COMBINED MULTISTAGE MICROBIAL PREPARATIONS AND METHOD OF THEIR APPLICATION

Abstract

Combined multistage microbial preparations for enhancement of the biological skin barrier and maintenance of healthy skin microbiota are disclosed. The preparations are useful in chronic problems associated with dysbiosis such as atopic dermatitis, acne, rosacea and vitiligo or acute problems caused by damage of the skin such as burns, cuts and contusions.

Claims

1. A method for treating dermatological conditions, comprising applying a multistage, microbial cosmetic preparation to a patient in need thereof, the preparation comprising four compositions for sequential application to the patient's skin, wherein the first stage composition comprises active substances that dissolve biofilms formed by skin pathogens and suppress the viability of the pathogenic microorganisms released from the biofilms, the active substances being cell-free extracts or lysates prepared from any of the commensal skin microorganisms selected from the bacteria of the genera Staphylococcus, Streptococcus, Corynebacterium, Propionibacterium and Proteobacterium, and any of the environmental microorganisms selected from the genera Trichoderma, Pythium, Nitrosomonas and Mycobacterium; the second stage composition comprises active substances that reduce inflammation and restore the biological skin barrier, the active substances being cell-free extracts or lysates prepared from any of the commensal skin microorganisms selected from the bacteria of the genera Staphylococcus, Streptococcus, Corynebacterium, Propionibacterium and Proteobacterium; the third stage composition comprises active substances that restore the normal skin microflora, the active substances being cell-free extracts or lysates prepared from any environmental bacteria selected from the genera Nitrosomonas and Mycobacterium; and the fourth stage composition comprises active substances that nourish skin and further supporting the colonization by commensal skin microorganisms while simultaneously suppressing the pathogens, in which the active substance is at least one compound selected from the group consisting of: xylitol, famesol, L-arginine, safflower oil, evening primrose oil, hemp oil, rapeseed oil, wheat germ oil, lactate, glycine, fructose, niacinamide, inositol, magnesium aspartate, zinc gluconate, and copper gluconate.

2. The method according to claim 1, wherein the method calms and regenerates irritated or burned skin and/or strengthens the biological component of the skin barrier and maintains normal skin microflora.

3. The method according to claim 1, wherein the dermatological conditions originate from skin imbalances, diseases or injuries.

4. The method according to claim 1, wherein the dermatological condition is selected from atopic dermatitis, acne, rosacea, psoriasis, vitiligo or skin damage due to the mechanical injury or burning.

5. The method according to claim 1, wherein the application is done in four subsequent periods, wherein in the first period the first stage combination is applied, in the second period the second stage combination is applied, in the third period the third stage combination is applied and in the fourth period the fourth stage combination is applied, wherein each of the first, second, and third period lasts for one to two weeks and the fourth period lasts for one to six weeks.

6. The method according to claim 5, wherein the application is done at least once a day by spraying or spreading of the application dose of the corresponding stage composition on affected sites or around the affected sites, or in case of very sensitive foci only in the surrounding of the affected sites.

7. A method of the cosmetic treatment of the skin characterized in that the first, the second, the third and the fourth composition are sequentially applied onto the skin in four consecutive periods, wherein in the first period the first composition is applied, in the second period the second composition is applied, in the third period the third composition is applied and in the fourth period the fourth composition is applied, wherein each of the first, second, and third period lasts for one to two weeks and the fourth period lasts for one to six weeks; and the first composition comprises Staphylococcus epidermidis and Pythium nunn cell-free extracts or lysates; the second composition comprises Staphylococcus epidermidis cell-free extract or lysate; the third composition comprises Nitrosomonas europaea cell-free extract or lysate; and the fourth composition comprises one or more of xylitol, hemp oil, rapeseed oil, glycerine, urea, glyceryl stearate citrate, olive oil, wheat germ oil, evening primrose oil, phenoxyethanol, polyacrylate crosspolymer-6, lavender extract, ethylhexylglycerin, Lactil, Sepitonic, D,L-tocopherol and amaranth A12385.

8. The method according to claim 7, wherein Staphylococcus epidermidis and Pythium nunn cell-free extracts or lysates comprise proteinase, laminarinase, cellulase and chitinase activities; Staphylococcus epidermidis cell-free extract or lysate comprises lipoteichoic acid, antimicrobial SH-lantibiotic peptides, antimicrobial γ-modulin and Esp proteinase; and Nitrosomonas europaea cell-free extract or lysate comprises low-molecular weight substances and protein complex comprising membrane complex oxidizing urea and producing nitric oxide.

