FORMULATIONS OF FUNCTIONAL ADDITIVES AND METHOD FOR ENCAPSULATING SAME IN A HYDROPHOBIC MATRIX

Abstract

The present invention is related to the inclusion of dehydrated and encapsulated functional additives formulations in food matrices.

For the encapsulation of the additives, molten hydrophobic mixtures of fatty acids and longchain saponified fatty acids were used under simple encapsulation techniques that require minimum residence times and early solidification.

These specific mixtures of coating materials and the manufacturing process confer physical and chemical resistance to the formulated additives, which allows their use as functional ingredients in industrial processes, such as the production of balanced foods, concentrated foods, dry or wet foods, for humans or animals; where extrusion, baking or pelletizing processes are used, without the additives losing their viability and activity.

Claims

1-12. (canceled)

13. A hydrophobic encapsulating matrix configured to protect functional additives, the hydrophobic encapsulating matrix comprising: a mixture of fatty acids and saponified fatty acids with divalent cations of magnesium (Mg) and/or calcium (Ca), in a ratio between 0.05 to 19, and long-chain saturated fatty acids comprising more than 10 carbon atoms, the long-chain saturated fatty acids selected from the group consisting of stearic acid (C18:0), palmitic acid (C16:0), myristic acid (C14:0), oleic acid (C18:1), arachidic acid (C20:0), lauric acid (C12:0) and capric acid (C10).

14. The hydrophobic encapsulating matrix as recited in claim 13 further comprising a mixture of fatty acids and saponified fatty acids of the type GRASS saturated and unsaturated with a melting point higher than 100° C.

15. The hydrophobic encapsulating matrix as recited in claim 13, wherein the hydrophobic encapsulating matrix is configured to protect dry functional additives, dry enzymes, encapsulated or absorbed essential oils on a dry matrix and organic minerals, wherein the mass ratio of the hydrophobic encapsulating matrix to the functional additive is between 40% to 90%, and preferably between 50% and 60%, by weight of a final encapsulated product.

16. An encapsulating method configured to protect functional additives, the method comprising the following steps: i) Providing a hydrophobic encapsulating matrix configured to protect functional additives, the hydrophobic encapsulating matrix comprising: a mixture of fatty acids and saponified fatty acids with divalent cations of magnesium (Mg) and/or calcium (Ca), in a ratio between 0.05 to 19, and long-chain saturated fatty acids comprising more than 10 carbon atoms, the long-chain saturated fatty acids selected from the group consisting of stearic acid (C18:0), palmitic acid (C16:0), myristic acid (C14:0), oleic acid (C18:1), arachidic acid (C20:0), lauric acid (C12:0) and capric acid (C10), wherein the functional additives are selected from the group consisting of dry functional additives, dry enzymes, encapsulated or absorbed essential oils on a dry matrix and organic minerals, and wherein the mass ratio of the hydrophobic encapsulating matrix to the functional additive is between 40% to 90%, and preferably between 50% and 60%, by weight of a final encapsulated product, ii) Melting the fatty acids in a pot and mixing them with the saponified fatty acids to obtain a melted mixture, iii) Adding the melted mixture of functional additives to a rotating chamber, and iv) Sprinkling or pouring the melted mixture of fatty acids and saponified fatty acids into a rotating chamber comprising a speed between 80 RMP to 200 RPM and a deflector with an inclination between 0° to 90° relative to the vertical plane of the rotating chamber.

17. The method as recited in claim 16 wherein sprinkling or pouring the melted mixture into a rotating chamber comprising a speed between 80 RMP to 200 RPM and a deflector with an inclination between 0° to 90° relative to the vertical plane of the rotating chamber further comprises sprinkling or pouring the melted mixture into a rotating chamber comprising a temperature between 0° C. to 90° C.

18. The method as recited in claim 16 wherein the functional additives comprise an average diameter between 20 .Math.m and 2000 .Math.m, and preferably between 500 .Math.m and 1300 .Math.m.

19. The method as recited in claim 16 further comprising uniformly adding the melted mixture with a conical-type droplet sprinkler with a hole or solid cone with a standard angle of dispersion and a nozzle hole between 0.030 inches to 0.2 inches in diameter.

20. The method as recited in claim 16 further comprising uniformly adding the melted mixture through a conical weir comprising a mouth diameter between ⅛ inch and 1 inch, and preferably between ¼ inch and ⅓ inch.

21. A formulation of multispecies strains used as a functional additive, the formulation comprising: a mixture of probiotic species selected from the group consisting of saccharomycescerevisiae 1.2 x 10.sup.9 Colony Forming Units (CFU)/g, saccharomycesc.var. boulardi 2 x 10.sup.8 CFU/g, Enterococcusfaecium 4x 10.sup.7 CFU/g, Lactobacilluscasei 3.7 x 10.sup.8 CFU/g and Lactobacillusacidophilus 3.7 x 10.sup.8 CFU/g; each one of the probiotic species coated with a hydrophobic encapsulating matrix comprising: a mixture of fatty acids and saponified fatty acids with divalent cations of magnesium (Mg) and/or calcium (Ca), in a ratio between 0.05 to 19, and long-chain saturated fatty acids comprising more than 10 carbon atoms, the long-chain saturated fatty acids selected from the group consisting of stearic acid (C18:0), palmitic acid (C16:0), myristic acid (C14:0), oleic acid (C18:1), arachidic acid (C20:0), lauric acid (C12:0) and capric acid (C10), and the percentage by weight of the hydrophobic encapsulating matrix to the final weight of the encapsulated probiotic species being between 40% and 60%.

22. The formulation as recited in claim 9 wherein the functional additive is added to a feed concentrate in proportions of 50 g/ton to 3000 g/ton.

23. A formulation of multispecies strains used as a functional additive, the formulation comprising: a mixture of probiotic species selected from the group consisting of saccharomyces cerevisiae type 1.2 x 10.sup.9 CFU/g, saccharomyces c. varBoulardii type 2 x 10.sup.8 CFU/g and Enterococcusfaecium type 4 x 10.sup.8 CFU/g, each one of the probiotic species coated with an encapsulating matrix comprising: a mixture of fatty acids and saponified fatty acids with divalent cations of magnesium (Mg) and/or calcium (Ca), in a ratio between 0.05 to 19, and long-chain saturated fatty acids comprising more than 10 carbon atoms, the long-chain saturated fatty acids selected from the group consisting of: stearic acid (C18:0), palmitic acid (C16:0), myristic acid (C14:0), oleic acid (C18:1), arachidic acid (C20:0), lauric acid (C12:0) and capric acid (C10), and the percentage by weight of the hydrophobic encapsulating matrix to the final weight of the encapsulated probiotic species being between 40% and 60%.

24. The formulation as recited in claim 23 wherein the functional additive is added to a feed concentrate requiring resistance to extrusion, pelletizing, or baking processes at temperatures of 70° C. to 120° C.; the functional additive being added to the feed concentrate in proportions of 50 g/ton to 3000 g/ton.

