WO2012101500A1 - Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections - Google Patents
Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections Download PDFInfo
- Publication number
- WO2012101500A1 WO2012101500A1 PCT/IB2012/000095 IB2012000095W WO2012101500A1 WO 2012101500 A1 WO2012101500 A1 WO 2012101500A1 IB 2012000095 W IB2012000095 W IB 2012000095W WO 2012101500 A1 WO2012101500 A1 WO 2012101500A1
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- Prior art keywords
- composition
- lactobacillus
- weight
- acid
- bicarbonate
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- MUPFEKGTMRGPLJ-ZQSKZDJDSA-N raffinose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)O)O1 MUPFEKGTMRGPLJ-ZQSKZDJDSA-N 0.000 description 1
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Classifications
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- A61K35/744—Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
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- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Definitions
- the present invention relates to an effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections. It is well known that the composition of intestinal and urogenital microflora represents a critical point for an individual's health and wellbeing.
- the vaginal ecosystem consists of epithelial cells that line the vagina and uterus, glandular cells that secrete into the lumen of the organ and complex bacterial flora represented by different species of microorganisms.
- microorganisms have the ability to ferment glycogen originating from the decomposition of parabasal cells of the eutrophic vaginal mucosa, with a consequent production of lactic acid, whose final effect is the establishment and maintenance of an acidic vaginal environment (with pH values of 4-4.5 under physiological conditions) .
- the H + deriving from lactic acid contribute to the formation of hydrogen peroxide.
- This molecule is toxic for a large number of bacterial species which lack the enzyme catalase. At the level of vaginal secretions, concentrations of 0.75-5 g/ml are easily reached and are abundantly sufficient in order for the toxic effect to be expressed.
- Candida albicans and glabrata and/or pathogenic microorganisms (e.g. Neisseria gonorrheae and Trichomonas vaginalis) which can lead to candidiasis, vaginitis or forms of vaginosis.
- pathogenic microorganisms e.g. Neisseria gonorrheae and Trichomonas vaginalis
- microorganisms capable of restoring the correct composition of vaginal microflora
- the mode of delivery of the microorganisms into the vaginal environment represents a very critical factor.
- soft gelatin capsules usually known as soft gels
- the oily matrix could exert a toxic effect on the microorganisms, to such a degree as to considerably reduce the number and viability thereof.
- the capsules may take a relatively long time to dissolve and in any case they do not assure an adequate dispersion of the active ingredient throughout the vaginal environment .
- hydrophilic suspensions or hydrogels
- the subjects must remain lying down for at least 20-30 minutes after applying them so as to prevent the product from leaking out .
- traditional vaginal tablets pose a problem of high mortality of the microorganisms during their manufacture and moreover they are not able to ensure an adequate distribution of microorganisms in the vaginal environment .
- composition which represents a valid alternative to antibiotic and/or fungicidal therapy and at the same represents an improvement over the known forms of administration .
- a probiotic formulation in the form of a suitably prepared solid composition is capable of solving the problems persisting in the prior art.
- Table 1 shows the bacterial strains tested by the Applicant and which form the subject matter of the present invention.
- Table 2 shows an example of a composition according to the invention.
- Table 3 shows the mortality data for the probiotic bacteria according to the different pressures exerted and stability of the tablets (expressed as the half- life of the bacterial load) after 2 years of storage thereof at 25°C.
- Table 4 shows a composition that is not in accordance with the present invention.
- Table 5 shows a composition in tablet form that is not in accordance with the present invention.
- the Applicant conducted lengthy, intense experimental research activity with the aim of identifying the optimal qualitative and quantitative composition for preparing the composition of the present invention, as well as the operating conditions for the preparation thereof .
- the composition of the present invention is an effervescent composition.
- the effervescence is due to the formation of carbon dioxide which occurs when an acid-base system comprising an organic acid and a salt of the carbonate and/or bicarbonate anion comes into contact with the water/moisture present in the vaginal cavity.
- the acid-base system is capable of maintaining the intravaginal pH stable within an interval comprised from 3 to 5.5, preferably from 4 to 5.
- the intravaginal pH is comprised from 4.2 to 4.5.
- composition of the present invention is an effervescent composition in solid form.
- the organic acid is in solid form, preferably a powder or granules
- the salt of the carbonate and/or bicarbonate anion is in solid form, preferably a powder or granules.
- the effervescent composition in solid form is in the form of a tablet, ovule, lozenge or granules .
- the organic acid is selected from the group consisting or, or alternatively comprising, citric acid, malic acid, tartaric acid, fumaric acid, lactic acid and mixtures thereof.
- the organic acid is citric acid.
- adipic and/or ascorbic acid as the organic acid present in the aforesaid acid-base system provokes a toxic effect on the microorganisms, resulting in the mortality thereof already at the time of preparation of the composition in solid form, for example as a powder or granules.
- said mortality occurs after the components are mixed to give a composition in solid form, for example as a powder or granules, but prior to compression. Therefore, the composition of the present invention does not contain adipic acid and/or ascorbic acid.
- the salt of the carbonate and/or bicarbonate anion is selected from the group consisting of or, alternatively, comprising: sodium carbonate, potassium carbonate, calcium carbonate, magnesium carbonate, sodium glycine carbonate, sodium bicarbonate, potassium bicarbonate, calcium bicarbonate, magnesium bicarbonate, sodium lactate, potassium lactate, carbonate lactate and mixtures thereof.
- said salt is selected from the group consisting of or, alternatively, comprising a salt of the bicarbonate anion.
- the salt is sodium bicarbonate .
- the amount of the salt of the carbonate or bicarbonate anion is comprised from 1 to 15% by weight, relative to the total weight of the composition.
- it is comprised from 3 to 13% by weight, relative to the total weight of the composition; even more preferably, it is comprised from 4 to 12% by weight, relative to the total weight of the composition.
- it is comprised from 5 to 10% by weight, relative to the total weight of the composition .
- the amount of sodium bicarbonate is comprised from 1 to 15% by weight, relative to the total weight of the composition.
- it is comprised from 3 to 13% by weight, relative to the total weight of the composition; even more preferably it is comprised from 5 to 10% by weight, relative to the total weight of the composition.
- it is comprised from 5 to 10% by weight, relative to the total weight of the composition .
- the acid-base system consists of citric acid and sodium bicarbonate in an amount by weight as described above.
- the Applicant has found that when the salt of the carbonate or bicarbonate anion, e.g. sodium bicarbonate, is more than 15% by weight, relative to the total weight of the composition, a toxic effect is manifested against the microorganisms due to an osmotic effect .
- the salt of the carbonate or bicarbonate anion e.g. sodium bicarbonate
- the amount of organic acid to be used in the acid-base system is calculated once the amount of the salt of the carbonate or bicarbonate anion used in accordance with the above-described concentrations has been determined.
- the amount of organic acid used is stoichiometric and is a function of the salt used and solely serves the purpose of forming carbon dioxide. In the presence of said salt, the organic acid is capable of developing effervescence, due to the formation of carbon dioxide, after hydration inside the vaginal cavity.
- the effervescent tablet is capable of delivering a large population of lactic bacteria for rapid colonization of the entire epithelium and vaginal mucosa. Thanks to the pH- controlled and stabilized effervescent system, the lactic bacteria are delivered into the vaginal cavity in a good physiological condition which enables them to grow and multiply.
- the composition of the present invention in the form of an effervescent tablet, is capable of ensuring an optimal distribution of the bacteria over the vaginal mucosa. Moreover, said composition is capable of ensuring and maintaining an anaerobic or microaerophilic environment inside the vaginal cavity thanks to the formation of carbon dioxide .
- a mixture comprising or, alternatively, consisting of [microcrystalline cellulose : arabinogalactan] , preferably in a ratio by weight of 1:1 to 3:1, is capable of preserving the number and viability of the cells of the microorganisms when it is desired to obtain a tablet from the composition in powder form.
- the composition of the present invention comprises a mixture containing [microcrystalline cellulose : arabinogalactan] in a ratio by weight of 1:1 to 3:1.
- arabinogalactan derived from plants is used.
- arabinogalactan derived from larch e.g. FiberAid ® , from the Larex ® range of products distributed by Lonza Inc. USA
- fiberAid ® from the Larex ® range of products distributed by Lonza Inc. USA
- the Applicant has likewise found that using corn starch as the aggregating substance in the composition of the present invention provides unsatisfactory results when the composition in powder form is used to prepare tablets, since the tablets obtained following compression of the powder are capped.
- the microcrystalline cellulose can be either partly or completely replaced by cellulose in powder form. Both microcrystalline cellulose and cellulose in powder form are present in the list of food additives as E460.
- Arabinogalactan is a biopolymer consisting of arabinose and galactose monomers. There are two classes of arabinogalactans : those derived from plants and those of microbial origin.
