JPS62132831A - Gelan gum for coating circumference of tablet or the like - Google Patents

Gelan gum for coating circumference of tablet or the like

Info

Publication number
JPS62132831A
JPS62132831A JP60273688A JP27368885A JPS62132831A JP S62132831 A JPS62132831 A JP S62132831A JP 60273688 A JP60273688 A JP 60273688A JP 27368885 A JP27368885 A JP 27368885A JP S62132831 A JPS62132831 A JP S62132831A
Authority
JP
Japan
Prior art keywords
tablet
resistance
drug
gelan gum
coating layer
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.)
Pending
Application number
JP60273688A
Other languages
Japanese (ja)
Inventor
Hiroki Iida
飯田 博樹
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.)
San Ei Kagaku Co Ltd
Sanei Kagaku Kogyo KK
Original Assignee
San Ei Kagaku Co Ltd
Sanei Kagaku Kogyo KK
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 San Ei Kagaku Co Ltd, Sanei Kagaku Kogyo KK filed Critical San Ei Kagaku Co Ltd
Priority to JP60273688A priority Critical patent/JPS62132831A/en
Publication of JPS62132831A publication Critical patent/JPS62132831A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To coat circumferential surface of tablet, tabletted granule, powder, etc., of food, drug, drug assistant, etc., with a coating layer resistance to heat, alkali and acid, by using a gelan gum which is a kind of polysaccharides as a component of the coating layer. CONSTITUTION:A fluid system consisting of a sol of an aqueous suspension containing <=2wt% gelan gum based on water or an incompletely gelled (solidified) suspension is applied at 35-85 deg.C to the circumferential surface of tablet, tabletted granule, etc., of a drug, etc., to be coated in a manner to form a layer of uniform thickness by an arbitrary method such as immersion, spraying, etc., to obtain a tablet, etc., resistant to deterioration of quality. The gelan gum coating layer has excellent heat-resistance, alkali-resistance and acid- resistance and is tasteless, odorless and colorless. Accordingly, it gives no adverse effect to the drug, etc. It has extremely low moisture-permeability.

Description

【発明の詳細な説明】 この発明は、食品ないし医薬品あるいは医薬助剤に係る
ものであり、これらの錠形物、拳粒錠物、粉状物、等の
周面に耐熱、耐アルカリ、耐酸性の被覆層を工業的に有
利に形成することを目的とする。
[Detailed Description of the Invention] This invention relates to foods, medicines, or pharmaceutical aids, and the peripheral surfaces of these tablets, fist tablets, powders, etc. are heat-resistant, alkali-resistant, and acid-resistant. The purpose of the present invention is to form a transparent coating layer industrially advantageously.

(従来の技術とその欠点) 錠形、顆粒形あるいは粗い粉状形の医薬、同助剤あるい
は食品であって、その周面を均一の厚さを持つ膠質ある
いは糊料層をもって被覆することは、広く知られている
。内容物の劣化防止、飲食のしやすさ、目減りの防止を
計るだめである。
(Prior art and its disadvantages) It is impossible to cover the peripheral surface of tablet-shaped, granular-shaped or coarsely powdered medicines, auxiliary agents, or foods with a colloid or glue layer of uniform thickness. , widely known. This is to prevent the contents from deteriorating, to make it easier to eat and drink, and to prevent loss of weight.

これらに採用する11g質ないし糊料としては寒天、カ
ラギナーン、アラビアガム、CMC,その他が知られて
いるが、これらの公知物質は耐酸性、耐アルカリ性、耐
熱性に劣るという欠点がある。
Agar, carrageenan, gum arabic, CMC, and others are known as the 11g substance or paste used in these materials, but these known substances have the disadvantage of being poor in acid resistance, alkali resistance, and heat resistance.

(この発明の課題) これらの欠点のない被覆物質の採用が当業者の課題であ
り、この発明はこの課題に対するーツの解答である。
OBJECT OF THE INVENTION It is a task for the person skilled in the art to adopt a coating material that does not have these drawbacks, and the present invention is an answer to this task.

この発明を以下に詳しく説明する。This invention will be explained in detail below.

(発明の構成) この発明は、被覆物質として多糖類の一種である。ジェ
ランガムを採用する。
(Structure of the Invention) This invention uses a type of polysaccharide as a coating material. Adopt gellan gum.

その使用の態様を説明すると、まずジェランガムの水性
懸濁系を作る。その使用量は水に対する約2%(重量、
以下同じ)以下量でよい。ジェランガムのこの水性系は
室温において高い粘性を示tその温度が上るにしたがっ
て、しだいに粘度を低下する。そして約85℃の温度に
いたったとき、ガムは分子状分散をおえてゾルになる。
To explain the mode of its use, first, an aqueous suspension system of gellan gum is made. The amount used is approximately 2% (weight,
(The same applies hereinafter) The following amount is sufficient. This aqueous system of gellan gum exhibits high viscosity at room temperature and gradually decreases in viscosity as the temperature increases. When the temperature reaches about 85°C, the gum undergoes molecular dispersion and becomes a sol.

