CN101069563A - 饮料组合物以及防止饮料中维生素降解的方法 - Google Patents
饮料组合物以及防止饮料中维生素降解的方法 Download PDFInfo
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- CN101069563A CN101069563A CNA200610130993XA CN200610130993A CN101069563A CN 101069563 A CN101069563 A CN 101069563A CN A200610130993X A CNA200610130993X A CN A200610130993XA CN 200610130993 A CN200610130993 A CN 200610130993A CN 101069563 A CN101069563 A CN 101069563A
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- Prior art keywords
- vitamin
- acid
- extract
- composition
- stabilizing agent
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- 238000000034 method Methods 0.000 title claims abstract description 12
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- OVVGHDNPYGTYIT-BNXXONSGSA-N rutinose Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)O1 OVVGHDNPYGTYIT-BNXXONSGSA-N 0.000 description 1
- 235000014214 soft drink Nutrition 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 235000011496 sports drink Nutrition 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 235000019605 sweet taste sensations Nutrition 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000012976 tarts Nutrition 0.000 description 1
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 description 1
- BWHOZHOGCMHOBV-BQYQJAHWSA-N trans-benzylideneacetone Chemical compound CC(=O)\C=C\C1=CC=CC=C1 BWHOZHOGCMHOBV-BQYQJAHWSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 150000002266 vitamin A derivatives Chemical class 0.000 description 1
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Abstract
提供一种维生素强化组合物,它包含防止维生素降解的维生素稳定剂,所述维生素稳定剂是C6-C3苯丙烯羰基化合物。另外,提供一种防止维生素强化组合物中维生素的降解的方法。
Description
技术领域
本发明涉及防止含维生素组合物中维生素降解的方法以及所获得的组合物,所述组合物可能是饮料。更具体地说,本发明组合物涉及含有维生素A、维生素D、维生素B12或其混合物以及一种维生素稳定剂的含维生素组合物。
背景技术
维生素是提供很多功能的必需营养素。维生素缺乏曾被作为被忽视的公共卫生问题提出。结果是,食品和饮料工业已制造出维生素强化组合物以提高消费者的维生素摄取量。然而,从含维生素产品离开生产设备并到达消费者时起,该产品可能会暴露于空气、光线、酸、温度以及其他组分的相互影响。遗憾是,暴露于任何上述因素均导致维生素的降解。
业已发现,穿透聚对苯二甲酸乙二醇酯(PET)和玻璃瓶的光线、特别是荧光,会使维生素A降解,所以商业期(trade age)维生素A含量标示并不满足推荐膳食标准(RDA)的要求。即使是3500国际单位(IU)这样高水平的维生素A,现有技术下的PET也不能使维生素A含量达到20%饮食参考摄入量(DRI)要求的1000IU。例如,新制备的装于20盎司PET瓶中的含3500IU维生素A的果汁,暴露于典型的商店荧光光线中(正如店内装设的展示型冰箱中发现的)一个星期后,可导致大约1000IU的剩余维生素A含量。至消费者购买时为止的平均商业期可能会明显更长。
因此,当组合物被装在透明或基本透明的瓶子,例如PET以及玻璃瓶中时,由于暴露于光线、尤其是荧光光线(正如店内装设的展示型冰箱中发现的),存在着防止含维生素组合物中维生素(包括维生素A在内)的降解的需求。
发明内容
