JPS6349977B2 - - Google Patents
Info
- Publication number
- JPS6349977B2 JPS6349977B2 JP57186709A JP18670982A JPS6349977B2 JP S6349977 B2 JPS6349977 B2 JP S6349977B2 JP 57186709 A JP57186709 A JP 57186709A JP 18670982 A JP18670982 A JP 18670982A JP S6349977 B2 JPS6349977 B2 JP S6349977B2
- Authority
- JP
- Japan
- Prior art keywords
- glucose
- jelly
- starch syrup
- acid
- pectin
- 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.)
- Expired
Links
- 235000000346 sugar Nutrition 0.000 claims description 21
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 20
- 239000008103 glucose Substances 0.000 claims description 20
- 235000015110 jellies Nutrition 0.000 claims description 18
- 239000008274 jelly Substances 0.000 claims description 18
- 229920002472 Starch Polymers 0.000 claims description 17
- 235000019698 starch Nutrition 0.000 claims description 17
- 239000008107 starch Substances 0.000 claims description 17
- 239000006188 syrup Substances 0.000 claims description 17
- 235000020357 syrup Nutrition 0.000 claims description 17
- 235000013305 food Nutrition 0.000 claims description 15
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 150000001720 carbohydrates Chemical class 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 claims description 6
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 claims description 6
- 235000014633 carbohydrates Nutrition 0.000 claims description 6
- 239000001814 pectin Substances 0.000 claims description 6
- 229920001277 pectin Polymers 0.000 claims description 6
- 235000010987 pectin Nutrition 0.000 claims description 6
- 208000007345 glycogen storage disease Diseases 0.000 claims description 4
- 150000007524 organic acids Chemical class 0.000 claims description 4
- 235000009508 confectionery Nutrition 0.000 claims description 3
- -1 organic acid salts Chemical class 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 2
- 235000005985 organic acids Nutrition 0.000 claims description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 239000008280 blood Substances 0.000 description 8
- 210000004369 blood Anatomy 0.000 description 8
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 7
- PYMYPHUHKUWMLA-UHFFFAOYSA-N 2,3,4,5-tetrahydroxypentanal Chemical compound OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 6
- 150000008163 sugars Chemical class 0.000 description 6
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 5
- 235000012054 meals Nutrition 0.000 description 5
- 238000001879 gelation Methods 0.000 description 4
- 239000003349 gelling agent Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 229920002527 Glycogen Polymers 0.000 description 3
- 208000013016 Hypoglycemia Diseases 0.000 description 3
- 229930006000 Sucrose Natural products 0.000 description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 229940096919 glycogen Drugs 0.000 description 3
- 230000002218 hypoglycaemic effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 235000011888 snacks Nutrition 0.000 description 3
- 239000001509 sodium citrate Substances 0.000 description 3
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000005720 sucrose Substances 0.000 description 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 description 2
- 206010010904 Convulsion Diseases 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 230000036461 convulsion Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 210000002784 stomach Anatomy 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 208000028782 Hereditary disease Diseases 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 208000026350 Inborn Genetic disease Diseases 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 208000024556 Mendelian disease Diseases 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 229930003270 Vitamin B Natural products 0.000 description 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000001800 adrenalinergic effect Effects 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 235000010419 agar Nutrition 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 210000002249 digestive system Anatomy 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 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 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 206010019847 hepatosplenomegaly Diseases 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 229960001790 sodium citrate Drugs 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 229940005581 sodium lactate Drugs 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
- 229940074404 sodium succinate Drugs 0.000 description 1
- ZDQYSKICYIVCPN-UHFFFAOYSA-L sodium succinate (anhydrous) Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O ZDQYSKICYIVCPN-UHFFFAOYSA-L 0.000 description 1
- PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 1
- 239000011755 sodium-L-ascorbate Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 235000019156 vitamin B Nutrition 0.000 description 1
- 239000011720 vitamin B Substances 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Landscapes
- Jellies, Jams, And Syrups (AREA)
Description
【発明の詳細な説明】
本発明は糖原病乳幼児の血糖値を維持するため
の食品に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a food for maintaining blood sugar levels in infants with glycogen storage disease.
