WO2017078024A1 - 乳酸カルシウムによる糖アルコール糖衣の糖衣形成促進方法 - Google Patents
乳酸カルシウムによる糖アルコール糖衣の糖衣形成促進方法 Download PDFInfo
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- WO2017078024A1 WO2017078024A1 PCT/JP2016/082473 JP2016082473W WO2017078024A1 WO 2017078024 A1 WO2017078024 A1 WO 2017078024A1 JP 2016082473 W JP2016082473 W JP 2016082473W WO 2017078024 A1 WO2017078024 A1 WO 2017078024A1
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- sugar
- coating
- sugar coating
- calcium lactate
- alcohol
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2806—Coating materials
- A61K9/282—Organic compounds, e.g. fats
- A61K9/2826—Sugars or sugar alcohols, e.g. sucrose; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/12—Carboxylic acids; Salts or anhydrides thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2893—Tablet coating processes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
Definitions
- the present invention relates to shortening the sugar coating time of a sugar alcohol sugar coating using calcium lactate. More specifically, the present invention relates to shortening of sugar coating formation time based on crystallization promotion of sugar alcohol by calcium lactate.
- sugar coating with maltitol is known as a typical sugarless sugar coating, and is widely practiced as a sugar coating to replace sucrose because of its excellent moisture absorption stability.
- Maltitol is a sugar alcohol obtained by hydrogenating maltose and reducing its carbonyl group. Maltitol has half the calorie of sucrose and has a sweetness of 80-90%, and its taste is similar to sucrose, so it is widely used as a low calorie sweetener as a substitute for sucrose.
- maltitol takes a longer time to precipitate crystals from a supersaturated solution than sucrose, in hard sugar coating with maltitol, it takes time in the process of precipitating crystals from the sugar coating liquid. Since it takes time to complete a sugar-coated tablet, attempts have been made to shorten the time for the sugar-coating process.
- Japanese Patent Application Laid-Open No. 7-132051 discloses an improved hard coating method capable of easily and quickly forming a hard coating (paragraph 0001).
- the problem is solved by combining an alcohol powder and a crystallizable syrup containing more than half of the same polyhydric alcohol with respect to the soluble dry material in each cycle (paragraph 0032), but adding the powder to each cycle
- the surface of the resulting sugar-coated tablets lacks smoothness, is easy to absorb moisture, and has no crunch properties.
- An object of the present invention is to shorten the time required for forming a sugar coating of a hard sugar coating with a sugar alcohol typified by maltitol and to form a smooth and practically sufficient sugar coating layer.
- the inventors of the present invention have only improved the smoothness of the sugar-coating layer as the spreadability of the sugar-coating liquid is improved by adding calcium lactate as a component of the sugar-alcohol sugar-coating liquid.
- the increase in the crystallization rate of sugar alcohols such as maltitol was confirmed, and it was found that the time required for the sugar coating process can be greatly shortened.
- the present invention is characterized in that calcium lactate is used for the sugar alcohol sugar coating liquid, but an example of using calcium lactate for sugar coating with ordinary sucrose is widely performed for the purpose of improving the sugar coating layer (for example, Japanese Patent Publication No. 48-37815, Japanese Patent No. 2759802, Japanese Patent Laid-Open No. 4-261118).
- an example of using calcium lactate for sugar coating with ordinary sucrose is widely performed for the purpose of improving the sugar coating layer (for example, Japanese Patent Publication No. 48-37815, Japanese Patent No. 2759802, Japanese Patent Laid-Open No. 4-261118).
- the effect of using calcium lactate in sugar coating with sucrose is to form a strong sugar coating layer by precipitating fine crystals of sucrose.
- Calcium lactate is a water-soluble calcium salt.
- the crystallization rate is slowed because the substance inhibits crystal precipitation.
- the time required for sucrose sugar coating was measured when calcium lactate was added and not added, about 10% more time was required until the sugar coated tablet was added with calcium lactate (Comparative Example 3 described later). 4).
- a problem with sugar alcohol sugar coating is that it takes a long time. This is due to the slow crystallization rate of sugar alcohols such as maltitol.
- a method of adding a solid such as a crystal nucleus has been performed for increasing the crystallization rate.