9. The method according to claim 8, wherein Staphylococcus epidermidis and Pythium nunn cell-free extracts or lysates comprise 0.23 mU of proteinases, 0.56 mU of laminarinases, 0.27 mU of cellulases and 0.47 mU chitinases per 1 ml; Staphylococcus epidermidis cell-free extract or lysate comprises 10 μg of lipoteichoic acid, 12 μg of antimicrobial SH-lantibiotic peptides, 38 μg of the antimicrobial γ-modulin and 5 μg of Esp proteinase per 1 ml; Nitrosomonas europaea cell-free extract or lysate comprises 60 μg of the substance mixture from Nitrosomonas europea per 3 ml application dose, the substance mixture consisting of about 45 μg of low-molecular weight substances and about 15 μg of protein complex comprising membrane complex oxidizing urea and producing nitric oxide; and the fourth composition contains 70.137% of water, 5.0% of xylitol, 5.0% of hemp oil, 5.0% of rapeseed oil, 4.0% of glycerine, 4.0% of urea, 2.0% of glyceryl stearate citrate, 1.0% of olive oil, 1.0% of wheat germ oil, 1.0% of evening primrose oil, 0.9% of phenoxyethanol, 0.25% of polyacrylate crosspolymer-6, 0.2% of lavender extract, 0.1% of ethylhexylglycerin, 0.1% of Lactil, 0.1% of Sepitonic, 0.01% of D,L-tocopherol, and 0.003% of amaranth A12385, wherein % is weight %.

10. The method according to any claim 7, wherein each of the compositions is applied at least once a day, during the corresponding period by spraying or spreading the corresponding composition on the affected sites or around the affected sites on the skin.

11. The method according to any claim 8, wherein each of the compositions is applied at least once a day, during the corresponding period by spraying or spreading the corresponding composition on the affected sites or around the affected sites on the skin.

12. The method according to any claim 9, wherein each of the compositions is applied at least once a day, during the corresponding period by spraying or spreading the corresponding composition on the affected sites or around the affected sites on the skin.

13. The method according to any claim 7, wherein each of the compositions is applied at least twice a day, during the corresponding period by spraying or spreading the corresponding composition on the affected sites or around the affected sites on the skin.

14. The method according to any claim 8, wherein each of the compositions is applied at least twice a day, during the corresponding period by spraying or spreading the corresponding composition on the affected sites or around the affected sites on the skin.

15. The method according to any claim 9, wherein each of the compositions is applied at least twice a day, during the corresponding period by spraying or spreading the corresponding composition on the affected sites or around the affected sites on the skin.

16. The method according to any claim 14, wherein each of the compositions is applied in the morning and again in the evening.

17. The method according to any claim 15, wherein each of the compositions is applied in the morning and again in the evening.

18. The method according to any claim 16, wherein each of the compositions is applied in the morning and again in the evening.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0025] The invention is further explained using the Examples and the enclosed drawings, wherein

[0026] FIGS. 1A-1B show the description of the preparation of the active substances for cleaning and disruption in the first stage, specifically

[0027] FIG. 1A shows the analyses of the individual fractions of proteins secreted by bacterium S. epidermidis strain ATCC_12228 after their concentration and transfer into the conservation buffer for the introduction into the formulation, wherein lanes 1 and 10 show the molecular standards and lanes 2 to 9 show eight different independent batches;

[0028] FIG. 1B shows the analysis of proteins secreted by the environment microorganism P. nunn strain CBS 808.96 after their concentration and transfer into the conservation buffer for the introduction into the formulation, wherein lanes 1 and 10 show the molecular standards and lanes 2 to 9 show eight different protein batches;

[0029] FIGS. 2A-2E show the method of preparation and concentration of active substance used for the calming of the immune system in the second stage, specifically

[0030] FIG. 2A shows the scheme for the fractionation of bacterial lysates from S. epidermidis strain ATCC_12228 using ammonium sulfate precipitation, after which the soluble compounds in the supernatant (“sup”) were further separated on phenyl-Sepharose® column, while the substances in the sediment (“sed”) were further separated on octadecyl silica column. The fractions separated according to these schemes are abbreviated as “F”.

[0031] FIGS. 2B to 2E show the electrophoretic and immunochemical analyses of the separated compound analyzed by 20% polyacrylamide electrophoresis in the presence of sodium dodecyl sulfate, wherein FIG. 2B and FIG. 2C show the compounds recovered from the supernatant after ammonium sulfate precipitation, where FIG. 2C specifically relates to the lipoteichoic acid (LTA), while FIG. 2D and FIG. 2E show the compounds recovered in the sediment after ammonium sulfate precipitation, where FIG. 2E specifically relates to the lantibiotic type antimicrobial peptides. The approximate molecular mass of the analyzed compounds is indicated at the right side of the gel. The fractions F1 and F2 not retained on the octadecylsilica column were also analyzed in 12% polyacrylamide/sodium dodecyl sulfate gels, wherein in FIG. 2D the band corresponding to Esp proteinase is marked by an arrow.

