Finasteride and minoxidil polymeric nanoparticle its process of preparation, aqueous suspension containing the same, pharmaceutical composition, and its use

Abstract

The present invention relates to a pharmaceutical composition for topical application for the treatment of alopecia, said composition comprising polymeric nanoparticles, preferably nanocapsules containing two active ingredients, finasteride and minoxidil, additives and a pharmaceutically acceptable carrier. The invention further includes a process for the preparation of polymeric nanoparticles, preferably nanocapsules of finasteride and minoxidil, a composition suitable for topical application for the treatment of alopecia, as well as the use of said nanocapsules for the preparation of a pharmaceutical composition.

Claims

1. A polymeric nanoparticle comprising the active ingredients finasteride and minoxidil, wherein said polymeric nanoparticle is in the form of a nanocapsoid formed from: (i) an organic phase comprising: (a) a hydrophobic polymer that is a biodegradable polymer from a group of polyesters having a melting point of less than 120 C., (b) a fixed oil, (c) a lipophilic surfactant having low hydrophilic-lipophilic balance (HLB), (d) an organic solvent, (e) a co-solvent, and (f) finasteride; and (ii) an aqueous phase comprising: (g) a hydrophilic surfactant, (h) minoxidil, and (i) water.

2. The polymeric nanoparticle according to claim 1, wherein said biodegradable polymer from the group of polyesters having a melting point of less than 120 C. is selected from the group consisting of a poly(lactide); poly(glycolide); copolymers of poly(lactide-co-glycolide); polycaprolactone; and a copolymer of polycaprolactone with a polyester, with a polyamide, with a polyurethane or with a vinyl polymer.

3. The polymeric nanoparticle according to claim 2, wherein said polycaprolactone is a poly (-caprolactone).

4. The polymeric nanoparticle according to claim 1, wherein said fixed oil is a medium-chain triglyceride.

5. The polymeric nanoparticle according to claim 4, wherein said medium-chain triglyceride is selected from the group consisting of capric and caprylic acids triglycerides, propylene glycol di(caprylate/caprate), and oleyl macrogolglycerides.

6. The polymeric nanoparticle according to claim 1, wherein said lipophilic surfactant of low HLB with a value in the range of 3 to 6 is selected from the group consisting of sorbitan monostearate, sorbitan distearate, sorbitan tristearate, capril caprylic macrogolglycerides, propylene glycol laurates, propylene glycol caprylates, glyceryl monostearate, and polyglyceryl oleates.

7. The polymeric nanoparticle according to claim 6, wherein said lipophilic surfactant of low HLB is sorbitan monostearate.

8. The polymeric nanoparticle according to claim 1, wherein said organic solvent is acetone.

9. The polymeric nanoparticle according to claim 1, wherein said co-solvent is ethanol.

10. The polymeric nanoparticle according to claim 1, wherein said hydrophilic surfactant is a neutral hydrophilic surfactant selected from the group consisting of polysorbate 20, polysorbate 60, polysorbate 80, macrogol stearate, macrogol cetostearyl ether, macrogol lauryl ether, macrogol oleyl ether, macrogol oleate, polyoxyl castor oil, hydrogenated polyoxyl castor oil, and mixtures thereof.

11. The polymeric nanoparticle according to claim 10, wherein said neutral hydrophilic surfactant is polysorbate 80.

12. The polymeric nanoparticles according to claim 1, wherein: (i) the organic phase comprises: (a) from 0.05% to 20.0% (w/w) of a poly (-caprolactone), (b) from 0.05% to 20.0% (w/w) of medium-chain triglycerides, (c) from 0.05% to 20.0% (w/w) of sorbitan monostearate, (d) from 10% to 80% (w/w) of acetone, (e) from 0.001% to 50% (w/w) of ethanol, and f) from 0.005% to 50.0% (w/w) of finasteride; and (ii) the aqueous phase comprises: (g) from 0.05% to 20.0% (w/w) of polysorbate 80, (h) from 0.005% to 50.0% (w/w) of minoxidil, and (i) from 10% to 90% (w/w) of water.

13. A pharmaceutical composition for the treatment of alopecia comprising: (A) the polymeric nanoparticle according to claim 1, and (B) a pharmaceutically acceptable carrier; wherein the polymeric nanoparticles are dispersed in said pharmaceutically acceptable carrier.