- microcrystalline cellulose (or cellulose in powder form) is present in amount comprised from 2 to 45% by weight, relative to the total weight of the composition, preferably from 5 to 25%.
- the arabinogalactan is present in amount comprised from 5 to 30% by weight, relative to the total weight of the composition, preferably from 10 to 20%.
- composition of the present invention can further comprise at least one additional component selected from the group comprising: sodium carboxymethyl cellulose, anhydrous calcium hydrogen phosphate and hydroxpropyl methylcellulose.
- Said at least one additional component is present in the composition of the present invention in a total amount that ranges from 3 to 70% w/w, more preferably from 6 to 40% w/w, and even more preferably from 10 to 25% w/w, relative to the total weight of the composition .
- the composition of the present invention further comprises magnesium stearate in an amount of 0.5% to 7% w/w, preferably 1% to 3.5% w/w, relative to the total weight of the composition.
- the composition of the present invention can further comprise silicon dioxide in an amount of 0.5% to 4% w/w, preferably 1% to 2% w/w, relative to the total weight of the composition.
- the composition of the present invention can further comprise sucrose palmitate in an amount of 0.5% to 7% w/w, preferably 1% to 3.5% w/w, relative to the total weight of the composition.
- the composition of the present invention can further comprise a mixture of glycerides (saponifiable fats) in an amount of 0.5% to 10% w/w, preferably 2% to 7% w/w, relative to the total weight of the composition.
- the composition can further comprise from 0.5% to 10% w/w, preferably from 1% to 5% w/w, of sucrose ester, the percentages being expressed relative to the total weight of the composition.
- composition of the invention is for vaginal applications for the treatment of vaginal infections such as vaginitis, vaginosis, candidiasis, gonorrhoea, herpes and venereal ulcer.
- the composition is in the form of a tablet.
- the tablet can be coated with one or more polymer materials known in the art .
- probiotic microorganisms used individually or in a mixture, even one consisting of different genera or species.
- Probiotic microorganisms are by definition microorganisms, prevalently bacteria of human origin, which are capable of inducing beneficial effects if taken regularly in a sufficient quantity and for an adequate amount of time.
- composition of the present invention comprises at least one probiotic bacterial strain having the ability to reduce and/or eliminate the presence of pathogenic agents selected from the group comprising: Candida albicans, Candida glabrata, Candida parapsilosis, Candida krusei, Candida tropicalis, Gardnerella vaginalis, Trichomonas vaginalis, Neisseria gonorrhoeae, Escherichia coli, Herpex simplex and Haemophilus ducreyi .
- pathogenic agents selected from the group comprising: Candida albicans, Candida glabrata, Candida parapsilosis, Candida krusei, Candida tropicalis, Gardnerella vaginalis, Trichomonas vaginalis, Neisseria gonorrhoeae, Escherichia coli, Herpex simplex and Haemophilus ducreyi .
- said bacterial strain belongs to at least one species selected from the group consisting of: Lactobacillus plantarum, Lactobacillus pentosus, Lactobacillus casei , Lactobacillus casei ssp. paracasei , Lactobacillus rhamnosus, Lactobacillus acidophilus, Lactobacillus delbrueckii , Lactobacillus delbrueckii ssp. bulgaricus, Lactobacillus delbrueckii ssp. delbrueckii , Lactobacillus fermentum,
- Lactobacillus gasseri Lactobacillus reuteri
- Bifidobacterium longum Bifidobacterium bifidum, Bifidobacterium breve, Bifidobacterium animalis ssp. lactis, Bifidobacterium adolescentis, Bifidobacterium pseudocatenulatum, Bifidobacterium catenulatum or Bifidobacterium infantis .
- the bacterial strains are selected from among: Lactobacillus salivarius CRL 1328, Lactobacillus paracasei CRL 1289, Lactobacillus gasseri CRL 1259, Lactobacillus crispatus CRL 1251, Lactobacillus crispatus CRL 1266, Lactobacillus acidphilus CRL 1294, Lactobacillus paracasei LPC 00, Lactobacillus plantarum LP 02 and Lactobacillus fermentum LF 10.
- composition of the present invention preferably in the form of a tablet, comprises at least two strains selected from the above- mentioned group.
- the composition of the present invention preferably in the form of a tablet, comprises at least three strains selected from the above-mentioned group.
- the composition of the present invention preferably in the form of a tablet, comprises at least four strains selected from the above-mentioned group.
- strains selected from among: Lactobacillus salivarius CRL 1328, Lactobacillus paracasei CRL 1289, Lactobacillus gasseri CRL 1259, Lactobacillus crispatus CRL 1266 and Lactobacillus fermentum LF 10 have demonstrated to be advantageous .
- the microorganisms preferably used in the form of a lyophilized culture having a viable count generally comprised from 10 to 200 billion colony forming units (CFU)/gram, are preferably present in an amount of 0.5 to 20% w/w, preferably 1 to 15% w/w, even more preferably 3 to 10% w/w, relative to the total weight of the tablet .
- CFU colony forming units
- prebiotic component is generally a non-digestible mixture of a saccharidic nature, at least partially soluble in water or in an aqueous solution, which stimulates the growth and/or activity of one or more probiotic bacterial strains as described above.
- prebiotic agents dietary fibres are preferred.
- said prebiotic fibre is selected from the group comprising: fructo-oligosaccharides (FOS) , galacto-oligosaccharides (GOS) , trans- galactooligosaccharides (TOS) , xylo-oligosaccharides (XOS) , chitosan oligosaccharides (COS) , o!-galactosides (such as raffinose and stachyose) , pectins, gums, partially hydrolyzed gums, inulin, psyllium, acacia, carob, oat or bamboo fibre, citrus fibres and, in general, fibres containing a soluble and an insoluble portion, in a variable ratio to each other.
- FOS fructo-oligosaccharides
- TOS trans- galactooligosaccharides
- XOS xylo-oligosaccharides
- COS chitosan oligosacc
- said prebiotic fibre is selected from among fructo-oligosaccharides (FOS) , galacto- oligosaccharides (GOS) and xylo-oligosaccharides (XOS) .
- FOS fructo-oligosaccharides
- GOS galacto- oligosaccharides
- XOS xylo-oligosaccharides
- the prebiotic component is present in the composition in an amount of up to 70% w/w, preferably comprised from 5 to 50% w/w, even more preferably from 10 to 30% w/w, relative to the total weight of the composition .
- the composition according to the invention can contain additional active components, e.g. vitamins, minerals, vegetable extracts or other compounds with an effect that is synergistic with or complementary to that of the population of microorganisms present in the formulations according to the invention.
- additional active components are present in the composition in an amount of up to 70% w/w, preferably comprised from 0.5 to 40% w/w, even more preferably from 1 to 20% w/w, relative to the total weight of the composition.
- the combination of technological excipients of compression and effervescence according to the present invention assures an adequate cohesiveness of the powders of the tablet and brings about the desired kinetics of release of the active ingredients after the intake thereof.
- the mixing of the various components can be done by adding the components in any order whatsoever, taking care to add the culture of microorganisms, preferably in the form of a lyophilizate , as the last ingredient, to prevent the possibility that an excessive mixing time may induce a mechanical shock in the wall of the bacterial cells, with consequent suffering and reduced stability of the final product.
- Formulations produced in accordance with the method of the present invention are characterized by excellent flowability, a parameter that favours uniform loading of the dies (i.e. the space dedicated to accommodating the specific amount of powder to be compressed) in the compression machines.
- Said compression machines typically comprise a device for loading the dies (generally represented by a hopper for delivering the powder mixture) and a metal disk of suitable radius, in whose thickness the dies themselves are obtained; these are present in variable number depending on the machine, and the step of compressing the powder takes place therein, thanks to the simultaneous, synergistic movement of two moving parts of the machine, defined as punches .
- Said compression machines further comprise a number of devices for controlling the main operating parameters (position of the lower punch at the start of the compression cycle, lowest position reached by the upper punch during the compression cycle, rotation speed of the disk in which the dies are present and so forth) .
- the main operating parameters position of the lower punch at the start of the compression cycle, lowest position reached by the upper punch during the compression cycle, rotation speed of the disk in which the dies are present and so forth.
- There exist alternative and rotary compression machines according to the machine's overall operating modes and, consequently, the number of tablets it is able to produce in a given unit of time. Tablets can thus be produced using compression machines known in the art and using punches of varying shape, preferably double-radius round convex and oval punches.
- Kp Keloponds
- N 9.807 Newtons
- the negative effect of compression on the population of microorganisms is manifested both when the applied forces are high, for example in tablets with a hardness of 10-12 Kp, and when they are low, such as, for example, in tablets with a hardness of 5-6 Kp .
- the disadvantage of using high forces is a larger reduction in the number of microorganisms, whereas with low forces a reduced cohesion of the tablet is generally obtained.
