CN112569323A - 一种解酒护肝的组合物及其应用 - Google Patents
一种解酒护肝的组合物及其应用 Download PDFInfo
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Abstract
本发明提供了一种解酒护肝的组合物及其应用,涉及保健品技术领域。本发明所述组合物包括药食同源的中药的水提物、益生菌、牛磺酸、维生素B和维生素C。本发明利用卫生部规定的药食两用生药原料,以及符合国家食品原料国标的营养强化剂原料制备所述组合物,兼具治疗和保健作用,可将其制备成具有相应功能的可长期食用的保健品,既有即时解酒又有长期服用保肝护肝的作用。
Description
技术领域
本发明属于保健品技术领域,具体涉及一种解酒护肝的组合物及其应用。
背景技术
世界卫生组织(WHO)指出,酒精中毒仍然是当今世界范围内的公害之一。饮酒过度现象以及由酒精所引发的疾病和问题也日益增多,且进入体内的乙醇大部分经肝脏代谢,对肝脏具有较强的毒性,例如使肝细胞膜表面的脂质过氧化以及破坏肝细胞膜,长期饮酒还会使肝细胞内的微管和线粒体等结构受到破坏,使细胞内的代谢紊乱,产生具有细胞毒性的代谢产物,导致肝细胞肿胀、坏死等等。
针对过量饮酒或酒精中毒等目前已有相关的化学药和中药,但是化学药本身也需要经肝脏代谢,代谢过程对肝脏同样具有毒性,故西药化学药只能在即时解决酒醉的不良反应,决不能作为长期调理的护肝保肝药物。同样的关于解酒的中药,大都是根据中药药味文献记载或古方文献记载,以及根据现代药理,提出的中药复方,虽能暂时缓解头晕、恶心等症状,但很多都含有使人兴奋的活性成分,只能治标不能治本。
虽然也有同时对脾气运化功能,肝气疏泄功能和肾气封藏功能的所谓标本兼治的中医理论,但鲜有现代药理实验证明,而且这类复方中药,都含有非药食两用的中药药味,即属治疗型,而不能长期服用调理。
发明内容
有鉴于此,本发明的目的在于提供一种解酒护肝的组合物及其应用,所述组合物既有解酒效果,又能长期服用,可制备成具有护肝保肝效果的食用保健品。
为了实现上述发明目的,本发明提供以下技术方案:
本发明提供了一种解酒护肝的组合物,所述组合物包括以下质量百分含量的组分:药食同源的中药的水提物66.3%~95.4%、益生菌2.5%~5.5%、牛磺酸0.15%~3.5%、维生素B 0.07%~0.75%和维生素C1%~4%。
优选的,所述组合物包括以下质量百分含量的组分:药食同源的中药的水提物72.7%~92.5%、益生菌3%~4%、牛磺酸2%~3%、维生素B 0.3%~0.45%和维生素C2%~3%。
优选的,所述药食同源的中药包括枳椇子、葛根、山楂、肉豆蔻、人参、菊花、高良姜和肉桂;且所述枳椇子、葛根、山楂、肉豆蔻、人参、菊花、高良姜和肉桂的质量比为(35~55):(18~30):(6~12):(3~12):(2~8):(2~7):(1.5~7):(0.6~4)。
优选的,所述枳椇子、葛根、山楂、肉豆蔻、人参、菊花、高良姜和肉桂的质量比为(40~47):(19~25):(8~10):(8~11):(3~6):(4~6):(4~6):(1~2)。