14. The pharmaceutical composition according to claim 13, comprising 0.01 to 1.0% (w/w) of finasteride and 0.01 to 2.0% (w/w) of minoxidil.

15. The pharmaceutical composition according to claim 13, wherein the pharmaceutical composition is in the form of a solution, gel or lotion for topical administration.

16. The pharmaceutical composition according to claim 13, wherein it further comprises additives selected from dispersants, surfactants, moisturizing agents, emollients, thickeners, sequestering agents, preservatives, antioxidants, and fragrances.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows a comparison of the physical profile of the finasteride nanocapsoids 0.20% and minoxidil 0.20% (n=3) [FIG. 1] and nanocapsoids of finasteride 0.25% (n=3) [Graphic 2].

(2) FIG. 2 shows a transmission electron microscopy of the 0.1% finasteride nanocapsoids.

(3) FIG. 3 shows photographs of the animals on day 1 (photo 1), day 15 (photo 2) and day 23 (photo 3) of treatment for the groups treated with: (A) nanocapsules of finasteride 0.25% (B) nanocapsoids of finasteride 0.20%, minoxidil 0.20% and (C) Pilexil.

(4) FIG. 4 illustrates the histopathological analysis of the skin removed from the back of the animals after 23 days of treatment with (A) nanocapsoids of finasteride 0.20%, minoxidil 0.20% and (B) Pilexil.

(5) FIG. 5 shows the mean number of mature follicles analyzed by histological specimen (n=12) animals treated with: (A) nanocapsules of finasteride 0.25%, (B) nanocapsoids of finasteride 0.20%, minoxidil 0.20% and (C) Pilexil.

DETAILED DESCRIPTION OF THE INVENTION

(6) The present invention relates to a pharmaceutical composition effective for the topical treatment of alopecia, said composition comprising nanoparticulate systems, preferably containing the nanocapsoids of finasteride and minoxidil, a pharmaceutically acceptable vehicle; and optionally containing additives.

(7) The term nanocapsoid, as used herein, means polymeric nanocapsules prepared by a nanoencapsulation process in which, in the organic phase, a solvent and a co-solvent are employed.

(8) The invention also includes a process for the preparation of polymeric nanoparticles, preferably nanocapsoids comprising finasteride and minoxidil, which are comprised by said composition.

(9) Finasteride is a synthetic azosteroid with potent selective antagonist action on 5-reductase type 2 enzymes. Finasteride acts by irreversibly binding to the enzyme, preventing the conversion of testosterone to its active metabolite, dihydrotestosterone (DHT). The use of finasteride was initially approved for the reduction of prostate size associated with urinary obstruction (benign prostatic hyperplasia), since DHT in men, although responsible for prostate development, can be involved in development of hyperplasia. However, it has been observed that patients taking this drug also presented a reversal in alopecia symptoms. For this reason, the development of studies to investigate the potential of finasteride in the treatment of baldness had begun (Sinclair, R D, Male androgenetic alopecia: Part II. The Journal of Men's Health & Gender, 2005, vol. 2, no. 1, p. 38-44). A study by Kaufmann et al (2008) with 1553 men aged 18 to 41 years evaluated the action of finasteride in doses of 1 mg daily against placebo for five years. The result of treatment with finasteride led to a decrease in the probability of visible hair loss, compared to the increased likelihood of visible hair loss in patients treated with placebo. In this study, at the end of the five years, 75% of placebo-treated patients developed baldness and only 10% of patients treated with finasteride developed the disease. A review of the safety and efficacy of finasteride use for treating androgenic alopecia in women showed in conclusion that this drug can be used safely and effectively in cases wherein topical treatment with minoxidil is not effective (Stout, S M; STUMPF, J L; Finasteride Treatment of Hair Loss in Women. The Annals of Pharmacotherapy, 2010, vol. 44, no. 6, p. 1090-1097).

