CN112998275A - Ready-to-eat probiotic composition - Google Patents
Ready-to-eat probiotic composition Download PDFInfo
- Publication number
- CN112998275A CN112998275A CN201911326592.5A CN201911326592A CN112998275A CN 112998275 A CN112998275 A CN 112998275A CN 201911326592 A CN201911326592 A CN 201911326592A CN 112998275 A CN112998275 A CN 112998275A
- Authority
- CN
- China
- Prior art keywords
- probiotic
- eat
- ready
- probiotic composition
- probiotics
- 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.)
- Pending
Links
- 239000006041 probiotic Substances 0.000 title claims abstract description 112
- 235000018291 probiotics Nutrition 0.000 title claims abstract description 112
- 230000000529 probiotic effect Effects 0.000 title claims abstract description 76
- 239000000203 mixture Substances 0.000 title claims abstract description 48
- 239000000843 powder Substances 0.000 claims abstract description 38
- 241000894006 Bacteria Species 0.000 claims abstract description 19
- WVXRAFOPTSTNLL-NKWVEPMBSA-N 2',3'-dideoxyadenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@H]1CC[C@@H](CO)O1 WVXRAFOPTSTNLL-NKWVEPMBSA-N 0.000 claims abstract description 13
- 240000001046 Lactobacillus acidophilus Species 0.000 claims abstract description 13
- 235000013956 Lactobacillus acidophilus Nutrition 0.000 claims abstract description 13
- 241000218588 Lactobacillus rhamnosus Species 0.000 claims abstract description 13
- 240000003394 Malpighia glabra Species 0.000 claims abstract description 13
- 235000014837 Malpighia glabra Nutrition 0.000 claims abstract description 13
- 239000001506 calcium phosphate Substances 0.000 claims abstract description 13
- 229940039695 lactobacillus acidophilus Drugs 0.000 claims abstract description 13
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 claims abstract description 13
- 229940078499 tricalcium phosphate Drugs 0.000 claims abstract description 13
- 229910000391 tricalcium phosphate Inorganic materials 0.000 claims abstract description 13
- 235000019731 tricalcium phosphate Nutrition 0.000 claims abstract description 13
- 241000901050 Bifidobacterium animalis subsp. lactis Species 0.000 claims abstract description 12
- 229940009289 bifidobacterium lactis Drugs 0.000 claims abstract description 12
- -1 oligoxylitol Substances 0.000 claims abstract description 12
- 150000005846 sugar alcohols Chemical class 0.000 claims abstract description 12
- 241000186016 Bifidobacterium bifidum Species 0.000 claims abstract description 11
- 241001608472 Bifidobacterium longum Species 0.000 claims abstract description 11
- 229940002008 bifidobacterium bifidum Drugs 0.000 claims abstract description 11
- 229940009291 bifidobacterium longum Drugs 0.000 claims abstract description 11
- 239000002131 composite material Substances 0.000 claims description 14
- 239000000832 lactitol Substances 0.000 claims description 10
- 235000010448 lactitol Nutrition 0.000 claims description 10
- VQHSOMBJVWLPSR-JVCRWLNRSA-N lactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-JVCRWLNRSA-N 0.000 claims description 10
- 229960003451 lactitol Drugs 0.000 claims description 10
- 238000009777 vacuum freeze-drying Methods 0.000 claims description 8
- 241000167854 Bourreria succulenta Species 0.000 claims description 6
- 235000019693 cherries Nutrition 0.000 claims description 6
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims description 5
- 230000001580 bacterial effect Effects 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims description 5
- 239000011148 porous material Substances 0.000 claims description 5
- 239000000811 xylitol Substances 0.000 claims description 5
- 235000010447 xylitol Nutrition 0.000 claims description 5
- 229960002675 xylitol Drugs 0.000 claims description 5
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims description 3
- SERLAGPUMNYUCK-DCUALPFSSA-N 1-O-alpha-D-glucopyranosyl-D-mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O SERLAGPUMNYUCK-DCUALPFSSA-N 0.000 claims description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 2
- 239000004386 Erythritol Substances 0.000 claims description 2
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 claims description 2
- 229930195725 Mannitol Natural products 0.000 claims description 2
- 239000002671 adjuvant Substances 0.000 claims description 2
- 235000019414 erythritol Nutrition 0.000 claims description 2