このゾルは、その温度を下降させると約35°Cの温度
においてゲル化を始める。このゾル糸ないしゲル化完了
前のゲル糸であって、固化を完了する前の流動糸を被覆
対象の囲薬品その他の錠形物、顆粒物その他の周面に均
一な厚さの層を形成させるように塗付する。塗付の要領
は浸漬、噴霧その他任意の方法によればよい。
This sol starts to gel at a temperature of about 35°C when its temperature is lowered. This sol thread or gel thread before completion of gelation, which is fluid thread before completion of solidification, is used to form a layer of uniform thickness on the surrounding surface of the drug, other tablets, granules, etc. to be coated. Apply as shown. The method of application may be dipping, spraying, or any other arbitrary method.

塗付をおえだ錠形物等を乾・操して目的の医薬物、食品
、その他が得られる。
By drying and manipulating the coated tablets, etc., the desired pharmaceuticals, foods, etc. can be obtained.

ここに、この発明はその目的を達しおえる。Here, this invention achieves its purpose.

(作用および効果) この発明のジェランガム被覆層は■耐酸、耐アルカリ、
#熱性に優れている。
(Functions and Effects) The gellan gum coating layer of this invention has ■acid resistance, alkali resistance,
#Excellent heat resistance.

さらに■このものは無味、無臭、無色であるから錠形物
その他の医薬等に、なんらの悪影響をおよぼさない。■
水分透過率がきわめて小さい。これらのことを以下の実
験例により証明する。
Furthermore, ■This product is tasteless, odorless, and colorless, so it does not have any adverse effects on tablets or other medicines. ■
Moisture permeability is extremely low. These points will be proven by the following experimental examples.

(発明の効果) 次に実験例に基づいて、この発明の詳細な説明する。(Effect of the invention) Next, the present invention will be explained in detail based on experimental examples.

(実験例1) 水99.6部(重量、以下同じ)に下記のゲル化惟物質
の試料0゜4部を溶解し、これを試液とし、シャーレに
入れて一20°Cで硬化し、同温度でシャーレを密閉せ
ず開放状態で保存して、3日後、1週間後の水分の蒸発
率を求めた。
(Experimental Example 1) Dissolve 0.4 parts of the following gelled material sample in 99.6 parts of water (weight, same below), use this as a test solution, put it in a petri dish and harden at -20°C. The petri dish was stored in an open state without being sealed at the same temperature, and the moisture evaporation rate was determined after 3 days and 1 week.

(結 果) (実験例2) ジェランガムの有効な粘性の証明試料0
.4部を95°Cの湯99.6部に10分間攪拌溶解し
その10°Cでの粘度を測定しその結果は次の通りであ
った。
(Results) (Experiment Example 2) Proof of effective viscosity of gellan gum Sample 0
.. 4 parts were stirred and dissolved in 99.6 parts of hot water at 95°C for 10 minutes, and the viscosity at 10°C was measured, and the results were as follows.

(実験例3) (耐熱性) 下記の各試料1部宛に、CaCl2・0.05部を夫々
前へ、夫々に水99.55部を加へ、何れをも沸騰させ
、5分間攪拌溶解後容器につめ7°Cの水槽で2時間冷
却ゲlし化させた。そのゲルを1辺2cmの立方体に切
シ出し、これを耐熱容器に入れ、さらにこれに水を10
0 yptf入れフタをして95°C160分間及び1
21 ’C115分間加熱後のゲルの状態を観察した。
(Experiment Example 3) (Heat resistance) Add 0.05 parts of CaCl2 and 99.55 parts of water to 1 part of each sample below, bring both to a boil, and stir and dissolve for 5 minutes. The mixture was then cooled in a 7°C water bath for 2 hours to form a gel. Cut the gel into cubes of 2 cm on each side, place them in a heat-resistant container, and add 10 cm of water to this.
0 Put the yptf in, cover and heat at 95°C for 160 minutes and 1
The state of the gel was observed after heating for 115 minutes at 21'C.

(実験例4) (耐酸、耐アルカリ性)下記の各試料1
部宛を夫々水99部に攪拌分散させて後、夫々を95°
C,5分間攪拌溶解した。
(Experiment Example 4) (Acid resistance, alkali resistance) Each sample 1 below
After stirring and dispersing each part in 99 parts of water, each part was heated at 95°.
C. Dissolved with stirring for 5 minutes.

