WO2024063543A1 - Composition pour la prévention ou le traitement du cancer à l'aide d'une polythérapie, comprenant une souche de lactobacillus plantarum et un médicament à base de plantes - Google Patents
Composition pour la prévention ou le traitement du cancer à l'aide d'une polythérapie, comprenant une souche de lactobacillus plantarum et un médicament à base de plantes Download PDFInfo
- Publication number
- WO2024063543A1 WO2024063543A1 PCT/KR2023/014310 KR2023014310W WO2024063543A1 WO 2024063543 A1 WO2024063543 A1 WO 2024063543A1 KR 2023014310 W KR2023014310 W KR 2023014310W WO 2024063543 A1 WO2024063543 A1 WO 2024063543A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cancer
- strain
- preventing
- herbal medicine
- active material
- Prior art date
Links
- 206010028980 Neoplasm Diseases 0.000 title claims abstract description 133
- 241000411851 herbal medicine Species 0.000 title claims abstract description 107
- 240000006024 Lactobacillus plantarum Species 0.000 title claims abstract description 84
- 201000011510 cancer Diseases 0.000 title claims abstract description 80
- 239000000203 mixture Substances 0.000 title claims abstract description 80
- 235000013965 Lactobacillus plantarum Nutrition 0.000 title claims abstract description 57
- 229940072205 lactobacillus plantarum Drugs 0.000 title claims abstract description 57
- 238000002648 combination therapy Methods 0.000 title abstract description 14
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 21
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 10
- 206010009944 Colon cancer Diseases 0.000 claims description 63
- 239000013543 active substance Substances 0.000 claims description 47
- 208000029742 colonic neoplasm Diseases 0.000 claims description 46
- 239000004480 active ingredient Substances 0.000 claims description 44
- 239000011149 active material Substances 0.000 claims description 40
- 230000036541 health Effects 0.000 claims description 36
- 235000013376 functional food Nutrition 0.000 claims description 33
- 239000006166 lysate Substances 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 27
- 235000001674 Agaricus brunnescens Nutrition 0.000 claims description 26
- 241001248610 Ophiocordyceps sinensis Species 0.000 claims description 24
- 238000002360 preparation method Methods 0.000 claims description 11
- 238000009472 formulation Methods 0.000 claims description 10
- 239000000843 powder Substances 0.000 claims description 9
- 108020004465 16S ribosomal RNA Proteins 0.000 claims description 8
- 239000002775 capsule Substances 0.000 claims description 8
- 230000006907 apoptotic process Effects 0.000 claims description 7
- 239000008187 granular material Substances 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000003826 tablet Substances 0.000 claims description 7
- 239000006187 pill Substances 0.000 claims description 6
- 239000000725 suspension Substances 0.000 claims description 6
- 230000002265 prevention Effects 0.000 claims description 5
- 235000020357 syrup Nutrition 0.000 claims description 5
- 239000006188 syrup Substances 0.000 claims description 5
- 230000001225 therapeutic effect Effects 0.000 claims description 5
- 208000000461 Esophageal Neoplasms Diseases 0.000 claims description 4
- 206010030155 Oesophageal carcinoma Diseases 0.000 claims description 4
- 208000015634 Rectal Neoplasms Diseases 0.000 claims description 4
- 208000005718 Stomach Neoplasms Diseases 0.000 claims description 4
- 201000004101 esophageal cancer Diseases 0.000 claims description 4
- 206010017758 gastric cancer Diseases 0.000 claims description 4
- 230000006872 improvement Effects 0.000 claims description 4
- 201000007270 liver cancer Diseases 0.000 claims description 4
- 208000014018 liver neoplasm Diseases 0.000 claims description 4
- 239000007937 lozenge Substances 0.000 claims description 4
- 206010038038 rectal cancer Diseases 0.000 claims description 4
- 201000001275 rectum cancer Diseases 0.000 claims description 4
- 201000011549 stomach cancer Diseases 0.000 claims description 4
- 230000004614 tumor growth Effects 0.000 claims description 4
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims description 3
- 206010061424 Anal cancer Diseases 0.000 claims description 3
- 208000007860 Anus Neoplasms Diseases 0.000 claims description 3
- 206010005003 Bladder cancer Diseases 0.000 claims description 3
- 208000003174 Brain Neoplasms Diseases 0.000 claims description 3
- 206010006187 Breast cancer Diseases 0.000 claims description 3
- 208000026310 Breast neoplasm Diseases 0.000 claims description 3
- 206010008342 Cervix carcinoma Diseases 0.000 claims description 3
- 208000022072 Gallbladder Neoplasms Diseases 0.000 claims description 3
- 208000008839 Kidney Neoplasms Diseases 0.000 claims description 3
- 206010023825 Laryngeal cancer Diseases 0.000 claims description 3
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 3
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 claims description 3
- 206010029260 Neuroblastoma Diseases 0.000 claims description 3
- 206010033128 Ovarian cancer Diseases 0.000 claims description 3
- 206010061535 Ovarian neoplasm Diseases 0.000 claims description 3
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims description 3
- 206010060862 Prostate cancer Diseases 0.000 claims description 3
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims description 3
- 206010038389 Renal cancer Diseases 0.000 claims description 3
- 201000000582 Retinoblastoma Diseases 0.000 claims description 3
- 208000004337 Salivary Gland Neoplasms Diseases 0.000 claims description 3
- 206010061934 Salivary gland cancer Diseases 0.000 claims description 3
- 208000000453 Skin Neoplasms Diseases 0.000 claims description 3
- 208000024770 Thyroid neoplasm Diseases 0.000 claims description 3
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims description 3
- 208000006105 Uterine Cervical Neoplasms Diseases 0.000 claims description 3
- 201000011165 anus cancer Diseases 0.000 claims description 3
- 210000001815 ascending colon Anatomy 0.000 claims description 3
- 201000009036 biliary tract cancer Diseases 0.000 claims description 3
- 208000020790 biliary tract neoplasm Diseases 0.000 claims description 3
- 201000010881 cervical cancer Diseases 0.000 claims description 3
- 210000001731 descending colon Anatomy 0.000 claims description 3
- 201000010175 gallbladder cancer Diseases 0.000 claims description 3
- 201000010536 head and neck cancer Diseases 0.000 claims description 3
- 208000014829 head and neck neoplasm Diseases 0.000 claims description 3
- 201000010982 kidney cancer Diseases 0.000 claims description 3
- 206010023841 laryngeal neoplasm Diseases 0.000 claims description 3
- 201000005202 lung cancer Diseases 0.000 claims description 3
- 208000020816 lung neoplasm Diseases 0.000 claims description 3
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims description 3
- 201000001441 melanoma Diseases 0.000 claims description 3
- 210000004877 mucosa Anatomy 0.000 claims description 3
- 208000008443 pancreatic carcinoma Diseases 0.000 claims description 3
- 230000002441 reversible effect Effects 0.000 claims description 3
- 210000001599 sigmoid colon Anatomy 0.000 claims description 3
- 201000000849 skin cancer Diseases 0.000 claims description 3
- 201000002314 small intestine cancer Diseases 0.000 claims description 3
- 201000002510 thyroid cancer Diseases 0.000 claims description 3
- 210000003384 transverse colon Anatomy 0.000 claims description 3
- 201000005112 urinary bladder cancer Diseases 0.000 claims description 3
- 239000008177 pharmaceutical agent Substances 0.000 claims description 2
- 241000332371 Abutilon x hybridum Species 0.000 claims 2
- 240000004270 Colocasia esculenta var. antiquorum Species 0.000 claims 2
- 201000005787 hematologic cancer Diseases 0.000 claims 2
- 208000024200 hematopoietic and lymphoid system neoplasm Diseases 0.000 claims 2
- 201000001244 rectum lymphoma Diseases 0.000 claims 2
- 239000001963 growth medium Substances 0.000 abstract description 11
- 230000002195 synergetic effect Effects 0.000 abstract description 8
- 230000034994 death Effects 0.000 abstract description 6
- 230000035755 proliferation Effects 0.000 abstract description 4
- 235000013402 health food Nutrition 0.000 abstract description 2
- 210000004027 cell Anatomy 0.000 description 74
- 230000000694 effects Effects 0.000 description 48
- 244000281702 Dioscorea villosa Species 0.000 description 29
- 235000004879 dioscorea Nutrition 0.000 description 29
- 241000703121 Campanula rotundifolia Species 0.000 description 28
- 239000012228 culture supernatant Substances 0.000 description 27
- 241000699666 Mus <mouse, genus> Species 0.000 description 22
- 230000001093 anti-cancer Effects 0.000 description 21
- 238000011282 treatment Methods 0.000 description 18
- 235000013305 food Nutrition 0.000 description 17
- 239000003814 drug Substances 0.000 description 16
- 239000002609 medium Substances 0.000 description 13
- 239000000047 product Substances 0.000 description 13
- 235000015872 dietary supplement Nutrition 0.000 description 12
- 229940079593 drug Drugs 0.000 description 11
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 10
- 239000000284 extract Substances 0.000 description 10
- 239000004615 ingredient Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 230000004083 survival effect Effects 0.000 description 10
- 238000011260 co-administration Methods 0.000 description 9
- 201000010099 disease Diseases 0.000 description 9
- 241000186660 Lactobacillus Species 0.000 description 8
- 241000699670 Mus sp. Species 0.000 description 8
- 239000000654 additive Substances 0.000 description 8
- 241000282412 Homo Species 0.000 description 7
- 229940039696 lactobacillus Drugs 0.000 description 7
- 239000000546 pharmaceutical excipient Substances 0.000 description 7
- 230000002829 reductive effect Effects 0.000 description 7
- 230000004044 response Effects 0.000 description 7
- 108090000672 Annexin A5 Proteins 0.000 description 6
- 241001465754 Metazoa Species 0.000 description 6
- 238000010171 animal model Methods 0.000 description 6
- 238000012790 confirmation Methods 0.000 description 6
- 238000012258 culturing Methods 0.000 description 6
- 239000003937 drug carrier Substances 0.000 description 6
- 239000000796 flavoring agent Substances 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 244000005700 microbiome Species 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 108700012813 7-aminoactinomycin D Proteins 0.000 description 5
- YXHLJMWYDTXDHS-IRFLANFNSA-N 7-aminoactinomycin D Chemical compound C[C@H]1OC(=O)[C@H](C(C)C)N(C)C(=O)CN(C)C(=O)[C@@H]2CCCN2C(=O)[C@@H](C(C)C)NC(=O)[C@H]1NC(=O)C1=C(N)C(=O)C(C)=C2OC(C(C)=C(N)C=C3C(=O)N[C@@H]4C(=O)N[C@@H](C(N5CCC[C@H]5C(=O)N(C)CC(=O)N(C)[C@@H](C(C)C)C(=O)O[C@@H]4C)=O)C(C)C)=C3N=C21 YXHLJMWYDTXDHS-IRFLANFNSA-N 0.000 description 5
- 102000004121 Annexin A5 Human genes 0.000 description 5
- 206010017993 Gastrointestinal neoplasms Diseases 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 239000003963 antioxidant agent Substances 0.000 description 5
- 235000006708 antioxidants Nutrition 0.000 description 5
- 150000001720 carbohydrates Chemical class 0.000 description 5
- 235000014633 carbohydrates Nutrition 0.000 description 5
- 238000005119 centrifugation Methods 0.000 description 5
- 239000003085 diluting agent Substances 0.000 description 5
- 235000013355 food flavoring agent Nutrition 0.000 description 5
