JP6433475B2 - Method for suppressing burning of fluid nutritional composition containing L-arginine - Google Patents

Method for suppressing burning of fluid nutritional composition containing L-arginine Download PDF

Info

Publication number
JP6433475B2
JP6433475B2 JP2016240150A JP2016240150A JP6433475B2 JP 6433475 B2 JP6433475 B2 JP 6433475B2 JP 2016240150 A JP2016240150 A JP 2016240150A JP 2016240150 A JP2016240150 A JP 2016240150A JP 6433475 B2 JP6433475 B2 JP 6433475B2
Authority
JP
Japan
Prior art keywords
arginine
composition
protein
calcium
caseinate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
JP2016240150A
Other languages
Japanese (ja)
Other versions
JP2017057214A (en
Inventor
浩平 宮野
浩平 宮野
未来 岡澤
未来 岡澤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Meiji Co Ltd
Original Assignee
Meiji Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Meiji Co Ltd filed Critical Meiji Co Ltd
Publication of JP2017057214A publication Critical patent/JP2017057214A/en
Application granted granted Critical
Publication of JP6433475B2 publication Critical patent/JP6433475B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/52Adding ingredients
    • A23L2/66Proteins
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/16Inorganic salts, minerals or trace elements
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/17Amino acids, peptides or proteins
    • A23L33/175Amino acids
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/17Amino acids, peptides or proteins
    • A23L33/19Dairy proteins
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/02Nutrients, e.g. vitamins, minerals
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Nutrition Science (AREA)
  • Engineering & Computer Science (AREA)
  • Polymers & Plastics (AREA)
  • Food Science & Technology (AREA)
  • Mycology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Diabetes (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Inorganic Chemistry (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Non-Alcoholic Beverages (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Description

本発明は、L−アルギニンを含む流動性栄養組成物の焦げ抑制方法に関する。   The present invention relates to a method for suppressing scorching of a fluid nutritional composition containing L-arginine.

近年、炎症性疾患や感染症、腎機能傷害に補給が必要なアミノ酸として、アルギニンが注目されている。アルギニンは非常に重要な生理機能を果たし、子供では必須アミノ酸として取り扱われている。例えば、アルギニンは、体内で生成されたアンモニアを尿素に変換する尿素サイクル(オルニチンサイクル)で利用され、細胞増殖や組織修復に必須であるポリアミンの合成に利用される。また、その代謝産物である一酸化窒素(NO)を介して、成長ホルモンの分泌促進、免疫機能の向上、脂肪代謝の促進など種々の機能に関与する。さらに、アルギニンを主要成分とした輸液が術後の回復を助け、感染性合併症の発生率低下に利用されている。この他にも、狭心症、末梢血管疾患、間質性膀胱炎の症状改善などに有効性が示唆されている。   In recent years, arginine has attracted attention as an amino acid that needs to be replenished for inflammatory diseases, infectious diseases, and impaired renal function. Arginine performs a very important physiological function and is treated as an essential amino acid in children. For example, arginine is used in a urea cycle (ornithine cycle) in which ammonia generated in the body is converted into urea, and is used for synthesis of a polyamine essential for cell growth and tissue repair. Furthermore, it is involved in various functions such as growth hormone secretion promotion, immune function enhancement, and fat metabolism promotion via its metabolite nitric oxide (NO). In addition, infusions containing arginine as the main ingredient help recovery after surgery and are used to reduce the incidence of infectious complications. In addition, it has been suggested to be effective for improving the symptoms of angina pectoris, peripheral vascular disease, and interstitial cystitis.

このような状況において、L−アルギニンを含む栄養組成物ないし嗜好品が種々提案されている。例えば、特許文献1(特表2007−515417号公報)には、組成物の総熱量の1.8%以下がアルギニン由来であり、タンパク質源が組成物の総熱量の少なくとも3%量のプロリンを含む栄養組成物が開示されている。この組成物は、創傷治癒のために適切な量のアルギニンが配合された組成物である。また、特許文献2(特開2002−186425号公報)には、コーヒー分とアルギニン及び乳分を含むコーヒー飲料が開示されている。当該コーヒー飲料は、アルギニンのような塩基性物質の添加により加熱殺菌により生じる沈殿物が抑えられた飲料である。特許文献3(特開2005−137266号公報)にも、L−ヒスチジン塩酸塩とL−アルギニン塩酸塩を含むコーヒー飲料が開示されている。当該コーヒー飲料では、L−アルギニン塩酸塩とL−アルギニン塩酸塩の相乗効果により、乳入りコーヒー飲料における異風味が抑制されている。さらに、特許文献4(特開平10−139681号公報)には、L−アルギニン及びグルタミン含有ペプチドを含む小麦グルテン分解物を含む経口水性乳化栄養組成物が開示されている。当該組成物は、L−アルギニンとグルタミンの配合によって生じる著しい苦みや加熱殺菌時に生じる着色などをグルタミン含有ペプチドの使用により改善した組成物である。   Under such circumstances, various nutritional compositions or luxury products containing L-arginine have been proposed. For example, in Patent Document 1 (Japanese Patent Publication No. 2007-515417), 1.8% or less of the total calorie of the composition is derived from arginine, and the protein source contains proline at least 3% of the total calorie of the composition. A nutritional composition comprising is disclosed. This composition is a composition containing an appropriate amount of arginine for wound healing. Patent Document 2 (Japanese Patent Application Laid-Open No. 2002-186425) discloses a coffee beverage containing coffee, arginine and milk. The coffee beverage is a beverage in which precipitates generated by heat sterilization are suppressed by the addition of a basic substance such as arginine. Patent Document 3 (Japanese Patent Application Laid-Open No. 2005-137266) also discloses a coffee beverage containing L-histidine hydrochloride and L-arginine hydrochloride. In the said coffee drink, the unusual flavor in the coffee drink containing milk is suppressed by the synergistic effect of L-arginine hydrochloride and L-arginine hydrochloride. Furthermore, Patent Document 4 (Japanese Patent Application Laid-Open No. 10-139681) discloses an oral aqueous emulsion nutrition composition containing a wheat gluten degradation product containing L-arginine and a glutamine-containing peptide. The said composition is the composition which improved the remarkable bitterness produced by the mixing | blending of L-arginine and glutamine, the coloring produced at the time of heat sterilization, etc. by use of a glutamine containing peptide.

