CN117941765A - Preparation method of various prebiotic tablet candy - Google Patents
Preparation method of various prebiotic tablet candy Download PDFInfo
- Publication number
- CN117941765A CN117941765A CN202410293184.9A CN202410293184A CN117941765A CN 117941765 A CN117941765 A CN 117941765A CN 202410293184 A CN202410293184 A CN 202410293184A CN 117941765 A CN117941765 A CN 117941765A
- Authority
- CN
- China
- Prior art keywords
- powder
- prebiotic
- oligosaccharide
- finished product
- semi
- 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
- 235000009508 confectionery Nutrition 0.000 title claims abstract description 94
- 235000013406 prebiotics Nutrition 0.000 title claims abstract description 76
- 238000002360 preparation method Methods 0.000 title abstract description 20
- 239000011265 semifinished product Substances 0.000 claims abstract description 67
- 238000002156 mixing Methods 0.000 claims abstract description 60
- 229920001202 Inulin Polymers 0.000 claims abstract description 31
- 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 claims abstract description 31
- 229940029339 inulin Drugs 0.000 claims abstract description 31
- 239000000463 material Substances 0.000 claims abstract description 30
- 229920001542 oligosaccharide Polymers 0.000 claims abstract description 27
- 150000002482 oligosaccharides Chemical class 0.000 claims abstract description 27
- 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 abstract description 26
- 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 abstract description 26
- 229920001353 Dextrin Polymers 0.000 claims abstract description 26
- 239000004375 Dextrin Substances 0.000 claims abstract description 26
- 235000012343 cottonseed oil Nutrition 0.000 claims abstract description 26
- HEBKCHPVOIAQTA-NGQZWQHPSA-N d-xylitol Chemical compound OC[C@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-NGQZWQHPSA-N 0.000 claims abstract description 26
- 235000019425 dextrin Nutrition 0.000 claims abstract description 26
- 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 claims abstract description 26
- 229940107187 fructooligosaccharide Drugs 0.000 claims abstract description 26
- 239000002245 particle Substances 0.000 claims abstract description 26
- 239000000600 sorbitol Substances 0.000 claims abstract description 26
- 239000000853 adhesive Substances 0.000 claims abstract description 17
- 230000001070 adhesive effect Effects 0.000 claims abstract description 17
- 238000001035 drying Methods 0.000 claims abstract description 13
- 239000000843 powder Substances 0.000 claims description 112
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 40
- 241000894006 Bacteria Species 0.000 claims description 31
- 239000000796 flavoring agent Substances 0.000 claims description 29
- 235000013355 food flavoring agent Nutrition 0.000 claims description 29
- 238000000576 coating method Methods 0.000 claims description 26
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims description 26
- 239000011248 coating agent Substances 0.000 claims description 25
- 241000186660 Lactobacillus Species 0.000 claims description 24
- 229940039696 lactobacillus Drugs 0.000 claims description 24
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims description 20
- 229930003268 Vitamin C Natural products 0.000 claims description 20
- 235000019154 vitamin C Nutrition 0.000 claims description 20
- 239000011718 vitamin C Substances 0.000 claims description 20
- 241000193749 Bacillus coagulans Species 0.000 claims description 16
- 229940054340 bacillus coagulans Drugs 0.000 claims description 16
- 238000007873 sieving Methods 0.000 claims description 16
- 244000078534 Vaccinium myrtillus Species 0.000 claims description 15
- 235000013399 edible fruits Nutrition 0.000 claims description 14
- 229920002472 Starch Polymers 0.000 claims description 13
- UEDUENGHJMELGK-HYDKPPNVSA-N Stevioside Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O UEDUENGHJMELGK-HYDKPPNVSA-N 0.000 claims description 13
- 235000019359 magnesium stearate Nutrition 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- 239000002002 slurry Substances 0.000 claims description 13
- 239000008107 starch Substances 0.000 claims description 13
- 235000019698 starch Nutrition 0.000 claims description 13
- OHHNJQXIOPOJSC-UHFFFAOYSA-N stevioside Natural products CC1(CCCC2(C)C3(C)CCC4(CC3(CCC12C)CC4=C)OC5OC(CO)C(O)C(O)C5OC6OC(CO)C(O)C(O)C6O)C(=O)OC7OC(CO)C(O)C(O)C7O OHHNJQXIOPOJSC-UHFFFAOYSA-N 0.000 claims description 13
- 229940013618 stevioside Drugs 0.000 claims description 13
- 235000019202 steviosides Nutrition 0.000 claims description 13
- 239000000047 product Substances 0.000 claims description 12
- 235000006040 Prunus persica var persica Nutrition 0.000 claims description 10
- 244000269722 Thea sinensis Species 0.000 claims description 10
- 239000011230 binding agent Substances 0.000 claims description 10
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 10
- 235000009569 green tea Nutrition 0.000 claims description 9
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims description 8
- 240000001890 Ribes hudsonianum Species 0.000 claims description 8
- 235000016954 Ribes hudsonianum Nutrition 0.000 claims description 8
- 235000001466 Ribes nigrum Nutrition 0.000 claims description 8
- 235000011941 Tilia x europaea Nutrition 0.000 claims description 8
- 235000003095 Vaccinium corymbosum Nutrition 0.000 claims description 8
- 235000017537 Vaccinium myrtillus Nutrition 0.000 claims description 8
- 235000021014 blueberries Nutrition 0.000 claims description 8
- 239000004571 lime Substances 0.000 claims description 8
- 235000011034 Rubus glaucus Nutrition 0.000 claims description 7
- 235000009122 Rubus idaeus Nutrition 0.000 claims description 7
- 240000001717 Vaccinium macrocarpon Species 0.000 claims description 7
- 235000012545 Vaccinium macrocarpon Nutrition 0.000 claims description 7
- 235000002118 Vaccinium oxycoccus Nutrition 0.000 claims description 7
- 235000004634 cranberry Nutrition 0.000 claims description 7
- 240000007651 Rubus glaucus Species 0.000 claims description 6
- 244000144730 Amygdalus persica Species 0.000 claims description 5
- 241000186018 Bifidobacterium adolescentis Species 0.000 claims description 5
- 241000186012 Bifidobacterium breve Species 0.000 claims description 5
- 241000186840 Lactobacillus fermentum Species 0.000 claims description 5
- 241000186604 Lactobacillus reuteri Species 0.000 claims description 5
- 241000218588 Lactobacillus rhamnosus Species 0.000 claims description 5
- 235000014655 lactic acid Nutrition 0.000 claims description 5
