adding any pharmaceutically acceptable
acid or alkali, of which the preferred choices are acetic acid, lactic acid,
or sodium hydroxide. The nature and concentration of such acid or alkali can
be readily determined by a person skilled in the art.
According to this invention, the composition may contain a viscous base. One
example of such base is Xanthan Gum with concentration of 1.0-2.2% (W/V),
and preferably of 1.4-2.0% (W/V). Xanthan Gum is able to keep the sugar in
uniform contact with vaginal mucosa and retain the product within the
vaginal vault for a long time due to its high adherence and stability
against changes of temperature and pH values, thus permit the compositions
to promote the growth of Gram-positive bacilli and increasing the production
of acid in vagina.
The composition can also be formulated into hydro-gel form or ointment with
other suitable viscous carrier bases, auxiliaries well known to a person
skilled in the art.
According to this invention, the composition also may not contain viscous
base, it may be administered by means of intravaginal tampon saturated with
the liquid composition. The intravaginal tampon may be composed of cotton
ball, gauze ball, ribbon gauze, etc. In this embodiment, the composition
according to the present invention can also stimulate the growth of
Gram-positive bacilli and increase the acidity in the vagina. The preferred
use of the composition of this invention does requires that the composition
of the invention stay in the vagina for some time before it can stimulate
the growth of Gram-positive bacilli and produce vaginal acidity in the
vagina. Therefore as a lotion without a viscous base, the composition can
not exhibit its therapeutic effect very well.
The saccharide(s) is/are the essential basic active components of the
composition of the invention, and can fulfill the object of this invention
when used with suitable pharmaceutically acceptable carriers. But these
saccharides can produce a better treatment effect if it is combined with
minor amount of amino-acid, vitamin or other similar substances, or yeast
extract rich in amino-acids and vitamins. The vaginal secretion naturally
contains sufficient amino-acids and vitamins. Such amino-acids or vitamins
are not available in conventional in vitro experiments and should be added
when in vitro experiments are carried out for the composition of the
invention.
Sucrose and/or maltose promote the growth of vaginal Gram-positive bacilli
and increase vaginal acidity, which would inhibit abnormal vaginal bacterial
flora except Gram-positive bacilli. In this way the reduced vaginal
Gram-positive bacilli and the disturbance of vaginal flora, vaginitis, or
bacterial vaginosis could be cured.
However, the inventor noticed further that in seldom cases Candida coexisted
with abnormal vaginal bacterial flora or even BV flora. Although increased
vaginal Gram-positive bacilli and vaginal acidity did inhibit abnormal
vaginal bacterial flora, it didn't inhibit Candida. Candida might grow
better in vagina as a result of inhibition of abnormal vaginal bacterial
flora. In order to treat such cases of reduced vaginal Gram-positive bacilli
or disturbance of vaginal flora or vaginits or bacterial vaginosis, the
inventor conducted further studies and this new composition comprising
sucrose and/or maltose and anti-fungi drugs was invented. As the anti-fungi
drugs may also be effective against bacteria, the preferred content of
anti-fungi drug in this invented composition is in low concentration so to
avoid inhibiting Gram-positive bacilli. Compared with some anti-fungi creams
available in market whose anti-fungi drugs concentration may be as high as
100 to 1000 times the drug's MIC against Candidal strains, in this invented
composition the content of anti-fungi drug may be as low as 0.1˜10 times the
drug's MIC.
The present application further relates to a composition for treating a
patient suffering from vaginitis, a disturbance of the vaginal bacterial
flora or bacterial vaginosis, wherein said vaginitis, disturbance of the
vaginal bacterial flora or bacterial vaginosis are accompanied with a
reduction of the number of Gram-positive bacilli, said composition
comprising:
 | (a) Sucrose and/or maltose in a concentration of from about 2.5% to
about 17% w/v based on the total volume of the composition, |
 | (b) Anti-fungi drug in a concentration of from about 0.0001% to about
5% w/v based on the total volume of the composition, and |
 | (c) A sufficient amount of a pharmaceutically acceptable acid or
alkali, which results in a pH of the composition from about 4.1 to about
7.2. |
The above mentioned composition may further comprise one or more saccharides
from the group consisting of glucose, fructose, galactose, mannose, lactose,
lactulose, mycose, cellobiose, melibiose, melitose, malto-oligosaccaride,
iso-malto-oligosaccharide and oligo-fructose, dextrin, starch and glycogen.
Preferably, the content of sucrose and/or maltose in said composition is
from about 8% to about 14% w/v, the content of anti-fungi drug in said
composition is from about 0.001% to about 0.5% w/v. More preferably, the
content of anti-fungi drug in said composition is in the range of 0.1 to 10
times of the drug's MIC against Candidal strains.
The anti-fungi drug in the above mentioned composition is selected from the
following group: Fluconazole, Terconazole, Tioconazole, Butoconazole,
Ketoconazole, Itraconazole, Econazole, Miconazole, and Cannitracin.