Description

DETAILED DESCRIPTION

[0030] The present invention is related to the encapsulation of dehydrated functional additive formulations in thermo-resistant matrices and their inclusion in processed or concentrated food.

[0031] For the encapsulation of the additives, the invention uses fused hydrophobic mixtures of fatty acids and long-chain saponified fatty acids under simple encapsulation techniques that require minimum residence times and early solidification. These specific mixtures of coating materials with the manufacturing method confer physical and chemical resistance to the formulated additives. That allows their use as functional ingredients in industrial processes, such as the production of balanced foods, concentrated foods, dry or humid foods, for humans or animals; where extrusion, baking, or pelletizing are used, without the additives losing their viability and activity. This encapsulation method allows, additionally, to protect functional additives from ruminal pH in polygastric animals and stomach acids in monogastric and polygastric animals, allowing their release in the intestine to exert their effect on the intestinal microbiota. The invention is implemented for dehydrated functional additives formulations of such as probiotics, prebiotics, enzymes, encapsulated essential oils or previously conveyed on a dry matrix, dehydrated natural active principles, organic acids, organic minerals, vitamins, as well as thermolabile molecules and their application in pharmaceutical, dietetic or food compositions.

[0032] The central idea of the present invention is related to mixtures of encapsulating materials, which include mixtures of fatty acids and saponified fatty acids with a long chain longer than 10 carbon atoms.

[0033] Saturated fatty acids are preferred over unsaturated ones due to their physicochemical properties, such as higher melting points and higher chemical stability understood as low reactivity under certain conditions. The encapsulating material, as it is composed of a physical mixture of fatty acids and saponified fatty acids with a long chain greater than 10 carbon atoms, allows the shell to resist temperatures between 70-120° C. used in the elaboration of food products in animal nutrition such as pelletized extrusion or baking.

[0034] Hence, it is ensured that the encapsulated additives, included in the concentrated food formulated in proportions of 50 g/ton up to 3000 g/ton, survive the host’s gastric system and, due to a combined effect of pH and enzymes, dissociate so that the additive fraction functionalities that include probiotics, enzymes, prebiotics, and other additives are released generating a positive change in the intestinal level.

[0035] An essential aspect of the present invention is that, due to the use of substances of a hydrophobic nature as coating material, it is possible to use encapsulated probiotic formulations and combine them with highly hygroscopic mineral salts, used mainly in livestock, without these salts affect the viability of the encapsulated microorganism by breaking the cell wall. In this way, the present invention makes it possible to include the specific combination of probiotic strains, dry natural extracts or absorbed on natural polymers, encapsulated prebiotics, and mineral salts with therapeutic or nutritional effects within the same food composition that confer benefits on the host’s health.

[0036] The encapsulation method of the present invention occurs inside a rotating chamber. First, there is a mass of microorganisms in permanent rotation. Then, the material is added uniformly through a micro-droplet sprinkler molten encapsulant. The chamber that contains the microorganisms to be coated is at room temperature, which is compatible with the survival of the more heat-sensitive microorganisms. The critical factor that controls the viability of the microorganisms in this stage is the solidification speed of the encapsulating material. This factor, due to the particle size of the drops that can be obtained with a sprinkler of the conical type with a hole or solid cone with dispersion angle standard and nozzle hole between 0.030 to 0.2 inches in diameter or a conical weir with a mouth diameter between ⅛” and 1” preferably between ¼” and ½” loses enough energy for immediate solidification on the additive, without causing significant loss of viability in dehydrated living microorganisms or measurable damage to the chemical structure of thermolabile molecules such as some natural extracts.

[0037] The formulations of the present invention are specific combinations of functional additives such as living thermosensitive microorganisms of a different probiotic nature, including Lactobacillusspp., Bifidobacteriumspp., Enterococcusfaecium, Saccharomycescerevisiaevar. Boulardii, SaccharomyCerevisiae, mixed with polysaccharide prebiotics such as fructooligosaccharides and mananooligosaccharides and yeast cell walls and in some cases natural dehydrated plant extracts or absorbed functional oils on natural flours or polymers such as cinnamaldehyde and garlic extract. The specific formulations of the present invention can be used as functional additives in the preparation of concentrated animal food, particularly in weaned piglets, allowing to improve performance and efficient replacement in the use of animal growth-promoting antibiotics.

[0038] The present invention provides a technology to elaborate or prepare hydrophobic encapsulating matrices, also known as coatings or shells or covering layers, highly stable, through specific mixtures of fatty acids and saponified fatty acids with a long chain greater than 10 atoms of Carbon to be used as an encapsulating material for functional additives due to its hydrophobic physical properties, its stability, its high melting point, and its dissociation in the intestine. The use of fatty acids mixed with saponified fatty acids represents a significant difference from traditional compositions for producing encapsulation matrices of living microorganisms and other functional additives. The term “saponified fatty acids” or “saponified lipids” or “soap” or “carboxylic salt” in the present invention refers to fatty acids bound to divalent cations such as magnesium (Mg2 +) or calcium (Ca2 +), generally produced by alkaline hydrolysis of glycerides. Especially, magnesium stearate or calcium palmitate, or calcium soaps produced by hydrolysis of palm stearin with calcium oxide or hydroxide are preferred, any saponified of the GRASS type fatty acids (Generally Recognized as Safe Substances) saturated and unsaturated with a high melting point higher than 100° C., preferably higher than 150° C.

[0039] Under gastric conditions, these dissociate or hydrolyze at pH less than 3, at temperatures between 37 and 39° C. and with the action of pepsins in times higher than 1 hour and a half, preferably 1 hour, to release the functional additive in the intestine and performs its function on the microbiota. As the functional additive is released, the encapsulating matrix is adsorbed in the body through the metabolic pathway of fats. Long-chain saturated fatty acids longer than 10 carbon atoms are preferred as fatty acids due to their high melting point, preferably stearic acid (C18:0), palmitic acid (C16:0), but is also useful myristic acid (C14:0), oleic acid (C18:1), arachidic acid (C20:0), lauric acid (C12:0), capric acid (C10:0).

[0040] The main characteristics of encapsulating matrices are their melting point that can be between 60 and 140° C., preferably between 70 and 120° C.; the ratio between fatty acid and saponified fatty acid that determines the melting point of the coating and that varies between 0.05 and 19, preferably between 1 and 19, understanding the ratio as the amount in mass units (g, Kg, ton) of saponified fatty acid per each mass unit (g, kg, ton) of fatty acid. For ratios close to 0.05, the coating may be inadequate for protection in extrusion processes because the melting point will be closer to the fatty acid than the saponified fatty acid. Another characteristic of encapsulating matrices is their physicochemical stability, understood as the ability not to react or break in the face of stressful environmental conditions such as relative humidity above 95% and even in aqueous solutions. The encapsulating matrix is stable when the solution has a pH greater than 3 and temperatures below 37° C. These encapsulating matrices do not affect ruminal metabolism; they are insoluble in the rumen and resist the enzymatic action of ruminal microorganisms, they do not affect fiber digestion, once they reach the abomasum they are hydrolyzed, and the fatty acids and the free ion are absorbed in the intestine.

