CN108617921A - A kind of lycopene preparation method cooperateing with ingredient containing pectin etc. and have repair to prostate - Google Patents
A kind of lycopene preparation method cooperateing with ingredient containing pectin etc. and have repair to prostate Download PDFInfo
- Publication number
- CN108617921A CN108617921A CN201710182540.XA CN201710182540A CN108617921A CN 108617921 A CN108617921 A CN 108617921A CN 201710182540 A CN201710182540 A CN 201710182540A CN 108617921 A CN108617921 A CN 108617921A
- Authority
- CN
- China
- Prior art keywords
- lycopene
- pectin
- prostate
- catsup
- powder
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- OAIJSZIZWZSQBC-GYZMGTAESA-N lycopene Chemical compound CC(C)=CCC\C(C)=C\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C=C(/C)CCC=C(C)C OAIJSZIZWZSQBC-GYZMGTAESA-N 0.000 title claims abstract description 93
- 235000010987 pectin Nutrition 0.000 title claims abstract description 75
- 239000001814 pectin Substances 0.000 title claims abstract description 75
- 229920001277 pectin Polymers 0.000 title claims abstract description 75
- 210000002307 prostate Anatomy 0.000 title claims abstract description 17
- 239000004615 ingredient Substances 0.000 title abstract description 10
- 238000002360 preparation method Methods 0.000 title abstract description 5
- 230000008439 repair process Effects 0.000 title abstract description 5
- UPYKUZBSLRQECL-UKMVMLAPSA-N Lycopene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1C(=C)CCCC1(C)C)C=CC=C(/C)C=CC2C(=C)CCCC2(C)C UPYKUZBSLRQECL-UKMVMLAPSA-N 0.000 claims abstract description 87
- JEVVKJMRZMXFBT-XWDZUXABSA-N Lycophyll Natural products OC/C(=C/CC/C(=C\C=C\C(=C/C=C/C(=C\C=C\C=C(/C=C/C=C(\C=C\C=C(/CC/C=C(/CO)\C)\C)/C)\C)/C)\C)/C)/C JEVVKJMRZMXFBT-XWDZUXABSA-N 0.000 claims abstract description 87
- 229960004999 lycopene Drugs 0.000 claims abstract description 87
- 235000012661 lycopene Nutrition 0.000 claims abstract description 87
- 239000001751 lycopene Substances 0.000 claims abstract description 87
- ZCIHMQAPACOQHT-ZGMPDRQDSA-N trans-isorenieratene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/c1c(C)ccc(C)c1C)C=CC=C(/C)C=Cc2c(C)ccc(C)c2C ZCIHMQAPACOQHT-ZGMPDRQDSA-N 0.000 claims abstract description 87
- 230000000694 effects Effects 0.000 claims abstract description 37
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 20
- 238000000034 method Methods 0.000 claims abstract description 17
- 238000000605 extraction Methods 0.000 claims abstract description 9
- 102000004190 Enzymes Human genes 0.000 claims abstract description 4
- 108090000790 Enzymes Proteins 0.000 claims abstract description 4
- 239000000843 powder Substances 0.000 claims description 62
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 45
- 239000000047 product Substances 0.000 claims description 23
- 235000007688 Lycopersicon esculentum Nutrition 0.000 claims description 21
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 16
- 239000007864 aqueous solution Substances 0.000 claims description 16
- 239000000706 filtrate Substances 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 239000012046 mixed solvent Substances 0.000 claims description 12
- 239000000243 solution Substances 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 7
- 230000036541 health Effects 0.000 claims description 7
- 238000004321 preservation Methods 0.000 claims description 5
- 208000026455 prostate symptom Diseases 0.000 claims description 5
- 206010060862 Prostate cancer Diseases 0.000 claims description 4
- 238000000874 microwave-assisted extraction Methods 0.000 claims description 4
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims description 3
- 230000002265 prevention Effects 0.000 claims description 3
- 238000004140 cleaning Methods 0.000 claims description 2
- 241000227653 Lycopersicon Species 0.000 claims 2
- 239000003814 drug Substances 0.000 abstract description 7
- 229940079593 drug Drugs 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract description 2
- 239000004480 active ingredient Substances 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000010178 pectin extract Substances 0.000 abstract 1
- 241000699666 Mus <mouse, genus> Species 0.000 description 25
- 240000003768 Solanum lycopersicum Species 0.000 description 19
- 206010028980 Neoplasm Diseases 0.000 description 17
- 201000011510 cancer Diseases 0.000 description 15
- 238000002474 experimental method Methods 0.000 description 10
- 230000006870 function Effects 0.000 description 9
- 238000011160 research Methods 0.000 description 9
- 230000002401 inhibitory effect Effects 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- 230000001093 anti-cancer Effects 0.000 description 6
- 230000000259 anti-tumor effect Effects 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 238000003304 gavage Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 4
- 241000207199 Citrus Species 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- 108091005804 Peptidases Proteins 0.000 description 3
- 239000004365 Protease Substances 0.000 description 3
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 3
- 235000020971 citrus fruits Nutrition 0.000 description 3
- 239000000284 extract Substances 0.000 description 3
- 235000013373 food additive Nutrition 0.000 description 3
- 239000002778 food additive Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 206010020718 hyperplasia Diseases 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 238000011552 rat model Methods 0.000 description 3
- 208000024891 symptom Diseases 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 208000007848 Alcoholism Diseases 0.000 description 2
- 206010003504 Aspiration Diseases 0.000 description 2
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 description 2
- AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 102000000802 Galectin 3 Human genes 0.000 description 2
- 108010001517 Galectin 3 Proteins 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- PDMMFKSKQVNJMI-BLQWBTBKSA-N Testosterone propionate Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](OC(=O)CC)[C@@]1(C)CC2 PDMMFKSKQVNJMI-BLQWBTBKSA-N 0.000 description 2