(10) Minoxidil was introduced as the therapy in the treatment of hypertension in 1965; however, it was observed that orally administered minoxidil caused hypertrichosis. Resulting from the evidence from this and subsequent studies, minoxidil was approved by the Food and Drug Administration (FDA) for treatment of androgenic alopecia in males (at a concentration of 5%) and women (at a concentration of 2%). However, although the topical solution of minoxidil presents proven safety and effectiveness, adverse effects may occur with its use. Friedman and colleagues (2002) reported cases of contact allergy, which included pruritus, erythema and dryness of the scalp. Some patients showed sensitivity to minoxidil, but mainly to the propylene glycol component present in the topical solution as a co-solvent and absorption enhancer (Friedman, E S, et al; Allergic contact dermatitis to topical minoxidil solution: Etiology and treatment. Journal of the American Academy of Dermatology, 2002, vol. 46, no. 2, p. 309-312).

(11) The present invention avoids the disadvantages and adverse effects associated with the systemic administration of finasteride and topical minoxidil and proposes a topical application composition of finasteride and minoxidil for the treatment of alopecia with reduced side effects caused by these two active ingredients.

(12) The invention is based on the preparation of polymeric nanoparticles, preferably nanocapsoids, of finasteride and minoxidil, by means of an interfacial deposition of preformed polymer, wherein it is firstly made the dissolution of finasteride, of a hydrophobic polymer, of a fixed oil and at least one low HLB surfactant (Hydrophilic Lipophilic Balance) in an organic solvent and a co-solvent, to form the organic phase; and dissolution of minoxidil, and at least one hydrophilic surfactant, preferably neutral, in water, to form the aqueous phase.

(13) Although nanoparticles, a term which includes nanospheres, nanocapsules and nanocapsoids, can be advantageously produced by the present invention, the invention is, preferably, particularly directed to the preparation of nanocapsoids, preferably carried out by the interfacial deposition method. However, it should be clear that other methods can be used to produce the nanocapsules of the invention.

(14) Said polymeric nanoparticles, preferably nanocapsoids are formed from the organic and aqueous phases, as follows: (i) The organic phase comprises: (a) a hydrophobic polymer, (b) a fixed oil, (c) at least one low HLB lipophilic surfactant, (d) a solvent, (e) a co-solvent and (f) finasteride; and (ii) The aqueous phase comprises: (g) at least one hydrophilic surfactant, (h) minoxidil and (i) water.

(15) Said polymer used to encapsulate finasteride is a hydrophobic polymer selected from the group consisting of vinyl polymers, polyesters, polyamides, polyurethanes and polycarbonates. Preferably, the hydrophobic polymer used is a biodegradable polymer from the group of polyesters having a melting point of less than 120 C. More preferably, the biodegradable hydrophobic polymer is from the group of polyesters, is a poly(lactide); a poly (glycolide); copolymers of poly(lactide-co-glycolide); a polycaprolactone; a copolymer of polycaprolactone with polyester, with polyamide, with polyurethane or with a vinyl polymer; and most preferably, it is the poly(-caprolactone).

(16) Said fixed oil used in the organic phase of the preparation of polymeric nanoparticles of the invention is selected from the group consisting of canola oil, soybean oil, olive oil and medium-chain triglycerides; with medium-chain triglycerides being preferably used. Among the medium-chain triglycerides selected from the group of triglycerides of capric and caprylic acid, propylene glycol dicaprylocaprate, macrogolglycerides of oleyl, laureola and linoleoyl. Still more preferably, the use as a fixed oil, of medium-chain triglycerides, are the triglycerides of capric and caprylic acid.

(17) The lipophilic surfactant used in said organic phase of preparation of polymeric nanoparticles of the invention is a surfactant of low HLB, preferably having a value in the range of 3 to 6, being solid or liquid, preferably solid, selected from the group consisting of sorbitan monostearate, sorbitan distearate, sorbitan tristearate, caprylocaproyl macrogolglycerides, propylene glycol laurates, propylene glycol caprylate, glyceryl monostearate, polyglyceryl oleate, or mixtures thereof. Preferably, the lipophilic surfactant used in the organic phase of the invention is sorbitan monostearate.

(18) The solvent used in the organic phase of preparation of the polymeric nanoparticles of the present invention is an organic solvent selected from the group consisting of acetone, dimethylsulfoxide, dimethylformamide, N-methylpyrrolidone, dioxane, acetonitrile, methyl ethyl ketone, or other solvent which presents physicochemical properties of intermolecular interaction with water. In a preferred embodiment of the invention, the organic solvent is preferably acetone.