特表2007−515417号公報Special table 2007-515417 特開2002−186425号公報JP 2002-186425 A 特開2005−137266号公報JP 2005-137266 A 特開平10−139681号公報Japanese Patent Laid-Open No. 10-139681

ところで、特許文献4にも記載されているようにL−アルギニンは特有の苦みを有する。これを改善するために糖質を組み合わせると、滅菌等のために加熱処理を行えば、アミノカルボニルとの反応を生じ、製品が著しい着色を生じるという問題がある。   By the way, as also described in Patent Document 4, L-arginine has a unique bitterness. When carbohydrates are combined to improve this, there is a problem that if heat treatment is performed for sterilization or the like, a reaction with aminocarbonyl occurs and the product is markedly colored.

また、乳タンパク質は、アミノ酸バランスがよく、カルシウムなどのミネラル分を含むので、良質なタンパク供給源となり得る。しかしながら、L−アルギニンは塩基性アミノ酸であるので、乳タンパク質を含む飲料に配合した場合には、苦みを抑えるためにも、また乳タンパク質の沈殿を防ぐためにも、多量の酸性pH調整剤が必要となる。しかしながら、アルギニンとクエン酸などの酸性pH調整剤と乳タンパク質を含む飲料を加熱処理した際には、焦げ付きが生じ、製品価値を失う場合があった。また、殺菌装置の流路内に残る焦げを除去するため、装置の洗浄に手間がかかっていた。これらの理由により、組成物の処方によって、高濃度のアルギニンを配合することができない場合があった。   Moreover, since milk protein has a good amino acid balance and contains minerals such as calcium, it can be a good protein source. However, since L-arginine is a basic amino acid, a large amount of an acidic pH adjuster is necessary to prevent bitterness and prevent precipitation of milk protein when blended in a beverage containing milk protein. It becomes. However, when a beverage containing an acidic pH adjusting agent such as arginine and citric acid and milk protein is heat-treated, it may be burnt and lose its product value. Moreover, in order to remove the burns remaining in the flow path of the sterilization apparatus, it takes time to clean the apparatus. For these reasons, there are cases where a high concentration of arginine cannot be blended depending on the formulation of the composition.

本発明は上記背景技術に鑑みてなされたものであって、本発明は、アルギニンとタンパク質、特に乳タンパク質を含む流動性栄養組成物において、苦みや加熱処理による焦げを抑えながら、より多くのアルギニンを配合可能にした栄養組成物を提供することを目的とする。   The present invention has been made in view of the above-described background art, and the present invention provides more arginine while suppressing bitterness and scorching due to heat treatment in a fluid nutrition composition containing arginine and protein, particularly milk protein. It is an object of the present invention to provide a nutritional composition that can be formulated.

上記課題を解決するために、本発明においては、ミセル非形成性のタンパク質と不溶性カルシウムを用いることによって、加熱処理による焦げや苦みを抑えて、風味を良好に保つことにしている。   In order to solve the above-described problems, in the present invention, by using a non-micelle-forming protein and insoluble calcium, it is possible to suppress scorching and bitterness due to heat treatment and maintain a good flavor.

つまり、本発明の方法は、アルギニンとタンパク源とカルシウム源と酸性pH調整剤を含む流動性栄養組成物を加熱することによって生じる焦げの抑制方法であって、前記組成物中のタンパク源として、その全部又はその一部にミセル非形成性タンパク質を用い、かつ、前記組成物中のカルシウム源として、その全部又はその一部に不溶性カルシウム化合物を用いる方法である。   That is, the method of the present invention is a method for suppressing scorching caused by heating a fluid nutrition composition containing arginine, a protein source, a calcium source, and an acidic pH adjuster, and as a protein source in the composition, In this method, a non-micelle-forming protein is used for all or part thereof, and an insoluble calcium compound is used for all or part thereof as a calcium source in the composition.