糖原病とは種々の臓器、組織中に異常に多量の
グリコーゲンを蓄積する疾病をいい、乳幼児に多
い遺伝性の疾患であるとされている。この疾病は
生後間もなく出現するグリコーゲン代謝異常に基
づくもので、体内に多量のグリコーゲンが貯蔵さ
れているにもかかわらず、低血糖、アドレナリン
作用欠如、肝脾腫などを起こすものである。現在
まで、これに対する特殊療法は知られておらず、
低血糖によるけいれん等を引き起こしている患児
に対してはぶどう糖を投与して血糖値を正常に戻
す等の手段が構じられているにすぎない。又、患
児は低血糖となる結果、血糖値を維持さすため食
事回数をふやし、ぶどう糖の補給を続ける必要が
あるが、度々の食事は保護者にとつて大きな負担
となるのみならず、このようにしても食事と食事
の間に血糖値が低下するものである。 Glycogen storage disease is a disease in which an abnormally large amount of glycogen accumulates in various organs and tissues, and is said to be a hereditary disease that is common in infants. This disease is based on abnormalities in glycogen metabolism that appear shortly after birth, and causes hypoglycemia, lack of adrenergic action, hepatosplenomegaly, etc. despite the large amount of glycogen stored in the body. To date, there are no known specific treatments for this.
For children suffering from convulsions due to hypoglycemia, measures such as administering glucose to return blood sugar levels to normal have been devised. In addition, as a result of hypoglycemia, the affected child must increase the number of meals and continue to replenish glucose in order to maintain blood sugar levels, but frequent meals not only place a heavy burden on parents, but also However, blood sugar levels drop between meals.
本発明は上記事情によりなされたもので、少量
のぶどう糖源の補給で食事と食事の間の血糖値の
低下を防止し、しかも患児が食い易い食品を得ん
と研究を進めた結果、患児が乳糖、フラクトー
ス、ガラクトース等の糖類を代謝できないことに
着目し、それらの糖類を排してぶどう糖又はぶど
う糖のみを構成成分とする糖類のみを原料とし、
これをゼリー化して患児が食べ易くすると共に間
食として与えると暫時消化器内にとどまつて徐々
に体内に吸収されぶどう糖を補給さすことにより
解決したのである。 The present invention was made in view of the above circumstances, and as a result of research to prevent the drop in blood sugar levels between meals by supplementing a small amount of glucose source, and to obtain a food that is easy for patients to eat, Focusing on the fact that sugars such as lactose, fructose, and galactose cannot be metabolized, we eliminate these sugars and use only glucose or glucose-based sugars as raw materials.
The problem was solved by making it into a jelly so that it was easier for the patient to eat, and when given as a snack, it remained in the digestive system for a while and was gradually absorbed into the body, replenishing glucose.
以下本発明を詳細説明すると、使用する糖質は
ぶどう糖又はぶどう糖のみを構成成分とする糖質
で、例えば結晶ぶどう糖、精製ぶどう糖、麦芽
糖、麦芽水飴、酸糖化水飴、粉飴等をあげること
ができる。 To explain the present invention in detail below, the carbohydrate used is glucose or a carbohydrate containing only glucose as a constituent, such as crystalline glucose, refined glucose, maltose, malt starch syrup, acid saccharified starch syrup, powdered candy, etc. .
上記糖類は単独使用し、ゲル化剤によりゼリー
状としてもよいが、消化器管での吸収、食べたと
きの食感等を考慮し、ぶどう糖、麦芽糖の如き糖
類と麦芽水飴、酸糖化水飴の如き粘性のある糖類
を適宜混合し、味覚を改良してゼリー化するとよ
い。このとき使用する麦芽水飴は分解率20〜40%
のものが主として使用され、酸糖化水飴はDE15
〜50のものが主として使用されるが、何れも粘性
を有し、ゲル化剤により容易に固化するものを使
用する。又ぶどう糖、麦芽糖の如き糖質と水飴類
の混合割合は、ゼリー食品のゼリー化度、易食
性、甘味度等を考慮して決定するのが良く、通常
後者の割合を多くし前者の割合を少なくする。 The above sugars may be used alone and made into a jelly with a gelling agent, but considering absorption in the gastrointestinal tract and texture when eaten, sugars such as glucose and maltose, malt starch syrup, and acid-saccharified starch syrup are used. It is recommended to mix viscous sugars such as saccharides as appropriate to improve the taste and make a jelly. The malt starch syrup used at this time has a decomposition rate of 20-40%.