优选的,所述益生菌中包括植物乳杆菌、嗜酸乳杆菌、干酪乳杆菌、副干酪乳杆菌、鼠李糖乳杆菌、发酵乳杆菌、唾液乳杆菌、瑞士乳杆菌、罗伊氏乳杆菌、格氏乳杆菌、卷曲乳杆菌、约氏乳杆菌、保加利亚乳杆菌、嗜热链球菌、乳双歧杆菌、长双歧杆菌、短双歧杆菌、婴儿双歧杆菌、芽孢杆粪链球菌、两歧双歧杆菌和青春双歧杆菌中的两种或两种以上的混合。
优选的,所述维生素B包括维生素B1、维生素B2和维生素B6;且所述维生素B1、维生素B2和维生素B6的质量比为(0.023~0.25):(0.023~0.25):(0.023~0.25)。
优选的,所述维生素B1、维生素B2和维生素B6的质量比为(0.10~0.15):(0.10~0.15):(0.10~0.15)。
本发明还提供了上述组合物在制备具有解酒护肝效果的保健品中的应用。
本发明还提供了一种具有解酒护肝效果的保健品,所述保健品的有效成分包括上述组合物。
优选的,所述保健品的剂型包括颗粒剂、片剂或胶囊剂。
本发明提供了一种解酒护肝的组合物,包括药食同源的中药的水提物、益生菌、牛磺酸、维生素B和维生素C。本发明所述组合物的原料属于卫生部规定的药食两用生药原料,兼具治疗和保健作用;且生药原料以外的其他原料,都为符合国家食品原料国标的营养强化剂原料,其添加量都在法规允许范围内,可将其制备成具有相应功能的可长期食用的保健品,既有即时解酒又有长期服用保肝护肝的作用。
本发明所述组合物和保健品通过多个途径参与乙醇的代谢过程,降低乙醇对机体的伤害(包括降低乙醇、氧自由基和乙醛对机体的伤害)、调节乙醇代谢过程相关键酶活性尤其是提高乙醇脱氢酶活性加速乙醇代谢、提高乙醛脱氢酶活性、降低乙醛对机体伤害,同时还可以增加抗氧化活性成分,减少因乙醇代谢过程产生的自由基对机体的伤害。
具体实施方式
本发明提供了一种解酒护肝的组合物,所述组合物包括以下质量百分含量的组分:药食同源的中药的水提物66.3%~95.4%、益生菌2.5%~5.5%、牛磺酸0.15%~3.5%、维生素B 0.07%~0.75%和维生素C1%~4%。
本发明所述组合物中药食同源的中药(也称生药)的水提物质量百分含量优选为72.7%~92.5%。本发明所述药食同源的中药优选包括枳椇子、葛根、山楂、肉豆蔻、人参、菊花、高良姜和肉桂;且所述枳椇子、葛根、山楂、肉豆蔻、人参、菊花、高良姜和肉桂的质量比优选为(35~55):(18~30):(6~12):(3~12):(2~8):(2~7):(1.5~7):(0.6~4),更优选为(40~47):(19~25):(8~10):(8~11):(3~6):(4~6):(4~6):(1~2)。
本发明对所述水提物(也称生药提取物)的制备方法并没有特殊限定,既可以将所述中药分别提取后混合,也可以混合后再共同提取,还可以任意两种或多种中药混合后提取;当分别提取时,各生药的提取方法相同,以枳椇子为例,进行说明,包括以下步骤:将生药枳椇子置于提取灌中,用8~12倍质量的饮用水进行微沸第一提取,并过60~100目筛;滤渣再经6~10倍质量的饮用水进行1~2次微沸提取,过60~100目筛;弃去滤渣,合并滤液,静置过夜,取上清液真空浓缩,至含固量约20%(或比重1.02~1.1(热测))的浸膏;喷雾干燥,制得生药的提取物;将利用上述方案制备得到的各生药的提取物混合后即可作为总生药提取物。当共同提取时,将所述生药按照上述比例混合后,依据上述方案进行相同的提取即可。