- 230000012010 growth Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000002773 nucleotide Substances 0.000 description 5
- 125000003729 nucleotide group Chemical group 0.000 description 5
- 235000015097 nutrients Nutrition 0.000 description 5
- 108090000623 proteins and genes Proteins 0.000 description 5
- 238000011160 research Methods 0.000 description 5
- 239000006228 supernatant Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 241000124008 Mammalia Species 0.000 description 4
- 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 4
- 230000009471 action Effects 0.000 description 4
- POJWUDADGALRAB-UHFFFAOYSA-N allantoin Chemical compound NC(=O)NC1NC(=O)NC1=O POJWUDADGALRAB-UHFFFAOYSA-N 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- -1 betasin Proteins 0.000 description 4
- 230000022131 cell cycle Effects 0.000 description 4
- 238000010835 comparative analysis Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 238000002955 isolation Methods 0.000 description 4
- 239000006872 mrs medium Substances 0.000 description 4
- 239000013642 negative control Substances 0.000 description 4
- 229940124597 therapeutic agent Drugs 0.000 description 4
- 229920001817 Agar Polymers 0.000 description 3
- 239000008272 agar Substances 0.000 description 3
- HAMNKKUPIHEESI-UHFFFAOYSA-N aminoguanidine Chemical compound NNC(N)=N HAMNKKUPIHEESI-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 235000013361 beverage Nutrition 0.000 description 3
- 230000005880 cancer cell killing Effects 0.000 description 3
- 230000030833 cell death Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000003636 conditioned culture medium Substances 0.000 description 3
- VLCYCQAOQCDTCN-UHFFFAOYSA-N eflornithine Chemical compound NCCCC(N)(C(F)F)C(O)=O VLCYCQAOQCDTCN-UHFFFAOYSA-N 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 235000013350 formula milk Nutrition 0.000 description 3
- 238000007918 intramuscular administration Methods 0.000 description 3
- 238000001990 intravenous administration Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 210000000056 organ Anatomy 0.000 description 3
- 230000001376 precipitating effect Effects 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 238000007920 subcutaneous administration Methods 0.000 description 3
- APTNOIWSCDBIAS-UHFFFAOYSA-N 5,10,11-trihydroxy-9,9-bis(hydroxymethyl)-2,2,6a,6b,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid Chemical compound C1C(O)C(O)C(CO)(CO)C2CCC3(C)C4(C)CC(O)C5(C(O)=O)CCC(C)(C)CC5C4=CCC3C21C APTNOIWSCDBIAS-UHFFFAOYSA-N 0.000 description 2
- POJWUDADGALRAB-PVQJCKRUSA-N Allantoin Natural products NC(=O)N[C@@H]1NC(=O)NC1=O POJWUDADGALRAB-PVQJCKRUSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 241001264174 Cordyceps militaris Species 0.000 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 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 description 2
- 206010061818 Disease progression Diseases 0.000 description 2
- 239000004386 Erythritol Substances 0.000 description 2
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 2
- 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 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 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 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- 230000002159 abnormal effect Effects 0.000 description 2
- 235000010443 alginic acid Nutrition 0.000 description 2
- 229920000615 alginic acid Polymers 0.000 description 2
- 229960000458 allantoin Drugs 0.000 description 2
- 230000003110 anti-inflammatory effect Effects 0.000 description 2
- 230000000259 anti-tumor effect Effects 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 239000001506 calcium phosphate Substances 0.000 description 2
- 229910000389 calcium phosphate Inorganic materials 0.000 description 2
- 235000011010 calcium phosphates Nutrition 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 230000010261 cell growth Effects 0.000 description 2
- 235000008504 concentrate Nutrition 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000001934 delay Effects 0.000 description 2
- 230000003111 delayed effect Effects 0.000 description 2
- 210000002249 digestive system Anatomy 0.000 description 2
- 230000005750 disease progression Effects 0.000 description 2
- 230000002500 effect on skin Effects 0.000 description 2
- 235000019414 erythritol Nutrition 0.000 description 2
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 2
- 229940009714 erythritol Drugs 0.000 description 2
- 230000003203 everyday effect Effects 0.000 description 2
- 230000029142 excretion Effects 0.000 description 2
- 238000000684 flow cytometry Methods 0.000 description 2
- MHMNJMPURVTYEJ-UHFFFAOYSA-N fluorescein-5-isothiocyanate Chemical compound O1C(=O)C2=CC(N=C=S)=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 MHMNJMPURVTYEJ-UHFFFAOYSA-N 0.000 description 2
- 210000001035 gastrointestinal tract Anatomy 0.000 description 2
- 230000002068 genetic effect Effects 0.000 description 2
- 229940093915 gynecological organic acid Drugs 0.000 description 2
- 238000011081 inoculation Methods 0.000 description 2
- 239000007951 isotonicity adjuster Substances 0.000 description 2
- MWDZOUNAPSSOEL-UHFFFAOYSA-N kaempferol Natural products OC1=C(C(=O)c2cc(O)cc(O)c2O1)c3ccc(O)cc3 MWDZOUNAPSSOEL-UHFFFAOYSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 238000010172 mouse model Methods 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 150000004804 polysaccharides Chemical class 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 239000006041 probiotic Substances 0.000 description 2
- 230000000529 probiotic effect Effects 0.000 description 2
- 235000018291 probiotics Nutrition 0.000 description 2
- XJMOSONTPMZWPB-UHFFFAOYSA-M propidium iodide Chemical compound [I-].[I-].C12=CC(N)=CC=C2C2=CC=C(N)C=C2[N+](CCC[N+](C)(CC)CC)=C1C1=CC=CC=C1 XJMOSONTPMZWPB-UHFFFAOYSA-M 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 229960001285 quercetin Drugs 0.000 description 2
- 235000005875 quercetin Nutrition 0.000 description 2
- HELXLJCILKEWJH-NCGAPWICSA-N rebaudioside A Chemical compound O([C@H]1[C@H](O)[C@@H](CO)O[C@H]([C@@H]1O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)O[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 HELXLJCILKEWJH-NCGAPWICSA-N 0.000 description 2
- 235000002020 sage Nutrition 0.000 description 2
- 229930182490 saponin Natural products 0.000 description 2
- 150000007949 saponins Chemical class 0.000 description 2
- 235000017709 saponins Nutrition 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 235000010356 sorbitol Nutrition 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 238000001356 surgical procedure Methods 0.000 description 2
- 239000000375 suspending agent Substances 0.000 description 2
- 208000024891 symptom Diseases 0.000 description 2
- 235000018553 tannin Nutrition 0.000 description 2
- 229920001864 tannin Polymers 0.000 description 2
- 239000001648 tannin Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 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 description 2
- 150000003648 triterpenes Chemical class 0.000 description 2
- 210000004881 tumor cell Anatomy 0.000 description 2
- 230000005740 tumor formation Effects 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 1
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 235000006491 Acacia senegal Nutrition 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 239000004382 Amylase Substances 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 102100034283 Annexin A5 Human genes 0.000 description 1
- 108010011485 Aspartame Proteins 0.000 description 1
- 241000304886 Bacilli Species 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 241000123667 Campanula Species 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- 244000003247 Caryota mitis Species 0.000 description 1
- 206010007953 Central nervous system lymphoma Diseases 0.000 description 1
- 241000282693 Cercopithecidae Species 0.000 description 1
- 241000931705 Cicada Species 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 208000001333 Colorectal Neoplasms Diseases 0.000 description 1
- KQLDDLUWUFBQHP-UHFFFAOYSA-N Cordycepin Natural products C1=NC=2C(N)=NC=NC=2N1C1OCC(CO)C1O KQLDDLUWUFBQHP-UHFFFAOYSA-N 0.000 description 1
- 229920002786 Corilagin Polymers 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- 102000004127 Cytokines Human genes 0.000 description 1
- 108090000695 Cytokines Proteins 0.000 description 1
- 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 description 1
- 108020004414 DNA Proteins 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 208000002699 Digestive System Neoplasms Diseases 0.000 description 1
- 240000008955 Dioscorea japonica Species 0.000 description 1
- 235000005251 Dioscorea japonica Nutrition 0.000 description 1
- 206010061825 Duodenal neoplasm Diseases 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000283086 Equidae Species 0.000 description 1
- 239000001512 FEMA 4601 Substances 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 241000208150 Geraniaceae Species 0.000 description 1
- 229920000061 Geraniin Polymers 0.000 description 1
- JQQBXPCJFAKSPG-SVYIMCMUSA-N Geraniin Chemical compound OC1=C(O)C(O)=CC(C(=O)O[C@H]2[C@@H]3OC(=O)C=4C=C(O)C(O)=C5O[C@@]6(O)C(=O)C=C([C@@H](C5=4)C6(O)O)C(=O)O[C@H]4[C@@H]3OC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC[C@H]4O2)=C1 JQQBXPCJFAKSPG-SVYIMCMUSA-N 0.000 description 1
- 244000275701 Geranium nepalense Species 0.000 description 1
- 239000004378 Glycyrrhizin Substances 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 241001632578 Hyacinthus orientalis Species 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 229920001202 Inulin Polymers 0.000 description 1
- PUPKKEQDLNREIM-UHFFFAOYSA-N Kaempferitin Natural products OC1C(O)C(O)C(C)OC1OC1=CC(O)=C2C(=O)C(OC3C(C(O)C(O)C(C)O3)O)=C(C=3C=CC(O)=CC=3)OC2=C1 PUPKKEQDLNREIM-UHFFFAOYSA-N 0.000 description 1
- 208000007766 Kaposi sarcoma Diseases 0.000 description 1
- 241000186612 Lactobacillus sakei Species 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 208000018142 Leiomyosarcoma Diseases 0.000 description 1
- 206010025323 Lymphomas Diseases 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 206010027476 Metastases Diseases 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 241000218213 Morus <angiosperm> Species 0.000 description 1
- 235000008708 Morus alba Nutrition 0.000 description 1
- 229920000715 Mucilage Polymers 0.000 description 1
- 208000034578 Multiple myelomas Diseases 0.000 description 1
- 241001656390 Ophiocordyceps sphecocephala Species 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 108020002230 Pancreatic Ribonuclease Proteins 0.000 description 1
- 102000005891 Pancreatic ribonuclease Human genes 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 229920002230 Pectic acid Polymers 0.000 description 1
- 206010035226 Plasma cell myeloma Diseases 0.000 description 1
- 244000274050 Platycodon grandiflorum Species 0.000 description 1
- 235000006753 Platycodon grandiflorum Nutrition 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- HELXLJCILKEWJH-SEAGSNCFSA-N Rebaudioside A Natural products O=C(O[C@H]1[C@@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1)[C@@]1(C)[C@@H]2[C@](C)([C@H]3[C@@]4(CC(=C)[C@@](O[C@H]5[C@H](O[C@H]6[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O6)[C@@H](O[C@H]6[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O6)[C@H](O)[C@@H](CO)O5)(C4)CC3)CC2)CCC1 HELXLJCILKEWJH-SEAGSNCFSA-N 0.000 description 1
