KR20030087726A - Composition for detoxifying toxic substances having Aloe vera gel - Google Patents
Composition for detoxifying toxic substances having Aloe vera gel Download PDFInfo
- Publication number
- KR20030087726A KR20030087726A KR1020020025602A KR20020025602A KR20030087726A KR 20030087726 A KR20030087726 A KR 20030087726A KR 1020020025602 A KR1020020025602 A KR 1020020025602A KR 20020025602 A KR20020025602 A KR 20020025602A KR 20030087726 A KR20030087726 A KR 20030087726A
- Authority
- KR
- South Korea
- Prior art keywords
- composition
- aloe vera
- vera gel
- blood
- detoxifying
- Prior art date
Links
- 235000011399 aloe vera Nutrition 0.000 title claims abstract description 54
- 239000000203 mixture Substances 0.000 title claims abstract description 42
- 235000002961 Aloe barbadensis Nutrition 0.000 title claims abstract description 40
- 239000003440 toxic substance Substances 0.000 title claims description 35
- 231100000614 poison Toxicity 0.000 title claims description 13
- 244000186892 Aloe vera Species 0.000 title 1
- 244000144927 Aloe barbadensis Species 0.000 claims abstract description 39
- FMMWHPNWAFZXNH-UHFFFAOYSA-N Benz[a]pyrene Chemical compound C1=C2C3=CC=CC=C3C=C(C=C3)C2=C2C3=CC=CC2=C1 FMMWHPNWAFZXNH-UHFFFAOYSA-N 0.000 claims abstract description 32
- DDRJAANPRJIHGJ-UHFFFAOYSA-N creatinine Chemical compound CN1CC(=O)NC1=N DDRJAANPRJIHGJ-UHFFFAOYSA-N 0.000 claims abstract description 28
- BPYKTIZUTYGOLE-IFADSCNNSA-N Bilirubin Chemical compound N1C(=O)C(C)=C(C=C)\C1=C\C1=C(C)C(CCC(O)=O)=C(CC2=C(C(C)=C(\C=C/3C(=C(C=C)C(=O)N\3)C)N2)CCC(O)=O)N1 BPYKTIZUTYGOLE-IFADSCNNSA-N 0.000 claims abstract description 26
- 210000004369 blood Anatomy 0.000 claims abstract description 21
- 239000008280 blood Substances 0.000 claims abstract description 21
- 230000000391 smoking effect Effects 0.000 claims abstract description 17
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 15
- 229940109239 creatinine Drugs 0.000 claims abstract description 14
- 201000010099 disease Diseases 0.000 claims abstract description 14
- 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 claims abstract description 11
- 239000008103 glucose Substances 0.000 claims abstract description 11
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 claims abstract description 10
- 229960002715 nicotine Drugs 0.000 claims abstract description 9
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 claims abstract description 9
- 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 claims abstract description 8
- 235000013305 food Nutrition 0.000 claims abstract description 7
- 235000013361 beverage Nutrition 0.000 claims abstract description 5
- 240000007594 Oryza sativa Species 0.000 claims abstract description 3
- 235000007164 Oryza sativa Nutrition 0.000 claims abstract description 3
- 244000269722 Thea sinensis Species 0.000 claims abstract description 3
- 235000008429 bread Nutrition 0.000 claims abstract description 3
- 235000009508 confectionery Nutrition 0.000 claims abstract description 3
- 235000015243 ice cream Nutrition 0.000 claims abstract description 3
- 235000015110 jellies Nutrition 0.000 claims abstract description 3
- 239000008274 jelly Substances 0.000 claims abstract description 3
- 235000012149 noodles Nutrition 0.000 claims abstract description 3
- 235000009566 rice Nutrition 0.000 claims abstract description 3
- 235000013616 tea Nutrition 0.000 claims abstract description 3
- 239000000499 gel Substances 0.000 claims description 35
- 231100000167 toxic agent Toxicity 0.000 claims description 22
- 208000014951 hematologic disease Diseases 0.000 claims description 5
- 235000013618 yogurt Nutrition 0.000 claims description 5
- 208000019838 Blood disease Diseases 0.000 claims description 4
- 208000018706 hematopoietic system disease Diseases 0.000 claims description 4
- YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 claims 1
- 239000003550 marker Substances 0.000 claims 1
- 230000029142 excretion Effects 0.000 abstract description 15
- 231100000331 toxic Toxicity 0.000 abstract description 7
- 230000002588 toxic effect Effects 0.000 abstract description 7
- 230000007613 environmental effect Effects 0.000 abstract description 4
- 239000003344 environmental pollutant Substances 0.000 abstract description 4
- 231100000719 pollutant Toxicity 0.000 abstract description 4
- 239000005556 hormone Substances 0.000 abstract description 3
- 229940088597 hormone Drugs 0.000 abstract description 3
- 239000000463 material Substances 0.000 abstract 3
- TXVHTIQJNYSSKO-UHFFFAOYSA-N BeP Natural products C1=CC=C2C3=CC=CC=C3C3=CC=CC4=CC=C1C2=C34 TXVHTIQJNYSSKO-UHFFFAOYSA-N 0.000 abstract 1
- 241001116389 Aloe Species 0.000 description 14
- 230000000694 effects Effects 0.000 description 13
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 10
- 241000208125 Nicotiana Species 0.000 description 9
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 9
- 239000002775 capsule Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- CVSVTCORWBXHQV-UHFFFAOYSA-N creatine Chemical compound NC(=[NH2+])N(C)CC([O-])=O CVSVTCORWBXHQV-UHFFFAOYSA-N 0.000 description 8
- 231100000357 carcinogen Toxicity 0.000 description 6
- 239000003183 carcinogenic agent Substances 0.000 description 6
- 238000001727 in vivo Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 210000002966 serum Anatomy 0.000 description 6
- UIKROCXWUNQSPJ-VIFPVBQESA-N (-)-cotinine Chemical compound C1CC(=O)N(C)[C@@H]1C1=CC=CN=C1 UIKROCXWUNQSPJ-VIFPVBQESA-N 0.000 description 5
- UIKROCXWUNQSPJ-UHFFFAOYSA-N Cotinine Natural products C1CC(=O)N(C)C1C1=CC=CN=C1 UIKROCXWUNQSPJ-UHFFFAOYSA-N 0.000 description 5
- 229950006073 cotinine Drugs 0.000 description 5
- 230000003247 decreasing effect Effects 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 210000002700 urine Anatomy 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 230000036765 blood level Effects 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 229960003624 creatine Drugs 0.000 description 4
- 239000006046 creatine Substances 0.000 description 4
- 238000001784 detoxification Methods 0.000 description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 230000001737 promoting effect Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000019504 cigarettes Nutrition 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
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 201000005202 lung cancer Diseases 0.000 description 3
- 208000020816 lung neoplasm Diseases 0.000 description 3
- 239000008213 purified water Substances 0.000 description 3
- 239000006228 supernatant Substances 0.000 description 3
- 210000005239 tubule Anatomy 0.000 description 3
- 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
- 235000005979 Citrus limon Nutrition 0.000 description 2
- 244000131522 Citrus pyriformis Species 0.000 description 2
- 206010023126 Jaundice Diseases 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000000711 cancerogenic effect Effects 0.000 description 2
- 230000034994 death Effects 0.000 description 2
- 231100000517 death Toxicity 0.000 description 2
- 206010012601 diabetes mellitus Diseases 0.000 description 2
- 239000003937 drug carrier Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 235000013376 functional food Nutrition 0.000 description 2
- 239000007903 gelatin capsule Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 2