[0041] According to the present invention, the encapsulating matrix includes dry functional additives, dry enzymes, essential oils encapsulated or absorbed on a dry matrix, dry natural active principles, organic acids, organic minerals, among others, where the mass ratio of the encapsulating matrix with the amount of functional additive it varies between 40 to 90% by weight of the final encapsulated product, preferably between 50 and 60%.

[0042] As used in the present invention, the term functional additive, includes dry or lyophilized thermolabile or thermosensitive microorganisms such as Lactobacillusspp., Bifidobacteriumspp, Enterococcusfaecium, Saccharomycescerevisiaevar. Boulardii, SaccharomyCerevisiae, and its combination with polysaccharide prebiotics such as fructooligosaccharides and mannanoligosaccharides, in addition to the yeast cell wall and some cases thermolabile natural extracts such as cinnamaldehyde extract or garlic extract, which, as proposed by the European Food Safety Authority, are considered as zootechnical additives, in the category of digestibility enhancers or stabilizers of the intestinal microbiota and GRASS.

[0043] The dried probiotic microorganisms of the present invention are living cells that have been dried by lyophilization or drying techniques that guarantee post-processing viability. Its shape can be spherical, ovoid, or elongated, smooth or rough, regular, or irregular, and whose size can be between 1 .Math.m and 1000 .Math.m in diameter.

[0044] Next are some important taxonomic genera:

A. BifidobacteriumSPP

[0045] Bifidobacteriumspp, found in the Bifidobacterium family, is a Gram-positive bacterium that is not mobile, anaerobic, and non-spore-forming. Instead, the bacterium is rod-shaped and can live in groups, pairs, or even independently. Most of the Bifidobacterium population has been found in the colon, lower small intestine, and breast milk; however, Bifidobacteriumspp is found mainly in the large intestine. Bifidobacteriumspp is found mainly in the large intestine. Bifidobacterium helps the body absorb calcium, iron, magnesium, vitamins, and minerals, and it also produces lactic and acetic acids to inhibit pathogenic bacteria. As a result, it can reduce the incidence of severe diarrhea in neonates and is beneficial in treating inflammatory bowel disease (colitis). The metabolic mechanism can be by heteromorphosis to ferment glucose, galactose, and fructose, to produce lactic and acetic acid, and to produce enzymes and vitamins. Bifidobacterium bifidum is the most popular probiotic Bifidobacterium and the most dominant in the intestine of neonates, which is why they are called in some cases “growth factors”.

B. LactobacillusSPP

[0046] Lactobacillusspp is a gram-positive bacterium rod-shaped and often found in the small intestine. It produces lactic acid, acetic acid, and antibiotics that protect against harmful bacteria. Lactobacillusspp is also Co-assistant in maintaining the balance of the intestinal microbiota and stimulating the immune system. Lactobacillusspp. is a homofermentative and microaerophilic species; it ferments sugars into lactic acid and multiplies at relatively low pH values (below pH 5.0); it has an optimal growth temperature of around 37° C. Lactobacillus is part of the natural microbiota in mammals located in the gastrointestinal tract, the animal mouth, and urinary tract. It has the typical character of lactic acid bacteria to produce lactic acid, acetic acid, and natural antimicrobials such as acidolin, acidophilin and aethocydon, which helps inhibit the other pathogenic bacteria. It can grow both in residual oxygen or not; although it grows better in an aerobic environment, it can even survive in media with nitrogen dioxide. It can also create lactase, an enzyme that turns lactose (milk sugar) into simple sugar.

C. EnterococcusFaecium

[0047] Enterococcusfaecium is a gram-positive bacterium that inhabits the gastrointestinal tracts of humans and other mammals. Enterococcusfaecium is an immobile, facultative anaerobic microbe; It ferments glucose without gas production, it does not produce the catalase reaction with hydrogen peroxide. It produces lactic acid, vitamins, enzymes, and antibacterial substances and inhibits the growth of E- coli, Salmonella, and Staphylococcusaureus. It strengthens the immune system, improves disease resistance, reduces digestive tract and respiratory diseases, lowers fecal ammonia concentrations, and improves breeding.

D. Saccharomycesspp

[0048] Saccharomycesspp belongs to the genus of yeasts of the saccharomycetaceae family; It is a eukaryotic cell different from prokaryotic bacteria; the cells are spheroidal, ellipsoidal, or cylindrical. S. cerevisiaevarBoulardii is widely used in monogastric nutrition due to its benefits at the intestinal level, its outstanding resistance to antibiotics, because it is a yeast and not a bacterium, and because of its wide growth range at different pH values. This yeast competes directly with Streptococcusbovis in sugar consumption, reducing the occurrence of this bacterium capable of destabilizing the intestines and rumen and associated in some cases with tumors or intestinal lacerations; this is a significant effect in the probiotic use of yeast.

[0049] A test to probe thermal resistance was performed by subjecting the encapsulating matrix of the present invention in conjunction with other encapsulating matrices developed from conventional compounds such as stearic acid. The thermal process was carried out at 70° C. and 2 hours, and losses of less than 10% were evidenced on a logarithmic basis of the matrix reported in this invention, and losses of complete viability for the other matrices. Another test of the thermal stability of probiotic bacteria covered by the shell described in the present invention was analyzed in an extrusion process to produce concentrated pet food where temperatures between 100 and 120° C. are used for up to 3 minutes. Again, the results showed the viability of the microorganism higher than 85% measured on a logarithmic basis, preferably between 85-90% after the process. The concentration of viable bacteria is expressed as CFU / g: the unit that forms a colony per gram of coated particles of the microorganism before and after each exposure. According to conventional techniques, the measurement method is based on the microbiological count of colonies after breaking the encapsulating matrix and an appropriate dilution.

[0050] In another test, ruminal, gastric, pancreatic stability, and intestinal release were analyzed for an encapsulated yeast by the technology described in the present invention. The results showed more than 75% viability, preferably between 80-90%, after ruminal, gastric, and pancreatic digestions. In addition, in a comparative in vivo test, it was possible to recover the additive from the fecal matter of a bovine supplemented with an encapsulated yeast described by the method of the present invention, a case that was not evidenced with the yeast encapsulated with stearic acid. The results showed the release and growth capacity of the additive in the intestine from the protection provided by the encapsulating matrix of this invention compared to other matrices used for the same purpose.

[0051] Otherwise, the variation of the physicochemical stability understood as the ability not to react, not solubilize and not break in time during storage and particular uses, was evaluated under harsh conditions when mixing additives encapsulated by the technology described in the present invention, with mineral salts for livestock containing 24% sodium chloride, 2.5% phosphorus, 13% calcium, 3% magnesium, 10% sulfur, 0.028% fluorine, 0.2% copper, zinc al 0.6%, iodine at 0.01% and cobalt at 0.01%, stored outdoors in open salting rooms and places with a relative humidity higher than 94%, specifically between 95-96%. For more than 5 days, the viability of the encapsulated additives was evaluated while the mixture was wetted to the point of deliquescence, where the mineral salts were solubilized. The results showed that 85% of the additive viability was preserved after testing, and the encapsulating matrix never hydrated or broke or solubilized or reacted with the mixture.