本発明によると、アルギニンによる苦みや加熱処理による焦げが抑えられた流動性組成物が提供される。また、ミセル形成性のタンパクや水溶性カルシウムを用いた場合に比べて、より多くのアルギニンが配合された流動性組成物が提供される。また、連続処理における流路となる配管内に焦げ付きが抑えられ、配管内の洗浄作業が簡便になる。   ADVANTAGE OF THE INVENTION According to this invention, the fluid composition in which the bitterness by arginine and the burning by heat processing were suppressed is provided. In addition, a fluid composition containing more arginine is provided as compared with the case where micelle-forming protein or water-soluble calcium is used. Moreover, scorching is suppressed in the piping that becomes the flow path in the continuous processing, and the cleaning work in the piping becomes simple.

本発明の方法により得られる流動性栄養組成物は、アルギニンとミセル非形成性タンパク質を含み、pHが6.0〜7.3である加熱処理された流動性栄養組成物であって、不溶性カルシウムの配合により、焦げが抑制され、かつ、風味が良好である流動性栄養組成物である。   The fluid nutrition composition obtained by the method of the present invention is a heat-treated fluid nutrition composition containing arginine and a non-micelle-forming protein and having a pH of 6.0 to 7.3, which is insoluble calcium. Is a fluid nutritional composition in which scorching is suppressed and the flavor is good.

当該流動性栄養組成物は、少なくともタンパク質源、好ましくは乳タンパク質を含み、室温(1〜30℃)において流動性を有する組成物を意味する。当該栄養組成物は、タンパク質源の他に糖質、脂質、ミネラル類、ビタミン類を含み得る。流動性栄養組成物は、例えば、飲料様の組成物、ゲル化剤の使用により粘性を有するゾル状の組成物であり得る。本発明の流動性栄養組成物は、主として経口される組成物であり、例えば、嗜好品である清涼飲料水やコーヒー飲料、スポーツドリンクのような飲料であり、健常人や病弱な人の体力維持、増進に必要な栄養を補給するための経口栄養剤や経口栄養流動食であり得る。また、経腸栄養流動食や経腸栄養剤や中心静脈栄養剤のように、経口以外の投与経路で投与される栄養組成物でもあり得る。   The fluid nutrition composition means a composition having at least a protein source, preferably milk protein, and fluidity at room temperature (1 to 30 ° C.). The nutritional composition may contain carbohydrates, lipids, minerals and vitamins in addition to the protein source. The fluid nutrition composition can be, for example, a beverage-like composition or a sol composition having viscosity due to the use of a gelling agent. The fluid nutrition composition of the present invention is a composition that is mainly orally administered, for example, beverages such as soft drinks, coffee beverages, and sports drinks, which are luxury products, and maintain the physical strength of healthy and sick people. It can be an oral nutritional supplement or a liquid nutritional diet for supplementing the nutrition required for enhancement. It may also be a nutritional composition administered by a route other than oral administration, such as enteral nutrition liquid food, enteral nutrition, and central parenteral nutrition.

本発明に係る組成物は、アルギニンとミセル非形成性タンパク質と不溶性カルシウムを必須成分とする。アルギニンはL−アルギニン、D−アルギニン、ラセミ体であるDL−アルギニンのいずれでもよいが、その有用性よりL−アルギニンが望ましい。また、アルギニンとして、遊離のアルギニンやアルギニンの塩の1種若しくは2種以上が用いられる。アルギニンの塩として、アルギニン塩酸塩、アルギニンリン酸塩、アルギニングルタミン酸塩が例示される。   The composition according to the present invention contains arginine, micelle-non-forming protein, and insoluble calcium as essential components. Arginine may be any of L-arginine, D-arginine, and racemic DL-arginine, but L-arginine is desirable from the viewpoint of its usefulness. As arginine, one or more of free arginine and arginine salts are used. Examples of arginine salts include arginine hydrochloride, arginine phosphate, and arginine glutamate.

ミセル非形成性タンパク質は、水及び油を含む系においてミセルを形成しないタンパク質である。ミセル非形成性タンパク質として、ナトリウムカゼイネート又はカリウムカゼイネートが例示される。本発明においては、良質なアミノ酸の供給源となることから、乳タンパク質由来のミセル非形成性タンパク質が好ましく用いられる。流動性栄養組成物に汎用し得る乳タンパク質として、MPC(乳タンパク濃縮物:milk protein concentrate)、脱脂粉乳、MPI(乳タンパク分離物:milk protein isolate)、カゼインやその塩であるカゼイネートが例示される。これらの乳タンパク質のうち、MPC、脱脂粉乳、MPIはミセルを形成する性質を有する。また、カゼイネートは、その塩によって性質が異なり、カルシウムカゼイネートやマグネシウムカゼイネートはミセルを形成するが、ナトリウムカゼイネートやカリウムカゼイネートはミセルを形成しない。もっとも、本発明の目的を逸脱しない範囲で、本発明の組成物では、タンパク源としてカゼイネート以外のミセル非形成性のタンパク質を用いることもできる。例えば、ホエイ、大豆タンパク質、ペプチドなどが例示される。   A non-micelle forming protein is a protein that does not form micelles in a system containing water and oil. Examples of non-micelle forming proteins include sodium caseinate and potassium caseinate. In the present invention, a non-micelle-forming protein derived from milk protein is preferably used because it serves as a source of good-quality amino acids. Examples of milk proteins that can be widely used in fluid nutritional compositions include MPC (milk protein concentrate), skim milk powder, MPI (milk protein isolate), casein and its caseinate. The Among these milk proteins, MPC, skim milk powder, and MPI have the property of forming micelles. Caseinate has different properties depending on its salt, and calcium caseinate and magnesium caseinate form micelles, but sodium caseinate and potassium caseinate do not form micelles. However, in the composition of the present invention, a non-micelle-forming protein other than caseinate can be used as a protein source without departing from the object of the present invention. For example, whey, soy protein, peptide and the like are exemplified.

