AU2002346897A1 - Low concentration of peroxide for treating or preventing vaginal infections - Google Patents
Low concentration of peroxide for treating or preventing vaginal infectionsInfo
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Description
LOW CONCENTRATION OF PEROXIDE FOR TREATING OR PREVENTING VAGINAL INFECTIONS
CROSS-REFERENCE TO RELATED APPLICATION This application claims the benefit of U.S. Provisional Application No.
60/330,683, filed October 29, 2001, the content of which is expressly incorporated herein by reference thereto.
FIELD OF THE INVENTION This invention relates to a pharmaceutical composition for treating or preventing vaginal infections. The pharmaceutical composition generally comprises a synergistic mix of a bioadhesive, extended release foπnulation that releases and maintains a very low concentration of peroxide over an extended period of time to provide benefits of oxygen release, while decreasing pH decrease over time, but without excessive peroxide concentrations. The invention also relates to a method of treating vaginal infections using the pharmaceutical composition disclosed herein.
BACKGROUND OF THE INVENTION
Vaginal infections are a common problem among women. Bacterial Vaginosis (BV) is the most common form of infectious vaginitis, accounting for 45% of symptomatic cases and estimated to be present in 15% of asymptomatic sexually active women. See Breeπ, J. ed., The Gynecologist and the Older Patient, pp. 304-305 (1988). It is a polymicrobial vaginal infection believed to be caused by an increase in the number of anaerobic organisms with a concomitant decrease in lactobacilli in the vagina. The decrease in the number of lactobacilli in the vagina has a dual effect, i.e., (i) a decreased competition for nutrients, and (ii) a decrease in the amount of lactic acid present, thus allowing for the multiplication of opportunistic pathogens in the vagina, whose growth is normally suppressed by the lactobacilli. The principal pathogens associated with BV are believed to be Gardnerella vaginalis and anaerobes of the Mobilαήcus species. However, numerous other pathogenic anaerobes are also believed to be involved in the etiology of vaginosis. See Kaufman et al., Benign Diseases of the Vulva and Vagina, 3rd ed., pp.401- 418 (1989). Thus, BV is considered a broad spectrum infection requiring a broad spectrum treatment.
In the United States discharge and foul smelling odor resulting from BV results in millions of women going to a physician's office each year in search of relief. An even larger number, estimated to be 30% of all adult American women, use douches that they purchase without a prescription. The idea of washing out the foul smelling discharge with an acid douche has a simplistic appeal. Medically, douching is frowned upon as studies have reported an association between douching and PID (Pelvic Inflammatory Disease), ectopic pregnancy, tubal infertility or reduced fertility. Furthermore, douching is unfavorable due to the fact that it also washes out normal and beneficial bacterial flora, leaving an environment prone to reoccurring BV. The most troublesome aspect of BV is its impact upon the quality oTfetal implantation and its potential to induce premature labor. The prevalence of BV in pregnant women has been reported to be 13 to 31%. BV during pregnancy is associated with increased risk of late miscarriage, pre-term labor, postpartum endometritis and low birth weight infants. In a recent study it was shown that BV is associated with an increased risk of miscarriage in the first trimester in women undergoing in-vitro fertilization..
U.S. Application No.09/748,753 discloses compositions useful in preventing miscarriage and premature labor associated with bacterial vaginosis by buffering the vaginal pH. The composition disclosed in the application comprises a therapeuticaily- effective amount of an aqueous pH-buffering bioadhesive water-insoluble, but water- swellable cross-linked polycarboxylic acid polymer, which provides the therapeutic effect without needing any additional treating agent, by itself buffering the vaginal pH to a normal, acidic pH, hostile to the infectant
Clinically, BV presents itself as a superficial vaginal infection with few irritative symptoms and no inflammatory response. Some noticeable symptoms include an unpleasant smell, an elevated vaginal pH greater than about 5.0, a thin homogeneous discharge, the presence of Gardnerella clue cells and a high succinate/lactate ratio (not less than 0.4). See, e.s., LivengθQd et ύ., "Bacterial Vaginosis: Diagnostic and Pathogenic findings during Topical Clindamycin Therapy " Am. J. Obstet GynecoL, Vol. 163, No. 2, p. 515 (August 1990). It is believed mat the composition of organic acids in the vagina shifts from primarily lactic acid (pKa=3.86) to succinic acid (pKftι=4.27, pK,2=5.64) as a result of the decrease in lactobacilli, which produce lactic acid, and a rise in Mobiluncus, which produce succinic acid. This shift in acid composition tends to raise the vaginal pH. It is unclear
whether the change in acidity is a cause or effect of the infectioa However, it is known that certain undesirable anaerobes grow better at a higher pH than is normally present in the vagina. It is thus believed that lowering the vaginal pH to a normal healthy level is an effective measure against symptoms of the infection, if not the infection itself. Moreover, the odor of the amines which are produced in the vagina during
BV is known to increase at higher pH's because unprotonated, volatile amines are more prevalent at higher pH — as the environment becomes more basic. Additionally, the higher pH level is thought to allow the undesirable anaerobes to grow and produce the odor- causing amines that are associated with a bacterial vaginosis infection. — , U. . Patent No, 6,017,521 (the "521 patent") discloses a method of-treatiπg
BV by topically contacting the lurnmal surface of vaginal epithelial cells with an effective pΞ buffering amount of an aqueous composition comprising water and an effective amount αf a water-swellable, but water-insoluble, cross-linked pH buffering bioadhesive polymer wherein at least 80% of the monomers comprising said polymer contain at least one carboxyl group. The composition is kept in contact with the vaginal cells for a time period sufficient to lower the pH of the vagina to an acidic pH. The composition taught by the '521 patent is free of any treating agents.