[0032] FIGS. 3A-3D show the laboratory tests of the antimicrobial efficiency of the prepared active substances towards the critical pathogens causing problems at the skin and mucosal surfaces, specifically

[0033] FIG. 3A shows the disc test for antimicrobial efficiency towards the pathogenic bacteria S. aureus strain ATCC_6538 wherein the substances applied onto the individual discs were as follows: in the first row from left to right the tested substances for the first stage SEF2K1 sequentially diluted 10×, 10.sup.2×, 10.sup.3× and 10.sup.4×, in the second row the tested substances for the second stage SELY diluted 10.sup.2×, 10.sup.3×, 10.sup.4× and 10.sup.5×, in the third row the tested substances for the third stage NIE1 diluted 10×, 10.sup.2×, 10.sup.3× and 10.sup.4×, the last row contained the positive control antibiotic tetracycline with a concentration of 0.5 μg/ml, 1 μg/ml, 2 μg/ml and 4 μg/ml. 5 μl of the tested substances were applied to all discs.

[0034] FIG. 3B shows the quantitative minimum inhibitory concentration (MIC) test for four different batches of the substances for the first stage SEF2 (samples 1 to 4), four different batches of the substances for the second stage SELY (samples 5 to 8), and four different batches NIE1, NIE2, NIE3 and NIE4 of extracts from the industrial wastewater cleaning bacterial communities containing Nitrosomonas species (samples 9 to 12) used for the third stage.

[0035] FIG. 3C and FIG. 3D shows the disc efficiency tests of the active compounds towards the pathogenic yeast Candida albicans strain ATCC_10231, wherein the Petri dish shown in FIG. 3C was incubated for 24 h at 30° C. and the same Petri dish shown in FIG. 3D was incubated for 48 h at 30° C. The volumes, compounds, and concentrations applied were identical to FIG. 3A except in the last row in which the chemical antifungal enilconazole was applied in concentrations 1 mg/ml, 2 mg/ml, 4 mg/ml and 8 mg/ml.

[0036] FIGS. 4A-4D show the results of the laboratory test of inhibition/disruption of biofilm formed by S. aureus ATCC_6538, specifically

[0037] FIG. 4A shows an example of the microtiter plate after incubation of the formed biofilm with the tested compounds for 24 h at 30° C., washing, and the detection of the remaining biofilm using crystal violet. Individual compound were tested in quadruplicates applied in 2×2 well squares in the neighbouring wells.

[0038] FIG. 4B shows the averaged values of the quadruplicate assessments as shown in FIG. 4A, wherein the biofilm intensity was measured in the conservation buffer only (C), or in the conservation buffer containing the compounds PNF1K1 secreted by P. nunn (PN), or in the conservation buffer containing the compounds SEF2K1 secreted by S. epidermidis (SE), or in the conservation buffer containing the S. epidermidis lysate SELY (LY), or in the conservation buffer containing the indicated combinations of the tested compounds (PNSELY, PNSE) using the tenfold serial dilutions (lx, 10×, 100×, 1000×).

[0039] FIG. 4C presents data identical to those in FIG. 4B but expressed as the % inhibition of the biofilm formation based on the formula % inhibition=[(A.sub.595 experiment−A.sub.595 background)/(A.sub.595 control−A.sub.595 background)]×100,

[0040] FIG. 4D shows the viability of the pathogenic bacterium S. aureus strain ATCC_6538 determined as CFU (colony forming units) after cultivation on recommended media where supernatants containing the bacteria released during the dissolution of biofilms were examined before the washing step in the protocol shown in FIG. 4A, the determined number of the viable bacteria was normalized per 10000 of the released bacteria.

[0041] FIGS. 5A-5D show the results of the application of the four stage preparation according to invention in case of a proband (man, 29 years) with atopic dermatitis localized at the ankle for the entire life of proband. Shown are photographs before the beginning (FIGS. 5A and 5B) of the application, and after 4 weeks (FIGS. 5C and 5D) of the application of the preparation, the composition for each stage being applied for one week. The state of the affection was characterized by the proband as significant calming

[0042] FIGS. 6A-6D show the result of the application in case of a proband (woman, 22 years) suffering by atopic dermatitis on her hands and forearms. Photographs show the status before the application (FIGS. 6A and 6B) and after 4 weeks of application (FIGS. 6C and 6D) of the four stage preparation according to the invention. The state of the affection was characterized by the proband as moderate improvement accompanied by a significant calming of the affected sites and a complete cessation of burning and itching,

[0043] FIGS. 7A-7D show the course of application in case of a proband (woman, 74 years) with recurrent fungal and yeast infections on the feet and the instep. The photographs show the status before the application (FIGS. 7A and 7D) of the product and after two weeks of applications (FIGS. 7C and 7D) involving the consecutive application of the composition for stage one and two, respectively. The state of the affection was characterized by the proband as a significant improvement contrary to the unsuccessful application of the standard creams and ointments available on the market.

