CS270801B1 - Method of lysine or tylosine containing stable bioconcentrates preparation - Google Patents
Method of lysine or tylosine containing stable bioconcentrates preparation Download PDFInfo
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- CS270801B1 CS270801B1 CS839769A CS976983A CS270801B1 CS 270801 B1 CS270801 B1 CS 270801B1 CS 839769 A CS839769 A CS 839769A CS 976983 A CS976983 A CS 976983A CS 270801 B1 CS270801 B1 CS 270801B1
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- lysine
- bioconcentrates
- preparation
- amount
- tylosin
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Links
- 239000004472 Lysine Substances 0.000 title claims abstract description 15
- 238000000034 method Methods 0.000 title claims abstract description 14
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 title claims abstract description 11
- WBPYTXDJUQJLPQ-VMXQISHHSA-N tylosin Chemical compound O([C@@H]1[C@@H](C)O[C@H]([C@@H]([C@H]1N(C)C)O)O[C@@H]1[C@@H](C)[C@H](O)CC(=O)O[C@@H]([C@H](/C=C(\C)/C=C/C(=O)[C@H](C)C[C@@H]1CC=O)CO[C@H]1[C@@H]([C@H](OC)[C@H](O)[C@@H](C)O1)OC)CC)[C@H]1C[C@@](C)(O)[C@@H](O)[C@H](C)O1 WBPYTXDJUQJLPQ-VMXQISHHSA-N 0.000 title claims abstract description 9
- 238000002360 preparation method Methods 0.000 title claims abstract description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 26
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 13
- 239000004182 Tylosin Substances 0.000 claims abstract description 9
- 229960004059 tylosin Drugs 0.000 claims abstract description 9
- 229930194936 Tylosin Natural products 0.000 claims abstract description 8
- 235000019375 tylosin Nutrition 0.000 claims abstract description 8
- 238000001035 drying Methods 0.000 claims abstract description 5
- 230000002209 hydrophobic effect Effects 0.000 claims description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 13
- 239000002028 Biomass Substances 0.000 claims description 10
- 239000000377 silicon dioxide Substances 0.000 claims description 6
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims description 5
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims 2
- 239000000126 substance Substances 0.000 abstract description 8
- 239000000047 product Substances 0.000 abstract description 7
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 238000001694 spray drying Methods 0.000 abstract description 2
- 239000013589 supplement Substances 0.000 abstract description 2
- 244000144972 livestock Species 0.000 abstract 1
- 230000000087 stabilizing effect Effects 0.000 abstract 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 15
- 235000018977 lysine Nutrition 0.000 description 7
- 239000002245 particle Substances 0.000 description 5
- 235000019766 L-Lysine Nutrition 0.000 description 4
- 238000000855 fermentation Methods 0.000 description 3
- 230000004151 fermentation Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000013543 active substance Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000007888 film coating Substances 0.000 description 2
- 238000009501 film coating Methods 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 108010001478 Bacitracin Proteins 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- -1 Sipermat 17 Chemical compound 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 229960003071 bacitracin Drugs 0.000 description 1
- 229930184125 bacitracin Natural products 0.000 description 1
- CLKOFPXJLQSYAH-ABRJDSQDSA-N bacitracin A Chemical compound C1SC([C@@H](N)[C@@H](C)CC)=N[C@@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]1C(=O)N[C@H](CCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2N=CNC=2)C(=O)N[C@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)NCCCC1 CLKOFPXJLQSYAH-ABRJDSQDSA-N 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 235000020776 essential amino acid Nutrition 0.000 description 1
- 239000003797 essential amino acid Substances 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000012051 hydrophobic carrier Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000003120 macrolide antibiotic agent Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
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- Fodder In General (AREA)
Abstract
Description
Vynález sa týká spůsobu přípravy stabilných biokoncentrátov s obsahom lyzínu alebo tylozínu.The invention relates to a process for preparing stable bioconcentrates containing lysine or tylosin.
