KR100464983B1 - Method of emulsifying feed oil and fat soluble vitamin by using lecithin and emulsifier - Google Patents
Method of emulsifying feed oil and fat soluble vitamin by using lecithin and emulsifier Download PDFInfo
- Publication number
- KR100464983B1 KR100464983B1 KR10-2002-0061760A KR20020061760A KR100464983B1 KR 100464983 B1 KR100464983 B1 KR 100464983B1 KR 20020061760 A KR20020061760 A KR 20020061760A KR 100464983 B1 KR100464983 B1 KR 100464983B1
- Authority
- KR
- South Korea
- Prior art keywords
- fat
- lecithin
- feed
- emulsifier
- oil
- Prior art date
Links
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 title claims abstract description 51
- 235000010445 lecithin Nutrition 0.000 title claims abstract description 51
- 239000000787 lecithin Substances 0.000 title claims abstract description 51
- 229940067606 lecithin Drugs 0.000 title claims abstract description 51
- 239000003995 emulsifying agent Substances 0.000 title claims abstract description 49
- 229930003231 vitamin Natural products 0.000 title claims abstract description 37
- 235000013343 vitamin Nutrition 0.000 title claims abstract description 37
- 229940088594 vitamin Drugs 0.000 title claims abstract description 37
- 239000011782 vitamin Substances 0.000 title claims abstract description 37
- 238000000034 method Methods 0.000 title claims abstract description 35
- 230000001804 emulsifying effect Effects 0.000 title claims description 11
- 150000003722 vitamin derivatives Chemical class 0.000 title description 4
- 239000003925 fat Substances 0.000 claims abstract description 59
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 31
- 238000003756 stirring Methods 0.000 claims description 16
- 235000013311 vegetables Nutrition 0.000 claims description 10
- DECIPOUIJURFOJ-UHFFFAOYSA-N ethoxyquin Chemical compound N1C(C)(C)C=C(C)C2=CC(OCC)=CC=C21 DECIPOUIJURFOJ-UHFFFAOYSA-N 0.000 claims description 9
- 238000010792 warming Methods 0.000 claims description 7
- 239000008346 aqueous phase Substances 0.000 claims 4
- 239000012071 phase Substances 0.000 claims 3
- 238000007789 sealing Methods 0.000 claims 1
- 239000003921 oil Substances 0.000 abstract description 52
- 235000019198 oils Nutrition 0.000 abstract description 51
- 239000012528 membrane Substances 0.000 abstract description 26
- 239000002245 particle Substances 0.000 abstract description 20
- 235000021323 fish oil Nutrition 0.000 abstract description 12
- 238000010521 absorption reaction Methods 0.000 abstract description 7
- 241001465754 Metazoa Species 0.000 abstract description 6
- 210000004211 gastric acid Anatomy 0.000 abstract description 6
- 239000007788 liquid Substances 0.000 abstract description 6
- 210000004185 liver Anatomy 0.000 abstract description 6
- 230000004060 metabolic process Effects 0.000 abstract description 6
- 239000000126 substance Substances 0.000 abstract description 6
- 241000238366 Cephalopoda Species 0.000 abstract description 5
- 210000000941 bile Anatomy 0.000 abstract description 3
- 210000001035 gastrointestinal tract Anatomy 0.000 abstract description 3
- 239000000693 micelle Substances 0.000 abstract description 3
- 235000019165 vitamin E Nutrition 0.000 abstract description 3
- 239000011709 vitamin E Substances 0.000 abstract description 3
- 210000005229 liver cell Anatomy 0.000 abstract description 2
- 238000012423 maintenance Methods 0.000 abstract description 2
- 238000007254 oxidation reaction Methods 0.000 abstract description 2
- 230000006378 damage Effects 0.000 abstract 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 abstract 2
- 210000000813 small intestine Anatomy 0.000 abstract 2
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 abstract 1
- 235000019482 Palm oil Nutrition 0.000 abstract 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 abstract 1
- 229930003316 Vitamin D Natural products 0.000 abstract 1
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 abstract 1
- 229930003427 Vitamin E Natural products 0.000 abstract 1
- 229930003448 Vitamin K Natural products 0.000 abstract 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 abstract 1
- 230000029087 digestion Effects 0.000 abstract 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 230000003020 moisturizing effect Effects 0.000 abstract 1
- 235000015097 nutrients Nutrition 0.000 abstract 1
- 235000016709 nutrition Nutrition 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 239000002540 palm oil Substances 0.000 abstract 1
- SHUZOJHMOBOZST-UHFFFAOYSA-N phylloquinone Natural products CC(C)CCCCC(C)CCC(C)CCCC(=CCC1=C(C)C(=O)c2ccccc2C1=O)C SHUZOJHMOBOZST-UHFFFAOYSA-N 0.000 abstract 1
- 235000015277 pork Nutrition 0.000 abstract 1
- 235000019155 vitamin A Nutrition 0.000 abstract 1
- 239000011719 vitamin A Substances 0.000 abstract 1
- 235000019166 vitamin D Nutrition 0.000 abstract 1
- 239000011710 vitamin D Substances 0.000 abstract 1
- 150000003710 vitamin D derivatives Chemical class 0.000 abstract 1
- 229940046009 vitamin E Drugs 0.000 abstract 1
- 235000019168 vitamin K Nutrition 0.000 abstract 1
- 239000011712 vitamin K Substances 0.000 abstract 1
- 150000003721 vitamin K derivatives Chemical class 0.000 abstract 1
- 229940045997 vitamin a Drugs 0.000 abstract 1
- 229940046008 vitamin d Drugs 0.000 abstract 1
- 229940046010 vitamin k Drugs 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 description 45
- 239000000203 mixture Substances 0.000 description 36
- 238000004945 emulsification Methods 0.000 description 31
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 12
- 238000004519 manufacturing process Methods 0.000 description 11
- 238000009472 formulation Methods 0.000 description 8
- 230000032683 aging Effects 0.000 description 7
- 238000004090 dissolution Methods 0.000 description 6
- 235000013773 glyceryl triacetate Nutrition 0.000 description 6
- 239000001087 glyceryl triacetate Substances 0.000 description 6
- 229960002622 triacetin Drugs 0.000 description 6
- 239000003963 antioxidant agent Substances 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- 235000006708 antioxidants Nutrition 0.000 description 4
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- 239000011259 mixed solution Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 3
- 230000001079 digestive effect Effects 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 235000014593 oils and fats Nutrition 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 150000003904 phospholipids Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 241000588724 Escherichia coli Species 0.000 description 1
- 239000004258 Ethoxyquin Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 206010047700 Vomiting Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 229940093500 ethoxyquin Drugs 0.000 description 1
- 235000019285 ethoxyquin Nutrition 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000009830 intercalation Methods 0.000 description 1
- 230000002687 intercalation Effects 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JMZOMFYRADAWOG-UHFFFAOYSA-N methyl 7-methoxy-4-(7-methoxy-5-methoxycarbonyl-1,3-benzodioxol-4-yl)-1,3-benzodioxole-5-carboxylate Chemical compound COC(=O)C1=CC(OC)=C2OCOC2=C1C1=C2OCOC2=C(OC)C=C1C(=O)OC JMZOMFYRADAWOG-UHFFFAOYSA-N 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 230000008673 vomiting Effects 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/158—Fatty acids; Fats; Products containing oils or fats
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/174—Vitamins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2250/00—Food ingredients
- A23V2250/18—Lipids
- A23V2250/184—Emulsifier
- A23V2250/1842—Lecithin
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Animal Husbandry (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Medicinal Preparation (AREA)
- Fodder In General (AREA)
- Edible Oils And Fats (AREA)
Abstract
본 발명은 사료용으로 이용되는 유지와 액상타입의 지용성 비타민을 레시틴과 유화제를 이용하여 O/W형으로 3중막을 형성하도록 유화함으로써 물에 잘 분산되도록 하고, 유화된 입자가 위산의 작용에 의해 깨지지 않고 소장까지 도달할 수 있도록 하여 위산에 의한 영양소의 파괴를 예방하는 한편, 담즙과 잘 결합하여 미셀을 이루게 함으로써 소화흡수율을 상승시키는 방법에 관한 것이다.The present invention emulsifies oil and liquid type fat-soluble vitamins used for feed to form a triple film in O / W form using lecithin and emulsifier to be dispersed well in water, and the emulsified particles are not broken by the action of gastric acid The present invention relates to a method for increasing digestion absorption by preventing the destruction of nutrients caused by gastric acid by allowing the small intestine to reach the small intestine and forming a micelle by combining with bile.