組成物におけるタンパク質の配合量は焦げや風味の低下を引き起こさない限り、任意である。その下限量は、例えば、組成物100ml中0.01gであり、0.1gであり、0.5gであり、1gであり得る。その上限量は、例えば、組成物100ml中50gであり、30gであり、20gであり、10gであり得る。また、病弱な人や術前術後の患者の栄養補給に用いられる組成物であれば、好ましくは組成物100ml中における総熱量に対するタンパク質由来の熱量が、2〜30%となるように調整される。   The blending amount of the protein in the composition is arbitrary as long as it does not cause burning or a decrease in flavor. The lower limit amount is, for example, 0.01 g in 100 ml of the composition, 0.1 g, 0.5 g, and 1 g. The upper limit amount is, for example, 50 g in 100 ml of the composition, 30 g, 20 g, or 10 g. Moreover, if it is a composition used for the nutritional supplementation of a sick person or a patient before and after surgery, it is preferably adjusted so that the amount of heat derived from protein relative to the total amount of heat in 100 ml of the composition is 2 to 30%. The

本発明に係る組成物は、不溶性カルシウム化合物を含む。不溶性カルシウム化合物を用いることにより、加熱時による焦げを防止できるからである。不溶性カルシウム化合物は、水にほとんど溶解しない物質であり、20℃における水に対する溶解度が0.05g/ml以下の物質、好ましくは0.01g/ml以下、望ましくは0.005g/ml以下の物質である。リン酸カルシウムや炭酸カルシウムが例示され、食品や医薬品に用いられるリン酸カルシウムが好ましく用いられる。不溶性カルシウム化合物は、MPCや脱脂粉乳、MPIなどの乳タンパク質に含まれるカルシウム分の代替としての意義を有し、栄養補給のために用いられる。不溶性カルシウム化合物の配合量は栄養補給の観点等から適宜定められる。その下限量は例えば組成物100ml中、0.0001gであり、0.001gであり、0.005gであり、0.01gであり、0.05gであり、0.1gであり得る。また、その上限量は例えば10gであり、5gであり、2gであり、1gであり得る。   The composition according to the present invention comprises an insoluble calcium compound. This is because the use of an insoluble calcium compound can prevent scorching due to heating. The insoluble calcium compound is a substance that hardly dissolves in water, and has a solubility in water at 20 ° C. of 0.05 g / ml or less, preferably 0.01 g / ml or less, desirably 0.005 g / ml or less. is there. Calcium phosphate and calcium carbonate are exemplified, and calcium phosphate used for foods and pharmaceuticals is preferably used. The insoluble calcium compound has significance as a substitute for calcium contained in milk proteins such as MPC, skim milk powder, and MPI, and is used for nutritional supplementation. The amount of the insoluble calcium compound is appropriately determined from the viewpoint of nutritional supplementation. The lower limit is, for example, 0.0001 g, 0.001 g, 0.005 g, 0.01 g, 0.05 g, and 0.1 g in 100 ml of the composition. Moreover, the upper limit amount is, for example, 10 g, 5 g, 2 g, and 1 g.

タンパク質の沈殿やアルギニンによる苦みを抑えるために酸性pH調整剤によって、組成物のpHが6.0〜7.3に調整される。組成物のpHが6.0未満であれば、加熱による滅菌時に焦げが生じるおそれがある。また、組成物のpHが7.3を越えると、アルギニンの苦みや焦げにより組成物の風味が損なわれるおそれがある。   In order to suppress protein precipitation and bitterness due to arginine, the pH of the composition is adjusted to 6.0 to 7.3 by an acidic pH adjuster. If the pH of the composition is less than 6.0, there is a risk of scorching during sterilization by heating. On the other hand, if the pH of the composition exceeds 7.3, the flavor of the composition may be impaired by the bitterness or scorching of arginine.

酸性pH調整剤は組成物のpHを調整する成分であって、主として塩基性成分であるアルギニンを中和する酸性物質である。酸性pH調整剤はリン酸、塩酸、硫酸などの無機酸や、クエン酸やシュウ酸、リンゴ酸、酢酸などの有機酸が例示される。本発明の組成物は栄養組成物であるので、リン酸やクエン酸、リンゴ酸、酢酸など食品添加物として使用され得る酸が好ましい。もっとも、アルギニン塩を構成する酸も当該酸性pH調整剤として利用され得る。   The acidic pH adjuster is a component that adjusts the pH of the composition, and is an acidic substance that mainly neutralizes arginine, which is a basic component. Examples of the acidic pH adjuster include inorganic acids such as phosphoric acid, hydrochloric acid, and sulfuric acid, and organic acids such as citric acid, oxalic acid, malic acid, and acetic acid. Since the composition of the present invention is a nutritional composition, acids that can be used as food additives such as phosphoric acid, citric acid, malic acid, and acetic acid are preferred. But the acid which comprises an arginine salt can also be utilized as the said acidic pH adjuster.