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 claims description 2
- 229940009714 erythritol Drugs 0.000 claims description 2
- 239000000905 isomalt Substances 0.000 claims description 2
- 235000010439 isomalt Nutrition 0.000 claims description 2
- HPIGCVXMBGOWTF-UHFFFAOYSA-N isomaltol Natural products CC(=O)C=1OC=CC=1O HPIGCVXMBGOWTF-UHFFFAOYSA-N 0.000 claims description 2
- 239000000845 maltitol Substances 0.000 claims description 2
- 235000010449 maltitol Nutrition 0.000 claims description 2
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 claims description 2
- 229940035436 maltitol Drugs 0.000 claims description 2
- 239000000594 mannitol Substances 0.000 claims description 2
- 235000010355 mannitol Nutrition 0.000 claims description 2
- 229960001855 mannitol Drugs 0.000 claims description 2
- 235000013406 prebiotics Nutrition 0.000 claims description 2
- 239000000600 sorbitol Substances 0.000 claims description 2
- 235000010356 sorbitol Nutrition 0.000 claims description 2
- 229960002920 sorbitol Drugs 0.000 claims description 2
- 229920001542 oligosaccharide Polymers 0.000 claims 2
- 230000004083 survival effect Effects 0.000 abstract description 12
- 238000000034 method Methods 0.000 abstract description 9
- 235000013305 food Nutrition 0.000 abstract description 5
- 230000008569 process Effects 0.000 abstract description 5
- 238000003860 storage Methods 0.000 abstract description 5
- 210000002421 cell wall Anatomy 0.000 abstract description 2
- 230000000968 intestinal effect Effects 0.000 description 17
- 210000001035 gastrointestinal tract Anatomy 0.000 description 10
- 230000036039 immunity Effects 0.000 description 10
- 210000004027 cell Anatomy 0.000 description 8
- 241000699670 Mus sp. Species 0.000 description 7
- 238000009472 formulation Methods 0.000 description 6
- 210000001519 tissue Anatomy 0.000 description 6
- 230000009286 beneficial effect Effects 0.000 description 5
- 239000002775 capsule Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000007910 chewable tablet Substances 0.000 description 4
- 244000005700 microbiome Species 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 3
- 239000003242 anti bacterial agent Substances 0.000 description 3
- 229940088710 antibiotic agent Drugs 0.000 description 3
- 229940068682 chewable tablet Drugs 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 230000003871 intestinal function Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- 241000186000 Bifidobacterium Species 0.000 description 2
- 208000027244 Dysbiosis Diseases 0.000 description 2
- 241000186660 Lactobacillus Species 0.000 description 2
- 241000194036 Lactococcus Species 0.000 description 2
- 241000699666 Mus <mouse, genus> Species 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 2
- 241000194017 Streptococcus Species 0.000 description 2
- 241000700605 Viruses Species 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 244000052616 bacterial pathogen Species 0.000 description 2
- 201000011510 cancer Diseases 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 230000007140 dysbiosis Effects 0.000 description 2
- 230000002550 fecal effect Effects 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 238000003304 gavage Methods 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 210000000987 immune system Anatomy 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- 229940039696 lactobacillus Drugs 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 230000004936 stimulating effect Effects 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 230000009044 synergistic interaction Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 208000019901 Anxiety disease Diseases 0.000 description 1
- 208000035143 Bacterial infection Diseases 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- 241000194033 Enterococcus Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 229920001202 Inulin Polymers 0.000 description 1
- 244000199866 Lactobacillus casei Species 0.000 description 1
- 235000013958 Lactobacillus casei Nutrition 0.000 description 1
- 229920002774 Maltodextrin Polymers 0.000 description 1
- 239000005913 Maltodextrin Substances 0.000 description 1
- 235000003805 Musa ABB Group Nutrition 0.000 description 1
- 240000008790 Musa x paradisiaca Species 0.000 description 1
- 102000015636 Oligopeptides Human genes 0.000 description 1