사료용 유지는 우지, 돈지, 팜유, 어유, 오징어유를 말하며 지용성 비타민은 비타민 A, 비타민 D, 비타민 K, 비타민 E를 말하며 액상형태를 사용한다.Fodder oil refers to Uji, pork, palm oil, fish oil, and squid oil. Fat-soluble vitamins refer to vitamin A, vitamin D, vitamin K, and vitamin E. They use liquid form.
액상타입의 레시틴은 동물사료에서 지방대사기능을 향상시키는 영양성 물질이지만 위산에 의하여 가수분해되어 파괴되거나 산화되어서 독성을 나타내는 단점 때문에 사용을 기피하여 왔다.Liquid type lecithin is a nutritional substance that improves fat metabolism in animal feeds, but it has been avoided because of its shortcomings due to its hydrolysis and destruction or oxidation caused by gastric acid.
본 발명에서는 레시틴이 사료용 유지에 잘 결합하는 성질을 이용하여 1차막을 형성하고 2차막과 3차막은 HLB 값이 14 전후인 친수성기가 강한 유화제를 사용하여 막을 구성하였다.In the present invention, the lecithin binds well to feed fats to form a primary membrane, and the secondary membrane and the tertiary membrane constitute a membrane using a strong hydrophilic group having an HLB value of about 14.
유화된 막은 3중 구조로서 강하게 결합되어 있기 때문에 위산으로부터 사료용 유지, 지용성 비타민, 레시틴이 파괴되지 않고 보존되며, 공기와 접촉이 차단된 상태이므로 더이상 산화되지 않아서 오랜시간 동안 역가 손실없이 보존할 수 있다.The emulsified membrane is a triple structure, so it is strongly bound and preserved from gastric acid for maintenance of fat, fat-soluble vitamins and lecithin without breaking, and because it is blocked from contact with air, it is not oxidized anymore and can be preserved without losing titer for a long time .
본 발명으로 제조된 것을 사료에 첨가했을 때 사료용 유지, 레시틴, 지용성비타민은 가공 공정에서 공기와 접촉이 없기 때문에 더 이상 산화되지 않고 유화제의 보습작용으로 사료의 물성을 부드럽게 개선할 수 있는 획기적인 발명이다.Feed fats, lecithin, and fat-soluble vitamins when added to the feed is a revolutionary invention that can not be oxidized anymore and smoothly improve the properties of the feed by the moisturizing action of the emulsifier because there is no contact with air in the processing process .
동물이 섭취했을 때는 담즙과 쉽게 미셀을 이루기 때문에 장관에서 흡수율이 높고 레시틴 성분이 파괴되지 않고 간세포에까지 도달하여 간장의 지방대사기능을 촉진하며, 지용성 비타민은 파괴되지 않고 간세포에까지 도달하여 대사되기 때문에 사료 품질의 개선에 있어서 획기적이라 할 수 있다.When the animal is ingested, it easily forms micelles with bile, so it has high absorption rate in the intestinal tract, reaches the liver cells without destroying lecithin, and promotes fat metabolism of the liver, and fat-soluble vitamins reach metabolism without reaching destruction. This is a breakthrough in quality improvement.
Description
본 발명은 레시틴과 유화제를 이용하여 사료용 유지 및 지용성 비타민을 유화시키는 방법에 관한 것으로, 더욱 상세하게는 레시틴과 유화제를 이용하여 유화된 입자의 막 구조가 3중으로 형성되도록 유화시켜 사료용 유지와 지용성 비타민의 유화된 입자가 오랜시간 동안 깨지지 않고 위산의 자극을 견디어 장관에서의 흡수 이용율이 향상된 사료용 유지와 지용성 비타민의 유화방법에 관한 것이다.종래 사료용 유지를 O/W형으로 유화하는 수준은 HLB가 7이상인 친수성 유화제를 사용하여 유화하고 유화 안정제로서 당류(구아검, 산탄검, 카제인, 젤라틴 등)를 첨가하였었다. 그런데 종래의 제조기법으로는 수일 내에 유화상이 깨지며 동물의 담즙과 미셀을 잘 형성하지 못하여 흡수율이 좋지 못한 단점이 있어 산업적으로 크게 이용되지는 못하였다.The present invention relates to a method for emulsifying feed fats and fat-soluble vitamins using lecithin and emulsifier, and more specifically, to emulsify the membrane structure of emulsified particles using triglycerides and emulsifiers to form triple layers. The emulsified particles of E. coli have a method of emulsifying feed fats and fat-soluble vitamins that have absorbed gastric acid irritation without breaking for a long time and have improved absorption rate in the intestinal tract. The above-mentioned hydrophilic emulsifier was emulsified, and sugars (guar gum, xanthan gum, casein, gelatin, etc.) were added as an emulsion stabilizer. However, in the conventional manufacturing method, the oily phase is broken within a few days and the bile and micelles of the animal are not formed well, and thus the absorption rate is not good.
유화상이 깨지는 원인과 형식은 다음과 같다.The cause and form of the broken oil image are as follows.
O/W형으로 유화되어 있는 상태에서 유화된 입자들끼리 서로 응집이 일어나서 큰덩어리로 합일되어서 커지게 되는데 유화제가 지방을 감싸고 견딜수 있는 한계를 초과하게 되면 막이 깨져서 물과 기름으로 분리된다.In the state of emulsification in O / W form, the emulsified particles coagulate with each other and coalesce into large chunks and become larger. When the emulsifier exceeds the limit of wrapping and enduring fat, the membrane is broken and separated into water and oil.
위와 같이 유화상이 깨져서 분리되는 원인은 유화된 입자들마다 유화제와 유지 사이에 결합력보다 유화된 입자 표면에 있는 유화제와 다른입자 표면에 있는 유화제 사이에 응집력이 더 강하여 시간이 갈수록 두개의 유화된 입자가 하나로 합쳐지는 응집이 일어나기 때문이다.The reason why the emulsified phase is broken and separated is that the emulsified particles are more cohesive between the emulsifier on the emulsified particle surface and the emulsifier on the other particle surface than the binding force between the emulsifier and the oil and fat. This is because aggregation occurs as one.