[0044] FIGS. 8A-8D show the course of the application of the first stage composition in case of a proband (man, 58 years) with burns on his hand. The composition was applied twice daily onto the ring finger with more severe burns using the middle finger as a control. Photographs before application (FIG. 8A), and 3 days, 7 days and 12 days after the beginning of the application (FIGS. 8D to 8D, respectively) are shown. A complete healing of the skin was observed at the same time for both the fingers without any scars, coloration or other damage of the skin.

EXAMPLES OF THE INVENTION

[0045] The invention is further demonstrated using the examples involving the biotechnological method used for the preparation of the active substances, the performed laboratory tests of the antimicrobial properties towards the critical pathogens on the skin and the mucosal surfaces, as well as practical examples of applications for some selected of skin problems potentially related to the dysbiosis of the skin microbiota. Examples are provided in order to demonstrate the principles, the substance and the practical verification of the present invention, but the invention is by no means limited only to the embodiments provided in the below given examples. The examples are provided to present the nature of the invention thoroughly and fully, and thus to justify the scope of the claims.

[0046] The examples are mostly based on methods and procedures that are common and known to the expert in the field. In order to culture and amplify the used microbial strains, the standard media were used but also some new media have been tested to suit better to the purpose of the individual cultivations. The cultures themselves were processed at various scales, from small cultures incubated in the laboratory shakers to fermentor cultures performed in 2×5 L laboratory scale fermenters. After the end of the culture, the cells were separated from the culture medium using a continuous flow centrifuge, and the sedimented biomass was used for the preparation of the bacterial lysates. The medium was initially filtered and then the clarified solution was concentrated by diafiltration (pressure filtration) through the cassettes with polyester sulfonate concentration membranes with 10 kDa molecular-weigh cut-off. The concentrated compounds were then transferred to conservation buffer containing preserving and stabilizing agents and having pH 4.7. The protein concentration was determined using the Bradford assay, proteinase activities using the azocasein method, and the glycohydrolase activities including the activity of laminarinase, cellulase, chitinase and amylase was determined by assaying the amount of the reducing sugars formed after the incubation with the respective substrates. One enzymatic unit (U) was defined for the purpose of the present invention as the amount of enzyme able to cleave 1 nmol of the substrate per minute under the given experimental conditions. This enzyme unit corresponds to one thousandth of the international enzyme unit. The bacterial biomass was lysed by the repeated sonication using the conservation buffer containing further detergents with saccharide hydrophilic component: methyl-6-O-(N-heptylkarbamoyl)-α-D-glucoside, N-oktanoyl-N-methylgluc-amine and 2-cyklohexylethyl-β-D-maltoside. The extracted mixtures of compounds were fractionated by ammonium sulfate precipitation after desalting to 75% (w/w) concentrations, and the obtained fractions were further separated on phenyl-Sepharose and octadecyl silica columns, respectively. Laboratory efficacy tests included antimicrobial assays against the key skin pathogens using the disc and minimum inhibitory concentration (MIC, ref. 8) assays while the ability to dissolve biofilms was tested using the microplate assay (ref. 16).

[0047] For further practical tests, restricted group of individuals with symptoms and problems associated with the damaged skin barriers and microbial skin dysbiosis was treated. These problems included atopic dermatitis (atopic eczema), skin infections by S. aureus, skin infections caused by fungi and pathogenic yeasts, as well as other damages of the skin of acute nature, such as skin burns. All tests were conducted on the basis of a signed informed consent. All data obtained during the study are anonymous, the results of the study in the form of questionnaires and the photo documentation are kept by the applicant in a secure repository.

Example 1

Preparation of Active Compounds for the First Stage Dissolving the Biofilms Formed by the Pathogenic Skin Microorganisms and Suppressing the Viability of the Released Pathogenic Bacteria