- 235000019359 magnesium stearate Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 230000003442 weekly effect Effects 0.000 description 2
- ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 2-phenyl-1h-imidazole Chemical compound C1=CNC(C=2C=CC=CC=2)=N1 ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 0.000 description 1
- 201000001320 Atherosclerosis Diseases 0.000 description 1
- 206010005003 Bladder cancer Diseases 0.000 description 1
- 206010008342 Cervix carcinoma Diseases 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 208000000461 Esophageal Neoplasms Diseases 0.000 description 1
- 229930091371 Fructose Natural products 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
- 239000005715 Fructose Substances 0.000 description 1
- 101000993347 Gallus gallus Ciliary neurotrophic factor Proteins 0.000 description 1
- 208000018522 Gastrointestinal disease Diseases 0.000 description 1
- 102000004877 Insulin Human genes 0.000 description 1
- 108090001061 Insulin Proteins 0.000 description 1
- 244000199885 Lactobacillus bulgaricus Species 0.000 description 1
- 235000013960 Lactobacillus bulgaricus Nutrition 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
- 241000234280 Liliaceae Species 0.000 description 1
- 206010030155 Oesophageal carcinoma Diseases 0.000 description 1
- 102000004316 Oxidoreductases Human genes 0.000 description 1
- 108090000854 Oxidoreductases Proteins 0.000 description 1
- 208000000453 Skin Neoplasms Diseases 0.000 description 1
- UZHDGDDPOPDJGM-UHFFFAOYSA-N Stigmatellin A Natural products COC1=CC(OC)=C2C(=O)C(C)=C(CCC(C)C(OC)C(C)C(C=CC=CC(C)=CC)OC)OC2=C1O UZHDGDDPOPDJGM-UHFFFAOYSA-N 0.000 description 1
- 208000005718 Stomach Neoplasms Diseases 0.000 description 1
- 208000006011 Stroke Diseases 0.000 description 1
- 238000000692 Student's t-test Methods 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 description 1
- 208000006105 Uterine Cervical Neoplasms Diseases 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 238000000540 analysis of variance Methods 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- 230000000975 bioactive effect Effects 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000010261 cell growth Effects 0.000 description 1
- 201000010881 cervical cancer Diseases 0.000 description 1
- 230000001447 compensatory effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000008278 cosmetic cream Substances 0.000 description 1
- 239000008341 cosmetic lotion Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 208000010643 digestive system disease Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 230000002124 endocrine Effects 0.000 description 1
- 210000000750 endocrine system Anatomy 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 201000004101 esophageal cancer Diseases 0.000 description 1
- 230000003090 exacerbative effect Effects 0.000 description 1
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
- 239000000576 food coloring agent Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 235000020510 functional beverage Nutrition 0.000 description 1
- 206010017758 gastric cancer Diseases 0.000 description 1
- 208000018685 gastrointestinal system disease Diseases 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 208000019622 heart disease Diseases 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002440 hepatic effect Effects 0.000 description 1
- 230000002519 immonomodulatory effect Effects 0.000 description 1
- 229940125396 insulin Drugs 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 230000003907 kidney function Effects 0.000 description 1
- 229940004208 lactobacillus bulgaricus Drugs 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229940041476 lactose 100 mg Drugs 0.000 description 1
- 208000032839 leukemia Diseases 0.000 description 1
- 201000007270 liver cancer Diseases 0.000 description 1
- 208000014018 liver neoplasm Diseases 0.000 description 1
- 230000007246 mechanism Effects 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
- 210000003205 muscle Anatomy 0.000 description 1
- 239000013642 negative control Substances 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 238000001543 one-way ANOVA Methods 0.000 description 1
- 239000008177 pharmaceutical agent Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 230000036470 plasma concentration Effects 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000013641 positive control Substances 0.000 description 1
- 230000003405 preventing effect Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- 201000000849 skin cancer Diseases 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 201000011549 stomach cancer Diseases 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 238000012353 t test Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- 231100000397 ulcer Toxicity 0.000 description 1
- 201000005112 urinary bladder cancer Diseases 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 230000029663 wound healing Effects 0.000 description 1
Classifications
-
- 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)
- A61K36/886—Aloeaceae (Aloe family), e.g. aloe vera
-
- 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
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2200/00—Function of food ingredients
- A23V2200/30—Foods, ingredients or supplements having a functional effect on health
- A23V2200/334—Foods, ingredients or supplements having a functional effect on health treating the effects of consuming alcohol, narcotics or other addictive behavior, e.g. treating hangover or reducing blood alcohol levels
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Botany (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Biotechnology (AREA)
- Alternative & Traditional Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Medical Informatics (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nutrition Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
Description
본 발명은 알로에 베라 겔을 포함하는 독성물질 해독용 조성물에 관한 것으로, 특히 흡연으로 인해 발생하는 독성물질을 해독할 수 있는 독성물질 해독용 조성물에 관한 것이다.The present invention relates to a composition for detoxifying a toxic substance including aloe vera gel, and more particularly to a composition for detoxifying a toxic substance caused by smoking.
현대 사회에서 가장 문제시되는 것은 흡연으로 인한 독성물질에 의한 질병이다. 예를 들면, 담배에 의해 발생하는 각종 질병의 원인은 4,000 여종 이상의 유해 독성물질(발암물질 포함) 때문이다. 최근 흡연은 직접 흡연자뿐만 아니라, 간접 흡연자의 건강을 크게 위협하고 있어, 흡연은 우리 모두의 문제로 부각되고 있다. 흡연은 암으로 죽어가는 전체 인구중 30%를 차지하며, 남성 폐암 사망자의 85%, 여성 폐암 사망자의 80%가 담배에 기인한다. 담배로 인한 암을 여성의 자궁경부암, 백혈병 등 다양하다. 뿐만 아니라, 위장질환, 심장질환, 뇌졸중 및 동맥경화증을 유발한다. 따라서, 담배독성물질의 작용을 억제하거나 배설을 촉진시켜 해독시킬 경우 흡연으로 인해 발생할 수 있는 여러 질병을 사전에 예방할 수 있다.The biggest problem in modern society is the disease caused by smoking toxic substances. For example, various diseases caused by tobacco are caused by more than 4,000 harmful toxins (including carcinogens). In recent years, smoking has threatened the health of not only direct smokers but also secondhand smokers, so smoking is a problem for all of us. Smoking accounts for 30% of the total population dying from cancer, with 85% of male lung cancer deaths and 80% of female lung cancer deaths. Cancers caused by tobacco are diverse, including cervical cancer and leukemia in women. In addition, it causes gastrointestinal disease, heart disease, stroke and atherosclerosis. Therefore, when the detoxification by inhibiting the action of tobacco toxic substances or by promoting the excretion can be prevented in advance a number of diseases caused by smoking.
