JP2003267893A - Lubricant for tableting - Google Patents

Lubricant for tableting

Info

Publication number
JP2003267893A
JP2003267893A JP2002073777A JP2002073777A JP2003267893A JP 2003267893 A JP2003267893 A JP 2003267893A JP 2002073777 A JP2002073777 A JP 2002073777A JP 2002073777 A JP2002073777 A JP 2002073777A JP 2003267893 A JP2003267893 A JP 2003267893A
Authority
JP
Japan
Prior art keywords
tableting
tablet
lubricant
peptide
sticking
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.)
Granted
Application number
JP2002073777A
Other languages
Japanese (ja)
Other versions
JP4315635B2 (en
Inventor
Eriko Fujikawa
恵理子 藤川
Kazuhito Uchida
一仁 内田
Yoshihiko Takase
嘉彦 高瀬
Tomoji Kato
友治 加藤
Nagahiro Yamazaki
長宏 山崎
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.)
Taiyo Kagaku KK
Original Assignee
Taiyo Kagaku 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 Taiyo Kagaku KK filed Critical Taiyo Kagaku KK
Priority to JP2002073777A priority Critical patent/JP4315635B2/en
Publication of JP2003267893A publication Critical patent/JP2003267893A/en
Application granted granted Critical
Publication of JP4315635B2 publication Critical patent/JP4315635B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

<P>PROBLEM TO BE SOLVED: To provide a lubricant for tableting, preventing capping, sticking and binding by improving binding force and lubrication effects when tableting a tablet or a tableted confectionery because sometimes the capping which is the phenomenon of peeling like a cap at the upper pestle side of the tablet when releasing the tablet from a mold, the sticking which is the phenomenon of damaging the surface of the tablet caused by sticking the powder to the pestle and hardly releasing the powder at tableting, and the binding which is the phenomenon of ill state when discharging the tablet after tableting because of large friction between the tablet and a mortar are caused, and they prevent smooth tableting when coming off badly. <P>SOLUTION: The lubricant for the tableting contains a peptide. <P>COPYRIGHT: (C)2003,JPO

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は打錠する際に結着
力、滑沢性を高めることにより、キャッピング、スティ
ッキング及びバインディング等を防止する打錠用滑沢剤
及びそれを用いた錠剤及び錠菓に関するものである。
TECHNICAL FIELD The present invention relates to a lubricant for tableting, which prevents binding such as capping, sticking and binding by improving binding force and lubricity during tableting, and tablets and confectionery using the same. It is about.

【0002】[0002]

【従来の技術】錠剤、錠菓において、粉末や粉状の原料
を打錠する必要がある。打錠においては、脱型の際に錠
剤の上杵側に帽子状にはがれるキャッピング、打錠中に
粉が杵に付着し杵離れが悪く、錠剤表面に傷がつくステ
ィッキング、錠剤と臼の摩擦が大きく打錠後の錠剤の排
出性が悪くなるバインディングを生じることがあり、こ
れがひどくなるとスムーズに打錠できなくなる。そこで
打錠においては滑沢剤を使用することにより、原料粉体
の流動性を向上させ、打錠機の臼に一定量が充填される
ようにすると同時に、打錠の際のキャッピング、スティ
ッキング及びバインディング等を防止し、打錠の表面に
光沢を与えることが望まれる。そのために従来から精製
タルク、ステアリン酸マグネシウム、植物硬化油、ポリ
グリセリン脂肪酸エステルやショ糖脂肪酸エステル等の
食品用乳化剤等が滑沢剤として使用されてきた。そのう
ち、ステアリン酸マグネシウムの場合は、少量の使用で
滑沢剤としての効果を出すことができるが、食品添加物
として認められていないためその用途が医薬品に限定さ
れる。精製タルクは、食品への使用量に制限があり、ま
た滑沢剤としての効果も小さいためあまり用いられな
い。また、食品用乳化剤は滑沢剤の効果が小さいため、
十分な効果を期待するためには多量添加をしなければな
らず、そのために錠剤の硬度低下や風味を悪くしたりす
る問題があった。
2. Description of the Related Art In tablets and tablet confectionery, it is necessary to compress raw materials in powder or powder form. During tableting, capping that peels off like a hat on the upper punch side of the tablet during demolding, sticking powder during punching to the punch, resulting in poor punch separation, sticking that scratches the tablet surface, and friction between the tablet and the mortar Is large, and binding that causes poor discharge of the tablet after tableting may occur, and when it becomes severe, tableting cannot be performed smoothly. Therefore, in tableting, a lubricant is used to improve the fluidity of the raw material powder so that a constant amount is filled in the die of the tableting machine, and at the same time, capping, sticking and It is desired to prevent binding and the like and give gloss to the surface of the tablet. Therefore, refined talc, magnesium stearate, hardened vegetable oil, food emulsifiers such as polyglycerin fatty acid ester and sucrose fatty acid ester have been used as lubricants. Among them, magnesium stearate can exert an effect as a lubricant with a small amount of use, but its use is limited to pharmaceuticals because it is not recognized as a food additive. Refined talc is rarely used because its amount used in foods is limited and its effect as a lubricant is small. In addition, since the effect of a lubricant on food emulsifiers is small,
In order to expect a sufficient effect, a large amount must be added, which causes problems such as a decrease in hardness of tablets and deterioration of flavor.