[0052] Another object of the present invention is the referred method for coating the functional additive. This method consists of several stages, as shown in FIG. 1:

[0053] (i) Encapsulating matrix: The fatty acid is previously melted in a pot at a controlled temperature between 60-75° C. Subsequently, the finely ground powdered saponified lipid is added to the pot to achieve the encapsulating mixture in the desired ratios according to the application, preferably in a mass ratio between 1-19 mass of saponified fatty acid per mass of fatty acid. Finally, the mixture is shaken for a specified time, between 2-20 minutes.

[0054] (ii) Functional additives: The dry functional additives, which may include microorganisms, are deposited in a rotating cylindrical chamber of 1.2 m in diameter equipped with a deflector with an inclination between 0 and 90° to the vertical wall chamber, preferably between 30°- 45°, and a drip sprinkler or weir. The chamber’s rotation speed is measured as revolutions per minute (rpm) is controlled by a variable frequency drive from 0 to 60 Hz, preferably between 20-40 Hz for a speed of rotation between 80-200 rpm.

[0055] (iii) encapsulation process: It is initiated by the controlled rotation of the mass of functional additives that hit the deflector, causing turbulence in the dry mass. After reaching a suitable rotation speed, the spraying of the encapsulating mixture is started at an average speed of 2-4 L/min, preferably between 3-3.5 L/min. The chamber’s temperature is at room temperature, which is compatible with the survival of the most thermo-sensitive or thermo-labile microorganisms. The inclination of the internal deflector to the vertical plane of the chamber and the speed of rotation determines the degree of dispersion and homogenization of the dry functional additives, which allows the molten encapsulating material to be added uniformly through a conical type sprinkler with a hole or solid cone with standard dispersion angle and nozzle hole between 0.030 to 0.2 inches in diameter or from a conical weir with a mouth diameter between ⅛ “and 1”, preferably between ¼ “- ½”. In addition, the deflector also controls the particle size since its degree of inclination and collision with the mass of additives breaks the aggregates of larger spheres, individualizing them into smaller spheres (iv).

[0056] Once the spraying operation is finished, the rotational movement of the chamber stops, and the encapsulated product is collected. The final temperature of the products is generally between 35 and 40° C.

[0057] For saponified fatty acid/fatty acid mass ratios of 0.05 and 1, it is also feasible to use encapsulation techniques such as those used in fluidized bed chambers.

[0058] Some ratios of fatty acids and saponified fatty acids that make up the encapsulating matrix affect its viscosity, making it necessary to use a conical weir instead of a droplet sprinkler with a mouth diameter between ⅛” and 1", preferably between ¼”-½”. Other mass ratios of the encapsulating matrix components can be highly viscous. Viscosity measurements can be determined among other methods through the MFI melt index. In cases where the MFI is lower than 16, the use of other conventional encapsulation techniques such as melt injection or melt extrusion is preferred in which functional additives are deposited on the molten encapsulating matrix and then injected through a filter or extrusion screw, preferably operating between 100 and 130° C. to form pellets. Sometimes, to apply these extrusion processes on the functional additives to be encapsulated, it is necessary to first carry out an initial coating with an encapsulating matrix such as the one described in this invention with a mass ratio between saponified fatty acids and fatty acids between 0.05 and 1.

[0059] As an important notation, the encapsulations obtained in the rotating chamber are different from those obtained in conventional spray towers or other rotating chambers. The technique to which the present invention refers prioritizes the relation between saponified fatty acids and fatty acids as a fundamental parameter to control the agglomeration of particles and to favor a determined particle size.

[0060] The encapsulated functional additive particles obtained through this method and with the encapsulating matrix technology have an average size between 20 and 2000 .Math.m in diameter, preferably between 500-1300 .Math.m, where the mechanical resistance is favored by the chemical structure of the shell and its homogeneous composition of hydrophobic material that does not show cavities on the surface allowing complex conditions of use.

[0061] In a particular essay, the use of an injection encapsulation method of melted mass was tested when the mass ratio of saponified fatty acids/fatty acids was higher than 9, preferably 17-19. The results shown that this method encapsulated additive and whit the encapsulating matrix of the present invention, conserved a high viability after the process.

[0062] Finally, when the specific combined use of certain functional additives that are encapsulated with the encapsulating matrix of the present invention are dosed on pelletized animal food, it confers benefits in the host’s health on a determined period of life and, they are a sustainable and natural alternative for profitable livestock production when substituting growth promoter antibiotics use. It was evidenced that encapsulation of several probiotic strains with the encapsulating matrix of the present invention promotes at an intestinal level a positive response on microbiota at a taxonomic genus level and species on weaned piglets in the pre-fattening stage during the first 70 days of life. Additionally, the consumption of these functional additives improves food conversion, and, at the same time, they replace the prophylactic animal growth-promoting antibiotics.

[0063] For instance, an important aspect of the present invention provides a formulation of substitutes functional additives of antibiotics on weaned piglets composed by encapsulated microorganisms such as, Saccharomycescerevisiae, Saccharomycesboulardii, Enterococcusfaecium, Lactobacilluscasei, Lactobacillus acidophilus, that once incorporated as functional additives in a pelletized concentrated food for weaned piglets based on grains such as corn and soy, lactose, fish meal, hemoglobin, amino acids, minerals, and vitamins; showed a significant improvement (P<0,05) in the food conversion factor compared to those foods that contained antibiotic additives such as animal growth promoters and foods that did not have probiotic or antibiotic additives. The food conversion factor is expressed as the relation between the food consumption in mass units and the pig’s weight gain in mass units in a given time; this period could be weekly, monthly, or stages.

[0064] Following are described examples of encapsulating mixtures of saponified fatty acids and fatty acids with different active ingredients applications with variations in both the correlation between fatty acids and saponified fatty acids and the connection between active ingredients and the encapsulating matrix, as well as different techniques used according to the rheology of the encapsulating mixture and its application, several specific formulations of encapsulated functional additives are also described that were evaluated to replace growth-promoting antibiotics and improve food conversion.

Example 1

[0065] Enterococcusfaecium coating with a stearic acid and magnesium stearate (saponified lipid) mixture with a melting point above 75° C.

[0066] Lyophilized Enterococcusfaecium bacteria powder, SF-GA12 strain, registered in the CCTCC with the number M 2015444, are introduced in a rotating cylindric chamber with a deflector.

[0067] The stearic acid was melted in a pot at a controlled temperature of 65-71° C. Once the stearic acid has melted, the magnesium stearate (melting point 150-160° C.) is added. This mixture was sprayed into the rotating chamber containing the lyophilized bacteria powder. The percentage of the encapsulating matrix is 48-50% of the final weight of the encapsulated product. Therefore, the ratio of the encapsulating mixture (g of magnesium stearate / g of stearic acid) is between 0.9-1.2.

