JP2023020776A - 胎盤抽出物および人参の実抽出物を含む食品組成物 - Google Patents
胎盤抽出物および人参の実抽出物を含む食品組成物 Download PDFInfo
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- JP2023020776A JP2023020776A JP2021139831A JP2021139831A JP2023020776A JP 2023020776 A JP2023020776 A JP 2023020776A JP 2021139831 A JP2021139831 A JP 2021139831A JP 2021139831 A JP2021139831 A JP 2021139831A JP 2023020776 A JP2023020776 A JP 2023020776A
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- placenta
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- A—HUMAN NECESSITIES
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Abstract
Description
人参の実抽出物および胎盤抽出物を含む食品組成物を提供する。
胎盤抽出物を含むカプセルの服用性を評価するために、下記の表1の組成によってすべての原料を混合器に入れて均質化した後、ハードカプセルに充填してカプセルを製造した。Biofac A/S社(Denmark、Kastrup)から豚胎盤抽出物を購入し、Nutrex社から人参の実抽出物を購入し、大東高麗参(Korea Rep、錦山)社から人参根抽出物を購入した。結晶セルロースは、当業界に普遍的に使用される原料であり、市中に流通する一般的な規格の製品を購入してカプセルの製造に使用した。
専門パネル10人を対象に、製造例1で製造したカプセルの服用性改善実験を実施した。実験は、対象者に比較例1~4、および実施例1~4のカプセルを水と共に摂取するようにした後、摂取による服用性を下記の表2の評価基準によって評価して表3に示した。
胎盤抽出物を含む飲料の服用性を評価するために、下記の表4の組成によってすべての原料を配合用撹拌機に入れて均質化した後、50mLガラス瓶で加熱殺菌して飲料を製造した。胎盤抽出物、人参の実抽出物および人参根抽出物は、製造例1と同じ経路で入手した。蜂蜜とクエン酸は、当業界に普遍的に使用される原料であり、市中に流通する一般的な規格の製品を購入して飲料の製造に使用した。
専門パネル10人を対象に、製造例2で製造した飲料の服用性改善実験を実施した。実験は、対象者に比較例5~8、および実施例5~8の飲料を水と共に摂取するようにした後、摂取による服用性を上記表2の評価基準によって評価して表5に示した。
胎盤抽出物を含む粉末の服用性を評価するために、下記の表6の組成によってすべての原料を造粒機に入れて均質化した後、アルミパウチに充填して粉末を製造した。胎盤抽出物、人参の実抽出物および人参根抽出物は、製造例1と同じ経路で入手した。結晶セルロースとマルチトールは、当業界に普遍的に使用される原料であり、市中に流通する一般的な規格の製品を購入して粉末の製造に使用した。
専門パネル10人を対象に、製造例3で製造した粉末の服用性改善実験を実施した。実験は、対象者に比較例9~12、および実施例9~12の粉末を水と共に摂取するようにした後、摂取による服用性を上記表2の評価基準によって評価して表7に示した。
酸化したタンパク質は、部分的にはレドックス恒常性(redox homeostasis)の弱化から起因する。また、酸化したタンパク質は、異味と異臭(off-flavor)を出して変質するので、製品の保管温度においての抽出物原料のタンパク質酸化実験を実施して鮮度が維持され得るかを確認した。胎盤抽出物の鮮度維持実験を行うために、下記の表8の組成によって胎盤抽出物の混合物を製造した。活性酸素を含んでいる試薬であるDPPH(2,2-diphenyl-1-picrylhydrazyl)が、抗酸化物質により活性酸素が除去されると、色が変わることを用いて、活性酸素が除去される程度を色濃度で測定した。前記実験は、テストチューブに試料および対照群と共にそれぞれDPPH溶液(sigma-Aldrich、USA)を入れて反応させた後、色濃度を測定し、色濃度は、分光光度計(microplate spectrophotometer;BioTek、USA)機器を用いて517nmで吸光度を測定した。この際、対照群としては、蒸留水を使用し、陽性対照群としては、アスコルビン酸100μMを使用した。DPPH消去能(%)は、下記の一般式によって計算した。
Claims (14)
- 人参の実抽出物および胎盤抽出物を含む食品組成物。
- 人参の実抽出物は、水、有機溶媒またはこれらの混合物から抽出されたものである、請求項1に記載の食品組成物。