응집된 유화 입자는 시간이 갈수록 큰 덩어리가 되는데 유화제가 이루고 있는 막이 견디지 못하고 깨지면서 물과 기름으로 분리된다. 그래서 O/W형으로 유화된 사료용 유지는 유화입자가 지속성이 없이 수일 내에 깨져서 유분리 현상이 발생한다.따라서, 부분적으로 산업에 이용되는 형식은 유지의 함량을 줄이고 물의 함량을 증가시킴으로서 유화된 입자가 서로 붙어있지 않도록 유지하여 응집이 일어나는 속도를 최대한 줄여서 생산하고 있다.이런 현상을 최소화하기 위하여 유화력이 강한 고가의 유화제를 사용하고 유지의 함량은 적기 때문에 제조가격이 높아서 식품 산업에서만 부분적으로 이용하고 있고 사료 산업에서는 이용이 불가능하였다.Aggregated emulsified particles become large lumps over time, and the membrane of the emulsifier becomes unbearable and breaks apart into water and oil. Thus, feed fats emulsified in O / W form have oil particles that break up within days without persistence, resulting in oil segregation. Thus, some types of industrial oils are emulsified by reducing fat content and increasing water content. In order to minimize this phenomenon, we use expensive emulsifiers with strong emulsifying power and low oil content to minimize this phenomenon. And not available in the feed industry.
본 발명은 종래의 문제점을 감안하여 개발한 것으로서, 사료용 유지, 지용성 비타민 및 레시틴을 O/W 타입으로 유화하는 기법에 관한 발명으로 사료용 유지를 70%까지 유화할 수 있고 오랜시간 동안 유화된 입자가 깨지지 않고 유지될 수 있도록 한 것이며 위산의 자극을 견딜 수 있어서 장관에서 흡수이용율을 높힐 수 있는 방법을 제공한다.The present invention has been developed in view of the conventional problems, the invention relates to a technique for emulsifying feed fats, fat-soluble vitamins and lecithin into O / W type, which can emulsify feed fats up to 70% and emulsified for a long time It is designed to remain unbreakable and to withstand the stimulation of stomach acid, providing a way for the gut to increase absorption.
본 발명은 유화된 입자의 막 구조가 3중으로 형성되도록 유화하는 것으로서, 사료용 유지와 지용성 비타민에 1차적으로 막을 형성하는 것은 레시틴이며 2차막과 3차막은 유화제로 구성되어 있어서 사료용 유지와 유화제의 결합력이 유화입자들간에 응집력보다 더 강력하게 유화막을 형성시킴으로써 유화 입자가 깨지지 않고 유지된다.The present invention is to emulsify the membrane structure of the emulsified particles to form a triple, the primary forming the membrane in the feed fat and fat-soluble vitamins is lecithin and the secondary membrane and the tertiary membrane is composed of an emulsifier binding force of the feed fat and emulsifier The emulsified particles are maintained without breaking by forming an emulsified film more strongly than the cohesive force between these emulsified particles.
사료용 유지, 지용성 비타민의 점성이 낮아지는 수준까지 가열한 상태에서 이들과 잘 혼합되고 결합성이 강한 식물성 레시틴(인지질 성분)을 첨가하여 교반기로 유화하면 식물성 레시틴은 사료용 유지, 지용성 비타민과 접촉면이 최고조에 이르게 되고 식물성 레시틴의 친유기가 사료용 유지, 지용성 비타민과 강력하게 결합된 상태가 되어서 1차막을 형성한다.Vegetable lecithin has the best contact with feed fat and fat-soluble vitamins when emulsified with stirrer by adding well mixed and highly bound vegetable lecithin (phospholipid component) while heated to a low viscosity of feed fat and fat-soluble vitamins. And lipophilic groups of vegetable lecithin are strongly combined with feed fats and fat-soluble vitamins to form primary membranes.
식물성 레시틴은 사료용 유지와 잘 결합하지만 HLB가 낮아서(친수성기가 적으므로) 사료용 유지를 물에 분산시키지는 못하므로 친수성기가 많아서 O/W 유화력이 높고 식물성 레시틴 분자들 사이에 끼워진 상태로 친유기가 사료용 유지와 결합하여 2차막을 형성할 수 있는 유화제를 사용하여 유화막과 사료용유지, 지용성 비타민 사이에 결합력을 향상시킨다.Vegetable lecithin binds well with feed fats, but because of its low HLB (low hydrophilicity), it does not disperse feed fats in water, so it has a high hydrophilicity, resulting in high O / W emulsification and intercalation between vegetable lecithin molecules. By using an emulsifier that can be combined to form a secondary membrane, it improves the binding force between the emulsion membrane, feed fats and fat-soluble vitamins.
2차막을 형성하는 유화제가 친수성기가 많다고 해서 레시틴 없이 유화시키고 검류를 첨가하여 유화 안정제로 사용한다면 유화막을 형성하는 유화제는 친수성기는 많지만 친유성기는 적기 때문에 사료용 유지와 강력하게 결합하지 못하여 사료용 유지와 유화제 사이에 결합력이 약해지고 유화입자들간에 응집력을 이겨낼 수 없게 된다. 수시간 이내에 O/W 유화상은 붕괴된다.If the emulsifier that forms the secondary membrane is emulsified without lecithin and is used as an emulsion stabilizer by adding gum, if the emulsifier that forms the secondary membrane is emulsified, the emulsifier that forms the emulsion membrane has many hydrophilic groups but few lipophilic groups, and thus it does not bind strongly to feed fats and fats. Cohesion is weakened between the cohesion between the emulsified particles will not be able to overcome. Within hours, the O / W oil phase collapses.
본 발명에서는 식물성 레시틴(식물성 인지질)이 친유기가 많아서 사료용 유지, 지용성 비타민과 잘 결합하고 동물의 간장에서 지방대사기능을 촉진하는 물질로 이용되기 때문에 식물성 레시틴으로 1차막을 형성하여 사료용 유지, 지용성 비타민을 강력하게 결합시켰다.In the present invention, since vegetable lecithin (vegetable phospholipid) has a lot of lipophilic groups, it is combined with fats and fats and fat-soluble vitamins for feed well and is used as a material for promoting fat metabolism in the liver of animals, thus forming a primary membrane with vegetable lecithin for fats and fats and fat-soluble vitamins. Combined strongly.
2차막을 형성하는 유화제는 사료용 유지와 결합하면서 레시틴과 친화성이 있어서 레시틴 분자들 사이에 끼워져서 사료용 유지와 결합할 수 있고 친수성기가 많아서(HLB가 14이상) 사료용 유지에 유화막을 형성할 때 친수성기를 충분히 보강해줄 수 있는 유화제로서 2차막을 형성한다.The emulsifier that forms the secondary membrane binds to feed fats and is affinity for lecithin, so that it can be sandwiched between lecithin molecules to bind to feed fats and bound, and has a high hydrophilic group (HLB is 14 or higher). The secondary film is formed as an emulsifier capable of sufficiently reinforcing.
3차막을 형성하는 유화제는 사료용 유지와 결합하면서 레시틴과 친수성 유화제(HLB 14이상)가 형성하고 있는 유화막에 친수성기를 더 보강하고 유화막의 점성을 상승시켜서 유화막을 안정화시킬 수 있는 유화제로서 3차막을 형성하며 3차막을 형성하는 유화제는 반드시 2차막을 형성하는 유화제보다 HLB 값이 높아야 한다(친수성기가 많아야 함).The emulsifier that forms the tertiary membrane is an emulsifier that can stabilize the emulsion membrane by further strengthening the hydrophilic group and increasing the viscosity of the emulsion membrane by combining with feed fats and oils to form the lecithin and the hydrophilic emulsifier (HLB 14 or higher). The emulsifier that forms and forms the tertiary membrane must have a higher HLB value than the emulsifier that forms the secondary membrane (the more hydrophilic groups).