- MUMGGOZAMZWBJJ-DYKIIFRCSA-N Testostosterone Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 MUMGGOZAMZWBJJ-DYKIIFRCSA-N 0.000 description 2
- 206010057362 Underdose Diseases 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- 201000007930 alcohol dependence Diseases 0.000 description 2
- 238000010171 animal model Methods 0.000 description 2
- 230000004663 cell proliferation Effects 0.000 description 2
- 239000006285 cell suspension Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 206010012601 diabetes mellitus Diseases 0.000 description 2
- 235000013325 dietary fiber Nutrition 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 231100000673 dose–response relationship Toxicity 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000001054 red pigment Substances 0.000 description 2
- 229960001712 testosterone propionate Drugs 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- 235000014101 wine Nutrition 0.000 description 2
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 description 1
- 201000001320 Atherosclerosis Diseases 0.000 description 1
- 208000012639 Balance disease Diseases 0.000 description 1
- 244000241235 Citrullus lanatus Species 0.000 description 1
- 235000012828 Citrullus lanatus var citroides Nutrition 0.000 description 1
- 244000276331 Citrus maxima Species 0.000 description 1
- 235000001759 Citrus maxima Nutrition 0.000 description 1
- 101800004637 Communis Proteins 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- 206010013457 Dissociation Diseases 0.000 description 1
- 244000283207 Indigofera tinctoria Species 0.000 description 1
- 240000008790 Musa x paradisiaca Species 0.000 description 1
- 235000018290 Musa x paradisiaca Nutrition 0.000 description 1
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 description 1
- 240000005373 Panax quinquefolius Species 0.000 description 1
- 235000003140 Panax quinquefolius Nutrition 0.000 description 1
- 241000531314 Premna microphylla Species 0.000 description 1
- 244000061458 Solanum melongena Species 0.000 description 1
- 235000002597 Solanum melongena Nutrition 0.000 description 1
- 241001593968 Vitis palmata Species 0.000 description 1
- 210000001015 abdomen Anatomy 0.000 description 1
- 206010000059 abdominal discomfort Diseases 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229940009456 adriamycin Drugs 0.000 description 1
- 230000001548 androgenic effect Effects 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 230000001142 anti-diarrhea Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000021028 berry Nutrition 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 235000021466 carotenoid Nutrition 0.000 description 1
- 150000001747 carotenoids Chemical class 0.000 description 1
- 239000006143 cell culture medium Substances 0.000 description 1
- 238000001516 cell proliferation assay Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 230000009514 concussion Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 208000018459 dissociative disease Diseases 0.000 description 1
- 208000002173 dizziness Diseases 0.000 description 1
- 231100000880 dysequilibrium Toxicity 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 229960005309 estradiol Drugs 0.000 description 1
- 229930182833 estradiol Natural products 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000000576 food coloring agent Substances 0.000 description 1
- 239000004459 forage Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 235000013376 functional food Nutrition 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 235000008434 ginseng Nutrition 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 230000027939 micturition Effects 0.000 description 1
- 239000002547 new drug Substances 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 238000001543 one-way ANOVA Methods 0.000 description 1
- 238000011022 operating instruction Methods 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 150000003180 prostaglandins Chemical class 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000012109 statistical procedure Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229960003604 testosterone Drugs 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000003202 urodynamic effect Effects 0.000 description 1
- 235000020097 white wine Nutrition 0.000 description 1
- 239000010151 yanghe Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
-
- 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
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/20—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents
- A23L29/206—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents of vegetable origin
- A23L29/231—Pectin; Derivatives thereof
-
- 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
- A23L3/00—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
- A23L3/40—Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by drying or kilning; Subsequent reconstitution
- A23L3/44—Freeze-drying
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Dispersion Chemistry (AREA)
- Botany (AREA)
- Mycology (AREA)
- Medicines Containing Plant Substances (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
The present invention discloses a kind of lycopene preparation method cooperateing with ingredient containing pectin etc. and have repair to prostate, using mixed organic solvents formulation and enzyme extraction method combination by catsup lycopene and pectin extract simultaneously, not only solve the loss of the active ingredients such as pectin in extraction process, also by pectin and lycopene relieve the effect of alcohol, the effect in terms of pre- preventing drunkenness and anti-prostate more efficiently cooperates with, combination efficacy and saferry is significantly better than single drug, plays better health-care effect in this way.The extracting method is industrially feasible, and technical process is simple, and the security performance of product is high, and yield is high.
Description
Technical field
The invention belongs to natural health care evaluation and exploration technology fields, and it is a kind of containing the collaboration ingredient such as pectin and right to be related to
Prostate has the lycopene preparation method of repair.