- the present invention is first a method for accelerating the formation of sugar coating of a sugar alcohol sugar coating using calcium lactate.
- the sugar coating formation promoting method according to the first aspect wherein the sugar coating liquid contains calcium lactate.
- the sugar coating formation promoting method according to the first or second aspect wherein the content of calcium lactate is 1 to 10% by weight of the sugar coating solution.
- a sugar alcohol sugar coating formation promoting composition containing calcium lactate is first a method for accelerating the formation of sugar coating of a sugar alcohol sugar coating using calcium lactate.
- the form of the sugar alcohol used in the present invention is not limited as long as a sugar coating layer can be formed.
- maltitol in the case of maltitol, it can be used in any form of a crystal product, a honey crystal product, and a liquid product. From the viewpoint of the smoothness and strength of the sugar coating layer, it is 90% or more, preferably 95 %, More preferably 98% or more of the purity can be advantageously used.
- sugar alcohols in the present invention include sorbitol, xylitol, lactitol, isomaltulose reduced products, and the like.
- the calcium lactate used in the present invention can be used in any form of a crystalline product or a liquid product, but from the viewpoint of operability, it is preferable to use a crystalline product.
- the content of calcium lactate in the present invention is preferably 1 to 10% by weight of the sugar coating liquid. If the content is 10% by weight or less, the solution viscosity is kept low and the operability is good. On the other hand, if it is 1% by weight or more, a sugar coating layer having good smoothness and usable sugar coating layer strength can be obtained.
- thickeners such as gum arabic, gelatin, pullulan, xanthan gum, hydroxymethyl cellulose, dietary fiber, and processed starch in the sugar coating liquid.
- the present invention by increasing the crystallization rate of sugar alcohol such as maltitol, the time required for the sugar-coating process of sugar-alcohol sugar coating can be greatly shortened, and a smooth and practically sufficient strength sugar coating layer can be formed. it can.
- calcium lactate indicates the content as a pentahydrate.
- Tableting machine VIRGO 0512SS2AZ (manufactured by Kikusui Seisakusho)
- Sugar coating machine 16DS (made by Kikusui Seisakusho Co., Ltd.)
- V mixer V mixer (manufactured by Ikeda Rika Co., Ltd.)
- oxidized starch 2 kg of water was added to 1 kg of tapioca starch (manufactured by Nippon Shokuhin Kako Co., Ltd.) and heated to 30 ° C. as a suspension. 3% aqueous sodium hydroxide solution was added to the suspension to adjust the pH to 11.0, and 150 ml of sodium hypochlorite solution containing 13% of effective chlorine was added for oxidation treatment for 1 hour. After neutralization, washing with water, dehydration and drying were performed to prepare oxidized tapioca starch. 30 parts by weight of the obtained oxidized tapioca starch and 70 parts by weight of potato starch (reagent grade 1, manufactured by Kanto Chemical Co., Ltd.) were mixed to obtain oxidized starch.
- the core material used in the present invention was prepared as follows. 2.5 parts by weight of magnesium stearate as a lubricant is added to 100 parts by weight of Amarty MR, and tableting is carried out under the conditions of dosage form 8 mm sugar coating R, unit weight 180 mg, vertical length 4 pieces, rotational speed 40 rpm, tableting pressure 770 kgf. The core material was manufactured.
- Step I-2 a relatively small amount of sugar-coating liquid is used, and sugar coating is performed until the peripheral portion of the tablet is covered with the sugar-coating layer.
- Step I-3 the amount of sugar-coating liquid is increased, and the sugar-coating rate is 35.
- Sugar coating was performed with the goal of%.
- the sugar coating liquid properties in each Example and Comparative Example are different, and the amount of sugar coating layer formation in one operation is different in each Example and Comparative Example. Therefore, in order to obtain a certain sugar coating rate, the operation is repeated. The number of times was different for each example and comparative example.
- sugar-coated tablets obtained in Examples and Comparative Examples were evaluated according to the items of sugar coating speed, sugar coating time, and 75 degree gloss.
- the sugar coating speed in the present invention is the sugar coating rate to the uncoated tablet per minute, and was calculated from the sugar coating time and the sugar coating rate.
- the sugar coating ratio is a percentage of the sugar coating layer weight with respect to the uncoated tablet weight and is calculated by measuring the weight of 10 tablets each of the uncoated tablet and the sugar coated tablet three times.