본 발명을 제조하는 기법으로는 2차막과 3차막을 구성하는 유화제, 물을 먼저 유화하여 제조된 친수성 유화 혼합제제와, 사료용 유지, 지용성 비타민, 레시틴을 유화하여 제조된 친유성 유화 혼합제제를 만들어야 하는데 친수성 유화 혼합제제를 제조하는데 있어서 친수성기가 많은 유화제는 흔히 결정성 분말 타입이나 응고되어 있는 형태로 시판되기 때문에 물에 용해 시키기 위해서는 용해되는 온도까지 온도를 상승시켜야만 물에 균일하게 분산되고 용해온도에서 교반기에서 물과 유화되어야만 친수성기가 물에 균일하게 결합한 상태로 친수성 유화 혼합제제가 제조된다.친유성 유화 혼합제제를 제조하는데 사용되는 사료용 유지, 지용성 비타민, 레시틴은 상온에서 분자들끼리 서로 엉켜있는 형태로서 물리적인 성상이 높은 점성을 가진 액체들이기 때문에 레시틴의 친유기와 유지를 균일하게 결합시키기 위해서는 엉킴을 풀어서 점성을 최대한 떨어뜨린 상태에서 교반기로 교반해야만 레시틴의 친유기와 사료용유지, 지용성 비타민의 접촉면이 증가하여 결합을 잘할 수 있다. 점성이 가장 낮아지는 수준까지 가열하여서 점성이 낮아진 상태에서 교반기로 유화하여 레시틴의 친유기가 사료용 유지, 지용성 비타민에 접촉율이 증가함에 따라서 균일하게 유화될 수 있도록 하여서 제조되어야만 강력한 1차막이 형성되고 유화 입자들간에 응집력을 이겨낼 수 있어서 유분리 현상을 예방할 수 있다.친수성 유화 혼합제제와 친유성 유화 혼합제제는 모두 가열된 상태에서 제조되었는데 이들의 온도를 40℃ 전후로 동일하게 보정하고 친수성 유화 혼합제제를 교반기에서 교반하면서 친유성 유화 혼합제제를 첨가하게 되면 친수성 유화제의 친유기가 레시틴 분자들 사이에서 사료용 유지, 지용성 비타민에 결합하게 된다.친유성 유화 혼합제제의 온도가 40℃ 전후를 유지하고 있어서 유지의 점성이 낮아진 상태이며 친수성 유화 혼합제제도 40℃ 전후로서 점성이 가장 낮아진 상태에서 교반기로 교반되기 때문에 친수성 유화 혼합제제의 친유기가 친유성 혼합제제의 유지성분에 결합할 수 있는 접촉율이 증가하기 때문에 친수성 유화 혼합제제가 균일하게 2차 및 3차막을 형성하게 된다.친수성 유화 혼합제제를 교반기로 교반하면서 친유성 유화 혼합제제를 투입하여 유화하는 공정을 마치면 유화는 이루워진 상태이지만 온도가 높아서 점성이 낮은 상태이기 때문에 유화제, 레시틴의 친유기가 유지와 견고하게 결합하지 않은 상태이다. 이 결합을 견고하게 하기 위해서는 유지와 유화제, 레시틴의 점성을 상승시켜야 하는데 점성의 상승을 위해서 온도를 다시 낮추게 되면 사료용유지, 지용성 비타민, 레시틴, 유화제의 점성이 상승하면서 유화막이 오므라들어서 유화막의 구조가 조밀해지고 3차 유화막이 강한 점성을 나타내기 때문에 유화막이 견고해지는 상태로 숙성이 되는데 숙성실 공기온도는 17-20℃ 사이에서 24시간 이상 숙성하여야 3차 유화막을 구성하는 유화제의 점성이 상승하게 되고 사료용 유지, 지용성 비타민이 응고되지 않는 상태에서 친수성 유화 혼합제제의 친유기가 사료용 유지, 지용성 비타민과 결합력을 유지하게 된다.유화막이 응집되어서 깨지지 않고 견딜 수 있는 강도는 사료용 유지와 지용성 비타민 혼합물을 70%까지 유화할 수 있으며 사료용 유지와 지용성 비타민의 함량을 줄이고 물의 양을 증가시키면 유화막은 좀 더 견고하게 형성된다.Techniques for preparing the present invention include the emulsifiers constituting the secondary and tertiary membranes, a hydrophilic emulsion mixture prepared by emulsifying water first, and a lipophilic emulsion mixture prepared by emulsifying feed fats, fat-soluble vitamins and lecithin. In the preparation of hydrophilic emulsified admixtures, emulsifiers with many hydrophilic groups are often commercially available in the form of crystalline powder or in a coagulated form, so in order to dissolve in water, the temperature must be raised to the temperature at which they are dissolved. The hydrophilic emulsified mixture formulation is produced only when the hydrophilic group is uniformly bound to the water when the hydrophilic group is emulsified in the stirrer. Feed fats, fat-soluble vitamins, and lecithin used to prepare the lipophilic emulsion mixture are entangled with molecules at room temperature. Viscous liquids with high physical properties Because there must be stirred with a stirrer while solving the entanglement possible knocking down the viscosity chinyugi the feed oil, the contact surface of the fat-soluble vitamins in combination with lecithin can do well to increase in order to uniformly bond the chinyugi and maintenance of lecithin. Emulsified with a stirrer in the state of low viscosity by heating up to the lowest viscosity, so that the lecithin lipophilic group can be uniformly emulsified as the contact rate of fats and fats is increased. The cohesion between particles can be overcome to prevent oil separation. Both hydrophilic emulsion mixtures and lipophilic emulsion mixtures were prepared in a heated state. When the lipophilic emulsion mixture is added while stirring in a stirrer, the lipophilic group of the hydrophilic emulsifier is bound to the feed fats and fat-soluble vitamins among the lecithin molecules. Hydrophilic emulsifier 40 ° C, the hydrophilic emulsified admixture is uniformly secondary and secondary because the contact rate at which the lipophilic group of the hydrophilic emulsified admixture can bind to the fat or oil component of the lipophilic admixture increases because the agitation is stirred with the stirrer at the lowest viscosity. When the hydrophilic emulsion mixture is stirred with a stirrer and the lipophilic emulsion mixture is added and emulsified, the emulsion is formed, but the temperature is high and the viscosity of the lecithin is low. It is not firmly combined with fat. In order to solidify this bond, the viscosity of fats and oils, emulsifiers and lecithin should be increased. When the temperature is lowered again to increase the viscosity, the viscosity of feed fats, fat-soluble vitamins, lecithin, and emulsifiers increases, and the emulsion film is retracted. As the dense and tertiary emulsion film exhibits a strong viscosity, the emulsion film is matured in a solid state. The air temperature of the aging chamber is aged between 17-20 ° C for at least 24 hours to increase the viscosity of the emulsifier constituting the tertiary emulsion film. In the absence of fat and fat-soluble vitamins, the lipophilic group of the hydrophilic emulsified mixture maintains the binding strength with the fat and fat-soluble vitamins for feed. Emulsifying, feed fat and fat soluble ratio Reducing the content of amine and increasing the amount of water makes the emulsion more firm.
