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for invention","granted":true,"earliest_filing_date":"2013-06-28","grant_date":"2017-10-31","anticipated_term_date":"2033-06-28","has_disclaimer":true,"patent_status":"ACTIVE","publication_count":3,"has_spc":false,"has_grant_event":true,"has_entry_into_national_phase":false},"abstract":{"en":[{"text":"A lipid composition comprising racecadotril, at least one surfactant and a lipid.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"}]},"abstract_lang":["en"],"has_abstract":true,"claim":{"en":[{"text":"1. A composition comprising: racecadotril, polyoxyl 35 castor oil USP/NF, glyceryl caprylate mono- and diglycerides USP/NF and caprylic/capric triglycerides, 70:30/C8:C10 USP/NF.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"2. The composition of claim 1 , wherein the composition is stable for about 40 weeks at 40° C.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"3. The composition of claim 1 , wherein the at least one surfactant is present in an amount from about 88 wt. % to about 91 wt. % in total per 100 ml of the composition.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"4. The composition of claim 1 , wherein the caprylic/capric triglycerides is present in an amount of from about 1 wt. % to about 2 wt. % lipid per 100 ml of the composition.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"5. The composition of claim 1 , further comprising an optional ingredient selected from the group consisting of preservatives, sweeteners, viscosity modifiers, colors, aromas, flavors, and mixtures thereof.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"6. The composition of claim 1 , further comprising an optional ingredient selected from the group consisting of citric acid, sodium benzoate, sucralose, flavors and mixtures thereof.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"7. A dosage form comprising the composition of claim 1 , wherein the dosage form is a soft shell dosage form, a hard shell dosage form, or a tablet dosage form.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"8. The composition of claim 1 , wherein the composition has a total water content of less than about 3.5 wt. % based on the total weight of the composition.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"9. The composition of claim 1 , further comprising a second active ingredient that is a digestive health active ingredient.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"10. A composition comprising: about 3.0 wt. % to about 7.0 wt. % racecadotril; about 40 wt. % to about 53 wt. % of polyoxyl 35 castor oil USP/NF, glyceryl caprylate mono- and diglycerides USP/NF in total; and about 40 wt. % to about 53 wt. % and caprylic/capric triglycerides, 70:30/C8:C10 USP/NF; wherein each wt. % is based upon 100 ml of the composition.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"11. A dosage form comprising the composition of claim 10 , wherein the dosage form is a soft shell dosage form, a hard shell dosage form, or a tablet dosage form.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"12. A method for treating a subject experiencing diarrhea comprising the step of orally administering to the subject a composition comprising racecadotril, polyoxyl 35 castor oil USP/NF, glyceryl caprylate mono- and diglycerides USP/NF and caprylic/capric triglycerides, 70:30/C8:C10 USP/NF.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"13. A composition comprising: racecadotril, polyoxyl 35 castor oil USP/NF, glyceryl caprylate mono- and diglycerides USP/NF and caprylic/capric triglycerides, 70:30/C8:C10 USP/NF, and a digestive health active ingredient selected from the group consisting of laxatives, antacids, proton pump inhibitors, anti-gas agents, antiemetics, H2 blockers, and antidiarrheal agents.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"14. The composition of claim 13 , wherein the anti-gas agent is simethicone.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"15. The composition of claim 13 , wherein the antidiarrheal agent is loperamide.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"16. A composition comprising: racecadotril, polyoxyl 35 castor oil USP/NF, glyceryl caprylate mono- and diglycerides USP/NF and caprylic/capric triglycerides, 70:30/C8:C10 USP/NF, wherein the racecadotril is present in amount from about 8% to about 10% by weight of a total weight of the composition.