- the sugar coating time is the work time required from the start of the sugar coating process to before the polishing process (from the process I-1 to the process I-6 or from the process II-1 to the process II-4).
- the 75 degree glossiness in the present invention is a value (JIS-Z8741-1983) measured with a gloss meter (Gloss Meter VG2000 (manufactured by Nippon Denshoku Industries Co., Ltd.)). Five samples were measured and the average value was taken as the measured value.
- step I-4 In the maltitol sugar coating shown as the comparative product 1, it is necessary to repeat the step (step I-4) 25 times in order to smooth the tablet surface.
- the step for smoothing the tablet surface (step I-4) can be simplified, and the smoothing time of the sugar coating is greatly reduced.
- the 75 degree glossiness which is an index of sexuality
- Example Product 1 was superior.
- the comparative product 2 using the same production method as the product 1 and not using calcium lactate the sugar coating time was long, and the 75 ° gloss was much inferior to that of the product. From this, it was confirmed that the use of calcium lactate shortened the sugar coating time and improved the glossiness with sugar alcohol.
- Comparative Example 3 and Comparative Example 4 show the effect on sucrose sugar coating by using calcium lactate, but Comparative Example 4 using calcium lactate is an index of smoothness compared to Comparative Example 3 not using calcium lactate. A certain 75 degree glossiness was lowered, and the sugar coating time also took a long time.
- the conventional technology for improving sucrose sugar coating by using calcium lactate in the sucrose sugar coating liquid is based on the formation of fine crystals of sucrose by using calcium lactate in sucrose. By using it, it has a technical background different from the present invention based on the finding that promotes crystallization of sugar alcohols such as maltitol.
- the sugar-coating process I (warm air blowing conditions) was carried out with the number of repetitions specified in the number of times specified for the sugar-coating process in Table 3 to obtain sugar-coated tablets (practical product 3).
- Table 3 shows the sugar-coating speed, sugar-coating time, and 75-degree glossiness of the resulting sugar-coated tablets.
- Example 2 and Example 3 were 1% by weight and 10% by weight, respectively, of the sugar-coating liquid, and the present invention was successfully implemented.
- the amount of calcium lactate used was 10% by weight, the viscosity of the sugar coating liquid was low and the operability was not affected. Further, in the case of 1% by weight, a sufficient glossiness was recognized as compared with Comparative Example 5.
