JP2004091485A - Vitamin b1 containing nutritive composition - Google Patents
Vitamin b1 containing nutritive composition Download PDFInfo
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- JP2004091485A JP2004091485A JP2003291288A JP2003291288A JP2004091485A JP 2004091485 A JP2004091485 A JP 2004091485A JP 2003291288 A JP2003291288 A JP 2003291288A JP 2003291288 A JP2003291288 A JP 2003291288A JP 2004091485 A JP2004091485 A JP 2004091485A
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- Prior art keywords
- vitamin
- nutritional composition
- blood
- nutritional
- kcal
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Abstract
Description
本発明は、経口あるいは経腸的な栄養補給を必要とする外科手術患者や高齢者、あるいは低栄養状態の患者に投与する栄養組成物に関する。さらに詳しくは、本発明は、蛋白質、脂質、糖質を主成分とし、ビタミンならびにミネラルを含有する、エネルギー0.5〜2.0kcal/mL、好ましくは1.0〜1.6kcal/mLの栄養組成物である。 The present invention relates to a nutritional composition to be administered to a surgical patient, an elderly person, or a malnourished patient requiring oral or enteral nutritional supplementation. More specifically, the present invention is a nutritional composition containing 0.5 to 2.0 kcal / mL, preferably 1.0 to 1.6 kcal / mL, which contains protein, lipid, and saccharide as main components and contains vitamins and minerals.
経腸栄養法は、投与経路により、経口栄養法と経鼻胃管または経鼻腸管、胃ろうや腸ろう等の強制的経腸栄養法がある。経腸栄養剤としては、窒素源の形態の違いや管腔内消化の必要性の有無により、成分栄養剤、消化態あるいは半消化態栄養剤、天然濃厚流動食等に分類される。経腸栄養は、静脈栄養と比べて生理的な栄養法であり、癌患者や重症熱傷患者、上部消化管通過障害や腸管不全の栄養管理に施行されているほか、消化器外科領域における術前・術後患者の栄養管理に用いられている。また、高齢者あるいは病後の人等喫食量の少ない人や嚥下能力が低下している人、嚥下機能訓練患者、水分制限患者において、経口摂取が不十分な低栄養患者等には、経腸栄養では主に液状の栄養剤が用いられているが、液状のものに限らずゲル状の栄養剤も同様にして用いられている。すなわち、咀嚼力が弱っている場合は、食材を細かく刻んだり、つぶした形態、嚥下機能が弱っている場合は、ゼリ−状やペ−スト状の形態と咀嚼力、嚥下機能の程度によって食べられる食事形態が異なってくるので、液状もしくはゲル状など、栄養を必要としている人に対して様々な形態の栄養組成物が広く用いられている。
消化器外科手術患者や高齢者において、蛋白質、エネルギー、ビタミンあるいはミネラル等の摂取不足状態が長く続くと、免疫機能の低下や新たな疾患の発症を誘引することがある。特に、ビタミンは健康的な生活を営むために、欠くことのできない栄養素の一つであり、その補酵素作用、代謝調節作用などが知られていたが、このほかに抗酸化作用、細胞間情報伝達作用等の栄養素以外の作用があることが判明してきた。そのため、ビタミンを適量に摂取することは重要である。
従来の栄養剤あるいは栄養組成物は、青壮年者におけるエネルギー所要量を投与した場合に、ビタミンの1日の所要量が充足できるように配合量が設定されている。そのため、エネルギー投与量の少ない場合にはビタミンは摂取不足状態となる。
Enteral nutrition includes oral nutrition and forced enteral nutrition, such as nasogastric or naso-intestinal tract, gastric fistula and intestinal fistula, depending on the administration route. Enteral nutrients are classified into component nutrients, digestive or semi-digestive nutrients, natural concentrated liquid foods, and the like, depending on the difference in the form of the nitrogen source and the necessity of intraluminal digestion. Enteral nutrition is more physiological than parenteral nutrition and is used for nutritional management of cancer patients, severe burns, upper gastrointestinal tract obstruction and intestinal insufficiency.・ It is used for nutrition management of postoperative patients. In addition, enteral nutrition is recommended for elderly people or those who have low consumption such as post-sick people, those who have reduced swallowing ability, those who have difficulty in swallowing training, and those who have poor oral intake in patients with limited water intake. Although liquid nutritional supplements are mainly used in the present invention, not only liquid nutritional supplements but also gel nutritional supplements are similarly used. In other words, when the chewing power is weak, the food is finely chopped or crushed, and when the swallowing function is weak, the food is eaten depending on the jelly-like or paste-like form, the chewing power, and the degree of the swallowing function. Since nutritional forms to be taken are different, various forms of nutritional compositions, such as liquid or gel, are widely used for people in need of nutrition.
In gastrointestinal surgery patients and the elderly, prolonged inadequate intake of proteins, energy, vitamins, minerals, etc. may lead to a decrease in immune function and the onset of new diseases. In particular, vitamins are one of the indispensable nutrients for living a healthy life, and their coenzyme action, metabolic regulation action, etc. were known, but in addition, antioxidant action, intercellular information It has been found that there is an action other than nutrients such as a transmission action. Therefore, it is important to take proper amounts of vitamins.
The amount of the conventional nutritional supplement or nutritional composition is set so that the required daily amount of vitamins can be satisfied when the energy requirement of the aged is administered. Therefore, when the energy dose is small, the vitamin is in a state of insufficient intake.