在本发明中,枳椇子“止呕逆”、“止咳除烦,去膈上热。润五脏,利大小便”,与李东垣的《脾胃论》对酒伤治疗所述“汗出则愈矣,其次莫如利小便”相符;葛根“解肌发表出汗”,同时“能治天行上气,呕逆,开胃下食,主解酒毒,止烦渴”,水提物中所含的葛根异黄酮等生物活性物质,能提高肝脏乙醇脱氢酶和乙醛脱氢酶的活性;过氧酶类等活性成分具有醒酒安神作用。葛根和枳椇子具有协同解酒作用。
在本发明中,山楂水提物中总黄酮含量可高达85%,可降低高脂饲料所致SD大鼠肝组织丙二醛(MDA)、总胆固醇(TC)等的含量,清除肝内堆积的三酰甘油,减少脂肪酸(FFA)对肝细胞毒性作用,能降低丙氨酸氨基转移酶(ALT)、天门冬酸氨基转移酶(AST)等肝功能指标,达到调节血脂、保肝作用;同时还具很强的抗氧化活性,对羟自由基和超氧阴离子有清除和抑制作用,且作用强度与浓度正相关;且能提高体内超氧化物歧化酶(SOD)活性。此外山楂水提物中还含多种有机酸,口服能增加胃中消化酶的分泌,增强脂肪酶、蛋白酶的活性。山楂还能促进肠道蠕动,对肠道功能紊乱有明显的双向调节作用。这些有对解酒护肝都具有很强的相关性作用。
在本发明中,肉豆蔻“消宿食,解酒毒”。动物试验证明,其能显著提高抗氧化酶系统中超氧化物歧化酶(SOD)活性,阻止自由基的脂质过氧化作用。显著降低脂质过氧化产物丙二醛(MDA)含量,从而显著降低对肝脏的损伤;能显著减少并降低因D-氨基半乳糖(GaIN)模型小鼠肝损伤模型造成的肝细胞变性、坏死。
在本发明中,人参能促进动物模型提高还原型谷胱甘肽(GSH)的含量和乙醇脱氢酶(ADH)含量,并显著降低乙醇模型小鼠血中乙醇浓度;同时人参可以促进葛根中的异黄酮类成分溶出,并增加人参皂苷的含量。葛根和人参混合提取比分别提取更有益于ADH活性增加,且两者混合提取液更有益于其他的体内酶活性的增加。
在本发明中,菊花主要活性成分为黄酮类化合物和绿原酸。具有疏风、清热、明目、解毒的功效,主要治疗头痛,眩晕,目赤,心胸烦热,疗疮,肿毒等症。《本草纲目》中称野菊花有“利五脉、调四肢,治头风热、脑骨肿痛、养目血、去翳膜,主肝气不足”。《药鉴》载其“解醉汉昏迷,易醒,共干葛(也叫葛花)煎汤”。同时,菊花具有较强的抗氧化作用,可提高小鼠谷胱甘肽过氧化物活性,清除氧自由基,具有保肝功能。
在本发明中,高良姜味辛热,有散寒止痛、温中止呕之功,“暖胃散寒,消食醒酒,治胃院冷痛”。在本发明所述组合物中,具有温中止呕,消化、健胃、止呕作用。药理学研究表明,其具有抗溃疡、抗腹泻、镇痛抗炎、抗血栓形成、抗氧化、抗菌等药理活性,姜能显著降低急性酒精性肝损伤小鼠血清GPT水平。
在本发明中,肉桂味辛、甘,性大热,能散寒通经、引火归源,而关于其解药毒之殊用,历代本草亦见散在记载。肉桂能制约金石等热药毒,这与其引火归元的特性相关,能发汗疏通血脉,宣导百药。肉桂辛以善行,热则温通,能导诸药通行于血脉经络,但凡药毒害人,其毒内结于血脉之中,无外泄之机,毒难排解,蓄积伤人,肉桂起到芳香宣导透毒外出,加速毒素代谢的作用。肉桂之宣透与其他解表透邪药又有所不同,其性能走能守,既能通经宣透,亦能补火助阳、引火归元。且肉桂的水提物有超强的抗氧化活性,具有很强的抗自由基活性,可提高超氧化物歧化酶(SOD)活性,能降低自由基代谢产物(MDA)含量,能提高神经生长因子(nerve growth factor,NGF)、脑源性神经生长因子(brainnerve growthfactor,BDNF)表达,改善血液流变学,改善慢性脑缺血大鼠的认知能力。