【0003】[0003]

【発明が解決しようとする課題】本発明は従来の技術の
課題を解決すべくなされたもので、錠剤、錠菓を打錠す
る際のキャッピング、スティッキング及びバインディン
グを防止する滑沢剤を提供することを目的とする。
SUMMARY OF THE INVENTION The present invention has been made to solve the problems of the prior art, and provides a lubricant for preventing capping, sticking and binding when tableting tablets and tablet confections. The purpose is to

【0004】[0004]

【課題を解決するための手段】本発明者は前記課題を解
決すべく鋭意研究を重ねた結果、植物性及び/又は動物
性ペプチドを使用することによって、結着力、滑沢性を
高め、キャッピング、スティッキング及びバインディン
グを起こさない錠剤、錠菓を得られる事を見出し、本発
明に至った。すなわち本発明は、植物及び/又は動物性
ペプチドを含有することを特徴とする打錠用滑沢剤に関
するものである。
Means for Solving the Problems As a result of intensive studies to solve the above-mentioned problems, the present inventor has improved binding force and smoothness by using a vegetable and / or animal peptide and capping. It was found that a tablet or confectionery free from sticking and binding can be obtained, and the present invention has been completed. That is, the present invention relates to a lubricant for tableting, which comprises a plant and / or animal peptide.

【0005】[0005]

【発明の実施の形態】以下本発明を詳細に説明する。本
発明におけるペプチドとは植物又は動物より分離した蛋
白質を酵素分解したものをいい、平均鎖長が2〜10、
好ましくは2〜6となるまで酵素分解されたオリゴペプ
チド(遊離アミノ酸及び未分解蛋白を除いたもの)を1
種又は2種以上混合したものである。
BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below. The peptide in the present invention means one obtained by enzymatically decomposing a protein isolated from a plant or an animal, and has an average chain length of 2 to 10,
It is preferable to use 1 as an oligopeptide (excluding free amino acids and undegraded protein) enzymatically decomposed to 2 to 6
One kind or a mixture of two or more kinds.