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"}]},"claim_lang":["en"],"has_claim":true,"description":{"en":{"text":"CROSS REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Application No. 61/665,470, filed on Jun. 28, 2012, U.S. Provisional Application No. 61/787,597, filed on Mar. 15, 2013 and U.S. Non-Provisional application Ser. No. 13/929,996, filed on Jun. 28, 2013 which are incorporated by reference in their entirety. BACKGROUND OF THE INVENTION Field of the Invention The present invention relates to lipid based microemulsion compositions. More particularly, the present invention relates to lipid based microemulsion compositions containing a pharmaceutical active ingredient and the method of making said compositions. Related Background Art Diarrhea is an intestinal disorder that is characterized by an increase in the frequency of watery bowel movements. It may result from a variety of causes including bacteria or viral induced diarrhea. Food intolerance caused by allergy or the consumption of foods such as fatty or spicy foods may result in diarrhea. Food poisoning may also lead to diarrhea. In some instances, diarrhea may be a symptom of other conditions and diseases. Diarrhea is symptomatic of an intestinal or other bodily function disorder. Various prescription and nonprescription products can be taken for relief. However, many of these products provide relief with some side effects. Racecadotril is also used in the treatment of diarrhea. It reduces (i) hypersecretion of water and electrolytes into the intestinal lumen, (ii) the incidence and duration of acute diarrhea and (iii) diarrhea-associated symptoms. Additionally, racecadotril is a pharmaceutical active ingredient that exhibits poor solubility and poor oral bioavailability. Presently, racecadotril is available in solid oral dosage forms. SUMMARY OF THE INVENTION The present invention is directed to a microemulsion composition comprising racecadotril, at least one surfactant and a lipid. In one embodiment, the inventive microemulsion composition comprises about 0.01 wt. % to about 24.0 wt. % racecadotril, about 1 wt. % to about 95 wt. % of surfactant in total, and about 0.01 wt. % to about 60 wt. % lipid, wherein each wt. % is based upon 100 ml of the composition. The present invention also includes a method for treating a subject experiencing diarrhea comprising the step of orally administering to the subject a composition comprising racecadotril, at least one surfactant, and a lipid. DETAILED DESCRIPTION OF THE INVENTION As used herein, a “microemulsion” refers to a liquid mixture of a lipid, water and at least one surfactant. A microemulsion is characterized by its clear, thermodynamically stable, and isotropic appearance. As used herein, “stable” refers to a composition that is clear to the naked eye and substantially free of chemical degradation of racecadotril, substantial color change, turbidity or oily globules. No phase separation should be observed in either aqueous and/or non-aqueous components for at least about 3 months at 40° C. More preferably, no phase separation should be observed in either aqueous and/or non-aqueous components for at least about 6 months at 40° C. In one embodiment, the total chemical degradant products of racecadotril should be less than 0.5 percent by weight (wt. %), e.g. less than 0.2 wt. % based on the total wt. % of racecadotril when stored at 3 months and 40° C. In another embodiment, the total chemical degradant products of racecadotril should be less than 0.5 percent by 6 months and 40° C. The percent degradation products are determined by calculating the % peak area of the degradation product peak areas relative to the peak areas of the Racecadotril peaks in the HPLC chromatograms. In one embodiment, the total chemical degradant products of racecadotril should be less than 0.5% of racecadotril, e.g. less than 0.2% based on of the total % of racecadotril when stored at 3 months and 40° C. As used herein, “self-microemulsifying drug delivery systems” (SMEDDS) are mixtures of oils, surfactants, and sometimes cosolvents. SMEDDS can be used for formulating systems to improve the oral absorption of highly lipophilic compounds. SMEDDS emulsify spontaneously using gentle agitation to produce fine oil-in-water emulsions when introduced into an aqueous phase. A drug in an SMEDDS appears in a small droplet size and exhibits increased dissolution and permeability. SMEDDS may be formulated for liquid or solid use. For solid use, the solids are packaged in capsules or tablets. Liquid filled or semi-solid filled capsules are a preferred dosage form by certain consumers, due to the perception of speed, visual appearance of the drug composition and ease of swallowing. The present invention is a microemulsion composition comprising racecadotril, at least one surfactant, and a lipid. Various studies have shown racecadotril to be efficacious in reducing the symptoms of diarrhea. One benefit of using racecadotril over other remedies is that racecadotril has been shown to have fewer side effects such as post-treatment constipation. Racecadotril has low water solubility, of about 10 micrograms/ml at room temperature conditions. In the inventive composition, the racecadotril may be solubilized in the microemulsion. Racecadotril is included in the microemulsion composition in an amount from about 0.01 wt. % to about 24.0 wt. % per 100 ml of the emulsion composition. Preferably, the racecadotril is about 0.01 wt. % to about 18.0 wt. %, and more preferably, about 0.01 wt. % to about 12.0 wt. % per 100 ml of the emulsion composition, and even more preferably, about 0.01 wt. % to about 10.0 wt. % per 100 ml of the emulsion composition. In one embodiment, the racecadotril is about 4.0 wt. % to about 24.0 wt. % per 100 ml of the emulsion composition. In another embodiment, the racecadotril