(19) Said co-solvent used in the organic phase of preparation of the polymeric nanoparticles, preferentially nanocapsoids, of the present invention is selected from the group consisting of methanol, ethanol, propanol, and isopropanol or other alcohol, mono-, di-, tri- or polyhydroxylated, glycerol, sorbitol, polyethylene glycol, mannitol or propylene glycol. In a preferred embodiment of the invention, the co-solvent is preferably ethanol. The use of ethanol in the organic phase as a co-solvent promotes the formation of nanocapsoids with unexpexted nanotechnological quality, since the polymer poly (-caprolactone) is insoluble in methanol or ethanol. However, to have nanoscopic granulometry, the components of the organic phase should be water soluble and employed below the saturation concentration.

(20) The aqueous phase contains at least one hydrophilic surfactant for the preparation of the nanoparticles, preferentially nanocapsoids, of the invention, preferably being an emulsifier such as polyoxygenated polymers, or ionic surfactants such as lecithin or a neutral surfactant selected from the group consisting of polysorbate 20, polysorbate 60 or polysorbate 80, macrogol stearate, macrogol cetostearyl ether, macrogol lauryl ether, macrogol oleyl ether, macrogol oleate, polyoxyl castor oil, hydrogenated polyoxyl castor oil, or mixtures thereof. Preferably, polysorbate is employed, and more preferably, polysorbate 80, for the aqueous phase of the preparation of the nanoparticles of the invention.

(21) The aqueous suspension of polymeric nanoparticles comprises: The organic phase (a) from 0.01% to 30.0% (w/w) of a hydrophobic polymer, (b) from 0.01% to 50.0% (w/w) of a fixed oil (c) from 0.01% to 50.0% (w/w) of at least one lipophilic surfactant of low HLB, preferably solid (d) from 10% to 80% (w/w) of organic solvent, (e) 0.001% to 50% (w/w) of a co-solvent; and (f)from 0.001% to 80.0% (w/w) of finasteride; and The aqueous phase (g) from 0.001% to 80.0% (w/w) of minoxidil, (h) from 0.05% to 20.0% (w/w) of at least one hydrophilic surfactant, (i) 10% to 90% (w/w) water.

(22) In a preferred formulation of the aqueous suspension, the polymeric nanoparticles, preferably nanocapsoids, comprise: in the organic phase (a) from 0.05% to 20.0% (w/w) of a hydrophobic polymer, preferably poly (caprolactone); (b) from 0.05% to 20.0% (w/w) of a fixed oil, preferably medium-chain triglycerides; (c) from 0.05% to 20.0% (w/w) of at least one lipophilic surfactant, preferably sorbitan monostearate; (d) from 10% to 80% (w/w) of an organic solvent, preferably acetone; (e) 0.001% to 50% (w/w) of a co-solvent, preferably ethanol; and (f) from 0.005% to 50.0% of finasteride; and in the aqueous phase (g) from 0.005% to 50.0% (w/w) minoxidil; (h) from 0.05% to 20.0% (w/w) of at least one hydrophilic surfactant, preferably polysorbate; and (i) from 10% to 90% (w/w) water.

(23) The pharmaceutical composition for the treatment of alopecia contains: (A) nanocapsids of the present invention, comprising (a) from 0.01% to 2.5% (w/w) of finasteride; (b) from 0.01% to 10.0% (w/w) minoxidil; (c) from 0.1% to 10.0% (w/w) of a hydrophobic polymer, preferably poly (-caprolactone ); (d) from 0.1% to 5.0% (w/w) of a fixed oil, preferably medium-chain triglycerides; (e) 0.1% to 5.0% (w/w) of at least one low HLB lipophilic surfactant, preferably sorbitan monostearate; (f) from 0.001% to 10% (w/w) of a hydrophilic surfactant, preferably polysorbate 80; and (B) a pharmaceutically acceptable carrier, wherein the amounts of the nanocapsoid components are a percentage of the final formulation and said nanocapsoids are dispersed in said pharmaceutically acceptable vehicle.

(24) A preferred pharmaceutical composition for treating alopecia of the present invention comprises from 0.01 to 1.0% (w/w) of finasteride and 0.01 to 2.0% (w/w) of minoxidil in the form of polymeric nanoparticles, preferably in the form of nanocapsoids, dispersed in a pharmaceutically acceptable vehicle.