- 239000004310 lactic acid Substances 0.000 claims description 5
- 229940012969 lactobacillus fermentum Drugs 0.000 claims description 5
- 229940001882 lactobacillus reuteri Drugs 0.000 claims description 5
- 238000004513 sizing Methods 0.000 claims description 5
- 235000011389 fruit/vegetable juice Nutrition 0.000 claims description 4
- 241000711295 Aeria Species 0.000 claims description 2
- 241001134770 Bifidobacterium animalis Species 0.000 claims description 2
- 241000901050 Bifidobacterium animalis subsp. lactis Species 0.000 claims description 2
- 229920002774 Maltodextrin Polymers 0.000 claims description 2
- 239000005913 Maltodextrin Substances 0.000 claims description 2
- 229940118852 bifidobacterium animalis Drugs 0.000 claims description 2
- 229940009289 bifidobacterium lactis Drugs 0.000 claims description 2
- 229940035034 maltodextrin Drugs 0.000 claims description 2
- 239000008188 pellet Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 10
- 235000016709 nutrition Nutrition 0.000 description 24
- 230000035764 nutrition Effects 0.000 description 16
- 235000019640 taste Nutrition 0.000 description 14
- 239000010410 layer Substances 0.000 description 10
- 239000003963 antioxidant agent Substances 0.000 description 9
- 235000006708 antioxidants Nutrition 0.000 description 9
- 230000009286 beneficial effect Effects 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 230000003078 antioxidant effect Effects 0.000 description 7
- 230000001965 increasing effect Effects 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 241000186000 Bifidobacterium Species 0.000 description 5
- 240000005809 Prunus persica Species 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 230000032683 aging Effects 0.000 description 4
- 230000001580 bacterial effect Effects 0.000 description 4
- 201000010099 disease Diseases 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- 230000036541 health Effects 0.000 description 4
- 230000036039 immunity Effects 0.000 description 4
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical class OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 3
- 241001147746 Lactobacillus delbrueckii subsp. lactis Species 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- 241001409305 Siraitia Species 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 235000010208 anthocyanin Nutrition 0.000 description 3
- 229930002877 anthocyanin Natural products 0.000 description 3
- 239000004410 anthocyanin Substances 0.000 description 3
- 150000004636 anthocyanins Chemical class 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000007407 health benefit Effects 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000012216 screening Methods 0.000 description 3
- 230000004083 survival effect Effects 0.000 description 3
- 235000019605 sweet taste sensations Nutrition 0.000 description 3
- 244000189548 Chrysanthemum x morifolium Species 0.000 description 2
- 235000005979 Citrus limon Nutrition 0.000 description 2
- 244000131522 Citrus pyriformis Species 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- REFJWTPEDVJJIY-UHFFFAOYSA-N Quercetin Chemical compound C=1C(O)=CC(O)=C(C(C=2O)=O)C=1OC=2C1=CC=C(O)C(O)=C1 REFJWTPEDVJJIY-UHFFFAOYSA-N 0.000 description 2
- GAMYVSCDDLXAQW-AOIWZFSPSA-N Thermopsosid Natural products O(C)c1c(O)ccc(C=2Oc3c(c(O)cc(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O4)c3)C(=O)C=2)c1 GAMYVSCDDLXAQW-AOIWZFSPSA-N 0.000 description 2
- 244000185386 Thladiantha grosvenorii Species 0.000 description 2
- 235000011171 Thladiantha grosvenorii Nutrition 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 230000003796 beauty Effects 0.000 description 2
- 230000005189 cardiac health Effects 0.000 description 2
- 230000036996 cardiovascular health Effects 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 235000013325 dietary fiber Nutrition 0.000 description 2
- 102000038379 digestive enzymes Human genes 0.000 description 2
- 108091007734 digestive enzymes Proteins 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000002708 enhancing effect Effects 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 229930003944 flavone Natural products 0.000 description 2
- 150000002212 flavone derivatives Chemical class 0.000 description 2
- 235000011949 flavones Nutrition 0.000 description 2
- 210000004211 gastric acid Anatomy 0.000 description 2
- 210000001035 gastrointestinal tract Anatomy 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 230000000968 intestinal effect Effects 0.000 description 2
- 210000004185 liver Anatomy 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 235000007686 potassium Nutrition 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 230000036559 skin health Effects 0.000 description 2
- 235000011888 snacks Nutrition 0.000 description 2
- 230000004936 stimulating effect Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 210000002784 stomach Anatomy 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
- 229940088594 vitamin Drugs 0.000 description 2
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 description 2
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 1
- 241000193830 Bacillus <bacterium> Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 235000007516 Chrysanthemum Nutrition 0.000 description 1
- 235000009604 Chrysanthemum X morifolium Nutrition 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 206010059866 Drug resistance Diseases 0.000 description 1
- 241000628997 Flos Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 201000005569 Gout Diseases 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 244000070406 Malus silvestris Species 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- ZVOLCUVKHLEPEV-UHFFFAOYSA-N Quercetagetin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=C(O)C(O)=C(O)C=C2O1 ZVOLCUVKHLEPEV-UHFFFAOYSA-N 0.000 description 1
- HWTZYBCRDDUBJY-UHFFFAOYSA-N Rhynchosin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=CC(O)=C(O)C=C2O1 HWTZYBCRDDUBJY-UHFFFAOYSA-N 0.000 description 1
- 244000235659 Rubus idaeus Species 0.000 description 1
- 206010039424 Salivary hypersecretion Diseases 0.000 description 1
- 102000002262 Thromboplastin Human genes 0.000 description 1
- 108010000499 Thromboplastin Proteins 0.000 description 1
- 244000291414 Vaccinium oxycoccus Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 208000007502 anemia Diseases 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 235000021016 apples Nutrition 0.000 description 1
- 206010003246 arthritis Diseases 0.000 description 1
- 210000000941 bile Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000001465 calcium Nutrition 0.000 description 1