【0006】また、本発明におけるペプチドの原料とな
る蛋白質は特に限定するものではないが、好ましくは大
豆、コーン、卵黄である。また、本発明における蛋白質
の分解に使用する酵素については、特に限定するもので
はないが、エンド型プロテアーゼ、エキソ型プロテアー
ゼ等が挙げられる。更に好ましくは、エンド型プロテア
ーゼ及びエキソ型プロテアーゼを共存したものが挙げら
れ、苦味が少なく好ましい。例えば、アスペルギルス・
オリーゼ起源の市販のプロテアーゼ「プロチンFN」
(大和化成(株)製)「FPC−30」(協和マイルス
(株)製)、ストレプトマイセス・グリセウス起源の市
販のプロテアーゼ「アクチナーゼ」(科研製薬(株)
製)等はエンド型プロテアーゼ及びエキソ型プロテアー
ゼが共存するので好ましい。また、本発明における食品
用乳化剤とはグリセリン脂肪酸エステル、プロピレング
リコール脂肪酸エステル、ソルビタン脂肪酸エステル、
ショ糖脂肪酸エステル等が例として挙げられ、その中で
もポリグリセリン脂肪酸エステル又はショ糖脂肪酸エス
テルを1種又は2種以上混合したものが好ましく、ポリ
グリセリン脂肪酸エステルを1種又は2種以上混合した
ものが更に好ましい。
The protein used as the raw material for the peptide in the present invention is not particularly limited, but soybean, corn and egg yolk are preferable. The enzyme used for degrading the protein in the present invention is not particularly limited, and examples thereof include endo-type protease and exo-type protease. More preferred are those in which an endo-type protease and an exo-type protease coexist, which is preferable because it has little bitterness. For example, Aspergillus
Commercial protease "Protin FN" originating from Olise
(Manufactured by Daiwa Kasei Co., Ltd.) “FPC-30” (manufactured by Kyowa Miles Co., Ltd.), a commercially available protease “Actinase” originating from Streptomyces griseus (Kaken Pharmaceutical Co., Ltd.)
(Manufactured) and the like are preferred because an endo-type protease and an exo-type protease coexist. Further, the food grade emulsifier in the present invention is glycerin fatty acid ester, propylene glycol fatty acid ester, sorbitan fatty acid ester,
Examples thereof include sucrose fatty acid ester and the like. Among them, polyglycerin fatty acid ester or sucrose fatty acid ester is preferably used as a mixture of one or more kinds, and polyglycerin fatty acid ester is mixed as one or more kinds. More preferable.

【0007】また、本発明におけるポリグリセリン脂肪
酸エステルは、特に限定されるものではないが、ポリグ
リセリンの脂肪酸の炭素数10〜22、重合度2〜20
で、水酸基価が100未満であるものが好ましい。炭素
数9以下のポリグリセリン脂肪酸エステルの場合には、
その融点が低くなりすぎるため微粉末にすることが困難
であり、滑沢剤としての効果が弱くなる。また、炭素数
23以上のポリグリセリン脂肪酸エステルでは、これを
使用して製造した錠剤、錠菓の硬度が低くなる。また、
重合度が21以上のポリグリセリンは、原料自体の粘度
が高すぎてエステル反応が著しく困難となるため、実用
的でない。また、エステルの水酸基価が100以上であ
ると打錠機への付着等により製品歩留まりが悪化する。
また、本発明のショ糖脂肪酸エステルは、特に限定され
るものではないが、ショ糖脂肪酸の炭素数が8〜22で
平均置換度が2以上であるものが好ましい。炭素数8未
満では融点が低くなりすぎるため微粉末にすることが困
難であり、滑沢剤としての効果が弱くなる。また、炭素
数が22をこえるものでは、これを使用して製造した錠
剤、錠菓の硬度が低くなる。平均置換度2未満のショ糖
脂肪酸エステルでは打錠機への付着等により製品歩留ま
りが悪化する。
The polyglycerin fatty acid ester in the present invention is not particularly limited, but the fatty acid of polyglycerin has 10 to 22 carbon atoms and a degree of polymerization of 2 to 20.
It is preferable that the hydroxyl value is less than 100. In the case of polyglycerin fatty acid ester having 9 or less carbon atoms,
Since its melting point becomes too low, it is difficult to make it into a fine powder, and the effect as a lubricant is weakened. Further, with the polyglycerin fatty acid ester having 23 or more carbon atoms, the hardness of tablets and tablet confectionery produced using the same becomes low. Also,
Polyglycerin having a degree of polymerization of 21 or more is not practical because the viscosity of the raw material itself is too high and the ester reaction becomes extremely difficult. Further, when the hydroxyl value of the ester is 100 or more, the product yield is deteriorated due to adhesion to the tableting machine and the like.
The sucrose fatty acid ester of the present invention is not particularly limited, but those having a carbon number of sucrose fatty acid of 8 to 22 and an average degree of substitution of 2 or more are preferable. If the carbon number is less than 8, the melting point will be too low, and it will be difficult to make a fine powder, and the effect as a lubricant will be weakened. If the carbon number exceeds 22, the hardness of tablets and confectionery produced using this will be low. With a sucrose fatty acid ester having an average degree of substitution of less than 2, the product yield is deteriorated due to adhesion to a tableting machine and the like.