(25) The pharmaceutical composition for the treatment of alopecia of the present invention is intended for topical administration and is in the form of a solution, gel or lotion.

(26) The pharmaceutical composition for the treatment of alopecia optionally contains additives such as dispersants, surfactants, moisturizing agents, emollients agents, thickeners, sequestering agents, preservatives, antioxidants, fragrances and the like.

(27) The following are specific embodiments of the invention. However, it should be understood that such examples are provided for illustrative purposes only, and that various modifications or changes, in light of the herein disclosed embodiments, will be suggestive to specialists in the art and must be included within the spirit and scope of this disclosure and the scope of the accompanying claims.

EXAMPLE 1

Preparation of Nanocapsoids of the Invention Containing Finasteride 0.20% and Minoxidil 0.20%

EXAMPLE 1.1

Preparation of Finasteride and Minoxidil Nanocapsoids

(28) The suspensions of nanocapsoids of finasteride were prepared from an organic solution of a mixture of acetone and ethanol containing poly (-caprolactone), medium chain triglycerides (triglycerides of capric and caprylic acids), sorbitan monostearate and finasteride employing the composition described in Table 1.

(29) TABLE-US-00001 TABLE 1 Composition of the suspensions of poly (-caprolactone) nanocapsoids containing finasteride 0.20% and minoxidil 0.20% based on the final formulation Quantity Organic Phase Triglycerides of capric and caprylic acids 3.30 ml Sorbitan monostearate 770 mg Poly(-caprolactone) 1000 mg Acetone 200 ml Ethanol 50 ml Finasteride 200 mg Aqueos Phase Polisorbate 80 770 mg Minoxidil 200 mg Distilled Water 500 ml

(30) The polymer (poly (-caprolactone)) was solubilized in the organic phase along with finasteride, triglycerides of caprylic and capric acid, and the low HLB surfactant (sorbitan monostearate) under moderate heating between 20 C. and 40 C. preferably at 40 C., employing acetone as the solvent and ethanol as the co-solvent. The neutral surfactant (polysorbate), and minoxidil were dissolved in water to form the aqueous phase. After solubilization of all components of the organic and aqueous phases, the organic phase was injected, using a funnel, on the aqueous phase.

(31) After the formation of the primary emulsion of nanocapsoids of the invention, it was maintained under moderate agitation for 10 minutes, and then concentrated to a final volume of 100 ml in a rotary evaporator under reduced pressure in a thermostatic bath in the evaporation flask between 10 C. and 80 C., preferably between 30 C. and 45 C. to eliminate the organic solvent and co-solvent and excess water, to adjust the final concentration of finasteride and minoxidil.

EXAMPLE 1.2

Characterization of the Formulation

(32) A. Determination of pH

(33) Determination of pH was performed in a potentiometer calibrated with a buffer of pH 4.0 and 7.0, directly in the suspensions, by the average of three repetitions.

(34) B. Determination of the Particle Diameter and Polydispersion Index by Multiple Light Scattering.

(35) For the determination of the diameter and polydispersity index of nanoparticle suspension by dynamic light scattering, the Zetasizer nano-device model ZEN 3600 ZS, Malvern, USA was used. For both, the samples were diluted in MilliQ water (filtered through a 0.45 micron filter, Millipore Millex-HP) 500 times at room temperature and the results were determined by the average of three repetitions.

(36) C. Determination of Particle Size Distribution by Laser Diffractometry

(37) To assess whether there is a concomitant presence of micrometer population, analyses of particle size were performed by laser diffraction (Mastersizer 2000, Malvern, UK). Analyses were carried out by adding a sample of the formulation in the accessory dispersion containing about 100 ml of distilled water. The amount added to that was enough to achieve obscuration between 0.02 and 0.10. To prevent interference of the background signal (from the water) it was measured before addition of the sample.

(38) D. Zeta Potential

(39) The zeta potential of the nanoparticle suspension was determined by electrophoresis methodology with the Zetasizer nano-ZS model ZEN 3600 device (Malvern, USA). The determination was carried out using 500 times dilution in 10 mM NaCl solution (filtered through a 0.45 micron filter, Millipore Millex-HP), and results obtained were the average of three determinations.

(40) E. Viscosity

(41) The viscosity of the suspensions was measured using a vibrational viscometer (SV-10, A & D Company, Japan). To achieve this, the viscosity was measured directly in the suspensions for 30 seconds with data collection every 5 seconds at a temperature of 251.0 C.