近年、ビタミン、ミネラルを強化した流動食が販売されている(商品名NT-3、NT-5、OKUNOS:商品名ハーモニック-M、エスエス・味の素ファルマ)。また、特許文献1には、蛋白質、ビタミン、ミネラルを含有した液状栄養組成物に粉砕した穀類を配合した栄養粥が提案されている。これらの流動食あるいは栄養粥は、栄養学的にはエネルギー1000kcalの摂取により栄養所要量のビタミン、ミネラルが充足できるとされている。しかしながら、これらの流動食に含まれるビタミンB1はエネルギー100kcalあたり0.18〜0.88mg、また栄養粥に含まれるビタミンB1は0.03〜0.4mg程度であり、さらに、これらの流動食あるいは栄養粥を摂取した場合の血中ビタミン濃度の検討等は全くなされていない。
ビタミンB1は、チアミン2-リン酸(TPP)の形で補酵素としてα-ケト酸の脱炭酸反応と、ヘキソースおよびペントースリン酸間でのトランスケトラーゼ反応系で働き、糖質や分枝鎖アミノ酸の代謝にあずかる。
ビタミンB2は、吸収後、補酵素型フラビンアデニンジヌクレオチドあるいはフラビンモノヌクレオチドに変換され、エネルギー代謝系や多くの酸化還元系において作用する。
ビタミンB6は、アミノ酸の代謝に関するトランスアミナーゼ、デカルボキシラーゼ等、補酵素として機能する。
Vitamin B1 acts as a coenzyme in the form of thiamine 2-phosphate (TPP) as a coenzyme in the decarboxylation reaction of α-keto acid and in the transketolase reaction between hexose and pentose phosphate, and acts as a sugar and branched-chain amino acid. Participates in the metabolism of
After absorption, vitamin B2 is converted to coenzyme type flavin adenine dinucleotide or flavin mononucleotide, and acts in energy metabolism and many redox systems.
Vitamin B6 functions as a coenzyme such as transaminase and decarboxylase related to amino acid metabolism.
消化器外科手術等により、生体に手術侵襲が加わると、手術後の侵襲下で代謝回転の促進による組織のビタミン需要量の増加が大きくなる。また、エピネフリン、ステロイドホルモン、グルカゴンなどの分泌が亢進する。また、膵からのインシュリン分泌は著明に抑制されることはないが、エピネフリンが末梢組織におけるインシュリン作用を阻害する。すなわち、術後は糖の利用が障害され、一種の糖尿病様状態となる。糖の利用障害がインシュリン分泌障害によるものでなく、末梢組織におけるインシュリンの作用障害であるため、外因性のインシュリンを投与しても奏効しない(術後代謝の基礎と臨床、真興交易医書出版部)。つまり術後早期は、高血糖を起こしやすく、投与エネルギー量は制限されることになる。
本発明の主たる目的は、潜在的なビタミン欠乏状態にある外科手術前後の患者や糖尿病患者、あるいは高齢者において、必要エネルギー投与量の1/5〜1/10量と少ない場合でも、ビタミンが十分量補給可能な栄養組成物を提供することにある。
本発明の他の目的は、経口あるいは経腸的な栄養補給を必要とする患者、中でも耐糖能異常に陥りやすい消化器外科手術患者や高齢者に対し、体内ビタミン充足率を上げ、血糖値上昇の抑制、体重増加、血清アルブミン濃度の改善を目的に、食事だけでは摂取不可能な栄養素補給を可能とする栄養組成物を提供することにある。
When surgical invasion is added to a living body by gastrointestinal surgery or the like, an increase in tissue vitamin demand due to promotion of turnover under invasion after surgery increases. In addition, secretion of epinephrine, steroid hormones, glucagon and the like is enhanced. In addition, insulin secretion from the pancreas is not significantly suppressed, but epinephrine inhibits insulin action in peripheral tissues. That is, the use of sugar is impaired after the operation, resulting in a kind of diabetes-like state. Because the impaired sugar utilization is not due to impaired insulin secretion but due to the impaired action of insulin in peripheral tissues, administration of exogenous insulin does not respond (Basic postoperative metabolism and clinical practice, Shinko Trading Medical Books) . That is, in the early postoperative period, hyperglycemia is likely to occur, and the amount of administered energy is limited.
The main object of the present invention is to provide a vitamin-deficient patient before and after surgery, a diabetic patient, or an elderly person, who has a sufficient amount of vitamins even if the required energy dose is as small as 1/5 to 1/10. It is to provide a nutritional composition that can be replenished in quantity.
Another object of the present invention is to increase the body's vitamin sufficiency and increase the blood glucose level in patients requiring oral or enteral nutritional supplementation, especially in gastrointestinal surgery patients and elderly people who are prone to impaired glucose tolerance. It is an object of the present invention to provide a nutritional composition capable of supplementing nutrients that cannot be taken only with meals, for the purpose of suppressing illness, increasing body weight, and improving serum albumin concentration.
本発明の課題は、以下の手段により解決される。
(1)蛋白質、糖質、脂質を主成分とし、ビタミンならびにミネラルを含有する栄養組成物であって、該栄養組成物100kcalあたり4mg以上のビタミンB1を含有する栄養組成物。
(2)ビタミンB1含有量が該栄養組成物100kcalあたり11mg以下である上記(1)に記載の栄養組成物。
(3)前記栄養組成物100kcalあたり0.1〜12mgのビタミンB2と0.12〜16mgのビタミンB6を含有する上記(1)または(2)に記載の栄養組成物。
(4)前記栄養組成物100kcalあたり0.13〜24μgのビタミンB12と6〜1000mgのビタミンCと10〜1000μgの葉酸を含有する上記(1)〜(3)のいずれかに記載の栄養組成物。
(5)前記栄養組成物100kcalあたりビタミンを次の割合で含有する上記(1)〜(4)のいずれかに記載の栄養組成物。
ビタミンK 120〜2000μg
ニコチン酸アミド 1〜30mg
パントテン酸 0.3〜50mg
ビタミンA 120〜5000IU
ビタミンD 10〜2000IU
ビタミンE 0.6〜600IU
(6)エネルギー0.5〜2.0kcal/mL、好ましくは1.0〜1.6kcal/mLである上記(1)〜(5)のいずれかに記載の栄養組成物。
(7)前記栄養組成物の粘度が5〜40mPa・s(25℃)の範囲であることを特徴とする上記(1)〜(6)のいずれかに記載の栄養組成物。
(8)前記栄養組成物のゲル強度が1×102〜1×105N/m2の範囲であることを特徴とする上記(1)〜(6)のいずれかに記載の栄養組成物。
The object of the present invention is solved by the following means.
(1) A nutritional composition containing proteins, carbohydrates, and lipids as main components and containing vitamins and minerals, wherein the nutritional composition contains 4 mg or more of vitamin B1 per 100 kcal of the nutritional composition.
(2) The nutritional composition according to the above (1), wherein the vitamin B1 content is 11 mg or less per 100 kcal of the nutritional composition.