is about 4.0 wt. % to about 18.0 wt. % per 100 ml of the emulsion composition. In yet another embodiment, the racecadotril is about 4.0 wt. % to about 12.0 wt. % per 100 ml of the emulsion composition. In still yet another embodiment, the racecadotril is about 4.0 wt. % to about 10.0 wt. % per 100 ml of the emulsion composition. The inventive microemulsion composition includes at least one surfactant. The surfactant may be, for example, a nonionic surfactant, cationic surfactant, anionic surfactant, or mixtures thereof. Suitable surfactants include, for example, water-insoluble surfactants having a hydrophilic-lipophilic balance (HLB) value less than 12 and water-soluble surfactants having a HLB value greater than 12. Surfactants that have a high HLB and hydrophilicity, aid the formation of oil-water droplets. The surfactants are amphiphilic in nature and are capable of dissolving or solubilizing relatively high amounts of hydrophobic drug compounds. Non-limiting examples, include, Tween, Dimethylacetamide (DMA), Dimethyl sulfoxide (DMSO), Ethanol, Glycerin, N-methyl-2-pyrrolidone (NMP), PEG 300, PEG 400, Poloxamer 407, Propylene glycol, Phospholipids, Hydrogenated soy phosphatidylcholine (HSPC), Distearoylphosphatidylglycerol (DSPG), L-α-dimyristoylphosphatidylcholine (DMPC), L-α-dimyristoylphosphatidylglycerol (DMPG), Polyoxyl 35 castor oil (CREMOPHOR EL, CREMOPHOR ELP), Polyoxyl 40 hydrogenated castor oil (Cremophor RH 40), Polyoxyl 60 hydrogenated castor oil (CREMOPHOR RH 60), Polysorbate 20 (TWEEN 20), Polysorbate 80 (TWEEN 80), d-α-tocopheryl polyethylene glycol 1000 succinate (TPGS), Solutol HS-15, Sorbitan monooleate (SPAN 20), PEG 300 caprylic/capric glycerides (SOFTIGEN 767), PEG 400 caprylic/capric glycerides (LABRASOL), PEG 300 oleic glycerides (LABRAFIL M-1944CS), Polyoxyl 35 Castor oil (ETOCAS 35), Glyceryl Caprylate (Mono- and Diglycerides) (IMWITOR), PEG 300 linoleic glycerides (LABRAFIL M-2125CS), Polyoxyl 8 stearate (PEG 400 monosterate), Polyoxyl 40 stearate (PEG 1750 monosterate), Peppermint oil, and combinations thereof. Additionally, suitable surfactants include, for example, polyoxyethylene derivative of sorbitan monolaurate such as polysorbate, caprylcaproyl macrogol glycerides, polyglycolyzed glycerides, and the like. In one embodiment, the surfactant is a combination of polyoxyl 35 castor oil and glyceryl caprylate (mono- and diglycerides) NF. In the inventive composition, the total weight percent of surfactant(s) is from about 1 wt. % to about 95 wt. % per 100 ml of the microemulsion composition. Preferably, the surfactant is about 25 wt. % to about 95 wt. %, and more preferably, about 30 wt. % to about 90 wt. % per 100 ml of the microemulsion composition. In one embodiment, the surfactant is about 45 wt. % to about 95 wt. % per 100 ml of the microemulsion composition. A lipid is another essential component of the inventive composition. The lipid aids in solubilizing the racecadotril and also facilitates the self-emulsification process. Suitable lipids include, for example, vegetable oils (modified and/or hydrolyzed), long-chain triglycerides and medium-chain triglycerides having different degrees of saturation, and combinations thereof may be used. In addition, monoglyceride, diglyceride, and/or triglyceride emulsifiers (fats and oils) that are lipophilic and insoluble in water (available from Abitec Corporation, sold under the tradename CAPMUL®) may be used as the lipid. For example, Beeswax, Oleic acid, Soy fatty acids, d-α-tocopherol (Vitamin E), Corn oil mono-di-tridiglycerides, Medium chain (C8/C10) mono- and diglycerides, Long-chain triglycerides, Castor oil, Corn oil, Cottonseed oil, Olive oil, Peanut oil, Peppermint oil, Safflower oil, Sesame oil, Soybean oil, Hydrogenated soybean oil, Hydrogenated vegetable oils, Medium-chain triglycerides, Caprylic/capric triglycerides derived from coconut oil, palm seed oil, and combinations thereof. The lipid is included in the composition in an amount from about 0.01 wt. % to about 60 wt. % per 100 ml of the emulsion composition. Preferably, the lipid is about 0.01 wt. % to about 50 wt. %. In another embodiment, the lipid is about 1 wt. % to about 20 wt. % per 100 ml of the emulsion composition, more preferably, about 1 wt. % to about 15 wt. % per 100 ml of the emulsion composition, and even more preferably, about 1 wt. % to about 10 wt. % per 100 ml of the emulsion composition. In one particular embodiment, the lipid is from about 1 wt. % to about 2 wt. % per 100 ml of the emulsion composition. It is desirable to minimize the amount of water in the composition. The amount of water in the composition will be largely determined by the water content of each component that is included in the composition. In one embodiment, the water content of the composition is less than about 3.5 wt. % based on the total wt. % of the composition. In another embodiment, the water content of the composition is less than about 2.5 wt. % based on the total wt. % of the composition. In yet another embodiment, the water content of the composition is less than about 0.5 wt. % based on the total wt. % of the composition. In still