- the sugar coating process II (room temperature blowing condition) was performed at the number of repetitions specified in the number of times specified in the sugar coating process of Table 5 to obtain sugar-coated tablets (practical product 5).
- Table 5 shows the sugar-coating speed, sugar-coating time, and 75-degree glossiness of the resulting sugar-coated tablets.
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Abstract
Description
第二に、糖衣液に乳酸カルシウムを含有する、上記第一に記載の糖衣形成促進方法である。
第三に、乳酸カルシウムの含有量が糖衣液の1~10重量%である、上記第一または第二に記載の糖衣形成促進方法である。
第四に、乳酸カルシウムを含有する糖アルコール糖衣形成促進用組成物である。
(1)糖衣層基材
結晶マルチトール: レシス(三菱商事フードテック株式会社製)
微粉マルチトール: レシス微粉(三菱商事フードテック株式会社製)
結晶キシリトール: キシリット(三菱商事フードテック株式会社製)
微粉キシリトール: キシリット微粉(三菱商事フードテック株式会社製)
乳酸カルシウム(五水和物): 乳酸カルシウム(昭和化工株式会社製)
結晶スクロース: グラニュ糖ME(大日本明治製糖株式会社製)
微粉スクロース: MGP粉糖(株式会社徳倉製)
(2)糖衣層配合剤
アラビアガム: アラビアゴム末(関東化学株式会社製)
酸化デンプン: 下記調製品を使用
(3)芯材原料
粉末マルチトール: アマルティMR(三菱商事フードテック株式会社製)
ステアリン酸マグネシウム: ステアリン酸マグネシウム(和光純薬工業株式会社製)
打錠機: VIRGO 0512SS2AZ(株式会社菊水製作所製)
糖衣機: No.16D-S(株式会社菊水製作所製)
Vミキサー: Vミキサー(池田理科株式会社製)
タピオカデンプン(日本食品化工株式会社製)1kgに水2kgを加えて懸濁液として30℃に加温した。その懸濁液に3%水酸化ナトリウム水溶液を加えてpHを11.0に調整し、有効塩素を13%含む次亜塩素酸ナトリウム溶液150mlを加えて1時間酸化処理を行った後、塩酸にて中和後、水洗・脱水・乾燥を行い酸化タピオカデンプンを調製した。得られた酸化タピオカデンプン30重量部と馬鈴薯澱粉(試薬1級、関東化学株式会社製)70重量部を混合し酸化デンプンとした。
本発明で用いた芯材は、下記のように作成した。
アマルティMR100重量部に滑沢剤としてステアリン酸マグネシウムを2.5重量部加え、剤型8mm糖衣R、単位重量180mg、杵たて数4本、回転数40rpm、打錠圧770kgfの条件で打錠を行い、芯材を製造した。
1試験区あたり300gの糖衣液を調製した。500mL容ビーカーに表1~7の各実施例および各比較例に示す質量比の3倍の質量(g)の糖衣液成分を採り混合した。精製水を加え全体に混合後、湯煎で加熱溶解した。精製水を加え300gとし、60℃に保温したものを糖衣液とした。
以下の工程I-1~I-7(工程I-2とI-3についてはそれぞれの実施例、比較例で指定した回数、表1-表3参照)を行い温風送風条件下糖衣を行った。
(工程I-1)
糖衣パンに芯材300gを投入し、30rpmで回転しながら糖衣液8gを添加し、引き続いて微粉マルチトール(比較例3、比較例4においては微粉スクロース)1gを添加し4分無風で糖衣液を展延させた後、45℃の温風を2分送風し糖衣液を乾燥させる操作を2回繰り返した。
(工程I-2)
糖衣液7gを添加し、4.5分無風で糖衣液を展延させた後、45℃の温風を2分送風し糖衣液を乾燥させる操作を指定回数繰り返した。
(工程I-3)
糖衣液9gを添加し、6分無風で糖衣液を展延させた後、45℃の温風を2分送風し糖衣液を乾燥させる操作を指定回数繰り返した。
(工程I-4)
糖衣層を平滑にするため糖衣液6gを添加し、6分無風で糖衣液を展延させた後、送風機のヒーターを切った状態で6分送風(22℃)し糖衣液を乾燥させる操作を2回(比較例1のみ25回)繰り返した。
(工程I-5)
糖衣液の添加量を6g、4g、3g、1.5gの順で変化させ、それぞれ12分、10分、8分、6分無風で乾燥させた。
(工程I-6)
糖衣パンの回転速度を12rpmに変え、糖衣液を1g添加し、糖衣パンの回転を30秒停止した。その後、糖衣パンを1回転させた後5秒停止させる操作を5回繰り返したのち、開口部を湿らせたペーパータオルで覆い8分40秒回転させた。
(工程I-7)
糖衣錠を別の糖衣パンに移し、糖衣パンを30rpmで回転させ、カルナバワックスを糖衣錠の総重量に対し0.03%添加したのち30分回転させる操作を2回繰り返した。
以下の工程II-1~II-5(工程II-2とII-3についてはそれぞれの実施例、比較例で指定した回数、表4-表7参照)を行い室温送風条件下糖衣を行った。
(工程II-1)
糖衣パンに芯材300gを投入し、30rpmで回転しながら糖衣液4gを添加し、引き続いて微粉マルチトール(若しくは微粉キシリトール)1gを添加し、1分無風で糖衣液を乾燥させた後、室温の風(22℃)を9分送風し、糖衣液を乾燥させる操作を5回繰り返した。
(工程II-2)
糖衣液4gを添加し、4分間無風で糖衣液を展延させた後、室温(22℃)の風を4分間送風し、糖衣液を乾燥させる操作を指定回数繰り返した。
(工程II-3)
糖衣液4gを添加し、6分間無風で糖衣液を展延させた後、室温(22℃)の風を2分間送風し糖衣液を乾燥させる操作を指定回数繰り返した。
(工程II-4)
糖衣パンの回転速度を12rpmに変え、糖衣液の添加量を1.5gとし、糖衣パンの回転を30秒停止した。その後、糖衣パンを1回転させた後5秒停止させる操作を5回繰り返したのち、開口部を湿らせたペーパータオルで覆い8分40秒回転させた。