- 235000005487 catechin Nutrition 0.000 description 1
- ADRVNXBAWSRFAJ-UHFFFAOYSA-N catechin Natural products OC1Cc2cc(O)cc(O)c2OC1c3ccc(O)c(O)c3 ADRVNXBAWSRFAJ-UHFFFAOYSA-N 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 230000001055 chewing effect Effects 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 229950001002 cianidanol Drugs 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- LOHQECMUTAPWAC-UHFFFAOYSA-N coagulin Natural products C1C(C)=C(CO)C(=O)OC1C1(C)C(C2(C)CCC3C4(C(=O)CC=CC4=CCC43)C)(O)CCC24O1 LOHQECMUTAPWAC-UHFFFAOYSA-N 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 235000021019 cranberries Nutrition 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 235000015872 dietary supplement Nutrition 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 230000004438 eyesight Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 210000004051 gastric juice Anatomy 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- MWDZOUNAPSSOEL-UHFFFAOYSA-N kaempferol Natural products OC1=C(C(=O)c2cc(O)cc(O)c2O1)c3ccc(O)cc3 MWDZOUNAPSSOEL-UHFFFAOYSA-N 0.000 description 1
- 230000003908 liver function Effects 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 235000001055 magnesium Nutrition 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000000050 nutritive effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 238000005502 peroxidation Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 235000014786 phosphorus Nutrition 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000006041 probiotic Substances 0.000 description 1
- 235000018291 probiotics Nutrition 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 235000005875 quercetin Nutrition 0.000 description 1
- 229960001285 quercetin Drugs 0.000 description 1
- 208000026451 salivation Diseases 0.000 description 1
- 235000019614 sour taste Nutrition 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 235000021147 sweet food Nutrition 0.000 description 1
- 238000009475 tablet pressing Methods 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 230000035922 thirst Effects 0.000 description 1
- 208000019206 urinary tract infection Diseases 0.000 description 1
Landscapes
- Medicinal Preparation (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
The invention discloses a preparation method of a plurality of prebiotics tabletting candies, S101, inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin are screened, and unqualified particles are removed; s102, mixing finely-screened inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin to obtain a mixed material; s103, adding an adhesive into the mixed materials, and drying and granulating to obtain a semi-finished product A. The invention relates to the technical field of prebiotic tablet candy. The preparation method of the multi-prebiotic tabletting candy can effectively improve the quality of the multi-prebiotic tabletting candy, can adjust the production cost of the multi-prebiotic tabletting candy according to the user group, reduces the selling price of the multi-prebiotic tabletting candy, can enable the multi-prebiotic tabletting candy to rapidly open the market, and is more suitable for popularization.
Description
Technical Field
The invention relates to the technical field of prebiotic tablet candy, in particular to a preparation method of a plurality of prebiotic tablet candy.
Background
Prebiotics are dietary supplements that improve the health of a host by selectively stimulating the growth and activity of bacteria in the colony to have a beneficial effect on the host. Prebiotics are functional oligosaccharides and dietary fibers are a dislike of the intestinal flora. They are dietary fibers that only bacteria like to eat.
In the prior art, the prebiotics improve the health of hosts by selectively stimulating the growth and activity of bacteria in bacterial colonies, and a large amount of antibacterial coagulin, lactic acid, amino acid, vitamins and various digestive enzymes are generated during the fermentation of bacillus coagulans, so that harmful bacteria can be effectively inhibited, and the growth and reproduction of beneficial bacteria such as bifidobacteria can be promoted, and therefore, the use effect of the prebiotics can be effectively improved by adding bacillus coagulans into the prebiotics.
Accordingly, one skilled in the art would be able to provide a method for preparing a variety of prebiotic tabletted confections that address the problems outlined in the background section above.
Disclosure of Invention
The invention aims to provide a preparation method of various prebiotic tablet candies, which aims to solve the problems in the background technology.
In order to achieve the above purpose, the present invention provides the following technical solutions:
the technical aim of the invention is realized by the following technical scheme:
a preparation method of a plurality of prebiotic tablet candy comprises the following steps:
s101, sieving inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin, and removing unqualified particles;
s102, mixing finely-screened inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin to obtain a mixed material;
S103, adding an adhesive into the mixed materials, and drying and granulating to obtain a semi-finished product A;
S104, mixing lactobacillus powder with vitamin C, stevioside, fruit powder and the like to obtain a semi-finished product B;
s105, uniformly mixing the semi-finished product A, the semi-finished product B, magnesium stearate and the flavoring agent, and tabletting to obtain a semi-finished product C;
And S106, coating a layer of coating on the outer wall of the semi-finished product C to obtain a finished product.
Further, based on S101, the number of screen meshes for sieving is 80 to 120 mesh.
Further, based on S102, the materials are mixed using a two-dimensional mixer or a three-dimensional mixer.
Further, based on S103, the binder is starch slurry with a concentration of 6% to 10% or maltodextrin with a concentration of 6% to 10%.
Further, the addition temperature of the binder was 70 ℃.
Further, based on S104, the lactic acid bacteria powder is formed by mixing bacteria powder a and bacteria powder B, wherein the bacteria powder a is bacillus coagulans, and the bacteria powder B is one or more of lactobacillus, bifidobacterium animalis, bifidobacterium lactis, lactobacillus rhamnosus, lactobacillus reuteri, lactobacillus fermentum, bifidobacterium breve and bifidobacterium adolescentis.
Further, based on S103, the number of screen meshes used for the sizing is 18 to 24 mesh.