依照本发明的一个方面,提供含有选自维生素A、维生素D、维生素B12及其混合物的维生素,以及至少一种维生素稳定剂的含维生素组合物。典型地,该稳定剂以提供至少一定的稳定作用以及提供防止存在于组合物中的维生素降解的有效量存在。该维生素稳定剂使组合物中的一种或多种维生素稳定,并能防止由于暴露于光线、特别是荧光光线中造成的维生素降解,并且所述维生素稳定剂包括这样一种维生素稳定剂,这种稳定剂包含由选自下组的式代表的C6-C3苯丙烯羰基结构:
及其混合物
图解1
依照本发明的另一个方面,提供一种在含维生素组合物中防止或至少减少由光线、特别是由荧光光线导致的维生素降解的方法。该方法包括添加至少一种维生素稳定剂,该稳定剂包含由图解1中任一式或其混合物所表示的C6-C3苯丙烯羰基结构。通常,所述至少一种维生素稳定剂的加入量能有效地提供至少一定的维生素稳定作用从而至少降低由于光线、尤其是荧光光线暴露导致的维生素降解速率。
具体实施方式
已发现苯丙烯羰基(phenylpropenoic carbonyl)化合物(C6-C3)能防止饮料中维生素的降解。C6-C3苯丙烯羰基化合物普遍存在于次级植物代谢物族中。这类化合物可以由许多植物物质衍生或由合成法制造。这些物质中有很多目前被批准用于食品和饮料。
虽然不希望被理论束缚,但据信,这些化合物通过充当维生素稳定剂而防止降解。维生素稳定剂是被称为自由基清除剂的很多物质之一。在光导致的成分降解中,自由基被认为是主要的活性物。当足够的自由基清除剂浓度维持在透明包装饮料中,光线导致的成分降解可以在饮料上架的整个期限中被降低到一定水平。据信,本发明的维生素稳定剂能清除在维生素A的荧光光线降解过程中饮料中产生的自由基。荧光光线暴露典型地发生在饮料储存在商店内安装的展示型冰箱中。
依照本发明的一个方面,提供包含至少一种维生素和至少一种维生素稳定剂的含维生素组合物。适合本发明的维生素包括,但不限于,维生素A及其棕榈酸酯、维生素D、维生素B12及其组合。这些维生素是本领域公知的并且容易由市售获得的。
所述一种或多种维生素可以所期望的量存在于组合物中。典型地,维生素以足够达到或超过推荐膳食标准(RDA)的量存在于本发明含维生素组合物中。然而,RDA是不时地可能需要修订的准则;因此,本领域普通技术人员会认识到,当这些准则逐步发展时或者当这些准则可能在任何时间点存在时,可以调节食品组合物中维生素的量以遵守这些准则。
最广义地,本发明的维生素稳定剂是在一个碳原子上既有(i)不饱和又有(ii)氧化的C6-C3苯丙烯羰基化合物。所述C6-C3苯丙烯羰基化合物可以是植物衍生的、也可以是合成法制备的。一般的C6-C3苯丙烯羰基结构可由下列异构式(a)、(b)和(c)中任一个来表示:
图解2
任何只具有这样结构的化合物,或任何具有这样结构作为更大结构的一部分的化合物,均适合作为C6-C3苯丙烯羰基化合物使用,即植物衍生或合成法制备的本发明维生素稳定剂,条件是它能提供至少一定的防止或减少维生素降解的作用。维生素稳定剂可由市售获得,也可以依照本领域公知的方法合成,或由植物或其提取物提供、衍生或分离或提取。代表性的提取方法包括B.Buszewski等,J.Pharm. Biomed.Anal.,第11卷,第3期,第211-215页(1993)公开的方法。
依照本发明的一个方面,适用于本发明的C6-C3苯丙烯羰基化合物包括,但不限于,迷迭香酸、绿原酸(chlorogenic acid)、菊苣酸、咖啡酸、香豆酸、肉桂酸、阿魏酸、芥子酸、caftaric acid、eichloric acid,松果菊苷(echinacoside)及其组合。从下列结构可清楚地看出,在诸如迷迭香酸、绿原酸和菊苣酸这样的物质中存在着所述一般结构图解2(a)。
图解3
从这些物质的结构还可以看出,对一般的C6-C3苯丙烯羰基结构图解2(a)的取代,以及对结构图解2(b)和结构图解2(c)的取代,只要在碳原子附近保留不饱和而且在碳原子处保留氧化,即是预期的。事实上,为获得各种各样的适宜维生素稳定剂,取代是必须的。适合的取代基包括但不限于,羟基、甲氧基以及在植物代谢物酚类中通常发现的其它取代基。进一步地,如果考虑到菊苣酸中存在着两个结构图解2(a),就可以轻易地理解,菊苣酸很可能是比列出的其它酸中的某些酸更有效的维生素稳定剂。通常,已发现在芳环上添加羟基增强了维生素稳定作用。因此,可以观察到,咖啡酸(2个羟基)的维生素稳定能力>阿魏酸>香豆酸>肉桂酸(无羟基)。
在本发明的某些优选实施方式中,上面列出的植物衍生的维生素稳定剂C6-C3苯丙烯羰基化合物通过植物提取物提供。适用于本发明的提取物包括但不限于:迷迭香提取物、生咖啡豆提取物、蓝莓提取物、杜鹃花提取物、向日葵仁提取物、菊苣叶提取物、紫松果菊提取物、莴苣提取物及其组合。更一般地说,唇形科、杜鹃科或紫菀科(asteraceae)中任一科的植物的提取物均适用。如下表1所示,上面提及的提取物中每一种均含有一种或多种充当维生素稳定剂的C6-C3苯丙烯羰基化合物。
表1
俗名 | 种 | C6-C3苯丙烯羰基化合物 |
迷迭香生咖啡豆蓝莓杜鹃花向日葵仁菊苣叶紫松果菊紫松果菊莴苣 | 迷迭香(Rosmarinus officianlis)小果咖啡(Coffea Arabica)Vaccinium vulgaris高加索杜鹃花(Rhododendroncaucasicum(Ungem)向日葵(Helianthus annuus)菊苣(Cichorium intybus)Echinacea angustifolia紫松果菊(Echinacea purpurea(Mench))莴苣(Lactuca sativa) | 迷迭香酸绿原酸绿原酸绿原酸绿原酸菊苣酸松果菊苷、菊苣酸、caftaricacid、eichloric acid菊苣酸、绿原酸、松果菊苷菊苣酸 |