【0008】また、本発明の滑沢剤のペプチドと食品用
乳化剤の混合割合はペプチド:食品用乳化剤=10:9
0〜90:10が好ましい。更に本発明の滑沢剤の粉体
粒径が大きいと、各粉末粒体と均一に分散せず流動性及
び製品の歩留まりが低下するので粒径が250μm以下
であることが必要である。錠剤、錠菓の製造過程は、粉
末又は顆粒を製造する造粒プロセスと、圧縮成型する打
錠プロセスに分けられるが、本発明における滑沢剤は一
般に造粒プロセス後に添加される。添加量は0.2〜5
重量%であるが、要求される機能によって添加量はその
限りでない。また、本発明における滑沢剤は直接錠剤製
造法、湿式錠剤製造法のどちらでも用いることができ
る。以下、実施例によって本発明を更に説明するが、本
発明の範囲はこれらのみに限定されるものではない。な
お、評価は肉眼観察により行った。
The mixing ratio of the peptide of the lubricant of the present invention and the food emulsifier is peptide: food emulsifier = 10: 9.
0 to 90:10 is preferable. Further, when the powder particle size of the lubricant of the present invention is large, it is not dispersed uniformly with each powder particle and the fluidity and the yield of the product are reduced, so the particle size is required to be 250 μm or less. The manufacturing process of tablets and tablet confectionery can be divided into a granulating process for manufacturing powder or granules and a tableting process for compression molding. The lubricant in the present invention is generally added after the granulating process. Addition amount is 0.2-5
Although the amount is% by weight, the amount added is not limited depending on the required function. Further, the lubricant in the present invention can be used in either a direct tablet manufacturing method or a wet tablet manufacturing method. Hereinafter, the present invention will be further described with reference to examples, but the scope of the present invention is not limited to these. The evaluation was performed by visual observation.

【0009】[0009]

【実施例】実施例1 滑沢剤実施例 原料を下記の割合で混合し本発明品(打錠用滑沢剤)1
〜7をそれぞれ20g調製した。 実施例1 大豆ペプチド=100 実施例2 大豆ペプチド:デカグリセリンデカステアレート=40:60 実施例3 大豆ペプチド:シュガートリステアレート=80:20 実施例4 大豆ペプチド:シュガートリステアレート=60:40 実施例5 ヨークペプチド:デカグリセリンデカステアレート=20:80 実施例6 ヨークペプチド:デカグリセリンデカベヘネート=50:50 実施例7 ヨークペプチド:デカグリセリンデカベヘネート=40:60 大豆ペプチド;不二製油(株)社製「ハイニュートSMS」 ヨークペプチド;太陽化学(株)社製「ヨークペプチドH−2」
Examples Example 1 Lubricants Example The raw materials were mixed in the following proportions to produce the product of the present invention (lubricant for tableting) 1
20g each of ~ 7 was prepared. Example 1 Soybean peptide = 100 Example 2 Soybean peptide: Decaglycerin Decasterate = 40: 60 Example 3 Soybean peptide: Sugar tristearate = 80: 20 Example 4 Soy peptide: Sugar tristearate = 60: 40 Example 5 York peptide: Decaglycerin decasterate = 20: 80 Example 6 York peptide: Decaglycerin decabehenate = 50: 50 Example 7 York peptide: Decaglycerin decabehenate = 40: 60 Soybean peptide; Fuji Oil refinery Co., Ltd. "High New SMS" York peptide; Taiyo Kagaku Co., Ltd. "Yoke peptide H-2"

【0010】比較例 下記の原料を用いて比較品(打錠用割沢剤)1〜4をそ
れぞれ20g調製した。 比較例1 デカグリセリンデカステアレート 比較例2 シュガートリステアレート 比較例3 ナタネ硬化油 比較例4 精製タルク
Comparative Example 20 g of comparative products (tabletting lubricants) 1 to 4 were prepared using the following raw materials. Comparative Example 1 Decaglycerin Decasterate Comparative Example 2 Sugar Tristearate Comparative Example 3 Rapeseed hydrogenated oil Comparative Example 4 Purified talc

