JP7112040B1 - Beverages containing placenta and iron - Google Patents
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- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
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- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
- A23L2/66—Proteins
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/70—Clarifying or fining of non-alcoholic beverages; Removing unwanted matter
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/16—Inorganic salts, minerals or trace elements
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/16—Inorganic salts, minerals or trace elements
- A23L33/165—Complexes or chelates
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/17—Amino acids, peptides or proteins
- A23L33/18—Peptides; Protein hydrolysates
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
- A61K35/48—Reproductive organs
- A61K35/50—Placenta; Placental stem cells; Amniotic fluid; Amnion; Amniotic stem cells
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- 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
- A61K47/02—Inorganic compounds
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- 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
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- 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
- A61K47/22—Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
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- 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
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/42—Proteins; Polypeptides; Degradation products thereof; Derivatives thereof, e.g. albumin, gelatin or zein
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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
- A61K9/08—Solutions
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
Abstract
本発明は、動物プラセンタエキス由来の沈殿生成を抑制した、炭水化物含有量の少ない飲料を提供することを課題とする。当該課題を解決した本発明の飲料は、動物プラセンタエキス、及び鉄化合物を含有し、炭水化物含有量が40w/v%以下であることを特徴とする。An object of the present invention is to provide a beverage containing less carbohydrates, in which precipitation derived from animal placenta extract is suppressed. The beverage of the present invention, which has solved the problem, is characterized by containing an animal placenta extract and an iron compound and having a carbohydrate content of 40 w/v % or less.
Description
本発明は、動物プラセンタエキスを含有する飲料に関し、医薬品、医薬部外品及び食品等の分野において利用されうる。 INDUSTRIAL APPLICABILITY The present invention relates to beverages containing animal placenta extracts, and can be used in fields such as pharmaceuticals, quasi-drugs and foods.
近年、動物プラセンタエキスを配合した飲料やサプリメントの人気が高まっている。動物プラセンタエキスはブタ、ウシ、ウマ、ヒト又はヒツジなどの哺乳動物の胎盤から抽出されたエキスである。哺乳動物の胎盤組織には、胎児の成長に不可欠な栄養素であるアミノ酸、活性ペプチド、ビタミン、ミネラル、糖類、酵素、核酸などが豊富に蓄えられており、前記哺乳動物の胎盤から抽出されたエキスをプラセンタエキスという(特許文献1)。動物プラセンタエキスは特有の味やにおいを有しているため、飲料として摂取する際のマスキング技術が報告されている(特許文献2)。 In recent years, the popularity of beverages and supplements containing animal placenta extracts has increased. Animal placenta extract is an extract extracted from the placenta of mammals such as porcine, bovine, equine, human or ovine. Placental tissues of mammals are rich in nutrients essential for fetal growth, such as amino acids, active peptides, vitamins, minerals, sugars, enzymes, nucleic acids, etc. Extracts extracted from the placenta of mammals. is called placenta extract (Patent Document 1). Since the animal placenta extract has a unique taste and smell, a masking technique has been reported when ingesting it as a beverage (Patent Document 2).
健康意識の高い消費者にとって、砂糖や果糖ぶどう糖液糖のような炭水化物を多く含んだ製品は好ましくない。そこで本発明者らは、動物プラセンタエキスを配合し、かつ、炭水化物の含有量の少ない飲料を調製したところ、沈殿が生成することを発見した。外観や舌触りといった商品性の観点から、沈殿の生成は少しでも抑制されるべきであるが、今までに、動物プラセンタエキスを炭水化物の含有量の少ない飲料に配合した際の、動物プラセンタエキス由来の沈殿生成を抑制する方法については報告されていない。 For health-conscious consumers, products containing a lot of carbohydrates, such as sugar and fructose corn syrup, are not desirable. Accordingly, the present inventors have found that precipitation occurs when a beverage containing animal placenta extract and containing a small amount of carbohydrates is prepared. From the viewpoint of marketability such as appearance and texture, the formation of precipitates should be suppressed as much as possible. No method for suppressing precipitation has been reported.
本発明の目的は、動物プラセンタエキス由来の沈殿生成を抑制した、炭水化物含有量の少ない飲料を提供することである。 SUMMARY OF THE INVENTION An object of the present invention is to provide a beverage with a low carbohydrate content that suppresses the formation of precipitates derived from animal placenta extracts.
本発明者らは、この問題を解決すべく鋭意検討を重ねた結果、意外にも、鉄化合物を配合すると沈殿生成を抑制できることを見出し、本発明を完成するに至った。また、鉄化合物とコラーゲンペプチドを配合すると、沈殿生成抑制効果が一層高まることを見出し、本発明を完成するに至った。 The inventors of the present invention conducted intensive studies to solve this problem, and unexpectedly found that the addition of an iron compound could suppress the formation of precipitates, and completed the present invention. In addition, the present inventors have found that the effect of inhibiting the formation of precipitates is further enhanced by blending an iron compound and a collagen peptide, and have completed the present invention.
かかる知見により得られた本発明の態様は次のとおりである。
(1)動物プラセンタエキス、及び鉄化合物を含有し、炭水化物含有量が40w/v%以下である飲料、
(2)さらにコラーゲンペプチドを含有する(1)に記載の飲料、
(3)鉄化合物の含有量が、鉄換算で0.0002~0.2w/v%である(1)に記載の飲料、
(4)鉄化合物が、フマル酸第一鉄、塩化第二鉄、クエン酸鉄、クエン酸鉄アンモニウム、クエン酸第一鉄ナトリウム、グルコン酸第一鉄、乳酸鉄、ピロリン酸第一鉄、ピロリン酸第二鉄、硫酸第一鉄およびヘム鉄からなる群から選ばれる少なくとも1種である(1)~(3)に記載の飲料、
(5)動物プラセンタエキスの含有量が、0.001~4w/v%である(1)~(4)に記載の飲料、
(6)動物プラセンタエキスの含有量が、胎盤換算で0.025~100w/v%である(1)~(5)に記載の飲料、
(7)コラーゲンペプチドの含有量が、0.02~20w/v%である(2)~(6)に記載の飲料、
(8)pHが2.5~4.5である(1)~(7)に記載の飲料、
(9)飲料が、液体飲料である(1)~(8)に記載の飲料、
(10)動物プラセンタエキスを含有する飲料において、鉄化合物を配合することを特徴とする沈殿生成抑制方法、
(11)動物プラセンタエキスを含有する飲料において、鉄化合物及びコラーゲンペプチドを特徴とする沈殿生成抑制方法、
である。The aspects of the present invention obtained from such findings are as follows.