本领域技术人员会容易认识到的是,C6-C3苯丙烯羰基化合物在给定提取物中存在的量会不同。本性不同的种可能含有不同量的C6-C3苯丙烯羰基化合物。该量也随给定植物的发育阶段的不同而变化。作为例子,下表2显示紫松果菊‘Magical Ruth’栽培种中绿原酸和松果菊苷含量的变化。
表2
紫松果菊栽培种‘Magical Ruth’的头状花序中松果菊苷和绿原酸含量的变化 | ||
花期 | 亲水组份(%) | |
绿原酸 | 松果菊苷 | |
I(早期)II(中期)III(成熟期)IV(盛开过的) | 0.0600.0240.0230.020 | 0.0120.0220.0150.016 |
*结果是从20株植物重复3次获得的;W.Letchamo.等,“Cichoric Acid...in Echinaceapurpurea as Influenced by Flower Dovelopmental Stages”,Perspectives on New Cropsand New Uses,J.Janick,编辑,ASHS出版社,Alexandria,VA,第494-498页(1999)。
另外,“Magical Ruth“中菊苣酸的含量从第I期的4.67%变化到笫IV期的1.42%。因此,早期培养似乎可以提供含最丰富量的所需维生素稳定剂的提取物。
适用于本发明的其它C6-C3苯丙烯羰基化合物,包括但不限于:肉桂酰酯类、香豆素类、查耳酮类、黄酮类、色酮类、异黄酮类及其组合。很多这些类型的化舍物可以衍生自一组叫做类黄酮的已知天然产物,其可以在水果、蔬菜、坚果、种子和花以及茶和葡萄酒中发现;已证明类黄酮具有很多生物学和药理学活性,例如抗细菌、抗真菌、抗病毒、抗氧化、抗炎、抗突变和抗变应性和对数种酶的抑制活性。从下面的结构可见:肉桂酰酯类图解4(a)、香豆素类图解4(b)、查耳酮类图解4(c)和黄酮类图式4(d)中每一个都含有一般的C6-C3结构图解2(a),色酮类图解4(e)含有一般的C6-C3结构图解2(c),而异黄酮类4(f)含有一般的C6-C3结构图解2(b)。
图解4
适用于本发明的肉桂酰酯(香料)包括但不限于:甲酸肉桂酯、乙酸肉桂酯、肉桂酸乙酯、丙酸肉桂酯、α-甲苯甲酸肉桂酯、2-氨基苯甲酸肉桂酯、邻氨基苯甲酸肉桂酯、苯甲酸肉桂酯、β-苯基丙烯酸肉桂酯、丁酸肉桂酯、肉桂酸肉桂酯、异丁酸肉桂酯、异戊酸肉桂酯、肉桂基甲基酮、邻氨基苯甲酸肉桂酯、苯乙酸肉桂酯、3-苯基丙烯酸肉桂酯及其组合。显然,在一般的结构图解4(a)上的取代,,只要在碳原子附近保留不饱和而且在碳原子处保留氧化,即是预期的。事实上,为获得各种各样的适宜维生素稳定剂,取代是必要的。一般结构图解4(a)的适宜取代基包括但不限于:包括线性的、非线性的、环状的和无环的烷基、以及非取代的和取代的烷基在内的任何烷基。
适用于本发明的香豆素类包括但不限于:香豆素、考迈斯托醇、黄檀素、瑞香素、七叶亭、柠檬油素、去甲黄檀素(noralbergin)、伞形酮、东莨菪亭、花椒毒酚、补骨脂素、佛手内酯、秦皮亭及其组合。显然,在一般结构图解4(b)上的取代,只要在碳原子附近保留不饱和而且在碳原子处保留氧化,即是预期的。事实上,为获得各种各样的适宜维生素稳定剂,取代是必须的。一般结构图解4(b)的适宜取代基包括但不限于:OH、OCH3、C6H4O2、Ph和CH2=CHO。下表3列出为上面列出的适用于本发明的香豆素化合物的取代基。
表3
有取代基位置的示范性香豆素
香豆素图解4(b)
名称 | 取代基位置 | |||||
3 | 4 | 5 | 6 | 7 | 8 | |
迈考斯托醇 | C6H4O2 | OH | ||||
黄檀素 | OH | OCH3 | ||||
瑞香素 | OH | OH | ||||
七叶亭 | OH | |||||
柠檬油素 | OCH3 | OCH3 | ||||
去甲黄檀素 | Ph | OH | OH | |||
伞形酮 | OH | |||||
东莨菪亭 | OCH3 | OH | ||||
花椒毒酚 | CH2=CHO | OH | ||||
补骨脂素 | CH2=CHO | |||||
佛手内酯 | OCH3 | CH2=CHO | ||||
秦皮亭 | OCH3 | OH |
注释:Ph=苯基
空白格=H
适用于本发明的查耳酮类包括但不限于:查耳酮、多羟基查耳酮、紫铆因、根皮苷、刺甘草查耳酮、马里苷、异甘草素、根皮素及其组合。显然,在一般结构图解4(c)上的取代,只要在碳原子附近保留不饱和而且在碳原子处保留氧化,即是预期的。事实上,为获得各种各样的适宜维生素稳定剂,取代是必须的。一般结构图解4(c)的适宜取代基包括但不限于:OH、OCH3和OGlc。下表4列出为上面列出的适用于本发明的查耳酮化合物的取代基。
表4
有取代基位置的示范性的查耳酮
查耳酮图解4(c)
名称 | 取代基位置 | ||||||
2 | 3 | 4 | 2′ | 3′ | 4′ | 6′ | |
紫铆因 | OH | OH | OH | OH | |||
根皮苷 | OH | OGlc | OH | OH | |||
刺甘草查耳酮 | OCH3 | OH | OH | ||||