Preferably, the antifungi drug is selected from Fluconazole, Terconazole,
and Tioconazole.
Said composition may be in the form of hydro-gel or ointment, or in the form
of liquid for preparing intravaginal tampon. Preferably, the composition is
in the form of hydro-gel or ointment, said composition further comprises
pharmaceutically acceptable viscous base, preferably, said pharmaceutically
acceptable viscous base is Xanthan gum.
The present application also relates to a method for treating a patient
suffering from vaginitis, a disturbance of the vaginal bacterial flora or
bacterial vaginosis, wherein said vaginitis, disturbance of the vaginal
bacterial flora or bacterial vaginosis are accompanied with a reduction of
the number of Gram-positive bacilli, said method comprising vaginally
administering to a subject in need of such treatment a therapeutically
effective amount of a composition comprising:
 | (a) Sucrose and/or maltose in a concentration of from about 2.5% to
about 17% w/v based on the total volume of the composition, |
 | (b)Anti-fungi drug in a concentration of from about 0.0001% to about
5% w/v based on the total volume of the composition, and |
 | (c) A sufficient amount of a pharmaceutically acceptable acid or
alkali, which results in a pH of the composition from about 4.1 to about
7.2; |
 | wherein said administration promotes selective growth of gram-positive
bacilli in the vagina of said subject. |
The present application further relates to a method for treating a patient
suffering from vaginitis, a disturbance of the vaginal bacterial flora or
bacterial vaginosis, wherein said vaginitis, disturbance of the vaginal
bacterial flora or bacterial vaginosis are accompanied with a reduction of
the number of Gram-positive bacilli, said method comprising, simultaneously
or sequentially, vaginally administering to a subject in need of such
treatment a therapeutically effective amount of a composition (A) and
composition (B),
 | Composition (A) comprising:
 | a) Sucrose and/or maltose in a concentration of from about 2.5% to
about 17% w/v based on the total volume of the composition, and |
 | b) A sufficient amount of a pharmaceutically acceptable acid or
alkali, which results in a pH of the composition from about 4.1 to about
7.2; |
|
 | Composition (B) comprising:
 | (a) Anti-fungi drug in a concentration of from about 0.0001% to
about 5% w/v based on the total volume of the composition, and |
 | (b) A sufficient amount of a pharmaceutically acceptable acid or
alkali, which results in a pH of the composition from about 4.1 to about
7.2. |
|
Preferably, composition (A) and composition (B) are vaginally administered
to a subject in need of such treatment simultaneously a therapeutically
effective amount of a composition (A) and composition (B).
The composition of the invention may also contain one or more anti-bacterial
agents that can suppress or kill Gram-negative bacteria but exert no effect
or only exert slight effect on Gram-positive bacilli. In this embodiment,
the composition of the invention may have an increased efficacy for treating
vaginal infection or inflammation. Such anti-bacterial agents may include,
but are not limited to polymyxin, metronidazole or aztreonam.
The composition of the invention can be prepared according to the processes
known to those skilled in the art.
If the saccharides used include little or no starch, such saccharide should
be mixed with viscous auxiliary substances homogeneously, and then distilled
water is added into the mixture, which are then stirred to dissolve the
saccharide and swell the viscous auxiliary substances until a homogeneous
viscous gel is formed. If starch is included, it is sufficient to heat
directly the mixture of saccharides and water to form a paste. In the latter
case, viscous auxiliary substances may be added or not. For adjusting the pH
to a predetermined value, lactic acid or sodium hydroxide solution is added
prior to sterilization treatment. Alternatively, sterilization treatment is
performed first, followed by adjustment of pH. For sterilization,
intermittent sterilization may be used, with the detailed steps described as
follows: sterilizing at 80° C. for 30 minutes, keeping at 36° C. for 8-12
hours, sterilizing at 80° C. for 30 minutes, keeping at 36° C. for 8-12
hours and finally sterilizing at 80° C. for 30 minutes. Alternatively, a
high-pressure sterilization may be performed for 15-20 minutes at 116° C. A
solution of saccharides may also be sterilized by filtering the solution.
Then the sterilized saccharide solution may be added to a viscous base in
the form of hydro-gel that has been sterilized at high pressure.
The composition of the invention also may be made into a solution by
dissolving the saccharides in water. The solution can be administered to a
patient by means of an intravaginal tampon soaked in it.
The composition of this invention uses sugar substances as active
ingredients, and has good stability during storage, but preferably it is
stored under refrigeration or in cool place. The near neutral pH value of
the composition is also helpful in stabilizing the sugar components.
The present invention also relates to the use of one or more of such
saccharides as defined above as active ingredients in the preparation of a
medicament for promoting the growth of Gram-positive bacilli and increasing
the acidity in the vagina. This invention uses D-type hexose, either amylose
or amylopectin.