The exact role ofH202-producing lactobacilli is at best unclear. This may be the result of several factors the most important of which is concentration. Being able to detect H2O2-producing lactobacilli does not mean they are present in sufficient concentration to oxygenize the vagina and make the environment hostile to anaerobes. The solution many investigators have proposed is to add H2Orproducing lactobacilli to the vagina in high concentration as a means of eh inating the infection. The technical difficulties involved in such a project have prevented any investigator from developing a truly viable therapy.
Other attempts have heen made to put H2O2 into a vaginal acidifier. However, those attempts have failed for two reasons. First, H2O2 is unstable in a gel and cannot be stored commercially. Second, the Hjθ2 concentration, which tends to be released quickly all at once, causing a "burst effect," not only obliterates the anaerobes, but also sterilizes the vagina making women more susceptible to reoccurring vaginal infections.
Such a treatment is disclosed in U.S. Pat. No. 5,741,525, (the "'525 patent"). The '525 patent discloses methods for ma taining or enhancing the normal protective function of vaginal flora by administering a therapeutically effective amount of a
composition that has hydrogen peroxide in an amount of about 0.1% to about 3.0%. The '525 patent teaches that peroxide "amounts below about 0.1% have been found to be unsuitable to have any meaningful inhibitory effect on a wide variety of microorganisms." (The '525 patent at column 5, lines 57-59). The concentrations of hydrogen peroxide taught by the '525 patent to be useful in treating BV, however, are often detrimental to the growth of beneficial bacterial and can cause severe vaginal irritation and even vaginal peroxide bums. Furthermore, the treatment simply supplies a sudden burst of peroxide, killing a substantial number of bacteria and leaving it to chance as to whether a beneficial bacterial flora will recolonize or there will be a reoccurrence of BV. Thus, there exists a need for an effective pharmaceutical composition jbj - treating vaginal infections such as BV that does not have a "burst effect" causing vaginal irritation and excessively inhibiting or destroying beneficial bacterial flora. Furthermore, there is a need for a pharmaceutical composition that treats BV without sterilizing or significantly killing the normally-desired local vaginal flora the vagina and leaving it susceptible to reoccurring BV. There is also a need for a pharmaceutical composition that is simple to use and still effectively achieves a balance between inhibiting undesirable microorganisms, while providing a favorable environment for desirable local flora. The present invention successfully addresses these needs as detailed below.
SUMMARY OF THE INVENTION "
The invention relates to a pharmaceutical composition for treating or preventing vaginal infections. The pharmaceutical composition includes a synergistic mix of a peroxide source and a bioadhesive, extended release polymer formulation, h one I embodiment of the invention, the synergistic mix is designed to release peroxide over a period of time, which is usually at least 12 hours and often more than 48 hours. In a further embodiment of the invention the synergistic mix releases peroxide in an amount less than 0.1% by weight per hour. In an additional embodiment of the invention the synergistic mix includes less than 0.1% by weight of peroxide. The peroxide released in each of these embodiments is in an amount sufficient to therapeutically increase oxygen concentration, while the extended release polymer reduces the pH, thereby sufficiently suppressin the growth of anaerobic organisms responsible for BV without also sterilizing the vagina or significantly killing the normally-desired local vaginal flora. So long as the anaerobic
organisms are not permitted to dominate the environment, BV should be prevented or treated.
The bioadhesive, extended release polymer formulation preferably includes a bioadhesive, water-swellable, water-insoluble, cross-linked polycarboxylic polymer. A non-limiting example of such a polymer is polycarbophil.
In one preferred embodiment, the synergistic mix includes carbamide peroxide as the peroxide source mixed with polycarbophil as the polymer.
The invention further relates to a method of treating or preventing a vaginal infection. The composition is vaginally administering to a subject in need of such treatment a therapeutically effective amount of the pharmaceutical vaginal compositions taught herein, without substantially adversely.affecting the normally-desired local flora,
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The present invention is based on the use of unexpectedly low concentrations of peroxide over an extended period of time to provide a beneficial effect by treating or preventing vaginal infections without the peroxide sterilizing the vagina, or significantly killing normally-desired local vaginal flora, or causing significant irritation of the sensitive tissues of the vagina,
I The phrase "normally-desired local vaginal flora" means bacteria which normally reside in the vagina of a healthy female. Normal flora include, for example the lactic acid family of bacteria in human subjects, such as, Tissier's bacillus. Microbes which constitute normal flora are well known ( e,g., see Principles and Practice of Infectious Diseases, 3rd EcL, 1990, G. Mandell et al., ed., Churchill Livingstone Inc. New York). The phrase "significantly killing" as used herein means substantially sterilizing die vagina of beneficial bacteria normally found in a healthy vaginal environment, wherein there is not a sufficient number of normally-desired local vaginal flora present and necessary to recolonize the vagina safely upon completion of the treatment regime.