[0048] In case of the commensal skin bacterium S. epidermidis the standard recommended medium (tryptone soya broth) was not optimal since it did not provide well defined composition and contained contaminating enzyme activities. An alternative medium containing a defined mixture of the necessary nutrients together with a cocktail of mineral and vitamins recommended for this bacterium was tested. In case of the oomycete P. nunn the standard minimal medium was satisfactory, provided that it was supplemented by the inducers of the required enzyme activities. While laminarin (an inducer of laminarinase, endo-β-1,3-glucosidase) and methylcellulose (an inducer of cellulase, endo-β-1,4-glucosidase) were used as described in the literature, the chitin as an inducer of chitinase cannot be used as such and it was used in the form of N-acetyl-D-glukosamin oligomers obtained by acid hydrolysis. As the starting biotechnological raw material, rough shrimp shells used for gardening purposes were used. Since this material also contained proteins, the mixture of N-acetyl-D-glukosamin oligomers and peptides after acid hydrolysis and neutralization was used advantageously as the inducer of both chitinases and proteinases as well as a source of nitrogen. At the end of the fermentation, the clarified medium was recovered by flowing the fermentation broth through a continuous flow centrifuge, while the sedimented microorganisms were obtained on a film inserted in a flow centrifuge cylinder. Overall, four fermentations were performed with the commensal skin bacterium S. epidermidis using the 5 L fermenters. The clarified cultivation medium was acidified to pH 4.7 using acetic acid, sterile filtered and frozen until further processing. The 2.5 L batches were thawed and concentrated about 25× using tangential flow filtration method with Minimate TFN cassette containing 10 kDa molecular weight cut-off polyester sulfonate membrane (PALL Inc.). The repeated cycles of dilution and concentration were then used to transfer the macromolecules to the conservation buffer described above. Finally, the protein mixture with a concentration of approximately 1 mg/ml was sterile filtered (Corning disposable filtration device with 0.22 μm cellulose acetate membrane) and stored at −20° C. until further use. The reproducibility of individual obtained protein fraction was confirmed by SDS polyacrylamide electrophoresis with silver staining of the fixed gels. Identical protein profile was observed for all processed batches except batch number 4 (SEF2K4), which was discarded (FIG. 1A). The proteins secreted by the microorganism P. nunn were also obtained in 8 batches having a protein concentration approximately 1 mg/ml under identical processing conditions (FIG. 1B). The protein concentration and enzymatic activities of proteinases, laminarinases, cellulases, and chitinases were determined in the final mixtures. These assays confirmed very good batch-to batch reproducibility with relative deviation approximately 10-20% for the enzymatic activities and about 30% for the protein concentrations. For the first stage of application, protein concentration is monitored as well as the enzyme activites providing the following amounts in the final application formulation: 15 μg/ml of protein, 0.23 mU/ml of acidic proteinases, 0.56 mU/ml of laminarinase, 0.27 mU/ml of cellulase, and 0.47 mU/ml of chitinase.

Example 2

The Preparation of Active Compounds for the Second Stage Calming the Skin Inflammation and Restoring the Biological Protective Skin Barrier

[0049] In the initial trials, an oil emulsion base was supplemented with the crude bacterial extract from S. epidermidis strain ATCC_12228 and crude γ-modulin modified by N-terminal formylation after the peptide synthesis. Nevertheless, since this crude composition caused undesired reaction on the skin of probands weakened by dysbiosis, further purification of the crude mixture was necessary. The adopted purification scheme is shown in FIG. 2A and included the precipitation of the detergent extract using 3 mol/L ammonium sulfate (final concentration, 75% saturation) followed by a separated processing of the supernatant and the sediment by reverse phase column chromatographies (phenyl-Sepharose, octadecyl silica) as indicated. The supernatant after ammonium sulfate precipitation was filtered and directly applied onto a column of phenyl-Sepharose (1.6×11 cm, 22 ml) equilibrated with 3 mol/L ammonium sulfate in the presence of 0.05 mol/L sodium acetate buffer pH 4.7. After the application of the sample, the column was washed with identical buffer and then eluted with the same acetate buffer without the ammonium sulfate and thereafter with 80% ethanol in the identical acetate buffer.

[0050] The material precipitated by ammonium sulfate was dissolved in the sodium acetate buffer and the concentration of ammonium sulfate was adjusted to 1 mol/L on the basis of conductometry. The material was spun, filtered and applied onto a column of octadecyl silica (1.6×13 cm, 26 ml, degree of modification by octadecyl was 20-22%, particle size 60-130 pin) equilibrated in the same buffer. After sample application and washing, the column was eluted with the acetate buffer without ammonium sulfate followed by a linear gradient from acetate buffer to 95% ethanol in acetate buffer, and fractions were collected 10 ml each. Fractions from both chromatographies were analyzed in 20% SDS polyacrylamide gels developed by silver staining and immunoblot. For immunoblotting, the compounds separated in the polyacrylamide gels were transferred onto PVDF membrane (0.2 μm) that was blocked with defatted milk, incubated with the primary antibody labelled with biotin, washed, incubated with the streptavidin-peroxidase and developed using 3-methyl-2-benzothiazolinonhydrazonu and 4-chloro-1-naphthol resulting in the formation of brown-red unsoluble complex (FIGS. 2B to 2E). 12% polyacrylamide gel was used for the detection of Esp proteinase because of the larger size of this molecule. The quantitative estimation of the compounds was performed using a comparison with the available standards (not shown) after photodocumentation and quantitative evaluation of the image. γ-modulin as a raw product of peptide synthesis comprising about 75% of the target peptide was purified on phenyl-Sepharose column using the published method (16) and its concentration determined spectrophotometrically using the predicted extinction coefficient (ProtParam tool at web.expasy.org). The concentration of Esp proteinase was estimated directly from the intensity of the signal on the gel. The application formulation for the second stage was prepared in a similar way as described for the first stage, and the second stage formulation thus contained the following 4 active substances in approximate concentrations as follows: lipoteichoic acid from S. epidermidis—10 μg/ml, specific Esp proteinase from S. epidermidis—5 μg/ml, SH-lantibiotic peptides from S. epidermidis—12 μg/ml, and γ-modulin from S. epidermidis—38 μg/ml. Reproducibility of the preparation of the individual batches in respect to the content of the active substances was satisfactory (relative deviation up to 10%).