本发明所述组合物中,所述益生菌的质量百分含量为2.5%~5.5%,优选为3%~4%,可满足每天人服用益生菌量≥360亿CFU/天·人即可。本发明所述益生菌中优选包括植物乳杆菌、嗜酸乳杆菌、干酪乳杆菌、副干酪乳杆菌、鼠李糖乳杆菌、发酵乳杆菌、唾液乳杆菌、瑞士乳杆菌、罗伊氏乳杆菌、格氏乳杆菌、卷曲乳杆菌、约氏乳杆菌、保加利亚乳杆菌、嗜热链球菌、乳双歧杆菌、长双歧杆菌、短双歧杆菌、婴儿双歧杆菌、凝结芽孢杆菌、两歧双歧杆菌和青春双歧杆菌中的两种或两种以上的混合。在本发明中,所述益生菌为一类活菌制剂,具有平衡肠道菌群、抑制潜在致病菌、增加肠黏膜抵抗力的作用,可在多个水平下调内源性炎症介质,同时利用益生菌还能改善肠道菌群结构,有利于慢性肝病动物模型恢复转氨酶水平、减少脂肪沉积、减轻肝脏炎症反应。本发明对上述益生菌的各菌种及来源并没有特殊限定,利用本领域的常规市售菌种即可。
本发明所述组合物中,维生素B的质量百分含量为0.07%~0.75%,优选为0.30~0.45%。本发明所述维生素B优选包括维生素B1、维生素B2和维生素B6;且所述维生素B1、维生素B2和维生素B6的质量比优选为(0.023~0.25):(0.023~0.25):(0.023~0.25),更优选为(0.10~0.15):(0.10~0.15):(0.10~0.15)。在本发明中,B族维生素可作为机体反应酶的合成原料,可改善脂肪蛋白质的代谢,助消化,并参与体内各种蛋白酶的作用和体内多种新陈代谢反应。充足的B族维生素,能避免肝脂肪变性,提高肝脏对乙醇的耐受力,消除乙醇和烟焦油等内毒素,保护肝脏,从而具有防止脂肪肝的功效和养肝功效。
本发明所述组合物中,牛磺酸的质量百分含量为0.15%~3.5%,优选为2%~3%。在本发明中,所述牛磺酸是细胞内含量最丰富的含磺酸基的β自由氨基酸,可以维持组织渗透压、稳定细胞膜、抗氧化应激、调节免疫力、维持细胞钙离子水平、保护线粒体、抑制肝细胞活性氧产生以及明显提高肝脏中乙醇脱氢酶和乙醛脱氢酶的活性,减少过氧化物酶的释放,可有效保护肝细胞。同时牛磺酸还可以抑制脂质过氧化,减少MDA并保护胰岛β细胞功能等广泛生物学效应;还具有加速乙醇的代谢、抗炎等多种生理功能。此外牛磺酸通过加速或对肝细胞极低密度脂蛋白分泌的保护作用,可防止高脂血清诱发的原代培养肝细胞脂肪变。牛磺酸还能减少造模大鼠肠道对高脂饮食中TG和TC的吸收,促进肝脏脂质代谢,从而防止高脂血症和肝脂肪变性的发生,能有效的保护肝脏因乙醇引起的伤害。
本发明所述组合物中,维生素C的质量百分含量为1%~4%,优选为2%~3%。在本发明中,所述维生素C是一种强还原剂,可以保护其他抗氧化剂,防止自由基对人体的伤害,保护细胞、解毒、保护肝脏。它还能促进许多体内抗氧化酶的氧化型转为还原型,从持续发挥抗氧化作用。
本发明所述组合物中优选还包括余量的辅料,所述辅料的质量优选为所述组合物质量的0~20%。本发明对所述辅料的种类和用量并没有特殊限定,优选根据不同的剂型进行常规选择即可。由此,本发明所述组合物通过多个途径参与乙醇的代谢过程,降低乙醇对机体的伤害,既有即时解酒又有长期服用保肝护肝作用。
本发明还提供了上述组合物在制备具有解酒护肝效果的保健品中的应用。
本发明还提供了一种具有解酒护肝效果的保健品,所述保健品的有效成分包括上述组合物。本发明所述保健品的剂型优选包括颗粒剂、片剂或胶囊剂。本发明所述保健品优选的每天服用5g,即每天服用益生菌活菌量为360~750亿/人·天。