- 229920000294 Resistant starch Polymers 0.000 description 1
- JUIYKRQGQJORHH-ZIIOQTAFSA-N Rhamnazin 3-rutinoside Natural products O(C[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](OC2=C(c3cc(OC)c(O)cc3)Oc3c(c(O)cc(OC)c3)C2=O)O1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](C)O1 JUIYKRQGQJORHH-ZIIOQTAFSA-N 0.000 description 1
- 206010054184 Small intestine carcinoma Diseases 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 244000228451 Stevia rebaudiana Species 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 241000001727 Tropicoporus linteus Species 0.000 description 1
- 206010046431 Urethral cancer Diseases 0.000 description 1
- 206010046458 Urethral neoplasms Diseases 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 230000035508 accumulation Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 208000009956 adenocarcinoma Diseases 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 210000001789 adipocyte Anatomy 0.000 description 1
- SOSLMHZOJATCCP-PADPQNGGSA-N afzelin Natural products O([C@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](C)O1)C1=C(c2ccc(O)cc2)Oc2c(c(O)cc(O)c2)C1=O SOSLMHZOJATCCP-PADPQNGGSA-N 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000001754 anti-pyretic effect Effects 0.000 description 1
- 230000000767 anti-ulcer Effects 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 229940041181 antineoplastic drug Drugs 0.000 description 1
- 239000002221 antipyretic Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 239000000605 aspartame Substances 0.000 description 1
- 235000010357 aspartame Nutrition 0.000 description 1
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 1
- 229960003438 aspartame Drugs 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 229920001222 biopolymer Polymers 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 235000012241 calcium silicate Nutrition 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 230000004611 cancer cell death Effects 0.000 description 1
- 230000005907 cancer growth Effects 0.000 description 1
- 235000014171 carbonated beverage Nutrition 0.000 description 1
- 231100000504 carcinogenesis Toxicity 0.000 description 1
- 208000002458 carcinoid tumor Diseases 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000013592 cell lysate Substances 0.000 description 1
- 238000002737 cell proliferation kit Methods 0.000 description 1
- 230000003833 cell viability Effects 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000011284 combination treatment Methods 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- OFEZSBMBBKLLBJ-BAJZRUMYSA-N cordycepin Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)C[C@H]1O OFEZSBMBBKLLBJ-BAJZRUMYSA-N 0.000 description 1
- OFEZSBMBBKLLBJ-UHFFFAOYSA-N cordycepine Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(CO)CC1O OFEZSBMBBKLLBJ-UHFFFAOYSA-N 0.000 description 1
- TUSDEZXZIZRFGC-XIGLUPEJSA-N corilagin Chemical compound O([C@H]1[C@H](O)[C@H]2OC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC[C@@H](O1)[C@H]2O)C(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-XIGLUPEJSA-N 0.000 description 1
- CPWYQGWOJMNXGJ-UHFFFAOYSA-N corilagin Natural products OC1C2COC(=O)c3c(O)c(O)c(O)c(O)c3c4c(O)c(O)c(O)c(O)c4C(=O)OC1C(O)C(OC(=O)c5cc(O)c(O)c(O)c5)O2 CPWYQGWOJMNXGJ-UHFFFAOYSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000001086 cytosolic effect Effects 0.000 description 1
- 231100000135 cytotoxicity Toxicity 0.000 description 1
- 230000003013 cytotoxicity Effects 0.000 description 1
- 238000007405 data analysis Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000001784 detoxification Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 235000013325 dietary fiber Nutrition 0.000 description 1
- 235000021245 dietary protein Nutrition 0.000 description 1
- 150000002016 disaccharides Chemical class 0.000 description 1
- 208000016097 disease of metabolism Diseases 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 238000012377 drug delivery Methods 0.000 description 1
- 201000000312 duodenum cancer Diseases 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- HELXLJCILKEWJH-UHFFFAOYSA-N entered according to Sigma 01432 Natural products C1CC2C3(C)CCCC(C)(C(=O)OC4C(C(O)C(O)C(CO)O4)O)C3CCC2(C2)CC(=C)C21OC(C1OC2C(C(O)C(O)C(CO)O2)O)OC(CO)C(O)C1OC1OC(CO)C(O)C(O)C1O HELXLJCILKEWJH-UHFFFAOYSA-N 0.000 description 1
- 210000003238 esophagus Anatomy 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000021107 fermented food Nutrition 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 239000005417 food ingredient Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- GJMUCSXZXBCQRZ-UHFFFAOYSA-N geraniin Natural products Oc1cc(cc(O)c1O)C(=O)OC2OC3COC(=O)c4cc(O)c(O)c(O)c4c5cc(C(=O)C67OC3C(O6)C2OC(=O)c8cc(O)c(O)c9OC%10(O)C(C(=CC(=O)C%10(O)O)C7=O)c89)c(O)c(O)c5O GJMUCSXZXBCQRZ-UHFFFAOYSA-N 0.000 description 1
- 208000005017 glioblastoma Diseases 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 108091005996 glycated proteins Proteins 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 102000035122 glycosylated proteins Human genes 0.000 description 1
- 108091005608 glycosylated proteins Proteins 0.000 description 1
- LPLVUJXQOOQHMX-UHFFFAOYSA-N glycyrrhetinic acid glycoside Natural products C1CC(C2C(C3(CCC4(C)CCC(C)(CC4C3=CC2=O)C(O)=O)C)(C)CC2)(C)C2C(C)(C)C1OC1OC(C(O)=O)C(O)C(O)C1OC1OC(C(O)=O)C(O)C(O)C1O LPLVUJXQOOQHMX-UHFFFAOYSA-N 0.000 description 1
- 229960004949 glycyrrhizic acid Drugs 0.000 description 1
- UYRUBYNTXSDKQT-UHFFFAOYSA-N glycyrrhizic acid Natural products CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(=O)O)OC6OC(C(O)C(O)C6OC7OC(O)C(O)C(O)C7C(=O)O)C(=O)O UYRUBYNTXSDKQT-UHFFFAOYSA-N 0.000 description 1
- 235000019410 glycyrrhizin Nutrition 0.000 description 1
- LPLVUJXQOOQHMX-QWBHMCJMSA-N glycyrrhizinic acid Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@H]1O[C@@H]1C([C@H]2[C@]([C@@H]3[C@@]([C@@]4(CC[C@@]5(C)CC[C@@](C)(C[C@H]5C4=CC3=O)C(O)=O)C)(C)CC2)(C)CC1)(C)C)C(O)=O)[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O LPLVUJXQOOQHMX-QWBHMCJMSA-N 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 230000005802 health problem Effects 0.000 description 1
- 230000002489 hematologic effect Effects 0.000 description 1
- 244000005702 human microbiome Species 0.000 description 1
- 229910052588 hydroxylapatite Inorganic materials 0.000 description 1
- 230000001900 immune effect Effects 0.000 description 1
- 230000036737 immune function Effects 0.000 description 1
- 230000028993 immune response Effects 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 230000028709 inflammatory response Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000001361 intraarterial administration Methods 0.000 description 1
- 230000003834 intracellular effect Effects 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 238000007913 intrathecal administration Methods 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
- ZMGSKTZDVIZXJS-UHFFFAOYSA-N kaempferitrin Natural products CC1OC(OC2C(Oc3cc(OC4OC(C)C(O)C(O)C4O)cc(O)c3C2=O)c5ccc(O)cc5)C(O)C(O)C1O ZMGSKTZDVIZXJS-UHFFFAOYSA-N 0.000 description 1
- PUPKKEQDLNREIM-QNSQPKOQSA-N kaempferol 3,7-di-O-alpha-L-rhamnoside Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1OC1=CC(O)=C2C(=O)C(O[C@H]3[C@@H]([C@H](O)[C@@H](O)[C@H](C)O3)O)=C(C=3C=CC(O)=CC=3)OC2=C1 PUPKKEQDLNREIM-QNSQPKOQSA-N 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 210000002429 large intestine Anatomy 0.000 description 1
- 208000032839 leukemia Diseases 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 210000001165 lymph node Anatomy 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 230000036210 malignancy Effects 0.000 description 1
- 230000003211 malignant effect Effects 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007721 medicinal effect Effects 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 208000030159 metabolic disease Diseases 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 230000009401 metastasis Effects 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical compound N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 description 1
- 230000009826 neoplastic cell growth Effects 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000021590 normal diet Nutrition 0.000 description 1
- 239000002417 nutraceutical Substances 0.000 description 1
- 235000021436 nutraceutical agent Nutrition 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 201000008968 osteosarcoma Diseases 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 201000002528 pancreatic cancer Diseases 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- LCLHHZYHLXDRQG-ZNKJPWOQSA-N pectic acid Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)O[C@H](C(O)=O)[C@@H]1OC1[C@H](O)[C@@H](O)[C@@H](OC2[C@@H]([C@@H](O)[C@@H](O)[C@H](O2)C(O)=O)O)[C@@H](C(O)=O)O1 LCLHHZYHLXDRQG-ZNKJPWOQSA-N 0.000 description 1
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229920000747 poly(lactic acid) Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000010318 polygalacturonic acid Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 235000021395 porridge Nutrition 0.000 description 1
- 235000008476 powdered milk Nutrition 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 235000019203 rebaudioside A Nutrition 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- 238000002271 resection Methods 0.000 description 1
- 235000021254 resistant starch Nutrition 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 238000007480 sanger sequencing Methods 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 210000000697 sensory organ Anatomy 0.000 description 1
- 235000020374 simple syrup Nutrition 0.000 description 1
- 210000000813 small intestine Anatomy 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229960002920 sorbitol Drugs 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 206010041823 squamous cell carcinoma Diseases 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 239000000892 thaumatin Substances 0.000 description 1
- 235000010436 thaumatin Nutrition 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000011277 treatment modality Methods 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Images
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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/06—Aluminium, calcium or magnesium; Compounds thereof, e.g. clay
- A61K33/10—Carbonates; Bicarbonates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/66—Microorganisms or materials therefrom
- A61K35/74—Bacteria
- A61K35/741—Probiotics
- A61K35/744—Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
- A61K35/747—Lactobacilli, e.g. L. acidophilus or L. brevis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/06—Fungi, e.g. yeasts
- A61K36/062—Ascomycota
- A61K36/066—Clavicipitaceae
- A61K36/068—Cordyceps
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/06—Fungi, e.g. yeasts
- A61K36/07—Basidiomycota, e.g. Cryptococcus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/34—Campanulaceae (Bellflower family)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/88—Liliopsida (monocotyledons)
- A61K36/894—Dioscoreaceae (Yam family)
- A61K36/8945—Dioscorea, e.g. yam, Chinese yam or water yam
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Definitions
- composition for treating cancer using combination therapy containing Lactobacillus plantarum strains and herbal medicine.