(3) The nutritional composition according to the above (1) or (2), comprising 0.1 to 12 mg of vitamin B2 and 0.12 to 16 mg of vitamin B6 per 100 kcal of the nutritional composition.
(4) The nutritional composition according to any one of (1) to (3) above, which contains 0.13 to 24 μg of vitamin B12, 6 to 1000 mg of vitamin C, and 10 to 1000 μg of folic acid per 100 kcal of the nutritional composition.
(5) The nutritional composition according to any one of the above (1) to (4), which contains vitamins in the following proportions per 100 kcal of the nutritional composition.
Vitamin K 120-2000μg
Nicotinamide 1-30mg
Pantothenic acid 0.3-50mg
Vitamin A 120-5000IU
Vitamin D 10-2000 IU
Vitamin E 0.6-600IU
(6) The nutritional composition according to any one of the above (1) to (5), which has an energy of 0.5 to 2.0 kcal / mL, preferably 1.0 to 1.6 kcal / mL.
(7) The nutritional composition according to any one of (1) to (6) above, wherein the viscosity of the nutritional composition is in a range of 5 to 40 mPa · s (25 ° C.).
(8) The nutritional composition according to any one of the above (1) to (6), wherein the nutritional composition has a gel strength in a range of 1 × 10 2 to 1 × 10 5 N / m 2 . .
本発明は、蛋白質、糖質、脂質を主成分とし、ビタミンならびにミネラルを含有する栄養組成物であって、該栄養組成物100kcalあたり4mg以上のビタミンB1を含有する栄養組成物であるので、血中ビタミンB1濃度を高値に維持することが可能であり、さらに血糖値の上昇を緩やかにできるものであるので、経口あるいは経腸的な栄養補給を必要とする患者、中でも耐糖能異常に陥りやすい消化器外科手術患者や高齢者に対し、体内ビタミン充足率を上げ、血糖値の上昇を緩やかにすることにより、投与エネルギーを制限することなく栄養補給が可能な栄養組成物を提供することができ、また、潜在的なビタミン欠乏状態にある外科手術前後の患者や糖尿病患者、あるいは高齢者において、必要エネルギー投与量の1/5〜1/10量と少ない場合でも、ビタミンが十分量補給可能な栄養組成物を提供することができる。 The present invention is a nutritional composition containing proteins, carbohydrates, and lipids as main components and containing vitamins and minerals. It can maintain high levels of middle vitamin B1 and can moderately increase blood sugar, so patients who need oral or enteral nutrition, especially those who have impaired glucose tolerance It is possible to provide a nutritional composition that can provide nutritional support to gastrointestinal surgery patients and the elderly by increasing the body's vitamin sufficiency rate and slowing the increase in blood sugar level without limiting the administration energy. In patients with potentially vitamin deficient pre- and post-surgical patients, diabetics, and the elderly, even small doses of 1/5 to 1/10 of the required energy Min can provide a sufficient amount of replenishing nutritional composition.
本発明者らは、上記課題を解決すべく鋭意検討した結果、従来の栄養組成物等に含まれるビタミンB1はエネルギー100kcalあたり0.88mgが最大であったが、1mg/100kcal配合しても本発明が想定する用途には適していないことを知見した。さらに検討を進めた結果、栄養組成物中のビタミンB1配合量を4mg/100kcal以上とすると、血中ビタミンB1濃度を高値に維持することが可能であり、さらに血糖値上昇の抑制、体重増加、血清アルブミン濃度上昇ができるという新たな知見を得て、本発明を完成するに至った。
また、高齢者ではビタミンB1保持能力が低下している可能性があり、良好なB1栄養状態を維持するためには継続的な補給が必要であることから、栄養組成物にB1を配合することは目的に適合する。
このビタミンB1は、水溶性ビタミンであり、過剰摂取しても尿中にすみやかに排出されるため、上記観点からはビタミンB1配合量に上限は設定されるものではないが、ビタミンB1には特有の臭いがあり、組成設定上マスキングが十分に行えない場合など、栄養組成物としての製剤上の理由で過剰配合が好ましくないことがある。また、栄養組成物を摂取した患者の体臭としてビタミンB1臭がすることがあり、これを不快に感じる場合もあり、QOLの観点から過剰配合が好ましくないことがある。さらに、患者に利用されることなく排出されてしまう分のビタミンB1を配合することは経済上好ましくなく、これらの点から上限は11mg/100kcalとすることが好ましい。
The present inventors have conducted intensive studies to solve the above problems, and found that the maximum amount of vitamin B1 contained in conventional nutritional compositions and the like was 0.88 mg per 100 kcal of energy. Was found to be unsuitable for the intended use. As a result of further study, when the vitamin B1 content in the nutritional composition is 4 mg / 100 kcal or more, it is possible to maintain the blood vitamin B1 concentration at a high value, and further suppress the increase in blood sugar level, increase the weight, The present inventors have obtained a new finding that the serum albumin concentration can be increased, and have completed the present invention.
In addition, vitamin B1 holding capacity may be reduced in elderly people, and continuous supplementation is necessary to maintain good B1 nutritional status. Fits the purpose.
Since this vitamin B1 is a water-soluble vitamin and is rapidly excreted in urine even if it is ingested excessively, the upper limit is not set for the amount of vitamin B1 from the above viewpoint, but it is unique to vitamin B1. For example, when the composition is set so that masking cannot be performed sufficiently, excessive blending may not be preferable for reasons of formulation as a nutritional composition. Further, the body odor of the patient who has taken the nutritional composition may have a vitamin B1 odor, which may be unpleasant, and an excessive combination may not be preferable from the viewpoint of QOL. Furthermore, it is not economically preferable to mix vitamin B1 that is excreted without being used by the patient, and from these points, the upper limit is preferably 11 mg / 100 kcal.