yet another embodiment, the water content of the composition is less than about 0.2 wt. % based on the total wt. % of the composition. Optionally, a variety of ingredients may be included in the emulsion composition of the present invention. Any coloring agent suitable for use in a food or pharmaceutical product may be used in the present invention. Typical coloring agents include, for example, azo dyes, quinopthalone dyes, triphenylmethane dyes, xanthene dyes, indigoid dyes, iron oxides, iron hydroxides, titanium dioxide, natural dyes, and mixtures thereof. More specifically, suitable colorants include, but are not limited to patent blue V, acid brilliant green BS, red 2G, azorubine, ponceau 4R, amaranth, D&C red 33, D&C red 22, D&C red 26, D&C red 28, D&C yellow 10, FD&C yellow 5, FD&C yellow 6, FD&C red 3, FD&C red 40, FD&C blue 1, FD&C blue 2, FD&C green 3, brilliant black BN, carbon black, iron oxide black, iron oxide red, iron oxide yellow, titanium dioxide, riboflavin, carotenes, antyhocyanines, turmeric, cochineal extract, clorophyllin, canthaxanthin, caramel, betanin, and mixtures thereof. Similarly, a flavor may be included in the emulsion composition. The amount of flavor added to the composition is dependent upon the desired taste characteristics. The composition may contain other ingredients or components, such as aromas; sweeteners such as sucralose, sorbitol, high fructose corn syrup, sugar, and the like; viscosity modifiers such as xanthan gum; preservatives such as sodium benzoate NF, buffers such as citric acid and/or sodium chloride; or mixtures thereof. The emulsion composition of the present invention may be made by any method known to those skilled in the art so long as it results in the desired composition. Suitable methods include, for example, combining each ingredient in a mixing kettle, where the ingredients may be added sequentially or in any manner so long as the intended result is achieved. Moreover, the mixing action should be sufficient to incorporate each ingredient into the composition. The primary means of assessing the stability of the emulsion is based on analytical degradation analysis. The efficiency of self-emulsification could be estimated by determining the rate of emulsification, droplet-size distribution and turbidity measurements. In addition, stability may be evaluated by measuring the turbidity of the emulsion. This evaluation helps to determine whether the emulsion reaches equilibrium quickly and in a reproducible time. Stability is also evaluated by checking for oversaturation (precipitation). The test is performed by placing 1 ml of formulation in a beaker with 250 ml of 0.1 N HCL. If a precipitation is formed, then the system is oversaturated. In one embodiment of the present invention, the microemulsion composition is administered as a packaged emulsion for direct oral consumption. In another embodiment, the microemulsion composition is administered in an oral soft gelatin capsule containing the microemulsion composition. In yet another embodiment the microemulsion composition is administered in a multiple of microgel beads containing the microemulsion composition. In still yet another embodiment the microemulsion composition is administered in a hard gelatin capsule containing the microemulsion composition. When the microemulsion composition is contained in the hard gelatin capsule, the hard gelatin capsule may be banded. In still yet another embodiment, the microemulstion composition is administered in a suppository or enema containing the microemulsion composition. Optionally, the microemulsion composition of the present invention comprises a second active ingredient. In one embodiment the second active ingredient is a digestive health active ingredient. Non-limiting examples, include, for example, laxatives, antacids, proton pump inhibitors, anti-gas agents, antiemetics, H2 blockers, or a second antidiarrheal agent. In one embodiment, the second active ingredient is incorporated into the microemulsion matrix. In another embodiment, the second active ingredient is present in another portion of the dosage form composition which is separate from the microemulsion composition. In yet another embodiment, the second active ingredient is microencapsulated. Suitable anti-gas agents include, but are not limited to simethicone. Suitable additional antidiarrheal agents include, but are not limited to loperamide. In one embodiment, the inventive microemulsion composition includes about 8.0 wt. % to about 10.0 wt. % racecadotril, about 88 wt. % to about 91 wt. % of surfactant in total, about 1 wt. % to about 2 wt. % lipid, wherein each wt. % is based upon 100 ml of the composition. In another embodiment, the inventive microemulsion composition includes about 0.01 wt. % to about 24.0 wt. % racecadotril, about 1 wt. % to about 95 wt. % of surfactant in total, about 0.01 wt. % to about 60 wt. % lipid, wherein each wt. % is based upon 100 ml of the composition. In yet another embodiment, the inventive microemulsion composition includes about 3.0 wt. % to about 7.0 wt. % racecadotril, about 40 wt. % to about 53 wt. % of surfactant in