Example 3

Preparation of Active Compounds for the Third Stage for the Restoration of the Normal Skin Microflora

[0051] The starting material for the preparation of the bacterial extract consisted of the microbial communities used in the wastewater treatment plants, the biomass was kindly provided to the inventors by Mgr. Jakub Hejnic PhD from Centre for Applied Investigations Dobříš(CAVD) and Ing. Pavel Pícha PhD from the Institute of Water and Environment of the University of Chemistry and Technology (VSCHT) Prague. The content of the bacteria belonging to Nitrosomonas family deprived from the human skin of modern population due to the use of soaps and detergents (www.aobiome-com) was estimated at 25-30%. The membrane complex comprising about 50% cell protein and 90% ubiquinone and cytochrome c oxidase was isolated as described previously (8) using freezing/thawing, clarification of the mixture by centrifugation at 20000×g.sub.av for 20 min The clear supernatant was discarded and the membrane complex was washed several times, centrifuged at 3000×g for 20 min and resuspended to a concentration of 5 mg/ml. The low molecular weight substances contained in the supernatant after the first centrifugation were purified on an octadecylsilicagel column as in Example 2. The fraction eluted from the column by 30% ethanol was carefully evaporated and the resulting material was added to the membrane fraction to a final concentration of 15 mg/ml. The extraction procedure was repeated four times to obtain extracts NIE1, NIE2, NIE3 and NIE4. The ability of the obtained extracts to decompose urea excreted by human skin into ammonia and further into nitrogen oxides, namely nitric oxide, was also confirmed at the specialized laboratory at the University of Chemistry and Technology Prague. The extracts were added to the third stage formulation after 1000× diluting at a final total concentration of 20 μg/ml. corresponding to enzyme concentration of approx. 78 mU/ml.

Example 4

Selection of Compounds for the Nutrition of the Skin and Stabilization of the Normal Microflora for the Fourth Stage Composition

[0052] Various compounds have been known to the experts in the field that are suitable for the nutrition of the skin, stabilization of the normal microflora on the skin, and suppression of the potential skin pathogens. In view of the considerable number of these compounds, some selection had to be made. We have found that compounds like xylitol, farnesol, L-arginin, safflower oil, evening primrose oil, hemp oil, rapeseed oil, wheat germ oil, lactate, glycin, fructose, niacinamide, inositol, magnesium aspartate, zinc gluconate, and copper gluconate might be the possible candidates. Considering our laboratory results, the price and availability of the above compounds, we decided to omit the farnesol and safflower oil, and to include the other components into the composition in the following concentrations (in % by weight), listed in the order of the decreasing abundance: xylitol 6%, hemp oil 5%, rapeseed oil 5%, L-arginine 1%, evening primrose oil 1%, wheat germ oil 1%. For the minor components such as lactate, glycine, fructose, niacinamid, inositol, magnesium asparate, zinc gluconate and copper gluconate, addition up to 0.1% (by weight) was sufficient for the given purpose.

Example 5

[0053] Examples of Suitable Cosmetic Formulations Compatible with the Active Substances and Results of the Stability Tests

[0054] In order to assure the compatibility with the active compounds and the long-term stability of the products, various formulations mostly on the basis of stabilized oil emulsions were tested for the development of skin lotions or skin emulsions as the final products. Some simple oil emulsions could not achieve the needed microbial contamination levels or creaming (separation and flotation of the oil components) occurred after the storage for 3 months at the recommended storage temperature (15-25° C.). Using the gradual increase in the complexity of the oil emulsion and the inclusion of new emulsifiers and stabilizers helped to increase the stability up to 9 months, but very high viscosity of the composition prevented its efficient application onto the affected sites. In the final round of optimization, the use of modern emulsifiers rather than some classical ones allowed to decrease their concentration as well as the concentration of some stabilizers, providing a composition stable for more than 12 months (1 year) at the recommended storage temperature (15-25° C.). Such a composition, emulsion No. 4, was then used for all the test formulations, and has been used for the manufacture of the commercial products.

[0055] The preparation of the optimized test emulsion proceeded in a standard way in which all the water soluble components represented one phase and all the oil soluble component represented the second phase. Both phases were heated and then mixed vigorously using the laboratory or industrial large scale blenders. Under the constant vigorous mixing (10000 rpm), the mixture was allowed to cool.