本発明の栄養組成物は、流動食など液状形態では、蛋白質、糖質、脂質、ビタミンならびにミネラルを含有しており、エネルギーが0.5〜2.0kcal/mL、好適範囲は1.0〜1.6kcal/mLである。投与経路に関しては、チューブによる経鼻胃管、経鼻腸管、胃ろう、腸ろうが考えられる。粘度は5〜40mPa・S・25℃、好適範囲は10〜30mPa・S・25℃であり、チューブにおける良好な流動性を有しているものが好ましい。また、ゲル状の栄養組成物では、蛋白質、糖質、脂質、ビタミン、ミネラルならびにゲル化剤を含有しており、エネルギーが0.5〜2.5kcal/mL、好適範囲は1.0〜1.6kcal/mLである。ゲル強度は1×102〜1×105N/m2、好適範囲は5×102〜5×104N/m2であり、経口摂取した場合に良好な喉越しを有しているものが好ましい。 The nutritional composition of the present invention, in a liquid form such as a liquid food, contains proteins, carbohydrates, lipids, vitamins and minerals, and has an energy of 0.5 to 2.0 kcal / mL, with a preferred range of 1.0 to 1.6 kcal / mL. is there. Regarding the administration route, a nasogastric tube, a nasal intestinal tube, a gastric fistula, and an intestinal fistula using a tube can be considered. The viscosity is 5 to 40 mPa · S · 25 ° C., the preferred range is 10 to 30 mPa · S · 25 ° C., and a tube having good fluidity is preferable. In addition, the gel-like nutritional composition contains proteins, carbohydrates, lipids, vitamins, minerals and a gelling agent, and has an energy of 0.5 to 2.5 kcal / mL, and a preferred range of 1.0 to 1.6 kcal / mL. . The gel strength is 1 × 10 2 to 1 × 10 5 N / m 2 , and the preferred range is 5 × 10 2 to 5 × 10 4 N / m 2 , and it has a good throat when taken orally. Are preferred.
蛋白質としては、動物性あるいは植物性蛋白質、これらの蛋白質加水分解物またはアミノ酸等が挙げられる。蛋白質の配合量は、栄養組成物100kcalあたり3〜5gが適当であり、これにより充分な蛋白質を摂取できる。
糖質としては、澱粉、デキストリン、乳糖、ショ糖、グルコース、フルクトース、マルトース、粉飴等が挙げられる。糖質の配合量としては、栄養組成物100kcalあたり10〜18gが適当であり、糖質のエネルギー比としては、40〜70%が好ましい。
脂質としては、大豆油、なたね油、コーン油、サフラワー油、キャノーラ油、ココヤシ油、ヒマワリ油、オリーブ油、シソ油、エゴマ油等の植物性油脂、牛脂、ラード等の動物性油脂、魚油、MCT油等が挙げられる。脂肪の配合量としては、栄養組成物100kcalあたり1〜4.5gが適当であり、脂肪のエネルギー比としては10〜40%が好ましい。
ミネラルとしては、ナトリウム、カルシウム、カリウム、マグネシウム、鉄、リン等が挙げられ、これら複数をできる限り組み合わせて配合するのが好ましい。ミネラルの配合量としては、栄養組成物100kcalあたり、下記の範囲が適当である。
ナトリウム 0〜400mg、好ましくは25〜200mg
カルシウム 0〜2500mg、好ましくは25〜80mg
鉄 0〜40mg、好ましくは0.5〜1.5mg
リン 0〜4000mg、好ましくは25〜65mg
マグネシウム 0〜650mg、好ましくは7〜45mg
カリウム 0〜2000mg、好ましくは25〜75mg
銅 0〜18mg、好ましくは0.1〜1mg
マンガン 0〜8mg、好ましくは0.1〜0.5mg
亜鉛 0〜30mg、好ましくは0.1〜1.5mg
Examples of proteins include animal or plant proteins, hydrolysates of these proteins or amino acids. An appropriate amount of protein is 3 to 5 g per 100 kcal of the nutritional composition, so that sufficient protein can be ingested.
Examples of the carbohydrate include starch, dextrin, lactose, sucrose, glucose, fructose, maltose, powdered candy and the like. An appropriate amount of sugar is 10 to 18 g per 100 kcal of the nutritional composition, and an energy ratio of sugar is preferably 40 to 70%.
As lipids, vegetable oils such as soybean oil, rapeseed oil, corn oil, safflower oil, canola oil, coconut oil, sunflower oil, olive oil, perilla oil, sesame oil, animal oils such as beef tallow, lard, fish oil, MCT Oil and the like. The amount of fat is suitably 1 to 4.5 g per 100 kcal of the nutritional composition, and the energy ratio of fat is preferably 10 to 40%.
Examples of the mineral include sodium, calcium, potassium, magnesium, iron, phosphorus and the like, and it is preferable to mix these as much as possible. The following ranges are appropriate for the amount of the mineral to be added per 100 kcal of the nutritional composition.
Sodium 0-400mg, preferably 25-200mg
Calcium 0-2500mg, preferably 25-80mg
Phosphorus 0-4000mg, preferably 25-65mg
Magnesium 0-650mg, preferably 7-45mg
Potassium 0-2000mg, preferably 25-75mg
Copper 0-18mg, preferably 0.1-1mg
Manganese 0-8 mg, preferably 0.1-0.5 mg
Zinc 0-30mg, preferably 0.1-1.5mg
ゲル化剤としては、ゼラチン、寒天、ペクチン、カラギーナン、グァーガム、ジェランガム、キサンタンガム、タマリンドガム、ローカストビーンガム、アルギン酸ナトリウム等が挙げられる。特性の異なる物を数種混合して使用することが好ましい。ゲル化剤の配合量は、組成物の総重量を基準として、0.2〜1.0重量%が適当である。栄養組成物100kcalあたり、下記の範囲が適当である。
ゼラチン 0.1〜3%、好ましくは0.5〜2%
寒天 0.1〜2.5%、好ましくは0.5〜2%
ペクチン 0.1〜4%、好ましくは2価陽イオンの存在によりゲル化能が増大するため、適時調整が必要。
カラギーナン 0.1〜2.5%、好ましくはミネラルの存在によりゲル化能が増大するため、適時調整が必要。
キサンタン−ガラクトマンナン系(グァーガム、ジェランガム、キサンタンガム、タマリンドガム、ローカストビーンガム、アルギン酸ナトリウム) 0.1〜3%、添加食材、種類、pH、加熱温度により変動があるために好ましくは2%以下が良い。
Examples of the gelling agent include gelatin, agar, pectin, carrageenan, guar gum, gellan gum, xanthan gum, tamarind gum, locust bean gum, sodium alginate and the like. It is preferable to use a mixture of several kinds having different characteristics. The amount of the gelling agent is suitably 0.2 to 1.0% by weight based on the total weight of the composition. The following range is appropriate per 100 kcal of the nutritional composition.