- the tablets of the present invention show a compression force comprised from 5 to 12 Kp, depending on the type of tablet it is desired to obtain .
- a mortality ranging from 4 to 15% was observed when the compression force applied was such as to obtain tablets with a hardness comprised from 5 to 6 Kp and a mortality ranging from 10 to 25% when the compression force applied was such as to obtain tablets with a hardness comprised from 10 to 12 Kp.
- Another advantage of the method according to the invention is that this enables the production of sufficiently cohesive tablets even at low compression forces, for example tablets with a hardness of 5-6 Kp .
- the tablets prepared in accordance with the present invention were tested in order to evaluate the disintegration time according to the European Pharmacopoeia, Ed. X, ref . 2.9.1.
- the friability of uncoated tablets was tested in accordance with ref. 2.9.7 and the resistance to crushing according to ref. 2.9.8.
- Table 2 shows an example of a composition in accordance with the invention.
- Table 3 shows the mortality data for the probiotic bacteria (composition shown in table 2) according to the different pressures exerted and the stability of the tablets (expressed as the half-life of the bacterial load) after 2 years of storage thereof at 25 °C.
- the tablets obtained with the formulations according to the invention had a thickness of about 7.7 mm in the case of tablets with a high degree of hardness and about 8.4 mm in the case of tablets with a low degree of hardness.
- stability is expressed as the half-life of the probiotic component of the formulation, i.e. the time that elapses before the initial viable cell count is halved.
- a powder composition an amount comprised from 1 to 4 grams of sample was resuspended in a suitable volume of a sterile liquid medium, generally a 0.85% sodium chloride saline solution, to which bacteriological peptone is added in a proportion of 1 g/litre.
- a sterile liquid medium generally a 0.85% sodium chloride saline solution, to which bacteriological peptone is added in a proportion of 1 g/litre.
- the number of cells/ml is reduced by means of subsequent base 10 serial dilutions.
- 1 ml of the most concentrated dilution is transferred each time, using a sterile pipette, into 9 ml of diluent; this operation is carried out a number of times that is sufficient to bring the quantity of microorganisms present per ml of diluent to a number comprised from 10 to 300, so that following their transfer into a Petri dish and the addition of a suitable agarized culture medium they form separate, and thus countable, colonies.
- a further advantageous aspect of the composition of the present invention is improved stability, over time, of the probiotic microorganisms (probiotic component) present therein compared to the typical stability of a prior art formulation.
- This advantage is due to the use of a mixture containing [microcrystalline cellulose : arabinogalactan] in a ratio by weight preferably comprised from 1:1 to 3:1. This mixture is capable of greatly limiting the mechanical damage caused to the probiotic bacterial cells by the compression step and allows tablets to be obtained with no occurrence of capping.
- the Applicant has found that the half-lives of the probiotic component in the powder composition and in the tablets of varying hardness manufactured with a formulation according to the invention are very similar, demonstrating the fact that the technological components used are able to minimize the mechanical damage caused by the compression step.
- the tablets according to the invention display a high rate of survival of the probiotic microorganisms even following the compression step.
- a further advantageous aspect is the ability to release carbon dioxide as the tablet disintegrates, resulting in the creation of an anaerobic or microaerophilic environment particularly favourable to vaginal colonization by the probiotics used.
- the effervescence is further capable of assuring an adequate and homogeneous distribution of the probiotic active ingredient in the vaginal environment by increasing the effectiveness of colonization.
- compositions of the present invention make it possible to obtain tablets containing probiotic microorganisms which are effective and stable over time, even at non-refrigerated temperatures, because the components forming the composition have been chosen and selected with the aim of reducing mortality due to mixing and mortality due to compression without impairing the cohesion of the powder.
- the composition of the present invention preferably in the form of a tablet, contains neither adipic acid nor ascorbic acid, the amount of the salt of the carbonate or bicarbonate anion present is lower than 15% by weight, relative to the total weight of the composition, and a mixture of microcrystalline cellulose and arabinogalactan is used instead of corn starch .
- composition of table 4 shows: 80.8% mortality due to mixing, 40.5% mortality due to compression and an overall mortality (mixing + compression) of 88.6%.
- composition of table 4 shows marked mortality already at the powder level, prior to compression.
- the pH of dissolution (in saline in a 1:10 ratio) is not a problem, as it is equal to 5.22 for the first formulation and 5.53 for the second one.
- Adipic acid was found to be toxic. But this toxicity accounts for only a certain portion of the mortality observed (about 60% of the total mortality) . Ascorbic acid was found to be toxic. But this toxicity accounts for a further portion of mortality. Removing ascorbic acid from the composition of table 4 reduces mortality from 73.8 to 26.7%. Adipic acid on its own is in any case toxic (45.8% at pH 4.24); its toxicity seems to increase in the presence of ascorbic acid. Ascorbic acid thus seems to show a toxicity synergistic with that of adipic acid.
- a degree of mortality was ascertained to be due to osmotic pressure, given by the bicarbonate present in an excessive amount. This mortality revealed to be equal to about 20%.
- Adipic acid, ascorbic acid and the osmotic effects mediated by bicarbonate are responsible for the toxicity observed. Bicarbonate in itself is not toxic: it becomes so only because of the osmotic effect .
- a composition (table 5) was prepared without adipic acid and ascorbic acid and with an amount of bicarbonate anion (e.g. sodium bicarbonate) less than 15% by weight, relative to the total weight of the composition .
- bicarbonate anion e.g. sodium bicarbonate
- 84 mg of sodium bicarbonate constitutes 1 millimole and the C0 2 that is released occupies a total volume of 25.4 ml at 37°C and under atmospheric pressure.
- the quantity of citric acid was chosen in such a manner as to ensure complete release of the C0 2 from the sodium bicarbonate at the pH values observed after the tablet's dissolution.
- composition of table 5 showed problems when subjected to a compression step in order to prepare the tablets .
- the powder (table 5) showed poor cohesive properties due to the use of corn starch in a formulation with a low moisture content. All of the tablets output by the compression machine were capped even before being passed through the deduster.
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Abstract
The present invention relates to an effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections.
Description
EFFERVESCENT COMPOSITION IN SOLID FORM FOR USE IN VAGINAL APPLICATIONS FOR THE TREATMENT OF VAGINAL INFECTIONS
DESCRIPTION
The present invention relates to an effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections. It is well known that the composition of intestinal and urogenital microflora represents a critical point for an individual's health and wellbeing. The vaginal ecosystem consists of epithelial cells that line the vagina and uterus, glandular cells that secrete into the lumen of the organ and complex bacterial flora represented by different species of microorganisms.
These microorganisms have the ability to ferment glycogen originating from the decomposition of parabasal cells of the eutrophic vaginal mucosa, with a consequent production of lactic acid, whose final effect is the establishment and maintenance of an acidic vaginal environment (with pH values of 4-4.5 under physiological conditions) .
The H+ deriving from lactic acid contribute to the formation of hydrogen peroxide. This molecule is toxic for a large number of bacterial species which lack the enzyme catalase. At the level of vaginal secretions,
concentrations of 0.75-5 g/ml are easily reached and are abundantly sufficient in order for the toxic effect to be expressed.
The combined action of hydrogen peroxide, uterine peroxidase (produced by the cervix and endometrium) and Cl" and I" ions also limits bacterial growth by directly activating polymorphonucleates, which exert a bactericidal action in epithelial intercellular spaces. In women, due to a variety of exogenous and endogenous factors, such as the intake of antibiotics, states of stress, hormonal modulations associated with pregnancy and the menstrual cycle or the intake of high concentrations of estrogen, an imbalance frequently occurs in the vaginal ecosystem. The alteration in the balance of the vaginal ecosystem leads to a prevalence of so-called "opportunistic" microorganisms (e.g. Candida albicans and glabrata) and/or pathogenic microorganisms (e.g. Neisseria gonorrheae and Trichomonas vaginalis) which can lead to candidiasis, vaginitis or forms of vaginosis.
Epidemiological data show that vaginal infections today affect over a billion women worldwide every year, with serious repercussions from a socioeconomic standpoint. The therapy generally adopted is an antibiotic and/or fungicidal one, which usually gives good results in the
short term, but shows to be incapable of preventing recurrent infections due to the ever increasing resistance of pathogens. Moreover, not all subjects who need to be treated are able to undertake and tolerate an antibiotic or fungicidal therapy.
The use of microorganisms capable of restoring the correct composition of vaginal microflora is known. However, the mode of delivery of the microorganisms into the vaginal environment represents a very critical factor. It is known, for example, that soft gelatin capsules, usually known as soft gels, entail suspending the probiotic component in an oily matrix which, after the product's application, tends to constitute a physical barrier capable of slowing down or almost totally inhibiting the capacity of said probiotic component to colonize the vaginal mucosa. Furthermore, the oily matrix could exert a toxic effect on the microorganisms, to such a degree as to considerably reduce the number and viability thereof.