In addition, the term "vaginal infection" includes any type of microorganism infecting the vagina of a patient which is not a normally-desired local vaginal flora, such as a bacterial or yeast infection, but specifically includes BV.
The term "peroxide source" as used herein is a compound fro which peroxide can be released. To illustrate the meaning of peroxide source in contrast to
peroxide, the following example is provided. If 0.1% to 0.25% by weight carbamide peroxide (peroxide source) is used in a pharmaceutical vaginal composition, the amount of peroxide, upon discounting the carbamide portion, would be about 0.034 to 0.085% by weight peroxide. The term "dose" or "dosage form" as used in the specification and claims means a physically discrete amount of the pharmaceutical composition suitable for use as dosages by human female subjects. Each dose contains a pre eteπnined quantity of peroxide source calculated to produce the desired therapeutic effect in association with the required pharmaceutical vehicle. The quantity of composition of peroxide in a dose, of course may be varied to provide release of peroxide in various concentrations or various quantities over different periods of time.
One embodiment of the present invention is a pharmaceutical vaginal composition useful in treatmg vaginal infections, especially BV. The composition typically comprises a synergistic mix of a bioadhesive, extended release formulation that contains a peroxide. The peroxide is released in an amount sufficient to therapeutically increase oxygen concentration while the extended release polymer also decreases the pH, allowing effective treatment or prevention of BV without sterilizing the vagina or substantially killing the normally-desired local vaginal flora.
In a particular embodiment, the vaginal composition is designed to release peroxide over a period of at least 12 hours, preferably over a period of at least 24 hours and even more preferably at least 48 hours. Other formulations of the composition are designed to release the peroxide over a period of at least 72 hours and at least 96 hours. The greater the period of time covered by one dose the less frequent dosing would be needed if sequential doses are desired. In a further non-limiting embodiment, the vaginal composition includes a synergistic mix that releases peroxide in an amount of less than 0.1% peroxide per hour. Preferably, the peroxide is released in an amount of less than 0.085% peroxide per hour. The compositions disclosed herein, which release low levels of peroxide, are surprisingly effective at treating and preventing vaginal infection without the negative effects of higher concentrations.
Some women lack a natural flora of peroxide-producing lactobacillus. In these women, the formulations disclosed herein are used to substitute for the function of
these organisms, and to provide a more favorable environment for the other normally- desired local vaginal flora.
In an alternative embodiment of the invention, the pharmaceutical vaginal composition includes less man 0.1% peroxide in the composition to be administered to the patient In this embodiment, the amount of peroxide being released over time is extremely low, while still being sufficient to treat or prevent vaginal infections.
The peroxide source may be selected from a variety of sources, both organic and inorganic. Typical forms of peroxide sources are those used for treating mucosa and related epithelial tissue, and particularly those used in dental bleaching application. Preferably the peroxide source is one of the following forms: hydrogen peroxide including its complexes (e.g., carbamide peroxide); alkyl peroxides (e.g., di t-butyl peroxide); benzyl peroxides (e.g., benzoyl peroxide); peroxyacids (e.g., m-chloroperbenzoic acid, peroxodisulfuric acid and its salts, peroxomonosulfuric acid and its salts); peroxyacid esters (e.g., t-butyl perbenzoate) dialkynitroxides (e.g., di t-butyl nitroxide). Preferred peroxide sources include carbamide peroxide, alkyl peroxides, benzyl peroxides or dialkynitroxides. Most preferably, however, the peroxide source is carbamide peroxide.
The preferred bioadhesive polymeric system of the invention has the advantage of being capable of being held in the vagina, and providing extended release of peroxide, for relatively lqng periods of time, i.e., 48 to 72 hours or more and providing pH buffering in the normal physiologic range. In contrast most drug delivery systems are sloughed off the vaginal walls in less than four hours. The polymer holds the peroxide source and slowly releases it over time. The preferred bioadhesive carrier includes a bioadhesive, water-swellable, water-insoluble, cross-linked polycarboxylic polymer. A particularly preferred bioadhesive, which may be in a gel formulation, contains a polycarbophil base designed to give controlled, extended release of peroxide over time.
The composition typically releases the peroxide over a period of at least 12 hours and preferably over a period of at least 24 hours. More preferably however the peroxide is released over a period of at least 48 hours and sometimes even more than 72 hours. Similar extended release formulations, albeit with other treating agents, are described in U.S. Patent Nos. 5,543,150 and 6,126,959, the contents of which are each expressly incorporated herein by reference.