- Microbiome refers to microorganisms and their entire genetic information existing in a specific environment. In addition to the human body, microbiome information is being used in various fields such as animals, agriculture, the ocean, and the environment. In particular, with the development of human microbiome research based on the development of genetic information analysis and data analysis technology, based on this, microbiome information is being used. The growth of the diagnostic and healthcare industries is expected.
- cancer is considered one of the major health problems.
- colon cancer is the fourth most common malignant tumor in the world and the third leading cause of cancer death.
- surgery is the most effective treatment method.
- the survival rate from early stage 1 to stage 3 reaches 70-90%, but in the final stage 4, the survival rate drops sharply to 15%.
- herbal medicine has been traditionally used to treat human diseases and protect the body for a long time.
- most of them are of plant origin and are mainly based on complex prescriptions of herbal medicinal ingredients. Therefore, interest is growing due to the chemical side effects of many synthetic drugs, which have complex effects and few side effects.
- Combination therapy is the use of two or more drugs or methods simultaneously or in relatively quick succession.
- the side effects of two or more treatment modalities used in combination therapy may be additive or less than additive, while the therapeutic effects may be additive or greater than additive.
- the effects that occur when each component is administered together can be expected to have a greater synergistic effect than the sum of the effects that occur when each component is administered alone. Therefore, there is a need for the development of combination therapy that can synergistically increase the effect of treatment using a single ingredient.
- One aspect includes as an active ingredient a first active material comprising a Lactobacillus plantarum strain, a culture of the strain, a lysate of the strain, or a mixture thereof, and a second active material containing a herbal medicine. do or;
- the present invention provides a pharmaceutical composition for preventing or treating cancer, which includes the first active substance as an active ingredient and the second active substance is administered in combination.
- Another aspect includes as an active ingredient a first active material comprising a Lactobacillus plantarum strain, a culture of the strain, a lysate of the strain, or a mixture thereof, and a second active material containing a herbal medicine. do or;
- the present invention provides a health functional food for preventing or improving cancer, which includes the first active substance as an active ingredient and the second active substance is administered in combination.
- a first active material containing a Lactobacillus plantarum strain, a culture of the strain, a lysate of the strain, or a mixture thereof, and a second active material containing a herbal medicine are used as active ingredients.
- a kit for preventing or treating cancer which includes the first active substance as an active ingredient and the second active substance is administered in combination.
- a first active material containing a Lactobacillus plantarum strain, a culture of the strain, a lysate of the strain, or a mixture thereof, and a second active material containing a herbal medicine are used as active ingredients.
- a first active material containing a Lactobacillus plantarum strain, a culture of the strain, a lysate of the strain, or a mixture thereof, and a second active material containing a herbal medicine are used as active ingredients.
- Another aspect is a first active material comprising an effective amount of a Lactobacillus plantarum strain, a culture of the strain, a lysate of the strain, or a mixture thereof, and a second active material comprising an effective amount of a herbal medicine.
- a first active material comprising an effective amount of a Lactobacillus plantarum strain, a culture of the strain, a lysate of the strain, or a mixture thereof
- a second active material comprising an effective amount of a herbal medicine.
- Another aspect includes Lactobacillus plantarum strains, cultures of the strains, lysates of the strains, or mixtures thereof for the production of pharmaceutical agents or health functional foods for preventing or treating cancer.
- a composition comprising as active ingredients a first active material and a second active material including an herbal medicine; Alternatively, it provides the use of a composition comprising the first active material as an active ingredient and the second active material being administered in combination.
- Lactobacillus genus strain specifically Lactobacillus plantarum GB104 strain, which has anticancer activity, for example, anticancer activity against colon cancer.
- Lactobacillus is a genus of aerobic or facultative anaerobic Gram-positive bacilli widely distributed in nature. Microorganisms belonging to the Lactobacillus genus include Lactobacillus plantarum and Sakei. As a result of research to develop a new strain with excellent anticancer effect, the present inventors selected Lactobacillus plantarum GB104 as an anticancer candidate strain. The strain was deposited at the Korea Research Institute of Bioscience and Biotechnology Biological Resources Center under the deposit number KCTC14107BP on January 14, 2020. The strain corresponds to a probiotic strain, is harmless to the human body, and can be used without side effects.
- Lactobacillus ( Lactobacillus ) has been renamed to Limosilactobacillus or Lactiplantibacillus , and the changed strain names in this specification can be used interchangeably.
- Lactobacillus plantarum was changed to Lactiplantibacillus plantarum .
- Lactobacillus plantarum GB104 may be used together with L. Plantarum GB104 strain or Lactobacillus plantarum GB104 strain (Accession Number: KCTC14107BP).
- the strain may be a strain deposited under accession number KCTC14107BP.
- the strain may be a strain containing a 16S rRNA gene consisting of the nucleotide sequence of SEQ ID NO: 1.
- the strain may be a strain having 16S rRNA comprising the nucleotide sequence of SEQ ID NO: 1 or a 16s rRNA comprising a nucleotide sequence having 97% or more nucleotide sequence identity thereto. Specifically, it has at least 93%, 95%, 96%, 97%, 98%, 99%, 99.5%, 99.8%, 99.9% or 100% homology with the nucleotide sequence consisting of SEQ ID NO: 1 of the present specification.
- the strain may be live cells, dead cells, or a cytoplasmic fraction obtained by disrupting the strain, and preferably may be live cells.
- the term “culture” may be used interchangeably with “culture supernatant,” “culture supernatant,” “conditioned culture,” or “conditioned medium,” and can be used interchangeably with “culture supernatant,” “conditioned culture medium,” or “conditioned medium” to allow strains of the genus Lactobacillus to grow and survive in vitro. It may refer to the entire medium containing the strain, its metabolites, extra nutrients, etc. obtained by culturing the strain in a medium capable of supplying nutrients for a certain period of time.
- the culture refers to a product obtained by culturing a probiotic strain in a known medium, and the product may or may not include the strain itself.
- the medium may be selected from known liquid media or solid media, for example, MRS liquid medium, GAM liquid medium, MRS agar medium, GAM agar medium, and BL agar medium, but is not limited thereto.
- lysate may be used interchangeably with “lysate”, meaning a solution or suspension of cells of a microorganism such as Lactobacillus plantarum in an aqueous medium o broken down.
- Cell lysates include, for example, macromolecules such as DNA, RNA, proteins, peptides, carbohydrates, lipids, etc. and/or micromolecules such as amino acids, sugars, fatty acids, etc., or fractions thereof.
- the lysate also contains cell debris, which may be smooth or granular in structure.
- the culture medium may include the culture medium itself, its concentrate, or freeze-dried product obtained by cultivating the strain, or the culture supernatant obtained by removing the strain from the culture medium, its concentrate, or freeze-dried product.
- the culture medium may be obtained by culturing Lactobacillus plantarum in an appropriate medium (e.g., MRS plate medium) at any temperature above 10°C or below 40°C for a certain period of time, for example, 4 to 50 hours. .
- an appropriate medium e.g., MRS plate medium
- the first active material comprising at least one member selected from the group consisting of the strain, a culture of the strain, a lysate of the strain, or an extract of the bacterium, culture, and lysate has anticancer activity. You can.
- the anticancer activity may be an activity that delays the development of a tumor or inhibits the growth rate of a tumor.
- the first active substance may have tumor growth inhibitory activity.
- the first active substance may induce apoptosis of cancer cells.
- the anticancer activity is a growth inhibitory activity of cancer cells, which reduces the cancer cell survival rate by 90% to 98% when the supernatant of Lactobacillus Plantarum GB104 strain is treated with colon cancer cells HCT116, or Lactobacillus Plantarum GB104
- the activity reduces tumor volume by 10% to 90% or tumor weight by 10% to 50% compared to the control group not administered the strain. It may be.
- the anti-cancer activity is an activity that induces apoptosis of cancer cells, and when the supernatant of Lactobacillus Plantarum GB104 strain was treated with colon cancer cells HCT116, the initial apoptosis induction of cancer cells was induced without administering the strain.
- the activity may be 5 to 9 times increased compared to the control group.
- the first active substance may have anticancer activity, specifically, anticancer activity against colon cancer.
- cancer refers to a physiological condition in animals, typically characterized by abnormal or uncontrolled cell growth. Cancer and cancer pathology include, for example, metastasis, interference with normally functioning surrounding cells, release of cytokines or other secreted products at abnormal levels, inhibition or enhancement of inflammatory or immunological responses, neoplasia, and premalignancy. ), malignancy, or involvement of surrounding or distant tissues or organs, such as lymph node invasion.
- the cancer may be gastrointestinal cancer or non-gastrointestinal cancer.
- the gastrointestinal cancer is a malignant tumor that occurs in the gastrointestinal tract, such as the esophagus, stomach, small intestine, or large intestine.
- the gastrointestinal cancer includes, for example, esophageal cancer, gallbladder cancer, liver cancer, biliary tract cancer, pancreatic cancer, stomach cancer, small intestine cancer, colon cancer, colon cancer, and anal cancer. It may be one or more cancers selected from the group consisting of rectal cancer, but is not limited thereto, and in one example, it may be colon cancer.
- the non-gastrointestinal cancer includes, without limitation, malignant tumors occurring in organs other than the gastrointestinal tract or digestive system, for example, hematological cancer, leukemia, acute myeloid leukemia, neuroblastoma, retinoblastoma, lung cancer, head and neck cancer, salivary gland cancer, melanoma, It may be, but is not limited to, laryngeal cancer, prostate cancer, breast cancer, bladder cancer, kidney cancer, multiple myeloma, cervical cancer, thyroid cancer, ovarian cancer, urethral cancer, skin cancer, osteosarcoma, glioblastoma, brain tumor, or lymphoma.
- malignant tumors occurring in organs other than the gastrointestinal tract or digestive system for example, hematological cancer, leukemia, acute myeloid leukemia, neuroblastoma, retinoblastoma, lung cancer, head and neck cancer, salivary gland cancer, melanoma
- It may be, but is not limited to, laryngeal cancer
- the cancer may be colon cancer, and the colon cancer includes occurring in one or more regions selected from the group consisting of ascending colon, transverse colon, descending colon, sigmoid colon, and rectal mucosa.
- the colon cancer may be one or more types selected from the group consisting of adenocarcinoma, lymphoma, malignant carcinoid, leiomyosarcoma, Kaposi's sarcoma, and squamous cell carcinoma, but is not limited thereto.