本発明では、タンパク源としてのミセル非形成性タンパク質と不溶性カルシウムの配合が、加熱による焦げを防止し、風味の維持を図る。このメカニズムは十分に解明されたものではないが、焦げの原因は、乳タンパクを用いた組成物では、アルギニンと共に配合される酸が乳タンパクのミセルを破壊し、それによりカルシウム(イオン)が遊離することであると考えられる。つまり、本発明の組成物は、ミセル非形成性タンパク質によるミセル形成の防止と不溶性カルシウムの使用によるカルシウムの遊離抑制が図られた組成物であると言える。この結果、液性の調整に使用しえる酸性pH調整剤の増量が可能となり、高濃度にアルギニンが配合され得ることになる。そして、さらに言い換えると、本発明の方法は、アルギニンとタンパク源とカルシウム源と酸性pH調整剤を含む流動性組成物を加熱した際に生じる焦げの発生を、当該組成物中のタンパク源としてその全部又はその一部にミセル非形成性タンパク質を用い、かつ、組成物中のカルシウム源としてその全部又はその一部に不溶性カルシウム化合物を用いて抑制する方法であると言える。   In the present invention, the combination of non-micelle-forming protein as a protein source and insoluble calcium prevents scorching due to heating and maintains the flavor. Although this mechanism has not been fully elucidated, in the composition using milk protein, the cause of scorching is that the acid mixed with arginine destroys the micelles of the milk protein, thereby releasing calcium (ions). It is thought to be. That is, it can be said that the composition of the present invention is a composition in which micelle formation is prevented by a non-micelle-forming protein and calcium release is suppressed by using insoluble calcium. As a result, it is possible to increase the amount of the acidic pH adjuster that can be used for adjusting the liquidity, and arginine can be blended at a high concentration. And in other words, the method of the present invention uses the occurrence of scorching that occurs when a fluid composition containing arginine, a protein source, a calcium source, and an acidic pH adjuster is heated as a protein source in the composition. It can be said that this is a method of inhibiting by using a micelle-non-forming protein for all or part thereof and using an insoluble calcium compound for all or part thereof as a calcium source in the composition.

本発明に係る組成物におけるアルギニンの配合量は、焦げが防止され、風味を良好に維持できる限り特に限定されるものではない。その下限は例えば遊離のアルギニンとして組成物100ml中、0.001gであり、0.01gであり、0.1gであり、0.5gであり、1.0g、1.5gであり得る。また、その上限は例えば組成物100ml中4.5gであり、4.0gであり、3.5gであり、3.0gであり得る。組成物100ml中4.5g以上になると、組成物の風味が低下するおそれがあるので、その配合量は組成物100ml中4.5g未満であるのが好ましい。   The blending amount of arginine in the composition according to the present invention is not particularly limited as long as scorch is prevented and the flavor can be maintained satisfactorily. The lower limit may be, for example, 0.001 g, 100 g, 0.1 g, 0.5 g, 1.0 g, 1.5 g as free arginine in 100 ml of the composition. Moreover, the upper limit is, for example, 4.5 g in 100 ml of the composition, 4.0 g, 3.5 g, and 3.0 g. If the amount is 4.5 g or more in 100 ml of the composition, the flavor of the composition may be lowered. Therefore, the blending amount is preferably less than 4.5 g in 100 ml of the composition.

本発明に係る組成物は、経口栄養用の組成物や経腸栄養用の組成物など、術前術後の栄養補給用の組成物としても用いられる。従って、当該組成物は、糖質、タンパク質、脂質、ミネラル、ビタミン類、ゲル化剤のような組成物の粘度調整剤を含み得る。しかしながら、タンパク質源としてミセル形成性タンパク質を用いた場合やミネラルであるカルシウム源として不溶性カルシウム以外のカルシウム化合物を用いた場合には、焦げを生じる場合や風味の低下を招く場合がある。従って、組成物中のタンパク質源が前記ミセル非形成性タンパク質のみであり、かつ、組成物中のカルシウム源が前記不溶性カルシウムのみであることが望まれる。もっとも、焦げを生じず、風味の維持が図られる限りにおいて、タンパク源としてミセル形成性タンパク質の配合が可能であり、カルシウム源として水溶性カルシウム化合物の配合も可能である。この場合、ミセル形成性タンパク質の配合量の上限は、組成物100ml中0.1gであり、0.05gであり、0.01gであり、0.005gであり得る。水溶性カルシウム化合物の配合量の上限は、組成物100ml中0.1gであり、0.05gであり、0.01gであり、0.005gであり得る。   The composition according to the present invention is also used as a composition for nutritional supplementation before and after surgery, such as a composition for oral nutrition and a composition for enteral nutrition. Accordingly, the composition may include a viscosity modifier for the composition such as carbohydrates, proteins, lipids, minerals, vitamins, gelling agents. However, when a micelle-forming protein is used as a protein source, or when a calcium compound other than insoluble calcium is used as a calcium source that is a mineral, there is a case where burnt or a decrease in flavor is caused. Therefore, it is desirable that the protein source in the composition is only the non-micelle-forming protein, and the calcium source in the composition is only the insoluble calcium. However, as long as the flavor is maintained without burning, micelle-forming protein can be blended as a protein source, and a water-soluble calcium compound can be blended as a calcium source. In this case, the upper limit of the amount of the micelle-forming protein is 0.1 g in 100 ml of the composition, 0.05 g, 0.01 g, and 0.005 g. The upper limit of the amount of the water-soluble calcium compound is 0.1 g in 100 ml of the composition, 0.05 g, 0.01 g, and 0.005 g.