马里苷 | OH | OH | OH | OH | OGlc | ||
异甘草素 | OH | OH | OH | ||||
根皮素 | OH | OH | OH | OH |
注释:Glc=葡萄糖
空白格=H
适用于本发明的黄酮类包括但不限于:野漆树苷、香叶木苷、芹菜苷、芹黄素、杨梅树皮素、山奈酚、木犀草素、桑色素、新香叶木苷、槲皮素、芸香苷、balcalein、柏木双黄酮、野麻根素、香叶木素、漆树黄酮、高良姜黄素、棉黄素、三叶草素、扁柏双黄酮、黄芩素、黄酮醇、报春花素、车轴草醇、洋槐黄素、万寿菊黄素、(OH)4黄酮、柑橘黄酮、橙黄酮、黄橘苷(fortunelin)、山柰甲黄素(kampferide)、金圣草黄素、异鼠李黄素、牡荆葡基黄酮及其组合。
黄酮类基本上是苦的(例如槲皮素)和不溶的。然而,在维生素稳定剂的使用水平下,通过调配的甜味和酸味,在使用的饮料基质中由于苦味混和抑制现象而感觉不到通常相关的苦味。采用常规实验,根据其在所需饮料基质中的溶解度,即可确定所有维生素稳定剂的最大优选使用水平。
从下列结构可以清楚地看到,一般结构图解4(d)存在于诸如野漆树苷和芸香苷这样的物质中。
图解5
从这些黄酮的结构还可以清楚地看到,在一般结构图解4(d)上的取代,只要在碳原子附近保留不饱和而且在碳原子处保留氧化,即是预期的。事实上,为获得各种各样的适宜维生素稳定剂,取代是必须的。合适的取代基包括但不限于:OH、ORut、OApioGlc、ONeoHesp、二聚体、OCH3和OGlc。下表5列出为上面列出的适用于本发明的黄酮化合物的取代基。
表5
有取代基位置的示范性的黄酮
黄酮图解4(d)
名称 | 取代基位置 | ||||||||
3 | 5 | 6 | 7 | 8 | 2′ | 3′ | 4′ | 5′ | |
野漆树苷 | OH | ONeoHesp | OH | ||||||
香叶木苷 | OH | ORut | OH | OCH3 | |||||
芹菜苷 | OApioGlc | OH | |||||||
芹黄素 | OH | OH | OH | OH | |||||
杨梅树皮素 | OH | OH | OH | OH | OH | OH | |||
山奈酚 | OH | OH | OH | OH | |||||
木犀草素 | OH | OH | OH | OH | |||||
桑色素 | OH | OH | OH | OH | OH | ||||
新香叶木苷 | OH | ONeoHesp | OH | OCH3 | |||||
槲皮素 | OH | OH | OH | OH | OH | ||||
芸香苷 | ORut | OH | OH | OH | OH | ||||
balcalein | OH | OH | OH | ||||||
柏木双黄酮 | OH | OH | 二聚体 | OH | |||||
野麻根素 | OH | OH | OH | OH | |||||
香叶木素 | OH | OH | OH | OCH3 | |||||
漆树黄酮 | OH | OH | OH | OH | |||||
高良姜黄素 | OH | OH | OH | ||||||
棉黄素 | OH | OH | OH | OH | OH | OH | |||
三叶草素 | OH | OH | OH | OCH3 | |||||
扁柏双黄酮 | OH | OGlc | OH | OH | OH |
有取代基位置的示范性的黄酮
黄酮图解4(d)
名称 | 取代基位置 | ||||||||
3 | 5 | 6 | 7 | 8 | 2′ | 3′ | 4′ | 5′ | |
黄芩素 | OH | OH | OH | OH | |||||
黄酮醇 | OH | ||||||||
报春花素 | OH | ||||||||
车轴草醇 | OH | ||||||||
洋槐黄素 | OH | OH | OH | OH | OH | ||||
万寿菊黄素 | OH | OH | OH | OH | OH | OH | |||
(OH)4黄酮 | OH | OH | OH | OH | |||||
柑橘黄酮 | OCH3 | OCH3 | OCH3 | OCH3 | OCH3 | ||||
橙黄酮 | OCH3 | OCH3 | OCH3 | OCH3 | OCH3 | ||||
金橘苷 | OH | OH | OCH3 | ||||||
山柰甲黄素 | OH | OH | OH | OCH3 | |||||
金圣草黄素 | OH | OH | OH | OCH3 | OH | ||||
异鼠李黄素 | OH | OH | OH | OH | OCH3 | ||||
牡荆葡基黄酮 | OH | OH | Glc | OH |
注释:Rut=芸香糖;NeoHesp=新橙皮糖;ApioGlc=芹菜糖-葡萄糖;Glc=葡萄糖
空白格=H
色酮类例如色酮适用于本发明。显然,在一般结构图解4(e)上的取代,只要象图解2(c)中那样碳原子附近保留不饱和而且碳原子处保留氧化,即是预期的。事实上,为获得各种各样的适宜维生素稳定剂,取代是必须的。适于一般结构图解4(e)的适宜取代基包括但不限于:OH、OCH3和OGlc,等等。