The specific peroxide delivery formulation chosen preferably includes a bioadhesive, water-insoluble, water-swellable, cross-linked polycarboxylic acid polymer formulation. An example of such a formulation in general is described in U.S. Patent No. 4,615,697 (the "'697 patent"), the content of which is expressly incorporated herein by reference thereto. Typically, at least about 80% of the monomers of the polymer in such a formulation should contain at least one carboxyl functionality. The cross-linking agent should be present at such an amount as to provide enough bioadhesion to allow the system to remain attached to the target epithelial surfaces for a sufficient time to allow the desired dosing to take place. For vaginal administration, the formulation preferably remains attachedjo the epithelial surfaces for a period of about 24 to 48 hours or more. Such results may be measured clinically over various periods of time, by testing samples from the vagina for pH reduction due to the continued presence of the polymer. This level of bioadhesion is generally attained when the cross-linking agent is present at about 0.1 to 6 weight percent of the polymer, preferably about 1 to 2 weight percent Bioadhesion can also be measured using commercially available surface tensiometers utilized to measure adhesive strength. The polymer formulation can be adjusted to control the release rate of the peroxide, by varying the amount of cross-linking agent in the polymer. Suitable cross- linking agents include divinyl glycol, divinylbenzene, N,N-diallylacrylamide, 3,4- dihydroxy-1 ,5-hexadiene, 2,5-dimethyl-l ,5-hexadiene, and similar agents.
A preferred polymer for use in such a formulation is polycarbophil, U.S.P., which is commercially available from Noveon, Inc., of Cleveland, Ohio under the trade name NOVEON®-AAl. Polycarbophil is a polyacrylic acid cross-linked with divinyl glycol. Other useful bioadhesive polymers that may be used in such a drug delivery system foπnulation are mentioned in the '697 patent. For example, these include polyacrylic acid polymers cross-linked with 3,4-dihydroxy-l,5-hexadiene, and polymethacrylic acid polymers cross-linked with divinyl benzene.
Typically, these polymers would not be used in their salt form, because this would significantly decrease their bioadhesive capability. Divalent salts, such as calcium salts, pose the greatest decrease in bioadhesion. Monovalent salts, such as sodium salts, do not tend to reduce bioadhesion as much.
Such bioadhesive polymers may be prepared by conventional free radical polymerization techniques utilizing initiators such as benzoyl peroxide, azobisisobutyronitrile, and the like. Exemplary preparations of useful bioadhesives are provided in the '697 patent The bioadhesive formulation may be in the form of a gel cream, tablet, pill, capsule, suppository, film, or any other pharmaceutically acceptable form that adheres to the mucosa and does not wash away easily. The preferred formulation for the present invention is in the form of a gel.
Additives such as those taught in the '697 patent may be mixed in with the cross-linked polymer in the foπnulation for maximum desired efficacy of the delivery system or for the comfort of the patient. Such additives, for example and without hmitation, include lubricants, plasticizing agents, preservatives, gel formers, tablet formers, pill formers, suppository formers, film formers, cream formers, disintegrating agents, coatings, binders, vehicles, coloring agents, taste and/or odor controlling agents, humectants, viscosity controlling agents, pH-adjusting agents, and similar agents.
Advantageously, the peroxide may be delivered, and the vaginal pH can be reduced, for an extended period of time by utilizing the bioadhesive polycarbophil. Polycarbophil is a polymer lightly cross-linked with divinyl glycol. Polycarbophil is also a weak poly-acid containing multiple carboxyl radicals, which are the source of its negative charges. These acid radicals peπnit hydrogen bonding witii the cell surface. Hydrogen bonds are weak, but in the case of polycarbophil they are numerous and therefore, tenacious. Polycarbophil is a water insoluble polymer and stays attached to the vaginal epithelial cells until they turnover, normally up to 3 to 5 days. Since polycarbophil is a weak poly-acid with an exceedingly high buffering capacity, it maintains the vaginal pH in the physiologic range, under 5, and thus, helps protect against infection. The effect has been shown to persist for more than 96 hours. Polycarbophil has a pKa of 4.3 and as with all good buffers it will adjust the environment close to its pKa.
The polymer described in the '697 patent may be adjusted to control the release rate of the peroxide, e.g., by varying the amount of cross-linking agent. Generally, the release rate of the peroxide source in the formulation is continuously about zero order release, relative to the amount of peroxide source present after a small burst of release initially. Accordingly, the composition would readily be formulated by one of skill in the
art softat the duration and release rate are adjusted to deliver an appropriate amount of peroxide. A typical composition of the polymer stays in place typically for about 48 hours.
A nonlimiting example of a suitable formulation for vaginal delivery of peroxide comprises polycarbophil, carbomer, Natrαsol® 250 HHX, glycerol, sorbic acid, methyl hydroxybenzoate, and purified water mixed with a peroxide source, preferably carbamide peroxide or benzoyl peroxide.
Sorbic acid and methyl hydroxybenzoate are preservatives, which maybe substituted by other known preservatives, such as benzoic acid, propylparaben, or propionic acid. - ,
Carbomer is a gel former, preferably Carbopol 974P, but may be substituted by other gel formers including, but not limited to Carbopol 934P, Carbopol 980, methyl' cellulose or ropyl cellulose.