For example, the capsules may take a relatively long time to dissolve and in any case they do not assure an adequate dispersion of the active ingredient throughout the vaginal environment .
For example, hydrophilic suspensions, or hydrogels, entail a mode of application that is neither easy nor
very comfortable. In fact, the subjects must remain lying down for at least 20-30 minutes after applying them so as to prevent the product from leaking out . Finally, traditional vaginal tablets pose a problem of high mortality of the microorganisms during their manufacture and moreover they are not able to ensure an adequate distribution of microorganisms in the vaginal environment .
Thus, there remains a need to have a composition capable of delivering probiotic bacteria into the vaginal environment and ensuring a complete dispersion/distribution thereof.
Moreover, there remains a need to have a pharmaceutical form that can be easily administered and is practical to use .
In particular, there remains a need to have a composition which represents a valid alternative to antibiotic and/or fungicidal therapy and at the same represents an improvement over the known forms of administration .
The Applicant has surprisingly found that a probiotic formulation in the form of a suitably prepared solid composition is capable of solving the problems persisting in the prior art.
The subject matter of the present invention is an
effervescent composition in solid form, as set forth in the appended independent claim.
Other preferred embodiments of the present invention are set forth in the appended dependent claims .
Table 1 shows the bacterial strains tested by the Applicant and which form the subject matter of the present invention.
Table 2 shows an example of a composition according to the invention.
Table 3 shows the mortality data for the probiotic bacteria according to the different pressures exerted and stability of the tablets (expressed as the half- life of the bacterial load) after 2 years of storage thereof at 25°C.
Table 4 shows a composition that is not in accordance with the present invention.
Table 5 shows a composition in tablet form that is not in accordance with the present invention.
The Applicant conducted lengthy, intense experimental research activity with the aim of identifying the optimal qualitative and quantitative composition for preparing the composition of the present invention, as well as the operating conditions for the preparation thereof .
The composition of the present invention is an
effervescent composition. The effervescence is due to the formation of carbon dioxide which occurs when an acid-base system comprising an organic acid and a salt of the carbonate and/or bicarbonate anion comes into contact with the water/moisture present in the vaginal cavity. The acid-base system is capable of maintaining the intravaginal pH stable within an interval comprised from 3 to 5.5, preferably from 4 to 5. Advantageously, the intravaginal pH is comprised from 4.2 to 4.5.
The composition of the present invention is an effervescent composition in solid form. In a preferred embodiment, the organic acid is in solid form, preferably a powder or granules, and the salt of the carbonate and/or bicarbonate anion is in solid form, preferably a powder or granules.
In a preferred embodiment, the effervescent composition in solid form is in the form of a tablet, ovule, lozenge or granules .
The organic acid is selected from the group consisting or, or alternatively comprising, citric acid, malic acid, tartaric acid, fumaric acid, lactic acid and mixtures thereof. In a preferred embodiment, the organic acid is citric acid.
The Applicant has found that the use of adipic and/or ascorbic acid as the organic acid present in the
aforesaid acid-base system provokes a toxic effect on the microorganisms, resulting in the mortality thereof already at the time of preparation of the composition in solid form, for example as a powder or granules. In the case of the preparation of a tablet, said mortality occurs after the components are mixed to give a composition in solid form, for example as a powder or granules, but prior to compression. Therefore, the composition of the present invention does not contain adipic acid and/or ascorbic acid.
The salt of the carbonate and/or bicarbonate anion is selected from the group consisting of or, alternatively, comprising: sodium carbonate, potassium carbonate, calcium carbonate, magnesium carbonate, sodium glycine carbonate, sodium bicarbonate, potassium bicarbonate, calcium bicarbonate, magnesium bicarbonate, sodium lactate, potassium lactate, carbonate lactate and mixtures thereof. Preferably, said salt is selected from the group consisting of or, alternatively, comprising a salt of the bicarbonate anion. In a preferred embodiment, the salt is sodium bicarbonate .
In a preferred embodiment, the amount of the salt of the carbonate or bicarbonate anion is comprised from 1 to 15% by weight, relative to the total weight of the
composition. Preferably, it is comprised from 3 to 13% by weight, relative to the total weight of the composition; even more preferably, it is comprised from 4 to 12% by weight, relative to the total weight of the composition. Advantageously, it is comprised from 5 to 10% by weight, relative to the total weight of the composition .
In a preferred embodiment, the amount of sodium bicarbonate is comprised from 1 to 15% by weight, relative to the total weight of the composition. Preferably, it is comprised from 3 to 13% by weight, relative to the total weight of the composition; even more preferably it is comprised from 5 to 10% by weight, relative to the total weight of the composition. Advantageously, it is comprised from 5 to 10% by weight, relative to the total weight of the composition .
In a preferred embodiment, the acid-base system consists of citric acid and sodium bicarbonate in an amount by weight as described above.
The Applicant has found that when the salt of the carbonate or bicarbonate anion, e.g. sodium bicarbonate, is more than 15% by weight, relative to the total weight of the composition, a toxic effect is manifested against the microorganisms due to an osmotic
effect .
The amount of organic acid to be used in the acid-base system is calculated once the amount of the salt of the carbonate or bicarbonate anion used in accordance with the above-described concentrations has been determined. The amount of organic acid used is stoichiometric and is a function of the salt used and solely serves the purpose of forming carbon dioxide. In the presence of said salt, the organic acid is capable of developing effervescence, due to the formation of carbon dioxide, after hydration inside the vaginal cavity.
The effervescent tablet, suitably formulated, is capable of delivering a large population of lactic bacteria for rapid colonization of the entire epithelium and vaginal mucosa. Thanks to the pH- controlled and stabilized effervescent system, the lactic bacteria are delivered into the vaginal cavity in a good physiological condition which enables them to grow and multiply.
Advantageously, the composition of the present invention, in the form of an effervescent tablet, is capable of ensuring an optimal distribution of the bacteria over the vaginal mucosa. Moreover, said composition is capable of ensuring and maintaining an anaerobic or microaerophilic environment inside the
vaginal cavity thanks to the formation of carbon dioxide .
The Applicant has found that a mixture comprising or, alternatively, consisting of [microcrystalline cellulose : arabinogalactan] , preferably in a ratio by weight of 1:1 to 3:1, is capable of preserving the number and viability of the cells of the microorganisms when it is desired to obtain a tablet from the composition in powder form.
In a preferred embodiment, the composition of the present invention comprises a mixture containing [microcrystalline cellulose : arabinogalactan] in a ratio by weight of 1:1 to 3:1.
Preferably, arabinogalactan derived from plants is used. Advantageously, arabinogalactan derived from larch (e.g. FiberAid®, from the Larex® range of products distributed by Lonza Inc. USA) is used.
The Applicant has likewise found that using corn starch as the aggregating substance in the composition of the present invention provides unsatisfactory results when the composition in powder form is used to prepare tablets, since the tablets obtained following compression of the powder are capped.
A mixture comprising or, alternatively, consisting of [microcrystalline cellulose : arabinogalactan] in a ratio
by weight of 1:1 to 1:3, on the contrary, allows tablets to be obtained with no occurrence of capping. Therefore, the tablets obtained from the composition of the present invention do not contain corn starch. In place of corn starch, a mixture containing [microcrystalline cellulose : arabinogalactan] is used in a ratio by weight preferably comprised from 1:1 to 3:1. The microcrystalline cellulose can be either partly or completely replaced by cellulose in powder form. Both microcrystalline cellulose and cellulose in powder form are present in the list of food additives as E460.
Arabinogalactan is a biopolymer consisting of arabinose and galactose monomers. There are two classes of arabinogalactans : those derived from plants and those of microbial origin.
The microcrystalline cellulose (or cellulose in powder form) is present in amount comprised from 2 to 45% by weight, relative to the total weight of the composition, preferably from 5 to 25%.
The arabinogalactan is present in amount comprised from 5 to 30% by weight, relative to the total weight of the composition, preferably from 10 to 20%.
Preferably, the composition of the present invention can further comprise at least one additional component selected from the group comprising: sodium
carboxymethyl cellulose, anhydrous calcium hydrogen phosphate and hydroxpropyl methylcellulose.
Said at least one additional component is present in the composition of the present invention in a total amount that ranges from 3 to 70% w/w, more preferably from 6 to 40% w/w, and even more preferably from 10 to 25% w/w, relative to the total weight of the composition .
According to a preferred embodiment of the invention, the composition of the present invention further comprises magnesium stearate in an amount of 0.5% to 7% w/w, preferably 1% to 3.5% w/w, relative to the total weight of the composition.
According to a preferred embodiment of the invention, the composition of the present invention can further comprise silicon dioxide in an amount of 0.5% to 4% w/w, preferably 1% to 2% w/w, relative to the total weight of the composition.