适用于本发明的异黄酮类包括但不限于:大豆黄苷、黄豆配基、鹰嘴豆素A、樱黄素、染料木苷、黄豆黄素、glycitin、染料木黄酮、6,7,4′-三(OH)异黄酮、7,3′,4′-三(OH)异黄酮及其组合。显然,在一般结构图解4(f)上的取代,只要象图解2(b)中那样在碳原子附近有不饱和而且在碳原子处有氧化,即是预期的。事实上,为获得各种各样的适宜维生素稳定剂,取代是必须的。适于一般结构图解4(f)的适宜取代基包括但不限于:OH、OCH3和OGlc。下表6列出为上面列出的适用于本发明的异黄酮化合物的取代基。
表6
有取代基位置的示范性的异黄酮
异黄酮图解4(f)
名称 | 取代基位置 | ||||
5 | 6 | 7 | 3′ | 4′ | |
大豆黄苷 | OGlc | OH | |||
黄豆配基 | OH | OCH3 | |||
鹰嘴豆素A | OH | OH | OH | ||
樱黄素 | OH | OCH3 | OH | ||
染料木苷 | OH | OGlc | OCH3 | OH | |
黄豆黄素 | OCH3 | OH | OH | OH | |
glycitin | OCH3 | OGlc | OH | ||
染料木黄酮 | OH | OH | OH | ||
6,7,4′-三(OH)异黄酮 | OH | OH | OH | ||
7,3′,4′-三(OH)异黄酮 | OH | OH | OH |
注释:Glc=葡萄糖
空白格=H
在本发明的某些优选实施方案中,上面提及的具有一般结构图解4(a)-(f)中任一种的C6-C3苯丙烯羰基化合物可以通过植物提取物来提供。适用于本发明的提取物包括但不限于:七叶树、蒲公英、桉树、红色澳洲桉树树皮、锯叶棕、忍冬、山楂、noni fruit、红三叶草、橙、葡萄柚、citrumelo、attani、pummelo、sour、orange、lemelo、Natsudaidai orange、荞麦、春黄菊及其组合。如下表7所示,上面提及的提取物中每一种均含有一种或多种充当植物衍生的维生素稳定剂的C6-C3苯丙烯羰基化合物。
表7
俗名 | 种 | C6-C3苯丙烯羰基化合物 |
七叶树 | 欧洲七叶树(Aesculus hippocastanum) | 芸香苷,七叶亭 |
蒲公英 | 蒲公英属(Taraxacum) | 七叶亭 |
桉树 | Eucalyptus oblique | 芸香苷,七叶亭 |
红色澳洲桉树树皮 | E.macrohyncha | 芸香苷,七叶亭 |
锯叶棕(sabal或shrub palmetto) | Arecaceae科中的锯齿棕(Serenoarepens) | 异槲皮苷,山柰酚-3-O-葡萄糖苷,野漆树苷 |
忍冬 | 金银花(Lonicera japonica) | 木犀草素,槲皮素,黄芪苷,异槲皮苷,香叶木素7-O-葡萄糖苷,野漆树苷,忍冬苷 |
山楂 | 山楂属的种(Crataegus specie) | 牡荆葡基黄酮 |
Noni fruit | 海巴戟(Morinda citrifolia) | 桑色素,芸香苷 |
红三叶草 | 红车轴草(Trifolium pretense) | 异黄酮 |
橙 | 甜橙(Citrus sinensis) | 芸香苷,黄酮类,查耳酮类,香豆素类 |
葡萄柚citrumeloAttani,pummelo,sour,orange,lemelo,Natsudaidai orange | P.trifoliata x C.paradise | 野漆树苷,异野漆树苷芸香,异野漆树苷,野漆树苷野漆树苷 |
荞麦 | 荞麦属的种(Fagopyrum specie) | 芸香苷 |
春黄菊 | 春黄菊属的种(Anthemis specie) | 芹黄素-7-葡萄糖苷 |
至于上面表7提及的植物,本领域技术人员会容易地认识到的是,C6-C3苯丙烯羰基化合物在给定提取物中存在的量会不同。本性不同的种可能含有不同量的C6-C3苯丙烯羰基化合物。该量还可能根据给定植物的发育阶段或者从其进行提取的植物部分而变化。例如,对很多柑橘类水果而言,叶子中的黄酮类和黄酮醇类比橘皮、白色内皮和果汁泡囊中的浓度更高。
典型地,上面提及的任何维生素稳定剂(一般结构图解2(a)-(c)和图解4(a)-(f))以足够提供饮料中从约10ppm到约500ppm的稳定剂的量出现在本发明含维生素组合物中,优选从约50ppm到约300ppm,更优选约100ppm到约200ppm。在维生素稳定剂是经植物提取物提供的情况下,该提取物在本发明含维生素组合物中存在的量足够在饮料中提供与上面提及的量相同量的稳定剂。需要注意的是,提取物中可能含有不同量的稳定剂。例如,一种提取物可能含有5%的活性成分或稳定剂;相应地,应用500ppm提取物可能导致应用25ppm的稳定剂。
本发明的第二个方面涉及防止含维生素饮料中维生素降解的方法,包括向所述饮料中加入维生素稳定量的维生素稳定剂。
所述饮料包括但不限于:充碳酸气的软饮料、汽水饮料、冰冻的立即可饮用的饮料、咖啡饮料、茶饮料、粉末状软饮料,以及液体浓缩物、加味水、维生素强化水、果汁和果汁加味饮料、运动饮料、奶制品和酒精制品。该饮料可以是充碳酸气或不充碳酸气的。该饮料可以被热灌装的。
该含维生素的饮料可能通过上面提及的维生素中的一种或多种的存在而得以强化。另外,维生素稳定剂可与上述本发明第一方面描述的相同。该含维生素组合物可以在饮料生产的任何阶段包含在内,即糖浆、浓缩物、成品饮料。