- 108010038807 Oligopeptides Proteins 0.000 description 1
- 235000015266 Plantago major Nutrition 0.000 description 1
- 206010035664 Pneumonia Diseases 0.000 description 1
- 240000000851 Vaccinium corymbosum Species 0.000 description 1
- 235000003095 Vaccinium corymbosum Nutrition 0.000 description 1
- 235000017537 Vaccinium myrtillus Nutrition 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000036506 anxiety Effects 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 208000022362 bacterial infectious disease Diseases 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 235000021014 blueberries Nutrition 0.000 description 1
- 206010006451 bronchitis Diseases 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000008260 defense mechanism Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000004064 dysfunction Effects 0.000 description 1
- 230000008451 emotion Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- FTSSQIKWUOOEGC-RULYVFMPSA-N fructooligosaccharide Chemical compound OC[C@H]1O[C@@](CO)(OC[C@@]2(OC[C@@]3(OC[C@@]4(OC[C@@]5(OC[C@@]6(OC[C@@]7(OC[C@@]8(OC[C@@]9(OC[C@@]%10(OC[C@@]%11(O[C@H]%12O[C@H](CO)[C@@H](O)[C@H](O)[C@H]%12O)O[C@H](CO)[C@@H](O)[C@@H]%11O)O[C@H](CO)[C@@H](O)[C@@H]%10O)O[C@H](CO)[C@@H](O)[C@@H]9O)O[C@H](CO)[C@@H](O)[C@@H]8O)O[C@H](CO)[C@@H](O)[C@@H]7O)O[C@H](CO)[C@@H](O)[C@@H]6O)O[C@H](CO)[C@@H](O)[C@@H]5O)O[C@H](CO)[C@@H](O)[C@@H]4O)O[C@H](CO)[C@@H](O)[C@@H]3O)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@@H](O)[C@@H]1O FTSSQIKWUOOEGC-RULYVFMPSA-N 0.000 description 1
- 229940107187 fructooligosaccharide Drugs 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 230000007407 health benefit Effects 0.000 description 1
- 230000002519 immonomodulatory effect Effects 0.000 description 1
- 210000002865 immune cell Anatomy 0.000 description 1
- 230000001900 immune effect Effects 0.000 description 1
- 230000036737 immune function Effects 0.000 description 1
- 208000026278 immune system disease Diseases 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- JYJIGFIDKWBXDU-MNNPPOADSA-N inulin Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@]1(OC[C@]2(OC[C@]3(OC[C@]4(OC[C@]5(OC[C@]6(OC[C@]7(OC[C@]8(OC[C@]9(OC[C@]%10(OC[C@]%11(OC[C@]%12(OC[C@]%13(OC[C@]%14(OC[C@]%15(OC[C@]%16(OC[C@]%17(OC[C@]%18(OC[C@]%19(OC[C@]%20(OC[C@]%21(OC[C@]%22(OC[C@]%23(OC[C@]%24(OC[C@]%25(OC[C@]%26(OC[C@]%27(OC[C@]%28(OC[C@]%29(OC[C@]%30(OC[C@]%31(OC[C@]%32(OC[C@]%33(OC[C@]%34(OC[C@]%35(OC[C@]%36(O[C@@H]%37[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O%37)O)[C@H]([C@H](O)[C@@H](CO)O%36)O)[C@H]([C@H](O)[C@@H](CO)O%35)O)[C@H]([C@H](O)[C@@H](CO)O%34)O)[C@H]([C@H](O)[C@@H](CO)O%33)O)[C@H]([C@H](O)[C@@H](CO)O%32)O)[C@H]([C@H](O)[C@@H](CO)O%31)O)[C@H]([C@H](O)[C@@H](CO)O%30)O)[C@H]([C@H](O)[C@@H](CO)O%29)O)[C@H]([C@H](O)[C@@H](CO)O%28)O)[C@H]([C@H](O)[C@@H](CO)O%27)O)[C@H]([C@H](O)[C@@H](CO)O%26)O)[C@H]([C@H](O)[C@@H](CO)O%25)O)[C@H]([C@H](O)[C@@H](CO)O%24)O)[C@H]([C@H](O)[C@@H](CO)O%23)O)[C@H]([C@H](O)[C@@H](CO)O%22)O)[C@H]([C@H](O)[C@@H](CO)O%21)O)[C@H]([C@H](O)[C@@H](CO)O%20)O)[C@H]([C@H](O)[C@@H](CO)O%19)O)[C@H]([C@H](O)[C@@H](CO)O%18)O)[C@H]([C@H](O)[C@@H](CO)O%17)O)[C@H]([C@H](O)[C@@H](CO)O%16)O)[C@H]([C@H](O)[C@@H](CO)O%15)O)[C@H]([C@H](O)[C@@H](CO)O%14)O)[C@H]([C@H](O)[C@@H](CO)O%13)O)[C@H]([C@H](O)[C@@H](CO)O%12)O)[C@H]([C@H](O)[C@@H](CO)O%11)O)[C@H]([C@H](O)[C@@H](CO)O%10)O)[C@H]([C@H](O)[C@@H](CO)O9)O)[C@H]([C@H](O)[C@@H](CO)O8)O)[C@H]([C@H](O)[C@@H](CO)O7)O)[C@H]([C@H](O)[C@@H](CO)O6)O)[C@H]([C@H](O)[C@@H](CO)O5)O)[C@H]([C@H](O)[C@@H](CO)O4)O)[C@H]([C@H](O)[C@@H](CO)O3)O)[C@H]([C@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 JYJIGFIDKWBXDU-MNNPPOADSA-N 0.000 description 1
- 229940029339 inulin Drugs 0.000 description 1
- 230000009545 invasion Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 229940017800 lactobacillus casei Drugs 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 229940035034 maltodextrin Drugs 0.000 description 1
- 150000003272 mannan oligosaccharides Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000003340 mental effect Effects 0.000 description 1
- 244000000010 microbial pathogen Species 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 210000000607 neurosecretory system Anatomy 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000007084 physiological dysfunction Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 210000004994 reproductive system Anatomy 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 206010044008 tonsillitis Diseases 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