上記の成分は水と共に、pHが6.0〜7.3となるように液体組成物に調製される。調製された液体組成物は加熱され、殺菌ないし滅菌される。加熱処理方法として、オートクレーブによるバッチ処理やスチームインジェクションによる連続処理が例示される。加熱処理後は、常温にまで冷却される。この結果、加熱処理中に焦げを生じず、風味が良好である流動性栄養組成物が得られる。また、連続処理における配管内に焦げ付きがなくなるので、製造ラインの洗浄作業が簡便になる。   The above components are prepared into a liquid composition together with water so that the pH is 6.0 to 7.3. The prepared liquid composition is heated and sterilized or sterilized. Examples of the heat treatment method include batch processing by autoclave and continuous processing by steam injection. After the heat treatment, it is cooled to room temperature. As a result, a fluid nutritional composition is obtained that does not burn during heat treatment and has a good flavor. Moreover, since there is no burning in the piping in the continuous processing, the cleaning operation of the production line becomes simple.

次に本発明について、下記の実施例に基づいて詳細に説明する。下記の実施例はあくまでも例示に過ぎず、本発明は下記の実施例に限られないのは言うまでもない。   Next, the present invention will be described in detail based on the following examples. The following embodiments are merely examples, and it goes without saying that the present invention is not limited to the following embodiments.

〔焦げの発生と使用タンパク質、カルシウムとの関係〕
L−アルギニン(協和発酵株式会社製)を配合した組成物における焦げの発生と、使用するタンパク質の種類、カルシウムの種類との関係について調べた。表1に示す配合量となるように水を加えて液状組成物を調整し、スチームインジェクション(145℃、5秒)による加熱後、45MPaで均質化して、その後冷却した。なお、脱脂粉乳は明治乳業株式会社製(たんぱく質含量34w/w%)、乳たんぱく質濃縮物(MPC)はフォンテラジャパン株式会社製(たんぱく質含量80w/w%)、リン酸カルシウムは丸尾カルシウム株式会社製のカルシウムスラリー(リン酸カルシウムとして21w/w%含有)、乳清カルシウムはフォンテラジャパン株式会社製乳清カルシウム(カルシウムとして30w/w%含有)を用いた。
[Relationship between scorching and protein and calcium used]
The relationship between the occurrence of scorch in the composition containing L-arginine (manufactured by Kyowa Hakko Co., Ltd.), the type of protein used, and the type of calcium was examined. Water was added to adjust the liquid composition so as to have the blending amounts shown in Table 1, and after heating by steam injection (145 ° C., 5 seconds), homogenized at 45 MPa, and then cooled. Skim milk powder is manufactured by Meiji Dairies Co., Ltd. (protein content 34 w / w%), milk protein concentrate (MPC) is manufactured by Fontera Japan Co., Ltd. (protein content 80 w / w%), and calcium phosphate is calcium manufactured by Maruo Calcium Co., Ltd. As the slurry (containing 21 w / w% as calcium phosphate) and whey calcium, whey calcium (containing 30 w / w% as calcium) manufactured by Fontera Japan Co., Ltd. was used.

Figure 0006433475
Figure 0006433475

これによると、1%以上のL−アルギニンとミセル形成性タンパク質、水溶性カルシウムを用いた場合には、ミセル非形成性のタンパク質の有無によらず、焦げ付きの発生が見られた。   According to this, when 1% or more of L-arginine, a micelle-forming protein, and water-soluble calcium were used, the occurrence of scorching was observed regardless of the presence or absence of a non-micelle-forming protein.

〔アルギニン添加量の検討〕
次に表2に示す配合量となるように水を加えて液状組成物を調整し、スチームインジェクション(145℃、5秒)による加熱後、45MPaで均質化して、その後冷却した。
[Examination of Arginine Addition Amount]
Next, water was added so that the blending amounts shown in Table 2 were added to prepare a liquid composition, which was heated by steam injection (145 ° C., 5 seconds), homogenized at 45 MPa, and then cooled.

Figure 0006433475
Figure 0006433475

これによると、4.5%未満のL−アルギニンを含む場合には焦げ付きの発生が見られなかったが、4.5%以上になるとL−アルギニンを含む場合に焦げ付きは見られないものの、風味が低下する場合があった。   According to this, when less than 4.5% of L-arginine was included, the occurrence of scorching was not observed, but when it was 4.5% or more, no scorching was observed when containing L-arginine, but the flavor May be reduced.