像上面提及的,一种“维生素稳定量”指足够充分减少或防止含维生素饮料中维生素降解的量。典型地,维生素稳定剂以从约10ppm到约500ppm,优选从约50ppm到约300ppm,更优选约100ppm到约200ppm的量加到含维生素饮料中。如果维生素稳定剂是经植物提取物提供的,该提取物在本发明含维生素食品组合物中存在的量足以在饮料中提供与上面提及的量相同量的稳定剂。
任选地,本发明防止含维生素饮料中维生素降解的方法,进一步包括向所述饮料中加入一种选自山梨酸、乌头酸、脱落酸、富马酸、马来酸或其任意组合的非-芳基烯醇羰基(non-aryl enoic carbonyl)化合物。当其存在时,非-芳基烯醇羰基化合物典型地以从约10ppm-约200ppm、优选从约25ppm-约100ppm的量加入饮料中。
本发明的第三个方面涉及一种稳定的含维生素饮料,该饮料包含维生素和维生素稳定量的维生素稳定剂。本发明第三个方面的稳定的含维生素饮料可任选地含有一种选自山梨酸、乌头酸、脱落酸、富马酸、马来酸或其任意组合的非-芳基烯醇羰基化合物。其中,维生素、维生素稳定剂和非-芳基烯醇羰基化合物各自的量,与上文对本发明第一和第二方面描述的相同。
实施例
表8
维生素A棕榈酸酯的IU
实施例1 | 实施例2 | 实施例3 | 实施例4 | |
黑亮33ppm芸香苷66ppm芸香苷100ppm芸香苷100ppm SanMelin AO-300033ppm蓝莓叶提取物 | 23005768781215--1400 | 1870548--856987- | 3215737-1824--- | 1500960---1261- |
实施例1装于透明玻璃瓶中的含维生素C和EDTA的清澈L/L CSD
制备含维生素C和乙二胺四乙酸(EDTA)的清澈的柠檬-酸橙(L/L)碳酸软饮料(CSD)。制备碳酸软饮料的七个样本,每个含有2500IU的可从Roche获得的维生素A棕榈酸酯,而芸香苷、SanMel in或蓝莓叶提取物的量列于表8。所有样本包装在透明玻璃容器中。黑和亮的样本各自不含芸香苷、SanMelin或蓝莓叶提取物。黑样本屏蔽了光线。所有其他样本,包括亮的样本暴露于典型的商店荧光光线。表中的值都是在一周测得的。
实施例2装于透明玻璃瓶中的含维生素C和EDTA的清澈L/L CSD
实施例2与实施例1的区别在于维生素A棕榈酸酯的初始量是2000IU。
实施例3装于PET瓶中的5%非充气粉红柠檬汁
制备由5%果汁组成的非充气粉红柠檬汁饮料。制备类似实施例1和2中的7个样本,不同的是维生素A棕榈酸酯的初始量为3500IU,并且样品装在PET容器中。
实施例4装于透明玻璃瓶中的杀菌的高酸乳制品
制备高酸乳制品。制备类似实施例2中的7个样本,每个含有2000IU的维生素A棕榈酸酯,并杀菌(retorted)。
虽然针对某些优选实施方案描述了本发明,但是对本领域技术人员可以理解的是,本发明可以有各种改变、改进和重新排列,而这些改变、改进和重新排列由后附权利要求书所涵概。
Claims (22)
2、根据权利要求1的含维生素组合物,其中维生素A是维生素A棕榈酸酯。
3、根据权利要求1的含维生素组合物,其中维生素稳定剂以足够在饮料中提供从约10ppm至约500ppm的维生素稳定剂的量存在。
4、根据权利要求3的含维生素组合物,其中维生素稳定剂以足够在饮料中提供从约50ppm至约300ppm的维生素稳定剂的量存在。
5、根据权利要求4的含维生素组合物,其中维生素稳定剂以足够在饮料中提供从约100ppm至约200ppm的维生素稳定剂的量存在。
6、根据权利要求1的含维生素组合物,其中维生素稳定剂是植物衍生的。
7、根据权利要求1的含维生素组合物,其中维生素稳定剂是合成衍生的。
8、根据权利要求1的含维生素组合物,其中C6-C3苯丙烯羰基化合物选自迷迭香酸、绿原酸、菊苣酸、咖啡酸、香豆酸、肉桂酸、阿魏酸、芥子酸、caftaric acid、eichloric acid、松果菊苷及其混合物。
9、根据权利要求1的含维生素组合物,其中C6-C3苯丙烯羰基化合物选自肉桂酰酯类、香豆素类、查耳酮类、黄酮类、色酮类、异黄酮类及其混合物。
10、根据权利要求9的含维生素组合物,其中肉桂酰酯选自甲酸肉桂酯、乙酸肉桂酯、肉桂酸乙酯、丙酸肉桂酯、α-甲苯甲酸肉桂酯、2-氨基苯甲酸肉桂酯、邻氨基苯甲酸肉桂酯、苯甲酸肉桂酯、β-苯基丙烯酸肉桂酯、丁酸肉桂酯、肉桂酸肉桂酯、异丁酸肉桂酯、异戊酸肉桂酯、肉桂酰甲基酮、邻氨基苯甲酸肉桂酯、苯乙酸肉桂酯、3-苯基丙烯酸肉桂酯及其混合物。
11、根据权利要求9的含维生素组合物,其中香豆素类选自香豆素、考迈斯托醇、黄檀素、瑞香素、七叶亭、柠檬油素、去甲黄檀素、伞形酮、东茛菪亭、花椒毒酚、补骨脂素、佛手内酯、秦皮亭及其混合物。
12、根据权利要求9的含维生素组合物,其中查耳酮类选自查耳酮、多羟基查耳酮类、紫铆因、根皮苷、刺甘草查耳酮、马里苷、异甘草素、根皮素及其混合物。
13、根据权利要求9的含维生素组合物,其中黄酮类选自野漆树苷、香叶木苷、芹菜苷、芹黄素、杨梅树皮素、山奈酚、木犀草素、桑色素、新香叶木苷、槲皮素、芸香苷、balcalein、柏木双黄酮、野麻根素、香叶木素、漆树黄酮、高良姜黄素、棉黄素、三叶草素、扁柏双黄酮、黄芩素、黄酮醇、报春花素、车轴草醇、洋槐黄素、万寿菊黄素、(OH)4黄酮、柑橘黄酮、橙黄酮、黄橘苷、山柰甲黄素、金圣草黄素、异鼠李黄素、牡荆葡基黄酮及其混合物。
14、根据权利要求9的含维生素组合物,其中色酮类是色酮。
15、根据权利要求9的含维生素组合物,其中异黄酮类选自大豆黄苷、黄豆配基、鹰嘴豆素A、樱黄素、染料木苷、黄豆黄素、glycitin、染料木黄酮、6,7,4′-三(OH)异黄酮、7,3′,4′-三(OH)异黄酮及其混合物。