Gelatin 0.1-3%, preferably 0.5-2%
Agar 0.1-2.5%, preferably 0.5-2%
Pectin 0.1 to 4%, preferably gelling ability is increased by the presence of divalent cations, so that appropriate adjustment is required.
Carrageenan 0.1-2.5%, preferably gelation ability is increased by the presence of minerals, so that timely adjustment is required.
Xanthan-galactomannan (guar gum, gellan gum, xanthan gum, tamarind gum, locust bean gum, sodium alginate) 0.1 to 3%, and preferably 2% or less because it varies depending on the added food material, type, pH, and heating temperature.
以下、実施例を挙げて本発明の栄養組成物を具体的に説明するが、本発明は以下の実施例のみに限定されるものではない。
表1に記載した組成に従って蒸留水に溶解後、この溶液を400mLずつ500mL容量のエチレン−酢酸ビニル共重合体製軟質容器(商品名「テルパック」テルモ(株)製)に充填し、密封後、121℃、10分間加熱滅菌した。その後、使用時までは、脱酸素剤とともにガスバリアー包材に入れ密閉包装した。この実施例1の栄養組成物の粘度は、粘度計(東機産業製:TV−30型)で測定したところ16mPa・s(25℃)であった。
Hereinafter, the nutritional composition of the present invention will be specifically described with reference to examples, but the present invention is not limited to only the following examples.
After dissolving in distilled water according to the composition described in Table 1, each 400 mL of the solution was filled into a 500 mL flexible container made of ethylene-vinyl acetate copolymer (trade name "Terpac" manufactured by Terumo Corporation), and sealed. Heat sterilization was performed at 121 ° C. for 10 minutes. After that, it was sealed in a gas barrier packaging material together with a deoxidizer until use. The viscosity of the nutritional composition of Example 1 was 16 mPa · s (25 ° C.) as measured with a viscometer (manufactured by Toki Sangyo: TV-30).
表2に記載した組成に従って蒸留水に溶解後、この溶液を400mLずつ500mL容量のエチレン−酢酸ビニル共重合体製軟質容器(商品名「テルパック」テルモ(株)製)に充填し、密封後、121℃、10分間加熱滅菌した。その後、使用時までは、脱酸素剤とともにガスバリアー包材に入れ密閉包装した。この比較例1の栄養組成物の粘度は、粘度計(東機産業製:TV−30型)で測定したところ15mPa・s(25℃)であった。 After dissolving in distilled water in accordance with the composition described in Table 2, the solution was filled into a 500 mL flexible container made of ethylene-vinyl acetate copolymer (trade name "Terpac" manufactured by Terumo Corporation) in a capacity of 500 mL, sealed, and then sealed. Heat sterilization was performed at 121 ° C. for 10 minutes. After that, it was sealed in a gas barrier packaging material together with a deoxidizer until use. The viscosity of the nutritional composition of Comparative Example 1 was 15 mPa · s (25 ° C.) as measured with a viscometer (manufactured by Toki Sangyo: TV-30).
表3に記載した組成に従って蒸留水に溶解後、この溶液を400mLずつ500mL容量のエチレン−酢酸ビニル共重合体製軟質容器(商品名「テルパック」テルモ(株)製)に充填し、密封後、121℃、10分間加熱滅菌した。その後、使用時までは、脱酸素剤とともにガスバリアー包材に入れ密閉包装した。この比較例2の栄養組成物の粘度は、粘度計(東機産業製:TV−30型)で測定したところ13mPa・s(25℃)であった。 After dissolving in distilled water in accordance with the composition described in Table 3, the solution was filled into flexible containers made of ethylene-vinyl acetate copolymer (trade name “Terpac” manufactured by Terumo Corporation) in a volume of 500 mL in a capacity of 500 mL, sealed, and then sealed. Heat sterilization was performed at 121 ° C. for 10 minutes. After that, it was sealed in a gas barrier packaging material together with a deoxidizer until use. The viscosity of the nutritional composition of Comparative Example 2 was 13 mPa · s (25 ° C.) as measured with a viscometer (manufactured by Toki Sangyo Co., Ltd., TV-30 type).
実施例1、比較例1、2で調製した栄養組成物を用いて、血中ビタミンB1濃度と血糖値に関する動物実験を行った。6週齢、体重180〜200gのSD系雄性ラットを用いて一夜絶食後に採血を行い、血中ビタミンB1濃度ならびに血糖値を測定した(pre値)。例数は実施例1、比較例1、2ともに5例とした。これらのラットのトライツ靱帯より肛門側5cmと回盲部より口側10cmを残し小腸の70%切除して消化器外科手術モデルとした後、胃内にカテーテルを留置した。カテーテルより各栄養組成物を無拘束下に270kcal/kg/dayで7日間持続投与した。投与終了後、下大動脈より採血して血中ビタミンB1濃度ならびに血糖値を測定した(post値)。
血中ビタミンB1濃度ならびに血糖値の結果を図1、2に示した。実施例1の栄養組成物を投与した群の血中ビタミンB1濃度はpre値の328ng/mLに比べてpost値は387ng/mLと上昇したが、比較例1の栄養組成物を投与した群はpre値の337ng/mLに比べて、post値は238ng/mLと低下した。また、比較例2の栄養組成物を投与した群はpre値の341ng/mLに比べて、post値は267ng/mLと低下した。
血糖値のpost値は、実施例1では85.9mg/dLと比較例1の98.3mg/dLあるいは比較例2の96.3mg/dLよりも低値を示した。
従って、ビタミンB1配合量を高くした実施例1の栄養組成物は、栄養素の消化吸収率の低下した消化器外科手術後にも血中ビタミンB1濃度を高値に維持し、さらに、血糖値を上昇させることなく栄養補給が可能であった。一方、ビタミンB1配合量の低い比較例1あるいは2の栄養組成物は、血中ビタミンB1濃度の低下が認められ、血糖値も高くなる傾向にあった。
Using the nutritional compositions prepared in Example 1 and Comparative Examples 1 and 2, animal experiments on blood vitamin B1 concentration and blood glucose level were performed. Blood was collected from 6-week-old, SD male rats weighing 180 to 200 g after overnight fasting, and the blood vitamin B1 concentration and blood glucose level were measured (pre value). The number of examples was set to 5 in both Example 1 and Comparative Examples 1 and 2. 70% of the small intestine was excised except for 5 cm anally from the ligament of Treitz and 10 cm from the ileocecal portion of these rats to make a gastrointestinal surgery model, and a catheter was placed in the stomach. Each nutrient composition was continuously administered from a catheter at 270 kcal / kg / day for 7 days without restraint. After the administration, blood was collected from the inferior aorta to measure the blood vitamin B1 concentration and blood glucose level (post value).