Further, based on S105, the flavoring agent is prepared by mixing cranberry powder, blackberry powder, blueberry juice powder and raspberry powder;
Based on S105, the flavoring agent is prepared by mixing green tea powder, fructus Siraitiae Grosvenorii powder and Hangzhou inulin;
Based on S105, the flavoring agent is prepared by mixing lime powder;
based on S105, the flavoring agent is prepared by mixing and modulating juicy peach powder;
based on S105, the flavoring agent is mixed and prepared from blackcurrant powder.
In summary, the present invention includes at least one of the following beneficial technical effects:
1. The preparation method of the multi-prebiotic tabletting candy can effectively improve the quality of the multi-prebiotic tabletting candy, can adjust the production cost of the multi-prebiotic tabletting candy according to the user group, reduces the selling price of the multi-prebiotic tabletting candy, can enable the multi-prebiotic tabletting candy to be rapidly opened in the market, and is more suitable for popularization;
2. According to the preparation method of the multiple prebiotic tabletting candy, different particle sizes of the multiple prebiotic tabletting candy are set, so that the multiple prebiotic tabletting candy can be used for producing multiple prebiotic tabletting candy of different types, and the nutritional ingredients of the multiple prebiotic tabletting candy are changed, so that the multiple prebiotic tabletting candy can be used for people in different stages, and the problem that nutrition of the multiple prebiotic tabletting candy is wasted due to the fact that nutrition is excessive and cannot be absorbed is solved;
3. according to the preparation method of the multi-prebiotic tablet candy, the nutritional content of the multi-prebiotic tablet candy can be increased by using the coating prepared by mixing and modulating the cranberry fruit powder, the blackberry fruit powder, the blueberry fruit juice powder and the raspberry powder, so that the multi-prebiotic tablet candy is more liked by women, and can be used for opening the female market;
4. the preparation method of the multi-prebiotic tabletting candy is characterized in that the coating prepared by mixing green tea powder, grosvener siraitia powder and Hangzhou inulin is used, so that the multi-prebiotic tabletting candy has good taste, rich nutrition, health benefits and the like, and is convenient for opening the male market.
Drawings
In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings that are needed in the embodiments will be briefly described below, and it is obvious that the drawings in the following description are only some embodiments of the present invention, and other drawings can be obtained according to these drawings without inventive effort for a person skilled in the art.
Figure 1 is a flow chart of a method of preparing a multi-prebiotic tableting confection of the present invention.
Figure 2 is a graph of the nutritional content of two coatings in a process for preparing a multi-prebiotic tableted confection of the present invention.
Detailed Description
The invention is further described below with reference to the accompanying drawings and detailed description:
embodiment one:
The invention discloses a preparation method of a plurality of prebiotic tablet candies, which comprises the following steps:
s101, sieving inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin, and removing unqualified particles;
s102, mixing finely-screened inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin to obtain a mixed material;
S103, adding an adhesive into the mixed materials, and drying and granulating to obtain a semi-finished product A;
S104, mixing lactobacillus powder with vitamin C, stevioside, fruit powder and the like to obtain a semi-finished product B;
s105, uniformly mixing the semi-finished product A, the semi-finished product B, magnesium stearate and the flavoring agent, and tabletting to obtain a semi-finished product C;
And S106, coating a layer of coating on the outer wall of the semi-finished product C to obtain a finished product.
Based on S101, the number of screens for sieving was 120 mesh.
Based on S102, the materials are mixed using a two-dimensional mixer or a three-dimensional mixer.
The binder was at a concentration of 6% based on S103.
The addition temperature of the binder was 70 ℃.
Based on S104, the lactobacillus powder is formed by mixing a bacterium powder A and a bacterium powder B, wherein the bacterium powder A is bacillus coagulans, and the bacterium powder B is one or more of lactobacillus, animal bifidobacterium, lactobacillus lactis, lactobacillus rhamnosus, lactobacillus reuteri, lactobacillus fermentum, bifidobacterium breve and bifidobacterium adolescentis.
In this example, when the number of the screening screens is 120, the powder particles are finer and finer, the content of the tablets after mixing is more uniform, and the tablets are finer and finer. The dissolution rate of the active ingredients is also greatly accelerated, and the absolute bioavailability of the fine powder can be improved by about 20 percent compared with the coarse powder. The smaller the particle size of the particles, the smaller the weight difference can be ensured, and the content distribution of the tabletting is uniform, thereby improving the dissolution performance of the tablet.
The screened powder particles are proportionally added into a two-dimensional mixer by a tray, and the powder particles are efficiently scattered and uniformly mixed by the two-dimensional mixer. In the step of mixing, in order to further improve the quality of the tabletting, a three-dimensional mixer with higher cost can be adopted, so that the mixing effect of powder particles is better, and the nutrition content distribution of the tabletting is more uniform.
In order to adsorb the mixed materials together, the starch slurry can be used as a mixing adhesive, and in order to ensure the viscosity of the starch slurry, the starch slurry needs to be heated to pasty state when being mixed with powder particles, and the common corn starch has a complete gelatinization temperature of 77 ℃, so that the starch slurry needs to be heated to more than 70 ℃ before being used, and the stability of the fructo-oligosaccharides adopted in the prebiotic tablet candy can be reduced when the temperature exceeds 70 ℃, so that the decomposition of the fructo-oligosaccharides can be accelerated, so that the fructo-oligosaccharides are prevented from being excessively decomposed, and meanwhile, the use temperature of the starch slurry is 70 ℃ in order to ensure the viscosity of the starch slurry.
The survival rate of the strain is almost linearly reduced along with the increase of the tabletting pressure, and when all strains are selected in the bacterial powder B in order to increase the nutrition components of the various prebiotic tabletting candies, the integral content of the various prebiotic tabletting candies is inevitably increased, and the compressibility of the adopted adhesive is poor, so that the adhesive adopts starch slurry with the concentration of 6 percent in order to avoid the hardness of the pressed prebiotic tabletting candies from greatly influencing the taste, and the strain death caused by the overpressure of the various prebiotic tabletting candies during tabletting can be avoided.