[0056] The overall composition of emulsion No. 4 was as follows (all numbers are %, by weight): water 70,137, xylitol 5.0, hemp (Cannabis sativa) oil 5.0, rapeseed (Brassica campestris) oil 5.0, glycerine 4.0, urea 4.0, glyceryl stearate citrate 2.0, olive (Olea europaea) oil 1.0, wheat germ oil 1.0, evening primrose (Oonothera biennis) oil 1.0, phenoxyethanol 0.9, polyacrylate crosspolymer-6 0.25, lavender extract 0.2, L-arginine 0.2, ethylhexylglycerin 0.1, Lactil® 0.1, Sepitonic® 0.1, D,L-tocopherol (vitamin E) 0.01, coloring agent amaranth A12385 (E123) 0.003.

[0057] The common practice in the manufacture of cosmetic and medicinal preparations such as skin lotion required that the components critical for the fourth stage composition providing the nutrition and stabilization of the skin microflora be a part of the above composition. Thus it represents the final formulation for the fourth stage composition.

[0058] The first stage composition thus typically contained, in the base formed by the above formulation, 0.03-0.06 mg of proteins, 0.47-0.94 mU of proteinases, 1.13-2.26 mU of laminarinases, 0.53-1.06 mU of cellulases and 0.93-1.86 mU of chitinases per 3 ml application dose.

[0059] The second stage composition contained 8-12 μg of lipoteichoic acid of the S epidermidis type, 30-40 μg of antimicrobial SH-lantibiotic peptide, 16-20 μg of antimicrobial γ-modulin, and 13-21 μg of Esp proteinase from S. epidermidis per 3 ml application dose.

[0060] Finally, the composition for the third stage contained 60 μg of the Nitrosomonas membrane complex (45 μg of low-molecular substances and 15 μg of protein complex) per 3 ml application dose.

Example 6

Laboratory Tests for Antimicrobial Activities

[0061] Antimicrobial and biofilm dissolving activities were tested using the appropriate laboratory tests, namely the disc test on Petri dishes (“disc test”), the minimum inhibitory concentration test on microtiter plates (“MIC test”) and the biofilm dissolution test in which the residual biofilm after an incubation with the test compounds is measured using crystal violet (“biofilm test”, see in the next Example 7).

[0062] We first tested the ability of the active compounds and formulations to inhibit the growth of the most common bacterial skin pathogen S. aureus. The particular laboratory strain used (ATCC_6538) is known to represent an aggressive strain commonly used as a standard in studies of disinfections and antiseptic biocides. The most profound effects in the disc test were achieved using the secreted proteins from S. epidermidis diluted a hundred fold, a lysate from this bacteria diluted hundred fold, and the membrane aminooxidase/hydroxylamine oxidase complex from the environmental bacteria Nitrosomonas sp. (FIG. 3A). These results were corroborated in the MIC test performed with four different batches of the active compounds. Here, three out of four batches of the secreted S. epidermidis proteins inhibited the growth of the pathogen S. aureus at concentrations as low as 0.1 μg/ml (determined as protein), while the lysate from the same bacterium provided very similar results (FIG. 3B). On the other hand, the Nitrosomonas membrane complex provided somewhat lower activities with inhibitions at 10 μg/ml (FIG. 3B). Finally, the antimicrobial activities were also tested towards the yeast Candida albicans that might acquire aggressive fibrillar forms in individuals with problematic skin and often occurs in co-infections with the other pathogens. The fast-growing aggressive strain ATCC_10231 used commonly as the sterilization control and in the tests of antifungal compounds. In case of this yeast, only secreted proteins and lysates from S. epidermidis provided efficient inhibition (FIGS. 3C and 3D).

Example 7

Demonstration of the Ability to Dissolve Biofilms in Laboratory Tests

[0063] The primary purpose for the biofilm test was to prove the ability of the active compounds to dissolve the biofilms formed by pathogenic microorganisms S. aureus and to determine if a simultaneous killing of the released pathogens determined as the reduction of their viability could be observed. The standard assay in which the residual biofilm in the microtiter wells is stained by crystal violet and determined spectrophotometrically at 595 nm after the extraction of the dye into ethanol was used. Because of the inherent variability in this biological assay, all experiments were performed in quadruplicates and the presented data thus represent the averaged values measured in the four adjacent wells (FIG. 4A). The ability of the tested mixtures to dissolve biofilms was measured at four different concentrations, when the 10× or even 100× diluted mixtures often provided the best results (FIG. 4B). The experiments covering the combinations of the active compounds appeared critical for the assessment of the final formulations. Here, the combinations involving the soluble secreted proteins from S. epidermidis and P. nunn appeared most (PNSE, FIGS. 4B and 4C). Another important parameter is the viability of pathogenic microorganisms released from biofilms: if the released bacteria remain viable, there is a risk of re-colonization and new biofilm formation after application. In order to assess the effect of the compounds on the viability of the pathogenic bacteria released from the biofilms, aliquots of the collected medium after incubation with the active compounds were cultured on Petri dishes under optimal conditions for 24 h and the number of viable microorganisms was expressed. This experiment clearly demonstrated that the microbial extracts not only have the ability to disrupt the biofilm, but also to kill (or at least significantly reduce the viability) of the released pathogenic bacteria. The best effects were achieved using the mixture of secreted proteins from both microorganisms diluted 100× or 1000× (FIG. 4D).