The results of blood vitamin B1 concentration and blood glucose level are shown in FIGS. In the group to which the nutritional composition of Example 1 was administered, the blood vitamin B1 concentration increased to a post value of 387 ng / mL as compared to the pre value of 328 ng / mL, but the group to which the nutritional composition of Comparative Example 1 was administered was: The post value decreased to 238 ng / mL compared to the pre value of 337 ng / mL. In the group to which the nutritional composition of Comparative Example 2 was administered, the post value was reduced to 267 ng / mL, compared to the pre value of 341 ng / mL.
The blood glucose post value was 85.9 mg / dL in Example 1 and lower than 98.3 mg / dL in Comparative Example 1 or 96.3 mg / dL in Comparative Example 2.
Therefore, the nutritional composition of Example 1 in which the amount of vitamin B1 was increased maintained the blood vitamin B1 concentration at a high level even after gastrointestinal surgery in which the digestion and absorption of nutrients decreased, and further increased the blood glucose level. Nutrition was possible without any. On the other hand, in the nutritional composition of Comparative Example 1 or 2 in which the amount of vitamin B1 was low, a decrease in the blood vitamin B1 concentration was observed, and the blood sugar level tended to increase.
表4に記載した組成に従って蒸留水に溶解後、この溶液を400mLずつ500mL容量のエチレン−酢酸ビニル共重合体製軟質容器(商品名「テルパック」テルモ(株)製)に充填し、密封後、121℃、10分間加熱滅菌した。その後、使用時までは、脱酸素剤とともにガスバリアー包材に入れ密閉包装した。 After dissolving in distilled water according to the composition described in Table 4, the solution was filled into a 500-mL flexible container made of ethylene-vinyl acetate copolymer (trade name "Terpac" manufactured by Terumo Corporation) in a capacity of 500 mL, and sealed. Heat sterilization was performed at 121 ° C. for 10 minutes. After that, it was sealed in a gas barrier packaging material together with a deoxidizer until use.
表5に記載した組成に従って蒸留水に溶解後、この溶液を400mLずつ500mL容量のエチレン−酢酸ビニル共重合体製軟質容器(商品名「テルパック」テルモ(株)製)に充填し、密封後、121℃、10分間加熱滅菌した。その後、使用時までは、脱酸素剤とともにガスバリアー包材に入れ密閉包装した。 After dissolving in distilled water in accordance with the composition described in Table 5, the solution was filled into a 500 mL flexible container made of ethylene-vinyl acetate copolymer (trade name "Terpac" manufactured by Terumo Corporation) in a capacity of 500 mL, and sealed. Heat sterilization was performed at 121 ° C. for 10 minutes. After that, it was sealed in a gas barrier packaging material together with a deoxidizer until use.
表6に記載した組成に従って蒸留水に溶解後、この溶液を400mLずつ500mL容量のエチレン−酢酸ビニル共重合体製軟質容器(商品名「テルパック」テルモ(株)製)に充填し、密封後、121℃、10分間加熱滅菌した。その後、使用時までは、脱酸素剤とともにガスバリアー包材に入れ密閉包装した。この実施例2、比較例3及び4の栄養組成物の粘度は、粘度計(東機産業製:TV−30型)で測定したところ各々15、11、18mPa・s(25℃)であった。 After dissolving in distilled water in accordance with the composition described in Table 6, the solution was filled into 500 mL ethylene-vinyl acetate copolymer flexible containers (trade name "Terpac" manufactured by Terumo Corporation) in a volume of 500 mL, and sealed. Heat sterilization was performed at 121 ° C. for 10 minutes. After that, it was sealed in a gas barrier packaging material together with a deoxidizer until use. The viscosities of the nutritional compositions of Example 2, Comparative Examples 3 and 4 were 15, 11, and 18 mPa · s (25 ° C.), respectively, as measured with a viscometer (manufactured by Toki Sangyo Co., Ltd., TV-30 type). .
実施例2、比較例3、4で調製した栄養組成物を用いて、血中ビタミンB1濃度と血糖値に関する動物実験を行った。10週齢、体重390〜430gのSD系雄性ラットを用いて、一夜絶食後に採血を行い、血中ビタミンB1濃度ならびに血糖値を測定した(pre値)。これらのラットの背部を剃毛し、半田ゴテにより体表面積の20%にIII度の熱傷を作製し、熱傷モデルとした。その後、胃内にカテーテルを留置した。カテーテルよりシリンジポンプを用いて、実施例2あるいは比較例3、4の栄養組成物を無拘束下に270kcal/kg/dayで3日間持続投与した。例数は実施例2、比較例3、4ともに5例とした。投与開始1日後から投与終了まで、毎日、血糖値を測定した。また、投与開始3日後に血中ビタミンB1濃度を測定した。
血中ビタミンB1濃度ならびに血糖値の結果を図3、4に示した。ビタミンB1配合量の低い比較例3あるいは4の栄養組成物を投与した群の血中ビタミンB1濃度は投与開始3日後にはpre値よりも低下した。血糖値は、投与開始1日後にはpre値に比べて上昇し、3日後には比較例3で159mg/dL、比較例4で151mg/dLとなった。これに対し、ビタミンB1配合量の高い実施例2の栄養組成物を投与した群では、投与開始3日後の血中ビタミンB1濃度は比較例3あるいは4と比べて451ng/mLと高値を示し、また投与期間を通して血糖値は比較例3あるいは4よりも低値で推移した。
従って、ビタミンB1配合量の高い実施例2の栄養組成物は、インシュリン抵抗性により高血糖を起こすと考えられている熱傷後にも、血中ビタミンB1を高値に維持し、血糖値の上昇を抑制できると考えられた。
Using the nutritional compositions prepared in Example 2 and Comparative Examples 3 and 4, animal experiments on blood vitamin B1 concentration and blood glucose level were performed. Blood was collected from 10-week-old male SD rats weighing 390-430 g after fasting overnight, and the blood vitamin B1 concentration and blood glucose level were measured (pre value). The backs of these rats were shaved, and a III-degree burn was made on 20% of the body surface area using a soldering iron, and used as a burn model. Thereafter, the catheter was placed in the stomach. The nutritional composition of Example 2 or Comparative Examples 3 and 4 was continuously administered at 270 kcal / kg / day without restriction using a syringe pump from a catheter for 3 days. The number of cases was 5 in each of Example 2, Comparative Examples 3 and 4. From one day after the start of the administration to the end of the administration, the blood glucose level was measured every day. Three days after the start of the administration, the blood vitamin B1 concentration was measured.