After the powder particles and the adhesive are mixed, adding lactobacillus powder for stirring when the powder particles and the adhesive are not completely cooled and solidified, avoiding massive death of the lactobacillus at high temperature, then continuously stirring until the lactobacillus powder is completely mixed with the lactobacillus powder, further ensuring the uniform nutrition content of various prebiotic tabletting candies, finally standing and cooling after the lactobacillus powder is mixed, and drying and granulating to obtain tablets after cooling.
After tabletting is finished, the embryonic form of the prebiotic tabletting candy is finished, and finally, a coating layer can be coated on the outer surface wall of the prebiotic tabletting candy according to the preference of a user.
Wherein, the bacillus coagulans is a gram-positive and rod-shaped bacterium and has the following characteristics:
no drug resistance: bacillus coagulans is sensitive to most antibacterial agents.
The metabolites are rich: bacillus coagulans is fermented to produce a large amount of antibacterial coagulants, lactic acid, amino acids, vitamins and various digestive enzymes, which can inhibit harmful bacteria and promote the growth and reproduction of beneficial bacteria such as bifidobacteria.
Gastric acid resistant: the bacillus coagulans has extremely strong acid condition tolerance to gastric juice, the survival of the bacillus coagulans is not affected, the bacillus coagulans is obviously superior to other microecologics, and the bacillus coagulans can smoothly pass through the stomach to enter the intestinal tract, thus being the only probiotics for resisting gastric acid and bile.
Stability is high: has extremely strong tolerance to temperature and pressure. Bacillus coagulans is facultative anaerobe, can grow in both aerobic and anaerobic environments, can adapt to low-oxygen intestinal environments, can form spores, and is favorable for restoring microecological balance of gastrointestinal tracts compared with other bacillus which does not produce lactic acid.
Therefore, the addition of bacillus coagulans can greatly improve the nutrition content of various prebiotic tablet candies.
Embodiment two:
The invention discloses a preparation method of a plurality of prebiotic tablet candies, which comprises the following steps:
s101, sieving inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin, and removing unqualified particles;
s102, mixing finely-screened inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin to obtain a mixed material;
S103, adding an adhesive into the mixed materials, and drying and granulating to obtain a semi-finished product A;
S104, mixing lactobacillus powder with vitamin C, stevioside, fruit powder and the like to obtain a semi-finished product B;
s105, uniformly mixing the semi-finished product A, the semi-finished product B, magnesium stearate and the flavoring agent, and tabletting to obtain a semi-finished product C;
And S106, coating a layer of coating on the outer wall of the semi-finished product C to obtain a finished product.
Based on S101, the number of screens for sieving was 100 mesh.
Based on S102, the materials are mixed using a two-dimensional mixer or a three-dimensional mixer.
The binder was 8% in concentration based on S103.
The addition temperature of the binder was 70 ℃.
Based on S104, the lactobacillus powder is formed by mixing a bacterium powder A and a bacterium powder B, wherein the bacterium powder A is bacillus coagulans, and the bacterium powder B is one or more of lactobacillus, animal bifidobacterium, lactobacillus lactis, lactobacillus rhamnosus, lactobacillus reuteri, lactobacillus fermentum, bifidobacterium breve and bifidobacterium adolescentis.
In this example, when the number of the screening screens is 100, the powder particles are finer and finer, the content of the tablets after mixing is more uniform, and the tablets are finer and finer. The dissolution rate of the active ingredients is also greatly accelerated, and the absolute bioavailability of the fine powder is improved by about 15 percent compared with that of coarse powder. Compared with 120 meshes, the 100-mesh screen mesh has the advantages that the requirement degree of powder particles is reduced, the grinding processing difficulty of inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol, resistant dextrin, vitamin C, stevioside and magnesium stearate can be reduced, the production cost of various prebiotic tabletting candies is reduced, and better control of the cost is facilitated.
The survival rate of the strain is almost linearly reduced along with the increase of tabletting pressure, and when more than one strain is selected in the bacterial powder B in order to increase the nutrition components of the various prebiotic tabletting candies, the integral content of the various prebiotic tabletting candies is increased slightly, so that the hardness of the various prebiotic tabletting candies is reduced when the concentration of starch slurry is 6%, the nutritional content of the various prebiotic tabletting candies is influenced due to the crushing of friction, extrusion, collision and the like in the production and transportation process, and the quality of the various prebiotic tabletting candies is reduced, so that the concentration of starch slurry is 8%, the hardness after powder tabletting can be effectively improved, and the quality of the various prebiotic tabletting candies is improved.
Embodiment III:
The invention discloses a preparation method of a plurality of prebiotic tablet candies, which comprises the following steps:
s101, sieving inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin, and removing unqualified particles;
s102, mixing finely-screened inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin to obtain a mixed material;
S103, adding an adhesive into the mixed materials, and drying and granulating to obtain a semi-finished product A;
S104, mixing lactobacillus powder with vitamin C, stevioside, fruit powder and the like to obtain a semi-finished product B;
s105, uniformly mixing the semi-finished product A, the semi-finished product B, magnesium stearate and the flavoring agent, and tabletting to obtain a semi-finished product C;
And S106, coating a layer of coating on the outer wall of the semi-finished product C to obtain a finished product.
Based on S101, the number of screens for sieving was 80 mesh.
Based on S102, the materials are mixed using a two-dimensional mixer or a three-dimensional mixer.
The binder was 10% in concentration based on S103.
The addition temperature of the binder was 70 ℃.
Based on S104, the lactobacillus powder is formed by mixing a bacterium powder A and a bacterium powder B, wherein the bacterium powder A is bacillus coagulans, and the bacterium powder B is one or more of lactobacillus, animal bifidobacterium, lactobacillus lactis, lactobacillus rhamnosus, lactobacillus reuteri, lactobacillus fermentum, bifidobacterium breve and bifidobacterium adolescentis.