(42) F. Assay of Finasteride in the Formulation

(43) For the assay of finasteride, the suspension of polymeric nanoparticles was treated with acetonitrile in ultrasson (for 30 min) resulting in the extraction of the drug from the formulation. The drug assay was then performed by high performance liquid chromatography (HPLC).

(44) The analysis was performed on the Perkin Elmer chromatograph Series 200, using ultraviolet-visible detector (with =210 nm for the finasteride), LiChrospher 100 RP-18 column (5 m, 2504 mm) pre-column of the same material (5 um) and isocratic mobile phase of acetonitrile: water (75:25), flow of 1 mL min 1, injection volume of 100 L.

(45) G. Assay of Minoxidil in the Formulation

(46) The assay of minoxidil was carried out in a spectrophotometer. For both, the polymeric nanoparticle suspension was treated with methanol in ultrasson (for 30 minutes) resulting in the extraction of the pharmacological formulation. Shortly after this, the samples were read in a spectrophotometer, at a wavelength of 248 nm, using a formulation of white nanocapsoides as a reference beam (prepared in the same manner without the presence of drugs).

(47) H. Checking for the Presence of Crystals

(48) To verify any simultaneous presence of crystals (drug dispersed in the aqueous phase) quantification by HPLC of a freshly prepared formulation of the drug was initially performed. After this formulation was divided into two samples: the first was allowed to be still and the second was stirred before the assay, which was performed again after 30 days. From the sample which was kept still, only one aliquot of the supernatant (preventing any movement) was collected. From the other, an aliquot (corresponding to 20% of the supernatant) was collected after vortexing for 15 seconds.

(49) I. In Vivo Assay for Determining the Ability of Hair Recovery

(50) The technique used was a modification of the technique described by Matias et al (1989), approved by the Ethics Committee of the Federal University of Rio Grande do Sul.

(51) For the experiments, B6CBAF1 hybrid female mice were used from the vivarium of the University of Vale do Itaja (UNIVALI). The animals were under standard conditions of temperature and relative humidity during the experiment, with light and dark cycles of 12 hours each. All animals received a subcutaneous injection of 1% testosterone dispersed in a mixture of polysorbate 80 in water (100 mg.Math.mL.sup.1) at a dose of 1 mg per day. There were five injections per week for 4 weeks.

(52) In the first week the animals received only injections of testosterone. On the first day of the second week of the experiment, all animals had the hair removed from their backs with Veet depilatory cream, for the total removal of hair. After removal of hair, daily injections of testosterone were maintained, and a daily topical application of the formulation was added to the treatment, depending on the treatment group (placebo, treatment, control). For the treatment groups, the optimized formulation containing the nanocapsoids of the present invention was used, which was compared with the results of the formulation of finasteride 0.25% disclosed in the co-pending patent application of the same Applicant of the present patent application. The formulation for topical treatment of androgenic alopecia, commercially available under the brand name Pilexil (Serenoa serrulata extract 22.0%, Valeant) was also tested.

(53) To monitor the growth of hair, photographs were taken on days 1, 15, and 23. On the 24th day the animals were sacrificed by cervical dislocation. A sample of skin from the backs of 4 animals of each group was removed and evaluated microscopically. To this end, the slides were sent to the Zanol laboratory, which were prepared and stained with hematoxylin-eosin. Then we proceeded to the analysis with a light microscope (ZeissPrimo Star coupled to the camera Canon Power Shot, PC1250) to determine which growth stage the hair was in. (MATIAS, J R, et al.; Animal models of androgen-dependent disorders of the pilosebaceous apparatus. 1. The androchronogenetic alopecia (AGA) mouse as a model for male-pattern baldness. Archives of Dermatological Research, v. 281, p. 247-253, 1989).

(54) To quantify the data obtained by histology, it was proceeded the counting of mature follicles (with pigmentation and inserted in the adipose tissue) of each of the histological slides from each group. Thus, we analyzed 4 slides per group, and the count was based on 3 different foci of the same slide, totaling 12 fields analyzed per group. For a comparison between the groups, statistical analysis by ANOVA (=0.05) was made.