Example 8

Practical Tests of the Multistage Preparations

[0064] Several rounds of practical tests were performed with the four-stage preparation formulated as the cosmetic product, skin milk (each stage active substances were formulated into basic emulsion No. 4 of Example 5).

[0065] The first round of testing was performed after obtaining a Report on the Cosmetic Product Safety. The preparation was administered in a four-week dosing regimen (each stage composition for one week in the morning and evening) in 10 healthy subjects with normal intact skin. With the exception of very mild pruritus in the first stage composition, no side or adverse reactions were observed after monthly administration. These results, together with those reported in the Safety Report, indicated the safety of the product when applied to the healthy skin of normal individuals.

[0066] Based on these results, in the second round the preparation was tested on individuals with skin problems related to dysbiosis (such as atopic dermatitis, acne, psoriasis and rosacea) or burn injury. The tests revealed (1) a greater sensitivity of these individuals to the former second stage composition of the preparation that was resolved by further purification, as described in Example 2, (2) beneficial effects even in severe cases of skin damage such as burns where the application of the cosmetic product around the burns proved salvatory in certain cases. The extensive hand burn associated with local sepsis was significantly improved after two weeks of application comprising the first and the second stage composition and the infection vanished.

[0067] In the third round of practical testing the restricted group of probands prone to skin dysbiosis were subjected to a treatment using the full four stages preparation according to the invention after the signing the informed consent.

[0068] 29 year-old man reported problems with atopic dermatitis from early childhood localized in the later period in the ankle area. The problem could not be solved using a large amount of preparations available on the cosmetics market. The four stage preparation was applied for 4 weeks twice daily. In 4 weeks the proband reported a significant improvement of the problem that is confirmed by photodocumentation (FIGS. 5A-5D). Subjectively the proband reported a significant calming effect although he found the time for absorption of the product (caused by the presence of the hydrated components) rather long.

[0069] 22 year-old woman suffered by atopic eczema on her hands that could not be managed by several means available for this diagnosis. The four stage preparation was intended as above, although only stage one and stage two formulations, one week each, were applied In two weeks, the proband describes a partial resolution of the problem accompanied with a significant calming, the calming and decrease in the extent of affection is obvious from the photographical documentation (FIGS. 6A-6D).

[0070] 74 year-old woman with diabetes and kidney damage, dependent on regular dialysis three times a week, suffered by long-term problems with fungi and yeasts on her legs accompanied by the cornering and cracking of the skin in the instep and on the sole. The four-stage preparation according to the invention was applied to the proband for four weeks. After 1 month of application, a significant decrease in the extent of infection was observed together with a complete cessation of the infection on about 80% of the affected area. The provided photodocumentation (FIGS. 7A-7D) was in support of the subjective evaluation by the proband and the doctor.

[0071] 58 year-old man reported the burns on his hand caused by a laboratory accident involving the formation of a deep, swollen burn on the ring finger of the left hand while the middle finger had a smaller injury (FIG. 8A). The application of the first stage composition was performed daily only on the ring finger protecting the middle finger from the application during the spraying, and the course of the healing was followed by photodocumentation (FIG. 8B to FIG. 8D). It could be observed and documented that after 12 days a nearly complete healing at both sides occurred, and only a mild redness could be observed at the sites of the original injuries (FIG. 8D). During the following two weeks a complete healing was finished without any scars or changes in the pigmentation on the burn fingers.

[0072] The inventors will perform practical tests under the supervision of the dermatologists with the aim to acquire a sufficient number of observations allowing the statistical evaluation as well as to get the relevant experience for the organization of more extensive clinical trials with medicinal use of the preparations.

INDUSTRIAL APPLICABILITY

[0073] The combined multistage microbial preparation according to the present invention can be used for the manufacturing of cosmetic products, functional cosmetics or medicinal cosmetics suitable for individuals prone to skin dysbiosis such as individuals with problems with atopic dermatitis, acne, rosacea, psoriasis, vitiligo and other skin problems as well as for the relief in case of acute skin problems such as burns, scratches etc. Also, the formulations and compositions described here might be useful for skin conditioning and prevention of the skin diseases strengthening the biological component of the skin barrier. An advanced manufacturing method may also be developed producing the formulations in the sterile form for their use in the treatment of atopic dermatitis, acne, rosacea, psoriasis, vitiligo, skin damages and acute skin infections in burned patients or patients the skin of whom has been otherwise damaged.

REFERENCES

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