[go: up one dir, main page]

JP2004081207A - Beverage - Google Patents

Beverage Download PDF

Info

Publication number
JP2004081207A
JP2004081207A JP2003180454A JP2003180454A JP2004081207A JP 2004081207 A JP2004081207 A JP 2004081207A JP 2003180454 A JP2003180454 A JP 2003180454A JP 2003180454 A JP2003180454 A JP 2003180454A JP 2004081207 A JP2004081207 A JP 2004081207A
Authority
JP
Japan
Prior art keywords
weight
acid
beverage
acids
component
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
JP2003180454A
Other languages
Japanese (ja)
Other versions
JP3769268B2 (en
Inventor
Yasushi Shioya
塩屋 靖
Tatsuya Kusaura
草浦 達也
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP2003180454A priority Critical patent/JP3769268B2/en
Publication of JP2004081207A publication Critical patent/JP2004081207A/en
Application granted granted Critical
Publication of JP3769268B2 publication Critical patent/JP3769268B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Non-Alcoholic Beverages (AREA)

Abstract

【解決手段】次の成分(a)、(b)及び(c):
(a)イソクロロゲン酸類を含むクロロゲン酸類混合物(ここで、成分(a)中のイソクロロゲン酸類含有重量比率は1/3〜1/20である)   0.05〜10重量%、
(b)野菜又は果物由来のフレーバー物質   0.65〜99重量%、
(c)水   99.3重量%以下
を含有する飲料。
【効果】本発明によれば、安定した血圧降下作用を有し、かつ味が良好で長期保存安定性の良好な飲料が得られる。
【選択図】   なし
The following components (a), (b) and (c):
(A) a mixture of chlorogenic acids containing isochlorogenic acids (where the weight ratio of isochlorogenic acids in component (a) is 1/3 to 1/20) 0.05 to 10% by weight;
(B) 0.65-99% by weight of a flavor substance derived from vegetables or fruits;
(C) A beverage containing 99.3% by weight or less of water.
According to the present invention, a beverage having a stable blood pressure lowering action, good taste and good long-term storage stability can be obtained.
[Selection diagram] None