Classifications
-
- 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
- A23L33/135—Bacteria or derivatives thereof, e.g. probiotics
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/11—Lactobacillus
- A23V2400/113—Acidophilus
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/11—Lactobacillus
- A23V2400/175—Rhamnosus
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/51—Bifidobacterium
- A23V2400/517—Bifidum
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/51—Bifidobacterium
- A23V2400/531—Lactis
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2400/00—Lactic or propionic acid bacteria
- A23V2400/51—Bifidobacterium
- A23V2400/533—Longum
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Mycology (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Medicinal Preparation (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
The invention relates to an instant probiotic composition, and solves the technical problems that the cell wall of probiotic is broken due to the force and temperature of a tablet press during tabletting of the probiotic composition in the prior art, the survival rate of the probiotic is low, the efficacy of the probiotic is reduced, and the stability of the probiotic in the storage process is poor. The invention provides a ready-to-eat probiotic composition, which comprises probiotics, sugar alcohol, oligoxylitol, tricalcium phosphate and acerola powder; the probiotic bacteria comprise Bifidobacterium bifidum, Bifidobacterium lactis, Bifidobacterium longum, Lactobacillus acidophilus, and Lactobacillus rhamnosus. The invention is widely applied to the technical field of health-care food.
Description
Technical Field
The invention relates to the technical field of health-care food, in particular to an instant probiotic composition.
Background
Immunity is the body's own defense mechanism, is the body's ability to resist external invasion, maintain the stability of the body's environment, and is the body's ability to recognize and eliminate any foreign body (virus, bacteria, etc.) invaded from the outside, to treat aged, damaged, dead, denatured self-cells, and to recognize and treat mutant cells and virus-infected cells in the body. When the human body has immune dysfunction or the immune system is not healthy, the body is easy to be infected, such as cold, tonsillitis, asthma, bronchitis, pneumonia, diarrhea and other repeated attacks, and serious diseases, such as cancer, are also easy to be induced. Modern medical science finds that immunity is a factor closely related to aging. According to related reports, the immunity function of the organism begins to be delayed when the organism is about 30 years old, and the number of people with low immunity tends to increase year by year due to factors such as rapid change of activities, irregular life, pressure of working and learning environments, lack of exercise and the like of modern life. Therefore, how to improve the immunity of people with low immunity becomes a hot spot of modern medical research.
Probiotics is a kind of active microorganisms beneficial to a host, and is a general term for active beneficial microorganisms which are planted in the intestinal tract and the reproductive system of a human body and can generate definite health efficacy so as to improve the micro-ecological balance of the host and play beneficial roles. The probiotic bacteria can enhance immunity, and can regulate too low or too high immunological activity to normal state by stimulating the immune function in intestinal tract. This immunomodulatory effect of probiotics is also thought to contribute to cancer resistance and inhibition of allergic diseases. Probiotics are "living microorganisms that, when administered in the correct amount, confer a health benefit to the host". Probiotics have been described in species belonging to the genera Lactobacillus (Lactobacillus), Bifidobacterium (Bifidobacterium), Streptococcus (Streptococcus) and Lactococcus (Lactococcus) commonly used in the dairy industry. It is believed that probiotics intervene at the level of the intestinal flora by hindering the growth of pathogenic microorganisms and/or by acting more directly on the immune system.