Natrosol® 250 HHX is a viscosity enhancing agent which may be substitued by other known viscosity enhancing agents, such as methyl cellulose or propyl cellulose. Natrosol® 250 HHX is commercially available from Hercules, Inc., located in ihnington, Delaware.
Glycerol is a humectant alternative humectants include, for example, propylene glycol and dipropylene glycol.
As will be apparent to those skilled in the art, the composition can be varied to affect certain properties. For example, the concentration of the bioadhesive polymer can be adjusted to provide greater or lesser bioadhesion. The viscosity can be varied by varying the pH or by changing the concentration of the polymer or gel former. The pH also can be varied as appropriate to affect the release rate or bioadhesiveness of the formulation. All ingredients are well known and readily available from supplier known in the industry.
In a preferred embodiment die invention includes a vaginal composition which includes a polycarbophil and carbamide peroxide in a synergistic mix formulated to release peroxide over at least 24 hours.
Preferred percentage of peroxide source included in the pharmaceutical composition ia typically between 0.01% and 15%, but more preferable between 0.1% and 10% and most preferably between 0.25% and 7%.
Generally, the peroxide source present in a dosage amount of pharmaceutical vaginal composition, wherein the dosage amount is between 0.5 g and 2.5 g, and the peroxide source is in an amount of about 0.01 mg and 500 mg. It is preferred, however, if
the peroxide source is present in the composition in an amount of between about 0.1 mg to 75 mg and more preferably in amount of 1 mg to 50 mg.
The amount of peroxide in the formulation is typically between 0.0035 mg to 350 mg. Preferably, however, the formulations usually contain between 0.01 rag to 100 mg i and more preferably between 0.1 mg and 75 mg peroxide.
The present invention further relates to a method of treating or preventing a vaginal infection in a subject The method involves inserting vaginally a synergistic mix of i a bioadhesive, extended release formulation that releases and maintains alow concentration of peroxide. ) The method can be used to mamtain normal vaginal floral activity. For " example, if a patient is pregnant, and especially if they are susceptible to miscarriage, the' l dosage amount of the pharmaceutical compositions described herein may be administered to the patient to treat or prevent BV. As discussed above, BV during pregnancy has an impact upon the quality of fetal implantation and its potential to induce premature labor. 5 The present invention is useful in preventing or treating BV in pregnant women or women attempting to become pregnant, and therefore reducing the risk of miscarriage and low birth
I weights of infants.
I The compositions described l herein may be administered to a patient by introducing it into the vaginal cavity by use of conventional applicators as known in the art,
0 such as (without limitation) plunger, douche, and manually. One method of delivery is to use a device similar to those described in U.S. Design Patents Nos. D345,211 and
D375,352. These devices are oblong hollow tube containers, with one end capable of being opened and the other end containing most of the composition to be delivered in a sealed container that may be used relatively easily by the patient The containers also maintain
!5 the foπnulation and treating agent in a sealed, sterile environment until used. Upon use, such a container is opened and the open end is inserted into the vagina, while the other end is squeezed to deliver the contents of the container into the vagina, such as tampon
, injectables or other coating or impregnating means. A Tαtf of the product can therefore contain a single dose or multiple doses of the product. 0 The quantity of pharmaceutical vaginal composition contained in a dose is generally at least about 0.5 g, and is not more than about 3 g. A typical and presently preferred dose is in a gel vehicle in the range of about 0.75 g to about 2 g and most preferably about l to 1.5 g per dose.
Advantageously, the dose may be formulated so that it may be taken as often as twice or more a day, or as infrequently as once or less per week. Preferably the dose is formulated so that the dose is taken only once a day and more preferably bi-weekly or even wecMy.
EXAMPLES
The following examples are illustrative of preferred formulations of the invention. All percentages are based on the percent by weight of the foπnulation prepared αnless otherwise indicated and all totals equal 100% by weight The peroxide sources used for illustrative purposes in these examples were carbamide peroxide and benzoyLpetoxide, but as explained above, several different peroxide sources can be used.