흡연 등에 의해 발생하는 대표적인 독성물질인 벤조[a]피렌(benzo[a]pyrene: BaP)은 유해 발암물질이고, 니코틴은 NNK 등 담배 특이적 발암물질을 만들어 내는 전구물질일 뿐만 아니라, 담배의 습관성 및 다양한 독성작용을 가지고 있다.Benzo [a] pyrene (BaP), a representative toxic substance caused by smoking, is a harmful carcinogen, and nicotine is not only a precursor for producing tobacco-specific carcinogens such as NNK, but also the habit of tobacco And various toxic effects.
상기 담배의 독성물질인 벤조[a]피렌은 또한 매연이나 자동차 배기가스중에 포함된 공해 물질이기도 하다. 산업사회의 발달과 더불어 인구의 집중화로 인한 환경오염은 날로 그 도를 더하고 있으며, 자동차 배기가스며 공단에서 배출되는 매연, 소각장 주변의 공해물질들은 여러 가지 형태와 경로를 통하여 환경조건을 악화시키고 있다. 최근에 부각되고 있는 내분비계 장애물질(일명 환경호르몬) 중에는 환경에서 유래되는 오염물질이 많은 부분을 차지하고 있는데, 이 중 어떤 것들은 미량으로 인체의 내분비계에 문제를 일으킬 수 있다. 자동차 배기가스 또한 발암물질의 집합체이며, 연료가 연소되면서 나오는 가스 속에는 특히 대표적인 유독성 물질인 벤조[a]피렌이 많이 들어 있는데, 벤조[a]피렌은 세포의 유전자에 붙어 돌연변이를 일으킴으로써 암세포로 변화시키는 물질로 알려져 있다. 아무리 적은 양이라도 벤조[a]피렌을 늘 들이마시게 되면 폐암, 간암, 위암, 방광암, 식도암, 피부암 등이 발생할 위험이 높다.Benzo [a] pyrene, a toxic substance of tobacco, is also a pollutant contained in soot or automobile exhaust. With the development of the industrial society, environmental pollution due to the concentration of the population is increasing day by day, and the pollutants around the incinerators and the exhaust emissions from automobiles, industrial complexes, etc. are exacerbating environmental conditions through various forms and routes. . Among the endocrine obstructions (aka environmental hormones), which are emerging recently, a lot of pollutants are derived from the environment, and some of them may cause problems in the human endocrine system. Automobile exhaust is also a collection of carcinogens, and the gas produced by burning fuel contains a number of toxic benzo [a] pyrenes, which are particularly representative of toxic substances. It is known to make a substance. Even small doses of benzo [a] pyrene are always at high risk for lung cancer, liver cancer, stomach cancer, bladder cancer, esophageal cancer and skin cancer.
또한 상기 독성물질로 인해 혈액의 질병과 관련된 인자들인 크레아티닌, 글루코스 및 빌리루빈 등의 혈중 농도가 증가되며, 증가된 상기 인자들의 농도가 인체에 질병을 유발한다.In addition, the toxic substance increases blood levels of creatinine, glucose, and bilirubin, which are factors related to the disease of blood, and the increased concentration of the factors causes disease in the human body.
크레아티닌(creatinine)은 단백질이 근육에서 에너지원으로 이용된 후 생긴 크레아틴(creatine)이 분해되어 생긴 노폐물로서 혈중으로 배출된 후 신장에서 여과되어 배출된다. 크레아틴, 크레아티닌은 사구체로부터 여과되나, 크레아틴은 세뇨관에서 완전히 재흡수되는데 반하여 크레아티닌은 세뇨관에서 재흡수가 안되고 혈중 농도가 높을 때는 오히려 세뇨관으로부터 분비된다. 이 때문에 혈중 크레아틴 농도는 신장기능의 척도로 임상적으로 중요시된다 또한 최근 성인에게서 많이 발생하는 당뇨병은 주로 인슐린 비의존성 당뇨병으로 스트레스와 운동부족, 폭음, 폭식 등에 의한 비만으로 인하여 인슐린 수용체가 기능을 상실하여 나타나며, 혈중 글루코스의 레벨을 측정하여 판정한다. 또한 빌리루빈(bilirubin)은 전간성 황달(prehepatic jaundice) 또는 간성 황달(hepatic jaundice) 등의 경우, 혈중농도가 증가한다.Creatinine is a waste product produced by the breakdown of creatine after protein is used as an energy source in muscles. It is discharged into the blood and then filtered out of the kidneys. Creatine and creatinine are filtered out of the glomeruli, but creatine is completely reabsorbed in the tubules, whereas creatinine is not resorbed in the tubules and is secreted from the tubules when blood levels are high. For this reason, blood creatine concentration is considered clinically important as a measure of renal function. In recent years, many diabetes mellitus in adults is mainly insulin-independent diabetes. Appears and is determined by measuring the level of glucose in the blood. In the case of bilirubin (bilirubin), in the case of prehepatic jaundice or hepatic jaundice, blood concentration increases.
알로에(Aloe)는 백합과(Liliaceae)에 속하는 약용식물로서 그의 다양한 약효로 인하여 고대로부터 민간에 널리 이용되어 왔다. 민간에서는 오래 전부터 알로에를 썬텐(suntan) 연고, 썬텐 분말, 화장품 크림, 로숀, 샴푸 등으로 다양하게 이용하고 있다. 그러나 이렇게 오래 전부터 이용되어 오던 알로에에 대해서 정확한 약효 및 작용기전에 대한 과학적인 연구는 비교적 최근에 와서야 이루어지고 있는 실정이다. 최근에 알로에에 대한 지속적인 연구 결과들로부터 알로에는 상처치유 효과와 소염활성, 궤양치료 활성, 항암활성, 항미생물활성, 면역조절활성, 세포성장촉진활성의 다양한 활성을 나타냄이 보고되어 있다.Aloe is a medicinal plant belonging to the family Liliaceae and has been widely used in folklore since ancient times because of its various effects. The civilian has long used aloe as a suntan ointment, suntan powder, cosmetic cream, lotion and shampoo. However, scientific researches on the exact effects and mechanisms of action of aloe, which have been used for a long time, have been made relatively recently. Recent studies on aloe have been reported to show a variety of activities such as wound healing, anti-inflammatory activity, ulcer treatment activity, anticancer activity, antimicrobial activity, immunomodulatory activity, cell growth promoting activity.