(1) a beverage containing an animal placenta extract and an iron compound and having a carbohydrate content of 40 w/v% or less;
(2) the beverage according to (1), which further contains collagen peptide;
(3) The beverage according to (1), wherein the iron compound content is 0.0002 to 0.2 w/v% in terms of iron,
(4) Iron compounds include ferrous fumarate, ferric chloride, iron citrate, ammonium ferric citrate, sodium ferrous citrate, ferrous gluconate, iron lactate, ferrous pyrophosphate, pyroline The beverage according to (1) to (3), which is at least one selected from the group consisting of ferric acid, ferrous sulfate and heme iron,
(5) The beverage according to (1) to (4), wherein the content of the animal placenta extract is 0.001 to 4 w/v%;
(6) The beverage according to (1) to (5), wherein the content of the animal placenta extract is 0.025 to 100 w/v% in terms of placenta;
(7) The beverage according to (2) to (6), wherein the content of collagen peptide is 0.02 to 20 w/v%,
(8) The beverage according to (1) to (7) having a pH of 2.5 to 4.5,
(9) The beverage according to (1) to (8), which is a liquid beverage,
(10) A method for suppressing precipitate formation, which comprises adding an iron compound to a beverage containing an animal placenta extract,
(11) A method for inhibiting precipitate formation in a beverage containing an animal placenta extract, characterized by an iron compound and a collagen peptide,
is.
本発明により、動物プラセンタエキスを配合し、沈殿生成が抑制された炭水化物含有量の少ない飲料を提供することが可能となった。 INDUSTRIAL APPLICABILITY According to the present invention, it has become possible to provide a beverage with a low carbohydrate content in which an animal placenta extract is blended and precipitation is suppressed.
本発明に用いる動物プラセンタエキスの原料である動物プラセンタは、特に限定されないが、例えば、適正に農場にて飼育された健康な動物の満期出産時に後産として得られる食用の胎盤で、子宮などの外的器官を含んでいないものや、魚などの卵巣膜に含まれる海洋性のプラセンタ様物質のことである。また、その起源についても特に限定されず、例えばヒト、牛、豚、馬、羊、鮭などが挙げられるが、好ましくは豚、馬、鮭であり、より好ましくは豚である。
動物プラセンタエキスの形態は特に制限されるものではなく、例えば、酵素分解、塩酸分解などの方法により分解後、抽出工程を経て得られた液体やペーストであり、凍結乾燥、噴霧乾燥などの方法により、水分を除去した粉末状のものであってもよい。The animal placenta, which is the raw material of the animal placenta extract used in the present invention, is not particularly limited. It is a marine placenta-like substance contained in the ovarian membranes of fish and the like that does not contain external organs. Also, the origin is not particularly limited, and examples thereof include humans, cattle, pigs, horses, sheep, and salmon. Pigs, horses, and salmon are preferred, and pigs are more preferred.
The form of animal placenta extract is not particularly limited. , it may be in the form of powder from which moisture has been removed.
本発明の動物プラセンタエキスは、市販品を用いてもよく、例えば、「豚プラセンタエキスAL-20」((株)三共バイオケミカルズ製)、「馬プラセンタエキスAL-20」((株)三共バイオケミカルズ製)、「食品用馬プラセンタエキス末(HPA)((株)ダード製)」「プラセンタエキスP-F」(一丸ファルコス(株)製)、「プラセンタパウダーT-100」(一丸ファルコス(株)製)、「P-プラセンタエキスG」(日本ハム(株)製)、「P-プラセンタリキッド」(日本ハム(株)製)、「P-プラセンタエキス」(日本ハム(株)製)、「SPFプラセンタT-AS」(東洋酵素化学(株)製)、「SPFプラセンタT-100S」(東洋酵素化学(株)製)「マリンプラセンタ(MP)(登録商標、(株)日本バリアフリー製)」等が挙げられる。 As the animal placenta extract of the present invention, commercially available products may be used. Chemicals), “Horse Placenta Extract Powder (HPA) for Food (Dard Co., Ltd.)”, “Placenta Extract P-F” (Ichimaru Pharcos Co., Ltd.), “Placenta Powder T-100” (Ichimaru Pharcos Co., Ltd.) ), “P-Placenta Extract G” (manufactured by Nippon Ham Co., Ltd.), “P-Placenta Liquid” (manufactured by Nippon Ham Co., Ltd.), “P-Placenta Extract” (manufactured by Nippon Ham Co., Ltd.), “SPF Placenta T-AS” (manufactured by Toyo Enzyme Chemical Co., Ltd.), “SPF Placenta T-100S” (manufactured by Toyo Enzyme Chemical Co., Ltd.) “Marine Placenta (MP) (registered trademark, manufactured by Japan Barrier Free Co., Ltd.) )” and the like.