The probiotic chewable tablet is prepared by preparing probiotic into powder, can enhance intestinal immune barrier function, relieve the penetration of pathogenic bacteria to mucous membrane, and help to enhance the physique of children and adults, and is convenient to take and good in compliance. However, the existing probiotic chewable tablets have low survival rate and low efficacy because the cell walls of the probiotics are broken by the force and the temperature of a tablet press during tabletting. Therefore, there is a need to provide a chewable tablet with a high survival rate of probiotics.
The gastrointestinal tract of a healthy person is populated by a wide variety of microorganisms, which are referred to as intestinal flora. The intestinal flora is combined according to a certain proportion, the bacteria are restricted and dependent with each other, an ecological balance is formed on the quality and quantity, once the internal and external environments of the organism change, the flora imbalance is caused, the normal physiological combination of the organism is destroyed, the pathological combination is generated, and the clinical symptoms are called the intestinal flora imbalance.
The amount of intestinal probiotics has become one of the criteria for testing the health of a human body. The physiological action of the medicine on human bodies is shown as follows: antibacterial property, which is to decompose organic acid in intestinal tract to reduce acidity of intestinal tract and inhibit putrefying bacteria; supplying vitamins to human body, generating various vitamins by probiotics, and inhibiting the decomposition of certain substances to ensure the supply; enhancing immunity, stimulating intestinal immune cells, and improving immunity. However, in daily life, the deterioration of environment and unhealthy life style are accompanied by the increase of life pressure, more and more people generate emotions such as anxiety, depression and the like due to excessive mental stress to cause dysfunction of neuroendocrine system, most of sensitive bacteria and normal flora can be inhibited or killed after the modern society uses a large amount of broad-spectrum antibiotics for a long time, while drug-resistant bacteria breed a large amount due to the selection function of the antibiotics, and the factors can cause physiological dysfunction of intestinal tracts, unbalance the micro-ecological environment in the intestinal tracts and further cause the aging of the intestinal tracts.
Chinese patent publication CN106659747A discloses the use of lactobacillus rhamnosus for promoting recovery of intestinal flora diversity after dysbiosis: by formulating lactobacillus rhamnosus in a form that can be administered orally for maintaining or increasing the intestinal flora diversity in a subject, for alleviating intestinal dysbiosis in a subject caused by antibiotics, for preventing intestinal bacterial infections and/or the development of diseases caused by pathogenic bacteria in the intestinal tract of a subject. However, the oral preparation containing probiotics prepared in the patent has few types of probiotics, cannot fully exert the synergistic effect among various probiotics, and does not fully consider the problems of survival rate and stability of the probiotics in the storage process in the preparation process.
Chinese patent publication CN106072657A discloses a probiotic composition and a preparation method thereof, wherein the probiotic composition is mainly prepared from the following substances in percentage by weight: 1-3% of lactobacillus acidophilus powder, 0.5-1.5% of lactobacillus casei powder, 1-3% of bifidobacterium lactis powder, 5-8% of mannan oligosaccharide, 3-5% of plantain seed powder, 40-60% of fructo-oligosaccharide, 2-5% of corn oligopeptide powder, 3-5% of inulin, 5-8% of blueberry powder and 10-25% of maltodextrin. The prepared probiotic composition can not only effectively regulate intestinal flora, but also enhance the immunity of human bodies. The invention does not carefully study the specific effects of various probiotic compositions on the diversity of the intestinal flora and still does not concern the stability of the probiotic compositions during storage.
Therefore, there is a need for an efficient large-scale production method of lactobacillus acidophilus; there is a need for an oral probiotic formulation that is shelf stable and that simultaneously contains multiple probiotics and is capable of improving the diversity of the intestinal flora.
Disclosure of Invention
The invention aims to overcome the defects of the prior art and provide the ready-to-eat probiotic composition which is simple and reasonable in raw material composition, scientific in compatibility, synergistic, high in survival rate of probiotics in probiotic powder, high in survival rate in a tabletting process and convenient to take.
The technical scheme adopted by the invention for solving the technical problem is as follows: the invention provides a ready-to-eat probiotic composition, which comprises probiotics, sugar alcohol, oligoxylitol, tricalcium phosphate and acerola powder; the probiotic bacteria comprise Bifidobacterium bifidum, Bifidobacterium lactis, Bifidobacterium longum, Lactobacillus acidophilus, and Lactobacillus rhamnosus.