これらのゾルをクエン酸、又は水酸化ナトリウム水溶液
でpH8,7,11に調整後90’C・20分間加熱し
、標準ゼリーカップに入れ7°Cの水槽に2時間つけゲ
ル化させ、そのゲル強度柩飯尾電機DIModel  
301)のカードメーターにて測定した。
These sols were adjusted to pH 8, 7, or 11 with citric acid or aqueous sodium hydroxide solution, heated at 90'C for 20 minutes, placed in a standard jelly cup, and placed in a 7°C water bath for 2 hours to gel. Strength Hitsugiio Electric DI Model
301) was measured using a card meter.

その結果は、次の通りであった。The results were as follows.

説明: pH7のもものゲル強度(? / 1* )を
100としだ。
Explanation: Calculate the gel strength (? / 1*) of peach at pH 7 as 100.

実施例1 白糖50gにβ−カロチン3部、ビタミンE1部、乳糖
45部及びジェランガム2部を加えて、さらに水100
部で分散混合したものを乳糖50部とL−アスコルビン
酸50部を混合打錠したものに、コートパンを用いて錠
剤コーディングを行い、乾燥させた。このものは、表面
のつやのあるアスコルビン酸の品質劣化の少ない錠剤か
えられた。
Example 1 Add 3 parts of β-carotene, 1 part of vitamin E, 45 parts of lactose, and 2 parts of gellan gum to 50 g of white sugar, and add 100 g of water.
A mixture of 50 parts of lactose and 50 parts of L-ascorbic acid was dispersed and mixed in 100 parts, and then tablet-coated using a coating pan and dried. This product was replaced by a tablet with a glossy surface and less deterioration in quality of ascorbic acid.

実施例2 乳糖50部と、L−アスコルビン酸50部を混合、打錠
して直径22間、高さ4mmの錠剤を試製し、これにあ
らかじめ水84.6部、エタノール15部の混液にジェ
ランガム0.4部を溶解したものを、噴霧塗布をし、乾
・斥させ(60°C)ついで60°Cフランキ内にて、
経日的に、L−アスコルビン酸の品質安定性を観察した
Example 2 50 parts of lactose and 50 parts of L-ascorbic acid were mixed and tableted to make tablets with a diameter of 22 mm and a height of 4 mm, and gellan gum was added in advance to a mixture of 84.6 parts of water and 15 parts of ethanol. A solution of 0.4 parts was applied by spraying, dried and repelled (at 60°C), and then placed in a 60°C Franchi.
The quality stability of L-ascorbic acid was observed over time.

Claims (1)

【特許請求の範囲】[Claims] 錠剤その他のものの周面を被覆してなることを特徴とす
るジェランガム。
Gellan gum is characterized by being made by coating the peripheral surface of tablets and other things.
JP60273688A 1985-12-03 1985-12-03 Gelan gum for coating circumference of tablet or the like Pending JPS62132831A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60273688A JPS62132831A (en) 1985-12-03 1985-12-03 Gelan gum for coating circumference of tablet or the like

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60273688A JPS62132831A (en) 1985-12-03 1985-12-03 Gelan gum for coating circumference of tablet or the like

Publications (1)

Publication Number Publication Date
JPS62132831A true JPS62132831A (en) 1987-06-16

Family

ID=17531163

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60273688A Pending JPS62132831A (en) 1985-12-03 1985-12-03 Gelan gum for coating circumference of tablet or the like

Country Status (1)

Country Link
JP (1) JPS62132831A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5888568A (en) * 1998-06-25 1999-03-30 Nestec S.A. Limitation of browning
WO2001026634A1 (en) * 1999-10-11 2001-04-19 Monsanto Company Tablets with a gellan gum coating
WO2002000268A1 (en) * 2000-06-28 2002-01-03 Bristol-Myers Squibb Company Sprayable wound care compositions
AU747099B2 (en) * 1997-10-31 2002-05-09 Pharmacia Corporation Gellan gum tablet coating

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU747099B2 (en) * 1997-10-31 2002-05-09 Pharmacia Corporation Gellan gum tablet coating
US6395298B1 (en) 1997-10-31 2002-05-28 Pharmacia Corporation Gellan gum tablet coating
US6627225B2 (en) 1997-10-31 2003-09-30 Pharmacia Corporation Gellan gum tablet coating
US6635282B1 (en) 1997-10-31 2003-10-21 Pharmacia Corporation Gellan gum tablet film coating
US5888568A (en) * 1998-06-25 1999-03-30 Nestec S.A. Limitation of browning
US6485747B1 (en) 1998-10-30 2002-11-26 Monsanto Company Coated active tablet(s)
WO2001026634A1 (en) * 1999-10-11 2001-04-19 Monsanto Company Tablets with a gellan gum coating
WO2002000268A1 (en) * 2000-06-28 2002-01-03 Bristol-Myers Squibb Company Sprayable wound care compositions

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