本発明の動物プラセンタエキスの含有量は、本発明の飲料中、0.001~4w/v%が好ましく、0.01~2w/v%がより好ましく、0.02~2w/v%がさらに好ましい。また、胎盤換算量で0.025~100w/v%が好ましく、0.25~50w/v%がより好ましい。ここで「胎盤換算量」とは、プラセンタエキスを得るために必要な胎盤量である。
プラセンタエキスの含有量は、本発明の効果の点から、後述する鉄化合物(鉄換算)で鉄1質量部に対して0.005~20000質量部が好ましく、0.025~2000質量部がより好ましく、0.5~1000質量部がさらに好ましく、10~200質量部が特に好ましい。また、胎盤換算では、鉄化合物(鉄換算)1質量部に対して0.125~500000質量部が好ましく、0.625~50000質量部がより好ましく、12.5~25000質量部が最も好ましい。The content of the animal placenta extract of the present invention is preferably 0.001 to 4 w/v%, more preferably 0.01 to 2 w/v%, and further preferably 0.02 to 2 w/v% in the beverage of the present invention. preferable. In addition, the amount in terms of placenta is preferably 0.025 to 100 w/v%, more preferably 0.25 to 50 w/v%. Here, the "placental equivalent amount" is the amount of placenta required to obtain the placenta extract.
From the viewpoint of the effect of the present invention, the content of the placenta extract is preferably 0.005 to 20000 parts by mass, more preferably 0.025 to 2000 parts by mass, relative to 1 part by mass of iron in terms of the iron compound (calculated as iron) described later. It is preferably 0.5 to 1000 parts by mass, and particularly preferably 10 to 200 parts by mass. In terms of placenta, 0.125 to 500,000 parts by mass is preferable, 0.625 to 50,000 parts by mass is more preferable, and 12.5 to 25,000 parts by mass is most preferable with respect to 1 part by mass of the iron compound (as iron).
本発明において「鉄化合物」としては、二価の鉄化合物及び三価の鉄化合物のいずれでもよく、例えばフマル酸第一鉄、塩化第二鉄、クエン酸鉄、クエン酸鉄アンモニウム、クエン酸第一鉄ナトリウム、グルコン酸第一鉄、乳酸鉄、ピロリン酸第一鉄、ピロリン酸第二鉄、硫酸第一鉄およびヘム鉄を挙げることができる。鉄化合物のみで沈殿生成を抑制する場合は、塩化第二鉄、クエン酸鉄、クエン酸鉄アンモニウム及びピロリン酸第二鉄等の三価の鉄化合物が好ましい。 In the present invention, the "iron compound" may be either a divalent iron compound or a trivalent iron compound. Mention may be made of sodium monoferrous, ferrous gluconate, iron lactate, ferrous pyrophosphate, ferric pyrophosphate, ferrous sulfate and heme iron. When suppressing precipitation with only an iron compound, trivalent iron compounds such as ferric chloride, iron citrate, ferric ammonium citrate and ferric pyrophosphate are preferred.
鉄化合物の含有量は、本発明の飲料中、鉄換算で0.0002~0.2w/v%が好ましく、0.001~0.1w/v%がより好ましく、0.002~0.04w/v%がさらに好ましい。また、鉄化合物としては、0.001~2.0w/v%が好ましく、0.005~1.2w/v%がより好ましく、0.01~0.5w/v%がさらに好ましい。また、風味の点から、鉄化合物の含有量は、本発明の飲料中、鉄換算としては上限値は0.2w/v%が好ましく、0.1w/v%がより好ましく、0.04w/v%が最も好ましい。 The content of the iron compound in the beverage of the present invention is preferably 0.0002 to 0.2 w/v% in terms of iron, more preferably 0.001 to 0.1 w/v%, and 0.002 to 0.04 w /v % is more preferred. The iron compound is preferably 0.001 to 2.0 w/v%, more preferably 0.005 to 1.2 w/v%, even more preferably 0.01 to 0.5 w/v%. In terms of flavor, the content of the iron compound in the beverage of the present invention, in terms of iron, is preferably 0.2 w/v%, more preferably 0.1 w/v%, and 0.04 w/v%. v% is most preferred.
また、本発明の飲料における鉄化合物の含有量は、好ましくは一回の経口摂取量当たり、鉄換算で、1mg~20mgがより好ましい。また、一回の経口摂取量とは、本発明の飲料が一度に経口摂取される量であり、例えば、30~200ml、典型的には30ml、50ml、100ml、150ml、200mlがその量であり、ゼリー状の形態である場合には、例えば15~200g、典型的には15g、30g、50g、100g、150g、150g、200gがその量である。また、経口液体用容器又は飲料用容器の形態は特に限定されない。容器の容量は特に限定されないが、例えば30ml~200ml(典型的には50ml、100ml、150ml、又は200ml)とすることができる。 Further, the content of the iron compound in the beverage of the present invention is more preferably 1 mg to 20 mg in terms of iron per oral intake. In addition, the amount of oral intake at one time is the amount of the beverage of the present invention that is orally ingested at one time, for example, 30 to 200 ml, typically 30 ml, 50 ml, 100 ml, 150 ml, and 200 ml. , in the form of jelly, the amount is, for example, 15 to 200 g, typically 15 g, 30 g, 50 g, 100 g, 150 g, 150 g, 200 g. Moreover, the form of the container for oral liquids or the container for beverages is not particularly limited. The capacity of the container is not particularly limited, but can be, for example, 30 ml to 200 ml (typically 50 ml, 100 ml, 150 ml, or 200 ml).