〔pHの検討〕
次に表3に示す配合量となるように水を加えて液状組成物を調整し、スチームインジェクション(145℃、5秒)による加熱後、45MPaで均質化して、その後冷却した。
[Investigation of pH]
Next, water was added so that the blending amounts shown in Table 3 were added, the liquid composition was adjusted, heated by steam injection (145 ° C., 5 seconds), homogenized at 45 MPa, and then cooled.

Figure 0006433475
Figure 0006433475

これによると、pHが6.0未満の場合には焦げ付きが見られた。一方、pHが7.3を越えると、焦げ付きは見られないものの、風味が悪くなる場合があった。   According to this, scorching was observed when the pH was less than 6.0. On the other hand, when the pH exceeded 7.3, although there was no scorch, the flavor sometimes deteriorated.

表4に示す成分から、本発明の組成物である飲料を製造した。当該組成物は焦げ付きがなく、また風味が良好であった。また、この飲料は経腸栄養組成物又は経口栄養組成物としても適したものであった。   From the components shown in Table 4, beverages that were the compositions of the present invention were produced. The composition was not burnt and had a good flavor. The beverage was also suitable as an enteral nutrition composition or an oral nutrition composition.

Figure 0006433475
Figure 0006433475

本発明は、少量の摂取量で比較的多量のアルギニンを摂取できる流動性栄養組成物を提供する。   The present invention provides a fluid nutrition composition capable of ingesting a relatively large amount of arginine with a small amount of intake.

Claims (2)

組成物100ml中に1.0g以上4.5g未満のアルギニンと、タンパク源と、カルシウム源と酸性pH調整剤を含み、ミセル形成性タンパク質及び水溶性カルシウム化合物を実質的に含まないpHが6.0〜7.3である流動性栄養組成物を加熱することによって生じる焦げの抑制方法であって、
前記タンパク源が、ナトリウムカゼイネート及び/又はカリウムカゼイネートであり、
前記カルシウム源が、リン酸カルシウム及び/又は炭酸カルシウムであり、
かつ、ナトリウムカゼイネート及びカリウムカゼイネートの合計量に対するアルギニンの配合比が質量比で5/71〜40/43の範囲内とする方法。
In 100 ml of the composition, 1.0 g or more and less than 4.5 g of arginine, a protein source, a calcium source and an acidic pH adjuster, and a pH substantially free of micelle-forming protein and water-soluble calcium compound is 6. A method for suppressing scorching caused by heating a fluid nutritional composition that is 0-7.3,
The protein source is sodium caseinate and / or potassium caseinate;
The calcium source is calcium phosphate and / or calcium carbonate;
And the method which makes the compounding ratio of arginine with respect to the total amount of sodium caseinate and potassium caseinate into the range of 5 / 71-40 / 43 by mass ratio.
アルギニンと、ナトリウムカゼイネート及び/又はカリウムカゼイネートと、リン酸カルシウム及び/又は炭酸カルシウムと、酸性pH調整剤を含み、pHが6.0〜7.3である流動性栄養組成物の製造方法であって、
ナトリウムカゼイネート及びカリウムカゼイネートの合計量に対するアルギニンの配合比が質量比で5/71〜40/43の範囲内であり、かつ、組成物100mlに1.0g以上4.5g未満のアルギニンと、加熱後の焦げが生じない程度にミセル形成性タンパク質及び水溶性カルシウム化合物が配合された組成物を加熱する工程を有する製造方法。
A method for producing a fluid nutritional composition comprising arginine, sodium caseinate and / or potassium caseinate, calcium phosphate and / or calcium carbonate, and an acidic pH adjuster and having a pH of 6.0 to 7.3. And
Arginine is mixed in a mass ratio of 5/71 to 40/43 with respect to the total amount of sodium caseinate and potassium caseinate, and 1.0 g or more and less than 4.5 g of arginine in 100 ml of the composition; The manufacturing method which has the process of heating the composition with which the micelle formation protein and the water-soluble calcium compound were mix | blended to such an extent that the charring after a heating does not arise.
JP2016240150A 2011-03-31 2016-12-12 Method for suppressing burning of fluid nutritional composition containing L-arginine Active JP6433475B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2011080721 2011-03-31
JP2011080721 2011-03-31

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2013507769A Division JP6313042B2 (en) 2011-03-31 2012-03-30 Fluid nutrition composition containing L-arginine and method for producing the same

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2018210094A Division JP2019037249A (en) 2011-03-31 2018-11-07 Method for suppressing scorch of flowable nutritional composition containing l-arginine

Publications (2)

Publication Number Publication Date
JP2017057214A JP2017057214A (en) 2017-03-23
JP6433475B2 true JP6433475B2 (en) 2018-12-05

Family

ID=46932022

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2013507769A Active JP6313042B2 (en) 2011-03-31 2012-03-30 Fluid nutrition composition containing L-arginine and method for producing the same
JP2016240150A Active JP6433475B2 (en) 2011-03-31 2016-12-12 Method for suppressing burning of fluid nutritional composition containing L-arginine
JP2018210094A Pending JP2019037249A (en) 2011-03-31 2018-11-07 Method for suppressing scorch of flowable nutritional composition containing l-arginine

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP2013507769A Active JP6313042B2 (en) 2011-03-31 2012-03-30 Fluid nutrition composition containing L-arginine and method for producing the same