CARBAMIDE PEROXIDE ALTERNATE FORMULATIONS
Carbamide Peroxide 0.10% 0.10% 0.25% 1.00% 0.25% Polycarbophil USP 1 2.00% 2.00% 2.00% 2.00% • 1.00% Carbopol 974P j 1.00% 1.00% 1.00% 1.00% Natw>sot,250HHX 2.00%
GlyceiolUSP/BP 12.90% 15.00% 12.90% 12.90% 12.90%
Sorbic acid NREP 0.08% 0.80% 0.08% 0.08% 0.08%
Methyl Hydroxybenzoate NF, EP 0.18% 0.18% 0.18% 0.18% 0.18%
Purified water USP/EP 83.74% 80.92% 83.59% 82.84% 83.59%
Total 100% 100% 100% 100% 100%
CARBAMIDE PEROXIDE ALTERNATE FORMULATIONS
Carbamide Peroxide 0.25% 5.00% 5.00% 10.00% 14.00%
Polycarbophil TJSP 1.00% 2.00% 1.00% 2.00% 2.00%
Carbopol 974P - 1.00% - 1.00% 1.00%
Natrosol* 250 HHX 2.00% . 2.00% - -
Glycerol USP/BP , 14.00% 12.90% 12.90% 12J0% 12.90%
Sorbic acid NF/EP 0.08% 0.08% 0.08% 0.08% 0.08%
Methyl Hydroxybenzoate NF, EP 0.18% 0.18% 0.18% 0.18% 0.18%
Purified water USP/EP 82.49% 78.84% 78.84% 73.84% 69.84%
Total 100% 100% 100% 100% 100%
BENZOYL PEROXIDE ALTERNATE FORMULATIONS
Benzoyi Peroxide 1 0.20% 0.20% 0.50% 0.50% 0.50%
Polycarbophil USP | 2.00% 2.00% 2.00% 1.00% 1.00%
Carbopol 974P 1.00% 1.00% 1.00% - -
Natrosol* 250 HHX - • 2.00% 2.00%
Glycerol USPBP 12.90% 15.00% 12.90% 12.90% 14.00%
Sorbic acid NF EP 0.08% 0.80% 0.08% 0.08% 0.08%
Methyl Hydroxybenzoate NF, EP 0.18% 0.18% 0.18% 0.18% 0.18%
Purified water USP/EP 83.64% 80.82% 83.34% 83.34% 82.24%
Total 100% 100% 100% 100% 100%
BENZOYL PEROXIDE ALTERNATE FORMULATIONS
Benzoyi Peroxide 1.00% 5.00% 5.00% 10.00% 14.00%
Porycarbopha USP 2.00% 2.00% 1.00% 2.00% 2.00%
Carbopol 974P 1.00% 1.00% - 1.00% 1.00%
Natrosol" 250 HHX . 2.00% - -
Glycerol USP/BP 12.90% 12.90% 12.90% 12.90% 12.90%
Sorbic acid NF/EP 0.08% 0.08% 0.08% 0.08% 0.08%
Methyl Hydroxybenzoate NF, EP 0.18% 0.18% 0.18% 0.18% 0.18%
Purified water USP/EP 82.84% 78.84% 78.84% 73.84% 69.84%
Total 100% 100% 100% 100% 100%
The above formulations can be adjusted to maximize die particular delivery system used. For example, note the foπnulation with 14% carbamide peroxide would typically be used with a dosage regime that requires less frequent administration of the I composition. With a composition having a high concentration of peroxide, a low concentration of peroxide could be released over longer duration, minimizing the number of dose adniinistrations needed daily or weekly.
Any and all publications and patent applications mentioned in this specification are indicative of the level of skill of those skilled in the art to which this i invention pertains. All publications and patent applications are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference.
It is to be understood that the invention is not to be limited to the exact configuration as illustrated and described herein. Accordingly, all expedient modifications readily attainable by one of ordinary skill in the art from the disclosure set forth herein, or
by routine experimentation therefrom, are deemed to be within the spirit and scope of the invention as defined by the appended claims.
Claims (43)
1. A pharmaceutical vaginal composition which comprises a source of peroxide and a bioadhesive, extended release formulation, the composition being formulated such that, upon local administration thereof to a patient the peroxide is released over a period of at least 12 hours in an amount sufficient to increase the concentration of oxygen in the vagina and the pH of the vagina is decreased therapeutically, without either sterilization of the vagina or a significant killing of the normally-desired local vaginal flora taking place.
2. The composition of claim 1, wherein the synergistic mix releases peroxide over a period of at least 24 hours.
3. The composition of claim 2, wherein said extended release formulation includes a bioadhesive, water-swellable, water-insohible, cross-linked polycarboxylic polymer.
4. The composition of claim 3, wherein the polymer is polycarbophil.
5. The composition of claim 2, wherein the peroxide source is present in an amount of about 0.01 mg to about 500 mg.
6. The composition of claim 4, wherein the peroxide source is present in an amount of about 0.1 mg to about 75 mg.
7. The composition of claim 2, wherein the peroxide source is carbamide peroxide.
8. The composition of claim 7, wherein the carbamide peroxide is present in an amount of about 0.01% to about 15% by weight
9. The composition of claim 8, wherein the polymer is polycarbophil.
10. The composition of claim 9, wherein the carbamide peroxide is in an amount of about 0.1% to about 025%.
11. The composition of claim 10, in single dosage form, wherein the composition is formulated to be administered in an amount of about 1 g to about 2 g per dose.
12. The composition of claim 2, wherein die synergistic mix releases peroxide over a period of at least 48 hours.
I I
13. The composition of claim 3, wherein (he synergistic mix releases peroxide over a period of at least 72 hours.
14. The composition of claim 2, wherein the peroxide amount in the composition is between 0.0035 mg to 350 mg.
15. The composition of claim 14, wherein the peroxide amount is between O.Ol mgto lOO mg.
16. A method of treating or preventing a vaginal infection comprising vaginally administering to a subject in need of such treatment a therapeutically effective amount of the vaginal composition of claim 1.
17. A method of treating or preventing a vaginal infection comprising vaginally administering to a subject in need of such treatment a therapeutically effective amount of the vaginal composition of claim 3.