Description

【0001】
【発明の属する技術分野】
本発明は、血圧降下作用等の生理効果を有し、味が良好で、かつ保存安定性の良好な飲料に関する。
【0002】
【従来の技術】
狭心症、心筋梗塞、心不全などの心疾患あるいは脳梗塞、脳出血、クモ膜下出血などの脳血管疾患は、高血圧と非常に深い関係があり、日本人の死因のそれぞれ第二位と第三位を占める。また、厚生省国民生活基礎調査(平成10年度)によれば、高血圧症で通院する患者数は我が国で千人あたり64人であり、病因の第一位を占めている。高血圧の対策としては、利尿薬、交感神経抑制薬、血管拡張薬、アンジオテンシン交換酵素阻害薬などの血圧降下医薬品が挙げられ、これらは主として重症高血圧患者に適用される。それに対して、食事療法、運動療法、飲酒・喫煙の制限などの生活習慣改善を目的とした一般療法は、軽症者から重症者までの高血圧者に広く適用されることから、一般療法の重要性が認識されている。なかでも食習慣の改善は重要であるといわれ、伝承として血圧降下作用を有すると言われる食品は数多く存在する。また従来から食品由来の血圧降下素材の探索が盛んに行われ、血圧降下作用を有する有効成分の分離・同定が数多くなされている。
【0003】
【発明が解決しようとする課題】
本出願人は食物素材の中から血圧降下作用を有する成分を検討し、クロロゲン酸類に優れた血圧降下作用があることを見出した(特許文献1、2)。しかしながら、クロロゲン酸類は、飲食品、特に飲料に配合した場合、苦味や渋味を与えるという問題があった。この苦味や渋味は、飲料において特に著しく、飲料を連続して飲用することが困難であった。
【0004】
【特許文献1】
特開2002−53464号公報
【特許文献2】
特開2002−87977号公報
【0005】
【発明が解決しようとする課題】
従って本発明の目的は、血圧降下作用を有するクロロゲン酸類を高濃度で含有し、かつ味が良好で毎日飲用でき、かつ保存安定性の良好な飲料を提供することにある。
【0006】
【課題を解決するための手段】
そこで本発明者は、クロロゲン酸類に一定量の野菜又は果物由来のフレーバー物質を配合し、かつクロロゲン酸類中のイソクロロゲン酸量を一定範囲に調整すると、渋味や苦味が改善され、フレッシュな味で飲用し易く、かつ長期間安定な飲料が得られることを見出した。
【0007】
すなわち、本発明は、次の成分(a)、(b)及び(c):
(a)イソクロロゲン酸類を含むクロロゲン酸類混合物(ここで、成分(a)中のイソクロロゲン酸類含有重量比率は1/3〜1/20である)   0.05〜10重量%、
(b)野菜又は果物由来のフレーバー物質   0.65〜99重量%、
(c)水   99.3重量%以下
を含有する飲料を提供するものである。
【0008】
【発明の実施の形態】
本発明の飲料に用いられるクロロゲン酸類混合物(成分(a))には、イソクロロゲン酸類、ネオクロロゲン酸、クリプトクロロゲン酸などのクロロゲン酸類及びそれらの誘導体が含まれる。ここで、クロロゲン酸は、キナ酸の5位の水酸基にカフェー酸がエステル結合した5−カフェオイルキナ酸であり、クリプトクロロゲン酸は、キナ酸の4位の水酸基にカフェー酸がエステル結合した4−カフェオイルキナ酸であり、ネオクロロゲン酸は、キナ酸の3位の水酸基にカフェー酸がエステル結合した3−カフェオイルキナ酸である。イソクロロゲン酸は、キナ酸の3位、4位及び5位の水酸基のうちの2つの水酸基にカフェー酸がエステル結合したジカフェオイルキナ酸(例えば3,4−ジカフェオイルキナ酸、3,5−ジカフェオイルキナ酸、4,5−ジカフェオイルキナ酸)である。その他のクロロゲン酸類としては、キナ酸の3位、4位及び5位の水酸基のうちの1つの水酸基にフェルラ酸がエステル結合したフェルリルキナ酸(例えば、5−フェルリルキナ酸)、キナ酸の3位、4位及び5位の水酸基のうちの2つの水酸基にカフェー酸とフェルラ酸がエステル結合したフェルリルカフェオイルキナ酸(例えば3−フェルリル−4−カフェオイルキナ酸)などが挙げられる。また、イソクロロゲン酸、クロロゲン酸等の誘導体としては、塩、糖エステル等の生理学的に許容されるものが挙げられる。このうち、イソクロロゲン酸、クロロゲン酸等の塩としては、ナトリウム塩、カリウム塩、カルシウム塩、マグネシウム塩等のアルカリ金属塩、アルカリ土類金属塩が挙げられる。
【0009】
成分(a)としては、植物抽出物が好ましい。成分(a)は単一植物又は植物の混合物のいずれかから抽出することができる。このうち、シソ、ヒマワリ、ヨモギ、サツマイモ、コーヒー生豆、南天の葉、リンゴ未熟果等の植物体から抽出したものが好ましく、さらにコーヒー生豆抽出物、特にアカネ科コーヒー(Coffea arabica LINNE)の種子より、温時アスコルビン酸、クエン酸酸性水溶液又は熱水で抽出して得られたものが好ましい。また抽出物を利用した成分(a)の化学修飾物をブレンドして使用してもよい。
【0010】
成分(a)中のイソクロロゲン酸量、すなわち成分(a)中のイソクロロゲン酸類含有重量比率は、1/3〜1/20であるが、1/4〜1/15がより好ましく、1/5〜1/10がさらに好ましい。この含有重量比率が1/3を超えると渋味と苦味が十分改善できず、一方、1/20未満だとオリが発生しやすくなり、飲料の安定性が良くない。含有重量比率の調整は、イソクロロゲン酸類の含有量の相違する植物抽出液をブレンドする方法;カラム分離、抽出、化学合成等によるクロロゲン酸類を用い、前記植物抽出物とブレンドする方法;特開平9−9603号記載のように樹脂への吸着・脱着処理等によりクロロゲン酸類を選択的に溶出し、これを前記植物抽出物とブレンドする方法等により行うことができる。
【0011】
本発明飲料中の成分(a)の含有量は、0.05〜10重量%であるが、0.07〜5.0重量%、特に0.10〜1.0重量%が好ましい。成分(a)の含有量が0.05重量%未満では十分な降圧効果が得られず、10重量%を超えると成分(a)による渋味や苦味が強くなる。
【0012】
本発明として用いられる野菜又は果物由来のフレーバー物質(成分(b))のうち、果物由来のフレーバー物質(フルーツフレーバー)としては、種子植物の食用生殖部分、特に種子に伴い甘味果肉を有する部分から得られるフレーバーが挙げられる。具体的には、例えば、オレンジ、ミカン、リンゴ、ブドウ、パイン、ピーチ、グレープフルーツ、レモン、和ナシ、洋ナシ、ウメ、ネーブル、イチゴ、パッションフルーツ、メロン、ライム、グアバ、アンズ、シークワーシャー、カボス、ポンカン、イヨカン、ハッサク、クランベリー、バナナ、スモモ、マンゴー、キウイフルーツ、カキ、アセロラ等から得られるフレーバーが挙げられる。また、フルーツフレーバーという用語は、天然源から得られるフルーツフレーバーを構成するために合成されたフレーバーも含まれる。特に好ましいフルーツフレーバーはオレンジ、レモン、ライム及びグレープフルーツフレーバーを含めたシトラスフレーバーである。アップル、グレープ、チェリー、パイナップル、ココナツ等のフルーツフレーバーも使用可能である。これらのフルーツフレーバーはフルーツジュース及び香油のような天然源から得ても又は合成してもよい。また、オレンジ、レモン、ライム、アップル及びグレープを含めたフルーツジュースもフレーバー成分として使用可能である。これらのフレーバー物質は濃縮物を使用するのが配合上好ましい。