실시예 1Example 1
예비 유화 공정 1 : 친유성 유화 혼합제제 제조 공정(유상 제조 공정)Preliminary emulsification step 1: lipophilic emulsion preparation formulation process (oil phase production process)
정제된 어유, 어간유, 오징어유, 오징어간유(이하 어유라고 함) 70%를 예비 탱크에 투입하였다. 여기에 레시틴(Lecithin) 5%, 에톡시퀸(Ethoxyquin)(산화방지제) 0.1%를 첨가하였다.온도를 70-80℃로 가온하면서 균일하게 혼합될 수 있도록 교반하였다. 상기 온도는 레시틴, 에톡시퀸, 어유의 점성이 가장 낮아져서 혼합이 잘되는 온도이었다. 그 후 온도를 30-40℃로 냉각하여 상기 온도로 유지하고 1000rpm으로 교반하였다. 상기 온도는 균일하게 혼합되어 있는 레시틴과 유지가 잘 결합하는 온도로 적당하였다.70% of refined fish oil, liver oil, squid oil and squid liver oil (hereinafter referred to as fish oil) were added to a reserve tank. To this was added 5% of Lecithin and 0.1% of Ethoxyquin (Antioxidant). The mixture was stirred to ensure uniform mixing while warming to 70-80 ° C. The temperature was the temperature at which the viscosity of the lecithin, ethoxyquine, fish oil was the lowest and the mixing was good. The temperature was then cooled to 30-40 ° C. and maintained at that temperature and stirred at 1000 rpm. The temperature was appropriate at a temperature at which lecithin and oils and fats were uniformly mixed.
예비 유화 공정 2 : 친수성 유화 혼합제제 제조 공정(수상 제조공정)Preliminary Emulsification Step 2: Hydrophilic Emulsion Mixture Preparation Process (Water Phase Manufacturing Process)
물 21.15%를 교반기에 투입하였다. HLB 값이 15인 친수성 유화제, HLB값이 16인 친수성 유화제 혼합물을 3.75% 투입하고 온도를 45-55℃로 가온하면서 3000rpm으로 교반하여 유화제를 물에 완전히 용해시켰다. 용해된 후에는 온도를 30-40℃로 유지시켰다. 단, 온도는 유상과 동일하여야 하였다.21.15% of water was added to the stirrer. 3.75% of a hydrophilic emulsifier mixture having an HLB value of 15 and a hydrophilic emulsifier mixture having an HLB value of 16 were added and stirred at 3000 rpm while the temperature was heated to 45-55 ° C. to completely dissolve the emulsifier in water. After dissolution, the temperature was maintained at 30-40 ° C. However, the temperature should be the same as the oil phase.
유화 공정Emulsification process
수상이 들어있는 교반기를 1000rpm으로 교반하면서 유상을 투입하였다. 투입속도는 10분 이상으로 서서히 하였으며 온도는 30-40℃로 유지시켰다. 한꺼번에 투입하게 되면 W/O형으로 유화될 수 있으므로 서서히 투입해야 했다. 유상이 모두 투입되고 나면 교반기를 3000rpm 이상으로 30분이상 교반하였다.완제품은 겔 타입으로 바뀌면서 친수성을 띤 유화오일로 완전히 바뀌었다.숙성 공정 The oil phase was added while stirring the stirrer containing the water phase at 1000 rpm. The feed rate was slowly over 10 minutes and the temperature was maintained at 30-40 ℃. If it was added all at once, it could be emulsified into W / O type, so it had to be slowly added. After the oil phase was added, the stirrer was stirred for 30 minutes or more at 3000 rpm or more. The finished product was changed into a gel type and completely changed into a hydrophilic emulsion oil. Aging process
상기 유화 공정에서 제조한 완제품을 공기의 접촉이 전혀 없도록 용기에 가득 채운 상태에서 마개로 밀봉하고 17-20℃에서 24시간 방치하였다. 상기 과정에서 친수성 유화 혼합 제제와 어유의 결합력이 증가되고 유화막이 수축하기 때문에 입자의 상이 충격에도 붕괴되지 않고 강해졌다.The finished product prepared in the emulsification process was sealed with a stopper in a state filled with a container so that there is no contact of air and left for 24 hours at 17-20 ℃. In this process, since the binding force between the hydrophilic emulsion mixed formulation and fish oil is increased and the emulsion film shrinks, the phase of the particles becomes stronger without collapsing even upon impact.
실시예 2Example 2
유화막을 좀더 견고하게 하기 위하여 하기와 같이 사료용 유지를 유화하였다.In order to make the emulsion more solid, the feed fat was emulsified as follows.
예비 유화 공정 1 : 유상 제조 공정Pre-emulsification process 1: oil phase manufacturing process
정제된 어유, 어간유, 오징어유, 오징어간유(이하 어유라고 함) 65%를 예비 탱크에 투입하였다. 여기에 레시틴 5%, 에톡시퀸(산화방지제) 0.1%를 첨가하였다.온도를 70-80℃로 가온하면서 균일하게 혼합될 수 있도록 교반하였다. 상기 온도는 레시틴, 에톡시퀸, 유지의 점성이 가장 낮아져서 혼합이 잘되는 온도이었다. 그 후 온도를 30-40℃로 냉각하여 상기 온도를 유지하고 1000rpm으로 교반하였다. 상기 온도에서는 균일하게 혼합되어 있는 레시틴과 유지가 잘 결합하였다.예비 유화 공정 2 : 수상 제조 공정 65% of refined fish oil, liver oil, squid oil and squid liver oil (hereinafter referred to as fish oil) were added to a reserve tank. To this was added 5% lecithin and 0.1% ethoxyquine (antioxidant). The mixture was stirred to ensure uniform mixing while warming to 70-80 ° C. The temperature was the temperature at which the viscosity of the lecithin, ethoxyquine and fats and oils was the lowest, and the mixing was good. The temperature was then cooled to 30-40 ° C. to maintain this temperature and stirred at 1000 rpm. At this temperature, the lecithin and oils and fats mixed uniformly were well combined. Preliminary Emulsification Process 2: Water Production Process
물 26.15%를 교반기에 투입하였다.26.15% of water was added to the stirrer.
HLB 값이 15인 친수성 유화제, HLB값이 16인 친수성 유화제 혼합물을 3.75% 투입하고 온도를 45-55℃로 가온하면서 3000rpm으로 교반하여 유화제를 물에 완전히 용해시켰다. 용해가 된 후에는 온도를 30-40℃로 유지시켰다. 단 온도는 유상과 동일하여야 하였다.유화 공정 3.75% of a hydrophilic emulsifier mixture having an HLB value of 15 and a hydrophilic emulsifier mixture having an HLB value of 16 were added and stirred at 3000 rpm while the temperature was heated to 45-55 ° C. to completely dissolve the emulsifier in water. After dissolution, the temperature was maintained at 30-40 ° C. However, the temperature should be the same as the oil phase. Emulsification process
수상이 들어있는 교반기를 1000rpm으로 믹싱하면서 유상을 투입하였다. 투입속도는 10분 이상으로 서서히 하였으며 온도는 30-40℃로 유지시켜야 했다. 한꺼번에 투입하게 되면 W/O형으로 유화될 수 있으므로 서서히 투입해야 했다. 유상이 모두 투입되고 나면 교반기를 3000rpm 이상으로 30분이상 교반하였다.완제품은 겔 타입으로 바뀌면서 친수성을 띤 유화오일로 완전히 바뀌었다.숙성 공정 The oil phase was added while mixing the stirrer containing the water phase at 1000 rpm. The feed rate was slowly over 10 minutes and the temperature had to be maintained at 30-40 ° C. If it was added all at once, it could be emulsified into W / O type, so it had to be slowly added. After the oil phase was added, the stirrer was stirred for 30 minutes or more at 3000 rpm or more. The finished product was changed into a gel type and completely changed into a hydrophilic emulsion oil. Aging process
상기 유화 공정에서 제조한 완제품을 공기의 접촉이 전혀 없도록 용기에 가득 채운 상태에서 마개로 밀봉하고 17-20℃로 24시간 방치하였다. 상기 과정에서 친수성 유화 혼합 제제와 어유의 결합력이 증가되고 유화막이 수축하기 때문에 입자의 상이 충격에도 붕괴되지 않고 강해졌다.The finished product prepared in the emulsification process was sealed with a stopper in a state filled with a container so that there is no contact of air and left at 17-20 ° C. for 24 hours. In this process, since the binding force between the hydrophilic emulsion mixed formulation and fish oil is increased and the emulsion film shrinks, the phase of the particles becomes stronger without collapsing even upon impact.