- 有機溶媒は、炭素数1~4の低級アルコール、ヘキサン、エーテル、グリセロール、プロピレングリコール、ブチレングリコール、エチルアセテート、メチルアセテート、ジクロロメタン、クロロホルム、ベンゼンおよびこれらの混合溶媒から選ばれるものである、請求項2に記載の食品組成物。
- 人参の実抽出物は、全体組成物100重量部を基準として0.0001~5重量部で含まれる、請求項1に記載の食品組成物。
- 胎盤抽出物は、全体組成物100重量部を基準として0.1~70重量部で含まれる、請求項1に記載の食品組成物。
- 胎盤抽出物は、胎盤抽出物を10~100倍濃縮した胎盤抽出物の濃縮物である、請求項1に記載の食品組成物。
- 胎盤抽出物と人参の実抽出物は、1:1~500:1の重量比で含まれる、請求項1に記載の食品組成物。
- 人参の実抽出物および胎盤抽出物のうち一つ以上は、発酵された発酵物である、請求項1に記載の食品組成物。
- 前記発酵物は、ラクトバチルス(Lactobacillus)属、ラクトコッカス(Lactococcus)属、エンテロコッカス(Enterococcus)属、ストレプトコッカス(Streptococcus)属、ロイコノストック(Leuconostoc)属およびビフィドバクテリウム(Bifidobacterium)属よりなる群から選ばれた一つ以上の乳酸菌により発酵されたものである、請求項8に記載の食品組成物。
- 食品組成物は、ビタミンBおよびアスタキサンチンのうち一つ以上を追加で含む、請求項1に記載の食品組成物。
- ビタミンBおよびアスタキサンチンは、それぞれ、全体組成物100重量部を基準として0.01~10重量部で含まれる、請求項10に記載の食品組成物。
- 前記食品組成物は、胎盤抽出物を含む食品の異臭および異味をマスキングするためのものである、請求項1に記載の食品組成物。
- 食品組成物は、カプセル、錠剤、丸剤、液剤またはドリンク剤である、請求項1に記載の食品組成物。
- 人参の実抽出物と胎盤抽出物を混合して食品組成物を製造する段階を含む、胎盤抽出物を含む食品の異臭および異味をマスキングする方法。
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JP2005185242A (ja) * | 2003-12-26 | 2005-07-14 | Takashi Kondo | プラセンタを含有した健康食品及びその製造方法 |
JP2005185240A (ja) * | 2003-12-26 | 2005-07-14 | Takashi Kondo | 発酵健康食品及びその製造方法 |
JP2017057155A (ja) * | 2015-09-16 | 2017-03-23 | 国立大学法人金沢大学 | 非アルコール性脂肪性肝疾患予防用又は治療用組成物の製造方法 |
CN107072229A (zh) * | 2014-10-17 | 2017-08-18 | 株式会社爱茉莉太平洋 | 人参苦味抑制剂及含有其的人参组合物 |
JP2019041696A (ja) * | 2017-09-04 | 2019-03-22 | 株式会社ノエビア | 経口用組成物 |
KR20200141766A (ko) * | 2019-06-11 | 2020-12-21 | 건국대학교 산학협력단 | 상이한 성숙 단계의 인삼 열매로부터 기능성 성분을 수득하는 방법 |
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KR101844591B1 (ko) | 2016-08-02 | 2018-04-02 | 류태경 | 진생 베리를 이용한 경옥고 제조방법 및 이에 따라 제조된 경옥고 |
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JP2005185242A (ja) * | 2003-12-26 | 2005-07-14 | Takashi Kondo | プラセンタを含有した健康食品及びその製造方法 |
JP2005185240A (ja) * | 2003-12-26 | 2005-07-14 | Takashi Kondo | 発酵健康食品及びその製造方法 |
CN107072229A (zh) * | 2014-10-17 | 2017-08-18 | 株式会社爱茉莉太平洋 | 人参苦味抑制剂及含有其的人参组合物 |
JP2017057155A (ja) * | 2015-09-16 | 2017-03-23 | 国立大学法人金沢大学 | 非アルコール性脂肪性肝疾患予防用又は治療用組成物の製造方法 |
JP2019041696A (ja) * | 2017-09-04 | 2019-03-22 | 株式会社ノエビア | 経口用組成物 |
KR20200141766A (ko) * | 2019-06-11 | 2020-12-21 | 건국대학교 산학협력단 | 상이한 성숙 단계의 인삼 열매로부터 기능성 성분을 수득하는 방법 |
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