【0013】
また、野菜由来のフレーバー物質としては、野菜の根、葉から得られるフレーバーが挙げられる。野菜フレーバー物質にも、フルーツフレーバー同様合成されたフレーバーも含まれる。具体的には、にんじん、トマト、ジェイレッド(甘藷)、アスパラガス、モロヘイヤ、パセリ、ほうれん草、小松菜、セロリ、キャベツ、ピーマン、ブロッコリー、大根葉、レタス、はくさい、だいこん、しょうが、かぼちゃ、アスパラガス、なす、ビート、クレソン等から得られるフレーバーが好ましい。これらのフレーバー物質も濃縮物を使用するのが配合上好ましい。
【0014】
本発明飲料中の成分(b)の含有量は、0.65〜99重量%であるが、5.0〜99重量%、特に10.0〜99重量%が好ましい。成分(b)が0.65重量%未満だと成分(a)の渋味、苦味改善効果が得られず、99重量%を超えると沈澱を生じやすくなる。
【0015】
本発明飲料には水(成分(c))を99.3重量%以下、好ましくは0.01〜99.3重量%、より好ましくは0.05〜99.3重量%含有する。
【0016】
本発明飲料には、さらにヒドロキシカルボン酸を含有させるのが渋味、苦味改善効果の点で好ましい。当該ヒドロキシカルボン酸としては、分子量60〜300のヒドロキシカルボン酸、例えば乳酸、クエン酸、グルコン酸、グリコール酸、リンゴ酸、酒石酸等が挙げられる。天然物、特に植物中に本来含有されているもの、抽出及び/又は分画の際の化学的処理によって交換したもの、及び化学的修飾を行ったものなども含まれる。この天然物に由来するものとしては、例えば日本農林規格で定められる醸造酢等あるいはその抽出物、果汁、その抽出物等が挙げられる。
【0017】
ヒドロキシカルボン酸は、渋味、苦味改善効果の点で成分(a)に対して5〜30重量倍、さらに、5〜20重量倍、特に5〜15重量倍含有するのが好ましい。またヒドロキシカルボン酸は飲料中に0.25〜15重量%、さらに0.25〜10重量%、特に0.35〜5重量%含有するのが好ましい。
【0018】
本発明の飲料のpHは生理効果を有する成分(a)の長期安定性の点から2〜5、さらに2.5〜5が好ましい。また炭酸飲料とする場合のpHは2.5〜4が好ましい。本発明飲料のpHの調整は食用酸又は有機食用酸の添加によって行われる。使用可能な食用有機酸としては前記ヒドロキシカルボン酸の他、フマル酸、アジピン酸、アスコルビン酸、酢酸又はそれらの混合物が挙げられる。これらの酸はそれらの非解離形でも又はそれら各々の塩としても存在することができる。ここで塩としては、ナトリウム塩、カリウム塩、リチウム塩、カルシウム塩、マグネシウム塩等の薬学上許容される塩が挙げられる。
【0019】
本発明の飲料には、前記成分の他、甘味料、増量剤、乳化剤、エマルション安定剤等を配合することができる。ここで甘味料としては、単糖、2糖甘味料、糖アルコール、無カロリー甘味料等が挙げられる。単糖、2糖類の例としてはスクロース、グルコース、フルクトース、高フルクトースコーンシロップ、転化シロップ、精製シロップ、コーンシロップ、マルトース、高マルトースシロップ及びそれらの混合物が挙げられる。好ましい糖類はスクロース及び高フルクトースコーンシロップである。糖アルコールとしてはソルビトール、マンニトール及びキシリトールが挙げられる。無カロリー甘味料の例としてはアスパルテーム、サッカリン、シクラメート類、アセトスルファム、L−アスパルチル−L−フェニルアラニン低級アルキルエステル甘味料、L−アスパルチル−D−アラニンアミド類(米国特許第4,411,925号)、L−アスパルチル−D−セリンアミド類(米国特許第4,399,163号)、L−アスパルチルヒドロキシメチルアルカンアミド甘味料(米国特許第4,338,346号)、L−アスパルチル−1−ヒドロキシエチルアルカンアミド甘味料(米国特許第4,423,029号)、グリセリン類、合成アルコキシ芳香族等が挙げられる。これらの甘味料は、糖度(Brix)が0.001〜40%、さらに0.01〜30%、特に0.1〜20%となるように配合するのが好ましい。
【0020】
乳化剤及びエマルション安定剤の例としては、臭素化植物油、ロジンエステル、ガム、ペクチン類、セルロース、ポリソルベート類、ソルビタンエステル類及びプロピレングリコールアルギネート類が挙げられる。
【0021】
本発明の飲料は、容器詰飲料とするのが好ましく、例えば成分(a)、(b)、(c)及びその他の成分を混合し、容器に充填し、殺菌して製造することができる。なお殺菌手段は、レトルト殺菌、UHT殺菌のいずれでもよい。
【0022】
本発明の飲料の形態としては、果汁又は野菜汁添加のジュース飲料、炭酸入り清涼飲料等が挙げられる。また容器としては、金属缶、PETボトル、紙パック、チューブパック、ビン等が挙げられる。
【0023】
【実施例】
以下の実施例においてヒドロキシカルボン酸及びクロロゲン酸類の分析は次のようにして行った。
ヒドロキシカルボン酸の分析法
厚生省環境衛生局食品化学課編:“食品中の食品添加物分析法”講談社サイエンティフィク(1998.8.1 第6刷)に準じ、ガスクロマトグラフィー法により定量する。
クロロゲン酸類の分析法
ODS−2逆相カラムを用い、溶離液A(0.05M酢酸 3vol%アセトニトリル水溶液)と溶離液B(0.05M酢酸 100vol%アセトニトリル溶液)にてグラジエントをかけて溶出した。標準品とRTを比較し、同定した。
【0024】
実施例1〜12及び比較例1〜8
表1及び2の組成の容器詰飲料を調製し、下記項目を評価した。
1.味(苦味、渋味、フレッシュ感によるおいしさ)
習熟したパネル10人を選んで官能評価を行った。
この場合、対照としてはクロロゲン酸類を添加していないプラセボ飲料を使用し、香味を評価した。その結果は表1のとおりである。
なお、表1及び2中の評価の点数は、下記の基準で採点(1〜4点)した各パネルの平均点である。(採点基準)渋味、苦味を非常に強く感じる:4点、異味を強く感じる:3点、異味を感じる:2点、異味を若干感じる:1点、異味を感じない:0点
2.おり発生抑制
透明の100mLびんに移し、ふたをしっかりとした後。
80℃に加熱したあと、25℃の部屋に放置徐冷した。
24時間後に、軽く振っておりの発生を評価した。
評点 ○;おりはみられない。
△;やや見られる。
×;はっきりとおりの発生が確認される。
【0025】
【表1】