Preferably, the ratio of the probiotics, the sugar alcohol, the xylitol oligomer, the tricalcium phosphate and the acerola cherry powder is as follows in parts by weight: the probiotics comprise lactitol, oligoxylitol, tricalcium phosphate, acerola cherry powder = (40-50), (40-90), (2-6), (2-4) and (1-10).
Preferably, the ratio of the probiotics in the probiotics is bifidobacterium bifidum, bifidobacterium lactis, bifidobacterium longum, lactobacillus acidophilus, lactobacillus rhamnosus = (10-20): (5-10): 1-5): 1-2 in parts by weight.
Preferably, the sugar alcohol has a pore volume of 0.005 to 0.05cm3A specific surface area of 1-10 cm3/g。
Preferably, the sugar alcohol is one or more of sorbitol, maltitol, mannitol, lactitol, erythritol, isomalt and xylitol.
Preferably, it further comprises prebiotics and/or dietetically acceptable adjuvants.
Preferably, the formulation of the ready-to-eat probiotic composition is composite probiotic freeze-dried powder; the composite probiotic freeze-dried powder is obtained by carrying out vacuum freeze-drying on bacterial liquid.
The invention has the beneficial effects that:
(1) the invention has scientific compatibility and synergistic interaction, ensures that the probiotic powder has high survival rate of the probiotics, high survival rate and high viable count in the tabletting process, increases the viable count of the probiotics cultured independently while ensuring the respective health-care effect, and embodies the unique superiority of the formula. . Compared with the commercial probiotic freeze-dried powder product, the compound probiotic composition formula obtains a special strain quantity ratio through research, so that the quantity of the bacteria planted in the intestinal tract is optimized. After being prepared into the enteric composite probiotic freeze-dried powder capsule, the capsule can be used for supplementing probiotics required by human bodies and balancing intestinal flora balance, is beneficial to preventing and treating certain diseases from bacteria, viruses, fungi and protozoa, and also has the effects of removing harmful substances, eliminating in-vivo toxins, purifying in-vivo environment and the like.
(2) The probiotic chewable tablet has the advantages of high particle porosity, large specific surface area, good compressibility and high hardness yield; the product is convenient to eat and has good taste; the storage time is long.
Detailed Description
The present invention will be further described with reference to specific examples to assist understanding of the invention. The method used in the invention is a conventional production method if no special provisions are made; the starting materials used, unless otherwise specified, are conventional commercial products.
Example 1
A ready-to-eat probiotic composition comprising probiotic bacteria, lactitol, oligolactitol, tricalcium phosphate and acerola powder; the probiotic bacteria comprise Bifidobacterium bifidum, Bifidobacterium lactis, Bifidobacterium longum, Lactobacillus acidophilus, and Lactobacillus rhamnosus; the probiotics comprise, by weight, lactitol, oligoxylitol, tricalcium phosphate and acerola cherry powder =40:40:2:4: 10; bifidobacterium bifidum, Bifidobacterium lactis, Bifidobacterium longum, Lactobacillus acidophilus and Lactobacillus rhamnosus =10:10:5:1: 1. The pore volume of the sugar alcohol is 0.005-0.05 cm3A specific surface area of 1-10 cm3/g。
The formulation of the ready-to-eat probiotic composition is composite probiotic freeze-dried powder; the composite probiotic freeze-dried powder is obtained by carrying out vacuum freeze-drying on bacterial liquid.
The damage to the structure and the characteristics of biological tissues and cells is small by adopting a vacuum freeze-drying technology, so that the biological tissues and the cell structures can rapidly enter a dormant state, and the stability of active ingredients of a plurality of heat-sensitive products such as probiotics is effectively protected. The invention also provides application of the composite probiotic freeze-dried powder capsule in health-care food for regulating intestinal functions.
Example 2
A ready-to-eat probiotic composition comprising probiotic bacteria, lactitol, oligolactitol, tricalcium phosphate and acerola powder; the probiotic bacteria comprise Bifidobacterium bifidum, Bifidobacterium lactis, Bifidobacterium longum, Lactobacillus acidophilus, and Lactobacillus rhamnosus; the probiotic comprises, by weight, lactitol, oligoxylitol, tricalcium phosphate and acerola cherry powder =50:90:6:2: 1; bifidobacterium bifidum, Bifidobacterium lactis, Bifidobacterium longum, Lactobacillus acidophilus and Lactobacillus rhamnosus =20:20:10:1: 2. The pore volume of the sugar alcohol is 0.005-0.05 cm3A specific surface area of 1-10 cm3/g。
The formulation of the ready-to-eat probiotic composition is composite probiotic freeze-dried powder; the composite probiotic freeze-dried powder is obtained by carrying out vacuum freeze-drying on bacterial liquid.