(工程II-5)
糖衣錠を別の糖衣パンに移し、糖衣パンを30rpmで回転させ、カルナバワックスを糖衣錠の総重量に対し0.03%添加したのち30分回転させる操作を2回繰り返した。
表1に示す糖衣液を用いて、表1の糖衣工程指定回数に指定した繰り返し回数で糖衣工程I(温風送風条件)を実施し、糖衣錠(実施品1)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表1に示す。
(マルチトール糖衣 工程I-4(25回)、温風送風条件)
表1に示す糖衣液を用いて、表1の糖衣工程指定回数に指定した繰り返し回数で糖衣工程I(温風送風条件)を実施し、糖衣錠(比較品1)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表1に示す。本比較例においてのみ工程I-4について25回繰り返した。(本比較例以外の温風送風条件での実施例、比較例における工程I-4の繰り返し回数は2回。)
(マルチトール糖衣 工程I-4(2回)、温風送風条件)
表1に示す糖衣液を用いて、表1の糖衣工程指定回数に指定した繰り返し回数で糖衣工程I(温風送風条件)を実施し、糖衣錠(比較品2)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表1に示す。
(スクロース糖衣、温風送風条件)
表2に示す糖衣液を用いて、表2の糖衣工程指定回数に指定した繰り返し回数で糖衣工程I(温風送風条件)を実施し、糖衣錠(比較品3)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表2に示す。
(乳酸カルシウムを用いたスクロース糖衣、温風送風条件)
表2に示す糖衣液を用いて、表2の糖衣工程指定回数に指定した繰り返し回数で糖衣工程I(温風送風条件)を実施し、糖衣錠(比較品4)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表2に示す。
表3に示す糖衣液を用いて、表3の糖衣工程指定回数に指定した繰り返し回数で糖衣工程I(温風送風条件)を実施し、糖衣錠(実施品2)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表3に示す。
表3に示す糖衣液を用いて、表3の糖衣工程指定回数に指定した繰り返し回数で糖衣工程I(温風送風条件)を実施し、糖衣錠(実施品3)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表3に示す。
(乳酸カルシウムを0.5重量%用いたマルチトール糖衣、温風送風条件)
表3に示す糖衣液を用いて、表3の糖衣工程指定回数に指定した繰り返し回数で糖衣工程I(温風送風条件)を実施し、糖衣錠(比較品5)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表3に示す。
表4に示す糖衣液を用いて、表4の糖衣工程指定回数に指定した繰り返し回数で糖衣工程II(室温送風条件)を実施し、糖衣錠(実施品4)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表4に示す。
(一般的なマルチトール糖衣、室温送風条件)
表4に示す糖衣液を用いて、表4の糖衣工程指定回数に指定した繰り返し回数で糖衣工程II(室温送風条件)を実施し、糖衣錠(比較品6)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表4に示す。
表5に示す糖衣液を用いて、表5の糖衣工程指定回数に指定した繰り返し回数で糖衣工程II(室温送風条件)を実施し、糖衣錠(実施品5)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表5に示す。
(酸化デンプンを用いたマルチトール糖衣、室温送風条件)
表5に示す糖衣液を用いて、表5の糖衣工程指定回数に指定した繰り返し回数で糖衣工程II(室温送風条件)を実施し、糖衣錠(比較品7)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表5に示す。
表6に示す糖衣液を用いて、表6の糖衣工程指定回数に指定した繰り返し回数で糖衣工程II(室温送風条件)を実施し、糖衣錠(実施品6)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表6に示す。
(アラビアガムを用いたキシリトール糖衣、室温送風条件)
表6に示す糖衣液を用いて、表6の糖衣工程指定回数に指定した繰り返し回数で糖衣工程II(室温送風条件)を実施し、糖衣錠(比較品8)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表6に示す。
表7に示す糖衣液を用いて、表7の糖衣工程指定回数に指定した繰り返し回数で糖衣工程II(室温送風条件)を実施し、糖衣錠(実施品7)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表7に示す。
(酸化デンプンを用いたキシリトール糖衣、室温送風条件)
表7に示す糖衣液を用いて、表7の糖衣工程指定回数に指定した繰り返し回数で糖衣工程II(室温送風条件)を実施し、糖衣錠(比較品9)を得た。得られた糖衣錠の糖衣速度、糖衣時間、75度光沢度を表7に示す。
Claims (4)
- 乳酸カルシウムを用いた糖アルコール糖衣の糖衣形成促進方法。
- 糖衣液に乳酸カルシウムを含有する、請求項1に記載の糖衣形成促進方法。
- 乳酸カルシウムの含有量が糖衣液の1~10重量%である、請求項1または2に記載の糖衣形成促進方法。
- 乳酸カルシウムを含有する糖アルコール糖衣形成促進用組成物。
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US15/772,769 US20180325824A1 (en) | 2015-11-02 | 2016-11-01 | Method for accelerating the sugar-coating formation of sugar alcohol coating with calcium lactate |