V súčasnej době sú esenciálně aminokyseliny okrem vitamínov najčastejšie používané látky při výživě poínohospodárskych, užitkových zvierat vo formě stabilizovaných biokoncentrátov ako doplňky biofaktorov, připadne domedikovaných krmných prípravkov a krmných zmesí. Pripravujú sa v prevažnej miere fermentáciou a následnou izoláciou buď kryštalizáciou z přečištěných roztokov alebo sprayovým sušením zahustenej biomasy na technické produkty. Při sprayovom sušení vyfermentovanej viac-menej zahustenej biomasy získané produkty sú z ekonomického a biologického híadiska veími výhodné, nakoíko odpadá energeticky, časovo náročná a pracná izolácia a s ňou spojené straty účinnej látky a hmota, ktorá je okrem účinnej látky přítomné v koncentráte je biologicky využitelná, nakoíko pozostáva z koagulovaných bielkovinových stien mikroorganienov z fermentačnej půdy. Značnou nevýhodou takýchto produktov je výrazná hygroskopicita, lepivosí a tým ovplyvnená ich stabilita. V krátkej době po sušení nastane agregácia častíc, zvýšenie povrchovej vlhkosti a nebezpečie mikrobiálnej kontaminácie vysušenej biomasy.At present, essential amino acids, in addition to vitamins, are the most commonly used substances in the nutrition of agricultural, utility animals in the form of stabilized bioconcentrates as biofactor supplements, possibly domedicated feed preparations and compound feeds. They are prepared predominantly by fermentation and subsequent isolation either by crystallization from purified solutions or by spray-drying of concentrated biomass to technical products. Spray-dried fermented, more or less thickened biomass products are very economically and biologically advantageous, since energy, time-consuming and laborious isolation and associated losses of the active substance are eliminated, and the material present in the concentrate is bioavailable, as it consists of coagulated protein walls of microorganisms from fermentation broth. A considerable disadvantage of such products is the pronounced hygroscopicity, tackiness and hence their stability. In a short time after drying, particle aggregation, increased surface moisture and a risk of microbial contamination of the dried biomass will occur.
Na znífcenie hygroskopicity prachov, kryštálov a granulátov sa používá niekoíko spůsobov. Najčastejšie je filmové obaíovanie častíc s filmotvornou látkou rozpuštěnou v organickom rozpúšladle. Technolgia je známa v bežnej farmaceutickéj praxi (E.L.Parrott: 'Pharmaceutical Technology, Burgess Publ. Compl, Minneapolis USA, 1970). Nevýhodou je komplikovaný proces, zdražovanie výroby, zvýšenie rizika nebezpečia výbuchu a ohrozenia zdravia obsluhujúceho personálu. Při filmovom obalovaní taktiež dochádza к zníženiu biologickej zúžitkovateínosti výživných látok z důvodu nerovnoměrněj hrůbky nanesenej filmotvornej látky. 'Several methods have been used to reduce the hygroscopicity of dusts, crystals and granules. Most often, the film coating of the particles with the film former is dissolved in an organic solvent. Technology is known in conventional pharmaceutical practice (E. L. Parrott: Pharmaceutical Technology, Burgess Publ. Compl, Minneapolis USA, 1970). The disadvantage is a complicated process, higher production costs, increased risk of explosion hazard and endangering the health of the operating personnel. Film coating also reduces the bioavailability of nutrients due to the uneven thickness of the applied film-forming substance. '
Předkládaný vynález rieši uvedené nedostatky při přípravě sušených technických produktov s obsahom lyzínu a tylozínu tak, že sa počas.sprayovania biomasy primiešava hydrofóbny materiál v práškovej formě, ktorý obalí hygroskopické hydrofilné částice sušeného biokoncentrátu. Takto vytvořený hydrofóbny film zabráni zlepeniu častíc, produkt je sypký a stabilnější voči vonkajším vplyvom. К lepšiemu rozdeleniu hydrofóbneho materiálu sa může používal nosič ní báze anorganickej zlúčeniny.The present invention addresses the above drawbacks in the preparation of dried lysine-tylosin-containing technical products by admixing a hydrophobic material in powder form which encapsulates the hygroscopic hydrophilic particles of the dried bioconcentrate during the biomass spraying. The hydrophobic film thus formed prevents the particles from sticking together, the product being free-flowing and more stable to external influences. A carrier base of the inorganic compound may be used to better distribute the hydrophobic material.
Ako najvhodnejší nosič sa ukázal uhličitan vápenatý, ktorý může byt plavený, zrážaný alebo mikromletý s maximálnou veíkoslou častíc do 100 /um. Povrchová úprava jemného uhličitanu vápenatého sa vyhotovuje metodou fyzikálneho miešania silné hydrofóbnej látky s velkých povrchom alebo súčasným mletím uhličitanu vápenatého s hydrofóbnou látkou s nižším bodom topenia, ktorá rovnoměrně obalí anorganický nosič. Hydrofóbne látky musia byl zdravotně nezávadné.Calcium carbonate has proven to be the most suitable carrier, which can be floated, precipitated or micronized with a maximum particle size of up to 100 µm. The surface treatment of the fine calcium carbonate is made by the physical mixing method of a strong hydrophobic substance with a large surface area or by simultaneous grinding of the calcium carbonate with a hydrophobic substance with a lower melting point which uniformly encapsulates the inorganic carrier. Hydrophobic substances must be harmless to health.