- the first active substance may contain Lactobacillus plantarum strain alone as an active ingredient, or may include one or more pharmaceutically acceptable carriers, excipients, or diluents.
- the second active material may include an herbal medicine.
- the herbal medicine may be one or more selected from the group consisting of Cordyceps sinensis, yam, bellflower root, Sanghwang mushroom, Hyeoncho, and combinations thereof.
- the term "herbal medicine” is defined in the Pharmaceutical Affairs Act as a raw medicinal material used to manufacture herbal medicine or herbal medicine preparations. Herbal medicines may have different medicinal properties depending on the processing laws and regulations, so processing and manufacturing methods are important.
- the herbal medicine may be Cordyceps sinensis, yam, bellflower root, Sanghwang mushroom, or Hyeoncho, but is not limited thereto. At this time, the herbal medicine may be used in powder or extract form.
- Cordyceps militaris in a broad sense refers to all types of mushrooms parasitic on insects, typically including Cordyceps militaris , whose host is a butterfly, C. sobolifera , whose host is a cicada, and bees.
- the host is Cordyceps sinensis ( C. sphecocephala ). It contains cordycepin, and has been reported to have anti-cancer, immune strengthening, skin beautification, fatigue recovery, and anti-aging effects.
- yam Dioscorea japonica
- yam Dioscorea japonica
- the rhizome of the yam contains amylase, betasin, mucin, mucilage, and allantoin ( It contains allantoin, saponin, tannin, and polyphenol, and has been reported to have antioxidant, anti-inflammatory, and anticancer effects.
- bellflower root ( Platycodon grandiflorum ) refers to a perennial herb or its root belonging to the Campanula family.
- Polysaccharides such as inulin, triterpenoids, triterpene, saponins such as platicodin, platycodigenin, polygalacin, etc. Containing a large amount of this, it has been reported to have effects such as immune enhancement, anti-inflammation, anti-ulcer, skin soothing effect, antipyretic, blood circulation, detoxification, and antibacterial effect.
- Phellinus linteus is a perennial wood-rot fungus that grows naturally on mulberry trees, etc., and is also called woody mud mushroom. It has been reported to have anticancer, immune, and antioxidant effects. Specifically, it has been reported that the pharmacological action of Sanghwa mushrooms enhances immune function when combined with chemotherapy after resection surgery for liver cancer, including gastric cancer, esophageal cancer, duodenal cancer, colon cancer, and rectal cancer, which are cancers of the digestive system.
- Hyeoncho refers to a perennial herb belonging to the Geranium nepalense subsp. Thunbergii family, Geraniaceae, and is also called Gwangjipul, Hyeoncho, and Hyeonchicho.
- the main components of Hyacinth herb extract include quercetin, geraniin, corilagin, tannin, and kaempferitrin.
- quercetin is an antioxidant. It is known.
- Hyeoncho has been reported to have the ability to inhibit the production of intracellular oxygen radicals and to scavenge free radicals in a concentration-dependent manner, and has antioxidant and anti-inflammatory effects.
- the herbal medicine of the present invention may be a mixture of one or more types.
- the herbal medicine may be a mixture of two types of herbal medicine.
- the herbal medicine may be a mixture of yam and Hyeoncho.
- the herbal medicine may be a mixture of yam and bellflower root.
- the herbal medicine may be a mixture of yam and Sanghwang mushroom.
- the herbal medicine may be a mixture of yam and Cordyceps sinensis.
- the herbal medicine may be a mixture of Hyeoncho and bellflower root.
- the herbal medicine may be a mixture of Hyeoncho and Sanghwang mushrooms.
- the herbal medicine may be a mixture of Hyeoncho and Cordyceps sinensis.
- the herbal medicine may be a mixture of bellflower root and Sanghwang mushroom. In one embodiment, the herbal medicine may be a mixture of bellflower root and Cordyceps sinensis. In one specific example, the herbal medicine may be a mixture of Sanghwang mushroom and Cordyceps sinensis.
- the herbal medicine may be a mixture of three types of herbal medicine.
- the herbal medicine may be a mixture of yam, Hyeoncho, and bellflower root.
- the herbal medicine may be a mixture of yam, Hyeoncho, and Sanghwang mushroom.
- the herbal medicine may be a mixture of yam, Hyeoncho and Cordyceps sinensis.
- the herbal medicine may be a mixture of yam, bellflower root, and sanghwang mushroom.
- the herbal medicine may be a mixture of yam, bellflower root, and Cordyceps sinensis.
- the herbal medicine may be a mixture of Hyeoncho, bellflower root, and Sanghwang mushroom.
- the herbal medicine may be a mixture of Hyeoncho, bellflower root, and Cordyceps sinensis.
- the herbal medicine may be a mixture of four types of herbal medicine.
- the herbal medicine may be a mixture of yam, Hyeoncho, bellflower root, and Sanghwang mushroom.
- the herbal medicine may be a mixture of yam, Hyeoncho, bellflower root, and Cordyceps sinensis.
- the herbal medicine may be a mixture of yam, Hyeoncho, Sanghwang mushroom, and Cordyceps sinensis.
- the herbal medicine may be a mixture of yam, bellflower root, Sanghwang mushroom, and Cordyceps sinensis.
- the herbal medicine may be a mixture of Hyeoncho, bellflower root, Sanghwang mushroom, and Cordyceps sinensis.
- the herbal medicine may be a mixture of five types of herbal medicine.
- the five types of herbal medicines such as yam, Hyeoncho, bellflower root, Sanghwang mushroom, and Cordyceps sinensis can be mixed in a predetermined ratio.
- the second active substance may include a herbal medicine alone as an active ingredient, or may include one or more pharmaceutically acceptable carriers, excipients, or diluents.
- the term "included as an active ingredient” means that strains of the Lactobacillus genus, lysate of the strain, culture medium, or extract of the culture medium are added, and various ingredients are added as sub-ingredients for drug delivery and stabilization. It means being formulated in various forms.
- the first active material and the second active material may be administered in combination simultaneously, sequentially, or in reverse order.
- the term “combination therapy” or “combination administration” or “in combination” refers to any form of simultaneous or concurrent treatment using at least two separate therapeutic agents.
- the components of the combination therapy may be administered simultaneously, sequentially, or in any order.
- the components may be administered in any suitable manner, in different doses or at different frequencies of administration or via different routes.
- the combined administration may be administering the Lactobacillus plantarum strain and herbal medicine simultaneously, or administering the herbal medicine after administering the Lactobacillus plantarum strain.
- the combination therapy according to the present invention is an efficacy that can be obtained by administering one or the rest of the components of the combination therapy at a conventional dose, for example, the efficacy measured through the degree of response, response rate, time to disease progression, or survival time. More therapeutically superior can be defined as being able to provide synergistic effects. For example, if the therapeutic efficacy is superior to the efficacy obtained by using each of the above alone, the efficacy of the combination treatment is synergistic.
- administered simultaneously is not particularly limited and means that the components of the combination therapy are administered substantially simultaneously, for example as a mixture or in an immediately following sequence.
- the term “sequentially administered” is not particularly limited and means that the components of the combination therapy are not administered simultaneously, but are administered one by one or in batches with a specific time interval between administrations.
- the time interval may be the same or different between the respective administrations of the components of the combination therapy and may be selected, for example, in the range of 2 minutes to 96 hours, 1 day to 7 days or 1 week, 2 weeks or 3 weeks.
- the time interval between administrations can range from minutes to hours, for example from 2 minutes to 72 hours, 30 minutes to 24 hours, or 1 to 12 hours. Additional examples include time intervals ranging from 24 to 96 hours, 12 to 36 hours, 8 to 24 hours, and 6 to 12 hours.
- Another aspect includes as an active ingredient a first active material comprising a Lactobacillus plantarum strain, a culture of the strain, a lysate of the strain, or a mixture thereof, and a second active material containing a herbal medicine. do or;
- the present invention provides a pharmaceutical composition for preventing or treating cancer, which includes the first active substance as an active ingredient and the second active substance is administered in combination.
- strain The “strain”, “first active substance”, “herbal medicine”, “second active substance”, “anticancer activity”, and “combined administration” are as described above.
- the pharmaceutical composition can be administered to mammals, including humans, through various routes.
- the administration method may be any commonly used method, for example, oral, dermal, intravenous, intramuscular or subcutaneous administration, and is preferably administered orally.
- it includes a first oral preparation containing a first active substance, and a second oral preparation containing a second active substance, and the first and second oral preparations may be administered orally.
- the oral preparation comes in the form of tablets, pills, capsules, lozenges, granules, powders, suspensions, and sachets. , or it may be in the form of syrups.
- prevention may refer to any action that suppresses the disease state of an individual or delays the onset of the disease by administering a pharmaceutical composition according to one aspect.
- treatment may refer to any action in which symptoms of an individual's disease state are improved or beneficially changed by administration of a pharmaceutical composition according to one aspect.
- the composition according to one embodiment may include 0.001% by weight to 80% by weight of the Lactobacillus plantarum strain based on the total weight of the composition. Additionally, the administered dose of the Lactobacillus plantarum strain may be 0.01 mg to 10,000 mg, 0.1 mg to 1000 mg, 1 mg to 100 mg, 0.01 mg to 1000 mg, 0.01 mg to 100 mg, 0.01 mg to 10 mg, or 0.01 mg to 1 mg. .
- the strain is included in the composition in a therapeutically effective amount or nutritionally effective concentration, for example, the strain is 10 3 to 10 16 CFU/g, 10 3 to 10 15 CFU/g, 10 3 to 10 14 CFU/g.
- 1x10 3 to 1x10 16 CFU/g of live or dead cells may be administered once or in divided doses.
- the dosage may be prescribed in various ways depending on factors such as formulation method, administration method, patient's age, weight, gender, pathological condition, food, administration time, administration route, excretion rate, and reaction sensitivity, and those skilled in the art will Taking these factors into consideration, the dosage can be adjusted appropriately.
- the number of administrations can be one time or two or more times within the range of clinically acceptable side effects, and the administration site can be administered at one or two or more places.
- the dosage per kg is the same as for humans, or, for example, the above-mentioned administration is based on the volume ratio (e.g., average value) of organs (e.g., heart, etc.) between the target animal and human.
- the converted dose can be administered.
- Possible routes of administration include oral, sublingual, parenteral (e.g., subcutaneous, intramuscular, intraarterial, intraperitoneal, intrathecal, or intravenous), rectal, topical (including transdermal), inhalation, and injection, or implantable device. Alternatively, it may include insertion of a substance.
- the composition includes killed dried strains, and can be administered in an amount of 1g to 10g, 0.5g to 1.5g, 2.5g to 3.5g, or 4.5g to 5.5g, once a day to 3 times. It may be administered once.