In this example, when the number of the screening screens is 80, the powder particles are finer and finer, the content of the tablets after mixing is more uniform, and the tablets are finer and finer. The dissolution rate of the active ingredients is also greatly accelerated, and the absolute bioavailability of the fine powder is improved by about 12 percent compared with that of coarse powder. Compared with 120 meshes and 100 meshes, the 80-mesh screen mesh has the advantages that the requirement degree of powder particles is reduced, the grinding processing difficulty of inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol, resistant dextrin, vitamin C, stevioside and magnesium stearate is further reduced, and the cost of the various prebiotic tabletting candies is reduced again under the condition of guaranteeing the quality.
When a strain is selected in the bacterial powder B, the total content of the prebiotic tablet candy is minimum, so that the prebiotic tablet candy cannot be compacted effectively when the concentration of starch slurry is 8%, the whole of the prebiotic tablet candy is loose, the hardness is extremely poor, the nutrition content of the prebiotic tablet candy can be influenced due to crushing such as friction, extrusion and collision in the production and transportation process, the quality of the prebiotic tablet candy is reduced, the concentration of starch slurry is 10%, the hardness after powder tablet pressing can be effectively improved, and the quality of the prebiotic tablet candy is improved.
Embodiment four:
The invention discloses a preparation method of a plurality of prebiotic tablet candies, which comprises the following steps:
s101, sieving inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin, and removing unqualified particles;
s102, mixing finely-screened inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin to obtain a mixed material;
S103, adding an adhesive into the mixed materials, and drying and granulating to obtain a semi-finished product A;
S104, mixing lactobacillus powder with vitamin C, stevioside, fruit powder and the like to obtain a semi-finished product B;
s105, uniformly mixing the semi-finished product A, the semi-finished product B, magnesium stearate and the flavoring agent, and tabletting to obtain a semi-finished product C;
And S106, coating a layer of coating on the outer wall of the semi-finished product C to obtain a finished product.
Based on S103, the number of screen meshes used for the sizing was 18 mesh.
In this embodiment, in order to improve the production efficiency of the various prebiotic tablet candies, the production line is generally used for automatic production, so that the nutritional ingredients contained in each produced various prebiotic tablet candies are basically the same, and the specifications of the nutritional ingredients which can be absorbed by users of different ages are not the same, so that the mesh number of the screens in the whole tablet is 18 meshes, thereby increasing the nutritional ingredients contained in the tablet, enabling the ingredients contained in one piece of various prebiotic tablet candies to meet the daily requirements of adults, and reducing the number of various prebiotic tablet candies taken by the adults at one time.
Fifth embodiment:
The invention discloses a preparation method of a plurality of prebiotic tablet candies, which comprises the following steps:
s101, sieving inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin, and removing unqualified particles;
s102, mixing finely-screened inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin to obtain a mixed material;
S103, adding an adhesive into the mixed materials, and drying and granulating to obtain a semi-finished product A;
S104, mixing lactobacillus powder with vitamin C, stevioside, fruit powder and the like to obtain a semi-finished product B;
s105, uniformly mixing the semi-finished product A, the semi-finished product B, magnesium stearate and the flavoring agent, and tabletting to obtain a semi-finished product C;
And S106, coating a layer of coating on the outer wall of the semi-finished product C to obtain a finished product.
The number of screen meshes used for the sizing is 20 mesh based on S103.
In this embodiment, since the nutritional components after the various prebiotic tablet candies are produced are fixed, and the nutritional requirement of young people is smaller, the various prebiotic tablet candies produced by 18 meshes are overabundant in nutrition, and the load of human bodies can be increased, so that the screen mesh number used in the process of finishing grains is 20 meshes for being suitable for better absorption of young people, the overall content of the various prebiotic tablet candies can be reduced, and the burden of the young people on the bodies caused by eating the various prebiotic tablet candies is avoided.
Example six:
The invention discloses a preparation method of a plurality of prebiotic tablet candies, which comprises the following steps:
s101, sieving inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin, and removing unqualified particles;
s102, mixing finely-screened inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin to obtain a mixed material;
S103, adding an adhesive into the mixed materials, and drying and granulating to obtain a semi-finished product A;
S104, mixing lactobacillus powder with vitamin C, stevioside, fruit powder and the like to obtain a semi-finished product B;
s105, uniformly mixing the semi-finished product A, the semi-finished product B, magnesium stearate and the flavoring agent, and tabletting to obtain a semi-finished product C;
And S106, coating a layer of coating on the outer wall of the semi-finished product C to obtain a finished product.
Based on S103, the screen mesh number used for the sizing was 24 mesh.
In this embodiment, the intestines and stomach of the elderly age because of the increase of age, so that the absorption efficiency of the elderly is lower, therefore, the absorption of the various prebiotic tablet candies is slower, the nutrition of the various prebiotic tablet candies can not be absorbed completely, the rest nutrition is discharged outside the body without being absorbed, the nutrition of the various prebiotic tablet candies is wasted, so that the various prebiotic tablet candies are produced by 24 meshes, the nutrition content of the various prebiotic tablet candies is reduced, the nutrition is prevented from being wasted, and the production cost of the various prebiotic tablet candies is reduced, thereby reducing the selling price of the elderly when buying the various prebiotic tablet candies.
Embodiment seven:
The invention discloses a preparation method of a plurality of prebiotic tablet candies, which comprises the following steps:
s101, sieving inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin, and removing unqualified particles;
s102, mixing finely-screened inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin to obtain a mixed material;
S103, adding an adhesive into the mixed materials, and drying and granulating to obtain a semi-finished product A;
S104, mixing lactobacillus powder with vitamin C, stevioside, fruit powder and the like to obtain a semi-finished product B;
s105, uniformly mixing the semi-finished product A, the semi-finished product B, magnesium stearate and the flavoring agent, and tabletting to obtain a semi-finished product C;
And S106, coating a layer of coating on the outer wall of the semi-finished product C to obtain a finished product.
Based on S105, the flavoring agent is prepared by mixing cranberry powder, blackberry powder, blueberry juice powder and raspberry powder.