Figure 2004081207
【0026】
【表2】
Figure 2004081207
【0027】
表1及び2から明らかなように、成分(a)中のイソクロロゲン酸量が1/3よりも多い場合(比較例2)は、味が強く、おりが発生し、一方、当該イソクロロゲン酸量が1/20よりも少ない場合(比較例1、比較例3、5〜8)は、おりが発生し、かつ味も苦い等の異味があり、飲料として適さなかった。
【0028】
これに対し、本発明飲料は、味も良好でかつおりの発生もなく長期間安定であった。
【0029】
実施例13 ゼリー状飲料
ローカストビーンガム0.35重量%、グレープフルーツの50%濃縮果汁30.0重量%、クエン酸0.05重量%、コーヒー豆抽出物(長谷川香料(株)製フレーバーホルダー(クロロゲン酸類混合物30重量%、イソクロロゲン酸:クロロゲン酸類混合物=0.16/1))1.8重量%を混合し、これに水を加えて100重量%に調整し、65℃で溶解した。さらに少量のグレープフルーツフーレバーを添加して85℃で5分間保持して殺菌処理後、100mLの容器に分注した。8時間静置して徐冷しながら5℃に冷却して、ゲル化させ、口に含んだ時に口溶け性が良好で、果実風味を有し食感良好なゼリー状飲料を得た。
【0030】
実施例14 果汁飲料
オレンジ100%果汁 70重量%
人参汁        25重量%
コーヒー豆抽出物(長谷川香料(株)製フレーバーホルダー(実施例5と同じ))            0.45重量%
レモン果汁       1重量%
はちみつ        1.5重量%
香料          0.1重量%
水           1.95重量%
上記組成の飲料は保存安定性も高く、また、風味もよく美味であった。
【0031】
実施例15 果汁飲料
リンゴ100%果汁  97.1重量%
コーヒー豆抽出物(実施例5と同じ) 0.25重量%
レモン果汁       1重量%
はちみつ        1.5重量%
香料          0.15重量%
【0032】
【発明の効果】
本発明によれば、安定した血圧降下作用を有し、かつ味が良好で長期保存安定性の良好な飲料が得られる。[0001]
TECHNICAL FIELD OF THE INVENTION
The present invention relates to a beverage that has a physiological effect such as a blood pressure lowering action, has a good taste, and has good storage stability.
[0002]
[Prior art]
Heart diseases such as angina pectoris, myocardial infarction, and heart failure or cerebrovascular diseases such as cerebral infarction, cerebral hemorrhage, and subarachnoid hemorrhage are very closely related to hypertension. Occupy the rank. According to the Ministry of Health and Welfare Basic Survey on Human Life (1998), the number of patients who go to the hospital for hypertension is 64 per 1,000 in Japan, which is the leading cause of the disease. Antihypertensive measures include antihypertensive drugs such as diuretics, sympathomimetic drugs, vasodilators, and angiotensin exchange enzyme inhibitors, which are mainly applied to patients with severe hypertension. In contrast, general therapies aimed at improving lifestyle, such as diet therapy, exercise therapy, and restriction of drinking and smoking, are widely applied to hypertensive people from mild to severely ill. Has been recognized. Above all, it is said that improving eating habits is important, and there are many foods that are said to have a blood pressure lowering effect as a tradition. Also, search for food-derived blood pressure lowering materials has been actively conducted, and many active ingredients having blood pressure lowering action have been separated and identified.
[0003]
[Problems to be solved by the invention]
The present applicant has examined components having a blood pressure lowering effect from food materials and found that chlorogenic acids have an excellent blood pressure lowering effect (Patent Documents 1 and 2). However, chlorogenic acids have the problem of imparting bitterness and astringency when blended in foods and drinks, especially beverages. The bitterness and astringency are particularly remarkable in beverages, and it is difficult to continuously drink the beverage.
[0004]
[Patent Document 1]
Japanese Patent Application Laid-Open No. 2002-53464 [Patent Document 2]
Japanese Patent Application Laid-Open No. 2002-87977
[Problems to be solved by the invention]
Accordingly, an object of the present invention is to provide a beverage which contains chlorogenic acids having a blood pressure lowering action at a high concentration, has good taste, can be drunk every day, and has good storage stability.
[0006]
[Means for Solving the Problems]
Therefore, the present inventor, by adding a certain amount of flavor substances derived from vegetables or fruits to chlorogenic acids, and adjusting the amount of isochlorogenic acid in the chlorogenic acids to a certain range, astringency and bitterness are improved, fresh taste It has been found that a drink which is easy to drink and stable for a long time can be obtained.
[0007]
That is, the present invention provides the following components (a), (b) and (c):
(A) a mixture of chlorogenic acids containing isochlorogenic acids (where the weight ratio of isochlorogenic acids in component (a) is 1/3 to 1/20) 0.05 to 10% by weight;
(B) 0.65 to 99% by weight of a flavor substance derived from vegetables or fruits;
(C) It provides a beverage containing 99.3% by weight or less of water.
[0008]
BEST MODE FOR CARRYING OUT THE INVENTION
The chlorogenic acids mixture (component (a)) used in the beverage of the present invention includes chlorogenic acids such as isochlorogenic acid, neochlorogenic acid, and cryptochlorogenic acid, and derivatives thereof. Here, chlorogenic acid is 5-caffeoylquinic acid in which caffeic acid is ester-bonded to the 5-hydroxyl group of quinic acid, and cryptochlorogenic acid is 4-caffeic acid in which caffeic acid is ester-bonded to the 4-hydroxyl group of quinic acid. -Caffeoylquinic acid, and neochlorogenic acid is 3-caffeoylquinic acid in which caffeic acid is ester-bonded to the 3-position hydroxyl group of quinic acid. Isochlorogenic acid is dicaffeoylquinic acid in which caffeic acid is ester-bonded to two of the 3-, 4-, and 5-hydroxyl groups of quinic acid (for example, 3,4-dicaffeoylquinic acid, 5-dicaffeoylquinic acid, 4,5-dicaffeoylquinic acid). Other chlorogenic acids include ferulyl quinic acid in which ferulic acid is ester-bonded to one of the hydroxyl groups at the 3-, 4- and 5-positions of quinic acid (for example, 5-ferryl quinic acid), 3-position of quinic acid, Ferulcaffeoylquinic acid (e.g., 3-ferryl-4-caffeoylquinic acid) in which caffeic acid and ferulic acid are ester-bonded to two of the 4- and 5-position hydroxyl groups is exemplified. Derivatives such as isochlorogenic acid and chlorogenic acid include physiologically acceptable derivatives such as salts and sugar esters. Among them, examples of the salt such as isochlorogenic acid and chlorogenic acid include alkali metal salts such as sodium salt, potassium salt, calcium salt and magnesium salt, and alkaline earth metal salts.
[0009]
As the component (a), a plant extract is preferable. Component (a) can be extracted from either a single plant or a mixture of plants. Among them, those extracted from plants such as perilla, sunflower, mugwort, sweet potato, green coffee beans, southern leaves, immature apples and the like are preferable, and further, green coffee bean extracts, in particular, Rubiaceae coffee (Coffea arabica LINEN) Those obtained by extracting with warm ascorbic acid, aqueous citric acid solution or hot water from seeds are preferable. Further, a chemically modified product of the component (a) using the extract may be blended and used.
[0010]
The amount of isochlorogenic acid in the component (a), that is, the weight ratio of isochlorogenic acids in the component (a) is 1/3 to 1/20, preferably 1/4 to 1/15, more preferably 1/15. 5 to 1/10 is more preferable. If the content ratio is more than 1/3, the astringency and bitterness cannot be sufficiently improved, while if it is less than 1/20, the liquor tends to be generated and the stability of the beverage is not good. Adjustment of the content weight ratio is achieved by a method of blending plant extracts having different contents of isochlorogenic acids; a method of blending with plant extracts using chlorogenic acids by column separation, extraction, chemical synthesis, and the like; As described in No. -9603, chlorogenic acids can be selectively eluted by adsorption / desorption treatment to a resin and the like, and the method can be carried out by a method of blending the chlorogenic acids with the plant extract.
[0011]
The content of the component (a) in the beverage of the present invention is 0.05 to 10% by weight, preferably 0.07 to 5.0% by weight, particularly preferably 0.10 to 1.0% by weight. If the content of the component (a) is less than 0.05% by weight, a sufficient pressure-reducing effect cannot be obtained, and if it exceeds 10% by weight, the astringency and bitterness of the component (a) become strong.
[0012]
Among the vegetable or fruit-derived flavor substances (component (b)) used in the present invention, the fruit-derived flavor substance (fruit flavor) includes edible reproductive parts of seed plants, particularly parts having sweet pulp accompanying seeds. And the resulting flavors. Specifically, for example, orange, tangerine, apple, grape, pine, peach, grapefruit, lemon, Japanese pear, pear, plum, navel, strawberry, passion fruit, melon, lime, guava, apricot, sikh washer, Flavors obtained from Cabos, Ponkan, Iyokan, Hassaku, Cranberry, Banana, Plum, Mango, Kiwifruit, Oyster, Acerola and the like. The term fruit flavor also includes flavors that have been synthesized to make up fruit flavors obtained from natural sources. Particularly preferred fruit flavors are citrus flavors, including orange, lemon, lime and grapefruit flavors. Fruit flavors such as apple, grape, cherry, pineapple and coconut can also be used. These fruit flavors may be obtained or synthesized from natural sources such as fruit juices and balms. Fruit juices, including orange, lemon, lime, apple and grape, can also be used as flavor ingredients. It is preferable to use a concentrate of these flavor substances in terms of formulation.
[0013]