Acid-saccharified starch syrup is DE15
-50 is mainly used, but all have viscosity and are easily solidified by gelling agents. The mixing ratio of carbohydrates such as glucose and maltose and starch syrup should be determined by taking into consideration the degree of jelly formation, ease of eating, sweetness, etc. of the jelly food, and usually the ratio of the latter should be increased and the ratio of the former should be determined. Reduce.
上記糖質は加水し、又は加水せず液状でゼリー
化剤を加え、加熱溶解し冷却してゼリー食品とす
るが、ゼリー化剤としてはペクチン、ゼラチン、
寒天、モデイフアイスターチ、アルギン酸塩等の
可食性ゲル化剤が使用され、好ましくはペクチン
で、ハイメトキシルペクチン及びローメトキシル
ペクチンが使用され特に好ましいのはハイメトキ
シルペクチンである。 The above-mentioned carbohydrates are made into jelly foods by adding hydration or non-hydration in liquid form, adding a jelly-forming agent, heating and dissolving, and cooling.
Edible gelling agents such as agar, modified starch, alginates are used, preferably pectin, high methoxyl pectin and low methoxyl pectin, with high methoxyl pectin being particularly preferred.
通常ハイメトキシルペクチンを使用し、菓子、
食品類を製造する場合は、蔗糖と酸の存在下でPH
3.5以下としゲル化するものであるが、本発明で
はぶどう糖や水飴等の存在下でゲル化さす関係上
必ずしもPH3.5以下とする必要はない。然し、で
きるだけ濃度を高くしてゲル化さす関係上得られ
たゼリー食品のゼリー強度は蔗糖のそれにくらべ
て弾性は劣るが剛性の大なるものとなる。又前記
ゲル化は水飴量が多くなるにつれ広範なPH域でゼ
リー食品とすることができる利点はあるが低糖濃
度では劣化するので実用的に前記糖質にゲル化剤
を全体の0.1〜3%程度溶解し、これを濃縮して
80%以上の全糖濃度となし、これに酸類を加えて
ゲル化するとよい。 Confectionery, usually using high methoxyl pectin,
When manufacturing food products, the pH should be adjusted in the presence of sucrose and acid.
Although gelation occurs when the pH is 3.5 or less, in the present invention, it is not necessarily necessary to set the pH to 3.5 or less because gelation occurs in the presence of glucose, starch syrup, etc. However, because gelation is achieved by increasing the concentration as much as possible, the jelly strength of the obtained jelly food is inferior to that of sucrose, but has greater rigidity, although its elasticity is inferior. In addition, as the amount of starch syrup increases, gelation has the advantage that jelly food can be made in a wide pH range, but it deteriorates at low sugar concentrations, so it is practical to add gelling agents to the sugar at 0.1 to 3% of the total sugar content. Dissolve it to a certain extent and concentrate it.
It is best to maintain a total sugar concentration of 80% or more and add acids to gel it.
添加する酸類としては、クエン酸、乳酸、酒石
酸の如き有機酸が望ましく、これらの酸に付加し
てクエン酸ナトリウム、コハク酸ナトリウム、乳
酸ナトリウム等の緩衝能を有する塩類を添加し、
PHの調整を行うとよい。又、ローメトキシルペク
チンを使用する場合には塩化カルシウム、硫酸カ
ルシウムを添加しても良い。又、製造中に所望の
工程でビタミン類を添加し強化をはかつてもよい
ものである。 The acids to be added are preferably organic acids such as citric acid, lactic acid, and tartaric acid, and salts having buffering capacity such as sodium citrate, sodium succinate, and sodium lactate are added to these acids.