The results of blood vitamin B1 concentration and blood glucose level are shown in FIGS. In the group to which the nutritional composition of Comparative Example 3 or 4 in which the amount of vitamin B1 was low was administered, the vitamin B1 concentration in blood was lower than the
Therefore, the nutritional composition of Example 2 having a high vitamin B1 content maintains blood vitamin B1 at a high level even after a burn which is considered to cause hyperglycemia due to insulin resistance, and suppresses an increase in blood glucose level. I thought it could be done.
表7に記載した組成に従って蒸留水に溶解後、この溶液を400mLずつ500mL容量のエチレン−酢酸ビニル共重合体製軟質容器(商品名「テルパック」テルモ(株)製)に充填し、密封後、121℃、10分間加熱滅菌した。その後、使用時までは、脱酸素剤とともにガスバリアー包材に入れ密閉包装した。 After dissolving in distilled water in accordance with the composition described in Table 7, the solution was filled into flexible containers made of ethylene-vinyl acetate copolymer (trade name “Terpac” manufactured by Terumo Corporation) in a capacity of 500 mL in a capacity of 500 mL, and sealed. Heat sterilization was performed at 121 ° C. for 10 minutes. After that, it was sealed in a gas barrier packaging material together with a deoxidizer until use.
表8に記載した組成に従って蒸留水に溶解後、この溶液を400mLずつ500mL容量のエチレン−酢酸ビニル共重合体製軟質容器(商品名「テルパック」テルモ(株)製)に充填し、密封後、121℃、10分間加熱滅菌した。その後、使用時までは、脱酸素剤とともにガスバリアー包材に入れ密閉包装した。 After dissolving in distilled water in accordance with the composition described in Table 8, the solution was filled into a flexible container made of ethylene-vinyl acetate copolymer (trade name "Terpac" manufactured by Terumo Corporation) in a volume of 500 mL in a capacity of 500 mL, and sealed. Heat sterilization was performed at 121 ° C. for 10 minutes. After that, it was sealed in a gas barrier packaging material together with a deoxidizer until use.
表9に記載した組成に従って蒸留水に溶解後、この溶液を400mLずつ500mL容量のエチレン−酢酸ビニル共重合体製軟質容器(商品名「テルパック」テルモ(株)製)に充填し、密封後、121℃、10分間加熱滅菌した。その後、使用時までは、脱酸素剤とともにガスバリアー包材に入れ密閉包装した。この実施例3、比較例5及び6の栄養組成物の粘度は、粘度計(東機産業製:TV−30型)で測定したところ各々14、15、12mPa・s(25℃)であった。 After dissolving in distilled water according to the composition described in Table 9, the solution was filled into 500 mL ethylene-vinyl acetate copolymer flexible containers (trade name “Terpac” manufactured by Terumo Corporation) in a volume of 500 mL, and sealed. Heat sterilization was performed at 121 ° C. for 10 minutes. After that, it was sealed in a gas barrier packaging material together with a deoxidizer until use. The viscosities of the nutritional compositions of Example 3, Comparative Examples 5 and 6 were 14, 15, and 12 mPa · s (25 ° C.), respectively, as measured with a viscometer (manufactured by Toki Sangyo Co., Ltd., TV-30 type). .
実施例3、比較例5、6で調整した栄養組成物を用いて、血中ビタミンB1濃度と耐糖能に関する動物実験を行った。7カ月齢、体重10kg前後のビーグル犬を用いて14日間、市販固形飼料5g/kg/dayの制限給餌を行い、低栄養状態とした。その後、市販固形飼料5g/kg/dayの制限給餌を継続しながら、実施例3あるいは比較例5、6の栄養組成物200kcal/head/dayを14日間経口摂取させた。制限給餌前後と栄養組成物投与後に血中ビタミンB1濃度の測定を行った。例数は実施例3、比較例5、6ともに5例とした。14日間の栄養組成物投与終了後、1昼夜絶食し、2g/kgのグルコース経口負荷により耐糖能試験を行った。
血中ビタミンB1濃度の結果を表10に示した。制限給餌により血中ビタミンB1の低下が認められたが、実施例3の栄養組成物を投与した群では制限給餌前値よりも高値を示した。これに対して、比較例5、6の栄養組成物を投与した群では、血中ビタミンB1濃度は低値であった。
Using the nutritional compositions prepared in Example 3 and Comparative Examples 5 and 6, animal experiments on blood vitamin B1 concentration and glucose tolerance were performed. A 7-month-old beagle dog weighing about 10 kg was fed with a restricted feed of a commercial solid feed of 5 g / kg / day for 14 days to reduce malnutrition. Thereafter, 200 kcal / head / day of the nutritional composition of Example 3 or Comparative Examples 5 and 6 was orally ingested for 14 days while continuing to limit the feed to 5 g / kg / day on the commercial solid feed. Blood vitamin B1 concentration was measured before and after restricted feeding and after administration of the nutritional composition. The number of examples was set to 5 in Example 3 and Comparative Examples 5 and 6. After the administration of the nutritional composition for 14 days, the animals were fasted all day and night, and a glucose tolerance test was performed by oral glucose load of 2 g / kg.
Table 10 shows the results of the blood vitamin B1 concentration. Blood vitamin B1 was reduced by restricted feeding, but in the group to which the nutritional composition of Example 3 was administered, the value was higher than the value before restricted feeding. On the other hand, in the groups to which the nutritional compositions of Comparative Examples 5 and 6 were administered, the blood vitamin B1 concentration was low.