本発明の飲料は、炭水化物の含有量0~40w/v%であり、より好ましくは0~20w/v%であり、さらに好ましくは0~15%w/v%であり、特に好ましくは0~10w/v%である。「炭水化物」としては、砂糖、異性化糖、果糖、果糖ぶどう糖液糖、ぶどう糖果糖液糖、はちみつ、水飴、粉飴、マルトデキストリン、ソルビトール、マルチトール、還元水飴、マルトース、トレハロース、黒糖等や、クエン酸やリンゴ酸等の有機酸が挙げられる。 The beverage of the present invention has a carbohydrate content of 0 to 40 w/v%, more preferably 0 to 20 w/v%, still more preferably 0 to 15% w/v%, particularly preferably 0 to 10 w/v%. "Carbohydrates" include sugar, isomerized sugar, fructose, high-fructose corn syrup, high-fructose corn syrup, honey, starch syrup, powdered syrup, maltodextrin, sorbitol, maltitol, reduced starch syrup, maltose, trehalose, brown sugar, etc. Organic acids such as citric acid and malic acid are included.
また、本発明の飲料のカロリーは、0~150kcal/100mlが好ましく、より好ましくは0~100kcal/100ml、さらにより好ましくは0~70kcal/100mlである。 The calorie content of the beverage of the present invention is preferably 0-150 kcal/100 ml, more preferably 0-100 kcal/100 ml, and even more preferably 0-70 kcal/100 ml.
本発明において「コラーゲンペプチド」とは、その起源は特に限定されず、合成であってもよく、牛や豚等の家畜や魚を加工する際に副生する皮、骨、靭帯、腱、軟骨等から抽出して製造されるコラーゲンペプチドであってもよいが、豚および魚由来のコラーゲンペプチドが好ましい。コラーゲンタンパク質を酵素や化学的処理等により分解して得られるコラーゲンペプチドが好ましい。
コラーゲンペプチドの平均分子量としては、特に限定されないが、500~50000であることが好ましく、1000~25000であることがより好ましい。本発明のコラーゲンペプチドは、市販品を用いてもよく、例えば「ニッピペプタイドPS-1」(登録商標、(株)ニッピ製)、「ニッピペプタイドPRA-P」(登録商標、(株)ニッピ製)、「ニッピペプタイドFCP-EX」(登録商標、(株)ニッピ製)、「HACP-CF」(ゼライス(株)製)、「HACP-TF」(ゼライス(株)製)、「コラペプPU」(登録商標、新田ゼラチン(株)製)、「コラペプJB」(登録商標、新田ゼラチン(株)製)、「HDL-50SP」(新田ゼラチン(株)製)、「SCP-3100」(新田ゼラチン(株)製)、「peptan P2000HD」(ルスロ(株)製)等が挙げられる。In the present invention, the "collagen peptide" is not particularly limited in its origin, may be synthetic, and is a by-product of processing livestock such as cattle and pigs and fish, skin, bone, ligament, tendon, and cartilage. Although it may be a collagen peptide produced by extracting it from, etc., collagen peptides derived from pigs and fish are preferred. Collagen peptides obtained by enzymatically or chemically degrading collagen proteins are preferred.
Although the average molecular weight of the collagen peptide is not particularly limited, it is preferably from 500 to 50,000, more preferably from 1,000 to 25,000. Collagen peptides of the present invention may be commercially available products, such as "Nippi Peptide PS-1" (registered trademark, manufactured by Nippi Co., Ltd.), "Nippi Peptide PRA-P" (registered trademark, manufactured by Nippi Co., Ltd.). ), “Nippi Peptide FCP-EX” (registered trademark, manufactured by Nippi Co., Ltd.), “HACP-CF” (manufactured by Zerais Co., Ltd.), “HACP-TF” (manufactured by Zerais Co., Ltd.), “Corapep PU” (registered trademark, manufactured by Nitta Gelatin Co., Ltd.), "Corapep JB" (registered trademark, manufactured by Nitta Gelatin Co., Ltd.), "HDL-50SP" (manufactured by Nitta Gelatin Co., Ltd.), "SCP-3100" (manufactured by Nitta Gelatin Co., Ltd.), "peptan P2000HD" (manufactured by Rousselot Co., Ltd.), and the like.
コラーゲンペプチドの含有量は、本発明の飲料中、0.02~20w/v%であることが好ましく、0.1~15w/v%がより好ましく、0.2~15w/v%がさらに好ましい。 The content of collagen peptide in the beverage of the present invention is preferably 0.02 to 20 w/v%, more preferably 0.1 to 15 w/v%, even more preferably 0.2 to 15 w/v%. .
コラーゲンペプチドの含有量は、本発明の効果の点から、鉄化合物(鉄換算)で鉄1質量部に対し0.1~100000質量部が好ましく、0.5~10000質量部がより好ましく、5~7500質量部がさらに好ましく、20~7500質量部が特に好ましい。また、プラセンタエキス1質量部に対して0.005~20000質量部が好ましく、0.01~1000質量部がより好ましく、0.1~750質量部がさらに好ましく、0.5~150質量部が特に好ましい。なお、プラセンタエキスを胎盤に換算すると、胎盤として1質量部に対し0.0002~800質量部が好ましく、0.002~40質量部がより好ましく、0.004~30質量部がさらに好ましく、0.02~6質量部が特に好ましい。 From the viewpoint of the effect of the present invention, the content of the collagen peptide is preferably 0.1 to 100000 parts by mass, more preferably 0.5 to 10000 parts by mass relative to 1 part by mass of iron in terms of iron compound (calculated as iron). More preferably up to 7500 parts by mass, particularly preferably 20 to 7500 parts by mass. Also, it is preferably 0.005 to 20000 parts by mass, more preferably 0.01 to 1000 parts by mass, still more preferably 0.1 to 750 parts by mass, and 0.5 to 150 parts by mass with respect to 1 part by mass of placenta extract. Especially preferred. When the placenta extract is converted to placenta, it is preferably 0.0002 to 800 parts by mass, more preferably 0.002 to 40 parts by mass, even more preferably 0.004 to 30 parts by mass, with respect to 1 part by mass of the placenta. 0.02 to 6 parts by weight is particularly preferred.