According to a preferred embodiment of the invention, the composition of the present invention can further comprise sucrose palmitate in an amount of 0.5% to 7% w/w, preferably 1% to 3.5% w/w, relative to the total weight of the composition.
According to a preferred embodiment of the invention, the composition of the present invention can further
comprise a mixture of glycerides (saponifiable fats) in an amount of 0.5% to 10% w/w, preferably 2% to 7% w/w, relative to the total weight of the composition.
According to a preferred embodiment of the invention, the composition can further comprise from 0.5% to 10% w/w, preferably from 1% to 5% w/w, of sucrose ester, the percentages being expressed relative to the total weight of the composition.
The composition of the invention is for vaginal applications for the treatment of vaginal infections such as vaginitis, vaginosis, candidiasis, gonorrhoea, herpes and venereal ulcer.
In a preferred embodiment, the composition is in the form of a tablet. Alternatively, the tablet can be coated with one or more polymer materials known in the art .
With regard to the microbial population of the formulations according to the present invention, it is advantageous to use probiotic microorganisms, used individually or in a mixture, even one consisting of different genera or species.
Probiotic microorganisms are by definition microorganisms, prevalently bacteria of human origin, which are capable of inducing beneficial effects if taken regularly in a sufficient quantity and for an
adequate amount of time.
The composition of the present invention comprises at least one probiotic bacterial strain having the ability to reduce and/or eliminate the presence of pathogenic agents selected from the group comprising: Candida albicans, Candida glabrata, Candida parapsilosis, Candida krusei, Candida tropicalis, Gardnerella vaginalis, Trichomonas vaginalis, Neisseria gonorrhoeae, Escherichia coli, Herpex simplex and Haemophilus ducreyi .
Preferably, said bacterial strain belongs to at least one species selected from the group consisting of: Lactobacillus plantarum, Lactobacillus pentosus, Lactobacillus casei , Lactobacillus casei ssp. paracasei , Lactobacillus rhamnosus, Lactobacillus acidophilus, Lactobacillus delbrueckii , Lactobacillus delbrueckii ssp. bulgaricus, Lactobacillus delbrueckii ssp. delbrueckii , Lactobacillus fermentum,
Lactobacillus gasseri, Lactobacillus reuteri,
Bifidobacterium longum, Bifidobacterium bifidum, Bifidobacterium breve, Bifidobacterium animalis ssp. lactis, Bifidobacterium adolescentis, Bifidobacterium pseudocatenulatum, Bifidobacterium catenulatum or Bifidobacterium infantis .
Among the above-mentioned bacterial species, the
bacterial strains listed in Table 1 have demonstrated to be particularly preferred.
In a preferred embodiment, the bacterial strains are selected from among: Lactobacillus salivarius CRL 1328, Lactobacillus paracasei CRL 1289, Lactobacillus gasseri CRL 1259, Lactobacillus crispatus CRL 1251, Lactobacillus crispatus CRL 1266, Lactobacillus acidphilus CRL 1294, Lactobacillus paracasei LPC 00, Lactobacillus plantarum LP 02 and Lactobacillus fermentum LF 10.
In a preferred embodiment, the composition of the present invention, preferably in the form of a tablet, comprises at least two strains selected from the above- mentioned group.
In a preferred embodiment, the composition of the present invention, preferably in the form of a tablet, comprises at least three strains selected from the above-mentioned group.
In a preferred embodiment, the composition of the present invention, preferably in the form of a tablet, comprises at least four strains selected from the above-mentioned group.
The strains selected from among: Lactobacillus salivarius CRL 1328, Lactobacillus paracasei CRL 1289, Lactobacillus gasseri CRL 1259, Lactobacillus crispatus
CRL 1266 and Lactobacillus fermentum LF 10 have demonstrated to be advantageous .
In the tablets according to the invention, the microorganisms, preferably used in the form of a lyophilized culture having a viable count generally comprised from 10 to 200 billion colony forming units (CFU)/gram, are preferably present in an amount of 0.5 to 20% w/w, preferably 1 to 15% w/w, even more preferably 3 to 10% w/w, relative to the total weight of the tablet .
In one of the preferred embodiments, in order to enhance the probiotic effectiveness of the formulations according to the present invention, specific prebiotic components are introduced into the powder mixture, so that a symbiotic composition is obtained. The prebiotic component is generally a non-digestible mixture of a saccharidic nature, at least partially soluble in water or in an aqueous solution, which stimulates the growth and/or activity of one or more probiotic bacterial strains as described above. Among these prebiotic agents, dietary fibres are preferred.
Preferably, said prebiotic fibre is selected from the group comprising: fructo-oligosaccharides (FOS) , galacto-oligosaccharides (GOS) , trans- galactooligosaccharides (TOS) , xylo-oligosaccharides
(XOS) , chitosan oligosaccharides (COS) , o!-galactosides (such as raffinose and stachyose) , pectins, gums, partially hydrolyzed gums, inulin, psyllium, acacia, carob, oat or bamboo fibre, citrus fibres and, in general, fibres containing a soluble and an insoluble portion, in a variable ratio to each other.
Advantageously, said prebiotic fibre is selected from among fructo-oligosaccharides (FOS) , galacto- oligosaccharides (GOS) and xylo-oligosaccharides (XOS) . These fibres are not used by yeasts of the Candida genera, which thus lends a competitive advantage to the bacterial strains present in the composition of the present invention.
Preferably, the prebiotic component is present in the composition in an amount of up to 70% w/w, preferably comprised from 5 to 50% w/w, even more preferably from 10 to 30% w/w, relative to the total weight of the composition .
In a preferred embodiment, the composition according to the invention can contain additional active components, e.g. vitamins, minerals, vegetable extracts or other compounds with an effect that is synergistic with or complementary to that of the population of microorganisms present in the formulations according to the invention.
Preferably, said additional active components are present in the composition in an amount of up to 70% w/w, preferably comprised from 0.5 to 40% w/w, even more preferably from 1 to 20% w/w, relative to the total weight of the composition.
The combination of technological excipients of compression and effervescence according to the present invention assures an adequate cohesiveness of the powders of the tablet and brings about the desired kinetics of release of the active ingredients after the intake thereof.
The mixing of the various components, generally in powder form, can be done by adding the components in any order whatsoever, taking care to add the culture of microorganisms, preferably in the form of a lyophilizate , as the last ingredient, to prevent the possibility that an excessive mixing time may induce a mechanical shock in the wall of the bacterial cells, with consequent suffering and reduced stability of the final product.
Formulations produced in accordance with the method of the present invention are characterized by excellent flowability, a parameter that favours uniform loading of the dies (i.e. the space dedicated to accommodating the specific amount of powder to be compressed) in the
compression machines. Said compression machines typically comprise a device for loading the dies (generally represented by a hopper for delivering the powder mixture) and a metal disk of suitable radius, in whose thickness the dies themselves are obtained; these are present in variable number depending on the machine, and the step of compressing the powder takes place therein, thanks to the simultaneous, synergistic movement of two moving parts of the machine, defined as punches .
During the compression step, the lower punch defines, with its position, the volume of the die (and thus the amount of powder loaded each time) , whereas the upper punch, positioned outside the die the during loading thereof with the powder mixture, is able to be lowered during the compression step and enter into contact with the powder present in the die, thus imposing, thanks to the force exerted, a more or less marked mechanical deformation on the particles making up the powder. At the end of the compression step, the upper punch rises, thus moving away from the die, and subsequently the lower punch also rises, expelling the newly formed tablet from the die.
Said compression machines further comprise a number of devices for controlling the main operating parameters
(position of the lower punch at the start of the compression cycle, lowest position reached by the upper punch during the compression cycle, rotation speed of the disk in which the dies are present and so forth) . There exist alternative and rotary compression machines, according to the machine's overall operating modes and, consequently, the number of tablets it is able to produce in a given unit of time. Tablets can thus be produced using compression machines known in the art and using punches of varying shape, preferably double-radius round convex and oval punches.
The compression force applied during manufacture is evaluated by quantifying, with a hardness tester, the force required to break a tablet. Said force is measured in Kp (Kiloponds) (1 Kp = 9.807 Newtons (N) ) . The negative effect of compression on the population of microorganisms is manifested both when the applied forces are high, for example in tablets with a hardness of 10-12 Kp, and when they are low, such as, for example, in tablets with a hardness of 5-6 Kp . The disadvantage of using high forces is a larger reduction in the number of microorganisms, whereas with low forces a reduced cohesion of the tablet is generally obtained. Advantageously, the tablets of the present invention show a compression force comprised from 5 to
12 Kp, depending on the type of tablet it is desired to obtain .
In manufacturing tests on tablets containing L. paracasei LPC 00, L. acidphilus LA 02 and L. salivarius CRL 1328 (table 2) , the Applicant obtained very positive results both in terms of survival and in terms of subsequent stability.