The damage to the structure and the characteristics of biological tissues and cells is small by adopting a vacuum freeze-drying technology, so that the biological tissues and the cell structures can rapidly enter a dormant state, and the stability of active ingredients of a plurality of heat-sensitive products such as probiotics is effectively protected. The invention also provides application of the composite probiotic freeze-dried powder capsule in health-care food for regulating intestinal functions.
Example 3
A ready-to-eat probiotic composition comprising probiotic bacteria, lactitol, oligolactitol, tricalcium phosphate and acerola powder; the probiotic bacteria comprise Bifidobacterium bifidum, Bifidobacterium lactis, Bifidobacterium longum, Lactobacillus acidophilus, and Lactobacillus rhamnosus; the probiotic comprises, by weight, lactitol, oligoxylitol, tricalcium phosphate and acerola cherry powder =45:80:5:3: 1; bifidobacterium bifidum, bifidobacterium lactis, bifidobacterium longum, lactobacillus acidophilus and lactobacillus rhamnosus =15:15:7:3: 1. The pore volume of the sugar alcohol is 0.005-0.05 cm3Table of the ratio of/gThe area is 1-10 cm3/g。
The formulation of the ready-to-eat probiotic composition is composite probiotic freeze-dried powder; the composite probiotic freeze-dried powder is obtained by carrying out vacuum freeze-drying on bacterial liquid.
The damage to the structure and the characteristics of biological tissues and cells is small by adopting a vacuum freeze-drying technology, so that the biological tissues and the cell structures can rapidly enter a dormant state, and the stability of active ingredients of a plurality of heat-sensitive products such as probiotics is effectively protected. The invention also provides application of the composite probiotic freeze-dried powder capsule in health-care food for regulating intestinal functions.
The efficacy of the ready-to-eat probiotic composition of the present invention is further illustrated by the experimental reports below.
1. Object and method
(1) The test substance: ready-to-eat probiotic compositions prepared according to the formulations given in examples 1 to 3 of the present invention were experimental samples.
(2) The method for measuring the abundance of the flora comprises the following steps: taking 110 mice with good and same growth state, randomly dividing the mice into 5 groups, each group comprising 20 mice, wherein 3 groups are experimental groups, 2 groups are control groups, uniformly feeding the mice under the same environment, and after feeding the mice for one week, carrying out continuous 7-day intragastric gavage on the mice, wherein the experimental groups adopt the composition of the embodiments 1-3 of the invention to carry out intragastric gavage. After the gastric lavage is finished for 7 days, collecting a fecal sample of the mouse, and using the fecal sample for the investigation and analysis of the 16SrRNA gene of the whole flora to detect the abundance of the flora in the mouse.
(3) The survival rate of the probiotics in the ready-to-eat probiotic composition refers to the survival rate of the ready-to-eat probiotic composition after the ready-to-eat probiotic composition is placed at 25 ℃ for 4 months.
The experimental result shows that the ready-to-eat probiotic composition can improve the abundance of the flora in mice from 400 to 448 and reduce the lgCFU/g value of enterococcus from 6.8 to below 6.0 by adding various probiotics into the composition, and has the obvious effects of improving the diversity of intestinal flora and reducing the content of harmful bacteria. When the addition of certain probiotics is omitted from the composition, the efficacy of the composition in increasing the abundance of the intestinal flora and in reducing the content of harmful bacteria may be reduced to different extents.
In conclusion, the experimental data results fully prove that the ready-to-eat probiotic composition has scientific compatibility and synergistic interaction, so that the survival rate of probiotics in the probiotic powder is high, and the survival rate and the viable count in the tabletting process are high; the product is convenient to eat and has good taste; the storage time is long.
However, the above description is only an embodiment of the present invention, and the scope of the present invention should not be limited by this, and all equivalent changes and modifications made in the claims of the present invention should be covered by the present invention.
Claims (7)
1. A ready-to-eat probiotic composition comprising probiotics, sugar alcohol, xylitol oligosaccharide, tricalcium phosphate and acerola powder; the probiotic bacteria comprise Bifidobacterium bifidum, Bifidobacterium lactis, Bifidobacterium longum, Lactobacillus acidophilus, and Lactobacillus rhamnosus.