下面结合实施例对本发明提供的一种解酒护肝的组合物及其应用进行详细的说明,但是不能把它们理解为对本发明保护范围的限定。
实施例1
1、按表1所示配制生药;
表1生药组成
生药名称 | 生药比例% |
枳椇子 | 47 |
葛根 | 25 |
山楂 | 8 |
肉豆蔻 | 8 |
人参 | 3 |
菊花 | 4 |
高良姜 | 4 |
肉桂 | 1 |
合计 | 100 |
2、生药原料提取(混合提取)
将表1所述生药混合一起置于提取灌中,加总生药重量10倍量饮用水,加热至沸,保持微沸2h,80目过滤,收集滤液;滤渣继续加水8倍,加热至沸,保持微沸1.5h,80目过滤,滤渣弃去,滤液与上述滤液合并,静置过夜,取上清液真空浓缩,至含固量约20%(或比重1.02~1.1左右(热测)的浸膏),将此浸膏喷雾干燥,控制进风温度为150~190℃,出风80~95℃,得浸膏粉;将此粉过100目筛,制得配方原料生药的混合提取物,即为总生药提取物。
3、产品制备(固体饮料,配方如表2)
表2固体饮料配方
名称 | 原辅料比例% |
总生药提取物 | 72.7 |
益生菌(规格:3×10<sup>11</sup>cfu/g) | 3 |
牛磺酸 | 2 |
维生素B1 | 0.1 |
维生素B2 | 0.1 |
维生素B6 | 0.1 |
维生素C | 2 |
赤藓糖醇、三氯蔗糖 | 20 |
合计 | 100 |
1)配方称量
按表2所述配方称取总生药提取物、益生菌(植物乳杆菌0.6%、嗜酸乳杆菌0.6%、鼠李糖乳杆菌0.6%、格氏乳杆菌0.6%、嗜热链球菌0.6%)、牛磺酸、维生素B1、维生素B2、维生素B6、维生素C和赤藓糖醇(19.5%)、三氯蔗糖(0.5%),为备用1。
2)混合制粒干燥
取已称取的备用1中的总生药提取物、牛磺酸、赤藓糖醇,置混合机混合均匀后,混合粉体置流化床,用水作粘合剂,进行制粒,至含水量3~5%,出料。经10目筛网摇摆式颗粒机整粒,得制粒颗粒。
3)总混:
取已称取的备用1中的益生菌、维生素B1、维生素B2、维生素B6、维生素C、三氯蔗糖先人工混合均匀,再与上述已制得的颗粒置混合机混合均匀,为备用2。
4)固体饮料灌装:
选择适当铝箔包装材料。调节灌装机至2.5克/支。取备用2灌装密封。装量误差符合相应包装食品要求。
5)产品活性检测
5.1)氧化自由基吸收能力(ORAC)分析检测结果,该产品ORAC值为3500(μmol TE/g)。
5.2)益生菌活菌含量检测:9×109(cfu/g),约225亿/支。
建议服用量:解酒:饮酒前后各服一次,每次1~2支,通常保健:每天2支。活菌每天服用量为450亿。
实施例2
1、按表3所示比例配置生药
表3生药配制比例
生药名称 | 生药比例% |
枳椇子 | 40 |
葛根 | 19 |
山楂 | 10 |
肉豆蔻 | 11 |
人参 | 6 |
菊花 | 6 |
高良姜 | 6 |
肉桂 | 2 |
合计 | 100 |
2、生药原料提取(混合提取)
除生药配制比例不同外,其余操作与实施例1相同。
3、产品制备(胶囊剂)
表4产品配方
1)配方称量