In particular, a mortality ranging from 4 to 15% was observed when the compression force applied was such as to obtain tablets with a hardness comprised from 5 to 6 Kp and a mortality ranging from 10 to 25% when the compression force applied was such as to obtain tablets with a hardness comprised from 10 to 12 Kp. Another advantage of the method according to the invention is that this enables the production of sufficiently cohesive tablets even at low compression forces, for example tablets with a hardness of 5-6 Kp .
The tablets prepared in accordance with the present invention were tested in order to evaluate the disintegration time according to the European Pharmacopoeia, Ed. X, ref . 2.9.1. The friability of uncoated tablets was tested in accordance with ref. 2.9.7 and the resistance to crushing according to ref. 2.9.8.
Table 2 shows an example of a composition in accordance
with the invention.
Table 3 shows the mortality data for the probiotic bacteria (composition shown in table 2) according to the different pressures exerted and the stability of the tablets (expressed as the half-life of the bacterial load) after 2 years of storage thereof at 25 °C. The tablets obtained with the formulations according to the invention had a thickness of about 7.7 mm in the case of tablets with a high degree of hardness and about 8.4 mm in the case of tablets with a low degree of hardness.
In table 3, stability is expressed as the half-life of the probiotic component of the formulation, i.e. the time that elapses before the initial viable cell count is halved.
The following were also measured:
(1) Number of viable cells lxlO9 CFU/g of powder expected at time zero
(2) Number of viable cells lxlO9 CFU/g of powder found at time zero
(3) % mortality due to compression
(4) Number of viable cells lxlO9 CFU/tablet after 2 years at 25 °C
(5) half-life in days
The above data were obtained by evaluating the number
of probiotic bacteria present in the powder composition and in the composition after compression using the viable plate count method, in accordance with methods known to persons skilled in the art.
In the case of the powder composition, an amount comprised from 1 to 4 grams of sample was resuspended in a suitable volume of a sterile liquid medium, generally a 0.85% sodium chloride saline solution, to which bacteriological peptone is added in a proportion of 1 g/litre.
After dissolution of the powder and subsequent homogenization with a suitable piston-driven instrument, the number of cells/ml is reduced by means of subsequent base 10 serial dilutions.
In practice, 1 ml of the most concentrated dilution is transferred each time, using a sterile pipette, into 9 ml of diluent; this operation is carried out a number of times that is sufficient to bring the quantity of microorganisms present per ml of diluent to a number comprised from 10 to 300, so that following their transfer into a Petri dish and the addition of a suitable agarized culture medium they form separate, and thus countable, colonies.
In the case of the tablets, a protocol was observed which provides for prior crushing of three to five
tablets and continuance of the analysis as described above for the powder composition.
The experimental data demonstrate a low mortality both in tablets with a high degree of hardness (approximately 16.4% of the initial population) and in those with a lower degree of hardness (approximately 8.2% of the initial population) . A further advantageous aspect of the composition of the present invention is improved stability, over time, of the probiotic microorganisms (probiotic component) present therein compared to the typical stability of a prior art formulation. This advantage is due to the use of a mixture containing [microcrystalline cellulose : arabinogalactan] in a ratio by weight preferably comprised from 1:1 to 3:1. This mixture is capable of greatly limiting the mechanical damage caused to the probiotic bacterial cells by the compression step and allows tablets to be obtained with no occurrence of capping.
The Applicant has found that the half-lives of the probiotic component in the powder composition and in the tablets of varying hardness manufactured with a formulation according to the invention are very similar, demonstrating the fact that the technological components used are able to minimize the mechanical
damage caused by the compression step.
Advantageously, the tablets according to the invention display a high rate of survival of the probiotic microorganisms even following the compression step. A further advantageous aspect is the ability to release carbon dioxide as the tablet disintegrates, resulting in the creation of an anaerobic or microaerophilic environment particularly favourable to vaginal colonization by the probiotics used.
The effervescence is further capable of assuring an adequate and homogeneous distribution of the probiotic active ingredient in the vaginal environment by increasing the effectiveness of colonization.
The compositions of the present invention make it possible to obtain tablets containing probiotic microorganisms which are effective and stable over time, even at non-refrigerated temperatures, because the components forming the composition have been chosen and selected with the aim of reducing mortality due to mixing and mortality due to compression without impairing the cohesion of the powder. For this reason, the composition of the present invention, preferably in the form of a tablet, contains neither adipic acid nor ascorbic acid, the amount of the salt of the carbonate or bicarbonate anion present is lower than 15% by
weight, relative to the total weight of the composition, and a mixture of microcrystalline cellulose and arabinogalactan is used instead of corn starch .
The Applicant arrived at these results starting off from a composition that demonstrated to be inadequate (table 4) .
The composition of table 4 shows: 80.8% mortality due to mixing, 40.5% mortality due to compression and an overall mortality (mixing + compression) of 88.6%.
The composition of table 4 shows marked mortality already at the powder level, prior to compression. The pH of dissolution (in saline in a 1:10 ratio) is not a problem, as it is equal to 5.22 for the first formulation and 5.53 for the second one.
Adipic acid was found to be toxic. But this toxicity accounts for only a certain portion of the mortality observed (about 60% of the total mortality) . Ascorbic acid was found to be toxic. But this toxicity accounts for a further portion of mortality. Removing ascorbic acid from the composition of table 4 reduces mortality from 73.8 to 26.7%. Adipic acid on its own is in any case toxic (45.8% at pH 4.24); its toxicity seems to increase in the presence of ascorbic acid. Ascorbic acid thus seems to show a toxicity synergistic with
that of adipic acid.
However, it is important to note that the sum of the toxicity due to adipic acid and ascorbic acid does not account for the overall mortality observed.
For this reason, the Applicant investigated the presence of other components capable of having a toxic effect with the aim of justifying the total toxicity observed in the composition of table 4.
Therefore, some other component (apart from pH, which was already considered) must justify the remaining toxicity in the same manner as adipic and ascorbic acid .
A degree of mortality was ascertained to be due to osmotic pressure, given by the bicarbonate present in an excessive amount. This mortality revealed to be equal to about 20%. Adipic acid, ascorbic acid and the osmotic effects mediated by bicarbonate are responsible for the toxicity observed. Bicarbonate in itself is not toxic: it becomes so only because of the osmotic effect .
Therefore, a composition (table 5) was prepared without adipic acid and ascorbic acid and with an amount of bicarbonate anion (e.g. sodium bicarbonate) less than 15% by weight, relative to the total weight of the composition .
For example, 84 mg of sodium bicarbonate constitutes 1 millimole and the C02 that is released occupies a total volume of 25.4 ml at 37°C and under atmospheric pressure. The quantity of citric acid was chosen in such a manner as to ensure complete release of the C02 from the sodium bicarbonate at the pH values observed after the tablet's dissolution.
The composition of table 5 showed problems when subjected to a compression step in order to prepare the tablets .
The powder (table 5) showed poor cohesive properties due to the use of corn starch in a formulation with a low moisture content. All of the tablets output by the compression machine were capped even before being passed through the deduster.
Following this compression test the Applicant proceeded to replace corn starch with a mixture containing [microcrystalline cellulose : arabinogalactan] in a ratio by weight preferably comprised from 1:1 to 3:1.
Claims
1. An effervescent composition in solid form comprising :
- an acid-base system comprising an organic acid and a salt of the carbonate and/or bicarbonate anion; said salt being present in an amount comprised from 1 to 15% by weight, relative to the total weight of the composition,
- a mixture comprising microcrystalline cellulose and arabinogalactan,
- at least one probiotic bacterial strain having the ability to reduce and/or eliminate the presence of pathogenic agents selected from the group comprising: Candida albicans, Candida glabrata, Candida parapsilosis, Candida krusei, Candida tropicalis, Gardnerella vaginalis, Trichomonas vaginalis, Neisseria gonorrhoeae, Escherichia coli, Herpes simplex and Haemophilus ducreyi ,
said composition being for use in vaginal applications for the treatment of vaginal infections.
2. The composition for use in accordance with claim 1, wherein said composition is in the form of a tablet, ovule, lozenge or granules.
3. The composition for use according to claim 1 or 2 , wherein the organic acid is selected from the group consisting of citric acid, malic acid, tartaric acid, fumaric acid, lactic acid and mixtures thereof; preferably, the organic acid is citric acid.
4. The composition for use according to any one of claims 1-3, wherein the salt of the carbonate and/or bicarbonate anion is selected from the group consisting of: sodium carbonate, potassium carbonate, calcium carbonate, magnesium carbonate, sodium glycine carbonate, sodium bicarbonate, potassium bicarbonate, calcium bicarbonate, magnesium bicarbonate, sodium lactate, potassium lactate, carbonate lactate and mixtures thereof; preferably, it is a salt of the bicarbonate anion.