실시예 3Example 3
산화가 잘되는 지용성 비타민을 안정화시키기 위하여 하기와 같이 유화막을 씌웠다.In order to stabilize the oxidized fat-soluble vitamins, an emulsion film was coated as follows.
예비 유화 공정 1 : 유상 제조 공정Pre-emulsification process 1: oil phase manufacturing process
액상 지용성 비타민(비타민 E, A, D3, K) 70%를 예비 탱크에 투입하였다. 여기에 레시틴 5%, 에톡시퀸(산화방지제) 0.1%를 첨가하였다.온도를 70-80℃로 가온하면서 균일하게 혼합될 수 있도록 교반하였다. 상기 온도는 레시틴, 에톡시퀸, 지용성 비타민의 점성이 가장 낮아져서 혼합이 잘되는 온도이었다. 그 후 온도를 30-40℃로 냉각하여 상기 온도를 유지하면서 1000rpm으로 교반하였다. 상기 온도에서 균일하게 혼합되어 있는 레시틴과 지용성 비타민이 잘 결합하였다.70% of the liquid fat-soluble vitamins (vitamins E, A, D3, K) were added to the reserve tank. To this was added 5% lecithin and 0.1% ethoxyquine (antioxidant). The mixture was stirred to ensure uniform mixing while warming to 70-80 ° C. The temperature was the temperature at which the viscosity of the lecithin, ethoxyquine, fat-soluble vitamin was the lowest, and the mixing was good. The temperature was then cooled to 30-40 ° C. and stirred at 1000 rpm while maintaining the temperature. At this temperature, the lecithin and fat soluble vitamins mixed uniformly were well combined.
예비 유화 공정 2 : 수상 제조 공정Preliminary Emulsification Process 2: Water Production Process
물 21.15%를 교반기에 투입하였다.21.15% of water was added to the stirrer.
HLB 값이 15인 친수성 유화제, HLB값이 16인 친수성 유화제 혼합물 3.75%를 투입하고 온도를 45-55℃로 가온하면서 3000rpm으로 교반하여 유화제를 물에 완전히 용해시켰다. 용해가 된 후에는 온도를 30-40℃로 유지시켰다. 단, 온도는 유상과 동일하여야 했다.A hydrophilic emulsifier having a HLB value of 15 and a 3.75% mixture of a hydrophilic emulsifier having a HLB value of 16 were charged and stirred at 3000 rpm while the temperature was heated to 45-55 ° C. to completely dissolve the emulsifier in water. After dissolution, the temperature was maintained at 30-40 ° C. However, the temperature had to be the same as the oil phase.
유화 공정Emulsification process
예비 유화 공정 1에서 생산된 것을 교반기에서 1000rpm으로 교반하면서 유상을 투입하였다. 투입속도는 10분 이상으로 서서히 하였다. 이 때 한꺼번에 투입하게 되면 W/O형으로 유화될 수 있으므로 서서히 투입해야 했다. 유상이 모두 투입되고 나면 3000rpm 이상으로 30분이상 교반하였다.완제품은 겔 타입으로 바뀌면서 친수성을 띤 유화오일로 완전히 바뀌었다.숙성 공정 What was produced in the preliminary emulsification step 1 was introduced into the oil phase while stirring at 1000 rpm with a stirrer. The feed rate was slowed to 10 minutes or more. At this time, if it was added all at once, it could be emulsified into W / O type, so it had to be slowly added. After the oil phase was added, the mixture was stirred for 30 minutes or more at 3000 rpm or more. The finished product was changed into a gel type and completely changed into a hydrophilic emulsion oil. Aging process
상기 유화 공정에서 제조한 완제품을 공기의 접촉이 전혀 없도록 용기에 가득 채운 상태에서 마개를 밀봉하고 17-20℃로 24시간 방치하였다. 상기 과정에서 친수성 유화 혼합 제제와 어유의 결합력이 증가되고 유화막이 수축하기 때문에 입자의 상이 충격에도 붕괴되지 않고 강해졌다.The finished product prepared in the emulsification process was sealed in a container filled with air so that there is no contact with air at all and left at 17-20 ° C. for 24 hours. In this process, since the binding force between the hydrophilic emulsion mixed formulation and fish oil is increased and the emulsion film shrinks, the phase of the particles becomes stronger without collapsing even upon impact.
실시예 4Example 4
유화막을 좀더 견고히 하기 위하여 하기와 같이 지용성 비타민을 유화하였다.In order to harden the emulsion film, the fat-soluble vitamin was emulsified as follows.
예비 유화 공정 1 : 유상 제조 공정Pre-emulsification process 1: oil phase manufacturing process
액상 지용성 비타민(비타민 E, A, D3, K) 65%를 예비탱크에 투입하였다. 여기에 레시틴 5%, 에톡시퀸(산화방지제) 0.1%를 첨가하였다.65% of liquid fat-soluble vitamins (vitamins E, A, D3, K) were added to the reserve tank. To this was added 5% lecithin and 0.1% ethoxyquine (antioxidant).
온도를 70-80℃로 가온하면서 균일하게 혼합될 수 있도록 교반하였다. 상기 온도에서 레시틴, 에톡시퀸, 지용성 비타민의 점성이 가장 낮아져서 혼합이 잘되었다. 그 후 온도를 30-40℃로 냉각하여 상기 온도를 유지하면서 1000rpm으로 교반 하였다. 상기 온도에서는 균일하게 혼합되어 있는 레시틴과 지용성 비타민이 잘 결합하였다.Stir to ensure uniform mixing while warming to 70-80 ° C. At this temperature, the lecithin, ethoxyquine, fat soluble vitamins were the lowest and the mixing was well. Thereafter, the temperature was cooled to 30-40 ° C. and stirred at 1000 rpm while maintaining the temperature. At this temperature, the lecithin and fat-soluble vitamins mixed uniformly were well combined.
예비 유화 공정 2 : 수상 제조 공정Preliminary Emulsification Process 2: Water Production Process
물 26.15%를 교반기에 투입하였다.26.15% of water was added to the stirrer.
HLB 값이 15인 친수성 유화제, HLB값이 16인 친수성 유화제 혼합물 3.75%를 투입하고 온도를 45-55℃로 가온하면서 3000rpm으로 교반하여 유화제를 물에 완전히 용해시켰다. 용해가 된 후에는 온도를 30-40℃로 유지시켰다. 단, 온도는 유상과 동일하여야 했다.A hydrophilic emulsifier having a HLB value of 15 and a 3.75% mixture of a hydrophilic emulsifier having a HLB value of 16 were charged and stirred at 3000 rpm while the temperature was heated to 45-55 ° C. to completely dissolve the emulsifier in water. After dissolution, the temperature was maintained at 30-40 ° C. However, the temperature had to be the same as the oil phase.