The vegetable-derived flavor substances include flavors obtained from vegetable roots and leaves. Vegetable flavor substances also include synthetic flavors as well as fruit flavors. Specifically, carrots, tomatoes, jay red (sweet potatoes), asparagus, moloheiya, parsley, spinach, komatsuna, celery, cabbage, peppers, broccoli, radish leaves, lettuce, hakusai, radish, ginger, pumpkin, asparagus, Flavors obtained from eggplant, beet, watercress and the like are preferred. It is preferable to use a concentrate of these flavor substances in terms of formulation.
[0014]
The content of the component (b) in the beverage of the present invention is from 0.65 to 99% by weight, preferably from 5.0 to 99% by weight, particularly preferably from 10.0 to 99% by weight. If the component (b) is less than 0.65% by weight, the effect of improving the astringency and bitterness of the component (a) cannot be obtained, and if it exceeds 99% by weight, precipitation tends to occur.
[0015]
The beverage of the present invention contains 99.3% by weight or less of water (component (c)), preferably 0.01 to 99.3% by weight, and more preferably 0.05 to 99.3% by weight.
[0016]
It is preferred that the beverage of the present invention further contain a hydroxycarboxylic acid from the viewpoint of an effect of improving astringency and bitterness. Examples of the hydroxycarboxylic acid include hydroxycarboxylic acids having a molecular weight of 60 to 300, such as lactic acid, citric acid, gluconic acid, glycolic acid, malic acid, and tartaric acid. Also included are natural products, particularly those originally contained in plants, those that have been exchanged by chemical treatment during extraction and / or fractionation, and those that have been chemically modified. Examples of those derived from the natural product include brewed vinegar and the like, extracts thereof, fruit juices and the extracts thereof, which are defined by Japanese Agricultural Standards.
[0017]
The hydroxycarboxylic acid is preferably contained in an amount of 5 to 30 times, more preferably 5 to 20 times, especially 5 to 15 times the weight of the component (a) from the viewpoint of improving the astringency and bitterness. Further, the hydroxycarboxylic acid is preferably contained in the beverage in an amount of 0.25 to 15% by weight, more preferably 0.25 to 10% by weight, particularly preferably 0.35 to 5% by weight.
[0018]
The pH of the beverage of the present invention is preferably from 2 to 5, more preferably from 2.5 to 5, from the viewpoint of the long-term stability of the component (a) having a physiological effect. The pH of the carbonated beverage is preferably 2.5 to 4. The pH of the beverage of the present invention is adjusted by adding a food acid or an organic food acid. Usable edible organic acids include fumaric acid, adipic acid, ascorbic acid, acetic acid, and mixtures thereof, in addition to the hydroxycarboxylic acids. These acids can exist in their undissociated form or as their respective salts. Here, examples of the salt include pharmaceutically acceptable salts such as a sodium salt, a potassium salt, a lithium salt, a calcium salt, and a magnesium salt.
[0019]
The beverage of the present invention may contain, in addition to the above components, a sweetener, a bulking agent, an emulsifier, an emulsion stabilizer, and the like. Here, examples of the sweetener include a monosaccharide, a disaccharide sweetener, a sugar alcohol, and a calorie-free sweetener. Examples of monosaccharides and disaccharides include sucrose, glucose, fructose, high fructose corn syrup, invert syrup, refined syrup, corn syrup, maltose, high maltose syrup and mixtures thereof. Preferred sugars are sucrose and high fructose corn syrup. Sugar alcohols include sorbitol, mannitol and xylitol. Examples of calorie-free sweeteners include aspartame, saccharin, cyclamate, acetosulfam, L-aspartyl-L-phenylalanine lower alkyl ester sweetener, L-aspartyl-D-alanineamides (US Pat. No. 4,411,925). L-aspartyl-D-serinamides (U.S. Pat. No. 4,399,163), L-aspartyl hydroxymethylalkaneamide sweetener (U.S. Pat. No. 4,338,346), L-aspartyl-1 -Hydroxyethylalkaneamide sweetener (U.S. Pat. No. 4,423,029), glycerins, synthetic alkoxy aromatics and the like. These sweeteners are preferably blended so that the sugar content (Brix) is 0.001 to 40%, more preferably 0.01 to 30%, and particularly preferably 0.1 to 20%.
[0020]
Examples of emulsifiers and emulsion stabilizers include brominated vegetable oils, rosin esters, gums, pectins, cellulose, polysorbates, sorbitan esters and propylene glycol alginate.
[0021]
The beverage of the present invention is preferably a packaged beverage, and can be produced, for example, by mixing the components (a), (b), (c) and other components, filling the mixture into a container, and sterilizing. The sterilization means may be either retort sterilization or UHT sterilization.
[0022]
Examples of the form of the beverage of the present invention include a juice beverage to which fruit juice or vegetable juice is added, a carbonated soft drink, and the like. Examples of the container include a metal can, a PET bottle, a paper pack, a tube pack, and a bottle.
[0023]
【Example】
In the following examples, analysis of hydroxycarboxylic acids and chlorogenic acids was performed as follows.
Analytical method of hydroxycarboxylic acid Gas chromatography method according to Kodansha Scientific (1998.8.1, 6th edition), "Analytical Method for Food Additives in Food," Ed., Food Chemistry Division, Environmental Health Bureau, Ministry of Health and Welfare Quantified by
Chlorogenic Acid Analysis Using a ODS-2 reverse phase column, elution was performed with a gradient using eluent A (0.05 M acetic acid, 3 vol% acetonitrile aqueous solution) and eluent B (0.05 M acetic acid, 100 vol% acetonitrile solution). RT was compared with a standard product and identified.
[0024]
Examples 1 to 12 and Comparative Examples 1 to 8
A packaged beverage having the composition shown in Tables 1 and 2 was prepared, and the following items were evaluated.
1. Taste (bitterness, astringency, taste due to freshness)
Sensory evaluation was performed by selecting 10 trained panels.
In this case, as a control, a placebo beverage to which no chlorogenic acids were added was used, and the flavor was evaluated. Table 1 shows the results.
The evaluation score in Tables 1 and 2 is the average score of each panel scored (1 to 4 points) based on the following criteria. (Scoring criteria) Very strong astringency and bitterness: 4 points, strong off-taste: 3 points, off-taste: 2 points, slight off-taste: 1 point, no off-taste: 0 point After transferring to a clear 100 mL bottle with a lid, the lid is firmly closed.
After heating to 80 ° C, it was left to cool slowly in a room at 25 ° C.
Twenty-four hours later, the occurrence of light shaking was evaluated.
Rating ○: No origami is observed.
Δ: Somewhat seen.
×: Clear occurrence is confirmed.
[0025]
[Table 1]
Figure 2004081207
[0026]
[Table 2]
Figure 2004081207
[0027]
As is clear from Tables 1 and 2, when the amount of isochlorogenic acid in the component (a) is more than 1/3 (Comparative Example 2), the taste is strong and a scent is generated. When the amount was less than 1/20 (Comparative Example 1, Comparative Examples 3, 5 to 8), a cage was generated and the taste had a bitter taste such as bitterness, and was not suitable as a beverage.
[0028]
On the other hand, the beverage of the present invention had good taste and was stable for a long time without occurrence of cage.
[0029]
Example 13 Jelly-like beverage Locust bean gum 0.35% by weight, grapefruit 50% concentrated fruit juice 30.0% by weight, citric acid 0.05% by weight, coffee bean extract (flavor holder manufactured by Hasegawa Koryo Co., Ltd. (chlorogen 30% by weight of an acid mixture and isochlorogenic acid: a mixture of chlorogenic acids = 0.16 / 1)) 1.8% by weight were mixed, and water was added thereto to adjust to 100% by weight, and the mixture was dissolved at 65 ° C. Further, a small amount of grapefruit fulever was added, sterilized by keeping at 85 ° C. for 5 minutes, and then dispensed into 100 mL containers. The mixture was allowed to stand for 8 hours and cooled to 5 ° C. while gradually cooling to form a gel, and a jelly-like beverage having a good mouth-melting property, a fruity flavor, and a good texture when contained in the mouth was obtained.
[0030]
Example 14 Juice Drink Orange 100% Juice 70% by Weight
Carrot juice 25% by weight
0.45% by weight of coffee bean extract (flavor holder (same as in Example 5) manufactured by Hasegawa Koryo Co., Ltd.)
Lemon juice 1% by weight
1.5% by weight honey
0.1% by weight of fragrance
1.95% by weight of water
The beverage having the above composition had high storage stability, and had good flavor and taste.
[0031]
Example 15 Juice Drink Apple 100% Juice 97.1% by Weight
Coffee bean extract (same as in Example 5) 0.25% by weight
Lemon juice 1% by weight
1.5% by weight honey
Spice 0.15% by weight
[0032]
【The invention's effect】
ADVANTAGE OF THE INVENTION According to this invention, the drink which has a stable blood pressure lowering effect, a favorable taste, and favorable long-term storage stability is obtained.