[0068] The coating operation was carried out according to the following parameters: [0069] Chamber rotation speed: 80-110 rpm [0070] Coating speed: 3-3.5 L/min. [0071] Stearic acid and magnesium stearate mixture temperature: 70-100° C. [0072] Product temperature when leaving the chamber: 35-40° C. [0073] Deflector angle: 45 °.

[0074] At the end of the operation, the particles are collected and stored in hermetic sachets.

[0075] The obtained particles have the following characteristics:

[0076] The average diameter of the particles is 1400 .Math.m, with 92% between 1000 and 1800 .Math.m in diameter.

[0077] The concentration of viable bacteria in the starting powder is between 2x10.sup.10 and 1.7x10.sup.10 CFU/g, and at the end of the operation, the coated particles have a concentration between 1.3x10.sup.10 and 1x10.sup.10 CFU/g. The result shows a recovery percentage of viable cells on a logarithmic basis of 98% according to the following formula:

[00001]$1-\frac{Log\left(2\times {10}^{10}\right)-\text{Log}\left(1.3\times {10}^{10}\right)}{Log\left(2\times {10}^{10}\right)}=0,98$

Example 2

[0078] Lactobacilluscasei coating with melting point above 90° C.

[0079] Lyophilized Lactobacilluscaseifaecium bacteria powder, LG-G11 strain, registered in the CCTCC with the number M 2013196, was introduced in the same rotating cylindric chamber with deflector as in example 1. The stearic acid was melted in a pot at a controlled temperature, as in example 1. Once the stearic acid had melted, the magnesium stearate (melting point 150-160° C.) was added. This mixture was sprayed into the rotating chamber as in example 1. The percentage of the encapsulating matrix is 48-50% of the final weight of the encapsulated product. Therefore, the ratio of the encapsulating mixture (g of magnesium stearate / g of stearic acid) is between 0.3-0.45.

[0080] The coating operation was carried out according to the following parameters: [0081] Chamber rotation speed: 80-120 rpm. [0082] Coating speed: 3-3.5 L/min. [0083] Stearic acid and magnesium stearate mixture temperature: 70-100° C. [0084] Product temperature when leaving the chamber: 35-40° C. [0085] Deflector angle: 70 °.

[0086] At the end of the operation, the particles are collected and stored in hermetic sachets.

[0087] The obtained particles have the following characteristics:

[0088] The average diameter of the particles is 800 .Math.m, with 92% between 500 and 1200 .Math.m in diameter.

[0089] The concentration of viable bacteria in the starting powder is between 1x10.sup.10 and 9x10.sup.10 CFU / g, and at the end of the operation, the coated particles have a concentration between 5x10.sup.9 and 4x10.sup.9 CFU / g. The result shows a recovery percentage of viable cells on a logarithmic basis of 97% according to the following formula:

[00002]$1-\frac{Log\left(1\times {10}^{10}\right)-\text{Log}\left(7\times {10}^9\right)}{Log\left(1\times {10}^{10}\right)}=0,97$

Example 3

[0090] Coating of a mixture of functional additives with a melting point above 90° C.

[0091] A formulation of the following lyophilized probiotics: Lactobacilluscasei, LactobacillusAcidophilus, BifidobacteriumBifidum, and Enterococcusfaecium, was previously mixed and homogenized in a powder mixer. Once finished the homogenization, this mixture was introduced in the same rotating chamber as in example 1. Subsequently, the mixture of molten encapsulating material formed by stearic acid and magnesium stearate was added. The mixture was previously carried out in a pot at a controlled temperature, as in Example 1. The percentage of the encapsulating matrix is 55-60% of the final weight of the encapsulated product. Therefore, the ratio of the encapsulating mixture (g of magnesium stearate / g of stearic acid) is 3.5-4.

[0092] The coating operation was carried out according to the following parameters: [0093] Chamber rotation speed: 80-120 rpm. [0094] Coating speed: 3-3.5 L/min. [0095] Stearic acid and magnesium stearate mixture temperature: 70-100° C. [0096] Product temperature when leaving the chamber: 35-40° C. [0097] Deflector angle: 35°

[0098] At the end of the operation, the particles are collected and stored in hermetic sachets.

[0099] The obtained particles have the following characteristics:

[0100] The average diameter of the particles is 900 .Math.m, with 90% between 600 and 1500 .Math.m in diameter.

[0101] The concentration of viable bacteria in the starting powder is lyophilized Lactobacilluscasei 2x10.sup.9 CFU/g, lyophilized LactobacillusAcidophilus 2x10.sup.9 CFU/g, lyophilized BifidobacteriumBifidum 2x10.sup.9 CFU/g, lyophilized Enterococcusfaecium 2x10.sup.9 CFU/g. After the encapsulation process, the average concentration of coated particles is 1x10.sup.9 CFU/g of each bacterium. The result shows a recovery percentage of viable cells on a logarithmic basis of 98% according to the following formula:

[00003]$1-\frac{Log\left(8\times {10}^9\right)-\text{Log}\left(5\times {10}^9\right)}{Log\left(8\times {10}^9\right)}=0,98$

Example 4

[0102] Saccharomycescerevisiae coating with a melting point above 90° C.

[0103] Commercial dry living yeast of the genus saccharomyces and the species cerevisiae were introduced in a rotating chamber with a deflector like in example 1. As in example 1, the mixture formed by stearic acid and magnesium stearate was prepared in a pot at a controlled temperature. Then, the mixture was sprayed into the rotating chamber, as in example 1. The percentage of the encapsulating matrix is 45-55% of the final weight of the encapsulated product. Therefore, the ratio of the encapsulating mixture (g of magnesium stearate / g of stearic acid) is between 1 - 2.

[0104] The coating operation was carried out according to the following parameters: [0105] Chamber rotation speed: 80-120 rpm [0106] Coating speed: 2-4 L/min. [0107] Stearic acid and magnesium stearate mixture temperature: 70-100° C. [0108] Product temperature when leaving the chamber: 35-40° C. [0109] Deflector angle: 40°

[0110] At the end of the operation, the particles are collected and stored in hermetic sachets.

[0111] The obtained particles have the following characteristics:

[0112] The average diameter of the particles is 1100 .Math.m, with 92% between 500 and 2200 .Math.m in diameter.

[0113] The concentration of viable bacteria in the starting powder is between 8.5x10.sup.9 and 9x10.sup.9 CFU/g, and at the end of the operation, the coated particles have a concentration between 7x10.sup.9 and 6x10.sup.9 CFU / g. The result shows a recovery percentage of viable cells on a logarithmic basis of 99% according to the following formula:

[00004]$1-\frac{Log\left(9\times {10}^9\right)-\text{Log}\left(7\times {10}^9\right)}{Log\left(9\times {10}^9\right)}=0,99$

Example 5

Comparative Thermal Stability

[0114] Dry yeast particles Saccharomycescerevisiae type were coated with stearic acid through a process carried out in a granulation chamber with rapid microdroplets cooling of coating substance. As in example 4, dry yeast particles Saccharomyces cerevisiae type were encapsulated. Both products were studied under the following conditions:

[0115] 3 g samples of each preparation were introduced into sealed tubes kept in a water bath at 75° C. A tube of each preparation was removed from the water bath after 1, 4, 7, and 24 hours to determine the concentration of viable cells.