Background technology
Lycopene (Lycopene) is a kind of fat-soluble natural pigment, is one kind of carotenoid, is widely present in certainly
It in right boundary, is primarily present in the plants such as ripe tomato, watermelon, the careless shaddock certain kind of berries, red grape, in recent years, research is found kind
Lycopene has various biological activity, has quenching activity oxygen, eliminates human free radical, slow down atherosclerosis, prevent
Kinds cancer, relieve the effect of alcohol (patent application publication number CN104800182A disclose lycopene make invention as main component have compared with
Good antialcoholism function) and the different physiological roles such as strengthen immunity.Lycopene can not only be used for the drug or related of anticancer, anti-cancer
Health products (patent application publication number CN104800181A discloses lycopene to be enhanced as the invention of main ingredient
There is good effect in terms of prostatic function), food additives, cosmetics, food coloring etc. are also can be used as, application prospect is wide
It is general.
The average content of lycopene is 8.5mg.l00g-1 in tamato fruit, but its biological value is not high, eats a life
Tomato can only absorb the lycopene of 0.05mg, and one day tomato that need to absorb 1-2kg of adult could meet normal physiology need
It asks, the unbalanced of diet must be caused in this way.From the perspective of development, lycopene is developed very necessary at drug.And
Currently, the exploitation of lycopene Healthy relevant products has become a hot spot of functional food in the world and new drug research.
For pectin as a kind of water-soluble dietary fiber, a kind of natural plant polyose is complicated, vdiverse in function.Currently,
Raw material for producing commodity pectin is mainly citrus and apple.In addition, there is numerous studies from premna microphylla, tomato and banana
Pectin is extracted in the by-products such as skin.Pectin is a kind of to be recommended as not limited by addition by FAO/WHO food additives joint committee
The food additives of amount, due to remarkable gelation and emulsion stability as a kind of important additive in food industry
In be used as thickener, gelling agent, can be shared individually or with other excipient in pharmaceuticals industry and prepare ointment, film, suppository, micro-
The pharmaceutical preparations such as capsule.Pharmaceutical research shows that pectin has anticancer, anti diar rhea as soluble dietary fiber, relieves the effect of alcohol (2014
It is relatively good that the researchs such as Li quintessences have shown that pectin has the function of in terms of relieving the effect of alcohol with pre- preventing drunkenness), treatment diabetes and other effects.More
Carry out the anticancer effect that target diversion is studied pectin by more scholars, it is found that pectin can be used as internal galectin-3
(Galectin-3) competitive inhibitor of ligand, preventing the formation of tumour, (researchs such as Lu Sheng people in 2012 have shown that fruit with development
Glue has the effect of that prostate gland cancer cell is inhibited to be proliferated well).China's research antitumor about pectin starts from 2005, main
Concentrate on the effect aspect of citrus low molecule pectin and ginseng pectin to tumour.Foreign countries are about antitumor seminar master
Concentrate on the U.S. and Japan, the U.S. in 1993 just about the antitumor patent of low molecule pectin, it is external in the past 20 years to close
Made rapid progress is achieved in the antitumor research of pectin, has large size pharmacy corporation and is applied to pectin to prepare targeting anti-tumor medicine
Object space face, wherein pectin adriamycin have been enter into preclinical phase.
Currently, the raw material of lycopene is mainly derived from tomato, the raw material of pectin is mainly derived from citrus and apple.This
Outside, some researches show that tomato is equally applied to as the source of pectin in the research of extracting method, and result of study is shown kind
Pectin content in eggplant is up to 0.72%.
Invention content
The purpose of the present invention is the above-mentioned deficiencies for the prior art, provide a kind of containing the collaboration ingredient such as pectin and to preceding
Row gland has the lycopene preparation method of repair.
What the present invention was achieved through the following technical solutions.
A kind of extracting method of the lycopene containing pectin, includes the following steps:
(1) fresh tomato, cleaning plus water are weighed, 100 DEG C of heat preservation 15min is heated to, smashs into catsup after being rinsed with water to pieces;
(2) it is added mixed solvent into catsup, the solid-liquid ratio of catsup and mixed solvent is 1:2.0~4.0, wherein
The mixed solvent is made of the aqueous solution of acid in ethyl acetate, and the volume ratio of sour aqueous solution and ethyl acetate is 1:0.5
~1.5;
(3) between the pH 2.0~3 for adjusting (2) solution, then biological enzyme is added into system, is heated to 40~60 DEG C, enzyme
For solution after 3~5 hours, the catsup liquid handled carries out Microwave Extraction, is filtered by vacuum after extraction, and filtrate is collected, and retains
Filter residue;
(4) filter residue ethyl acetate, sour aqueous solution filter after extracting successively, merge with filtrate in (3);
(5) filtrate, the lycopene powder product for being freeze-dried containing pectin are concentrated.
Wherein in step (1), 2~4 times of the preferred tomato weight of water weight of addition.
In step (2), the preferred hydrochloric acid of acid, and a concentration of 0.2mol/L of the aqueous acid medium of acid.
In step (3), Microwave Extraction time preferably 10~35min, ultrasonic power 100-200W.
The mass ratio of pectin and lycopene is in the lycopene powder product containing pectin:1:1~
100。
The pectous lycopene prepared according to above-mentioned extracting method.
Pectous lycopene of the present invention is preparing anti-prostate cancer, is improving male prostate symptom, prevention
The drunk application in the health products to relieve the effect of alcohol.
A kind of to improve male prostate function, the health products that relieve the effect of alcohol, it is characterised in that containing of the present invention containing pectin
Lycopene.