Claims (4)

次の成分(a)、(b)及び(c):
(a)イソクロロゲン酸類を含むクロロゲン酸類混合物(ここで、成分(a)中のイソクロロゲン酸類含有重量比率は1/3〜1/20である)   0.05〜10重量%、
(b)野菜又は果物由来のフレーバー物質   0.65〜99重量%、
(c)水   99.3重量%以下
を含有する飲料。
The following components (a), (b) and (c):
(A) a mixture of chlorogenic acids containing isochlorogenic acids (where the weight ratio of isochlorogenic acids in component (a) is 1/3 to 1/20) 0.05 to 10% by weight;
(B) 0.65-99% by weight of a flavor substance derived from vegetables or fruits;
(C) A beverage containing 99.3% by weight or less of water.
成分(b)が、果物由来のフレーバー物質である請求項1記載の飲料。The beverage according to claim 1, wherein the component (b) is a fruit-derived flavor substance. 成分(a)が、植物抽出物である請求項1又は2記載の飲料。The beverage according to claim 1 or 2, wherein the component (a) is a plant extract. 容器詰飲料である請求項1〜3のいずれか1項記載の飲料。The beverage according to any one of claims 1 to 3, which is a packaged beverage.
JP2003180454A 2002-06-28 2003-06-25 Beverage Expired - Lifetime JP3769268B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2003180454A JP3769268B2 (en) 2002-06-28 2003-06-25 Beverage