16、根据权利要求13的含维生素组合物,其中芸香苷是酶修饰的异槲皮苷。
17、根据权利要求6的含维生素组合物,其中植物衍生的维生素稳定剂是由植物提取物提供的。
18、根据权利要求17的含维生素组合物,其中提取物选自迷迭香提取物、生咖啡豆提取物、蓝莓提取物、杜鹃花提取物、向日葵仁提取物、菊苣叶提取物、紫松果菊提取物、莴苣提取物及其混合物。
19、根据权利要求17的含维生素组合物,其中提取物选自七叶树提取物、蒲公英提取物、桉树提取物、澳洲桉树树皮提取物、锯叶棕提取物、忍冬提取物、山楂提取物、noni fruit提取物、红三叶草提取物、橙提取物、荞麦提取物、春黄菊提取物及其混合物。
20、根据权利要求1的含维生素组合物,进一步包含选自山梨酸、乌头酸、脱落酸、富马酸、马来酸及其混合物的非-芳基烯羰基化合物。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/267,376 US7767238B2 (en) | 2005-11-04 | 2005-11-04 | Beverage composition and method of preventing degradation of vitamins in beverages |
US11/267,376 | 2005-11-04 |
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CN101069563A true CN101069563A (zh) | 2007-11-14 |
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EP (1) | EP1782701B1 (zh) |
JP (2) | JP2007125018A (zh) |
CN (1) | CN101069563B (zh) |
CA (1) | CA2567000A1 (zh) |
ES (1) | ES2400723T3 (zh) |
MX (1) | MXPA06012784A (zh) |
PL (1) | PL1782701T3 (zh) |
RU (1) | RU2337593C2 (zh) |
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CN104146300A (zh) * | 2014-08-06 | 2014-11-19 | 河南钧鼎生物科技有限公司 | 复合诺丽果浆及其制备方法 |
CN105338832A (zh) * | 2013-06-27 | 2016-02-17 | 弗门尼舍有限公司 | 用于改变味道的成分 |
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US20070275140A1 (en) * | 2006-05-26 | 2007-11-29 | Paula Safko | Beverage compositions comprising a preservative system |
US8293299B2 (en) | 2009-09-11 | 2012-10-23 | Kraft Foods Global Brands Llc | Containers and methods for dispensing multiple doses of a concentrated liquid, and shelf stable Concentrated liquids |
JP5393367B2 (ja) * | 2009-09-14 | 2014-01-22 | サントリー食品インターナショナル株式会社 | 呈味付与剤 |
AU2012315782B2 (en) | 2011-09-30 | 2015-10-29 | Perio Sciences, Llc | Antioxidant compositions for treatment of inflammation or oxidative damage |
JP5128710B1 (ja) * | 2012-03-23 | 2013-01-23 | 株式会社 伊藤園 | 容器詰飲料及びその製造方法 |
US11013248B2 (en) | 2012-05-25 | 2021-05-25 | Kraft Foods Group Brands Llc | Shelf stable, concentrated, liquid flavorings and methods of preparing beverages with the concentrated liquid flavorings |
JP2020536537A (ja) | 2017-10-06 | 2020-12-17 | カーギル インコーポレイテッド | 易溶解性ステビオールグリコシド組成物 |
US20210022372A1 (en) * | 2018-06-22 | 2021-01-28 | "Bio 8", Limited Liability Company | Dry concentrate for preparation of a protein cocktail |