本発明は、動物プラセンタエキス由来の沈殿物の生成を、鉄化合物を配合することで抑制できる。また、さらにコラーゲンペプチドを配合すると、動物プラセンタエキス由来の沈殿物の生成抑制効果は大きくなる。動物プラセンタとしては特に限定されないが、鉄化合物のみで沈殿の生成を抑制する場合、豚由来動物プラセンタが特に好ましい。 INDUSTRIAL APPLICABILITY The present invention can suppress the formation of animal placenta extract-derived precipitates by adding an iron compound. In addition, when a collagen peptide is added, the effect of suppressing the formation of animal placenta extract-derived precipitates is increased. The animal placenta is not particularly limited, but pig-derived animal placenta is particularly preferable when the formation of precipitates is suppressed only with an iron compound.
本発明における飲料とは、経口摂取できる液体であれば特に制限はなく、医薬品、医薬部外品、又は食品(一般の食品だけでなく、栄養機能性食品や特定保健用食品、機能性表示食品も含む)を挙げることができる。医薬品及び医薬部外品としては、例えば内服液剤、ドリンク剤等を挙げることができる。食品としては、清涼飲料水、炭酸飲料、スポーツ・機能性飲料、ノンアルコール飲料、乳飲料、茶飲料、コーヒー飲料、果実・野菜系飲料、ゼリー飲料等が挙げられる。より好ましくは、医薬品及び医薬部外品であれば内服液剤、ドリンク剤、食品であれば、栄養機能性食品、特定保健用食品等の各種飲料、炭酸飲料、ゼリー飲料である。 The beverage in the present invention is not particularly limited as long as it is a liquid that can be taken orally, and is not limited to pharmaceuticals, quasi-drugs, or foods (not only general foods, but also nutritional functional foods, specified health foods, and functionally labeled foods). also included) can be mentioned. Examples of pharmaceuticals and quasi-drugs include internal liquids and drinks. Foods include soft drinks, carbonated drinks, sports/functional drinks, non-alcoholic drinks, milk drinks, tea drinks, coffee drinks, fruit/vegetable drinks, jelly drinks and the like. More preferably, pharmaceuticals and quasi-drugs are oral liquid preparations and drinks, and foods are various beverages such as nutritional functional foods and foods for specified health uses, carbonated beverages, and jelly beverages.
本発明の飲料のpHは、特に限定されないが、口当たりの良さという点から2.5~4.5が好ましく、3.0~4.0がより好ましい。pHを上記範囲に保つために、必要に応じて有機酸等のpH調整剤を配合することができる。 The pH of the beverage of the present invention is not particularly limited, but is preferably 2.5 to 4.5, more preferably 3.0 to 4.0, from the viewpoint of good taste. In order to maintain the pH within the above range, a pH adjuster such as an organic acid may be blended as necessary.
本発明の飲料は、常法により製造することができ、その方法は特に限定されるものではない。通常、各成分を量りとり、適量の精製水で溶解、撹拌した後、pHを調整し、さらに精製水を加えて容量調整し、必要に応じてろ過、殺菌処理を施すことにより得られる。 The beverage of the present invention can be produced by a conventional method, and the method is not particularly limited. Usually, each component is weighed, dissolved in an appropriate amount of purified water, stirred, then the pH is adjusted, purified water is added to adjust the volume, and if necessary, filtration and sterilization are performed.
また、本発明の飲料には、その他の成分として、ビタミン類、ミネラル類、アミノ酸及びその塩類、生薬、生薬抽出物、カフェイン、ローヤルゼリー、デキストリン等を本発明の効果を損なわない範囲で適宜に配合することができる。さらに必要に応じて、抗酸化剤、着色剤、香料、矯味剤、保存剤、甘味料、酸味剤等の添加物を本発明の効果を損なわない範囲で適宜に配合することができる。 In addition, the beverage of the present invention may contain other ingredients such as vitamins, minerals, amino acids and their salts, herbal medicines, herbal extracts, caffeine, royal jelly, dextrin, etc. as appropriate within the range that does not impair the effects of the present invention. can be compounded. Furthermore, if necessary, additives such as antioxidants, coloring agents, flavoring agents, corrigents, preservatives, sweeteners, acidulants and the like can be appropriately blended within limits that do not impair the effects of the present invention.
以下に、実施例、比較例を挙げ、本発明を更に詳細に説明する。 EXAMPLES The present invention will be described in more detail below with reference to examples and comparative examples.
下記表1に記載の処方の飲料を次の方法に従い調製した。まず、クエン酸(クエン酸一水和物)と安息香酸ナトリウムを精製水で溶解し、全量の60v/v%に容量調整し酸味剤液を得た。次に、クエン酸鉄アンモニウムを精製水で溶解し、鉄として0.2~0.4w/v%含むように容量調整し、鉄溶液を得た。酸味剤液に、表に示した処方となるように必要に応じて、鉄溶液または鉄化合物、豚由来動物プラセンタエキス(日本ハム(株)製 P-プラセンタエキス)を添加し、全量の90v/v%程度となるように精製水を加え、十分に撹拌した。十分に撹拌後、塩酸または水酸化ナトリウムを用いてpHを調整し、精製水を加えて全量とし、飲料を得た(実施例1-1~4-1)。
これらの飲料をスクリュー管No.7((株)マルエム製)に50ml充填し、80℃25分の殺菌を行った。クエン酸鉄アンモニウムを添加しない飲料(比較例1~4)を対照とした。
上記の通り調製した飲料を65℃で7日間保存し、沈殿を目視により観察した。表2の基準で沈殿生成度合いを評価した。Beverages having the formulations shown in Table 1 below were prepared according to the following method. First, citric acid (citric acid monohydrate) and sodium benzoate were dissolved in purified water, and the volume was adjusted to 60 v/v % of the total amount to obtain an acidulant liquid. Next, ammonium ferric citrate was dissolved in purified water, and the volume was adjusted so as to contain 0.2 to 0.4 w/v% iron to obtain an iron solution. To the acidulant liquid, iron solution or iron compound, pig-derived animal placenta extract (P-placenta extract manufactured by Nippon Ham Co., Ltd.) is added as necessary so that the formulation shown in the table is obtained, and the total amount is 90 v / Purified water was added so as to make it about v%, and the mixture was sufficiently stirred. After sufficient stirring, the pH was adjusted using hydrochloric acid or sodium hydroxide, and purified water was added to make up the total volume to obtain beverages (Examples 1-1 to 4-1).