Advantageous effect:
Lycopene powder containing pectin composition made of of the invention, had both remained the healthcare functions such as lycopene, had
There are anti-oxidant, anticancer, anti-aging, relieve the effect of alcohol and the effects that pre- preventing drunkenness;The healthcare function for also supplementing pectin simultaneously has anti-
The effects that diarrhea, anticancer, treatment diabetes.Wherein lycopene and pectin, which all have, relieves the effect of alcohol, before pre- preventing drunkenness and prevention
The function of row parathyrine cancer, and the present invention is made lycopene powder and contains pectin and lycopene simultaneously, the two ingredients are total to
With in the presence of collaboration improve human body relieve the effect of alcohol, pre- preventing drunkenness and the ability for preventing prostaglandin cancer etc..Extract tomato red
Pectin with synergy is proposed to have many advantages, such as to reduce extraction cost while plain, it is easy to operate;Using vacuum refrigeration
This dry physical method is dried, and reduces chemical contamination;The method of the present invention is simple, and the course of work is easily operated;The present invention
Raw material sources are extensive, cheap, and production cost is low, and working condition is mild, and environmental pollution is small.
Specific implementation mode
The invention will be further described by the following examples.
Embodiment 1
Fresh tomato 500g is weighed, is positioned in beaker after washing with water, the water of 2 times of tomato weight is added, is heated to 100
DEG C heat preservation 15min, smash into catsup after being rinsed with water to pieces.Mixed solvent is added into catsup (i.e. containing ethyl acetate
The aqueous solution of 0.2mol/L hydrochloric acid), the wherein aqueous solution of hydrochloric acid:Ethyl acetate=1:0.5 (V/V), catsup and mixed solvent
Solid-liquid ratio be 1:2.0(g/mL);Between the pH 2.0 for adjusting solution, then protease is added into system, heating temperature 50
DEG C, enzymolysis is after 3 hours, and processing obtains catsup liquid input microwave device, and (it is public that day wawter bloom justifies pharmaceutical equipment science and technology Limited Liability
Department) it extracts, microwave mixing time is 10min, and ultrasonic power 150W is filtered by vacuum after extraction, collects filtrate, is protected
Stay filter residue;Filter residue ethyl acetate, sour aqueous solution filter after extracting successively, merge with above-mentioned gained filtrate;Filtrate is concentrated, it is cold
Be lyophilized it is dry, weigh lycopene powder 40g, HPLC method to measure wherein lycopene content be 28g, pectin content is
3.7g。
Embodiment 2
Fresh tomato 1Kg is weighed, is positioned in beaker after washing with water, the water of 3 times of tomato weight is added, is heated to 100
DEG C heat preservation 15min, smash into catsup after being rinsed with water to pieces.Mixed solvent is added into catsup (i.e. containing ethyl acetate
The aqueous solution of 0.2mol/L hydrochloric acid), the wherein aqueous solution of hydrochloric acid:Ethyl acetate=1:1 (V/V), catsup and mixed solvent
Solid-liquid ratio is 1:3.0(g/mL);Between the pH 2.5 for adjusting solution, then protease being added into system, heating temperature is 40 DEG C,
Enzymolysis 4 hours after, processing obtain catsup liquid input microwave device (Huayuan Pharmaceutical Equipment Science & Technology Co., Ltd., Tianshui) into
Row extraction, microwave mixing time are 30min, and ultrasonic power 100W is filtered by vacuum after extraction, collect filtrate, retain filter
Slag;Filter residue ethyl acetate, sour aqueous solution filter after extracting successively, merge with above-mentioned gained filtrate;Filtrate is concentrated, freezing is dry
Dry, weighing obtains lycopene powder 0.13Kg, HPLC method and measures wherein lycopene content to be 0.094Kg, and pectin contains
Amount is 12.1g.
Embodiment 3
Fresh tomato 10Kg is weighed, is positioned in beaker after washing with water, the water of 4 times of tomato weight is added, is heated to 100
DEG C heat preservation 15min, smash into catsup after being rinsed with water to pieces.Mixed solvent is added into catsup (i.e. containing ethyl acetate
The aqueous solution of 0.2mol/L hydrochloric acid), the wherein aqueous solution of hydrochloric acid:Ethyl acetate=1:1.5 (V/V), catsup and mixed solvent
Solid-liquid ratio be 1:4.0(g/mL);Between the pH 3.0 for adjusting solution, then protease is added into system, heating temperature 60
DEG C, enzymolysis is after 5 hours, and processing obtains catsup liquid input microwave device, and (it is public that day wawter bloom justifies pharmaceutical equipment science and technology Limited Liability
Department) it extracts, microwave mixing time is 20min, and ultrasonic power 200W is filtered by vacuum after extraction, collects filtrate, is protected
Stay filter residue;Filter residue ethyl acetate, sour aqueous solution filter after extracting successively, merge with above-mentioned gained filtrate;Filtrate is concentrated, it is cold
Be lyophilized it is dry, weighing obtain lycopene powder 1.44Kg, HPLC method and measure lycopene content wherein in powder be
1.24Kg, pectin content 139.8g.
The lycopene of ingredient is cooperateed with to have containing pectin below by way of being further illustrated the present invention to specific test of pesticide effectiveness example
There is prostatic function.
Embodiment 4
Anti-prostate cancer cell in vivo studies
1, materials and methods
1.1 sample
The lycopene powder that ingredient is cooperateed with containing pectin of the present invention;Pure lycopene powder identical as content of the present invention
End;Pure pectin powder identical as content of the present invention.