total, about 40 wt. % to about 53 wt. % lipid, wherein each wt. % is based upon 100 ml of the composition. The inventive microemulsion composition may be delivered in any suitable delivery system. For example, in one embodiment, the microemulsion composition is delivered orally. In another embodiment, the microemulsion composition is delivered in a soft shell dosage form. In still another embodiment, the microemulsion composition is delivered in a hard shell dosage form. In still yet another embodiment, a tablet dosage form is used to deliver the microemulsion composition. In addition, the droplet size of the inventive composition was measured using a Horiba SZ-100 Nanoparticle Size Analyzer by dynamic light scattering (DLS) at a scattering angle of 90 degrees. Samples were kept in a temperature control chamber at 25° C. during measurement. Immediately prior to measurement the instrument performance was checked with a nominal 100 nm polystyrene latex (PSL) size standard in 10 mM NaCl. Count rates for these measurements ranged from 1 million to 3 million counts per second. The measurements were performed for one minute each. Data were analyzed using the cumulant technique. The droplet size was also measured on a Nicomp 380 Nanoparticle Size Analyzer by dynamic light scattering (DLS) with a scattering angle of 90 degrees at Particle Sizing Systems (PSS). All measurements were performed at 23° C. After warming up, the instrument was challenged with a NIST traceable standard (i.e., polystyrene latex) to check for accuracy. A scattering intensity of 150-500 kHz was targeted during sample measurement which lasted for 15 minutes. Data were analyzed using the cumulant technique. The present invention also includes a method for treating a subject experiencing diarrhea comprising the step of orally administering to the subject a composition comprising racecadotril, at least one surfactant, and a lipid. The following example is provided to further illustrate the compositions and methods of the present invention. It should be understood that the present invention is not limited to the examples described. EXAMPLE 1 Concentrated Racecadotril Lipid Composition: For Use in Liquid Filled Gelatin Capsule TABLE 1Racecadotril Lipid Based Composition as a percentage of the composition:Triglyceride Type 1Formula 1Formula 3Formula 5Ingredient(% w/w)(% w/w)(% w/w)Racecadotril9.609.318.34Polyoxyl 35 Castor oil 179.5552.6027.50Glyceryl Caprylate (Mono- and9.0436.2762.33Diglycerides) NF 2Medium Chain Triglycerides 31.811.811.83Total100100100Racecadotril Assay (mg/mL)96.0493.1483.371 Commercially available from CRODA Healthcare as ETOCAS ® 35 USP/NF, EP, JP2 Commercially available from CREMER as IMWITOR ® 988 USP/NF, EP, JP3 Commercially available from CREMER as MIGLYOL ® 810N (Caprylic/Capric Triglycerides; 70:30/C8:C10) USP/NF, EP, JP TABLE 2Racecadotril Lipid Based Composition as a percentage of the composition:Triglyceride Type 2Formula 2Formula 4Formula 6Ingredient(% w/w)(% w/w)(% w/w)Racecadotril9.478.988.33Polyoxyl 35 Castor oil 179.6752.7927.50Glyceryl Caprylate (Mono- and9.0536.4162.33Diglycerides) NF 2Medium Chain Triglycerides 31.811.821.83Total100100100Racecadotril Assay (mg/mL)94.6889.7783.341 Commercially available from CRODA Healthcare as ETOCAS ® 35 USP/NF, EP, JP2 Commercially available from CREMER as IMWITOR ® 988 USP/NF, EP, JP3 Commercially available from CREMER as MIGLYOL ® 812N (Caprylic/Capric Triglycerides; 60:40/C8:C10) USP/NF, EP, JP Utilizing the materials in Table 1 and Table 2, the following mixing steps were taken to form the microemulsion. A total of 6 mixtures were prepared including 3 ratios, with each prepared with MIGLYOL 810N (Table 1) and MIGLYOL 812N (Table 2). Step 1: In a suitable vessel, a mixture of the Polyoxyl 35 Castor oil (ETOCAS® 35), Glyceryl Caprylate (IMWITOR® 988) and Medium Chain triglycerides (MIGLYOL® 810N & 812N) was prepared in three separate mixtures in the following weight ratios: 88:10:2 (Ratio 1), 58:40:2 (Ratio 2), and 30:68:2 (Ratio 3). Step 2: The mixture(s) from Step 1 were mixed utilizing a vortex mixer. Step 3: The Racecadotril was slowly added to the mixture(s) from Step 2 utilizing the vortex mixer, and mixed for 5 minutes. Step 4: The mixture from Step 3 was placed into a laboratory shaker and mixed for 36 hours until a clear solution was formed. Stability of Racecadotril Lipid Formulation The chemical stability of the formulations prepared in Example 1 was examined for racecadotril degradation when stored for 40.1 weeks at 40° C. in sealed bottles, and is shown in Table 3. TABLE 3Stability Data for lipid-based Formulations;Formula 1, Formula 3, Formula 5RAC (%)Benzyl Alcohol (%)Impurity C (%)Impurity G (%)Form.Form.Form.Form.Form.Form.Form.Form.Form.Form.Form.Form.Time135135135135Initial99.9599.9499.95NDNDNDNDNDNDNDNDND6wk99.6799.2399.000.060.290.29NDND0.010.010.020.0212wk99.4698.4598.610.130.480.32NDND0.040.010.020.0216wk99.1597.8297.790.180.660.49NDND0.100.020.020.0240.1wk98.8696.8996.860.260.850.740.070.110.260.020.090.01Formula 2, Formula 4, Formula 6RAC (%)Benzyl Alcohol (%)Impurity C (%)Impurity G (%)Form.Form.Form.Form.Form.Form.Form.Form.Form.Form.Form.Form.Time246246246246Intial99.9599.9499.94NDNDNDNDNDNDNDNDND6wk99.6699.1198.940.050.300.34NDNDND0.020.020.0212wk99.4198.3798.490.120.520.45NDNDND0.020.020.0216wk99.0997.7897.860.150.650.57NDND0.050.020.020.0240.1wk98.7496.9596.850.270.870.790.140.080.220.020.06NDThere was no Impurity A, thiorphan, or Impurity E in Form. 1, Form. 2, Form. 3, Form. 4, Form. 5, Form. 6ND: not detectableFormula:1. 