These beverages were passed through screw tube no. 7 (manufactured by Maruem Co., Ltd.) was filled with 50 ml and sterilized at 80° C. for 25 minutes. Beverages to which ferric ammonium citrate was not added (Comparative Examples 1 to 4) served as controls.
Beverages prepared as described above were stored at 65° C. for 7 days, and precipitation was visually observed. The degree of precipitate formation was evaluated according to the criteria in Table 2.
表1に示した通り、動物プラセンタエキスの配合により沈殿が生じ(比較例1、2、3-1、4)、動物プラセンタエキスの濃度が高まると沈殿生成の割合も増加した(比較例1~3-1)。一方、比較例1に対して実施例1-1、比較例2に対して実施例2-1~実施例2-3、比較例3-1に対して実施例3-1~3-5、比較例4に対して実施例4-1を比較して明白なように、鉄化合物を配合することにより沈殿生成が抑制された。 As shown in Table 1, the addition of the animal placenta extract caused precipitation (Comparative Examples 1, 2, 3-1, 4), and the higher the concentration of the animal placenta extract, the higher the percentage of precipitate formation (Comparative Examples 1 to 4). 3-1). On the other hand, Example 1-1 for Comparative Example 1, Examples 2-1 to 2-3 for Comparative Example 2, Examples 3-1 to 3-5 for Comparative Example 3-1, As is clear from the comparison of Example 4-1 with Comparative Example 4, the addition of the iron compound suppressed the formation of precipitates.
下記表3、表4に記載の処方の飲料を次の方法に従い調製した。まず、クエン酸(クエン酸一水和物)と安息香酸ナトリウムを精製水で溶解し、精製水で全量の60v/v%に容量調整し、酸味剤液を得た。次に、クエン酸鉄アンモニウムを精製水で溶解し、鉄として0.2~0.4w/v%含むように容量調整し、鉄溶液を得た。酸味剤液に、表に示した処方となるように、必要に応じて鉄溶液または鉄化合物を添加し、豚由来動物プラセンタエキス(日本ハム(株)製 P-プラセンタエキス)及びコラーゲンペプチドを添加し、全量の90v/v%程度となるように精製水を加え、十分に撹拌した。十分に撹拌後、塩酸または水酸化ナトリウムを用いてpHを調整し、精製水を加えて全量とし、飲料を得た(実施例1-2、実施例2-4、実施例3-6~3-13、実施例4-2)。豚由来コラーゲンペプチド(分子量約5000)はコラぺプJB(登録商標、新田ゼラチン(株)製)、豚由来コラーゲンペプチド(分子量約4000―12000)はニッピペプタイドPRA-P(登録商標、株式会社ニッピ製)、魚由来コラーゲンペプチド(分子量約4000)はニッピペプタイドFCP-EX(登録商標、株式会社ニッピ製)を使用した。
これらの飲料をスクリュー管No.7((株)マルエム製)に50ml充填し、80℃25分の殺菌を行った。クエン酸鉄アンモニウム及びコラーゲンペプチドを添加しない飲料(比較例1~4)を対照とした。
上記の通り調製した飲料を65℃で7日間保存し、沈殿を目視により観察した。表2の基準で沈殿生成度合いを評価した。Beverages having the formulations shown in Tables 3 and 4 below were prepared according to the following method. First, citric acid (citric acid monohydrate) and sodium benzoate were dissolved in purified water, and the volume was adjusted to 60 v/v % of the total amount with purified water to obtain an acidulant liquid. Next, ammonium ferric citrate was dissolved in purified water, and the volume was adjusted so as to contain 0.2 to 0.4 w/v% iron to obtain an iron solution. An iron solution or an iron compound is added to the acidulant liquid as required to achieve the formulation shown in the table, and a porcine-derived animal placenta extract (P-placenta extract manufactured by Nippon Ham Co., Ltd.) and collagen peptide are added. Then, purified water was added so as to be about 90 v/v% of the total amount, and the mixture was sufficiently stirred. After sufficient stirring, the pH was adjusted using hydrochloric acid or sodium hydroxide, purified water was added to make the total amount, and beverages were obtained (Example 1-2, Example 2-4, Example 3-6 to 3 -13, Example 4-2). Pig-derived collagen peptide (molecular weight about 5000) is Korapep JB (registered trademark, manufactured by Nitta Gelatin Co., Ltd.), and pig-derived collagen peptide (molecular weight about 4000-12000) is Nippi Peptide PRA-P (registered trademark, Co., Ltd.). Nippi Co., Ltd.), and fish-derived collagen peptide (molecular weight: about 4000) was Nippi Peptide FCP-EX (registered trademark, Nippi Co., Ltd.).
These beverages were passed through screw tube no. 7 (manufactured by Maruem Co., Ltd.) was filled with 50 ml and sterilized at 80° C. for 25 minutes. Beverages containing no ammonium ferric citrate or collagen peptide (Comparative Examples 1 to 4) were used as controls.
Beverages prepared as described above were stored at 65° C. for 7 days, and precipitation was visually observed. The degree of precipitate formation was evaluated according to the criteria in Table 2.