본 발명자들은 알로에에 대한 연구를 예의 수행한 결과, 알로에 베라 겔이 독성물질, 특히 벤조[a]피렌과 같이 흡연이나 자동차 배기가스로 인해 발생하는 독성물질의 해독 작용을 갖는 것을 처음으로 발견하여 본 발명을 완성하였다.As a result of diligent research on aloe, the present inventors have found for the first time that aloe vera gel has a detoxifying effect of toxic substances, particularly toxic substances caused by smoking or automobile exhaust, such as benzo [a] pyrene. The invention has been completed.
본 발명의 목적은 알로에 베라 겔을 포함하는 독성물질 해독용 조성물을 제공하는 것이다.It is an object of the present invention to provide a composition for detoxifying a toxic substance comprising aloe vera gel.
도 1은 알로에 베라 겔 투여에 대한 인비보(in vivo) 상의 벤조[a]피렌의 배설효과를 나타낸 그래프이고,1 is a graph showing the excretion effect of benzo [a] pyrene on in vivo ( in vivo ) for aloe vera gel administration,
도 2는 알로에 베라 겔 투여에 대한 인비보상의 코티닌의 배설효과를 나타낸 그래프이며,Figure 2 is a graph showing the excretory effect of cotinine in vivo on aloe vera gel administration,
도 3은 알로에 베라 겔 투여에 대한 인비보상의 크레아티닌의 혈중 농도를 나타낸 그래프이고,Figure 3 is a graph showing the blood concentration of creatinine in vivo for aloe vera gel administration,
도 4는 알로에 베라 겔 투여에 대한 인비보상의 글루코스의 혈중 농도를 나타낸 그래프이며,Figure 4 is a graph showing the blood concentration of in vivo compensatory glucose for aloe vera gel administration,
도 5는 알로에 베라 겔 투여에 대한 인비보상의 빌리루빈의 혈중 농도를 나타낸 그래프이다,Figure 5 is a graph showing the blood concentration of bilirubin in vivo for administration of aloe vera gel,
본 발명은 알로에 베라 겔을 포함하는 독성물질 해독용 조성물을 제공한다.The present invention provides a composition for detoxifying a toxic substance including aloe vera gel.
본 발명은 특히, 흡연으로 인해 발생하는 독성물질을 해독할 수 있는 독성물질 해독용 조성물을 제공하며, 또한 상기 독성물질은 예컨대, 벤조[a]피렌, 니코틴, 타르 등이다.In particular, the present invention provides a composition for detoxifying a toxic substance which can be detoxified due to smoking, and the toxic substance is, for example, benzo [a] pyrene, nicotine, tar and the like.
본 발명은 또한 혈중 질병 지표 물질을 감소시키는 것을 특징으로 하는 독성물질 해독용 조성물을 제공한다. 상기 혈중 질병 지표 물질은 크레아티닌, 빌리루빈 또는 글루코스 등이다.The present invention also provides a composition for detoxifying a toxic substance, which reduces blood disease markers. The blood disease indicator is creatinine, bilirubin or glucose and the like.
본 발명은 또한 알로에 베라 겔을 포함하는 독성물질 해독 효과를 갖는 식품학적 조성물을 제공한다.The present invention also provides a food composition having a detoxifying effect including aloe vera gel.
이하, 본 발명을 상세하게 설명한다.EMBODIMENT OF THE INVENTION Hereinafter, this invention is demonstrated in detail.
본 발명의 첫 번째 양상은 알로에 베라 겔을 포함하는 독성물질 해독용 조성물을 제공하는 것이다.A first aspect of the present invention is to provide a composition for detoxifying a toxic substance comprising aloe vera gel.
본 발명의 조성물에 포함되는 알로에 베라 겔은 바람직하게는 알로에 베라로부터 얻어진 겔(gel)을 단독으로 사용하거나, 알로에 베라 겔을 분말화시켜 사용하거나, 또는 알로에 베라 겔과 분말을 적합한 비율로 혼합한 것을 사용할 수 있다. 또한 알로에의 생리활성효과가 높은 성분을 다량 함유하는 가공된 시판 알로에 제품을 사용할 수도 있고, 특히 액티브 알로에TM(알로콥(Aloecorp), 미국) 등을 사용할 수 있다. 상기 액티브 알로에TM는 알로에의 생리활성효과가 가장 높은 중간 범위의 다당류가 알로에 생초보다도 많이 함유되어 있는 제품으로, 알로에 베라 겔의 200배 농축 분말이다.The aloe vera gel included in the composition of the present invention is preferably a gel obtained from aloe vera alone, or powdered aloe vera gel, or a mixture of aloe vera gel and powder in a suitable ratio. Can be used. In addition, a commercially available aloe product containing a large amount of the high physiological activity effect of aloe may be used, and in particular, active aloe TM (Aloecorp, USA) and the like may be used. The active aloe TM is a product containing more of the middle range of polysaccharides with the highest bioactive activity of aloe than aloe vera, and is 200 times concentrated powder of aloe vera gel.
본 발명의 조성물은 알로에 베라 겔만을 함유할 수 있으나, 투여의 용이를 위해 약제학적으로 허용되는 공지의 담체 등을 포함할 수 있다.The composition of the present invention may contain only aloe vera gel, but may include a pharmaceutically acceptable carrier or the like for ease of administration.
본 발명의 조성물은 약제학적 분야에서 공지의 방법의 의해 제제화될 수 있고, 그 자체 또는 약제학적으로 허용되는 담체, 부형제 등과 혼합하여 약제학적으로 통상으로 허용되는 약학적 제제, 예를 들면 액제, 시럽제, 캡슐제 등으로 제제화될 수 있으며, 이들은 경구 또는 비경구로 투여될 수 있다. 본 발명의 조성물은 분말로써 경구 투여하는 것이 바람직하다.The compositions of the present invention may be formulated by methods known in the pharmaceutical art, and may be mixed with themselves or with a pharmaceutically acceptable carrier, excipient, and the like to be a pharmaceutically conventionally acceptable pharmaceutical agent such as a liquid or a syrup. , Capsules and the like, which can be administered orally or parenterally. The composition of the present invention is preferably administered orally as a powder.
상기 본 발명의 조성물을 포함하는 액제, 캡슐제 등은 건강기능식품으로 사용하는 것이 바람직하며, 본 발명에서 사용된, 용어 "건강기능식품"이라 함은 인체에 유용한 기능성을 가진 원료나 성분을 사용하여 정제, 캅셀, 분말, 과립, 액상, 환 등의 형태로 제조 가공한 식품을 말한다.The liquid, capsules and the like containing the composition of the present invention is preferably used as a health functional food, the term "health functional food" used in the present invention is used as a raw material or ingredient having a useful functionality to the human body Refers to food products manufactured and processed in the form of tablets, capsules, powders, granules, liquids, and pills.