- the term "therapeutically effective amount” refers to an herbal medicine or method of the present invention for the method and use of the present invention that elicits a biological or medical response or desired therapeutic effect in a patient that researchers, doctors, or other clinicians wish to obtain. and the amount of a pharmaceutical composition containing herbal medicine for use.
- the therapeutically effective amount of a herbal medicine may vary depending on factors such as the disease state, age, sex and weight of the individual, and the ability of the herbal medicine to elicit the desired response in the individual.
- a therapeutically effective amount is also an amount in which the therapeutically beneficial effects outweigh any toxic or harmful effects.
- the pharmaceutical composition according to one embodiment may include a pharmaceutically acceptable carrier and/or additive.
- a pharmaceutically acceptable carrier and/or additive for example, sterilized water, physiological saline, common buffers (phosphoric acid, citric acid, other organic acids, etc.), stabilizers, salts, antioxidants (ascorbic acid, etc.), surfactants, suspending agents, isotonic agents, or preservatives.
- it may also include combinations with organic materials such as biopolymers and inorganic materials such as hydroxyapatite, specifically collagen matrices, polylactic acid polymers or copolymers, polyethylene glycol polymers or copolymers, and chemical derivatives thereof. You can.
- the Lactobacillus bacteria may be dissolved or dispersed in a pharmaceutically acceptable carrier, or may be frozen in a dissolved or dispersed solution state. .
- the pharmaceutical composition may be used as a suspending agent, solubilizing agent, stabilizer, isotonic agent, preservative, anti-adsorption agent, surfactant, diluent, excipient, pH adjuster, analgesic agent, etc., if necessary depending on the administration method or formulation. Buffers, reducing agents, antioxidants, etc. may be appropriately included.
- Pharmaceutically acceptable carriers and agents suitable for the present invention including those exemplified above, are described in detail in Remington's Pharmaceutical Sciences, 19th ed., 1995.
- the pharmaceutical composition according to one embodiment is formulated in unit dosage form using a pharmaceutically acceptable carrier and/or excipient according to a method that can be easily performed by a person skilled in the art to which the invention pertains. It can be manufactured by or by placing it in a multi-capacity container.
- the formulation may be in the form of a solution, suspension or emulsion in an oil or aqueous medium, or in the form of powder, granules, tablets or capsules.
- the pharmaceutical composition is administered in a pharmaceutically effective amount.
- pharmaceutically effective amount means an amount sufficient to treat the disease with a reasonable benefit/risk ratio applicable to medical treatment, and the effective dose level is determined by the type, severity, activity of the drug, and the type and severity of the patient's disease. It can be determined based on factors including sensitivity to the drug, time of administration, route of administration and excretion rate, duration of treatment, drugs used simultaneously, and other factors well known in the medical field.
- the composition of the present invention may be administered as an individual therapeutic agent or in combination with other therapeutic agents, may be administered sequentially or simultaneously with conventional therapeutic agents, and may be administered singly or multiple times. Considering all of the above factors, it is important to administer an amount that can achieve maximum effect with the minimum amount without side effects, and this can be easily determined by a person skilled in the art.
- the anticancer activity of the first active material may be more effective when administered in combination with the second active material.
- Lactobacillus plantarum GB104 strain and the herbal medicines Cordyceps sinensis, yam, bellflower root, or Sanghwang mushroom are administered in combination to a tumor animal model transplanted with the mouse colon cancer cell line CT26, Lactobacillus plantarum GB104 strain It showed increased anticancer effect compared to when administered alone. Specifically, the effect of inhibiting the growth and progression of colon cancer tumors was confirmed. On average, compared to the control group, the experimental group administered GB104 and herbal medicine in combination showed a reduction in tumor volume by 10% to 90% or tumor weight by 10% to 50%.
- the colon cancer tumor volume is 90% based on 100% of the colon cancer tumor volume of the negative control group that did not administer the strain or herbal medicine.
- the colon cancer tumor weight is reduced by 50% based on 100% of the colon cancer tumor weight of the negative control group that did not administer the strain or herbal medicine. or less, 45% or less, 40% or less, 35% or less, 10 to 50%, 10 to 45%, 10 to 40%, 10 to 35%, 10 to 30%, 15 to 50%, 15 to 45%, 15 It may have activity that decreases to 40%, 15 to 35%, 15 to 30%, 20 to 50%, 20 to 45%, 20 to 40%, 20 to 35%, or 20 to 30%. .
- Lactobacillus Plantarum GB104 strain and herbal medicine specifically, Herbal Root
- a tumor animal model transplanted with the mouse colon cancer cell line MC-38 when the Lactobacillus Plantarum GB104 strain is administered alone. It showed increased anti-cancer effect. Specifically, the effect of inhibiting the growth and progression of colon cancer tumors was confirmed. On average, compared to the control group, in the experimental group administered GB104 and herbal medicine together, the tumor volume was reduced by 10% to 90% and the tumor weight was reduced by 10% to 50%.
- the colon cancer tumor volume is 90% based on 100% of the colon cancer tumor volume of the negative control group that did not administer the strain or herbal medicine.
- the colon cancer tumor weight is reduced by 50% based on 100% of the colon cancer tumor weight of the negative control group that did not administer the strain or herbal medicine. or less, 45% or less, 40% or less, 35% or less, 10 to 50%, 10 to 45%, 10 to 40%, 10 to 35%, 10 to 30%, 15 to 50%, 15 to 45%, 15 It may have activity that decreases to 40%, 15 to 35%, 15 to 30%, 20 to 50%, 20 to 45%, 20 to 40%, 20 to 35%, or 20 to 30%. .
- Another aspect is a first activity comprising at least one member selected from the group consisting of Lactobacillus plantarum strains, cultures of the strains, lysates of the strains, or extracts of the cells, cultures, and lysates. or containing a second active substance including a substance and herbal medicine as an active ingredient;
- the present invention provides a health functional food for preventing or improving cancer, which includes the first active substance as an active ingredient and the second active substance is administered in combination.
- Another aspect is a first activity comprising at least one member selected from the group consisting of Lactobacillus plantarum strains, cultures of the strains, lysates of the strains, or extracts of the cells, cultures, and lysates. or containing a second active substance including a substance and herbal medicine as an active ingredient;
- the present invention provides a food composition for preventing or improving cancer, which includes the first active substance as an active ingredient and the second active substance is administered in combination.
- strain The “strain”, “first active substance”, “herbal medicine”, “second active substance”, “anticancer activity”, and “combined administration” are as described above.
- the food composition can be administered to mammals, including humans, through various routes.
- the administration method may be any commonly used method, for example, oral, dermal, intravenous, intramuscular or subcutaneous administration, and is preferably administered orally.
- it includes a first oral preparation containing a first active substance, and a second oral preparation containing a second active substance, and the first and second oral preparations may be administered orally.
- the oral preparation comes in the form of tablets, pills, capsules, lozenges, granules, powders, suspensions, and sachets. , or it may be in the form of syrups.
- the health functional food may further include a foodologically acceptable carrier.
- the term “foodologically acceptable” means that the compound exhibits non-toxic properties to cells or humans exposed to the compound.
- the term “improvement” may refer to any action that at least reduces the severity of a parameter related to the condition being treated, for example, a symptom.
- the health functional food can be used simultaneously or separately with a drug for treatment before or after the onset of the disease in order to prevent or improve cancer.
- the active ingredient can be added directly to the food or used together with other foods or food ingredients, and can be used appropriately according to conventional methods.
- the mixing amount of the active ingredient can be appropriately determined depending on the purpose of use (prevention or improvement).
- the health functional food may be added in an amount of about 15% by weight or less, more specifically about 10% by weight or less, based on the raw materials.
- the amount may be below the above range.
- the health functional food may be formulated with one selected from the group consisting of tablets, pills, powders, granules, powders, capsules, and liquid formulations, further including one or more of carriers, diluents, excipients, and additives.
- Foods to which compounds according to one aspect can be added include various foods, powders, granules, tablets, capsules, syrups, beverages, gum, tea, vitamin complexes, health functional foods, etc.
- the carriers, excipients, diluents and additives include lactose, dextrose, sucrose, sorbitol, mannitol, erythritol, starch, gum acacia, calcium phosphate, alginate, gelatin, calcium phosphate, calcium silicate, microcrystalline cellulose. , polyvinylpyrrolidone, cellulose, polyvinylpyrrolidone, methylcellulose, water, sugar syrup, methylcellulose, methylhydroxy benzoate, propylhydroxy benzoate, talc, magnesium stearate and mineral oil. It may be at least one selected from.
- the health functional food may contain other ingredients as essential ingredients without any particular restrictions.
- the health functional food may contain various flavoring agents or natural carbohydrates as additional ingredients.
- natural carbohydrates include monosaccharides such as glucose, fructose, etc.; disaccharides such as maltose, sucrose, etc.; and polysaccharides, such as common sugars such as dextrin and cyclodextrin, and sugar alcohols such as xylitol, sorbitol, and erythritol.
- natural flavoring agents thaumatin, stevia extract (e.g., rebaudioside A, glycyrrhizin, etc.)
- synthetic flavoring agents sacharin, aspartame, etc.
- the ratio of the natural carbohydrates can be appropriately determined by the selection of a person skilled in the art.
- health functional foods include various nutrients, vitamins, minerals (electrolytes), flavoring agents such as synthetic and natural flavors, colorants and thickening agents (cheese, chocolate, etc.), pectic acid and salts thereof. , alginic acid and its salts, organic acids, protective colloidal thickeners, pH adjusters, stabilizers, preservatives, glycerin, alcohol, carbonating agents used in carbonated beverages, etc. These components can be used independently or in combination, and the proportions of these additives can also be appropriately selected by those skilled in the art.
- the health functional food may be provided by mixing with conventionally known health functional food for preventing or improving cancer or other existing health functional food, and the health functional food for preventing or improving cancer is known to be a metabolic disease. It may be a health functional food for the prevention or improvement of, an existing health functional food, or a newly developed health functional food.
- the health functional food contains other health functional foods that have the effect of preventing or improving cancer, it is important to mix the amount to obtain the maximum effect with the minimum amount without side effects, and this can be easily determined by a person skilled in the art. there is.
- the food composition for preventing or improving cancer includes all forms such as functional food, nutritional supplement, health food, and food additives, and the above type of food composition It can be manufactured in various forms according to conventional methods known in the art.
- compositions herein may be considered food supplements.
- Food supplements also known as dietary supplements or nutritional supplements, can be considered another pharmaceutical product. It is intended to supplement the diet and provide nutrients or beneficial ingredients that may not be available or consumed in sufficient amounts in the normal diet.
- Most food supplements are considered foods, but sometimes they are considered drugs, natural health products, or nutraceutical products.
- food supplements include health functional foods. Food supplements are usually sold over the counter without a prescription. When food supplements take the form of pills or capsules, they contain the same excipients used in pharmaceuticals. However, food supplements may take the form of food fortified with some nutrients (e.g. infant formula). Accordingly, in certain embodiments, the compositions of the present invention are food supplements.