[0116] The results listed in the following table refer to CFU/g concentrations for a given time range and its viability loss through time taking as reference base the concentration reported in t=0h.

TABLE-US-00001 Time (h) 0 1 4 7 24 Sample 1 (Encapsulated yeast with stearic acid) 1 × 10.sup.10 1 × 10.sup.3 No count No count No count Sample 2 (Encapsulated yeast from example 4) 1 × 10.sup.10 1 × 10.sup.10 1 × 10.sup.10 9 × 10.sup.9 8 × 10.sup.9

[0117] When both samples reached 67° C., the encapsulated yeast with stearic acid (sample 1) began to melt its coating leaving the yeast exposed, thus promoting the viability loss in each sampling. After 4 hours of being under the test conditions, sample 1 completely lost its viability. On the other hand, sample 2 yeast continued stable during the 24 h of the entire experiment. Thus, superior hydrophobic protection is demonstrated using of the mixture of fatty acid and long-chain saponified fatty acid as encapsulating material.

Example 6

[0118] Thermal stability, recovery in extruded food.

[0119] The encapsulation additives formulation from example 3 was dosed at a rate of 500 g of encapsulated additives per ton of food in the industrial production of an extruded pet food processed in a single crew extruder that operates at a temperature between 100-120° C. Subsequently to the food production process, the food was sampled and analyzed in the laboratory to count CFU/g. The Table 2 presents the results and are compared with the initial formulation.

TABLE-US-00002 Additive formulations Average concentration Encapsulated lactic acid bacteria formulation (LAB) from example 3 before adding to the extruded food. 2.5 × 10.sup.6 CFU/g of extruded food. Encapsulated lactic acid bacteria formulation (LAB) encapsulated in extruded food after production. 8 × 10.sup.5 CFU/g of extruded food.

[0120] The fatty acids and saponified fatty acids from example 3 allowed the formulation of additives composed of lactic acid bacteria to hold the extrusion process and maintain an appropriate concentration of viable cells for commercial use.

Example 7

[0121] Coating of a Saccharomycescerevisiae yeast with a mixture of palm stearin (palmitic acid) and palm stearin saponified with calcium hydroxide (calcium palmitate) with a melting temperature higher than 120° C. through melt injection.

[0122] Encapsulated yeast particles from Example 4 were coated through a mix by injection with a molten viscous mass composed of palm stearin and calcium palmitate. The mixture was let into an extrusion screw that works between 100 and 120° C. to form pellets. The percentage of the encapsulating matrix is 40-70% of the final weight of the encapsulated product. Therefore, the mass ratio of the encapsulating mixture (g of palm stearin / g of calcium palmitate) is between 0.1 - 0.3.

[0123] The coating operation was carried out according to the following parameters: [0124] Screw rotor frequency: 15-50 Hz. [0125] Palm stearin and calcium palmitate mixture temperature: 80-140° C. [0126] Product temperature when leaving the chamber: 50-60° C.

[0127] At the end of the operation, the pellets are collected and stored in hermetic sachets.

[0128] The obtained particles have the following characteristics:

[0129] The average diameter of the particles is 2000 .Math.m, with 92% between 1000 and 2900 .Math.m in diameter.

[0130] The concentration of viable bacteria in the starting powder is between 2x10.sup.9 and 2.8x10.sup.9 CFU/g, and at the end of the operation, the coated particles have a concentration between 1x10.sup.9 and 1.2x10.sup.9 CFU / g. The result shows a recovery percentage of viable cells on a logarithmic basis of 97% according to the following formula:

[00005]$1-\frac{Log\left(2\times {10}^9\right)-\text{Log}\left(1\times {10}^9\right)}{Log\left(2\times {10}^9\right)}=0,97$

Example 8

[0131] Weatherability of the encapsulation matrix in hygroscopic media with mineral salts.

[0132] Dry yeast particles Saccharomyces cerevisiae type microsphere shape, deposited species in the CNCM with the number NCYC Sc 47 1-440 (sample 1), and encapsulated dry yeast particles Saccharomyces cerevisiae type according to example 4 (sample 2) were studied with the following conditions:

[0133] 10 grams of each sample were homogeneously mixed with 150 g of a mineralized salt for fattening cattle composed of 24% sodium chloride, 2.5% phosphorus, 13% calcium, 3% magnesium, 10% sulfur, 0.028% fluorine, 0.2% copper, 0.6% zinc, 0.01 % iodine and 0.01 % cobalt. Subsequently, the salts mixtures with yeasts are left open weather where the relative humidity is 95% in an open saltshaker for 4 days. Every 24 h, a 5 g sample was taken from each trial, and the CFU / g were evaluated.

[0134] The results listed in the following table refer to CFU/g concentrations for a given time range and its viability loss through time taking as reference base the concentration reported in t=0h.

TABLE-US-00003 Time 0 24 h 48 h 72 h 96 h Commercial dry yeast 1 × 10.sup.11 1 × 10.sup.5 1 × 10.sup.1 No count No count Encapsulated yeast from example 4 7 × 10.sup.9 7 × 10.sup.9 7 × 10.sup.9 6 × 10.sup.9 6 × 10.sup.9

[0135] After 24 h commercial dry yeast, began to rapidly lose activity (CFU/g) and after 72 h it didn’t show activity. On the other hand, the encapsulated yeast with the hydrophobic mixture of fatty acids and saponified fatty acids described in the present invention showed activity throughout the test, remaining functional for its final use.

Example 9

[0136] Ruminal, gastric, and pancreatic stability, with study of release in the intestine and recovery in feces.

[0137] Encapsulated yeast samples from example 4 were used in an in vitro test developed in three phases and an application in situ:

First Phase: Ruminal Digestion

[0138] 1.5 g encapsulated yeast samples were taken according to example 4 and packed in 20 ANKOM F57 bags, specially designed for this type of incubation with a pore size of 50 .Math.m. Before placing the sample inside, the bags were labeled and weighed. Furthermore, incubation in the ruminal liquid was realized during 48 h with regular shaking and at a controlled temperature of 39° C. in DAISY II equipment, ANKOM Technology. Ruminal digestion used culture media with microorganisms and a McDougall buffer solution (NaHCO3 (9.8 g/L), Na2HPO4 (2.44 g/L), KCI (0.57 g/L), NaCl (0.47 g/L), MgS04.sub.' 7H2O (0.12 g/L), CaCI2 2H2O(0.16 g/L)) to keep a constant pH. The ruminal content was taken from 4 animals cannulated to the rumen.

[0139] Subsequently, the bags were taken to the laboratory where the CFU/g of encapsulated yeast were measured. Data are presented in the following table:

TABLE-US-00004 CFU/g before digestion CFU/g after ruminal digestion 5 × 10.sup.10 1 × 10.sup.10

[0140] The samples with the encapsulated coating reported in the present invention showed their capacity to resists ruminal conditions, showing matrix physicochemical stability to neutral pH and microbiological action of ruminal microbiota.