88% Super Refined Etocas 35, 10% Imwitor 988, 2% Miglyol 810N (Ratio 1)2. 88% Super Refined Etocas 35, 10% Imwitor 988, 2% Miglyol 812N (Ratio 1)3. 58% Super Refined Etocas 35, 40% Imwitor 988, 2% Miglyol 810N (Ratio 2)4. 58% Super Refined Etocas 35, 40% Imwitor 988, 2% Miglyol 812N (Ratio 2)5. 30% Super Refined Etocas 35, 68% Imwitor 988, 2% Miglyol 810N (Ratio 3)6. 30% Super Refined Etocas 35, 68% Imwitor 988, 2% Miglyol 812N (Ratio 3)ND—Not detectableIngredient:A.Super Refined Etocas 35 (NF, EP, JP):Manufactured by CRODA Health CarePolyoxyl 35 Castor OilHLB value of 14B.Imwitor 988: Medium Chain Partial GlyceridesManufactured by CREMERGlyceryl Caprylate (Mono- and Diglycerides)Melting Point ~25° C.HLB value of 4C.Imwitor 742: Medium Chain Partial GlyceridesManufactured by CREMERCaprylic/Capric GlyceridesMelting Point ~25° C.HLB value of 3-4D.Miglyol: Medium Chain Triglycerides (MCT Oils, Fractionated Coconut Oil)Manufactured by CREMERCaprylic (C8)/Capric (C10) Triglycerides810N - 70:30 C8/C10 blend812N - 60:40 C8/C10 blendConversion based on the density of each formula:Formula 1/Formula 2:1.042 g/mlFormula 3/Formula 4:1.028 g/mlFormula 5/Formula 6:1.016 g/mlWater Content (% w/w):Racecadotril0.5%Super Refined Etocas 0-3% (EP):0%Super Refined Etocas 0-1% (JP):0%Imwitor 988:0.2%Miglyol 810N:0.01%Miglyol 812N:0.01%Water ContentFormula(% w/w)10.0220.0230.0840.0850.1360.1370.0980.0990.10100.10 EXAMPLE 2 Concentrated Racecadotril Lipid Composition: For Use in Liquid Filled Gelatin Capsule TABLE 4Formula 7Formula 8Ingredient(% w/w) a(% w/w)Racecadotril4.614.25Glyceryl Caprylate (Mono- and Diglycerides) NF 147.9548.00Medium Chain Triglycerides 247.44—Medium Chain Triglycerides 3—47.75Total100100Racecadotril Assay (mg/mL)46.1142.491 Commercially available from CREMER as IMWITOR 742 ® USP/NF, EP, JP2 Commercially available from CREMER as MIGLYOL ® 810N (Caprylic/Capric Triglycerides; 70:30/C8:C10) USP/NF, EP, JP3 Commercially available from CREMER as MIGLYOL ® 812N (Caprylic/Capric Triglycerides; 60:40/C8:C10) USP/NF, EP, JP TABLE 5Formula 9Formula 10Ingredient(51.5:48.5) a(51.4:48.6)Racecadotril5.285.59Glyceryl Caprylate (Mono- and48.8348.54Diglycerides) NF 1Medium Chain Triglycerides 245.90—Medium Chain Triglycerides 3—45.87Total100100Racecadotril Assay (mg/mL)52.7855.931 Commercially available from CREMER as IMWITOR 988 ® USP/NF, EP, JP2 Commercially available from CREMER as MIGLYOL ® 810N (Caprylic/Capric Triglycerides; 70:30/C8:C10) USP/NF, EP, JP3 Commercially available from CREMER as MIGLYOL ® 812N (Caprylic/Capric Triglycerides; 60:40/C8:C10) USP/NF, EP, JP Testing Methods: Sample Preparation: (in Acetonitrile) 1. Pipet 1 mL of Racecadotril lipid solution into a 100 mL volumetric flask (V.F.)2. Dilute to volume with Acetonitrile. Add about 20 mL of Dimethylacetamide if necessary.3. Further dilute the sample solution to about 0.1 mg/mL with acetonitrile if necessary. Sample AnalysisInject reference standards (0.1 mg/mL of Racecadotril in Acetonitrile) and samples onto a suitable HPLC system under conditions similar to those suggested below. Parameters may be modified to optimize chromatography.Determine the assay of Racecadotril using the Racecadotril peak areas of the sample solutions under test in comparison with the Racecadotril peak areas of the standard solution. The degradation products levels are determined by % peak area relative to the Racecadotril peak. Chromatographic conditions(European Pharmacopoeia Racecadotril method):Column:Phenomenex Luna 5 μm C18 (2), 100 Å;250 mm × 4.6 mm ID (Column ID in EP is 4.0 mm)Column heater:30° C.Wavelength:210 nmInj. Vol.:10 μLFlow rate:1 mL/min Gradient Table:Time (min)flow% A% BInitial1.0604051.06040251.02080351.02080361.06040451.06040 Mobil Phase A: Phosphate buffer, pH 2.5 (Buffer prep: dissolve 1 g of potassium dihydrogen phosphate in water, adjust to pH 2.5 with phosphoric acid, dilute to 1000 mL with water) Mobil Phase B: 100% Acetonitrile EXAMPLE 3 Racecadotril Lipid Composition: Droplet Size Procedure The droplet size was measured on a Horiba SZ-100 Nanoparticle Size Analyzer by dynamic light scattering (DLS) at a scattering angle of 90 degrees. During measurement, samples were kept in a temperature control chamber at 25° C. Immediately prior to measurement the instrument performance was checked with a nominal 100 nm polystyrene latex (PSL) size standard in 10 mM NaCl. Count rates for these measurements ranged from 1 million to 3 million counts per second. The measurements were performed for one minute each. Data were analyzed using the cumulant technique. Solubility and Droplet Size for lipid-based formulations**Formula 1, Formula 3, Formula 5Form. 1Form. 3Form. 5Solubility (mg/mL)96.093.183.4Solubility (mg/g)92.2 290.6 382.1 4Droplet Size (nm)*18.1 525.1 648.3 7(Z-avg Diameter) 1**Formula 2, Formula 4, Formula 6Form. 2Form. 4Form. 6Solubility (mg/mL)94.789.883.3Solubility (mg/g)90.7 287.7 382.1 4Droplet Size (nm)*19.4 825.3 947.2 10(Z-avg Diameter) 1*Determined by dynamic light scattering (DLS) with a Horiba SZ-100 Nanoparticle Size Analyzer, average of three determinations (n = 3)1 General procedure: 0.08 g of each formulation and 15 mL of 0.1N HCl were combined and mixed by vortex2 Calculated based on density of 1.042 g/mL3 Calculated based on density of 1.028 g/mL4 Calculated based on density of 1.016 g/mL5 Concentration of racecadotril ~0.53 mg/mL6 Concentration of racecadotril ~0.55 mg/mL7 Concentration of racecadotril ~0.44 mg/mL8 Concentration of racecadotril ~0.60 mg/mL9 Concentration of racecadotril ~0.43 mg/mL10 Concentration of racecadotril ~0.46 mg/mL**See Example 1 for Formula The droplet size was also measured on a Nicomp 380 Nanoparticle Size Analyzer by dynamic light scattering (DLS) with a scattering angle of 90 degrees at Particle Sizing Systems (PSS). All measurements were performed at 23° C. After warming up, the instrument was challenged with a NIST traceable standard (i.e., polystyrene latex) to check for accuracy. A scattering intensity of 150-500 kHz was targeted during sample measurement which lasted for 15 minutes. Data were analyzed using the cumulant technique. **Formula 1, Formula 3, Formula 5Form. 1Form. 3Form. 5Solubility (mg/mL)96.093.183.4Solubility (mg/g)92.2 290.6 382.1 4Droplet Size (nm)*17.2 522.9 656.6 7(Z-avg Diameter) 1Determinations (n =)211**Formula 2, Formula 4, Formula 6Form. 2Form. 4Form. 6Solubility (mg/mL)94.789.883.3Solubility (mg/g)90.7 287.7 382.1 4Droplet Size (nm)*17.8 824.7 947.4 10(Z-avg Diameter) 1Determinations (n =)122*Determined by dynamic light scattering (DLS) with a Nicomp 380 Nanoparticle Size Analyzer.1 General procedure: 0.2 mL of formulation and 4.8 mL of 0.1N HCl were combined and mixed for Formula 1 and 3; 0.1 mL of formulation and 4.9 mL of 0.1N HCl were combined and mixed for Formula 2 and 4; 0.1 mL of formulation and 4.9 mL of 0.1N HCl were combined and mixed, then 2.5 mL of dilution was added to 2.5 mL of 0.1N HCl for Formula 5 and 6.2 Calculated based on density of 1.042 g/mL3 Calculated based on density of 1.028 g/mL4 Calculated based on density of 1.016 g/mL5 Concentration of racecadotril ~3.84 mg/mL6 Concentration of racecadotril ~3.72 mg/mL7 Concentration of racecadotril ~0.83 mg/mL8 Concentration of racecadotril ~1.89 mg/mL9 Concentration of racecadotril ~1.80 mg/mL10 Concentration of racecadotril ~0.83 mg/mL**See Example 1 for Formula While the invention has been described above with reference to specific embodiments thereof, it is apparent that many changes, modifications, and variations can be made without departing from the inventive concept disclosed herein. Accordingly, it is intended to embrace all such changes, modifications, and variations that fall within the spirit and broad scope of the appended claims. All patent applications, patents, and other publications cited herein are incorporated by reference in their entirety.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"}},"description_lang":["en"],"has_description":true,"has_docdb":true,"has_inpadoc":true,"has_full_text":true,"biblio_lang":"en"},"jurisdiction":"US","collections":[],"usersTags":[],"lensId":"007-451-743-482-942","publicationKey":"US_9801819_B2","displayKey":"US 9801819 B2","docAssets":{"lensId":"007-451-743-482-942","pdfUrl":"https://www.lens.org/images/patent/US/9801819/B2/US_9801819_B2.pdf","images":[{"thumb":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/10pc/00000001.png","full":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/full/00000001.png"},{"thumb":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/10pc/00000002.png","full":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/full/00000002.png"},{"thumb":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/10pc/00000003.png","full":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/full/00000003.png"},{"thumb":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/10pc/00000004.png","full":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/full/00000004.png"},{"thumb":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/10pc/00000005.png","full":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/full/00000005.png"},{"thumb":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/10pc/00000006.png","full":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/full/00000006.png"},{"thumb":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/10pc/00000007.png","full":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/full/00000007.png"},{"thumb":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/10pc/00000008.png","full":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/full/00000008.png"},{"thumb":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/10pc/00000009.png","full":"https://s3-us-west-2.amazonaws.com/lens-resource/patent/US/B2/9801/9801819/image/page/full/00000009.png"}],"fallover":false},"countryName":"USA","inventorModel":{"inventors":[{"name":{"value":"LEE DER-YANG","valueNormalised":"Lee Der-yang"},"inventorship":null}],"inventorships":[],"unmatchedInventorships":[],"activeUserHasInventorship":false},"simpleFamilyId":186212704,"citesPatentCount":40,"countrySpec":{"countryName":"USA","description":"GRANTED PATENT AS SECOND PUBLICATION [FROM 2001 ONWARDS]","rule":"pubdate:AFTER:01-01-2001","docType":"GRANTED_PATENT"},"pageTitle":"US 9801819 B2 - Racecadotril compositions","documentTitle":"Racecadotril compositions"},"claims":{"source":"xml_claims","claims":[{"lines":["A composition comprising:\n