表3、4に示した通り、動物プラセンタエキスの配合により沈殿が生じた(比較例1、2、3-1、4)。比較例1と実施例1-2、比較例2と実施例2-4、比較例3-1と実施例3-6~3-11、比較例4と実施例4-2を比較して明白なように、鉄化合物およびコラーゲンペプチドを配合することにより沈殿生成が抑制された。
また、表1の実施例3-2と比較して実施例3-7、実施例3-3と比較して実施例3-8、実施例3-4と比較して実施例3-9、実施例3-5と比較して実施例3-11で沈殿生成が抑制されており、鉄化合物とコラーゲンペプチドを組み合わせることで沈殿生成抑制効果が向上した。As shown in Tables 3 and 4, the addition of the animal placenta extract caused precipitation (Comparative Examples 1, 2, 3-1, 4). Clear by comparing Comparative Example 1 and Example 1-2, Comparative Example 2 and Example 2-4, Comparative Example 3-1 and Examples 3-6 to 3-11, Comparative Example 4 and Example 4-2 As shown above, precipitation formation was suppressed by adding an iron compound and collagen peptide.
In addition, in comparison with Example 3-2 in Table 1, Example 3-7, Example 3-8 in comparison with Example 3-3, Example 3-9 in comparison with Example 3-4, Precipitate formation was suppressed in Example 3-11 as compared with Example 3-5, and the effect of suppressing precipitate formation was improved by combining the iron compound and the collagen peptide.
下記表5に記載の処方の飲料を次の方法に従い調製した。まず、クエン酸(クエン酸一水和物)と安息香酸ナトリウムを精製水で溶解し、全量の60v/v%程度の精製水で容量調整し、酸味剤液を得た。次に、クエン酸第一鉄ナトリウム、豚由来動物プラセンタエキス(日本ハム(株)製 P-プラセンタエキス)及びコラーゲンペプチドを順に添加し、全量の90v/v%程度となるように精製水を加え、十分に撹拌した。十分に撹拌後、塩酸または水酸化ナトリウムを用いてpHを調整し、精製水を加えて全量とし、飲料を得た(実施例3-14)。
これらの飲料をスクリュー管No.7((株)マルエム製)に50ml充填し、80℃25分の殺菌を行った。上記の通り調製した飲料を65℃で7日間保存し、沈殿を目視により観察した。表2の基準で沈殿生成度合いを評価した。
クエン酸第一鉄ナトリウム及びコラーゲンペプチドを添加しない飲料(比較例3-1)を対照とした。Beverages having the formulations shown in Table 5 below were prepared according to the following method. First, citric acid (citric acid monohydrate) and sodium benzoate were dissolved in purified water, and the volume was adjusted with purified water to about 60 v/v% of the total amount to obtain an acidulant liquid. Next, sodium ferrous citrate, pig-derived animal placenta extract (P-placenta extract manufactured by Nippon Ham Co., Ltd.) and collagen peptide are added in order, and purified water is added so that the total amount becomes about 90 v / v%. , stirred well. After sufficient stirring, hydrochloric acid or sodium hydroxide was used to adjust the pH, and purified water was added to make up the total volume to obtain beverages (Examples 3-14).
These beverages were passed through screw tube no. 7 (manufactured by Maruem Co., Ltd.) was filled with 50 ml and sterilized at 80° C. for 25 minutes. Beverages prepared as described above were stored at 65° C. for 7 days, and precipitation was visually observed. The degree of precipitate formation was evaluated according to the criteria in Table 2.
A beverage containing no sodium ferrous citrate or collagen peptide (Comparative Example 3-1) was used as a control.
表5に示す通り、クエン酸鉄アンモニウムの代わりにクエン酸第一鉄ナトリウムを配合した場合、鉄化合物の配合だけでは沈殿生成抑制効果は見られなかったが(比較例3-2)、比較例3-1と実施例3-14に示した通り、コラーゲンペプチドを配合することで、クエン酸第一鉄ナトリウム及びコラーゲンを配合しない処方(比較例3-1)と比較して沈殿生成が抑制された(実施例3-14)。 As shown in Table 5, when sodium ferrous citrate was blended instead of ammonium ferric citrate, the effect of suppressing precipitation formation was not observed only by blending the iron compound (Comparative Example 3-2). As shown in 3-1 and Example 3-14, by blending the collagen peptide, precipitation formation was suppressed compared to the formulation (Comparative Example 3-1) that did not blend sodium ferrous citrate and collagen. (Examples 3-14).
下記表6に記載の処方の飲料を次の方法に従い調製した。まず、クエン酸(クエン酸一水和物)と安息香酸ナトリウムを精製水で溶解し、精製水で全量の60v/v%に容量調整し、酸味剤液を得た。次に、クエン酸鉄アンモニウムを精製水で溶解し、鉄として0.4w/v%含むように容量調整し、鉄溶液を得た。酸味剤液に、表に示した処方となるように鉄溶液を添加し、鮭由来プラセンタエキス((株)日本バリアフリー製 マリンプラセンタ(MP))または馬由来プラセンタエキス((株)ダード製 馬由来プラセンタエキス末)及び必要に応じてコラーゲンペプチドを添加し、全量の90v/v%程度となるように精製水を加え、十分に撹拌した。十分に撹拌後、塩酸または水酸化ナトリウムを用いてpHを調整し、精製水を加えて全量とし、飲料を得た(比較例5-2、6-2、実施例5、6)。
これらの飲料をスクリュー管No.7((株)マルエム製)に50ml充填し、80℃25分の殺菌を行った。クエン酸鉄アンモニウム及びコラーゲンペプチドを添加しない飲料(比較例5-1、6-1)を対照とした。
上記の通り調製した飲料を65℃で7日間保存し、沈殿を目視により観察した。表2の基準で沈殿生成度合いを評価した。Beverages having the formulations shown in Table 6 below were prepared according to the following method. First, citric acid (citric acid monohydrate) and sodium benzoate were dissolved in purified water, and the volume was adjusted to 60 v/v % of the total amount with purified water to obtain an acidulant liquid. Next, ammonium ferric citrate was dissolved in purified water, and the volume was adjusted so as to contain 0.4 w/v % iron to obtain an iron solution. An iron solution was added to the acidulant liquid so as to have the formulation shown in the table, and salmon-derived placenta extract (Marine Placenta (MP), manufactured by Nihon Barrier Free Co., Ltd.) or horse-derived placenta extract (Dard Co., Ltd., horse). derived placenta extract powder) and, if necessary, collagen peptides were added, and purified water was added so as to make the total amount about 90 v/v%, and the mixture was sufficiently stirred. After sufficient stirring, hydrochloric acid or sodium hydroxide was used to adjust the pH, and purified water was added to make up the total volume to obtain beverages (Comparative Examples 5-2, 6-2, Examples 5, 6).