It is a good idea to adjust the pH. Furthermore, when using rhomethoxyl pectin, calcium chloride or calcium sulfate may be added. It is also a good idea to add vitamins at a desired step during production to fortify the product.
次に本発明の好ましい配合例を第1表に示す。 Next, Table 1 shows preferred formulation examples of the present invention.
第 1 表
配 合 物 %
ぶどう糖又は麦芽糖 10〜20
麦芽水飴又は酸糖化水飴 50〜65
ハイメトキシルペクチン 0.2〜0.4
有機酸 0.5〜1.0
有機酸塩 0.3〜0.7
水 15〜20
上記配合物よりゼリー食品を製造するに際して
は、ペクチン、ぶどう糖、麦芽糖を混合し、水を
加え加熱して溶解し、これに有機酸塩を混合し均
一に撹拌する。次いで麦芽水飴、酸糖化水飴を加
熱溶解する。通常このように調製した溶液は糖濃
度50〜80%であり、そのまゝゲル化すると軟質と
なつて本発明の目的とするゼリー食品とはならな
いので、これを糖濃度80%以上に減圧濃縮する。
濃縮が完了すると熱い中に少量の水に溶解した有
機酸を加え撹拌し、所望の形状の型に流し込んで
冷却する。冷却後取り出すと固化しゼリー食品が
得られる。 Table 1 Compounds % Glucose or maltose 10-20 Malt starch syrup or acid saccharified starch syrup 50-65 High methoxyl pectin 0.2-0.4 Organic acid 0.5-1.0 Organic acid salt 0.3-0.7 Water 15-20 Jelly foods are made from the above formulations. When producing it, pectin, glucose, and maltose are mixed, water is added and heated to dissolve, and an organic acid salt is mixed with this and stirred uniformly. Next, malt starch syrup and acid-saccharified starch syrup are heated and dissolved. Usually, the solution prepared in this way has a sugar concentration of 50 to 80%, and if it gels as it is, it will become soft and will not become the jelly food that is the object of the present invention, so it is concentrated under reduced pressure to a sugar concentration of 80% or more. do.
When the concentration is complete, a small amount of organic acid dissolved in water is added to the hot mixture, stirred, poured into a mold of the desired shape, and cooled. When taken out after cooling, it solidifies and a jelly food is obtained.
上記ゼリー食品は乳幼児でも食べ易く、通常の
蔗糖を原料とするゼリーにくらべ剛性があり、胃
の中に入つても直に糖質を放出することはないの
で、徐々に溶解し体内に吸収せられる。 The above jelly foods are easy to eat even for infants and young children, and they are more rigid than regular jelly made from sucrose, and do not release carbohydrates directly even when they enter the stomach, so they are gradually dissolved and absorbed into the body. It will be done.
本発明の製品は患児の間食に供し血糖低下を防
止するもので、通常患児体重1Kg当り5〜10gを
食間にあたえるとよい。このように少量であるか
ら胃への負担もかけず、必要なぶどう糖を補給で
きるので糖原病治療用食品として極めて有効で、
常用により血糖値の異常低下を防止し、けいれん
等を起こさない。 The product of the present invention is used as snacks for infants to prevent blood sugar drop, and it is usually advisable to give 5 to 10 g per 1 kg of infant's body weight between meals. Because it is in such a small amount, it does not put a burden on the stomach and can supply the necessary glucose, making it extremely effective as a food for treating glycogen storage diseases.
Regular use prevents abnormal drops in blood sugar levels and does not cause convulsions.
以下実施例により本発明を説明する。 The present invention will be explained below with reference to Examples.
実施例 1 原料の配合割合は下表に示す割合とした。Example 1 The mixing ratio of raw materials was as shown in the table below.