Při přípravě hydrofobizovaného anorganického nosiča, keó sa jedná o úpravu pomocou mechanického zmiešania sa výhodné může používal hydrofóbny kysličník křemičitý (napr. Sipermat 0 17, Aerosil R 972 a pod.), alebo sa anorganický nosič hydrofobizuje hydrofóbnymi látkami s nižším bodom topenia jeho mletím za tepla. *In the preparation of a hydrophobic inorganic carrier, such as by mechanical mixing, hydrophobic silica (e.g., Sipermat 17, Aerosil R 972 and the like) may be advantageously used, or the inorganic carrier may be hydrophobized with hydrophobic substances with a lower melting point by grinding it heat. *
Podstata vynálezu spočívá v dávkovaní hydrofobizovaného uhličitanu vápenatého na atomizovanú zahustenú biomasu v množstve 10 až 30 % hmot, s obsahom lyzinu alebo tylozínu počas sušiaceho procesu, při teplote 85 až 110° C.SUMMARY OF THE INVENTION The invention is based on the addition of hydrophobized calcium carbonate to an atomized concentrated biomass in an amount of 10 to 30% by weight, containing lysine or tylosin during the drying process, at a temperature of 85 to 110 ° C.
Sypnosl upraveného, hydrofobizovaného technického lyzínu sa skúšala metodou podía Kleina (Klein,K.: Seifen-01e-Fette-Wachse, 94, 12, 1968). Pri tejto metóde sa hmoty vyhodnocujú faktormi od 1 do 6, kde nižšie číslo znamená vždy vyššie a výhodnejšie sypné vlastnosti skúšenej látky.The loosening of the treated, hydrophobized technical lysine was tested by the Klein method (Klein, K., Seifen-01e-Fette-Wachse, 94, 12, 1968). In this method, the masses are evaluated by factors ranging from 1 to 6, where the lower number always indicates the higher and more preferably the flow properties of the test substance.
CS 270 801 B1CS 270 801 B1
Při pokusoch sme používali ako modelové látku aminokyseliny ako např. technický lyzín, antibiotiká ako např. tylozín, bacitracin, ktoré sú veími obtiažne spracovateíné do suchej formy, ale postup, ktorý uvádzame, je použitelný aj pre ostatně biologicky aktivně materiály technickej kvality, t.j. v prípadoch ked účinná látka sa suší priamo spolu s biomasou.In the experiments we used amino acids such as e.g. technical lysine, antibiotics such as e.g. tylosin, bacitracin, which are very difficult to process into a dry form, but the process we present is also applicable to other biologically active materials of technical quality, i. in cases where the active substance is dried directly together with the biomass.
Technický lyzín, neupravovaný hydrofóbnym anorganickým nosičom sa nedal vyhodnocoval uvedenou metodou, nakoíko niekoíko minút pri uchovávaní na Petriho miske při relatívnej vlhkosti 80 %, teplote 25° C sa vytvořil tuhý agregát.Technical lysine, untreated with a hydrophobic inorganic carrier, was not evaluated by the above method, as a solid aggregate was formed for several minutes when stored on a Petri dish at a relative humidity of 80% at 25 ° C.
Při modelovom pokuse bol použitý vyfermentovaný lyzín (obsah sušiny 42 %) a ako hydrofóbny nosič uhličitan vápenatý hydrofobizovaný hydrofóbnym kysličníkom křemičitým a v druhom případe stearínom.In the model experiment, fermented lysine (42% solids content) was used and as a hydrophobic carrier calcium carbonate hydrophobized with hydrophobic silica and in the second case with stearin.
Při tých istých podmienkach uchovávané homogenizáty technického lyzínu s rfiznymi koncentráciami hydrofobizovaného uhličitanu vápenatého vykazovali následovně hodnoty:Under the same conditions, stored lysine technical homogenates with close concentrations of hydrophobized calcium carbonate exhibited the following values:
AA
Koncentrácia hydrofobizovaného uhličitanu vápenatého (% hmot.) (úprava s 10 4 hmot.Concentration of hydrophobized calcium carbonate (% by weight) (10 4 wt.
val : .val:.
Příklad 1 .Example 1.