グルコース経口負荷による耐糖能試験の結果を図5に示した。実施例3の栄養組成物を投与した群では、比較例5、6の栄養組成物を投与した群に比べて血糖値は常に低値で推移した。
従って、補食として実施例3の栄養組成物を摂取した場合にも、血中ビタミンB1濃度を高値に維持し、血糖値の上昇を抑制できると考えられた。
FIG. 5 shows the results of a glucose tolerance test using an oral glucose load. In the group to which the nutritional composition of Example 3 was administered, the blood sugar level was always lower than in the groups to which the nutritional composition of Comparative Examples 5 and 6 was administered.
Therefore, even when the nutritional composition of Example 3 was ingested as a dietary supplement, it was considered that the blood vitamin B1 concentration could be maintained at a high level, and an increase in blood sugar level could be suppressed.
表11に記載した組成に従って蒸留水に溶解後、151℃、2秒間直接蒸気滅菌した後、この溶液を125mLずつ125mL容量のポリエチレン−紙−アルミ箔ラミネ−ト紙質容器(商品名「テトラブリック(登録商標)アセプティック」テトラ(株)製)に無菌充填密封包装した。この実施例4の栄養組成物の粘度は、粘度計(東機産業製:TV−30型)で測定したところ11mPa・s(25℃)であった。 After dissolving in distilled water in accordance with the composition described in Table 11 and then directly steam sterilizing at 151 ° C. for 2 seconds, the solution was placed in polyethylene-paper-aluminum foil laminated paper containers (trade name “Tetrabrick (trade name)) in 125 mL volumes of 125 mL each. (Registered trademark) Aseptic "manufactured by Tetra Corporation. The viscosity of the nutritional composition of Example 4 was 11 mPa · s (25 ° C.) as measured with a viscometer (manufactured by Toki Sangyo: TV-30).
実施例4で調整した栄養組成物を用いて、血中ビタミンB1濃度と栄養改善に関する臨床評価を行った。老人保健施設入所後期高齢者(平均87.8歳)10例に1本/日を8週間にわたり飲用したときの栄養改善を評価した。投与前後の血中ビタミンB1濃度、血清アルブミン濃度、体重の測定を行った。
血中ビタミンB1濃度の結果を図6に示した。老人保健施設入所後期高齢者は、6例/10例(60%)で血中ビタミンB1濃度が基準下限値以下(28ng/ml)であったが、実施例4の栄養組成物の投与4週後では全例が基準下限値以上となった。また、血清アルブミン値が3.5mg/dl以下の場合、低栄養状態であるといわれている。血清アルブミン値の結果を図7に示した。低栄養状態が認められた3例/10例(30%)については、実施例4の栄養組成物の投与により血清アルブミンの増加が認められた。体重の結果を図8に示した。実施例4の栄養組成物の投与により体重の増加が認められた。
Using the nutritional composition prepared in Example 4, clinical evaluation was conducted on the blood vitamin B1 concentration and nutritional improvement. Nutrition improvement was evaluated for 10 elderly people (average 87.8 years old) who entered the geriatric health facility after drinking 1 bottle / day for 8 weeks. Blood vitamin B1 concentration, serum albumin concentration, and body weight before and after administration were measured.
The results of the blood vitamin B1 concentration are shown in FIG. In the late-elderly patients entering the geriatric health facility, the blood vitamin B1 concentration was lower than the lower reference limit (28 ng / ml) in 6/10 (60%), but 4 weeks of administration of the nutritional composition of Example 4. Later, all cases exceeded the reference lower limit. When the serum albumin value is 3.5 mg / dl or less, it is said that the patient is undernourished. The results of the serum albumin level are shown in FIG. Regarding 3/10 cases (30%) in which undernutrition was observed, administration of the nutritional composition of Example 4 caused an increase in serum albumin. The results of body weight are shown in FIG. An increase in body weight was observed by administration of the nutritional composition of Example 4.
表12に記載した組成に従って蒸留水に溶解後、80℃で完全に溶解する。作製した溶解液を68g容量の耐レトルト容器に充填した後レトルト殺菌を行う。この実施例5の栄養組成物のゲル強度は1×104N/m2(測定機器:クリ−プメ−タ−TPU−2S:(株)山電製)であり、経口摂取した場合に良好な喉越しを有していた。 After dissolving in distilled water according to the composition shown in Table 12, it is completely dissolved at 80 ° C. After filling the prepared solution in a 68 g capacity retort-resistant container, retort sterilization is performed. The gel strength of the nutritional composition of Example 5 was 1 × 10 4 N / m 2 (measurement instrument: Creepmeter-TPU-2S: manufactured by Yamaden Corporation), which was good when taken orally. Had a great throat.
Claims (2)
The nutritional composition according to claim 1, wherein the vitamin B1 content is 11 mg or less per 100 kcal of the nutritional composition.
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| WO2006033349A1 (en) | 2004-09-22 | 2006-03-30 | Ajinomoto Co., Inc. | Total enteral nutritious composition |
| WO2008010472A1 (en) * | 2006-07-18 | 2008-01-24 | Ajinomoto Co., Inc. | Total enteral nutrition composition |
| WO2008032432A1 (en) * | 2006-09-13 | 2008-03-20 | En Otsuka Pharmaceutical Co., Ltd. | Gel type enteric nutrient |
| WO2009087987A1 (en) * | 2008-01-10 | 2009-07-16 | Nutri Co., Ltd. | Composition for improving nutritional status, reducing frequency of fever and/or increasing immunocompetence of elderly |
| JPWO2009139167A1 (en) * | 2008-05-15 | 2011-09-15 | 株式会社明治 | Nutritional composition that can adjust the amount of energy, the amount of water and the amount converted to salt |
| WO2012141018A1 (en) * | 2011-04-15 | 2012-10-18 | ライオン株式会社 | Composition, glucose metabolism-improving agent, and method for improving glucose metabolism |
| US9872515B2 (en) | 2009-01-19 | 2018-01-23 | Nutri Co., Ltd. | Low-concentration nutritional composition |
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| WO2012141018A1 (en) * | 2011-04-15 | 2012-10-18 | ライオン株式会社 | Composition, glucose metabolism-improving agent, and method for improving glucose metabolism |
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