5. The composition for use according to claim 5, wherein the salt of the carbonate and/or bicarbonate anion is present in an amount comprised from 3 to 13% by weight, relative to the total weight of the composition; preferably in an amount comprised from 4 to 12% by weight, relative to the total weight of the composition; even more preferably in an amount comprised from 5 to 10% by weight, relative to the total weight of the composition.
6. The composition for use according to any one of claims 1-5, wherein the acid-base system consists of sodium bicarbonate and citric acid, and wherein the sodium bicarbonate is present in an amount comprised from 3 to 13% by weight, relative to the total weight of the composition; preferably in an amount comprised from 4 to 12% by weight, relative to the total weight of the composition; even more preferably in an amount comprised from 5 to 10% by weight, relative to the total weight of the composition.
7. The composition for use according to claim 1, wherein said microcrystalline cellulose and arabinogalactan are present in a ratio by weight comprised from 1:1 to 3:1.
8. The composition for use according to any one of claims 1-7, wherein said at least one probiotic bacterial strain belongs to at least one species selected from the group consisting of: Lactobacillus plantarum, Lactobacillus pentosus, Lactobacillus casei, Lactobacillus casei ssp. paracasei , Lactobacillus rhamnosus, Lactobacillus acidophilus, Lactobacillus delbrueckii , Lactobacillus delbrueckii ssp. bulgaricus, Lactobacillus delbrueckii ssp. delbrueckii , Lactobacillus fermentum, Lactobacillus gasseri, Lactobacillus reuteri , Bifidobacterium longum, Bifidobacterium bifidum, Bifidobacterium breve, Bifidobacterium animalis ssp. lactis, Bifidobacterium adolescentis, Bifidobacterium pseudocatenulatum,
Bifidobacterium catenulatum or Bifidobacterium infantis; said at least one bacterial strain is preferably selected from among: Lactobacillus salivarius CRL 1328, Lactobacillus paracasei CRL 1289, Lactobacillus gasseri CRL 1259, Lactobacillus crispatus CRL 1251, Lactobacillus crispatus CRL 1266, Lactobacillus acidophilus CRL 1294, Lactobacillus paracasei LPC 00, Lactobacillus plantarum LP 02 e Lactobacillus fermentum LF 10.
9. The composition for use according to any one of claims 1-8, wherein said composition is for the treatment of vaginitis, vaginosis, candidiasis, gonorrhoea, herpes and venereal ulcer.
10. An effervescent tablet in solid form comprising:
- an acid-base system comprising sodium bicarbonate and citric acid; said bicarbonate being present in an amount comprised from 1 to 15% by weight, relative to the total weight of the composition,
- a mixture comprising microcrystalline cellulose and arabinogalactan in un ratio by weight comprised from 1:1 to 3:1,
- at least one probiotic bacterial strain having the ability to reduce and/or eliminate the presence of pathogenic agents selected from the group comprising: Candida albicans, Candida glabrata, Candida parapsilosis, Candida krusei, Candida tropicalis, Gardnerella vaginalis, Trichomonas vaginalis, Neisseria gonorrhoeae, Escherichia coli, Herpes simplex and Haemophilus ducreyi, said composition being for use in vaginal applications for the treatment of vaginal infections .
Priority Applications (17)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| UAA201309615A UA114888C2 (en) | 2011-01-28 | 2012-01-24 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections |
| MX2013008547A MX347165B (en) | 2011-01-28 | 2012-01-24 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections. |
| US13/982,255 US9492377B2 (en) | 2011-01-28 | 2012-01-24 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections |
| RU2013137656/15A RU2587717C2 (en) | 2011-01-28 | 2012-01-24 | Effervescent composition in solid form for use in vaginal applications for treating vaginal infections |
| CN201280015994.3A CN104519866A (en) | 2011-01-28 | 2012-01-24 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections |
| KR1020137022730A KR101913797B1 (en) | 2011-01-28 | 2012-01-24 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections |
| EP12706669.4A EP2667849B1 (en) | 2011-01-28 | 2012-01-24 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections |
| NZ614002A NZ614002B2 (en) | 2012-01-24 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections | |
| BR112013018953-3A BR112013018953B1 (en) | 2011-01-28 | 2012-01-24 | EFERVESCENT COMPOSITION IN SOLID FORM FOR USE IN VAGINAL APPLICATIONS FOR THE TREATMENT OF VAGINAL INFECTIONS |
| ES12706669T ES2751416T3 (en) | 2011-01-28 | 2012-01-24 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections |
| DK12706669T DK2667849T3 (en) | 2011-01-28 | 2012-01-24 | RUSHING COMPOSITION IN SOLID FORM FOR VAGINAL USE TO TREAT VAGINAL INFECTIONS |
| AU2012210296A AU2012210296B2 (en) | 2011-01-28 | 2012-01-24 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections |
| PL12706669T PL2667849T3 (en) | 2011-01-28 | 2012-01-24 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections |
| JP2013550962A JP5992446B2 (en) | 2011-01-28 | 2012-01-24 | Foam composition in solid form for use in vaginal applications to treat vaginal infections |
| TNP2013000310A TN2013000310A1 (en) | 2011-01-28 | 2013-07-23 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections |
| MA36208A MA34926B1 (en) | 2011-01-28 | 2013-08-27 | EFFERVESCENT COMPOSITION IN SOLID FORM FOR USE IN VAGINAL APPLICATIONS FOR THE TREATMENT OF VAGINAL INFECTIONS |
| US15/265,706 US20170014335A1 (en) | 2011-01-28 | 2016-09-14 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ITMI2011A000107A IT1403661B1 (en) | 2011-01-28 | 2011-01-28 | EFFERVESCENT COMPOSITION IN THE SOLID FORM FOR USE IN VAGINAL APPLICATIONS FOR THE TREATMENT OF VAGINAL INFECTIONS. |
| ITMI2011A000107 | 2011-01-28 | ||
| IT000316A ITMI20110316A1 (en) | 2011-01-28 | 2011-03-01 | EFFERVESCENT COMPOSITION IN SOLID FORM FOR USE IN VAGINAL APPLICATIONS FOR THE TREATMENT OF VAGINAL INFECTIONS. |
| ITMI2011A000316 | 2011-03-01 |
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| US15/265,706 Division US20170014335A1 (en) | 2011-01-28 | 2016-09-14 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections |
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| PCT/IB2012/000095 WO2012101500A1 (en) | 2011-01-28 | 2012-01-24 | Effervescent composition in solid form for use in vaginal applications for the treatment of vaginal infections |
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| EP (1) | EP2667849B1 (en) |
| JP (1) | JP5992446B2 (en) |
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Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4853211A (en) * | 1982-03-05 | 1989-08-01 | Eisai Co., Ltd. | Stable, effervescent vaginal suppositories |
| EP0956858A1 (en) * | 1998-04-30 | 1999-11-17 | Renata Maria Anna Cavaliere Vesely | Pharmaceutical compositions containing lactobacilli for treatment of vaginal infections |
| WO2004089278A2 (en) * | 2003-04-09 | 2004-10-21 | Dolhay Klinika Egészségügyi Kft. | Sexual hygienic composition |
| WO2008065492A2 (en) * | 2006-11-28 | 2008-06-05 | Probiotical S.P.A. | A composition for the administration of biologically active principles in gynaecologic and rectal field and uses thereof |
Family Cites Families (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3819838A (en) | 1970-08-04 | 1974-06-25 | Bush Boake Allen Ltd | Encapsulated flavoring composition |
| JPS53121949A (en) | 1977-03-31 | 1978-10-24 | Yakult Honsha Kk | Production of drink and food containing bifidobacterium cells |