본 발명의 조성물은 체내에서 활성성분의 흡수도, 배설속도, 환자의 연령 및 체중, 성별 및 상태, 치료할 질병의 중증정도 등에 따라 적절히 선택되나, 일반적으로 성인에게 1일 10∼5,000mg/일, 바람직하게는 100∼2,000mg/일로 투여하는 것이 바람직하다. 이렇게 제형화된 단위투여형 제제는 필요에 따라 일정시간 간격으로 수회 투여할 수 있다.The composition of the present invention is appropriately selected according to the absorption of the active ingredient in the body, the rate of excretion, the age and weight of the patient, the sex and condition, the severity of the disease to be treated, etc., but generally in adults 10 to 5,000mg / day, It is preferable to administer at 100 to 2,000 mg / day. The unit dosage form so formulated may be administered several times at regular time intervals as needed.
이하, 본 발명을 인체에 가장 많은 종류의 유해 독성 물질에 노출되는 흡연자를 대상으로 하여 알로에의 흡연독성 예방, 억제, 유해 독성 물질의 배설 촉진 또는 해독작용에 대해 기술하나, 예시된 벤조[a]피렌은 담배연기 뿐만 아니라 자동차 배기가스 등에도 존재하므로, 본 발명의 독성물질 해독용 조성물이 흡연으로 인한 독성물질의 해독에만 한정되는 것은 아니다.Hereinafter, the present invention will be described for a smoker who is exposed to the most harmful toxic substance to the human body, preventing, inhibiting, promoting the excretion or detoxification of toxic toxic substances in aloe, but exemplified benzo [a] Since pyrene is present not only in cigarette smoke but also in automobile exhaust, etc., the composition for detoxifying the toxic substance of the present invention is not limited to the detoxification of toxic substances due to smoking.
상기와 같이, 흡연 등에 의해 발생하는 대표적인 독성물질인 벤조[a]피렌은 유해 발암물질이고, 다른 독성물질인 니코틴은 NNK 등 담배 특이적 발암물질을 만들어 내는 전구물질일 뿐만 아니라, 담배의 습관성 및 다양한 독성작용을 가지고 있다.As described above, benzo [a] pyrene, which is a representative toxic substance caused by smoking, is a harmful carcinogen, and nicotine, another toxic substance, is not only a precursor for producing tobacco-specific carcinogens such as NNK, but also habits of tobacco and It has a variety of toxic effects.
본 발명의 조성물은 상기와 같은 벤조[a]피렌, 니코틴 등의 독성물질의 배설을 촉진함으로써 해독작용을 나타낸다.The composition of the present invention exhibits detoxification by promoting the excretion of toxic substances such as benzo [a] pyrene and nicotine.
본 발명의 두 번째 양상은 혈중 질병 지표 물질을 감소시키는 것을 특징으로 하는 독성물질 해독용 조성물을 제공하는 것이다.A second aspect of the present invention is to provide a composition for detoxifying a toxic substance, which reduces blood disease markers.
본 발명의 조성물은 하기 실험예의 혈액의 질병과 관련된 인자들의 생화학적 지표 연구에서도 월등한 효과를 나타냈다. 따라서, 본 발명의 조성물은 상기와 같이 혈액의 질병과 관련된 인자, 즉, 크레아티닌, 글루코스, 빌리루빈의 혈중 농도를 저하시켜 상기 인자들의 증가로 발생되는 질환 또는 질환으로 인해 발생되는 비정상적인 증가 현상을 정상화시킴으로써 질병치료 및 예방효과를 기대할 수 있다.The composition of the present invention showed an excellent effect even in the study of biochemical indicators of factors related to the disease of the blood of the following experimental example. Thus, the composition of the present invention by lowering the blood concentration of factors associated with the disease of the blood, ie creatinine, glucose, bilirubin as described above to normalize the abnormal increase caused by the disease or disorder caused by the increase of these factors It can be expected to treat and prevent diseases.
본 발명은 세 번째 양상은 알로에 베라 겔을 포함하는 독성물질 해독 효과를 갖는 식품학적 조성물을 제공하는 것이다.The third aspect of the present invention is to provide a food composition having a toxic substance detoxifying effect including aloe vera gel.
상기 식품학적 조성물은 음료, 요구르트, 차(tea), 아이스크림, 캔디, 젤리, 빵, 떡 또는 국수 등이 바람직하며, 이에 제한되지는 않는다.The food composition is preferably a beverage, yogurt, tea, ice cream, candy, jelly, bread, rice cake or noodles, but is not limited thereto.
이하, 본 발명을 하기 실시예를 통하여 더욱 상세히 설명한다. 이들 실시예는 본 발명의 예시 목적을 위한 것이며, 본 발명의 보호범위를 제한하고자 하는 것은 아니다.Hereinafter, the present invention will be described in more detail with reference to the following examples. These examples are for illustrative purposes of the present invention and are not intended to limit the protection scope of the present invention.
실험예 1. 벤조[a]피렌의 배설 측정Experimental Example 1. Measurement of excretion of benzo [a] pyrene
하루 1갑 이상의 담배를 피우는 흡연자 10명을 대상으로 1달 동안 시판 액티브 알로에TM(알로콥(Aloecorp), 미국)를 600mg/일의 용량으로 하루 두 번(아침, 저녁) 경구 투여하고, 1주 간격으로 아침에(8∼9시) 뇨(urine)를 채취하였다. 상기 액티브 알로에를 투여하지 않은 하루 1갑 이상의 담배를 피우는 흡연자 10명을 양성대조군으로 하고, 비흡연자 10명을 음성대조군으로 하여, 상기와 마찬가지 방법으로 뇨를 채취하였다.For 10 smokers who smoke one or more packs of cigarettes daily, oral administration of commercially active Aloe TM (Aloecorp, USA) twice daily (morning and evening) at a dose of 600 mg / day for 1 month, and 1 week Urine was collected in the morning (8-9 hours) at intervals. Urine was collected in the same manner as above, with 10 smokers who smoked one or more packs of cigarettes per day that were not administered the active aloe as positive controls and 10 non-smokers as negative controls.
4ml 뇨 샘플에 내부 표준 BaP-7,8-디하이드로디올(네셔날 캔서 인스티튜트, Bethesda, MD) 150㎕(200ng/ml)를 첨가하였다. 여기에 4ml의 클로로포름을 가하고, 1시간동안 진탕시켰다. 그후, 10분동안 원심분리시키고(3,500×g), 3ml의 유기상을 취하여 N2가스로 건고시켰다. 다시 300㎕ 메탄올에 녹인 후, 0.45um 필터로 여과하여 샘플을 제조하였다.To 4 ml urine sample 150 μl (200 ng / ml) of internal standard BaP-7,8-dihydrodiol (National Cancer Institute, Bethesda, MD) was added. 4 ml of chloroform was added thereto and shaken for 1 hour. Thereafter, it was centrifuged for 10 minutes (3,500 x g), and 3 ml of the organic phase was taken and dried with N 2 gas. After dissolving in 300 μl methanol and filtering with a 0.45um filter to prepare a sample.