按表4所示配方称取总生药提取物、益生菌(鼠李糖乳杆菌0.8%、乳双歧杆菌0.8%、长双歧杆菌0.8%、短双歧杆菌0.8%、凝结芽孢杆菌0.8%)、牛磺酸、维生素B1、维生素B2、维生素B6、维生素C和硬脂酸镁,为备用1。
2)混合制粒干燥
取已称取的备用1中的总生药提取物、牛磺酸、置混合机混合均匀后,混合粉体置流化床,用水作粘合剂,进行制粒,至含水量3~5%,出料。经10目筛网摇摆式颗粒机整粒,得制粒颗粒。
3)总混:
取已称取的备用1中的益生菌、维生素B1、维生素B2、维生素B6、维生素C、硬脂酸镁,先人工混合均匀,再与上述已制得的颗粒置混合机混合均匀,为备用2。
4)灌装:
选择0#号硬胶囊囊壳。调节灌装至0.5g/粒。灌装胶囊。装量误差符合相应保健食品要求。
5)产品活性检测
5.1)氧化自由基吸收能力(ORAC)分析检测结果,该产品ORAC值为4300(μmol TE/g)。
5.2)益生菌活菌含量检测:9×109(cfu/g),约45亿/粒。
建议服用量:解酒:饮酒前后各服一次,每次4~5粒,通常保健:每天2次,每次3~4粒。活菌每天服用量约为360~480亿/天·人。
实施例3
1、按表5所示比例配制生药
表5生药配制比例
生药名称 | 生药比例% |
枳椇子 | 45 |
葛根 | 22 |
山楂 | 8 |
肉豆蔻 | 9 |
人参 | 5 |
菊花 | 5 |
高良姜 | 4.5 |
肉桂 | 1.5 |
合计 | 100 |
2、生药原料提取(各生药分别提取)
按表5所示配方分别称取生药枳椇子、葛根、山楂、高良姜、肉豆蔻、菊花、肉桂、人参。分别置提取灌中,分别加该种生药重量10倍量饮用水,加热至沸,保持微沸1.5h,80目过滤,收集滤液;滤渣继续加水8倍,加热至沸,保持微沸1h,80目过滤,滤渣弃去,滤液与上述滤液合并,静置过夜,取上清液真空浓缩,至含固量约20%(或比重1.02~1.1左右(热测)的浸膏);将此浸膏喷雾干燥,控制进风温度为150~190℃,出风80~95℃,得浸膏粉;将此粉过100目筛,制得各味生药的提取物,将制得的各生药提取物混合后作为总生药提取物。
3、产品制备(片剂):
表6产品配方
1)配方称量
按表6所示配方称取总生药提取物、益生菌(干酪乳杆菌0.8%、副干酪乳杆菌0.8%、发酵乳杆菌0.8%、两歧双歧杆菌0.8%、凝结芽孢杆菌0.8%)、牛磺酸、维生素B1、维生素B2、维生素B6、维生素C和微晶纤维素(10%)、硬脂酸镁(0.55%),为备用1。
2)混合制粒干燥
取已称取的备用1中的总生药提取物、牛磺酸、及微晶纤维素,置混合机混合均匀后,混合粉体置流化床,用水作粘合剂,进行制粒,至含水量3~5%,出料。经10目筛网摇摆式颗粒机整粒,得制粒颗粒。
3)总混:
取已称取的备用1中的益生菌、维生素B1、维生素B2、维生素B6、维生素C和硬脂酸镁,先人工混合均匀,再与上述已制得的颗粒置混合机混合均匀,为备用2。
4)压片:
选用合适片型及片重的冲头,调节片重至0.75g/片,进行压片,片剂要求硬度为大于5kg,崩解时间在60min以内。压片后,再进行薄膜包衣,包衣粉用量为素片重量的3%。
5)产品活性检测
5.1)氧化自由基吸收能力(ORAC)分析检测结果,该产品ORAC值为3900(μmol TE/g)。
5.2)益生菌活菌含量检测:1.2×1010(cfu/g),约90亿/片。
建议服用量:解酒:饮酒前后各服一次,每次3~4片。通常保健:每天2次,每次2~3片。活菌每天服用量约为360~540亿/天·人。