2. The ready-to-eat probiotic composition according to claim 1, wherein the ratio of the probiotics to the sugar alcohol, the xylitol oligosaccharide, the tricalcium phosphate and the acerola powder is as follows: the probiotics comprise lactitol, oligoxylitol, tricalcium phosphate, acerola cherry powder = (40-50), (40-90), (2-6), (2-4) and (1-10).
3. The ready-to-eat probiotic composition according to claim 2, wherein the ratio of the probiotics in the probiotic composition is Bifidobacterium bifidum, Bifidobacterium lactis, Bifidobacterium longum, Lactobacillus acidophilus, Lactobacillus rhamnosus = (10-20): 5-10): 1-5): 1-2.
4. A ready-to-eat probiotic composition according to claim 1 or 2, characterized in that said sugar alcohol has a pore volume of 0.005-0.05 cm3A specific surface area of 1-10 cm3/g。
5. The ready-to-eat probiotic composition according to claim 1, characterized in that said sugar alcohol is one or more of sorbitol, maltitol, mannitol, lactitol, erythritol, isomalt, xylitol.
6. A ready-to-eat probiotic composition according to claim 1, characterized in that it also comprises prebiotics and/or dietetically acceptable adjuvants.
7. The ready-to-eat probiotic composition according to claim 6, wherein the ready-to-eat probiotic composition is in the form of composite probiotic freeze-dried powder; the composite probiotic freeze-dried powder is obtained by carrying out vacuum freeze-drying on bacterial liquid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201911326592.5A CN112998275A (en) | 2019-12-20 | 2019-12-20 | Ready-to-eat probiotic composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201911326592.5A CN112998275A (en) | 2019-12-20 | 2019-12-20 | Ready-to-eat probiotic composition |
Publications (1)
Publication Number | Publication Date |
---|---|
CN112998275A true CN112998275A (en) | 2021-06-22 |
Family
ID=76382699
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201911326592.5A Pending CN112998275A (en) | 2019-12-20 | 2019-12-20 | Ready-to-eat probiotic composition |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN112998275A (en) |
-
2019
- 2019-12-20 CN CN201911326592.5A patent/CN112998275A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102905712B (en) | Be used for the treatment of the probiotic composition of enteritis | |
JP2015512936A (en) | Prebiotic composition and method of use thereof | |
AU2014291777B2 (en) | A composition having a prebiotic effect | |
CN1480528A (en) | Bifidobacterium and products contg same | |
KR101104397B1 (en) | Antiviral composition of fermented milk from lactic bacteria and its therof | |
CN111528479A (en) | Probiotics and prebiotics composition for relieving atopic dermatitis function and application | |
EP3781185B1 (en) | Method for alleviating tobacco or nicotine withdrawal symptoms | |
KR20210112342A (en) | Strain, composition and method of use | |
US20130309212A1 (en) | Lactobacillus salivarius and method for preparing metabolite thereof, composition of lactobacillus salivarius and metabolite thereof and use of the composition | |
CN107854495B (en) | Application of bacillus coagulans in preparation of preparation for reducing hematuria | |
JP2018532380A (en) | Enterobacteriaceae butyric acid intestini and uses thereof | |
WO2015140299A1 (en) | Oronasopharyngeal probiotics | |
WO2019227414A1 (en) | Composition and uses thereof | |
CN109414465B (en) | Probiotic compositions and uses thereof | |
KR101849424B1 (en) | Use of a fermented soy extract for manufacture of a prebiotic composition | |
CN112998275A (en) | Ready-to-eat probiotic composition | |
CN116396884A (en) | Lactobacillus rhamnosus and a composition for inhibiting helicobacter pylori | |
KR102480131B1 (en) | Lactobacillus rhamnosus with cognitive function improvement | |
KR102480136B1 (en) | Lactobacillus paracasei with cognitive function improvement | |
EP3691665B1 (en) | A pharmaceutical composition comprising a probiotic and a prebiotic to prevent acquisition of or treat drug resistant infections | |
CN111560335A (en) | Bifidobacterium lactis for relieving asthma and application thereof | |
WO2019227417A1 (en) | Composition and uses thereof | |
US20240050493A1 (en) | Strains, compositions and methods of use | |
KR102685867B1 (en) | Pharmaceutical composition for preventing or treating the acquisition of drug-resistant infections comprising a combination of probiotics and prebiotics | |
EP1900371A1 (en) | Method for treating and/or preventing intestinal bacterial imbalance |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
WD01 | Invention patent application deemed withdrawn after publication | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20210622 |