상기 샘플(20㎕)을 HPLC system을 이용하여 벤조[a]피렌을 정량하였다. HPLC 분석 조건은 다음과 같다The sample (20 μl) was quantified benzo [a] pyrene using an HPLC system. HPLC analysis conditions are as follows.
1. HITACHI-Model L-7200 Autosampler; 2. Model L-7100 Pump; 3. Model L-7610 Degasser; 4. Model D-7000/6000 Interfadce Module; 5. Model FP-920 Fluorescence Detector(JASCO); 6. colume, Novapak C18 컬럼(15×0.37(i.d.)), 4um paricle, waters); 7. 용매 구배 0분-A용매(80%), B용매(20%), 20분-A용매(12%), B용매(88%)(선형 구배)(A용매-50:50(물:메탄올)/B용매-메탄올); 8. 유출 속도-1.2ml/분.1.HITACHI-Model L-7200 Autosampler; 2.Model L-7100 Pump; 3.Model L-7610 Degasser; 4.Model D-7000 / 6000 Interfadce Module; 5. Model FP-920 Fluorescence Detector (JASCO); 6. colume, Novapak C18 column (15 × 0.37 (i.d.)), 4um paricle, waters; 7. Solvent gradient 0 min-A solvent (80%), B solvent (20%), 20 min-A solvent (12%), B solvent (88%) (linear gradient) (A solvent-50: 50 (water : Methanol) / B solvent-methanol); 8. Spill rate-1.2 ml / min.
BaP의 양은 Fluorescence Detector(exi/emi:265/450nm)에 의한 높이 비로 계산하였으며, 단위는 ng/ml로 나타내었고, 그 결과를 도 1에 나타내었다. 통계학적 분석은 one-way analysis of variance(ANOVA)의 Bonferroni t-test와 Dunnett's 방법에 의한 통계적 유의성을 검토하였다(*: p<0.05, **: p<0.01, ***: p<0.001)The amount of BaP was calculated by the height ratio by Fluorescence Detector (exi / emi: 265 / 450nm), and the unit was expressed in ng / ml, and the results are shown in FIG. 1. Statistical analysis examined the statistical significance of Bonferroni t-test and Dunnett's method of one-way analysis of variance (ANOVA) (*: p <0.05, **: p <0.01, ***: p <0.001).
도 1에서 알 수 있는 바와 같이, 본 발명의 알로에 베라 겔 투여군은 대조군에 비하여 알로에 베라 겔 투여후 2주 째부터 유의성있게(p<0.001) 벤조[a]피렌의 배설이 촉진되었으며, 투여후 3, 4주 째에도 유의성있게(p<0.001) 벤조[a]피렌의 배설이 촉진되었다.As can be seen in Figure 1, the aloe vera gel administration group of the present invention was significantly (p <0.001) benzo [a] pyrene excretion was promoted from the second week after aloe vera gel administration compared to the control group, 3 The excretion of benzo [a] pyrene was also accelerated significantly at week 4 (p <0.001).
실험예 2. 코티닌의 배설 측정Experimental Example 2. Measurement of excretion of cotinine
상기 실험예 1과 같이, 흡연자 2군에 1달 동안 액티브 알로에TM(알로콥(Aloecorp), 미국)(600mg/일)를 투여하고, 1주 간격으로 아침에(8∼9시) 뇨(urine)를 채취하였다.As in Experiment 1, two groups of smokers were administered with active Aloe TM (Aloecorp, USA) (600 mg / day) for one month, and urine in the morning (8-9 hours) at weekly intervals. ) Was collected.
4ml 뇨 샘플에 2ml NaOH(5몰/L)를 가하고 내부 표준으로서 100㎕의 2-페닐이미다졸(20㎍/ml. 시그마사(St. Louis, MO))을 첨가하였다. 여기에 4ml의 클로로포름을 가하고, 1시간동안 진탕시켰다. 그후, 10분동안 원심분리시키고(3,500×g), 3ml의 유기상을 취하여 N2가스로 건고시켰다. 다시 300㎕ 메탄올에 녹인 후, 0.45um 필터로 여과하여 샘플을 제조하였다.2 ml NaOH (5 mol / L) was added to a 4 ml urine sample and 100 μl of 2-phenylimidazole (20 μg / ml. Stig. Louis, Mo.) was added as an internal standard. 4 ml of chloroform was added thereto and shaken for 1 hour. Thereafter, it was centrifuged for 10 minutes (3,500 x g), and 3 ml of the organic phase was taken and dried with N 2 gas. After dissolving in 300 μl methanol and filtering with a 0.45um filter to prepare a sample.
상기 샘플(20㎕)을 실험예 1과 같은 HPLC system으로 코티닌을 정량하고, 그 결과를 도 2에 나타내었다.Cotinine was quantified in the sample (20 μl) using the same HPLC system as in Experimental Example 1, and the results are shown in FIG. 2.
도 2에서 알 수 있는 바와 같이, 본 발명의 알로에 베라 겔 투여군이 흡연 대조군에 비하여 알로에 베라 겔 투여후 3주 째부터 유의성있게(p<0.001) 코티닌의 배설이 촉진되었으며, 투여후 4주 째에도 유의성있게(p<0.001) 코티닌의 배설이 촉진되었다.As can be seen in Figure 2, the aloe vera gel administration group of the present invention was significantly (p <0.001) promoted the excretion of cotinine from the third week after aloe vera gel administration compared to the smoking control, even at 4 weeks after administration Significantly (p <0.001) the excretion of cotinine was promoted.
이와같이 알로에 베라 겔이 니코틴의 대사물인 코티닌의 배설을 촉진시키므로, 담배의 중독성분인 니코틴의 배설을 촉진시킴을 알 수 있다.In this way, aloe vera gel promotes the excretion of nicotine, a metabolite of nicotine, and thus, promotes the excretion of nicotine, a poisoning component of tobacco.
실험예 3. 크레아티닌, 글루코스 및 빌리루빈의 혈중농도 측정Experimental Example 3 Measurement of Blood Levels of Creatinine, Glucose and Bilirubin
상기 실험예 1과 같이, 흡연자 2군에 1달 동안 액티브 알로에TM(알로콥(Aloecorp), 미국)(600mg/일)를 투여하고, 1주 간격으로 아침에(8∼9시) 혈액을 채취하였다. 크레아티닌, 글루코스 및 빌리루빈의 혈중농도의 측정법은 하기와 같다As in Experiment 1, two groups of smokers were administered with active Aloe TM (Aloecorp, USA) (600 mg / day) for one month, and blood was collected in the morning (8-9 hours) at weekly intervals. It was. The measurement of blood levels of creatinine, glucose and bilirubin is as follows.