- composition according to the present invention can be administered as is or mixed with a suitable edible liquid or solid or in the form of tablets, pills, capsules, lozenges, granules, powders. ), suspensions, sachets, syrups, or may be freeze-dried in the form of unit doses. It may also be in the form of monodoses of a lyophilized composition that are mixed in a separate liquid container provided prior to administration.
- composition of the present invention may be included in various edible foods and foods such as milk products for infants.
- the term "edible product” has a broad sense and includes any product that can be ingested by an animal, in any form (e.g., a product that can be consumed by the sense organs). products that can be imported).
- the term "food product” is understood as an edible product that provides nutritional support to the body.
- Foods of particular interest are food supplements and infant formulas.
- Foods preferably include oatmeal porridge, lactic acid fermented foods, resistant starch, dietary fibers, carbohydrates, proteins and glycated proteins. Includes carrier materials such as glycosylated proteins.
- bacterial cells of the invention are homogenized with other ingredients, such as cereals or powdered milk, to form infant formula.
- Another aspect is a first activity comprising at least one member selected from the group consisting of Lactobacillus plantarum strains, cultures of the strains, lysates of the strains, or extracts of the cells, cultures, and lysates. or containing a second active substance including a substance and herbal medicine as an active ingredient;
- the present invention provides a kit for preventing or treating cancer, which includes the first active substance as an active ingredient and the second active substance is administered in combination.
- Another aspect is a first activity comprising at least one member selected from the group consisting of Lactobacillus plantarum strains, cultures of the strains, lysates of the strains, or extracts of the cells, cultures, and lysates. or containing a second active substance including a substance and herbal medicine as an active ingredient;
- a first activity comprising at least one member selected from the group consisting of Lactobacillus plantarum strains, cultures of the strains, lysates of the strains, or extracts of the cells, cultures, and lysates. or containing a second active substance including a substance and herbal medicine as an active ingredient;
- it provides a method of delivering a drug into a subject comprising administering to an subject in need a composition containing the first active substance as an active ingredient and co-administering the second active substance.
- Another aspect is a first activity comprising at least one member selected from the group consisting of Lactobacillus plantarum strains, cultures of the strains, lysates of the strains, or extracts of the cells, cultures, and lysates. or containing a second active substance including a substance and herbal medicine as an active ingredient; Alternatively, it provides a method for preventing or treating cancer, comprising administering to an individual in need a composition containing the first active ingredient as an active ingredient and administering the second active ingredient in combination.
- strain The “strain”, “first active substance”, “herbal medicine”, “second active substance”, “anticancer activity”, and “combined administration” are as described above.
- the individual may be an individual suffering from cancer. Additionally, the subject may be a mammal, and preferably may be a human.
- the administration route, dosage, and frequency of administration of the Lactobacillus Plantarum GB104 strain and herbal medicine can be administered to the subject in various methods and amounts depending on the patient's condition and the presence or absence of side effects, and the optimal administration method, dosage, and administration The number of times can be selected within an appropriate range by a person skilled in the art.
- it may be administered in combination with other drugs known to have therapeutic effects on cancer diseases (e.g., the herbal medicine described above) or physiologically active substances, or may be formulated in the form of a combination preparation with other drugs. .
- Lactobacillus plantarum strain or the culture medium of the strain, can not only inhibit the proliferation of cancer cells or induce the death of cancer cells, but when administered in combination with herbal medicine, it has a synergistic effect on inhibiting the proliferation of cancer cells and tumors. It can be usefully used to prevent, treat or improve cancer in the form of a composition or health functional food.
- Figure 1 is a graph showing the results of analyzing the cell survival rate after treating the human colon cancer cell line HCT116 with culture supernatants of GB104 and other strains, respectively.
- Figure 2 is a graph showing the results of confirming the cell cycle after treating the human colon cancer cell line HCT116 with culture supernatants of GB104 and the comparison strain (GBCC_F0077), respectively.
- Figure 3 is a graph showing the results of confirming cell death after treating the human colon cancer cell line HCT116 with culture supernatants of GB104 and the comparison strain (GBCC_F0077), respectively.
- Figure 4 is a graph showing the results of analyzing the synergistic effect by measuring tumor volume after co-administration of GB104 and herbal medicine (Cordyceps sinensis, yam, bellflower root, and Sanghwang mushroom) in an allograft CT26 mouse colon carcinoma model.
- Figure 5 is a graph showing the results of analyzing the synergy effect by measuring tumor weight after co-administration of GB104 and herbal medicine (Cordyceps sinensis, yam, bellflower root, and Sanghwang mushroom) in an allograft CT26 mouse colon carcinoma model.
- Figure 6 is a graph showing the results of comparative analysis by measuring tumor volume after single and combined administration of GB104 and herbal medicine (yam, bellflower root) in an allograft CT26 mouse colon carcinoma model.
- Figure 7 is a graph showing the results of analyzing the synergy effect by measuring the tumor volume after co-administration of GB104 and herbal medicine (Hyeoncho) in the allograft MC-38 mouse colon carcinoma model.
- Figure 8 is a graph showing the results of analyzing the synergy effect by measuring tumor weight after co-administration of GB104 and herbal medicine (Hyeoncho) in the allograft MC-38 mouse colon carcinoma model.
- Figure 9 is a graph showing the results of comparative analysis by measuring tumor volume after single and combined administration of GB104 and herbal medicine (Hyeoncho) in the allograft MC-38 mouse colon carcinoma model.
- Lactobacillus Plantarum GB104 was isolated from a vaginal sample of a healthy woman who visited the hospital for health checkup. First, vaginal samples were collected with a swab, inoculated into Rogosa SL (MRS) plate medium, and cultured in an anaerobic chamber at 37°C for 48 hours. When bacterial colonies grew, single colonies were subcultured onto new MRS plate medium for pure isolation. After pure isolation, the strain was cultured using MRS medium. Next, among the cultured strains, Lactobacillus plantarum has an inhibitory effect on fat cell accumulation and has low cytotoxicity. Strain GB104 was finally selected.
- MRS Rogosa SL
- the 16S rRNA gene sequence obtained through PCR using primers targeting the 16S rRNA gene was analyzed by Sanger sequencing method, and Lactobacillus Plantarum
- the 16S rRNA sequence of GB104 is shown as SEQ ID NO: 1.
- the present inventors named the GB104 strain as " Lactobacillus plantarum GB104" (Accession number: KCTC 14107BP) and transferred it to the Korean collection for type cultures (KCTC) at the Korea Research Institute of Bioscience and Biotechnology in 2020. It was deposited on the 14th of February.
- Lactobacillus plantarum was changed to Lactiplantibacillus plantarum .
- the changed strain names of existing strains are described interchangeably.
- L. Plantarum culture supernatants including L. Plantarum GB104 strain
- L. Plantarum GB104 strain were treated using human colon cancer cell lines, and cell viability was screened through MTT analysis.
- Human colon cancer cell line HCT116 cells were dispensed into each well of a 96-well plate at 2 ⁇ 10 3 cells and cultured for 24 hours. Then, 10% culture supernatant of various L. Plantarum strains was added in a culture medium supplemented with DFMO and aminoguanidine. concentration and cultured for 72 hours under conditions of 37°C and 5% CO 2 . The culture supernatant was obtained by culturing the L. Plantarum strain in MRS medium, precipitating the strain by centrifugation, collecting only the supernatant, and filtering it through a 0.22 ⁇ m filter.
- MTT Cell Proliferation Kit I
- Figure 1 is a graph showing the results of analyzing the cell survival rate after treating the human colon cancer cell line HCT116 with culture supernatants of GB104 and other strains, respectively.
- L. Plantarum GB104 culture supernatant was treated using the human colon cancer cell line, and changes in the cancer cell cycle were confirmed through flow cytometry.
- Human colon cancer cell line HCT116 cells were dispensed into each well of a 6-well plate at 5 ⁇ 10 4 cells and cultured for 24 hours. Then, 10% of the culture supernatant of the L. Plantarum GB104 strain was added in a culture medium supplemented with DFMO and aminoguanidine. concentration and cultured for 48 hours under conditions of 37°C and 5% CO 2 . The culture supernatant was obtained by culturing the L. Plantarum strain in MRS medium, precipitating the strain by centrifugation, collecting only the supernatant, and filtering it through a 0.22 ⁇ m filter.
- Figure 2 is a graph showing the results of confirming the cell cycle after treating the human colon cancer cell line HCT116 with culture supernatants of GB104 and the comparison strain (GBCC_F0077), respectively.
- L. Plantarum GB104 culture supernatant was treated using human colon cancer cell line, and the cancer cell killing effect was confirmed through flow cytometry.
- Human colon cancer cell line HCT116 cells were dispensed into each well of a 6-well plate at 5 ⁇ 10 4 cells and cultured for 24 hours. Then, 10% of the culture supernatant of the L. Plantarum GB104 strain was added in a culture medium supplemented with DFMO and aminoguanidine. concentration and cultured for 48 hours under conditions of 37°C and 5% CO 2 . The culture supernatant was obtained by culturing the L. Plantarum strain in MRS medium, precipitating the strain by centrifugation, collecting only the supernatant, and filtering it through a 0.22 ⁇ m filter. After 48 hours, the cells were removed by treatment with trypsin-EDTA and then harvested by centrifugation.
- Figure 3 is a graph showing the results of confirming cell death after treating the human colon cancer cell line HCT116 with culture supernatants of GB104 and the comparison strain (GBCC_F0077), respectively.
- mice with tumor sizes within a certain range were selected and classified so that the average tumor size of each group was the same.
- L. Plantarum GB104 strain alone, L. Plantarum GB104 strain and Cordyceps sinensis, yam, and bellflower root were treated.
- each of the Sanghwang mushrooms was orally administered to the animal model every day until just before the end of the test.
- the concentration of the administered strain was 1x109 CFU per mouse, and all herbal medicines were administered at 1mg per mouse.
- Table 1 shows the mean and standard deviation of the tumor size of mice in each group at 5, 7, 9, 11, 13, 15, and 17 days after injection of the colon cancer cell line CT26.
- Figure 4 is a graph showing the results of analyzing the synergistic effect by measuring tumor volume after co-administration of GB104 and herbal medicine (Cordyceps sinensis, yam, bellflower root, and Sanghwang mushroom) in an allograft CT26 mouse colon carcinoma model.
- Figure 5 is a graph showing the results of analyzing the synergy effect by measuring tumor weight after co-administration of GB104 and herbal medicine (Cordyceps sinensis, yam, bellflower root, and Sanghwang mushroom) in an allograft CT26 mouse colon carcinoma model.
- Figure 6 is a graph showing the results of comparative analysis by measuring tumor volume after single and combined administration of GB104 and herbal medicine (yam, bellflower root) in an allograft CT26 mouse colon carcinoma model.
- mice with tumor sizes within a certain range were selected and classified so that the average tumor size of each group was the same.