유화 공정Emulsification process
예비 유화 공정 1에서 생산된 것을 1000rpm으로 교반하면서 유상을 투입하였다. 투입속도는 10분 이상으로 서서히 했다. 한꺼번에 투입하게 되면 W/O형으로 유화될 수 있으므로 서서히 투입해야 했다. 유상이 모두 투입되고 나면 3000rpm 이상으로 30분 이상 교반하였다.완제품은 겔 타입으로 바뀌면서 친수성을 띤 유화오일로 완전히 바뀌었다.숙성 공정 The oil phase was added while stirring what was produced in the preliminary emulsification process 1 at 1000 rpm. The feed rate was settled to 10 minutes or more. If it was added all at once, it could be emulsified into W / O type, so it had to be slowly added. After the oil phase was added, the mixture was stirred for 30 minutes or more at 3000 rpm or more. The finished product was changed into a gel type and completely changed into a hydrophilic emulsified oil. Aging process
상기 유화 공정에서 제조한 완제품을 공기의 접촉이 전혀 없도록 용기에 가득 채운 상태에서 마개로 밀봉하고 17-20℃로 24시간 방치하였다. 상기 과정에서 친수성 유화 혼합 제제와 어유의 결합력이 증가되고 유화막이 수축하기 때문에 입자의 상이 충격에도 붕괴되지 않고 강해졌다.The finished product prepared in the emulsification process was sealed with a stopper in a state filled with a container so that there is no contact of air and left at 17-20 ° C. for 24 hours. In this process, since the binding force between the hydrophilic emulsion mixed formulation and fish oil is increased and the emulsion film shrinks, the phase of the particles becomes stronger without collapsing even upon impact.
실시예 5Example 5
난용성 물질인 바이페닐 디메틸 디카르복실레이트(Biphenyl Dimethyl Dicarboxylate; 이하 비디디 라고 함)는 소화흡수율이 너무 낮아서 동물이 섭취했을 때 소화장애로 인한 구토증세를 일으키므로 가용화시키기 위하여 유기용매로 용해 시킨 후에 유화시켰다.예비 유화 공정 1 : 유상을 제조하는 공정 Diphenyl Dimethyl Dicarboxylate, a poorly water-soluble substance, has a low digestive absorption rate and causes vomiting due to digestive disorders when ingested by animals. After emulsification. Preliminary emulsification step 1: process for producing oil phase
사료용 유지 : 트리아세틴(Triacetin)을 1.5 : 1로 혼합한 혼합용액 70%를 60℃의 온도에서 1000rpm으로 교반하였다. 여기에서 트리아세틴(Triacetin)은 유기용매로 사용하였다. 상기 교반된 용액에 비디디(BDD) 0.7%(혼합용액의 1/100배)를 첨가하였다. 첨가한 후에 온도를 60℃로 상승시키면서 3000rpm으로 10분간 교반하였다. 여기에 레시틴을 5% 첨가하여 3000rpm에서 10분간 교반하였다.예비 유화 공정 2 : 수상 제조 공정 Feed fat: 70% of a mixed solution of triacetin (1.5: 1) was stirred at 1000 rpm at a temperature of 60 ℃. Here triacetin (Triacetin) was used as an organic solvent. To the stirred solution was added 0.7% of BDD (1/100 times of the mixed solution). After addition, the mixture was stirred at 3000 rpm for 10 minutes while the temperature was raised to 60 ° C. 5% of lecithin was added thereto, followed by stirring for 10 minutes at 3000 rpm. Preliminary Emulsification Process 2: Water Production Process
물 20.55%를 교반기에 투입하였다.20.55% of water was added to the stirrer.
HLB 값이 15-16인 친수성 유화혼합제 3.75%를 투입하고 온도를 45-55℃로 가온하면서 3000rpm으로 교반하여 유화제를 물에 완전히 용해시켰다. 용해가 된 후에는 온도를 30-40℃로 유지시켰다. 단, 온도는 유상과 동일하여야 했다.3.75% of a hydrophilic emulsion mixture having an HLB value of 15-16 was added thereto, and the emulsion was completely dissolved in water by stirring at 3000 rpm while warming the temperature to 45-55 ° C. After dissolution, the temperature was maintained at 30-40 ° C. However, the temperature had to be the same as the oil phase.
유화 공정Emulsification process
예비 유화 공정 1에서 생산된 것을 교반기에서 1000rpm으로 교반하면서 유상을 투입하였다. 투입속도는 10분 이상으로 서서히 하였다. 한꺼번에 투입하게 되면 W/O형으로 유화될 수 있으므로 서서히 투입해야 했다. 유상이 모두 투입되고 나면 3000rpm 이상으로 30분 이상 교반하였다.숙성 공정 What was produced in the preliminary emulsification step 1 was introduced into the oil phase while stirring at 1000 rpm with a stirrer. The feed rate was slowed to 10 minutes or more. If it was added all at once, it could be emulsified into W / O type, so it had to be slowly added. After all the oil phase was added, the mixture was stirred for 30 minutes or more at 3000 rpm or more. Aging process
상기 유화 공정에서 제조한 완제품을 공기의 접촉이 전혀 없도록 용기에 가득 채운 상태에서 마개로 밀봉하고 17-20℃로 24시간 방치하였다. 이 과정에서 친수성 유화 혼합 제제와 어유의 결합력이 증가되고 유화막이 수축하기 때문에 입자의 상이 충격에도 붕괴되지 않고 강해졌다.The finished product prepared in the emulsification process was sealed with a stopper in a state filled with a container so that there is no contact of air and left at 17-20 ° C. for 24 hours. In this process, the binding force between the hydrophilic emulsion mixed formulation and the fish oil is increased and the emulsion film shrinks, so that the phase of the particles is stronger without impact collapse.
실시예 6Example 6
유화막을 좀더 견고히 하기 위하여 하기와 같이 사료용 유지를 유화시켰다.예비 유화 공정 1 : 유상을 제조하는 공정 To further solidify the emulsion, feed fat was emulsified as follows. Preliminary emulsification step 1: process for producing oil phase
사료용 유지 : 트리아세틴(Triacetin)을 1.5 : 1로 혼합한 혼합용액 65%를 60℃에서 1000rpm으로 교반하였다. 여기서 트리아세틴은 유기용매로 사용하였다. 상기 교반된 용액에 비디디(BDD) 0.65%(혼합용액의 1/100배)를 첨가하였다. 첨가한 후에 온도를 60℃로 상승시키면서 3000rpm으로 10분간 교반하였다. 여기에 레시틴 5%를 첨가하여 3000rpm으로 10분간 교반하였다.예비 유화 공정 2 : 수상 제조 공정 Feed fat: 65% of the mixed solution of triacetin (Triacetin) 1.5: 1 was stirred at 1000rpm at 60 ℃. Here triacetin was used as the organic solvent. To the stirred solution was added 0.65% of BDD (1/100 times of the mixed solution). After addition, the mixture was stirred at 3000 rpm for 10 minutes while the temperature was raised to 60 ° C. Lecithin 5% was added thereto and stirred at 3000 rpm for 10 minutes. Preliminary Emulsification Process 2: Water Production Process
물 25.6%를 교반기에 투입하였다.25.6% of water was added to the stirrer.