(55) J. In Vivo Assay for Determining the Ability of Hair Recovery

(56) The analyses were performed with a transmission electron microscope (JEOL, JEM 1200 Exll, Electron Microscopy CenterUFRGS) operating at 80 kV. The diluted suspensions were deposited on the carbon support film in grids, negatively stained with uranyl acetate solution (2% w/v) and observed using a magnitude of 250,000 times.

EXAMPLE 1.3

Physicochemical Characterization of the Nanocapsoid Formulation Containing Finasteride 0.20% and Minoxidil 0.20%

(57) Table 2 shows the diameter values (for multiple light scattering), polydispersion index, zeta potential, pH and viscosity for the nanocapsoids formulation of the invention containing the combination of finasteride and minoxidil.

(58) TABLE-US-00002 TABLE 2 Physicochemical characterization of the nanocapsoids formulation containing the combination of finasteride and minoxidil (finasteride 0.20% and minoxidil 0.20%) of the invention, compared with the characterization of the formulation of finasteride 0.25% (as disclosed in application co-pending from the same Applicant of the present application) Formulation 0.20% finasteride and Formulation 0.25% Analysis 0.20% minoxidil finasteride Average diameter (nm) 255 2 221 3 Polydispersion index 0.22 0.02 0.14 0.03 Zeta potencial (mV) 11.7 1.2 14.9 2.7 pH 6.4 0.1 4.6 0.1 Viscosity (mPa .Math. s) 1.25 0.19 1.21 0.07

(59) This formulation containing the two active ingredients, finasteride and minoxidil, presented physicochemical characteristics close to those of the formulation containing only finasteride (nanocapsules of poly (caprolactone) containing 0.25% of the active ingredient), as, for example, the diameter and the zeta potential. However, the pH was shown to be closer to the neutral value, probably due to the presence of the minoxidil solution in the external aqueous phase.

(60) FIG. 1 shows a comparison between the granulometryprofile of the nanocapsoids of finasteride and minoxidil (finasteride 0.20% and minoxidil 0.20%) of the invention and of the nanocapsules of finasteride (finasteride 0.25%). As noted, the nanocapsoids of the invention containing the combination have a slightly decreased micrometer population compared to the nanometer. To facilitate this view, the profiles of the triplicate of each formulation lot were presented separately in FIG. 1.

(61) For a better evaluation of the morphological characteristics of the formulation, analysis of transmission with electron microscopy as shown in FIG. 2 was performed.

EXAMPLE 1.4

Assay for Determining the Capillary Recovery Capacity of the Nanocapsoids of Finasteride and Minoxidil of the Invention

(62) The improvement in efficiency of the capillary recovery capacity by use of the nanocapsoid formulation containing the combination of the drugs finasteride and minoxidil of the invention, was assessed with an in vivo assay with this formulation, and was compared to the results using the nanocapsule formulation containing 0.25% finasteride and the use of a formulation available in the market having antiandrogen action indicated for the treatment of alopecia: Pilexil (Valeant), with the active ingredient Serenoa serrulata extract.

(63) To perform the test, animals of the B6CBAF1 lineage were treated for a week with subcutaneous injections of testosterone, and in the second week, had the back depilated for treatment and determination, thus, the capillary recovery capacity of the tested formulations. FIG. 3 shows the comparison of treatments through the pictures of the representative animals from each group on days 1, 15 and 23; treated with (A) the nanocapsule formulation containing 0.25% finasteride, as disclosed in the co-pending application of the same Applicant of the present application; (B) the formulation of the invention containing nanocapsoids comprising finasteride 0.20% and minoxidil 0.20%; and (C) Pilexil.

(64) As noted, the formulation of the present invention presented a visual result well superior to the product in the market for the treatment of androgenetic alopecia (Pilexil).

(65) When compared with the formulation of nanocapsules containing finasteride 0.25%, the result was slightly higher. This result can be best observed when all the animals of the groups were analyzed together. One can observe a more complete covering of hair on all the animals treated with the formulation of the present invention. In turn, in the group treated with the formulation of nanocapsules containing 0.25% finasteride, some animals still showed some areas without full coverage by the new coat of hair.

(66) The histopathological analysis, shown in FIG. 4, and cell counts, shown in FIG. 5, from the slide images showed significant differences between the groups (ANOVA, =0.05).