(1) 크레아티닌의 농도 측정법(1) How to measure the concentration of creatinine
혈액을 실험군으로부터 수집하여 원심분리(3,000rpm, 15분) 하고, 상등액(serum)을 분리하였다. 혈청 15ul 주입하여 Autoanalyzer Hitachi 7170을 이용하여 분석하였다. 분석법은 Jaffe Kinetic법을 이용하였다.Blood was collected from the experimental group, centrifuged (3,000 rpm, 15 minutes), and the supernatant (serum) was separated. 15ul serum was injected and analyzed using Autoanalyzer Hitachi 7170. Jaffe Kinetic method was used for the analysis.
(2) 글루코스의 농도 측정법(2) measuring the concentration of glucose
혈액을 실험군으로부터 수집하여 원심분리(3,000rpm, 15분)하고, 상등액(serum)을 분리하였다. 혈청 2.5ul 주입하여 Autoanalyzer Hitachi 7170을이용하여 분석하였다. 분석법은 oxidase법을 이용하였다.Blood was collected from the experimental group, centrifuged (3,000 rpm, 15 minutes), and the supernatant (serum) was separated. 2.5ul of serum was injected and analyzed using Autoanalyzer Hitachi 7170. Assay, oxidase method was used.
(3) 빌리루빈의 농도 측정법(3) method for measuring the concentration of bilirubin
혈액을 실험군으로부터 수집하여 원심분리(3,000rpm, 15분)하고, 상등액(serum)을 분리하였다. 혈청 4ul 주입하여 Autoanalyzer Hitachi 7170을 이용하여 분석하였다. 분석법은 Jendrassick-Cleghorn법을 이용하였다.Blood was collected from the experimental group, centrifuged (3,000 rpm, 15 minutes), and the supernatant (serum) was separated. 4ul of serum was injected and analyzed using Autoanalyzer Hitachi 7170. Jendrassick-Cleghorn method was used for the analysis.
상기 샘플(20㎕)의 크레아티닌, 글루코스 및 빌리루빈의 혈중농도 측정하여, 대조군과 비교하였고, 그 결과를 도 3, 4 및 5에 나타내었다.Plasma concentrations of creatinine, glucose and bilirubin of the sample (20 μl) were measured and compared with the control group, and the results are shown in FIGS. 3, 4 and 5.
도 3과 같이, 본 발명의 알로에 베라 겔 투여군이 대조군에 비하여 알로에 베라 겔 투여후 3주 째에 흡연 대조군에 비해 혈중 크레아티닌 농도가 유의성있게(p<0.01) 감소하였으며, 4주 째에도 유의성있게(p<0.001) 감소하였다.As shown in FIG. 3, the aloe vera gel-administered group of the present invention significantly decreased (p <0.01) the blood creatinine concentration at 3 weeks after the aloe vera gel administration compared to the control group, and also significantly at 4 weeks ( p <0.001) decreased.
또한 도 4와 같이, 본 발명의 알로에 베라 겔 투여군이 흡연 대조군에 비하여 알로에 베라 겔 투여후 2, 3, 4주에 걸쳐 유의성있게(p<0.001) 감소하였다.In addition, as shown in Figure 4, the aloe vera gel administration group of the present invention significantly decreased (p <0.001) over 2, 3, 4 weeks after aloe vera gel administration compared to the smoking control.
또한 도 5와 같이, 본 발명의 알로에 베라 겔 투여군이 흡연 대조군에 비하여 알로에 베라 겔 투여후 1주 째부터 대조군에 비해 혈중 빌리루빈 농도가 유의성있게(p<0.05) 감소하였으며, 2, 3, 4주 째에도 유의성있게(p<0.001) 감소하였다.In addition, as shown in Figure 5, the aloe vera gel administration group of the present invention significantly decreased (p <0.05) blood bilirubin concentration from the first week after the aloe vera gel administration compared to the smoking control group, 2, 3, 4 weeks Also decreased significantly (p <0.001).
상기 도 3, 4, 5와 같이, 알로에 베라 겔의 투여로 의해 혈액의 질병에 관련된 상기 인자 모두의 혈중농도를 저하시켜, 상기 인자들의 증가로 발생되는 질환의 치료 및 예방 효과도 기대할 수 있다.3, 4, and 5, the administration of aloe vera gel lowers the blood concentration of all the factors related to the disease of the blood, it can also be expected to treat and prevent the disease caused by the increase of the factors.
다음에 실시예로서 본 발명을 더욱 상세히 설명한다.Next, the present invention will be described in more detail by way of examples.
실시예 1 : 캡슐제의 제조Example 1 Preparation of Capsule
액티브 알로에TM600mgActive Aloe TM 600mg
유당 50mgLactose 50mg
전분 50mgStarch 50mg
탈크 2mgTalc 2mg
스테아린산마그네슘 적량Magnesium stearate appropriate amount
상기의 성분을 혼합하고 통상의 캡슐제의 제조방법에 따라서 젤라틴 캡슐에 충진하여 캡슐제를 제조하였다.The capsules were prepared by mixing the above ingredients and filling gelatin capsules according to a conventional method for preparing capsules.
실시예 2 : 캡슐제의 제조Example 2 Preparation of Capsules
알로에 베라 겔 추출물 200mgAloe Vera Gel Extract 200 mg
유당 100mgLactose 100mg
전분 93mgStarch 93mg
탈크 2mgTalc 2mg
스테아린산 마그네슘 적량Magnesium stearate proper amount
상기의 성분을 혼합하고 통상의 캡슐제의 제조방법에 따라서 젤라틴 캡슐에 충진하여 캡슐제를 제조하였다. 상기 알로에 베라 겔 추출물은 알로에 베라를 통상의 방법으로 추출하여 얻었다.The capsules were prepared by mixing the above ingredients and filling gelatin capsules according to a conventional method for preparing capsules. The aloe vera gel extract was obtained by extracting the aloe vera in a conventional manner.
실시예 3 : 액제의 제조Example 3 Preparation of Liquid
액티브 알로에TM600mgActive Aloe TM 600mg
설탕 20g20 g of sugar
이성화당 20g20 g of isomerized sugar
레몬향 적량Lemon flavor
정제수를 가하여 전체 100mlAdd 100 ml of purified water
상기의 성분을 통상의 액제의 제조방법에 따라서 혼합하고 100ml의 갈색병에 충진하고 멸균시켜서 액제를 제조하였다.The above components were mixed according to a conventional method for preparing a liquid, and filled into 100 ml brown bottles and sterilized to prepare a liquid.
실시예 4 : 액제의 제조Example 4 Preparation of Liquid
알로에 베라 겔 추출물 1,200mgAloe Vera Gel Extract 1,200 mg
설탕 20g20 g of sugar
이성화당 20g20 g of isomerized sugar
레몬향 적량Lemon flavor
정제수를 가하여 전체 100mlAdd 100 ml of purified water
상기의 성분을 통상의 액제의 제조방법에 따라서 혼합하고 100ml의 갈색병에 충진하고 멸균시켜서 액제를 제조하였다. 실시예 2과 마찬가지로, 상기 알로에 베라 겔 추출물은 알로에 베라를 통상의 방법으로 추출하여 얻었다.The above components were mixed according to a conventional method for preparing a liquid, and filled into 100 ml brown bottles and sterilized to prepare a liquid. As in Example 2, the aloe vera gel extract was obtained by extracting the aloe vera in a conventional manner.