1.2 cell
Human prostata cancer PC3 cells are purchased from Chinese Academy of Sciences's Shanghai cell bank
The selection of 1.3 dosage
The lycopene powder of embodiment 3, pure lycopene powder, pure pectin powder are prepared as sample with DMSO (AR)
The solution example of product, each powder is as follows:
Lycopene powder (a of embodiment 31):10309ug/mL、5155ug/mL、2557ug/mL、1031ug/mL;
Pure lycopene powder (a2):8876ug/mL、4438ug/mL、2202ug/mL、888ug/mL;
Pure pectin powder (a3):1000ug/mL、500ug/mL、250ug/mL、100ug/mL;
2, test method
By the good human prostata cancer PC3 cell dissociations of growth conditions, human prostata cancer PC3 cell suspensions are obtained, and carry out
Cell concentration is adjusted to 1 × 10 by cell count according to counting5A/mL;According to the volume in the holes 180uL/ by a concentration of 1 × 105
The human prostata cancer PC3 cell suspension inoculations of a/mL are cultivated for 24 hours in 96 orifice plates in 5%CO2,37 DEG C of cell incubators;
The solution example of tri- kinds of powder of 20uL is added in 96 orifice plates again, three multiple holes are arranged in each concentration gradient, are averaged, with not
The blanc cell culture medium of dosing is blank control group.In 5%CO2, cultivate for 24 hours in 37 DEG C of cell incubators;5 are added per hole
Mg/mL MTT solution 10uL, are placed in 4h in incubator, abandon supernatant, and the holes DMSO 100uL/ are added, and concussion 15min makes purple
Crystallization is completely dissolved, and 96 orifice plates are placed in microplate reader, selects wavelength for 570nm, measures OD values.
3, calculation formula
Human prostata cancer PC3 cell inhibitory rates (%)=OD0-ODJ/OD0
ODJFor the absorbance of test group (dosing);
OD0For the absorbance of normal group (not dosing).
4, statistical procedures use SPSS statistical packages, data to be indicated with x ± s.One-way analysis of variance, group difference
It is examined using t.
5, result
As shown in Table 1, using the cell that is not loaded as blank control, when sample amount pure lycopene under four concentration
Ability with certain inhibition human prostata cancer PC3 cell Proliferations, inhibiting rate reaches 50% or more, and certain agent is presented
Measure dependence.And the lycopene powder (a of embodiment 31) in high dose (P=is significantly stronger than to the inhibiting effect of cancer cell
0.0213<0.05, with a2Compare) as the pure lycopene (a of sample amount2)。
As shown in Table 2, using the cell that is not loaded as blank control, when the pure pectin of sample amount all has under four concentration
The ability of certain inhibition human prostata cancer PC3 cell Proliferations, and certain dose dependent is presented.And the tomato of embodiment 3
Red pigment powder (a1) in high dose to the inhibiting effect of cancer cell compared with the pure pectin (a when sample amount3) extremely significantly increase (P=
0.003<0.01, with a3Compare).
3 sample a in Tables 1 and 21、a2、a3It shows that human prostata cancer PC3 cells is inhibited to increase under doses
The ability grown, and the inhibiting effect of a1 is greater than single a2 or a3.
Table 1 is when sample amount lycopene is to human prostata cancer PC3 cell inhibitory rates
*P<0.05, * * P<0.01
Table 2 is when sample amount pectin is to human prostata cancer PC3 cell inhibitory rates
*P<0.05, * * P<0.01
Embodiment 5 improves mouse prostate hyperplasia, the pre- preventing drunkenness of mouse and mouse and relieves the effect of alcohol experiment
One, improve mouse prostate Proliferation Assays
1.1 sample
The lycopene powder that ingredient is cooperateed with containing pectin of the present invention;Pure lycopene powder identical with content of the present invention
End;Pure pectin powder identical with content of the present invention.
1.2 experimental animal
ICR male mices 60,18~22g of weight (animal cards number:SCXK (Shanghai) 2007-0005)
The selection of 1.3 dosage
The lycopene powder of embodiment 3, pure lycopene powder, pure pectin powder are made with physiological saline (pH7.0)
Standby is sample, and the solution example of each powder is as follows:
Lycopene powder (the b of embodiment 31):3000mg/kg、1000mg/kg、500mg/kg、200mg/kg;
Pure lycopene powder (b2):2583mg/kg、861mg/kg、430.5mg/kg、232.3mg/kg;
Pure pectin powder (b3):291.3mg/kg、97.1mg/kg、48.55mg/kg、19.42mg/kg;
1.4 method
Mouse 65 is only randomly divided into 13 groups, 13 groups of Normal group 1 and experiment.Mouse routinely forage feed one week
Afterwards, in addition to Normal group, testosterone propionate is subcutaneously injected according to 5mg/kg daily in remaining mouse, and (Shanghai GM medicine company share is limited
Company produces, lot number 070102) modeling, while remaining 12 groups of gavage gives drug 1 time, continuous 21d.Last time administration is for 24 hours
Afterwards, it is put to death after each group animal being weighed, wins prostate and claim weight in wet base, calculate prostate index, prostate index=prostate is wet
Weight (mg)/mouse weight (g).It takes blood in cleaned glass test tube through arteria carotis communis, stands overnight, next day takes serum, by kit
(being purchased from Beijing North Institute of Biological Technology) operating instruction, detects testosterone (T) and estradiol (E in prostate2) horizontal.