18. A pharmaceutical vaginal composition which comprises a source of peroxide and a bioadhesive, extended release formulation, the composition being formulated such that upon local administration thereof to a patient the peroxide is released in an amount of less than 0.1 % by weight per hour and the pH of the vagina is decreased therapeutically, without either sterilization of the vagina or significant killing of the normally-desired local vaginal flora taking place.
19. The composition of claim 18, wherein said extended release formulation includes a bioadhesive, water-swellable, water-insoluble, cross-linked porycarboxylic polymer.
20. The composition of claim 19, wherein the polymer is polycarbophil.
21. The composition of claim 20, wherein the peroxide source is present in an amount of about 0.01 mg to about 500 mg.
22. The composition of claim 21, wherein the peroxide source is present in an amount of about 0.1 mg to about 75 mg.
23. The composition of claim 22, in single dosage form, wherein the composition is formulated to be administered in an amount of about 1 g to about 2.5 g per dose and the peroxide amount in the composition is about 0.01 mg to about 100 mg.
24. The composition of claim 23, wherein the peroxide amount is about 0.1 to about 75 mg.
25. The composition of claim 18, wherein the peroxide source is carbamide peroxide. .
26. The composition of claim 25, wherein the carbamide peroxide is present in an amount of about 0.01 % to about 15% by weight
27. The composition of claim 19, wherein the synergistic mix releases peroxide over a period of at least 24 hours.
28. The composition of claim 20, wherein the synergistic mix releases peroxide over a period of at least 48 hours.
29. A method of treating or preventing a vaginal infection comprising vaginally administering to a subject in need of such treatment a therapeutically effective amount of the vaginal composition of claim 18.
-
30. A method of treating or preventing a vaginal infection comprising vaginally administering to a subject of need of such treatment a therapeutically effective amount of the vaginal composition of claim 24.
31. A pharmaceutical vaginal composition which comprises a source of . ; peroxide and a bioadhesive, extended release formulation, the composition contairύngjess than 0.1% by weight of peroxide and being formulated such that upon local aώninistration thereof to a patient die concentration of oxygen in the vagina increases therapeutically and the pH of the vagina decreases therapeutically, without either sterilization of the vagina or significant killing of the normally-desired local vaginal flora taking place.
32. The composition of claim 31, wherein said extended release formulation includes a bioadhesive, water-sweilable, water-insoluble, cross-linked polycarboxylic polymer.
33. The composition of claim 32, wherein the polymer is polycarbophil.
.
34. The composition of claim 33, wherein the peroxide source is carbamide peroxide.
35. The composition of claim 34, wherein the peroxide is in an amount of about 0.034% to about 0.085% by weight.
36. The composition of claim 31, in dosage form, wherein the composition is formulated to be administered in an amount of about 1 g to about 2.5 g per single dosage.
37. The composition of claim 31 , wherein the peroxide amount in d e foπnulation is 0.01 mg to 100 mg.
38. A composition according to claims 1, 18, or 31, wherein the source of peroxide and the bioadhesive, extended release formulation are present in synergistically effective amounts.
39. A composition according to any one of claims 1, 18, or 31 for use in a method of medical treatment of the human or animal body by therapy.
40. Use of a source of peroxide and a bioadhesive, extended release foπnulation in the manufacture of a medicament for vaginal administration in the treatment orprevention of a vaginal infection, the medicament being formulated such that upon administration thereof to a patient, the peroxide is released over a period of at least 12 hours in an amount sufficient to increase the concentration of oxygen in the vagina and the pH of the vagina is decreased therapeutically, without either sterilization of the vagina or a significant killing of the normally-desired local vaginal flora taking place.
41. Use of a source of peroxide and a bioadhesive, extended release foπnulation in the manufacture of a medicament for vaginal administration in the treatmen or prevention of a vaginal infection, the medicament being formulated such that upon administration thereof to a patient, the peroxide is released in an amount of less than 0.1% by weight per hour and the pH of the vagina is decreased therapeutically, without either sterilization of the vagina or a substantial reduction in the levels of normally-desired local vaginal flora taking place.
1
42. Use of a source of peroxide and a bioadhesive, extended release formulation in the manufacture of a medicament for vaginal administration in the treatment or prevention of a vaginal infection, the medicament containing less than 0.1% by weight of peroxide and being formulated such that upon administration thereof to a patient the concentration of oxygen in the vagina increases therapeutically and the pH of the vagina decreases therapeutically, without either sterilization of the vagina or a substantial reduction in the levels of normally-desired local vaginal flora taking place.