【0011】試験例 乳糖800g、粉糖180g、本発明品又は比較品20
gを混合後、直接打錠法により打錠機で一定の成形圧力
を加えて(300±8)mg/錠で打錠を行った。打錠
時間は10分とし、キャッピング、スティッキング及び
バインディングの評価を肉眼観察により行った。結果を
表1に示す。
Test Example Lactose 800 g, powdered sugar 180 g, product of the present invention or comparative product 20
After mixing g, a constant molding pressure was applied by a tableting machine by the direct tableting method to give tablets at (300 ± 8) mg / tablet. The tableting time was 10 minutes, and capping, sticking and binding were evaluated by visual observation. The results are shown in Table 1.

【0012】[0012]

【表1】 [Table 1]

【0013】評価基準:◎ 全くなし、○ 若干あり、
△ あり、× 非常にあり 表1の評価結果に示したごとく本発明によるペプチドを
含有することを特徴とする打錠用滑沢剤は従来品に比べ
てキャッピング、スティッキング及びバインディングを
起こさない、結着性のよい錠菓が得られた。
Evaluation criteria: ◎ None, ○ Some
Δ Yes, × Very Yes As shown in the evaluation results in Table 1, the tableting lubricant characterized by containing the peptide according to the present invention does not cause capping, sticking and binding as compared with conventional products. A tablet confectionery having good wearing property was obtained.

【0014】[0014]

【発明の効果】本発明によれば、錠剤、錠菓を打錠する
際に結着力、滑沢性を高めることにより、キャッピン
グ、スティッキング及びバインディングを防止する打錠
用滑沢剤を得ることができる。
INDUSTRIAL APPLICABILITY According to the present invention, a tableting lubricant capable of preventing capping, sticking and binding can be obtained by enhancing binding force and lubricity when tableting tablets and tablet confections. it can.

フロントページの続き (72)発明者 加藤 友治 三重県四日市市赤堀新町9番5号 太陽化 学株式会社内 (72)発明者 山崎 長宏 三重県四日市市赤堀新町9番5号 太陽化 学株式会社内 Fターム(参考) 4B014 GB08 GK07 GL09 4C076 AA37 BB01 EE41C FF43 GG01 Continued front page    (72) Inventor Yuji Kato             9-5 Akahori Shinmachi, Yokkaichi-shi, Mie Solarization             Gaku Co., Ltd. (72) Inventor Nagahiro Yamazaki             9-5 Akahori Shinmachi, Yokkaichi-shi, Mie Solarization             Gaku Co., Ltd. F-term (reference) 4B014 GB08 GK07 GL09                 4C076 AA37 BB01 EE41C FF43                       GG01

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】ペプチドを含有することを特徴とする打錠
用滑沢剤。
1. A lubricant for tableting, which comprises a peptide.
【請求項2】ペプチドと食品用乳化剤を併用することを
特徴とする請求項1記載の打錠用滑沢剤。
2. The tableting lubricant according to claim 1, wherein the peptide and a food-grade emulsifier are used in combination.
【請求項3】ペプチドと食品用乳化剤が粉末であること
を特徴とする請求項2記載の打錠用滑沢剤。
3. The lubricant for tableting according to claim 2, wherein the peptide and the emulsifier for food are powders.
【請求項4】請求項1〜3いずれか記載の滑沢剤を添加
してなることを特徴とする錠剤又は錠菓。
4. A tablet or confectionery containing the lubricant according to any one of claims 1 to 3.
JP2002073777A 2002-03-18 2002-03-18 Tableting lubricant Expired - Fee Related JP4315635B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2002073777A JP4315635B2 (en) 2002-03-18 2002-03-18 Tableting lubricant

Publications (2)

Publication Number Publication Date
JP2003267893A true JP2003267893A (en) 2003-09-25
JP4315635B2 JP4315635B2 (en) 2009-08-19

Family

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Family Applications (1)

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Country Status (1)

Country Link
JP (1) JP4315635B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101519911B (en) * 2008-12-29 2013-05-15 青建集团股份公司 Multifunctional special template for top angle
CN101525941B (en) * 2008-12-29 2013-05-15 青建集团股份公司 Combined top angle molding plate

Also Published As

Publication number Publication date
JP4315635B2 (en) 2009-08-19

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