The medicament prepared according to the use of the invention can be used
for promoting the growth of Gram-positive bacilli and increasing the acidity
in the vagina, and reversing decreased numbers of Gram-positive bacilli,
diminished vaginal acidity (pH value above 4.6) as well as treating
vaginitis and the disturbance of vaginal bacterial flora accompanied with
the reduction of Gram-positive bacilli, especially bacterial vaginosis.
The experiments in vitro and in vivo have proven that the composition of the
invention can strongly stimulate the growth of Gram-positive bacilli and
increase the acidity in the vagina, and can be used for the reversal of the
reduction of Gram-positive bacilli, diminished vaginal acidity and treatment
of vaginitis and the disturbance of vaginal bacterial flora accompanied with
reduction of Gram-positive bacilli, especially bacterial vaginosis.
Therefore, this invention also relates to a method for promoting the growth
of Gram-positive bacilli and increasing vaginal acidity, reversing the
reduction of Gram-positive bacilli, increasing vaginal acidity and treatment
of vaginitis and the disturbance of vaginal bacterial flora that accompanied
with reduction of Gram-positive bacilli, especially bacterial vaginosis,
wherein the subject in need of such treatment is given a medically-effective
amount of the pharmaceutical composition according to the invention.
The administration method of the composition is to administer the
composition locally inside the vagina. The composition of the invention
containing a tissue viscous base or other carriers may be applied directly
to the lumen of the vagina. If the composition of the invention is in the
form of a solution, an intravaginal tampon is soaked in the solution, then
the tampon is placed inside the vagina.
For the composition and method of treatment according to the invention, the
medicament is administered according to the following dosage. For the
composition of this invention containing 8-14% (W/V) of saccharides as
active ingredients, such composition is applied inside the vagina 1-3 times
daily in doses of 1-5 ml, with the total sugar amount controlled to 0.08-2.1
grams daily dosage, generally applied before sleep at night or after arising
in the morning, with an additional dose applied at noon for a few patients.
For the patients suffering from severely abnormal vaginal bacterial flora
and with the pH value of the vaginal secretion greater than 5.0, and if the
vaginal Gram smear shows few or no Gram-positive bacilli, more extensive
treatment is required with the sugar amount above 0.8 grams daily. For the
patients having less severe disease with the pH value of vaginal secretion
between 5.0 and 4.6, or if the vaginal Gram smear reveals Gram-positive
bacilli, but in lesser abundance than that of any of Gram-negative bacilli,
Gram-negative cocci, or Gram-positive cocci, a smaller dosage is used and
the total sugar amount is limited to 0.8 grams or less.
During treatment with this composition, clinical symptoms may be observed
daily and the vaginal pH value checked for change. Moreover, the vaginal
Gram smear may be performed in order to check the change of bacterial flora
and adjust the treatment accordingly if necessary. Generally, the
composition of this invention can produce remarkable therapeutic effects 1-3
days after beginning of use, with symptoms improved significantly even
disappearing, and pH values in the vagina reduced to normal levels and the
Gram-positive bacilli in the vagina restored to dominance in the vaginal
bacterial flora, at which time therapy with the composition should be
stopped or the dosage be reduced, or the treatment continued at a low
maintenance dosage.
For the method of this invention, the patients are provided with the
composition containing only the saccharides of this invention as active
ingredients, or the composition containing the saccharides, anti-fungal
agent and/or anti-bacterial agent. Alternatively, the composition containing
the saccharides of this invention as its active ingredients is administered
in conjunction with suitable anti-fungal agent or anti-bacterial agent. For
the latter case, the composition of this invention can be administered
simultaneously with the anti-fungal and/or anti-bacterial agent or
before/after the administration of the anti-fungal and/or anti-bacterial
agent.
After the administration of this composition, the clinical symptoms of
patients can be alleviated quickly, the numbers of Gram-positive bacilli are
increased in the vagina, vaginal acidity is raised with the pH value reduced
to 4.0-4.6, while the Gram-negative bacilli, Gram-negative cocci and other
harmful abnormal bacteria are reduced substantially or even disappear. The
composition of this invention is easy to prepare and to use with reliable
effects.
Claim 1 of 19 Claims
1. A method for treating a patient suffering from vaginitis, a disturbance
of the vaginal bacterial flora or bacterial vaginosis, wherein said
vaginitis, disturbance of the vaginal bacterial flora or bacterial
vaginosis are accompanied with a reduction of the number of Gram-positive
bacilli, said method comprising vaginally administering to a subject in
need of such treatment a therapeutically effective amount of a composition
comprising:
a) sucrose and/or maltose in a concentration of from about 2.5% to about
17% w/v based on the total volume of the composition,
b) anti-fungal drug in a concentration of from about 0.0001% to about 5%
w/v based on the total volume of the composition, and
c) a sufficient amount of a pharmaceutically acceptable acid or alkali,
which results in a pH of the composition from about 4.1 to about 7.2;
wherein said administration promotes selective growth of gram-positive
bacilli in the vagina of said subject.
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