实施例4
除益生菌组成与实施例3不同外,其余均相同,本实施例中的益生菌(4%,规格3×1011cfu/g)组成为:青春双歧杆菌1%、长双歧杆菌1%、短双歧杆菌1%、凝结芽孢杆菌1%。
实施例5
除益生菌组成与实施例3不同外,其余均相同,本实施例中的益生菌(4%,规格3×1011cfu/g)组成为:植物乳杆菌0.4%、嗜酸乳杆菌0.4%、鼠李糖乳杆菌0.4%、格氏乳杆菌0.4%、嗜热链球菌0.4%、干酪乳杆菌0.4%、副干酪乳杆菌0.4%、发酵乳杆菌0.4%、两歧双歧杆菌0.4%和凝结芽孢杆菌0.4%。
实施例6
除益生菌组成与实施例3不同外,其余均相同,本实施例中的益生菌(4%,规格3×1011cfu/g)组成为:鼠李糖乳杆菌0.40%、乳双歧杆菌0.40%、长双歧杆菌0.40%、短双歧杆菌0.40%、凝结芽孢杆菌0.40%、青春双歧杆菌0.40%、长双歧杆菌0.40%、短双歧杆菌0.40%、两歧双歧杆菌0.40%和凝结芽孢杆菌0.40%。
实施例7
除总生药提取物占比、益生菌组成及占比与实施例3不同外,其余均相同,本实施例中的总生药提取物(80%),益生菌(3%,规格3×1011cfu/g)组成为:长双歧杆菌1%、短双歧杆菌1%、凝结芽孢杆菌1%。
对实施例2和实施例3制备得到的保健品进行动物试验:
构建小鼠醉酒模型:适应性饲养后,小鼠随机分成7组(正常组、醉酒组、醉酒+海王金樽、醉酒+受试物组,每组10个动物。
分组信息如下:正常对照组(n=10),不做处理;模型对照组(n=10),等体积赋形剂;阳性对照1(n=10),海王金樽(1.5g/kg);受试样品(1.5和3g/kg,n=10)。
试验当日,各组小鼠给予赋形剂、海王金樽或受试物灌胃(体积25ml/kg),半小时后,各组小鼠给予乙醇(浓度50%)20ml/kg体重,记录醉酒潜伏期(灌酒后至翻正反射消失)、醉酒时间(反射消失至反射恢复)。
苏醒后:
摘眼球取血,分离血清,测定肝功能指标(ALT(IU/L)、AST(IU/L)、TBIL(μmol/L)、ALP(IU/L));
实验样品小鼠服用量为人体的20倍,其中解酒试验指标包括:反射消失时长和反射恢复时间;对肝脏影响的指标包括:谷丙转氨酶、谷草转氨酶、总胆红素、碱性磷酸酶。并以市售的海王金樽作为阳性对照。其中实施例2和实施例3两个样品的各项指标(表7~12)都优于阳性对照海王金樽,且与模型组比较,经统计分析,都具显著性,P值*<0.05和极显著性,P值**<0.01。
表7保健品对反射消失时长的影响(用量均为3g/kg)
反射消失时长(min) | 模型 | 海王金樽 | 实施例2* | 实施例3** |
mean均值 | 18.4 | 13.6 | 35 | 28 |
SD方差 | 5.680375574 | 4.788875999 | 19.24693338 | 4.666666667 |
显著性P值 | 0.025000651 | 0.002173431 |
表8保健品对反射恢复时长的影响(用量均为3g/kg)
反射恢复时间(min) | 模型 | 海王金樽 | 实施例2* | 实施例3* |
mean均值 | 744.5 | 708 | 616.1111111 | 623.7777778 |