1.5 result
By table 3 and table 4 it is found that compared with Normal group, T and E in model group rats prostata tissue2It is horizontal significantly to rise
Height makes rat prostate group hyperplasia occur under exogenous androgenic effect.Compared with model group, when the lycopene of sample amount
(b2) or pectin (b3) T and E in four dosage the following groups can reduce rat model prostate2It is horizontal.The tomato red of embodiment 3
Plain powder (b1) in high dose compared with the lycopene (b when sample amount2) it can extremely significantly decrease T and E in rat model2It is horizontal
(P=0.0078 or 0.0092<0.01, with b2Compare), and relatively work as the pectin (b of sample amount3) although rat model can be reduced
Middle T and E2Level, but the not notable (P=0.147 or 0.221 of otherness>0.05 and b3Compare).3 samples in table 3 and table 4
Product b1、b2、b3It can inhibit the mouse prostate hyperplasia induced by testosterone propionate under doses, it is equal to hyperplasia of prostate
There is certain therapeutic effect.
Table 3, the T and E in sample amount lycopene is to mouse prostate weight in wet base and serum2Influence
(*P<0.05, * * P<0.01)
Table 4, the T and E in sample amount pectin is to mouse prostate weight in wet base and serum2Influence
(*P<0.05, * * P<0.01)
Two, the pre- preventing drunkenness of mouse and experiment of relieving the effect of alcohol
2.1 sample
The lycopene powder that ingredient is cooperateed with containing pectin of the present invention;Pure lycopene powder identical with content of the present invention
End;Pure pectin powder identical with content of the present invention.
2.2 experimental animal
ICR mouse 100 (half male and half females), 18~22g of weight (animal cards number:SCXK (Shanghai) 2007-0005)
The selection of 2.3 dosage
Lycopene powder (the c of embodiment 31):116mg、290mg、580mg;
Pure lycopene powder (c2):100mg、250mg、500mg;
Pure pectin powder (c3):11.3mg、28.2mg、56.6mg.
Gavage volume is the product suspension per 100g mouse weights 1.5mL (1.5mL/100g).Solvent is 1%CMNa.
The pre- preventing drunkenness experiment of 2.4 mouse
Mouse 50 is only randomly divided into 10 groups, 91 group of control, experiment groups.Fasting 1 night (12h) before experiment.Each group is distinguished
Gavage 1.5mL/100g 1%CMNa, the lycopene powder of embodiment 3, pure lycopene powder, pure pectin powder 30min
Afterwards.Each group is gavaged with 52 ° of Red Star Erguotou wines with 1.5mL/100g weight.The drunk rate of mouse is observed and recorded, and is observed small
The death rate in mouse 24 hours.The activity condition for observing mouse, being creeped with mouse, unstable, rear abdomen mops floor, hair is loose, closing one's eyes is ignorant of
For drunk index.With activity freely, flexibly, spirit, hair it is smooth to sober up index.
The 2.5 mouse test mice 50 that relieves the effect of alcohol only is randomly divided into 10 groups, 91 group of control, experiment groups.1 night of fasting before experiment
(12h).Each group is gavaged with 52 ° of Red Star Erguotou wines with 1.5mL/100g weight.After 30min is all drunk, except control group uses
Gavage 1%CMNa, remaining 3 groups of difference gavage 1.5mL/100g 1%CMNa, the lycopene powder of embodiment 3, pure tomato red
Plain powder, pure pectin powder.Relieving the effect of alcohol the time for mouse is observed and recorded, and observes the dead number of elements of mouse in for 24 hours.
2.6 experimental result
2.6.1 the pre- preventing drunkenness test result of mouse
By table 5 and table 6 it is found that compared with Normal group, the lycopene powder (c of embodiment 31), pure lycopene
Powder (c2), pure pectin powder (c3) there is apparent pre- preventing drunkenness effect at the highest dose, and certain dose-dependant is presented
Property (compared with normal group).
Table 5 compares drunk effect when sample amount lycopene
(*P<0.05, * * P<0.01)
Table 6 compares drunk effect when sample amount pectin
(*P<0.05, * * P<0.01)
The test result 2.6.2 mouse is relieved the effect of alcohol
By table 7 and table 8 it is found that compared with Normal group, the lycopene powder (c of embodiment 31), pure lycopene
Powder (c2), pure pectin powder (c3) under three dosage there is dispelling effects of alcohol, as the increase of sample concentration time of sobering up becomes
It is short, and certain dose dependent is presented.The time of relieving the effect of alcohol in high dose of the lycopene powder of embodiment 3 is considerably shorter than pure
Lycopene powder or pure pectin powder (P=0.0217<0.05, with c2Compare;P=0.0412<0.05, with c3)。
Table 7 is when sample amount lycopene is to sober up effect comparison sheet
*P<0.05, * * P<0.01
Table 8 is when sample amount pectin is to sober up effect comparison sheet
*P<0.05, * * P<0.01
Embodiment 6 improves male prostate symptom and male and relieves the effect of alcohol experiment
One, improve the experiment of male prostate symptom
60 hyperplasia of prostate middle-aging male (cardinal symptoms confirmed through hospital:Average urination 8~10 times daily, put down
Get up in the night to urinate number 2~4 times, and with urodynamic sense), it is divided into 3 groups, every group is divided into 20 people;First group, continuously take the present invention
3 product of embodiment, 3 lycopene powder dose of embodiment 23.2mg/ days, 60 days;Second group:Continuously take and embodiment 3
The pure lycopene product of equal volume, pure lycopene dose 20mg/ days, 60 days;Third group:It is continuous to take and embodiment
The pure pectin powder product of 3 equal volumes, pure lycopene dose 2.3mg/ days, 60 days.