실시예 5 : 음료의 제조Example 5 Preparation of Beverages
액티브 알로에TM5 중량%와 식용색소 0.05 중량%, 오렌지 에센스 0.05 중량%, 과당 7.0 중량%, 구연산 0.1중량%, 비타민 C 0.05 중량%를 포함하는 일반 기능성 음료 베이스를 첨가한 조성물을 제조한 다음, 정제수를 첨가하여 음료를 제조하였다.To prepare a composition comprising a general functional beverage base comprising 5% by weight active aloe TM and 0.05% food coloring, 0.05% orange essence, 7.0% fructose, 0.1% citric acid, 0.05% vitamin C, Purified water was added to prepare a beverage.
실시예 6 : 요구르트의 제조Example 6: Preparation of Yogurt
통상의 탈지분유(서울우유제품)에 본 발명의 액티브 알로에TM1 중량%를 첨가하여 균질화시킨 후 80℃에서 30분간 가열처리하였다. 37℃로 냉각시킨 후 요구르트 균주 락토바실러스 불가리쿠스를 접종하고, 37℃ 항온기에서 12시간 발효시킨 후, 4℃에서 냉장보관하여 숙성시켜 요구르트를 제조하였다.1% by weight of the active aloe TM of the present invention was added to a common skimmed milk powder (Seoul Milk Products), followed by heat treatment at 80 ° C. for 30 minutes. After cooling to 37 ℃ yogurt strain inoculated with Lactobacillus Bulgaricus, fermented in a 37 ℃ thermostat for 12 hours, and then refrigerated at 4 ℃ to prepare the yogurt.
이상에서 알 수 있는 바와 같이, 본 발명의 알로에 베라 겔을 포함하는 독성물질 해독용 조성물은 벤조[a]피렌, 니코틴 등의 독성물질의 배설을 촉진함으로써 우수한 독성물질 해독 효과를 가지며, 혈액의 질병과 관련된 인자들의 생화학적 지표 연구에서도 월등한 효과를 나타내어, 현대 사회의 각종 공해로 인한 독성물질, 환경호르몬 및 흡연 등으로 인한 독성물질을 해독할 수 있다.As can be seen from the above, the composition for detoxifying a toxic substance comprising the aloe vera gel of the present invention has an excellent toxic substance detoxifying effect by promoting the excretion of toxic substances such as benzo [a] pyrene, nicotine, and blood diseases. Biochemical indicators of related factors also show superior effects, which can detoxify toxic substances caused by various pollutions in modern society, environmental hormones and smoking.
Claims (8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020020025602A KR20030087726A (en) | 2002-05-09 | 2002-05-09 | Composition for detoxifying toxic substances having Aloe vera gel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020020025602A KR20030087726A (en) | 2002-05-09 | 2002-05-09 | Composition for detoxifying toxic substances having Aloe vera gel |
Publications (1)
Publication Number | Publication Date |
---|---|
KR20030087726A true KR20030087726A (en) | 2003-11-15 |
Family
ID=32382181
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020020025602A KR20030087726A (en) | 2002-05-09 | 2002-05-09 | Composition for detoxifying toxic substances having Aloe vera gel |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR20030087726A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100691605B1 (en) * | 2005-03-15 | 2007-03-09 | 숙명여자대학교산학협력단 | Food for preventing PAHs-related cancer diseases and a Method to define the same |
KR101127454B1 (en) * | 2008-01-25 | 2012-03-23 | 주식회사 유니베라 | Pharmaceutical composition comprising processed Aloe vera gel for preventing or treating type II diabetes |
-
2002
- 2002-05-09 KR KR1020020025602A patent/KR20030087726A/en not_active Application Discontinuation
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100691605B1 (en) * | 2005-03-15 | 2007-03-09 | 숙명여자대학교산학협력단 | Food for preventing PAHs-related cancer diseases and a Method to define the same |
KR101127454B1 (en) * | 2008-01-25 | 2012-03-23 | 주식회사 유니베라 | Pharmaceutical composition comprising processed Aloe vera gel for preventing or treating type II diabetes |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6030447B2 (en) | Composition containing green tea extract | |
Melis | Renal excretion of stevioside in rats | |
JP3730522B2 (en) | Smoking craving suppression composition | |
WO2020239035A1 (en) | Cigarette additive, preparation method therefor and application thereof | |
KR100526760B1 (en) | An oriental herb extracts composition having detoxification effect on the nicotine and dioxin | |
KR101325122B1 (en) | Composition for aid to stop smoking having effect of nicotine elimination and its manufacturing method | |
CN113616688B (en) | Anserine composition for repairing kidney injury and application thereof | |
JPH10508880A (en) | Pharmaceutical composition for diabetes | |
KR20030087728A (en) | Composition for detoxifying toxic substances having Aloe vera gel and propolis | |
KR20030087726A (en) | Composition for detoxifying toxic substances having Aloe vera gel | |
JPH0434382B2 (en) | ||
CN110719774A (en) | Composition for improving, preventing or treating sleep disorder or inhibiting tolerance to or reducing side effects of an agonist of the benzodiazepine binding site of GABA-A receptor, each composition comprising phloroglucinol as an active ingredient | |
KR100512912B1 (en) | Alcohol metabolism herbal medicine accelerator | |
JP2005023008A (en) | Internal liquid medicine composition containing vitamin b group | |
JP4706174B2 (en) | α-Glucosidase inhibitor | |
JP2006193501A (en) | Adiponectin regulating agent and food, drink, food additive and medicine containing the same | |
KR102421081B1 (en) | A composition for anti-smoke comprising niacin | |
KR102687132B1 (en) | A composition for the prevention or treatment of pain containin Plantago asiatica L extract | |
RU2257221C1 (en) | Helminthicide species | |
KR20040092232A (en) | Composition of Korean Red Ginseng for Improving Sexual Function, Manufacturing Method the Same and Its Use | |
JPH092966A (en) | Amylase inhibitor obtained from moutan cortex and diet food containing the same | |
CN102198166B (en) | New use of chemical ingredients of eucommia bark as nephroprotective agents | |
CN111773274A (en) | Application of coleus blumei and plantain seed composition in preparation of pharmaceutical composition for reducing blood sugar and blood pressure | |
CN111773352A (en) | Application of turmeric and plantain seed composition in preparation of pharmaceutical composition for reducing blood sugar and blood pressure | |
WO1998044937A1 (en) | Preventive or remedy for kidney diseases |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WITN | Withdrawal due to no request for examination |