Second Phase: Gastric Digestion

[0141] 1.5 g encapsulated yeast samples were taken according to example 4 and packed in 20 ANKOM F57 bags, specially designed for this type of incubation with a pore size of 50 .Math.m. Before placing the sample inside, the bags were labeled and weighed. Furthermore, incubation in the ruminal liquid was realized during 1h in chlorohydric acid solution 0.1 M (HCI) pH2, under pepsin action at 37-39° C. with regular shaking, simulating stomachal digestion conditions. After 2 h of incubation, the bags were taken to the laboratory to make microbiological culture. Data are presented in the following table:

TABLE-US-00005 CFU/g before digestion CFU/g after gastric digestion, solid phase CFU/g after gastric digestion, liquid phase 5 × 10.sup.10 1 × 10.sup.10 3 × 10.sup.8

[0142] The evidence of the effectiveness of the coating by the encapsulating mixture became evident during the first hour, the encapsulating matrix was able to preserve 60% of the initial weight of encapsulated additive located in the respective bags, after the first hour, the acid hydrolyzed the encapsulating material evidenced by a greater loss in mass and a reduction in the size of the encapsulated additives, at 2 h a CFU / g counting was made of the residual solid phase and the liquid phase, the colony counting demonstrates the protection that the coating achieves over the encapsulated additives at those pH conditions over time. Monogastric animals have stomach transit times close to 1 hour for which it is expected that the encapsulated content will be released in the intestine which is located immediately after the stomach system.

Third Phase: Pancreatic Digestion

[0143] 10 resulting samples from the acid digestion and their liquid content were taken; an incubation was carried out in a potassium phosphate solution (KH2PO4) with pancreatin (an enzyme with lipase activity) in a period of 4-8 h. Subsequently, the samples were cultured in Sabouraud dextrose Agar, and after 48 h, the colony counting was done.

TABLE-US-00006 CFU/g before digestion and after acid digestion CFU/g after pancreatic digestion solid phase CFU/g after pancreatic digestion liquid phase 1 × 10.sup.10 1 × 10.sup.9 2 × 10.sup.8

[0144] This pancreatic digestion test simulates a part of the intestine where enzymes are liberated with lipase activity to hydrolyze triglycerides and release fatty acids. The conclusion was that the comminated action of acids and stomachal enzymes with the pancreatic lipases could unfold the encapsulating matrix releasing functional additives at the intestinal level to produce their effect on the intestinal microbiota.

In Vivo Test

[0145] Dry yeast particles Saccharomyces cerevisiae type coated with fatty acids, obtained as in example 4, were studied under the following conditions:

[0146] In vivo test of cattle prolonged exposure to encapsulated living yeast supplementation with stearic acid and encapsulated yeast as in example 4 was done. For 26 days, 2 bovines were inoculated with 1 g/day of living encapsulated yeast with stearic acid, and 2 bovines were inoculated with 1 g/day of living yeast with encapsulating matrix of the present invention prepared as in example 4. In addition, on days 22, 23, 24, 255, and 26, feces samples were taken and cultured to identify the recovery of Saccharomyces cerevisiae using the API 20 C AUX method from bioMerieux SA.

[0147] The results showed that Saccharomyces cerevisiae was recovered from the bovines’ feces supplemented with living encapsulated yeast, as in example 4. On the other hand, it was impossible to recover the living encapsulated yeast with stearic acid of any bovine supplemented with this sample. Thus, this test demonstrated the efficiency and protection capacity and controlled release of the encapsulated additives with the encapsulated matrix of this invention, which guarantees the beneficial effects on the intestinal microbiota of polygastric animals.

Example 10

[0148] Application of two specific formulations of encapsulated additives to replace animal growth-promoting antibiotics.

[0149] In vivo test with weaned piglets divided into 4 groups, with four different diets (D1, D2, D3, and D4), evaluated the effect in the food conversion, the intestinal microbiota composition, and the replacement of animal growth-promoting antibiotics from day 21 (weaning) until the day 70 of life. Each group had an average of 9,52 animals and three (3) replications of the entire trial, for 111 evaluated animals in total, where 27,75 animals were evaluated on average per diet. Following, the conditions and the results of the trial are shown.

Diet 1 (D1)

[0150] Pelletized concentrated food for weaned piglets based on grains such as corn and soy, lactose, fish meal, hemoglobin, amino acids, minerals, and vitamins, plus a specific formulation of functional additives incorporated in the 500 g/ton dose of food base. The specific formulation 1 of functional additives contains:

[0151] Saccharomycescerevisiae 1.2 x 10.sup.9 CFU/g encapsulated as in example 4, S. Boulardii 2 x 10.sup.8 UFC/g y E. faecium 4 x 10.sup.8 UFC/g encapsulated as in example 1 of the present invention.

[0152] [00184] Pelletized concentrated food for weaned piglets based on grains such as corn and soy, lactose, fish meal, hemoglobin, amino acids, minerals, and vitamins, plus a specific formulation of functional additives incorporated in the 500 g/ton dose of food base. The specific formulation 2 of functional additives contains:

Diet 2 (D2)

[0153] Encapsulated Saccharomycescerevisiae 1.2 x 10.sup.9 CFU/g as in example 4, S. Boulardii 2 x 10.sup.8 CFU/g, E. faecium 4 x 10.sup.7 CFU/g, Lactobacilluscasei 3.7 x 10.sup.8 CFU/g and encapsulated Lactobacillusacidophilus 3.7 x 10.sup.8 CFU/g as in example 3.

Diet 3 (D3)

[0154] Pelletized concentrated food for weaned piglets based on grains such as corn and soy, lactose, fish meal, hemoglobin, amino acids, minerals, and vitamins, plus the following animal growth-promoting antibiotics: Doxycycline 0.08% of the formulation, Zinc bacitracin 0.05% of the formulation, valosin 0.04% and neomycin 0.02% of the formulation.

Diet 4 (D4)

[0155] Pelletized concentrated food for weaned piglets based on grains such as corn and soy, lactose, fish meal, hemoglobin, amino acids, minerals, and vitamins, without the addition of probiotic or antibiotic additives.

[0156] Evaluation conversion factor results (CF) for each one of the 4 diets are listed in Table 4. The diets with functional additives content D1 and D2 were those where the piglets had to be fed with less concentrate to gain 1.0 kg of body mass.

TABLE-US-00007 Diets Average cumulative food conversion from day 21 to day 70 of life Total number of animals evaluated in the three repetitions Diet 1 1.48 29 Diet 2 1.51 28 Diet 3 1.58 27 Diet 4 1.57 27

[0157] In the trial, the supplemented diets with encapsulated functional additives improved the food conversion for diet 1 between 5% and 8%, preferably between 6% and 7%, according to the antibiotics diet, this when is compared to diet 3, showing efficacy in the zootechnic response of the specific formulation of encapsulated functional additives trough the described techniques in the present invention.