- L. Plantarum GB104 strain alone, L. Plantarum GB104 strain and sage root combination were treated as described above. It was orally administered to the animal model every day until just before the end of the test. The concentration of the administered strain was 1x109 CFU per mouse, and Hyeoncho was administered at 1 mg per mouse.
- Table 2 shows the mean and standard deviation of the tumor size of mice in each group at 6, 9, 12, 14, 16, 19, and 21 days after injection of the colon cancer cell line MC-38.
- Figure 7 is a graph showing the results of analyzing the synergy effect by measuring the tumor volume after co-administration of GB104 and herbal medicine (Hyeoncho) in the allograft MC-38 mouse colon carcinoma model.
- Figure 8 is a graph showing the results of analyzing the synergy effect by measuring tumor weight after co-administration of GB104 and herbal medicine (Hyeoncho) in the allograft MC-38 mouse colon carcinoma model.
- Figure 9 is a graph showing the results of comparative analysis by measuring tumor volume after single and combined administration of GB104 and herbal medicine (Hyeoncho) in the allograft MC-38 mouse colon carcinoma model.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Chemical & Material Sciences (AREA)
- Mycology (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Microbiology (AREA)
- Engineering & Computer Science (AREA)
- Botany (AREA)
- Medical Informatics (AREA)
- Biotechnology (AREA)
- Alternative & Traditional Medicine (AREA)
- Molecular Biology (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Nutrition Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Abstract
La présente invention concerne une composition pour le traitement du cancer à l'aide d'une polythérapie, comprenant une souche de Lactobacillus plantarum et un médicament à base de plantes. La souche de Lactobacillus plantarum ou un milieu de culture de la souche peut non seulement inhiber la prolifération des cellules cancéreuses ou induire la mort des cellules cancéreuses, mais présente également, lorsqu'elle est administrée en combinaison avec un médicament à base de plantes, un effet synergique sur l'inhibition de la prolifération des cellules cancéreuses et des tumeurs, et peut ainsi être utilement utilisée pour prévenir, traiter ou soulager le cancer sous la forme d'une composition pharmaceutique ou d'un aliment fonctionnel de santé.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2022-0118923 | 2022-09-20 | ||
KR20220118923 | 2022-09-20 | ||
KR1020230125600A KR20240040655A (ko) | 2022-09-20 | 2023-09-20 | 락토바실러스 플란타룸 균주 및 한약재를 포함하는 병용 요법을 이용한 암 예방 또는 치료용 조성물 |
KR10-2023-0125600 | 2023-09-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2024063543A1 true WO2024063543A1 (fr) | 2024-03-28 |
Family
ID=90454984
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/KR2023/014310 WO2024063543A1 (fr) | 2022-09-20 | 2023-09-20 | Composition pour la prévention ou le traitement du cancer à l'aide d'une polythérapie, comprenant une souche de lactobacillus plantarum et un médicament à base de plantes |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2024063543A1 (fr) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100911115B1 (ko) * | 2007-06-15 | 2009-08-11 | 주식회사 씨티씨바이오 | 내산성, 내담즙산성 및 항균 효과를 가진 신규한 유산균 및 이를 포함하는 조성물 |
KR20100079303A (ko) * | 2008-12-31 | 2010-07-08 | 주식회사한국신약 | 상황버섯과 동충하초를 포함하는 항암용 건강식품 |
CN104127443A (zh) * | 2014-07-25 | 2014-11-05 | 吉林省农业科学院 | 一种乳酸菌与人参多糖组合物及其制备方法与应用 |
KR20180105842A (ko) * | 2017-03-16 | 2018-10-01 | 주식회사 알엔에이 | 약리학적 활성성분이 축적된 미생물 제제 |
KR20210086540A (ko) * | 2019-12-31 | 2021-07-08 | 주식회사 지아이바이옴 | 락토바실러스 플란타럼 균주 및 이를 포함하는 대사질환의 예방 또는 치료용 조성물 |
KR20210090570A (ko) * | 2020-01-10 | 2021-07-20 | 이뮤노바이옴 주식회사 | 신규한 락토바실러스 플란타룸(Lactobacillus plantarum) 균주, 균주 유래 다당체 및 이의 용도 |
KR20220028943A (ko) * | 2020-08-31 | 2022-03-08 | 주식회사 리비옴 | 항암 활성을 갖는 락토바실러스 플란타룸 미생물, 그를 포함하는 조성물 및 그를 이용한 암 예방 또는 치료 방법 |
KR20220131844A (ko) * | 2021-03-22 | 2022-09-29 | 주식회사 지아이바이옴 | 락토바실러스 플란타럼 gb104 균주 및 이를 포함하는 암 예방 또는 치료용 조성물 |
-
2023
- 2023-09-20 WO PCT/KR2023/014310 patent/WO2024063543A1/fr unknown
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100911115B1 (ko) * | 2007-06-15 | 2009-08-11 | 주식회사 씨티씨바이오 | 내산성, 내담즙산성 및 항균 효과를 가진 신규한 유산균 및 이를 포함하는 조성물 |
KR20100079303A (ko) * | 2008-12-31 | 2010-07-08 | 주식회사한국신약 | 상황버섯과 동충하초를 포함하는 항암용 건강식품 |
CN104127443A (zh) * | 2014-07-25 | 2014-11-05 | 吉林省农业科学院 | 一种乳酸菌与人参多糖组合物及其制备方法与应用 |
KR20180105842A (ko) * | 2017-03-16 | 2018-10-01 | 주식회사 알엔에이 | 약리학적 활성성분이 축적된 미생물 제제 |
KR20210086540A (ko) * | 2019-12-31 | 2021-07-08 | 주식회사 지아이바이옴 | 락토바실러스 플란타럼 균주 및 이를 포함하는 대사질환의 예방 또는 치료용 조성물 |
KR20210090570A (ko) * | 2020-01-10 | 2021-07-20 | 이뮤노바이옴 주식회사 | 신규한 락토바실러스 플란타룸(Lactobacillus plantarum) 균주, 균주 유래 다당체 및 이의 용도 |
KR20220028943A (ko) * | 2020-08-31 | 2022-03-08 | 주식회사 리비옴 | 항암 활성을 갖는 락토바실러스 플란타룸 미생물, 그를 포함하는 조성물 및 그를 이용한 암 예방 또는 치료 방법 |
KR20220131844A (ko) * | 2021-03-22 | 2022-09-29 | 주식회사 지아이바이옴 | 락토바실러스 플란타럼 gb104 균주 및 이를 포함하는 암 예방 또는 치료용 조성물 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7785581B2 (en) | Composition and method for reducing feces toxins and treating digestive disorders | |
WO2019199094A1 (fr) | Nouvelle souche de bifidobacterium longum ou de lactobacillus rhamnosus ayant pour effet de prévenir ou de traiter l'obésité, et utilisation correspondante | |
WO2022203303A1 (fr) | Souche de lactobacillus plantarum gb104 et composition la comprenant destinée à la prévention ou au traitement du cancer | |
KR102173168B1 (ko) | 류코노스톡속 균주를 포함하는 장 기능 개선용 조성물 | |
WO2015030283A1 (fr) | Composition destinée à prévenir et traiter la fatigue liée au cancer contenant de la poudre de ginseng traitée ou de l'extrait de ginseng traité comprenant un constituant de ginsénoside amélioré | |
WO2018090983A9 (fr) | Composé de saponine pour améliorer la microflore intestinale, son procédé de préparation et son utilisation | |
KR102041916B1 (ko) | 신장질환 진행 억제 및 예방용 프로바이오틱스 및 이를 포함하는 신장질환 진행 억제 및 예방용 조성물 | |
WO2017183902A1 (fr) | Composition contenant des extraits de artemisia capillaris, sanguisorba officinalis et curcuma longa et un agent antiviral, en tant que principes actifs, destinée à prévenir ou traiter une maladie du foie | |
WO2016190566A9 (fr) | Composition pharmaceutique ou aliment naturel fonctionnel pour la prévention et le traitement de maladies métaboliques, contenant un extrait aqueux de pleurotus eryngii var. ferulae (pf.) en tant que principe actif | |
WO2016072655A1 (fr) | Composition pour améliorer, traiter ou prévenir la constipation comprenant un produit fermenté renfermant des bactéries lactiques de graines de cassia comme ingrédient efficace, et son procédé de préparation | |
WO2020226467A1 (fr) | Souche d'enterococcus lactis wik0107 ayant des effets de régulation des fonctions immunitaires et d'atténuation des maladies inflammatoires chroniques intestinales et son utilisation | |
WO2020226468A1 (fr) | Souche de pediococcus inopinatus wikim0108 ayant un effet de régulation de la fonction immunitaire et de soulagement d'une maladie intestinale inflammatoire et son utilisation | |
WO2020139020A2 (fr) | Kimchi pour la prévention ou le traitement de maladies associées à helicobacter pylori | |
WO2024063543A1 (fr) | Composition pour la prévention ou le traitement du cancer à l'aide d'une polythérapie, comprenant une souche de lactobacillus plantarum et un médicament à base de plantes | |
WO2023068855A1 (fr) | Composition pour le soulagement, la prévention ou le traitement du cancer à l'aide d'une souche de veillonella parvula ayant une activité anticancéreuse | |
WO2016093613A2 (fr) | Composition pour la prévention ou le traitement d'une perte de poids anormale, contenant un extrait de pelure de mandarine satsuma | |
WO2023058801A1 (fr) | Composition pour soulager, prévenir ou traiter un trouble intestinal, comprenant une souche de lactobacillus acidophilus kbl402 ou kbl409 | |
WO2022039514A1 (fr) | Composition pour le traitement de maladies cérébrales comprenant lactobacillus sakei ou des vésicules extracellulaires dérivées de celui-ci en tant que principe actif | |
WO2021261929A1 (fr) | Nouvelle souche de lactobacillus reuteri et utilisation associée | |
KR20240040655A (ko) | 락토바실러스 플란타룸 균주 및 한약재를 포함하는 병용 요법을 이용한 암 예방 또는 치료용 조성물 | |
KR20130131973A (ko) | 오리나무 수피 추출물 및 유산균을 포함하는 항우식성 조성물 | |
WO2024063545A1 (fr) | Composition comprenant une souche de lactobacillus plantarum pour améliorer la composition de métabolite intestinal | |
WO2024058320A1 (fr) | Composition pour prévenir, soulager ou traiter une maladie intestinale | |
WO2023229263A1 (fr) | Composition pour prévenir, traiter ou atténuer des maladies métaboliques comprenant une souche de lactobacillus plantarum nchbl-004 ou un milieu de culture de celle-ci | |
WO2022158922A2 (fr) | Composition comprenant une souche de propionibacterium freudenreichii mj2 utilisée en tant que principe actif pour la prévention, le traitement ou l'atténuation de la polyarthrite rhumatoïde |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 23868595 Country of ref document: EP Kind code of ref document: A1 |