Test result shows as follows:As shown in Table 9:The lycopene or pectin phase of product of the present invention and single component
Than middle-aging male isuria frequency, number of averagely getting up in the night to urinate are substantially reduced, and antalgesic state is substantially reduced, and illustrates this hair
Bright lycopene powder has better effect in terms of improving male prostate symptom.
Table 9 improves male prostate symptomatic consequence comparison sheet
Two, human body liver-protecting and alcoholism-relieving is tested
The male female volunteers of 30 health of subject, are randomly divided into 3 groups, every group of 10 people;First group, take the production of embodiment 3
Product lycopene powder (55.8mg);Second group, the pure lycopene (48mg) with 3 equal volume of embodiment;Third group, with reality
Apply the pure pectin (5.4mg) of 3 equal volume of example;Indigo plant 42 ° of 100~300mL of white wine that the above volunteer drinks Yanghe River sea are differed, and half
After hour, there is phenomena such as different degrees of facial flushes in three groups of volunteers, have part dysequilibrium, dizziness, language occur
The drunk symptom such as unclear, respectively warm water takes product lycopene powder of the present invention, tomato to the one two three group of volunteer immediately
Red pigment, pectin, pay a return visit volunteer and continue to observe at the case where observing and recording volunteer after 30min, 60min, 90min afterwards for 24 hours.
Experimental result:As shown in Table 10, product of the present invention is compared with the lycopene of single component or pectin, 30min
Afterwards, three groups of volunteer's septum resets are rubescent, the symptoms such as drunk are mitigated or disappeared;3 product lycopene of embodiment after 60min
The drunk aspiration disease 80% of powder group restores normal, and pure lycopene group is 70%;3 product lycopene of embodiment after 120min
The drunk aspiration disease of powder group is restored normally, and pure lycopene group 90% restores normal, and pure pectin group 60% restores normal.24h
After pay a return visit volunteer, the one or two group of phenomena such as not being still drank after a night, volunteer's night does not occur reaction of having a stomach upset, and sleep is good
Good, third group occurs sleeping slightly weaker phenomenon.The above result shows that product of the present invention compared with single component lycopene or
Person's pectin has the effect of stronger liver-protecting and alcoholism-relieving.
Table 10, human body dispelling effects of alcohol compare
Claims (8)
1. a kind of extracting method of the lycopene containing pectin, it is characterised in that include the following steps:
(1) fresh tomato is weighed, water is added after cleaning, 100 DEG C of heat preservation 15min is heated to, smashs into catsup after being rinsed with water to pieces;
(2) it is added mixed solvent into catsup, the solid-liquid ratio of catsup and mixed solvent is 1:2.0~4.0, wherein described
Mixed solvent be made of in ethyl acetate the aqueous solution of acid, the volume ratio of sour aqueous solution and ethyl acetate is 1:0.5~
1.5;
(3) pH of (2) solution is adjusted to 2.0~3, then biological enzyme is added into system, is heated to 40~60 DEG C, enzymolysis 3~5 is small
Shi Hou, the catsup liquid handled carry out Microwave Extraction, are filtered by vacuum after extraction, collect filtrate, retain filter residue;
(4) filter residue ethyl acetate, sour aqueous solution filter after extracting successively, and filtrate merges with filtrate in (3);
(5) filtrate, the lycopene powder product for being freeze-dried containing pectin are concentrated.
2. extracting method according to claim 1, it is characterised in that:In step (1), the water weight of addition is tomato weight
2~4 times.
3. extracting method according to claim 1, it is characterised in that in step (2), acid is hydrochloric acid, and in the aqueous solution of acid
A concentration of 0.2mol/L of acid.
4. extracting method according to claim 1, it is characterised in that:The Microwave Extraction time is 10~35min, ultrasonic power
For 100-200W.
5. extracting method according to claim 1, it is characterised in that:The lycopene powder product containing pectin
The mass ratio of middle pectin and lycopene is 1:1~100.
6. the pectous lycopene prepared according to the extracting method described in any one of claim 1-5.
7. the pectous lycopene described in claim 6 is preparing anti-prostate cancer, is improving male prostate symptom, prevention
The drunk application in the health products to relieve the effect of alcohol.