racecadotril, polyoxyl 35 castor oil USP/NF, glyceryl caprylate mono- and diglycerides USP/NF and caprylic/capric triglycerides, 70:30/C8:C10 USP/NF."],"number":1,"annotation":false,"title":false,"claim":true},{"lines":["The composition of claim 1, wherein the composition is stable for about 40 weeks at 40° C."],"number":2,"annotation":false,"title":false,"claim":true},{"lines":["The composition of claim 1, wherein the at least one surfactant is present in an amount from about 88 wt. % to about 91 wt. % in total per 100 ml of the composition."],"number":3,"annotation":false,"title":false,"claim":true},{"lines":["The composition of claim 1, wherein the caprylic/capric triglycerides is present in an amount of from about 1 wt. % to about 2 wt. % lipid per 100 ml of the composition."],"number":4,"annotation":false,"title":false,"claim":true},{"lines":["The composition of claim 1, further comprising an optional ingredient selected from the group consisting of preservatives, sweeteners, viscosity modifiers, colors, aromas, flavors, and mixtures thereof."],"number":5,"annotation":false,"title":false,"claim":true},{"lines":["The composition of claim 1, further comprising an optional ingredient selected from the group consisting of citric acid, sodium benzoate, sucralose, flavors and mixtures thereof."],"number":6,"annotation":false,"title":false,"claim":true},{"lines":["A dosage form comprising the composition of claim 1, wherein the dosage form is a soft shell dosage form, a hard shell dosage form, or a tablet dosage form."],"number":7,"annotation":false,"title":false,"claim":true},{"lines":["The composition of claim 1, wherein the composition has a total water content of less than about 3.5 wt. % based on the total weight of the composition."],"number":8,"annotation":false,"title":false,"claim":true},{"lines":["The composition of claim 1, further comprising a second active ingredient that is a digestive health active ingredient."],"number":9,"annotation":false,"title":false,"claim":true},{"lines":["A composition comprising:\n
about 3.0 wt. % to about 7.0 wt. % racecadotril;\n
about 40 wt. % to about 53 wt. % of polyoxyl 35 castor oil USP/NF, glyceryl caprylate mono- and diglycerides USP/NF in total; and\n
about 40 wt. % to about 53 wt. % and caprylic/capric triglycerides, 70:30/C8:C10 USP/NF;\n
wherein each wt. % is based upon 100 ml of the composition."],"number":10,"annotation":false,"title":false,"claim":true},{"lines":["A dosage form comprising the composition of claim 10, wherein the dosage form is a soft shell dosage form, a hard shell dosage form, or a tablet dosage form."],"number":11,"annotation":false,"title":false,"claim":true},{"lines":["A method for treating a subject experiencing diarrhea comprising the step of orally administering to the subject a composition comprising racecadotril, polyoxyl 35 castor oil USP/NF, glyceryl caprylate mono- and diglycerides USP/NF and caprylic/capric triglycerides, 70:30/C8:C10 USP/NF."],"number":12,"annotation":false,"title":false,"claim":true},{"lines":["A composition comprising:\n
racecadotril, polyoxyl 35 castor oil USP/NF, glyceryl caprylate mono- and diglycerides USP/NF and caprylic/capric triglycerides, 70:30/C8:C10 USP/NF, and a digestive health active ingredient selected from the group consisting of laxatives, antacids, proton pump inhibitors, anti-gas agents, antiemetics, H2 blockers, and antidiarrheal agents."],"number":13,"annotation":false,"title":false,"claim":true},{"lines":["The composition of claim 13, wherein the anti-gas agent is simethicone."],"number":14,"annotation":false,"title":false,"claim":true},{"lines":["The composition of claim 13, wherein the antidiarrheal agent is loperamide."],"number":15,"annotation":false,"title":false,"claim":true},{"lines":["A composition comprising:\n
racecadotril, polyoxyl 35 castor oil USP/NF, glyceryl caprylate mono- and diglycerides USP/NF and caprylic/capric triglycerides, 70:30/C8:C10 USP/NF,\n
wherein the racecadotril is present in amount from about 8% to about 10% by weight of a total weight of the composition."],"number":16,"annotation":false,"title":false,"claim":true}]}},"filters":{"npl":[],"notNpl":[],"applicant":[],"notApplicant":[],"inventor":[],"notInventor":[],"owner":[],"notOwner":[],"tags":[],"dates":[],"types":[],"notTypes":[],"j":[],"notJ":[],"fj":[],"notFj":[],"classIpcr":[],"notClassIpcr":[],"classNat":[],"notClassNat":[],"classCpc":[],"notClassCpc":[],"so":[],"notSo":[],"sat":[]},"sequenceFilters":{"s":"SEQIDNO","d":"ASCENDING","p":0,"n":10,"sp":[],"si":[],"len":[],"t":[],"loc":[]}}