JP2017548778A JP6827945B2 (ja) | 2015-11-02 | 2016-11-01 | 乳酸カルシウムによる糖アルコール糖衣の糖衣形成促進方法 |
EP16862084.7A EP3372245A4 (en) | 2015-11-02 | 2016-11-01 | METHOD FOR ACCELERATING THE SUGAR COATING FOR FORMING SUGAR COATING OF SUGAR ALCOHOL WITH CALCIUM LACTATE |
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JP2015215371 | 2015-11-02 | ||
JP2015-215371 | 2015-11-02 |
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US (1) | US20180325824A1 (ja) |
EP (1) | EP3372245A4 (ja) |
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FR3125719A1 (fr) * | 2021-07-30 | 2023-02-03 | Roquette Freres | Procédé de dragéification amélioré comprenant un amidon hydrolysé et fonctionnalisé |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2759802B2 (ja) * | 1988-08-31 | 1998-05-28 | 山之内製薬株式会社 | 薬剤被覆用材料 |
WO1998028987A1 (en) * | 1996-12-30 | 1998-07-09 | Wm. Wrigley Jr. Company | Comestible coated with a poorly water-soluble salt and process for making |
JP2002179559A (ja) * | 2000-10-06 | 2002-06-26 | Takeda Chem Ind Ltd | 薄層糖衣錠およびその製造方法 |
JP2009073814A (ja) * | 2007-08-31 | 2009-04-09 | Taisho Pharmaceutical Co Ltd | エリスリトール配合糖衣液 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04261118A (ja) * | 1991-02-13 | 1992-09-17 | Zeria Pharmaceut Co Ltd | 固形製剤の糖衣被覆用組成物 |
US20070275129A1 (en) * | 2006-04-21 | 2007-11-29 | Cadbury Adams Usa Llc | Coating compositions, confectionery and chewing gum compositions and methods |
-
2016
- 2016-11-01 JP JP2017548778A patent/JP6827945B2/ja active Active
- 2016-11-01 EP EP16862084.7A patent/EP3372245A4/en not_active Withdrawn
- 2016-11-01 WO PCT/JP2016/082473 patent/WO2017078024A1/ja active Application Filing
- 2016-11-01 US US15/772,769 patent/US20180325824A1/en not_active Abandoned
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2759802B2 (ja) * | 1988-08-31 | 1998-05-28 | 山之内製薬株式会社 | 薬剤被覆用材料 |
WO1998028987A1 (en) * | 1996-12-30 | 1998-07-09 | Wm. Wrigley Jr. Company | Comestible coated with a poorly water-soluble salt and process for making |
JP2002179559A (ja) * | 2000-10-06 | 2002-06-26 | Takeda Chem Ind Ltd | 薄層糖衣錠およびその製造方法 |
JP2009073814A (ja) * | 2007-08-31 | 2009-04-09 | Taisho Pharmaceutical Co Ltd | エリスリトール配合糖衣液 |
Non-Patent Citations (1)
Title |
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See also references of EP3372245A4 * |
Also Published As
Publication number | Publication date |
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JP6827945B2 (ja) | 2021-02-10 |
US20180325824A1 (en) | 2018-11-15 |
JPWO2017078024A1 (ja) | 2018-08-30 |
EP3372245A4 (en) | 2019-07-10 |
EP3372245A1 (en) | 2018-09-12 |
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