(67) The nanocapsoid formulation with a combination of the drugs finasteride and minoxidil of the present invention exhibited a number of follicles per field significantly higher than that of the Pilexil formulation, being similar to that shown by the formulation of nanocapsules containing 0.25% finasteride (ANOVA, =0.05).

(68) Although the visual results, through the accompanying photographs, of hair growth using the nanocapsoids formulation containing minoxidil and finasteride of the present invention have been slightly higher compared to those presented by the use of the nanocapsule formulation containing 0.25% finasteride, the results of the cell counts showed similarity between these two formulations. Thus, it can be concluded that the addition of minoxidil assists in accelerating the growth of the hair (revival) without favoring however the development (maturation) thereof. That is, minoxidil accelerates the growth of hair, but does not reverse the capillary involution that occurring in androgenic alopecia; this reversal is provided by finasteride.

EXAMPLE 2

Pharmaceutical Compositions Comprising Minoxidil and Finasteride Nanocapsoids

EXAMPLE 2.A

Formulation in the Form of Topical Solution

(69) Nanocapsoids of finasteride and minoxidil are prepared as described in Example 1.1. The topical solution is prepared resulting in the formulation in Table 3.

(70) TABLE-US-00003 TABLE 3 Formulation in form of a topical solution containing the nanocapsoids suspension containing 0.025% finasteride and 0.20% minoxidil. Components Percentage Triglycerides of capric and caprylic acids 3.23 Sorbitan monostearate 0.77 Poly(-caprolactone) 1.00 Finasteride 0.025 Polisorbate 80 0.77 Minoxidil 0.20 Distilled water 94.005

EXAMPLE 2.B

Formulation in the Form of Topical Gel

(71) Nanocapsoids of finasteride and minoxidil are prepared as described in Example 1.1.

(72) The nanocapsoid suspensions, prepared as described in Example 2.A, were thickened with 0.2% Carbopol 940. Triethanolamine qs was added to obtain a suitable viscosity for topical application. The resulting gel has the formulation shown in Table 4.

(73) TABLE-US-00004 TABLE 4 Formulation in form of a topical gel containing the nanocapsoid suspension of 0.05% finasteride and 0.25% minoxidil. Components Percentage Triglycerides of capric and caprylic acids 3.23 Sorbitan monostearate 0.77 Poly(-caprolactone) 1.00 Finasteride 0.05 Polisorbate 80 0.77 Carbopol 940 0.20 Distilled water 93.73 Triethanolamine qs

EXAMPLE 2.C

Formulation in Form of a Topical Lotion

(74) Initially, phase 1 is prepared as described in Example 2.A, and the composition was employed from phase 1 in Table 5. Separately, the components were merged from phase 2 in a water bath at 50 C. and removed from heating after fusion. Next, add phase 3 to phase 1 and disperse under constant magnetic stirring. Add this mixture of phases 1 and 3 in the molten phase 2 and cool to 40 C. under moderate mechanical agitation to avoid air incorporation.

(75) TABLE-US-00005 TABLE 5 Formulation in form of a topical lotion containing the nanocapsoid suspension containing 0.1% finasteride and 0.3% minoxidil. Percentage (%) Components Phase 1 Triglycerides of capric and caprylic acids 3.23 Sorbitan monostearate 0.77 Poly(-caprolactone) 1.00 Finasteride 0.10 Polisorbate 80 0.77 Minoxidil 0.30 Distilled water 89.53 Components Phase 2 Coconut oil 2.0 Propylparaben 0.2 Methylparaben 0.1 Components Phase 3 Salcare SC91 (INCI: Polyacrylamide 2.0 and C13-14 Isoparaffin and Laureth-7)

(76) All publications and patent applications mentioned in this specification are indicative of the level of those skilled in the art to which the invention relates. All publications and patent applications are incorporated herein by reference to the same extent as if each individual publication or patent application were each specifically and individually indicated to be incorporated for ease of reference.

(77) Although certain embodiments have been described, they are presented in an exemplary mode only, and are not intended to limit the scope of the invention. In fact, the new embodiments described herein may be implemented in a variety of other forms; more than that, various omissions, substitutions and changes in the form of the embodiments described herein may be made without diverging from the spirit of the invention. The claims and their equivalents accompanying this description are considered to cover such forms or modifications as they may be within the scope and spirit of the invention.