原 料
水 136.16g
ぶどう糖 70.50g
ペクチン(ハイメトキシルペクチン) 7.10g
クエン酸ナトリウム 1.33g
麦芽水飴 282.04g
ビタミンE 20.00mg
ビタミンB1塩酸塩 1.50mg
L−アスコルビン酸ナトリウム 335.00mg
クエン酸 2.50g
上記配合中ペクチンはぶどう糖と混合した後、
130gの水を加え90〜100℃に加熱溶解した。この
溶液にクエン酸ナトリウムを全量加え、よく混合
し、溶解後麦芽水飴を全量添加し混合した。混合
溶液は減圧濃縮器に入れ固形分濃度が約75%にな
るまで濃縮し、別にビタミン類を70%エタノール
の少量に溶解したものを添加し、更に濃縮を続
け、固形分濃度80%内外の濃縮時にクエン酸全量
を6.16gの水に溶解して添加し、更に濃縮を続け
て最終固形分濃度82%とした。次いで、200×160
×30mmの型に流し込み放冷して5時間後取り出し
約35×15×1mmの大きさに切断し、1個平均7g
のゼリー食品とした。このゼリー食品は間食とし
て毎回数個食べさせて乳幼児の血糖値低下が予防
できた。 Raw water 136.16g Glucose 70.50g Pectin (high methoxyl pectin) 7.10g Sodium citrate 1.33g Malt starch syrup 282.04g Vitamin E 20.00mg Vitamin B monohydrochloride 1.50mg Sodium L - ascorbate 335.00mg Citric acid 2.50g In the above combination After pectin is mixed with glucose,
130g of water was added and dissolved by heating at 90-100°C. The entire amount of sodium citrate was added to this solution and mixed well. After dissolving, the entire amount of malt starch syrup was added and mixed. The mixed solution is placed in a vacuum concentrator and concentrated until the solid content concentration is approximately 75%. Vitamins dissolved in a small amount of 70% ethanol are added separately, and concentration is continued until the solid content concentration is around 80%. During concentration, the entire amount of citric acid was dissolved in 6.16 g of water and added, and concentration was continued to give a final solid concentration of 82%. Then 200×160
Pour into a 30mm mold, leave to cool, take out after 5 hours, cut into pieces approximately 35x15x1mm, each weighing an average of 7g.
It was made into a jelly food. This jelly food was able to prevent a drop in blood sugar levels in infants by allowing them to eat several pieces each time as a snack.
Claims (1)
水飴、酸糖化水飴、粉飴等のぶどう糖のみから構
成された糖質の1種又は2種以上を50〜65%、ペ
クチン0.2〜0.4%、有機酸0.5〜1.0%、有機酸塩
0.3〜0.7%、水15〜20%からなる配合物を80%以
上の糖濃度に濃縮し、ついでゼリー化してなる糖
原病治療用ゼリー食品。1 10-20% glucose and/or maltose, 50-65% one or more carbohydrates composed only of glucose such as malt starch syrup, acid saccharified starch syrup, powdered candy, etc., 0.2-0.4% pectin, Organic acids 0.5-1.0%, organic acid salts
A jelly food for treating glycogen storage diseases made by concentrating a compound consisting of 0.3 to 0.7% and 15 to 20% water to a sugar concentration of 80% or more and then turning it into jelly.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57186709A JPS5978653A (en) | 1982-10-26 | 1982-10-26 | Jelly food for treating glycogenosis |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57186709A JPS5978653A (en) | 1982-10-26 | 1982-10-26 | Jelly food for treating glycogenosis |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5978653A JPS5978653A (en) | 1984-05-07 |
JPS6349977B2 true JPS6349977B2 (en) | 1988-10-06 |
Family
ID=16193261
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57186709A Granted JPS5978653A (en) | 1982-10-26 | 1982-10-26 | Jelly food for treating glycogenosis |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5978653A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2937904B2 (en) * | 1995-11-15 | 1999-08-23 | 日本たばこ産業株式会社 | Coated jelly and its manufacturing method |
JPWO2004080469A1 (en) * | 2003-03-11 | 2006-06-08 | アークレイ株式会社 | Supplements for recovery of hypoglycemia symptoms |
-
1982
- 1982-10-26 JP JP57186709A patent/JPS5978653A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5978653A (en) | 1984-05-07 |
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