These beverages were passed through screw tube no. 7 (manufactured by Maruem Co., Ltd.) was filled with 50 ml and sterilized at 80° C. for 25 minutes. Beverages containing no ammonium ferric citrate and collagen peptide (Comparative Examples 5-1 and 6-1) were used as controls.
Beverages prepared as described above were stored at 65° C. for 7 days, and precipitation was visually observed. The degree of precipitate formation was evaluated according to the criteria in Table 2.
表6に示したように、動物プラセンタである鮭由来プラセンタエキス、馬由来プラセンタエキスを配合すると沈殿が生じた(比較例5-1、6-1)。鮭由来プラセンタエキス、馬由来プラセンタエキスの沈殿生成はクエン酸鉄アンモニウムの配合だけでは抑制できなかったが(比較例5-2、6-2)、比較例5-1と実施例5、比較例6-1と実施例6を比較して明白なように、鉄化合物にさらにコラーゲンを配合することで沈殿生成が抑制された。 As shown in Table 6, when animal placenta such as salmon-derived placenta extract and horse-derived placenta extract were blended, precipitation occurred (Comparative Examples 5-1 and 6-1). Precipitation of the salmon-derived placenta extract and the horse-derived placenta extract could not be suppressed only by the addition of ferric ammonium citrate (Comparative Examples 5-2 and 6-2). As is clear from the comparison of 6-1 and Example 6, the addition of collagen to the iron compound suppressed the formation of precipitates.
表6の通り、豚由来動物プラセンタエキスに代えて、メロン胎座由来植物プラセンタエキスを配合し表1又は表3の調製と同様の方法にて飲料を得た(比較例7-1~8-2)。
これらの飲料をスクリュー管No.7((株)マルエム製)に50ml充填し、80℃25分の殺菌を行った。上記の通り調製した飲料を65℃で7日間保存し、沈殿を目視により観察した。表2の基準で沈殿生成度合いを評価した。
クエン酸鉄アンモニウム及びコラーゲンペプチドを添加しない飲料(比較例7-1、8-1)を対照とした。
These beverages were passed through screw tube no. 7 (manufactured by Maruem Co., Ltd.) was filled with 50 ml and sterilized at 80° C. for 25 minutes. Beverages prepared as described above were stored at 65° C. for 7 days, and precipitation was visually observed. The degree of precipitate formation was evaluated according to the criteria in Table 2.
Beverages containing no ammonium ferric citrate and collagen peptide (Comparative Examples 7-1 and 8-1) were used as controls.
表7に示した通り、植物プラセンタエキスの配合により沈殿が生じたが(比較例7-1、8-1)、鉄化合物およびコラーゲンペプチドを配合した場合でも沈殿生成抑制効果は得られなかった(比較例7-2~7-4、8-2)。 As shown in Table 7, precipitation occurred by blending the plant placenta extract (Comparative Examples 7-1 and 8-1), but even when the iron compound and collagen peptide were blended, no precipitate formation inhibitory effect was obtained ( Comparative Examples 7-2 to 7-4, 8-2).
本発明により、飲料中における動物プラセンタエキス由来の沈殿を抑制することが可能となったので、医薬品、医薬部外品及び食品の分野において、商品性の高い動物プラセンタエキス含有飲料を提供することが期待される。 INDUSTRIAL APPLICABILITY According to the present invention, precipitation of animal placenta extracts in beverages can be suppressed. Therefore, beverages containing animal placenta extracts with high marketability can be provided in the fields of pharmaceuticals, quasi-drugs and foods. Be expected.
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JPH11221047A (en) * | 1997-10-29 | 1999-08-17 | Masakazu Matsushima | Placenta extract-containing liquid agent |
WO2005107734A1 (en) * | 2004-05-06 | 2005-11-17 | Taiyokagaku Co., Ltd. | Alcohol metabolism accelerating composition, and food or drink containing the composition |
JP4715078B2 (en) * | 2003-04-16 | 2011-07-06 | 大正製薬株式会社 | Liquid composition for internal use containing iron compounds |
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JPH11221047A (en) * | 1997-10-29 | 1999-08-17 | Masakazu Matsushima | Placenta extract-containing liquid agent |
JP4715078B2 (en) * | 2003-04-16 | 2011-07-06 | 大正製薬株式会社 | Liquid composition for internal use containing iron compounds |
WO2005107734A1 (en) * | 2004-05-06 | 2005-11-17 | Taiyokagaku Co., Ltd. | Alcohol metabolism accelerating composition, and food or drink containing the composition |
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BERRY YOGURT FLAVOUR VEGEFUL RED SMOOTHIE, 記録番号(ID#) 2983875, MINTEL GNPD, 2015, [ONLINE], [RETR, JPN6021051493, ISSN: 0004733271 * |
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