HLB 값이 15-16인 친수성 유화혼합제 3.75%를 투입하고 온도를 45-55℃로 가온하면서 3000rpm으로 교반하여 유화제를 물에 완전히 용해시켰다. 용해가 된 후에는 온도를 30-40℃로 유지시켰다. 단, 온도는 유상과 동일하여야 했다.3.75% of a hydrophilic emulsion mixture having an HLB value of 15-16 was added thereto, and the emulsion was completely dissolved in water by stirring at 3000 rpm while warming the temperature to 45-55 ° C. After dissolution, the temperature was maintained at 30-40 ° C. However, the temperature had to be the same as the oil phase.
유화 공정Emulsification process
예비 유화 공정 1에서 생산된 것을 교반기에서 1000rpm으로 교반하면서 유상을 투입하였다. 투입속도는 10분 이상으로 서서히 하였다. 한꺼번에 투입하게 되면 W/O형으로 유화될 수 있으므로 서서히 투입해야 했다. 유상이 모두 투입되고 나면 3000rpm 이상으로 30분 이상 교반하였다.숙성 공정 What was produced in the preliminary emulsification step 1 was introduced into the oil phase while stirring at 1000 rpm with a stirrer. The feed rate was slowed to 10 minutes or more. If it was added all at once, it could be emulsified into W / O type, so it had to be slowly added. After all the oil phase was added, the mixture was stirred for 30 minutes or more at 3000 rpm or more. Aging process
상기 유화 공정에서 제조한 완제품을 공기의 접촉이 전혀 없도록 용기에 가득 채운 상태에서 마개로 밀봉하고 17-20℃로 24시간 방치하였다. 이 과정에서 친수성 유화 혼합 제제와 어유의 결합력이 증가되고 유화막이 수축하기 때문에 입자의 상이 충격에도 붕괴되지 않고 강해졌다.The finished product prepared in the emulsification process was sealed with a stopper in a state filled with a container so that there is no contact of air and left at 17-20 ° C. for 24 hours. In this process, the binding force between the hydrophilic emulsion mixed formulation and the fish oil is increased and the emulsion film shrinks, so that the phase of the particles is stronger without impact collapse.
이상에서와 같이 본 발명에 따르면 사료용 유지, 지용성 비타민, 난용성 물질을 레시틴과 유화제를 이용하여 O/W형으로 유화시킬 수 있어 사료에 첨가하는 지방의 산화 반응응 근본적으로 막을수 있으며 사료용 유지, 지용성 비타민, 레시틴, 난용성 물질이 위산에 의해 파괴되는 것을 막을 수 있고 레시틴의 작용으로 간세포의 지방 대사기능을 활성화하여 사료용 유지, 지용성 비타민, 난용성 물질의 대사량을 증가시킴으로써 동물의 건강을 증진시키고 지용성 비타민의 첨가량을 절감하는 한편 비디디와 같은 난용성 물질의 흡수 이용율을 높혀서 질병의 치료에 효과적으로도 이용할 수 있다.As described above, according to the present invention, it is possible to emulsify feed fats, fat-soluble vitamins, and poorly soluble substances into O / W type using lecithin and emulsifiers, thereby fundamentally preventing the oxidation reaction of fats added to the feeds. Vitamin, lecithin, and poorly soluble substances can be prevented from being destroyed by gastric acid, and lecithin promotes the fat metabolism of liver cells, thereby increasing the metabolism of feed fats, fat-soluble vitamins, and poorly soluble substances, thereby improving animal health and fat-soluble In addition to reducing the amount of vitamins added to the absorption rate of poorly soluble substances such as video, it can be effectively used in the treatment of diseases.
Claims (2)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2002-0061760A KR100464983B1 (en) | 2002-10-10 | 2002-10-10 | Method of emulsifying feed oil and fat soluble vitamin by using lecithin and emulsifier |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2002-0061760A KR100464983B1 (en) | 2002-10-10 | 2002-10-10 | Method of emulsifying feed oil and fat soluble vitamin by using lecithin and emulsifier |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20040032562A KR20040032562A (en) | 2004-04-17 |
KR100464983B1 true KR100464983B1 (en) | 2005-01-05 |
Family
ID=37332446
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR10-2002-0061760A KR100464983B1 (en) | 2002-10-10 | 2002-10-10 | Method of emulsifying feed oil and fat soluble vitamin by using lecithin and emulsifier |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR100464983B1 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100581076B1 (en) * | 2004-12-28 | 2006-05-16 | 주식회사 마니커 | Refined fish oil, feed composition and feeding method of broiler for enriching docosa hexaenoic acid in broiler meat |
KR101149441B1 (en) * | 2009-09-28 | 2012-06-27 | 대한민국 | Feed additive including distilled soybean fatty acid from soybean oil manufacturing |
CN104304679B (en) * | 2014-10-27 | 2017-07-11 | 广东金品动物营养有限公司 | A kind of B B-complex C, E immune polysaccharide microemulsion preparation and its preparation method and application |
KR102695644B1 (en) * | 2021-01-25 | 2024-08-21 | 주식회사 노즈워크 | Paste composition for companion animals and method thereof |
KR102689220B1 (en) * | 2023-02-02 | 2024-07-30 | 주식회사 대호 | Composition of functional coating solution for animal pellet feed |
CN117837676A (en) * | 2023-12-27 | 2024-04-09 | 江苏四新界面剂科技有限公司 | Preparation method of probiotics emulsifier for feed production |
-
2002
- 2002-10-10 KR KR10-2002-0061760A patent/KR100464983B1/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
KR20040032562A (en) | 2004-04-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN109481402B (en) | Preparation method of water-in-oil-in-water double emulsion gel with stable starch-based nanoparticles | |
EP2296494B2 (en) | Infant milk formula with fat gradient | |
JPH0759523B2 (en) | Modified release composition | |
KR100951706B1 (en) | Nanoemulsion, nanoparticle containing resveratrol and method of production thereof | |
KR100464983B1 (en) | Method of emulsifying feed oil and fat soluble vitamin by using lecithin and emulsifier | |
JPS63185350A (en) | Emulsification of fats of oils in aqueous phase consisting essentially of soy sauce | |
EP0352144A1 (en) | Protein product | |
KR100395791B1 (en) | Water dispersive mastic gum compound and preparation method thereof | |
WO2012081545A1 (en) | Water-in-oil emulsion and method of producing the same | |
EP2793614B1 (en) | Dispersion comprising protein particles, food product comprising such dispersion and use of such dispersion | |
JP3011530B2 (en) | Spreads and how to make them | |
JPH0550251B2 (en) | ||
JP2008178381A (en) | Method of preparing oil-in-water type emulsified food | |
JPS6159110B2 (en) | ||
CN113558237A (en) | Preparation method of capsaicin-loaded two-phase network water-in-oil high internal phase emulsion | |
JPH0342866B2 (en) | ||
JP2003213290A (en) | Double-emulsified oil and fat composition and method for producing the same | |
JP3325197B2 (en) | Water-in-oil type emulsified fat composition and method for producing the same | |
US6153248A (en) | Low-fat spread | |
WO2019029370A1 (en) | Microcapsule oil and preparation method therefor | |
EP0356094A2 (en) | Food product | |
JPS62221629A (en) | Production of phospholipid emulsion | |
JPH02182149A (en) | Cream, product made by churning milk therefrom, and making thereof | |
KR102653457B1 (en) | Method for preparing Quercetin powder composition improving mucosal adhesive capacity and Quercetin powder composition prepared by the same | |
JPH01132336A (en) | Production of milk fat-containing plastic oil and fat composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
N231 | Notification of change of applicant | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
LAPS | Lapse due to unpaid annual fee |