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2002190690 2002-06-28
JP2003180454A JP3769268B2 (en) 2002-06-28 2003-06-25 Beverage

Publications (2)

Publication Number Publication Date
JP2004081207A true JP2004081207A (en) 2004-03-18
JP3769268B2 JP3769268B2 (en) 2006-04-19

Family

ID=32071833

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003180454A Expired - Lifetime JP3769268B2 (en) 2002-06-28 2003-06-25 Beverage

Country Status (1)

Country Link
JP (1) JP3769268B2 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005306793A (en) * 2004-04-22 2005-11-04 Maruzen Pharmaceut Co Ltd Ampelopsis extract composition, ampelopsis extract-containing food/drink, and method for ameliorating taste of ampelopsis extract
JP2006042624A (en) * 2004-08-02 2006-02-16 Ajinomoto General Foods Inc Chlorogenic acid-containing beverage
JP2009165498A (en) * 2009-05-07 2009-07-30 Ajinomoto General Foods Inc Beverage containing chlorogenic acid
US8263149B2 (en) 2005-07-29 2012-09-11 Kao Corporation Container-packed milk coffee beverage
US8282973B2 (en) 2005-07-29 2012-10-09 Kao Corporation Container-packed milk coffee beverage
US9055753B2 (en) 2005-07-29 2015-06-16 Kao Corporation Container-packed black coffee beverage

Citations (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07285876A (en) * 1993-12-06 1995-10-31 Nikka Uisukii Kk Fruit polyphenols and methods for producing the same, antioxidants, antihypertensive agents, antimutagenic agents, allergy suppressants, anticaries agents and deodorants
JPH0823939A (en) * 1994-07-14 1996-01-30 Sanei Gen F F I Inc Preventing agent for flavor of beverage from deteriorating and prevention of flavor of beverage from deteriorating
JPH08319433A (en) * 1995-05-29 1996-12-03 Nikka Uisukii Kk Apple red pigment and its manufacturing method, antioxidant, antihypertensive agent, allergy suppressant, anticaries agent and deodorant
JPH09143465A (en) * 1995-11-21 1997-06-03 Dainippon Ink & Chem Inc Antioxidant composition
JP2000063827A (en) * 1998-08-26 2000-02-29 Dainippon Ink & Chem Inc Method for producing antioxidant
JP2000270807A (en) * 1999-01-22 2000-10-03 Sanei Gen Ffi Inc Fading preventing agent for anthocyanin-based coloring matter and food containing the same
JP2000342219A (en) * 1999-06-02 2000-12-12 Sanei Gen Ffi Inc Pigment discoloration-preventing agent and food containing the same
JP2002047196A (en) * 1993-12-06 2002-02-12 Nikka Whisky Distilling Co Ltd Fruit polyphenols, antioxidants, antihypertensives, anti-mutagenic agents, allergy inhibitors, anti-carious agents and deodorants
JP2002053464A (en) * 2000-08-07 2002-02-19 Kao Corp Antihypertensive agent
JP2002080357A (en) * 2000-09-05 2002-03-19 Kao Corp Hypertension prevention / amelioration / treatment agent
JP2002095450A (en) * 2000-09-22 2002-04-02 Asahi Soft Drinks Co Ltd Beverages containing apple polyphenols
JP2002154977A (en) * 2000-09-05 2002-05-28 Kao Corp Food composition
JP2002233333A (en) * 2001-02-09 2002-08-20 Umai Kk Polyphenol-containing food
JP2002255803A (en) * 2001-03-05 2002-09-11 Nippon Menaade Keshohin Kk Phototoxicity inhibitor comprising extract from tussilago farfara l.
JP2002308766A (en) * 2001-04-13 2002-10-23 Kao Corp Prophylactic and ameliorative agent for life style- related diseases
JP2003079335A (en) * 2001-09-12 2003-03-18 Ogawa & Co Ltd Food flavor determination inhibitor and inhibition method
JP2003137803A (en) * 2001-10-30 2003-05-14 Ryuukyuu Cement Kk Medicine containing cane sugar polyphenol-containing material as active ingredient, and its use
JP2003261444A (en) * 2002-03-06 2003-09-16 Kao Corp Vascular endothelial function improver
JP2004033023A (en) * 2002-06-28 2004-02-05 Kao Corp Beverage
JP2005506353A (en) * 2001-10-15 2005-03-03 ルドルフ ヴィルト ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディトゲゼルシャフト Concentrate, method for producing the same, and method of using the concentrate