In this embodiment, in order to increase the popularity of the prebiotic tablet candy, the prebiotic tablet candy can be better driven into the mass market, so that the outer surface wall of the prebiotic tablet candy can be coated with a flavoring agent for increasing the taste.
Cranberry: the active substances and the A-type procyanidine contained in the composition can reduce the adhesion of bacteria in vivo, and are beneficial to improving urinary tract infection. Meanwhile, the content of the antioxidant component of the cranberry is high, for example, 25% higher than that of the blueberry, and is more than 4 times of that of apples and peaches. These characteristics make cranberries considered beneficial to female health.
Blackberry: blackberry contains rich nutrients such as vitamin C, potassium, cellulose and the like, has the functions of resisting oxidation and inflammation, and is beneficial to protecting cardiovascular health and preventing certain diseases.
Blueberry: blueberry is rich in antioxidants, helps to slow down the aging process, protects heart health, enhances immunity, and potentially improves memory.
Raspberry: raspberry is rich in vitamin C, manganese, fiber and antioxidant, and helps to reduce cholesterol, protect heart health, and promote digestion and control blood glucose.
In general, these four fruits are rich in nutrients and have many health benefits, and are therefore favored by females. Therefore, the coating of the tablet candy with the prebiotics is prepared by mixing cranberry powder, blackberry powder, blueberry juice powder and raspberry powder, and can be used for opening the female market.
Example eight:
The invention discloses a preparation method of a plurality of prebiotic tablet candies, which comprises the following steps:
s101, sieving inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin, and removing unqualified particles;
s102, mixing finely-screened inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin to obtain a mixed material;
S103, adding an adhesive into the mixed materials, and drying and granulating to obtain a semi-finished product A;
S104, mixing lactobacillus powder with vitamin C, stevioside, fruit powder and the like to obtain a semi-finished product B;
s105, uniformly mixing the semi-finished product A, the semi-finished product B, magnesium stearate and the flavoring agent, and tabletting to obtain a semi-finished product C;
And S106, coating a layer of coating on the outer wall of the semi-finished product C to obtain a finished product.
Based on S105, the flavoring agent is prepared by mixing green tea powder, grosvener siraitia powder and Hangzhou inulin.
In this example, green tea: has light taste, refreshing taste, and can relieve fatigue and refresh mind. In addition, green tea is rich in antioxidants, helping to prevent aging and protect cardiovascular health. These characteristics make green tea popular and tougher for many men. Meanwhile, in east Asian culture, green tea drinking is considered as a way of teaching and maintenance, and therefore has cultural appeal.
Momordica grosvenori: momordica grosvenori has effects of clearing heat, moistening lung, promoting salivation, quenching thirst, etc., and is beneficial to human body. The taste is unique, sweet and popular with many people.
Chrysanthemum morifolium ramat: the flos Chrysanthemi has effects of clearing heat and detoxicating, dispelling pathogenic wind and heat, removing liver fire and improving eyesight. Meanwhile, the chrysanthemum tea is drunk, has faint scent taste and is also liked by a plurality of people.
In general, these three foods or drinks have respective advantages such as good taste, rich nutrition, health benefits, etc., and are thus very popular among men.
Therefore, the taste of the flavoring agent prepared by mixing green tea powder, grosvener siraitia powder and Hangzhou inulin is more liked by the male population, and the flavoring agent can be used for opening the male market.
Example nine:
The invention discloses a preparation method of a plurality of prebiotic tablet candies, which comprises the following steps:
s101, sieving inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin, and removing unqualified particles;
s102, mixing finely-screened inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin to obtain a mixed material;
S103, adding an adhesive into the mixed materials, and drying and granulating to obtain a semi-finished product A;
S104, mixing lactobacillus powder with vitamin C, stevioside, fruit powder and the like to obtain a semi-finished product B;
s105, uniformly mixing the semi-finished product A, the semi-finished product B, magnesium stearate and the flavoring agent, and tabletting to obtain a semi-finished product C;
And S106, coating a layer of coating on the outer wall of the semi-finished product C to obtain a finished product.
Based on S105, the flavoring agent is prepared by mixing lime powder;
based on S105, the flavoring agent is prepared by mixing and modulating juicy peach powder;
based on S105, the flavoring agent is mixed and prepared from blackcurrant powder.
In this example, the audience group of lime is very broad, including the following:
people with strong health consciousness: the green lemon is rich in vitamin C and antioxidant substances, has good effects of enhancing immunity and preventing diseases, and is favored by many people focusing on healthy life style.
People who like fresh taste: the lime has unique sour taste and can bring fresh taste, so the lime is popular with many people who like to try new taste.
Beauty and skin care fan: the lime contains abundant antioxidant substances, can help resist free radical attack and protect skin health, so that the lime is favored by a plurality of women who pay attention to skin care.
Children: green lemon is also commonly used as a child snack or drink because it is sweet and sour in taste and easy to chew.
The favorite people of the juicy peach mainly comprise the following groups:
Healthy lifestyle pursuers: juicy peaches are rich in vitamin C and antioxidant substances, help to enhance immunity and prevent diseases, and are thus favored by many people focusing on healthy lifestyles.
People who like sweet taste: the juicy peach has tender meat quality and sweet taste, and is suitable for people who like sweet food.
Beauty and skin care fan: juicy peaches are rich in vitamin C and antioxidant substances, and help to protect skin health, so that juicy peaches are favored by many women who pay attention to skin care.
Children: juicy peaches are also commonly used as children's snacks or drinks because of their sweet taste and ease of chewing.
The blackcurrant audience population mainly includes the following categories:
Healthy lifestyle pursuers: blackcurrants contain rich vitamin C, magnesium, potassium, calcium, phosphorus, anthocyanin, phenolic substances and the like, and have rich nutritive value. These components can be used for enhancing immunity, and preventing anemia, gout, arthritis, edema, rheumatism, oral and throat diseases, etc.
Liver protection demander: anthocyanin, vitamin C, flavone and phenolic antioxidant actives in blackcurrant can resist peroxidation, and are important for protecting liver function.