Vyfermentovaná, zahuštěná biomasa s obsahom L-lyzínu 62 kg.m-^ sa dávkuje do rozprašovacej sušiarne rýchlosfou 34,6 kg.h“1 pri teplote 210° C na vstupe a 106° C na výstupe. Zároveň sa tryskou v protisměre rozprašuje zdravotně nezávadným hydrofóbnym kysličníkom křemičitým hydrofobizovaný uhličitan^vápenatý rýchlosíou 1,4 kg.h'1. Uhličitan vápenatý bol hydrofobizovaný zmiešaním s hydrofóbnym kysličníkom krémičitým v hmotnostnom pomere 10 í 1 v homogenizačnom zariadení. Připravený stabilný biokoncentrát technickej kvality s obsahom L-lyzínu 40 až 43 % hmot, sa adjustuje běžným spčsom.The fermented, concentrated biomass with an L-lysine content of 62 kg.m - 1 is fed to the spray dryer at a rate of 34.6 kg.h -1 at 210 ° C inlet and 106 ° C at outlet. At the same time, hydrophobised calcium carbonate is sprayed in a counter-direction through the nozzle at a rate of 1.4 kg.h- 1 with non-toxic hydrophobic silica. The calcium carbonate was hydrophobised by mixing with a hydrophobic cream of 10 µl in a homogenizer. The prepared, stable, technical grade bioconcentrate with an L-lysine content of 40 to 43% by weight is adjusted by conventional means.
Příklad 2 . ’Example 2. '
Biomasa po fermentácii s obsahom makrolidového anitobiotika tylozínu o sušině 7 % hmot, sa atomizuje v sprayovej sušiarni pri teplote na vstupe 195° C, 102° C na výstupe řýchlosťou 23 kg.h1. Do sušiaceho priestoru sa súčasne tryskou v protisměre přidává hydrofóbnym kysličníkom křemičitým hydrofobizovaný uhličitan vápenatý v pomere 100 : 8 rýchlosťou 0,32 kg.h“^. Připravený stabilný technický biokoncentrát s obsahom antibiotika tylozínu sa adjustuje běžným spósobom pře ďalšie spracovanie do krmných zmesí pre veterinárně použitie.After fermentation, the biomass containing 7% by weight of the macrolide anitobiotics tylosin is atomized in a spray dryer at an inlet temperature of 195 ° C, 102 ° C at an outlet at a rate of 23 kg.h 1 . Hydrophobic calcium carbonate in a ratio of 100: 8 at the rate of 0.32 kg.h -1 is simultaneously added to the drying space through the nozzle in the opposite direction by hydrophobic silica. The prepared stable technical bioconcentrate containing the antibiotic tylosin is adjusted in a conventional manner before further processing into compound feed for veterinary use.
CS 270 801 B1CS 270 801 B1
Příklad 3Example 3
Vyfermentovaná, zahuštěná biomasa s obsahom L-lyzínu 60 kg.m·5 sa dávkuje do rozprašovacej sušiarne rýchlosťou 35 kg.h”^ při teplote na vstupe 210° C, 106° C na výstupe, zároveň sa v protisměre do sušiaceho priestoru rozprašuje stearínom hydrofobizovaný uhličitan vápenatý v pomere 1 : 99 rýchlosíou 2,8 kg.h”^. Připravený technický biokoncentrát s obsahom L-lyzínu sa adjustuje běžným spósobom.The fermented, concentrated biomass with L-lysine content of 60 kg.m · 5 is fed to the spray dryer at a rate of 35 kg.h-1 at the inlet temperature of 210 ° C, 106 ° C at the outlet, and sprayed with stearin in the opposite direction hydrophobised calcium carbonate at a ratio of 1: 99 at a rate of 2.8 kg.h -1. The prepared technical bioconcentrate containing L-lysine is adjusted in a conventional manner.
Claims (3)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS839769A CS270801B1 (en) | 1983-12-22 | 1983-12-22 | Method of lysine or tylosine containing stable bioconcentrates preparation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS839769A CS270801B1 (en) | 1983-12-22 | 1983-12-22 | Method of lysine or tylosine containing stable bioconcentrates preparation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS976983A1 CS976983A1 (en) | 1989-07-12 |
| CS270801B1 true CS270801B1 (en) | 1990-08-14 |
Family
ID=5446464
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS839769A CS270801B1 (en) | 1983-12-22 | 1983-12-22 | Method of lysine or tylosine containing stable bioconcentrates preparation |
Country Status (1)
| Country | Link |
|---|---|
| CS (1) | CS270801B1 (en) |
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1983
- 1983-12-22 CS CS839769A patent/CS270801B1/en unknown
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| Publication number | Publication date |
|---|---|
| CS976983A1 (en) | 1989-07-12 |
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