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2018210094A Pending JP2019037249A (en) 2011-03-31 2018-11-07 Method for suppressing scorch of flowable nutritional composition containing l-arginine

Country Status (6)

Country Link
JP (3) JP6313042B2 (en)
CN (1) CN103458711B (en)
HK (1) HK1189334A1 (en)
SG (1) SG193588A1 (en)
TW (1) TWI561175B (en)
WO (1) WO2012133746A2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI561175B (en) * 2011-03-31 2016-12-11 Meiji Co Ltd Flowable nutrition composition containing l-arginine and method for producing the same
CN104883895B (en) * 2012-12-28 2017-12-29 花王株式会社 Beverage containing di-coffee mesitoyl quinine acid
JP6378513B2 (en) * 2014-03-24 2018-08-22 アサヒ飲料株式会社 Hesperidin-containing beverage, bitterness improving agent, and bitterness improving method

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2474829B1 (en) * 1980-02-01 1983-09-09 Agronomique Inst Nat Rech PROCESS FOR THE TREATMENT OF A CASEIN MATERIAL CONTAINING PHOSPHOCASEINATES OF MONOVALENT CATIONS OR DERIVATIVES THEREOF, PRODUCTS OBTAINED AND APPLICATIONS
JP3981991B2 (en) * 1996-11-05 2007-09-26 日本油脂株式会社 Aqueous emulsified nutritional composition and use thereof
JPH10139683A (en) * 1996-11-14 1998-05-26 Otsuka Pharmaceut Co Ltd Immunopotentiating nutrient supplying composition
EP0891719A1 (en) * 1997-07-14 1999-01-20 N.V. Nutricia Nutritional composition containing methionine
GB9923048D0 (en) * 1999-09-29 1999-12-01 Nestle Sa Composition comprising casein protein and whey protein
JP2004097034A (en) * 2002-09-05 2004-04-02 Howaizu:Kk L-arginine powder and food containing the same
DK1543735T3 (en) * 2003-12-20 2015-11-02 Nestec Sa FOOD COMPOSITION FOR HEALTH CARE
JP2009106217A (en) * 2007-10-31 2009-05-21 Ajinomoto Co Inc Food composition containing thickener and amino acid
US8361534B2 (en) * 2007-12-20 2013-01-29 Abbott Laboratories Stable nutritional powder
JP5665009B2 (en) * 2008-11-21 2015-02-04 味の素株式会社 Liquid emulsified nutritional composition
TWI561175B (en) * 2011-03-31 2016-12-11 Meiji Co Ltd Flowable nutrition composition containing l-arginine and method for producing the same

Also Published As

Publication number Publication date
TW201242519A (en) 2012-11-01
JP2017057214A (en) 2017-03-23
CN103458711A (en) 2013-12-18
SG193588A1 (en) 2013-10-30
CN103458711B (en) 2015-08-19
JPWO2012133746A1 (en) 2014-07-28
JP2019037249A (en) 2019-03-14
HK1189334A1 (en) 2014-06-06
TWI561175B (en) 2016-12-11
WO2012133746A3 (en) 2012-11-29
JP6313042B2 (en) 2018-04-18
WO2012133746A2 (en) 2012-10-04

Similar Documents

Publication Publication Date Title
ES2837050T3 (en) Liquid nutritional composition comprising micellar casein and hydrolyzed whey protein
EP2651249B1 (en) Method for making whey protein composition with a reduced astringency
TWI301052B (en) Infant formula compositions comprising increased amounts of alpha-lactalbumin
EP2699251B1 (en) Infant formula for use in the prevention of cardiovascular diseases
JP2003510059A (en) Composition comprising casein protein and whey protein
JPH04267864A (en) Highly acidic nutrition mixture
JP2019037249A (en) Method for suppressing scorch of flowable nutritional composition containing l-arginine
JP4972308B2 (en) Gelling nutrient and method for producing the same
JP2017518078A (en) Potato-based protein mixture and nutritional composition containing potato protein
SE1350804A1 (en) New prophylactic use
JP5421769B2 (en) Liquid nutrition composition containing sodium in high concentration and method for producing the same
JP6586414B2 (en) Nutritional composition
JP2001316278A (en) Liquid enteral nutrition composition
JP6961569B2 (en) Hydration agent
JPS595111A (en) Prepared nutritious substance for infant with phenylketonuria
KR102050578B1 (en) Composition of infant liquid formula including goat milk
JP6439681B2 (en) Semi-solid high nutrition food
JP5377202B2 (en) Food material for fortification
JP4484010B2 (en) Liquid liquid food
JP2023069186A (en) Nutritive composition, manufacturing method of nutritive composition, and evaluation method of bioavailability of copper in nutritive composition
CN117297113A (en) Method for improving stability of whey protein and application of whey protein in special medical food
JP2021065164A (en) Nutritive composition for infants
JPWO2009116636A1 (en) Mineral fortified soy protein solution
NZ623027B2 (en) Sterilized liquid protein supplement

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20170105

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20171003

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20171115

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20180201

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20180410

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20180604

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20180808

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20180828

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20181026

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20181106

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20181106

R150 Certificate of patent or registration of utility model

Ref document number: 6433475

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150