SD方差 | 69.72732606 | 108.012345 | 88.17375523 | 69.77961339 |
存活率% | 60 | 70 | 90 | 90 |
显著性P值 | 0.239323573 | 0.026232911 | 0.017284511 |
表9保健品对谷丙转氨酶的影响(用量均为1.5g/kg)
表10保健品对谷草转氨酶的影响(用量均为1.5g/kg)
表11保健品对总胆红素的影响(用量均为1.5g/kg)
表12保健品对碱性磷酸酶的影响(用量均为1.5g/kg)
以上所述仅是本发明的优选实施方式,应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明原理的前提下,还可以做出若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。
Claims (10)
1.一种解酒护肝的组合物,其特征在于,所述组合物包括以下质量百分含量的组分:药食同源的中药的水提物66.3%~95.4%、益生菌2.5%~5.5%、牛磺酸0.15%~3.5%、维生素B 0.07%~0.75%和维生素C1%~4%。
2.根据权利要求1所述组合物,其特征在于,所述组合物包括以下质量百分含量的组分:药食同源的中药的水提物72.7%~92.5%、益生菌3%~4%、牛磺酸2%~3%、维生素B0.3%~0.45%和维生素C 2%~3%。
3.根据权利要求1或2所述组合物,其特征在于,所述药食同源的中药包括枳椇子、葛根、山楂、肉豆蔻、人参、菊花、高良姜和肉桂;且所述枳椇子、葛根、山楂、肉豆蔻、人参、菊花、高良姜和肉桂的质量比为(35~55):(18~30):(6~12):(3~12):(2~8):(2~7):(1.5~7):(0.6~4)。
4.根据权利要求3所述组合物,其特征在于,所述枳椇子、葛根、山楂、肉豆蔻、人参、菊花、高良姜和肉桂的质量比为(40~47):(19~25):(8~10):(8~11):(3~6):(4~6):(4~6):(1~2)。
5.根据权利要求1所述组合物,其特征在于,所述益生菌中包括植物乳杆菌、嗜酸乳杆菌、干酪乳杆菌、副干酪乳杆菌、鼠李糖乳杆菌、发酵乳杆菌、唾液乳杆菌、瑞士乳杆菌、罗伊氏乳杆菌、格氏乳杆菌、卷曲乳杆菌、约氏乳杆菌、保加利亚乳杆菌、嗜热链球菌、乳双歧杆菌、长双歧杆菌、短双歧杆菌、婴儿双歧杆菌、芽孢杆粪链球菌、两歧双歧杆菌和青春双歧杆菌中的两种或两种以上的混合。
6.根据权利要求1所述组合物,其特征在于,所述维生素B包括维生素B1、维生素B2和维生素B6;且所述维生素B1、维生素B2和维生素B6的质量比为(0.023~0.25):(0.023~0.25):(0.023~0.25)。
7.根据权利要求6所述组合物,其特征在于,所述维生素B1、维生素B2和维生素B6的质量比为(0.10~0.15):(0.10~0.15):(0.10~0.15)。
8.权利要求1~7任一项所述组合物在制备具有解酒护肝效果的保健品中的应用。
9.一种具有解酒护肝效果的保健品,其特征在于,所述保健品的有效成分包括权利要求1~7任一项所述组合物。
10.根据权利要求9所述保健品,其特征在于,所述保健品的剂型包括颗粒剂、片剂或胶囊剂。
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