8. a kind of to improve male prostate function, the health products that relieve the effect of alcohol, it is characterised in that containing containing pectin described in claim 6
Lycopene.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710182540.XA CN108617921A (en) | 2017-03-24 | 2017-03-24 | A kind of lycopene preparation method cooperateing with ingredient containing pectin etc. and have repair to prostate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710182540.XA CN108617921A (en) | 2017-03-24 | 2017-03-24 | A kind of lycopene preparation method cooperateing with ingredient containing pectin etc. and have repair to prostate |
Publications (1)
Publication Number | Publication Date |
---|---|
CN108617921A true CN108617921A (en) | 2018-10-09 |
Family
ID=63707773
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201710182540.XA Pending CN108617921A (en) | 2017-03-24 | 2017-03-24 | A kind of lycopene preparation method cooperateing with ingredient containing pectin etc. and have repair to prostate |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN108617921A (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1398186A (en) * | 1999-12-24 | 2003-02-19 | 株式会社韩国新科学技术中心 | Pharmaceutical compsn. comprising pectin effective in inhibiting male productive toxxicity |
CN102070392A (en) * | 2009-11-23 | 2011-05-25 | 湖州来色生物基因工程有限公司 | Microwave-assisted method for extracting lycopene |
CN102858190A (en) * | 2010-05-03 | 2013-01-02 | 荷兰联合利华有限公司 | Tomato-derived thickening agent |
CN103449952A (en) * | 2013-09-18 | 2013-12-18 | 南京通泽农业科技有限公司 | Preparation method of high-purity lycopene |
CN104892342A (en) * | 2015-05-27 | 2015-09-09 | 合肥卓元科技服务有限公司 | Extraction method of lycopene |
-
2017
- 2017-03-24 CN CN201710182540.XA patent/CN108617921A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1398186A (en) * | 1999-12-24 | 2003-02-19 | 株式会社韩国新科学技术中心 | Pharmaceutical compsn. comprising pectin effective in inhibiting male productive toxxicity |
CN102070392A (en) * | 2009-11-23 | 2011-05-25 | 湖州来色生物基因工程有限公司 | Microwave-assisted method for extracting lycopene |
CN102858190A (en) * | 2010-05-03 | 2013-01-02 | 荷兰联合利华有限公司 | Tomato-derived thickening agent |
CN103449952A (en) * | 2013-09-18 | 2013-12-18 | 南京通泽农业科技有限公司 | Preparation method of high-purity lycopene |
CN104892342A (en) * | 2015-05-27 | 2015-09-09 | 合肥卓元科技服务有限公司 | Extraction method of lycopene |
Non-Patent Citations (8)
Title |
---|
JUN YAN: "PectaSol-C Modified Citrus Pectin Induces Apoptosis and Inhibition of Proliferation in Human and Mouse Androgen-Dependent and -Independent Prostate Cancer Cells", 《INTEGRATIVE CANCER THERAPIES》 * |
李云飞: "《食品工程原理》", 30 June 2014, 中国农业大学出版社 * |
李英华: "不同酯化度和分子量的果胶解酒效果比较研究", 《天然产物研究与开发》 * |
林华娟: "番茄果实打浆温度对番茄酱中果胶物质的影响", 《食品工业科技》 * |
汪多仁: "《绿色发酵与生物化学品》", 31 August 2007, 科学技术文献出版社 * |
王芳: "番茄果胶提取方法和含量分析研究", 《光谱实验室》 * |
粟萍: "《果蔬加工技术》", 30 November 2010, 天津大学出版社 * |
金青哲: "《功能性脂质》", 31 August 2013, 中国轻工业出版社 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104432012B (en) | A kind of stem of noble dendrobium composite superfine powder and its preparation method | |
CN100450495C (en) | Method for processing ginseng and the uses of extract of processed ginseng | |
CN103750328B (en) | A kind of freeze drying compound berry Ultramicro-powder and production method thereof | |
CN100423727C (en) | Antineoplastic composition, and process for preparing the same | |
CN102242044A (en) | Cordyceps cicadae wine and preparation method thereof | |
CN109938332B (en) | Hericium erinaceus health product preparation containing ergothioneine and preparation method thereof | |
CN102349963A (en) | Health care product for preventing microthrombus from forming and preparation method thereof | |
CN102631405A (en) | Compound apigenin nanoemulsion antihypertensive drug | |
CN105707637A (en) | Solid beverage capable of reduce blood glucose, and preparation method thereof | |
KR101330411B1 (en) | Composition for improving atopic dermatitis comprising extract of steamed green tea | |
CN108210547B (en) | Preparation method of phyllanthus emblica leaf extract, preparation and anti-artemisia application thereof | |
CN114032273A (en) | Multifunctional American ginseng hydrolyzed peptide and preparation method and application thereof | |
CN108813465A (en) | A kind of fig function chewable tablets and preparation method thereof | |
CN107996913A (en) | A kind of juice functional additive and preparation method and application | |
KR20140062249A (en) | Composition for improving condition of hair and preventing hair loss | |
CN108617921A (en) | A kind of lycopene preparation method cooperateing with ingredient containing pectin etc. and have repair to prostate | |
CN102626418B (en) | Application of pyrola polysaccharide in preparing immunity-enhancing medicaments and health food | |
CN101480407A (en) | Hyaluronidase inhibitor as well as preparation method and use thereof | |
CN101077873B (en) | Novel NEO-clerodane type diterpene compound and application thereof | |
CN101948453A (en) | Novel NEO-clerodane typed diterpene compound and application thereof | |
CN101962394A (en) | Method for preparing 1,2,3,4,6-penta-O-galloyl-beta-D-glucose (PGG) | |
CN114886945B (en) | Supermolecule medicine for regulating purine metabolism and application thereof | |
KR20200108125A (en) | Anti-atopic dermatitis composition comprising mixture of plant extract as effective component | |
CN104056159A (en) | Alpinia zerumbet volatile oil dropping pill and preparation method thereof | |
CN103497871A (en) | Formulation method for blood-nourishing yin-nourishing health-care wine |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20181009 |
|
RJ01 | Rejection of invention patent application after publication |