Patent Citations (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002047196A (en) * 1993-12-06 2002-02-12 Nikka Whisky Distilling Co Ltd Fruit polyphenols, antioxidants, antihypertensives, anti-mutagenic agents, allergy inhibitors, anti-carious agents and deodorants
JPH07285876A (en) * 1993-12-06 1995-10-31 Nikka Uisukii Kk Fruit polyphenols and methods for producing the same, antioxidants, antihypertensive agents, antimutagenic agents, allergy suppressants, anticaries agents and deodorants
JPH0823939A (en) * 1994-07-14 1996-01-30 Sanei Gen F F I Inc Preventing agent for flavor of beverage from deteriorating and prevention of flavor of beverage from deteriorating
JPH08319433A (en) * 1995-05-29 1996-12-03 Nikka Uisukii Kk Apple red pigment and its manufacturing method, antioxidant, antihypertensive agent, allergy suppressant, anticaries agent and deodorant
JPH09143465A (en) * 1995-11-21 1997-06-03 Dainippon Ink & Chem Inc Antioxidant composition
JP2000063827A (en) * 1998-08-26 2000-02-29 Dainippon Ink & Chem Inc Method for producing antioxidant
JP2000270807A (en) * 1999-01-22 2000-10-03 Sanei Gen Ffi Inc Fading preventing agent for anthocyanin-based coloring matter and food containing the same
JP2000342219A (en) * 1999-06-02 2000-12-12 Sanei Gen Ffi Inc Pigment discoloration-preventing agent and food containing the same
JP2002053464A (en) * 2000-08-07 2002-02-19 Kao Corp Antihypertensive agent
JP2002154977A (en) * 2000-09-05 2002-05-28 Kao Corp Food composition
JP2002080357A (en) * 2000-09-05 2002-03-19 Kao Corp Hypertension prevention / amelioration / treatment agent
JP2002095450A (en) * 2000-09-22 2002-04-02 Asahi Soft Drinks Co Ltd Beverages containing apple polyphenols
JP2002233333A (en) * 2001-02-09 2002-08-20 Umai Kk Polyphenol-containing food
JP2002255803A (en) * 2001-03-05 2002-09-11 Nippon Menaade Keshohin Kk Phototoxicity inhibitor comprising extract from tussilago farfara l.
JP2002308766A (en) * 2001-04-13 2002-10-23 Kao Corp Prophylactic and ameliorative agent for life style- related diseases
JP2003079335A (en) * 2001-09-12 2003-03-18 Ogawa & Co Ltd Food flavor determination inhibitor and inhibition method
JP2005506353A (en) * 2001-10-15 2005-03-03 ルドルフ ヴィルト ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディトゲゼルシャフト Concentrate, method for producing the same, and method of using the concentrate
JP2003137803A (en) * 2001-10-30 2003-05-14 Ryuukyuu Cement Kk Medicine containing cane sugar polyphenol-containing material as active ingredient, and its use
JP2003261444A (en) * 2002-03-06 2003-09-16 Kao Corp Vascular endothelial function improver
JP2004033023A (en) * 2002-06-28 2004-02-05 Kao Corp Beverage

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005306793A (en) * 2004-04-22 2005-11-04 Maruzen Pharmaceut Co Ltd Ampelopsis extract composition, ampelopsis extract-containing food/drink, and method for ameliorating taste of ampelopsis extract
JP2006042624A (en) * 2004-08-02 2006-02-16 Ajinomoto General Foods Inc Chlorogenic acid-containing beverage
US8263149B2 (en) 2005-07-29 2012-09-11 Kao Corporation Container-packed milk coffee beverage
US8282973B2 (en) 2005-07-29 2012-10-09 Kao Corporation Container-packed milk coffee beverage
US9055753B2 (en) 2005-07-29 2015-06-16 Kao Corporation Container-packed black coffee beverage
JP2009165498A (en) * 2009-05-07 2009-07-30 Ajinomoto General Foods Inc Beverage containing chlorogenic acid

Also Published As

Publication number Publication date
JP3769268B2 (en) 2006-04-19

Similar Documents

Publication Publication Date Title
JP6659891B2 (en) Rebaudioside sweetener composition and food product imparted with sweetness using the rebaudioside sweetener composition
DE69434354T2 (en) sweeteners
JP4324761B2 (en) Carbonated drink
JP3498505B2 (en) Acidic beverage
KR101057287B1 (en) beverage
JP2010521174A (en) Beverages sweetened with rebaudioside A, erythritol, and D-tagatose
JP2012143254A (en) Long-chain fatty acid for reducing off-taste of non-nutritive sweetener
JP2010521171A (en) Beverages sweetened with non-nutritive sweetener along with coconut milk
JP4838669B2 (en) Flavor improving agent, flavor improving method using the same, and food and drink
JP2019528732A (en) Compositions and methods for improving the taste of non-nutritive sweeteners
JP2004073197A (en) Sweetening composition and food containing the same
JP3662555B2 (en) Beverage
JP6291317B2 (en) Flavor improver, perfume composition and food and drink containing these
JP2001095541A (en) Bitter carbonated drink
JP4667514B2 (en) Chlorogenic acid-containing beverage
JP3769268B2 (en) Beverage
JP2001299264A (en) Flavor improving agent
JP2017500050A (en) Control of bitterness and mouthfeel by synergistic mixtures of long chain fatty acids
TW201831095A (en) Sweetness enhancer and flavor composition for enhancing sweetness
JP2006042624A (en) Chlorogenic acid-containing beverage
JP6839629B2 (en) Food and drink containing spinach juice
JP2013226128A (en) Vegetable beverage packed in container, manufacturing method and harsh taste reducing method for vegetable beverage
JP4943770B2 (en) Container drink
US20230013964A1 (en) Rare Sugars in Food and Beverage Products
KR20100047951A (en) Preparation method of beverage comprising extracts of c. tora and the beverage composition

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20040914

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20060120

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20060131

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20060203

R151 Written notification of patent or utility model registration

Ref document number: 3769268

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R151

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100210

Year of fee payment: 4

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100210

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110210

Year of fee payment: 5

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120210

Year of fee payment: 6

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120210

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130210

Year of fee payment: 7

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20140210

Year of fee payment: 8

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

EXPY Cancellation because of completion of term