[0158] In diet 2 trial, supplemented with encapsulated functional additives improved the food conversion for diet 1 between 3% and 7%, preferably between 5% and 6%, according to the antibiotics diet, showing efficacy in the zootechnic response of the specific formulation of encapsulated functional additives trough the described techniques in the present invention.

[0159] Additionally, during trial 36 feces samplings were taken to determine fecal microbiota of the piglets and seek for changes at the level of bacterial communities that could be related with the use of different diets. The sampling of the animals and the sequencing technique used are described below.

[0160] Additionally, during the test, 36 fecal matter samples were taken to determine the fecal microbiota of the piglets and look for changes at the level of bacterial communities that could be related to the use of different diets. The sampling of the animals and the sequencing technique used are described below.

[0161] From each of the four diets, 9 animals were randomly chosen, divided into groups of three according to the different growth stages of the trial; for greater clarity, the following sampling table is presented.

TABLE-US-00008 Diet Piglet’s stage 1= first weaning week Piglet’s stage 2 = third weaning week Piglet’s stage 3 = seventh weaning week Total sampled animals Diet 1 M1, M2, M3 M4, M5, M6 M7, M8, M9 9 Diet 2 M10, M11, M12 M13, M14, M15 M16, M17, M18 9 Diet 3 M19, M20, M21 M22, M23, M24 M25, M25, M26 9 Diet 4 M27, M28, M29 M30, M31, M32 M33, M34, M35 9

[0162] Single or paired-end sequence reads were generated using the Illumina NovaSeq 6000 or MiSeq system. The generated sequences with the MiSeq system were realized under accreditation according to the scope of the provider. (L457; NEN-EN-ISO / IEC 17025). When the paired-end sequencing is made, the “Reading numbers” refers to reading pairs.

[0163] The files of FAST sequences were generated using bcl2fastq2, 2.18 version. The initial quality evaluation was based on data through the Illumina Chastity filter. Subsequently, the sequences that contained the PhiX control signal were eliminated using an internal device of filter protocol. Moreover, sequences containing (partial) adapters) were trimmed (to a minimum reading length of 50 bp).

[0164] The second quality evaluation was based on the remaining sequences using the quality control tool FASTQC 0.11.5 version.

[0165] Paired-end sequences were collapsed into the so-called pseudo threads using sequence overlap with USEARCH 9.2 version (Edgar, 2010).

[0166] The pseudo-processes classification is accomplished in function of the alienation results with SNAP 1.0.23 version (Zaharia et al., 2011) against the database RDP (Cole et al., 2014) for bacterial organisms, while the fungal organisms are classified using the genes database UNITE ITS (Abarenkov et al., 2010).

[0167] Results showed that many of the encapsulated species with the encapsulated matrix of the present invention were identified mostly (higher probability of finding) in the animals that consumed these diets, compared to the animals that consumed other diets.

[0168] Results showed that many of the encapsulated species with the present invention’s encapsulated matrix were primarily identified (higher probability of finding) in the animals that consumed these diets, compared to those that consumed other diets.

TABLE-US-00009 Lactobacilluacidophilus Diet Piglet’s stage 1 Piglet’s stage 2 Piglet’s stage 3 Total positive simples for L. Acidophilus Diet 1 0/3 1/3 1/3 2 (22%) Diet 2 3/3 3/3 2/3 8 (89%) Diet 3 1/3 1/3 0/3 2 (22%) Diet 4 3/3 1/3 0/3 4 (44%)

TABLE-US-00010 Lactobacilluscasei Diet Piglet’s stage 1 Piglet’s stage 2 Piglet’s stage 3 Total positive samples for L. casei Diet 1 0/3 0/3 0/3 0 (0%) Diet 2 1/3 0/3 0/3 1 (11.1%) Diet 3 0/3 0/3 0/3 0 (0%) Diet 4 0/3 0/3 0/3 0 (0%)

TABLE-US-00011 Enterococcusfaecium Diet Piglet’s stage 1 Piglet’s stage 2 Piglet’s stage 3 Total positive samples for E. Faecium Diet 1 0/3 1/3 0/3 1 (11.1%) Diet 2 1/3 0/3 0/3 1 (11.1%) Diet 3 1/3 0/3 0/3 1 (11.1%) Diet 4 0/3 0/3 0/3 0 (0%)

[0169] The main conclusion of this analysis is that animals that consumed diet 2 (D2) showed a higher probability in their feces of detecting sequences of encapsulated bacterial strains, which is strongly related with the formulation of these in said diet.

[0170] The main conclusion of this analysis is that animals that consumed diet 2 (D2) showed a higher probability in their feces of detecting sequences of encapsulated bacterial strains, which is strongly related to the formulation of these in the said diet.

[0171] Regarding the bacterial diversity understood as the richness and relative abundance of the intestinal microbiota of the animals associated with the different diets, it was found that the animals that consumed Diet D2 supplemented with encapsulated additives had greater bacterial diversity (p <0, 05) compared to basal diet D4 when analyzing Shannon’s entropy.

[0172] In the same diet D2, a higher bacterial richness (p <0.05) was observed compared to the other diets when analyzing the Chao index, the analysis were carried out using a one-factor ANOVA and a Tukey HSD test, while the antibiotic diet had a higher probability (66.6%) of reducing bacterial diversity compared to the other diets when using the Simpson index in a probability analysis by quartiles, in this same analysis, it was found that 77.7% of the samples of the diet D2 were located in the first two quartiles (50%) with a value between 0.0135 and 0.0461 of Simpson indices, while 44.4% of Simpson indices of diets D1 and D4 were in the first two quartiles and 55% in the last two. For clarity, check the following table:

TABLE-US-00012 Diets Simpson indices (D) Shannon entropy Chao index D2 0.0135 7.24 557.2 D2 0.0172 6.88 517.7 D3 0.0239 6.57 413.9 D3 0.0276 6.29 409.9 D2 0.0293 6.47 484.4 D2 0.0302 6.31 461.5 D2 0.0306 6.06 403 D4 0.0331 6.17 431.3 D1 0.0338 6.1 414.6 D1 0.0358 6.33 482.1 D2 0.0364 6.17 424.9 D4 0.0367 6.25 469.8 D3 0.0393 5.86 312.2 D4 0.0398 5.96 391.5 D1 0.0422 5.76 334.4 D4 0.0435 5.8 354.6 D2 0.0457 6.02 408.1 D1 0.0461 5.97 411.3 D4 0.0465 5.2 218.4 D4 0.0471 5.48 276.8 D1 0.0512 5.69 283.7 D1 0.0531 5.42 253.1 D3 0.0604 5.18 248.1 D3 0.061 5.03 205.6 D2 0.0615 5.87 433.5 D4 0.0621 5.45 256.3 D1 0.0645 5.24 280.8 D3 0.0689 5.46 394.4 D2 0.0728 5.61 375.5 D1 0.0774 5.24 283.2 D3 0.0867 4.99 302.4 D3 0.0926 4.8 183.2 D3 0.123 4.36 208.8 D4 0.134 4.22 200.7 D1 0.23 3.77 156.2 D4 0.254 3.05 108.1