43. Use according to any one of claims 39 to 42 wherein the medicament contains the source of peroxide and the bioadhesive, extended release foπnulation in synergistically effective amounts.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
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US33068301P | 2001-10-29 | 2001-10-29 | |
US60/330,683 | 2001-10-29 | ||
US10/278,910 US7709026B2 (en) | 2001-10-29 | 2002-10-24 | Low concentration of peroxide for treating or preventing vaginal infections |
US10/278,910 | 2002-10-24 | ||
PCT/EP2002/012043 WO2003037382A1 (en) | 2001-10-29 | 2002-10-28 | Low concentration of peroxide for treating or preventing vaginal infections |
Publications (2)
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AU2002346897A1 true AU2002346897A1 (en) | 2003-07-10 |
AU2002346897B2 AU2002346897B2 (en) | 2008-04-17 |
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AU2002346897A Ceased AU2002346897B2 (en) | 2001-10-29 | 2002-10-28 | Low concentration of peroxide for treating or preventing vaginal infections |
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US (1) | US7709026B2 (en) |
EP (1) | EP1441769B1 (en) |
JP (2) | JP5153049B2 (en) |
KR (1) | KR101009146B1 (en) |
CN (1) | CN1578676A (en) |
AR (1) | AR037047A1 (en) |
AT (1) | ATE297222T1 (en) |
AU (1) | AU2002346897B2 (en) |
BR (1) | BR0213584A (en) |
CA (1) | CA2465133C (en) |
DE (1) | DE60204584T2 (en) |
DK (1) | DK1441769T3 (en) |
ES (1) | ES2243772T3 (en) |
HK (1) | HK1063290A1 (en) |
HR (1) | HRP20040480B1 (en) |
HU (1) | HU229487B1 (en) |
IL (2) | IL161512A0 (en) |
MA (1) | MA26289A1 (en) |
ME (1) | MEP34608A (en) |
MX (1) | MXPA04003977A (en) |
MY (1) | MY137791A (en) |
NO (1) | NO20042199L (en) |
NZ (1) | NZ532294A (en) |
PE (1) | PE20030492A1 (en) |
PL (2) | PL402550A1 (en) |
PT (1) | PT1441769E (en) |
RS (1) | RS51154B (en) |
RU (1) | RU2329829C2 (en) |
SI (1) | SI1441769T1 (en) |
WO (1) | WO2003037382A1 (en) |
ZA (1) | ZA200402943B (en) |
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2002
- 2002-10-24 US US10/278,910 patent/US7709026B2/en not_active Expired - Lifetime
- 2002-10-28 PL PL402550A patent/PL402550A1/en not_active Application Discontinuation
- 2002-10-28 ES ES02783026T patent/ES2243772T3/en not_active Expired - Lifetime
- 2002-10-28 NZ NZ532294A patent/NZ532294A/en not_active IP Right Cessation
- 2002-10-28 PE PE2002001057A patent/PE20030492A1/en not_active Application Discontinuation
- 2002-10-28 JP JP2003539722A patent/JP5153049B2/en not_active Expired - Fee Related
- 2002-10-28 RS YUP-366/04A patent/RS51154B/en unknown
- 2002-10-28 BR BR0213584-1A patent/BR0213584A/en not_active Application Discontinuation
- 2002-10-28 AU AU2002346897A patent/AU2002346897B2/en not_active Ceased
- 2002-10-28 PL PL369725A patent/PL216746B1/en not_active IP Right Cessation
- 2002-10-28 CN CNA028215664A patent/CN1578676A/en active Pending
- 2002-10-28 KR KR1020047006272A patent/KR101009146B1/en not_active IP Right Cessation
- 2002-10-28 RU RU2004116312/15A patent/RU2329829C2/en not_active IP Right Cessation
- 2002-10-28 PT PT02783026T patent/PT1441769E/en unknown
- 2002-10-28 HU HU0401672A patent/HU229487B1/en unknown
- 2002-10-28 SI SI200230172T patent/SI1441769T1/en unknown
- 2002-10-28 EP EP02783026A patent/EP1441769B1/en not_active Expired - Lifetime
- 2002-10-28 AR ARP020104078A patent/AR037047A1/en not_active Application Discontinuation
- 2002-10-28 CA CA2465133A patent/CA2465133C/en not_active Expired - Lifetime
- 2002-10-28 DE DE60204584T patent/DE60204584T2/en not_active Expired - Lifetime
- 2002-10-28 DK DK02783026T patent/DK1441769T3/en active
- 2002-10-28 AT AT02783026T patent/ATE297222T1/en active
- 2002-10-28 IL IL16151202A patent/IL161512A0/en unknown
- 2002-10-28 WO PCT/EP2002/012043 patent/WO2003037382A1/en active IP Right Grant
- 2002-10-28 MX MXPA04003977A patent/MXPA04003977A/en active IP Right Grant
- 2002-10-28 ME MEP-346/08A patent/MEP34608A/en unknown
- 2002-10-28 MY MYPI20024019A patent/MY137791A/en unknown
-
2004
- 2004-04-19 IL IL161512A patent/IL161512A/en not_active IP Right Cessation
- 2004-04-19 ZA ZA2004/02943A patent/ZA200402943B/en unknown
- 2004-04-29 MA MA27664A patent/MA26289A1/en unknown
- 2004-05-26 NO NO20042199A patent/NO20042199L/en not_active Application Discontinuation
- 2004-05-27 HR HR20040480A patent/HRP20040480B1/en not_active IP Right Cessation
- 2004-08-12 HK HK04106057A patent/HK1063290A1/en not_active IP Right Cessation
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2010
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