EP3952667A1 (en) | 2019-04-06 | 2022-02-16 | Cargill, Incorporated | Sensory modifiers |
CA3135584A1 (en) | 2019-04-06 | 2020-10-15 | Cargill, Incorporated | Methods for making botanical extract composition |
EP4362704A1 (en) * | 2021-06-29 | 2024-05-08 | Firmenich SA | Licorice compounds and their use as flavor modifiers |
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JPS62278969A (ja) * | 1986-05-28 | 1987-12-03 | Yagieiji Shoten:Kk | そば炒り煎茶の製造法 |
JPH03272643A (ja) | 1990-03-20 | 1991-12-04 | Calpis Food Ind Co Ltd:The | 乳含有酸性飲料 |
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US20060051472A1 (en) * | 2004-05-07 | 2006-03-09 | San-Ei Gen F.F.I., Inc. | Method for suppressing fading of tar colorant, and fading-suppressed tar colorant-containing composition |
-
2005
- 2005-11-04 US US11/267,376 patent/US7767238B2/en active Active
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2006
- 2006-11-01 CA CA002567000A patent/CA2567000A1/en not_active Abandoned
- 2006-11-02 CN CN200610130993XA patent/CN101069563B/zh active Active
- 2006-11-02 JP JP2006298834A patent/JP2007125018A/ja active Pending
- 2006-11-03 PL PL06255667T patent/PL1782701T3/pl unknown
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- 2006-11-03 ES ES06255667T patent/ES2400723T3/es active Active
- 2006-11-03 RU RU2006139014/13A patent/RU2337593C2/ru active
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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CN105338832A (zh) * | 2013-06-27 | 2016-02-17 | 弗门尼舍有限公司 | 用于改变味道的成分 |
CN108271962A (zh) * | 2013-06-27 | 2018-07-13 | 弗门尼舍有限公司 | 用于改变味道的成分 |
CN104146300A (zh) * | 2014-08-06 | 2014-11-19 | 河南钧鼎生物科技有限公司 | 复合诺丽果浆及其制备方法 |
CN104146300B (zh) * | 2014-08-06 | 2015-09-09 | 河南钧鼎生物科技有限公司 | 复合诺丽果浆及其制备方法 |
Also Published As
Publication number | Publication date |
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US7767238B2 (en) | 2010-08-03 |
PL1782701T3 (pl) | 2013-05-31 |
EP1782701B1 (en) | 2013-01-02 |
EP1782701A1 (en) | 2007-05-09 |
US20070110851A1 (en) | 2007-05-17 |
CA2567000A1 (en) | 2007-05-04 |
RU2337593C2 (ru) | 2008-11-10 |
JP2007125018A (ja) | 2007-05-24 |
MXPA06012784A (es) | 2007-10-10 |
RU2006139014A (ru) | 2008-05-20 |
ES2400723T3 (es) | 2013-04-11 |
CN101069563B (zh) | 2012-07-25 |
JP2011067221A (ja) | 2011-04-07 |
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