| DE2757370A1 (en) | 1977-12-22 | 1979-07-05 | Bayer Ag | GAS-TIGHT PLASTIC-ALUMINUM COMPOSITE FILMS |
| CH637297A5 (en) | 1978-12-05 | 1983-07-29 | Nestle Sa | MICROBALL COMPRISING A MICROORGANISM AND ITS MANUFACTURING METHOD. |
| US4670272A (en) | 1985-11-08 | 1987-06-02 | Frito-Lay, Inc. | Thermostable creme |
| US5343672A (en) | 1992-12-01 | 1994-09-06 | Scherer Ltd R P | Method for manufacturing freeze dried dosages in a multilaminate blister pack |
| CN1211188A (en) * | 1996-02-14 | 1999-03-17 | 普罗克特和甘保尔公司 | Urogenital and intestinal compositions |
| EP0845350A1 (en) | 1996-11-29 | 1998-06-03 | Alusuisse Technology & Management AG | Cold formable laminated film |
| ES2258841T3 (en) | 1998-04-01 | 2006-09-01 | Ganeden Biotech, Inc. | PROCEDURES TO REDUCE CHOLESTEROL WITH SPACES OF BACILLUS COAGULANS, SYSTEMS AND ASSOCIATED COMPOSITIONS. |
| RU2150268C1 (en) | 1998-12-25 | 2000-06-10 | Быков Валерий Алексеевич | Lactobacterium-containing suppository for treatment of patient with vagina dysbacteriosis |
| IT1309427B1 (en) | 1999-05-28 | 2002-01-23 | Mendes S U R L | DIETARY OR PHARMACEUTICAL COMPOSITION USEFUL FOR THE PREVENTION OR TREATMENT OF HYPEROXIDE AND ITS USE |
| CN1234373C (en) * | 2000-09-28 | 2006-01-04 | 信谊药厂 | Medicinal preparation containing lactobacillus acidophilus and preparation process thereof |
| CA2559596A1 (en) | 2003-03-13 | 2004-11-25 | Universite De Moncton (Bureau De Soutien A L'innovation) | Antioxidant producing bacterium and uses thereof |
| US20040185032A1 (en) | 2003-03-18 | 2004-09-23 | David Burrell | Compositions and methods for treating colic |
| DK1675481T3 (en) | 2003-10-24 | 2009-01-19 | Nutricia Nv | Synbiotic preparation for children |
| ATE289514T1 (en) | 2003-11-03 | 2005-03-15 | Peter-Hansen Volkmann | VAGINAL CARE COMPOSITION |
| GB0330009D0 (en) * | 2003-12-24 | 2004-01-28 | Ferrosan As | Probiotic tablet formulations |
| GB0405406D0 (en) | 2004-03-10 | 2004-04-21 | Edko Pazarlama Tanitim Ltd Sti | Anti-vaginitis compositions |
| DE602004027120D1 (en) | 2004-05-25 | 2010-06-24 | Cognis Ip Man Gmbh | Oral and / or topical preparations |
| EP1600060A1 (en) | 2004-05-25 | 2005-11-30 | Cognis IP Management GmbH | Oral and/or topical compositions comprising prebiotics and fatty acid |
| CN101039687A (en) | 2004-08-05 | 2007-09-19 | 安尼德拉尔有限公司 | Folic acid producing bifidobacterium bacterial strains, formulations and use thereof |
| US20060039973A1 (en) * | 2004-08-19 | 2006-02-23 | Mary Aldritt | Effervescent composition including water soluble dietary fiber |
| US7468182B2 (en) | 2004-10-27 | 2008-12-23 | North Carolina State University | Lactobacillus acidophilus nucleic acids and uses thereof |
| KR100661032B1 (en) | 2005-04-19 | 2006-12-22 | 주식회사한국야쿠르트 | Composition for Improving Liver Function, Reduction of Serum Ethanol Level, and Antioxidation |
| WO2007100765A2 (en) | 2006-02-28 | 2007-09-07 | Childrens Memorial Hospital | Lysozyme-modified probiotic components and uses thereof |
| RU2318523C2 (en) | 2006-03-13 | 2008-03-10 | Лев Давидович Раснецов | Antibacterial agent |
| WO2007125558A1 (en) | 2006-05-03 | 2007-11-08 | Anidral S.R.L. | Symbiotic composition comprising non-digestible polysaccharides and bifidobacteria which metabolize them and its uses |
| ITMI20061841A1 (en) | 2006-09-27 | 2008-03-28 | Mofin S R L | MICROBIAL LIQUID CULTIVATIONS WITH HIGH STABILITY AND FERMENTATIVE ACTIVITY |
| US20080175899A1 (en) | 2007-01-19 | 2008-07-24 | Ross Mairi R | Formulation for promoting sinus health in nasal cavities |
| US20080187628A1 (en) | 2007-02-02 | 2008-08-07 | Champion Melinda L | Water-Soluble, Quick-Dissolve Flavor Tablets |
| PL210465B1 (en) | 2007-06-04 | 2012-01-31 | Inst Biotechnologii Surowic I Szczepionek Biomed Społka Akcyjna | Composition of strains type Lactobacillus and application of the composition of strains type Lactobacillus |
| WO2008153377A1 (en) | 2007-06-15 | 2008-12-18 | N.V. Nutricia | Nutrition with non-viable bifidobacterium and non-digestible oligosaccharide |
| DE102008023952A1 (en) | 2008-05-16 | 2009-12-03 | Alcan Technology & Management Ag | Packaging cover film, container, packaging and packaging product unit |
| BRPI0917172A2 (en) | 2008-08-28 | 2015-08-04 | Chr Hansen As | Bacterial composition |
| US9283252B2 (en) | 2008-09-30 | 2016-03-15 | Meiji Co., Ltd. | Lactic acid bacterium having high oxalic acid decomposition ability |
| RU2011139211A (en) | 2009-03-05 | 2013-04-10 | Пробиотикал С.п.А. | BACTERIAL STRAINS HAVING HIGH ANTI-INFLAMMATORY ACTIVITY |
| IT1400821B1 (en) | 2009-03-09 | 2013-07-02 | Probiotical Spa | OIL SUSPENSION CONTAINING PROBIOTIC BACTERIA FOR PEDIATRIC USE |
| FI20095550A0 (en) | 2009-05-19 | 2009-05-19 | Bayer Schering Pharma Oy | Vaginal delivery system |
| IT1397566B1 (en) | 2009-05-27 | 2013-01-16 | Probiotical Spa | LACTOBACILLUS PENTOSUS MANUFACTURER OF BACTERIOCINES, FOOD AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME AND ITS USE |
| IN2012DN00713A (en) | 2009-07-27 | 2015-05-22 | Nestec Sa | |
| WO2011012932A1 (en) | 2009-07-30 | 2011-02-03 | Compagnie Gervais Danone | Use of coated sterol or stanol particles for the preparation of food compositions having a low fat content and being essentially emulsifier-free |
| IT1398553B1 (en) | 2010-03-08 | 2013-03-01 | Probiotical Spa | COMPOSITION INCLUDING PROBIOTIC BACTERIA FOR THE TREATMENT OF PATHOLOGIES ASSOCIATED WITH THE ALTERATION OF THE IMMUNE SYSTEM. |
| WO2012001440A1 (en) | 2010-06-28 | 2012-01-05 | Probiotical S.P.A. | Use of lactobacilli inhibiting gas producing coliform bacteria isolated from infants affected by colic |
| IT1403661B1 (en) | 2011-01-28 | 2013-10-31 | Probiotical Spa | EFFERVESCENT COMPOSITION IN THE SOLID FORM FOR USE IN VAGINAL APPLICATIONS FOR THE TREATMENT OF VAGINAL INFECTIONS. |
| ITMI20110791A1 (en) | 2011-05-09 | 2012-11-10 | Probiotical Spa | BACTERIA OF BACTERIA ABLE TO METABOLIZE THE OXALATES. |
| ITRM20110477A1 (en) | 2011-09-09 | 2013-03-10 | Giovanni Mogna | COMPOSITION INCLUDING N-ACETYLCISTEIN AND / OR LYSOZYME MICROINCAPSULATE GASTROPROTECT IN ASSOCIATION WITH PROBIOTIC BACTERES ABLE TO RESTORE THE BARRIER EFFECT OF THE STOMACH THAT IS LOST DURING THE PHARMACOLOGICAL TREATMENT OF |
| ITRM20110475A1 (en) | 2011-09-09 | 2013-03-10 | Probiotical Spa | BACTERIA OF LACTIC AND / OR BIFIED BACTERIA BACTERIA, OPTIONALLY ADDED TO N-ACETYLCISTEIN AND / OR LYSOZYME MICROINCAPSULATE GASTROPROTETTO, HAVING INHIBITION ACTIVITIES / REDUCTION OF THE GROWTH OF DIFFERENT E.COLI BIOTYPES, INCLUDING E.COLI O157: H7 E |
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- 2013-07-26 CL CL2013002148A patent/CL2013002148A1/en unknown
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- 2013-08-20 EC ECSP13012844 patent/ECSP13012844A/en unknown
- 2013-08-27 MA MA36208A patent/MA34926B1/en unknown
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4853211A (en) * | 1982-03-05 | 1989-08-01 | Eisai Co., Ltd. | Stable, effervescent vaginal suppositories |
| EP0956858A1 (en) * | 1998-04-30 | 1999-11-17 | Renata Maria Anna Cavaliere Vesely | Pharmaceutical compositions containing lactobacilli for treatment of vaginal infections |
| WO2004089278A2 (en) * | 2003-04-09 | 2004-10-21 | Dolhay Klinika Egészségügyi Kft. | Sexual hygienic composition |
| WO2008065492A2 (en) * | 2006-11-28 | 2008-06-05 | Probiotical S.P.A. | A composition for the administration of biologically active principles in gynaecologic and rectal field and uses thereof |
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