Delaying aging in the people in need of: blackcurrants contain various antioxidant substances such as anthocyanin, quercetin, flavone, catechin, blackcurrant polysaccharide and the like, and can help human body to remove free radicals and delay human body aging.
The above is only a part of the possible audience population, and it is seen that the development of prebiotic tablet candies with multiple tastes is extremely important for the expansion of the market.
Although embodiments of the present invention have been shown and described, it will be understood by those skilled in the art that various changes, modifications, substitutions and alterations can be made therein without departing from the principles and spirit of the invention, the scope of which is defined in the appended claims and their equivalents.
Claims (8)
1. A method for preparing a plurality of prebiotic tablet candies, which is characterized by comprising the following steps:
s101, sieving inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin, and removing unqualified particles;
s102, mixing finely-screened inulin, fructo-oligosaccharide, xylo-oligosaccharide, cottonseed oligosaccharide, sorbitol and resistant dextrin to obtain a mixed material;
S103, adding an adhesive into the mixed materials, and drying and granulating to obtain a semi-finished product A;
S104, mixing lactobacillus powder with vitamin C, stevioside, fruit powder and the like to obtain a semi-finished product B;
s105, uniformly mixing the semi-finished product A, the semi-finished product B, magnesium stearate and the flavoring agent, and tabletting to obtain a semi-finished product C;
And S106, coating a layer of coating on the outer wall of the semi-finished product C to obtain a finished product.
2. The method of producing a pressed candy product according to claim 1, wherein the number of screens for sieving is 80 to 120 mesh based on S101.
3. The method of preparing a plurality of prebiotic pellet candy as claimed in claim 1 wherein the materials are mixed using a two dimensional mixer or a three dimensional mixer based on S102.
4. The method of preparing a multi-prebiotic tableting confection of claim 1, wherein the binder is 6-10% starch slurry or 6-10% maltodextrin based on S103.
5. The method of claim 4, wherein the binder is added at a temperature of about 70 ℃.
6. The method for preparing the multi-prebiotic tablet candy according to claim 1, wherein based on S104, the lactic acid bacteria powder is formed by mixing bacteria powder a and bacteria powder B, wherein the bacteria powder a is bacillus coagulans, and the bacteria powder B is one or more of lactobacillus, bifidobacterium animalis, bifidobacterium lactis, lactobacillus rhamnosus, lactobacillus reuteri, lactobacillus fermentum, bifidobacterium breve and bifidobacterium adolescentis.
7. The method for preparing a plurality of prebiotic tablet candy according to claim 1, wherein the number of screen meshes used for the sizing is 18-24 mesh based on S103.
8. The method of preparing a multi-prebiotic pressed candy as recited in claim 1, wherein the flavoring agent is mixed and blended from cranberry powder, blackberry powder, blueberry juice powder and raspberry powder based on S105;
Based on S105, the flavoring agent is prepared by mixing green tea powder, fructus Siraitiae Grosvenorii powder and Hangzhou inulin;
Based on S105, the flavoring agent is prepared by mixing lime powder;
based on S105, the flavoring agent is prepared by mixing and modulating juicy peach powder;
based on S105, the flavoring agent is mixed and prepared from blackcurrant powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202410293184.9A CN117941765A (en) | 2024-03-14 | 2024-03-14 | Preparation method of various prebiotic tablet candy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202410293184.9A CN117941765A (en) | 2024-03-14 | 2024-03-14 | Preparation method of various prebiotic tablet candy |
Publications (1)
Publication Number | Publication Date |
---|---|
CN117941765A true CN117941765A (en) | 2024-04-30 |
Family
ID=90803880
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202410293184.9A Pending CN117941765A (en) | 2024-03-14 | 2024-03-14 | Preparation method of various prebiotic tablet candy |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN117941765A (en) |
-
2024
- 2024-03-14 CN CN202410293184.9A patent/CN117941765A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2367446B1 (en) | Food-based supplement delivery system | |
AU2007300461B2 (en) | Probiotic oral dosage forms | |
CN103431134A (en) | Tablet candy containing prebiotics and preparation method thereof | |
KR101773249B1 (en) | The manufacturing method of Herbal Food Products from the Leaves and Berries of Korean Cudrania tricuspidata | |
CN106954856A (en) | A kind of ferment dietary fiber and its preparation technology | |
WO2018181380A1 (en) | Edible composition for intestinal bacteria | |
CN105249480A (en) | Chewable tablet with dietary fiber and bifidobacteria and preparing method thereof | |
CN108634151A (en) | A kind of probiotics egg nutrient powder and preparation method thereof | |
CN114376235B (en) | Weight-losing probiotics and prebiotic composition for controlling body fat and preparation method thereof | |
CN108813068A (en) | A kind of compound probiotic pressed candy and its preparation process | |
CN103005259A (en) | Xylitol puerarin chewable tablet and preparation technique thereof | |
CN114208989A (en) | Ketogenic meal replacement nutrition powder solid beverage and preparation method thereof | |
CN113040253A (en) | Tabletting candy for relaxing bowels and preparation method thereof | |
KR20190001448A (en) | Oval solid yogurt and method for manufacturing thereof | |
CN112136894A (en) | Nutritional dietary supplement food beneficial to cardiovascular health and preparation method and application thereof | |
CN116671569A (en) | Active probiotic antioxidation soft sweet and preparation method thereof | |
JP2006325486A (en) | Functional food and functional drink | |
CN117941765A (en) | Preparation method of various prebiotic tablet candy | |
CN115316479A (en) | Tablet candy containing probiotics and preparation method thereof | |
CN102293380B (en) | Chewable banana tablet and preparation method thereof | |
CN108936265A (en) | A kind of nutritional meal replacement and its preparation method and application of dark hair brighten the hair | |
KR20220058176A (en) | Prebiotics composition for improving intestinal microflora | |
CN112189843A (en) | Raspberry nutritional chewable tablet and preparation method thereof | |
CN111466579A (en) | Probiotic inulin tablet and preparation method thereof | |
CN111264739A (en) | Probiotic solid beverage and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination |