CN108850407A - A kind of chewing gum of the extract containing hairystalk loosestrife herb is improving the application on oral environment - Google Patents
A kind of chewing gum of the extract containing hairystalk loosestrife herb is improving the application on oral environment Download PDFInfo
- Publication number
- CN108850407A CN108850407A CN201810946666.4A CN201810946666A CN108850407A CN 108850407 A CN108850407 A CN 108850407A CN 201810946666 A CN201810946666 A CN 201810946666A CN 108850407 A CN108850407 A CN 108850407A
- Authority
- CN
- China
- Prior art keywords
- parts
- chewing gum
- loosestrife herb
- hairystalk loosestrife
- extract
- 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
- 235000015218 chewing gum Nutrition 0.000 title claims abstract description 43
- 229940112822 chewing gum Drugs 0.000 title claims abstract description 40
- 241000219991 Lythraceae Species 0.000 title claims abstract description 31
- PCSWXVJAIHCTMO-UHFFFAOYSA-P dequalinium Chemical compound C1=CC=C2[N+](CCCCCCCCCC[N+]3=C4C=CC=CC4=C(N)C=C3C)=C(C)C=C(N)C2=C1 PCSWXVJAIHCTMO-UHFFFAOYSA-P 0.000 claims abstract description 24
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 21
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
- 239000011159 matrix material Substances 0.000 claims description 13
- 239000002994 raw material Substances 0.000 claims description 9
- 235000019441 ethanol Nutrition 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 8
- 108010011485 Aspartame Proteins 0.000 claims description 7
- 229920002472 Starch Polymers 0.000 claims description 7
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims description 7
- 239000000605 aspartame Substances 0.000 claims description 7
- 235000010357 aspartame Nutrition 0.000 claims description 7
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 claims description 7
- 229960003438 aspartame Drugs 0.000 claims description 7
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 7
- 235000019698 starch Nutrition 0.000 claims description 7
- 239000008107 starch Substances 0.000 claims description 7
- 239000000811 xylitol Substances 0.000 claims description 7
- 235000010447 xylitol Nutrition 0.000 claims description 7
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims description 7
- 229960002675 xylitol Drugs 0.000 claims description 7
- 239000000845 maltitol Substances 0.000 claims description 6
- 235000010449 maltitol Nutrition 0.000 claims description 6
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 claims description 6
- 229940035436 maltitol Drugs 0.000 claims description 6
- 210000001161 mammalian embryo Anatomy 0.000 claims description 6
- 238000000605 extraction Methods 0.000 claims description 4
- 238000001914 filtration Methods 0.000 claims description 4
- 238000010992 reflux Methods 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 3
- 230000003020 moisturizing effect Effects 0.000 claims description 3
- 239000012467 final product Substances 0.000 claims description 2
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 claims 1
- 150000005846 sugar alcohols Chemical class 0.000 claims 1
- 238000012360 testing method Methods 0.000 abstract description 12
- 239000000203 mixture Substances 0.000 abstract description 8
- 206010061218 Inflammation Diseases 0.000 abstract description 6
- 230000004054 inflammatory process Effects 0.000 abstract description 6
- 235000001674 Agaricus brunnescens Nutrition 0.000 abstract description 2
- 230000001954 sterilising effect Effects 0.000 abstract description 2
- 241000894006 Bacteria Species 0.000 description 22
- 241000590002 Helicobacter pylori Species 0.000 description 12
- 229940037467 helicobacter pylori Drugs 0.000 description 11
- 230000001580 bacterial effect Effects 0.000 description 8
- 201000001245 periodontitis Diseases 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000005764 inhibitory process Effects 0.000 description 7
- WZUVPPKBWHMQCE-UHFFFAOYSA-N Haematoxylin Chemical compound C12=CC(O)=C(O)C=C2CC2(O)C1C1=CC=C(O)C(O)=C1OC2 WZUVPPKBWHMQCE-UHFFFAOYSA-N 0.000 description 6
- 241000700159 Rattus Species 0.000 description 6
- 210000000214 mouth Anatomy 0.000 description 6
- 230000000844 anti-bacterial effect Effects 0.000 description 5
- 238000004140 cleaning Methods 0.000 description 5
- 210000003296 saliva Anatomy 0.000 description 5
- 241000588747 Klebsiella pneumoniae Species 0.000 description 4
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000006916 nutrient agar Substances 0.000 description 4
- 230000028327 secretion Effects 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 241001164374 Calyx Species 0.000 description 3
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 3
- 208000006558 Dental Calculus Diseases 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 206010044029 Tooth deposit Diseases 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000036541 health Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- 206010011224 Cough Diseases 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000001154 acute effect Effects 0.000 description 2
- 230000002308 calcification Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000001055 chewing effect Effects 0.000 description 2
- 230000007665 chronic toxicity Effects 0.000 description 2
- 231100000160 chronic toxicity Toxicity 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 230000037308 hair color Effects 0.000 description 2
- 210000002216 heart Anatomy 0.000 description 2
- 210000004400 mucous membrane Anatomy 0.000 description 2
- 210000000056 organ Anatomy 0.000 description 2
- 230000001575 pathological effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 230000002110 toxicologic effect Effects 0.000 description 2
- 231100000027 toxicology Toxicity 0.000 description 2
- 210000001364 upper extremity Anatomy 0.000 description 2
- 239000012224 working solution Substances 0.000 description 2
- 206010002383 Angina Pectoris Diseases 0.000 description 1
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 1
- 241001573881 Corolla Species 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000589989 Helicobacter Species 0.000 description 1
- 208000032843 Hemorrhage Diseases 0.000 description 1
- 206010020565 Hyperaemia Diseases 0.000 description 1
- 241000588748 Klebsiella Species 0.000 description 1
- 241000186660 Lactobacillus Species 0.000 description 1
- 244000178870 Lavandula angustifolia Species 0.000 description 1
- 235000010663 Lavandula angustifolia Nutrition 0.000 description 1
- 208000037093 Menstruation Disturbances Diseases 0.000 description 1
- 206010027339 Menstruation irregular Diseases 0.000 description 1
- QZYVWCYNDZZJQD-UHFFFAOYSA-N N1=CC=CC2=CC=CC=C12.NCl Chemical compound N1=CC=CC2=CC=CC=C12.NCl QZYVWCYNDZZJQD-UHFFFAOYSA-N 0.000 description 1
- 241000588653 Neisseria Species 0.000 description 1
- 208000007443 Neurasthenia Diseases 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- 208000002193 Pain Diseases 0.000 description 1
- 241000192035 Peptostreptococcus anaerobius Species 0.000 description 1
- 206010035664 Pneumonia Diseases 0.000 description 1
- 241000191940 Staphylococcus Species 0.000 description 1
- 241000194017 Streptococcus Species 0.000 description 1
- 241000194019 Streptococcus mutans Species 0.000 description 1
- 206010044302 Tracheitis Diseases 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 231100000215 acute (single dose) toxicity testing Toxicity 0.000 description 1
- 210000000577 adipose tissue Anatomy 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 206010003549 asthenia Diseases 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 208000034158 bleeding Diseases 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 230000017531 blood circulation Effects 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 235000015111 chews Nutrition 0.000 description 1
- 208000037976 chronic inflammation Diseases 0.000 description 1
- 230000006020 chronic inflammation Effects 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- NWFNSTOSIVLCJA-UHFFFAOYSA-L copper;diacetate;hydrate Chemical compound O.[Cu+2].CC([O-])=O.CC([O-])=O NWFNSTOSIVLCJA-UHFFFAOYSA-L 0.000 description 1
- 238000003113 dilution method Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000002224 dissection Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000010794 food waste Substances 0.000 description 1
- 238000003304 gavage Methods 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 229940039696 lactobacillus Drugs 0.000 description 1
- 239000001102 lavandula vera Substances 0.000 description 1
- 235000018219 lavender Nutrition 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 231100001252 long-term toxicity Toxicity 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 230000005906 menstruation Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 238000011169 microbiological contamination Methods 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000002715 modification method Methods 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000021590 normal diet Nutrition 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 210000004681 ovum Anatomy 0.000 description 1
- 230000003239 periodontal effect Effects 0.000 description 1
- 210000004261 periodontium Anatomy 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 210000001187 pylorus Anatomy 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 210000000952 spleen Anatomy 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000820 toxicity test Toxicity 0.000 description 1
- 210000004291 uterus Anatomy 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
- A23G4/06—Chewing gum characterised by the composition containing organic or inorganic compounds
- A23G4/068—Chewing gum characterised by the composition containing organic or inorganic compounds containing plants or parts thereof, e.g. fruits, seeds, extracts
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G4/00—Chewing gum
- A23G4/06—Chewing gum characterised by the composition containing organic or inorganic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Food Science & Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Inorganic Chemistry (AREA)
- Botany (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Alternative & Traditional Medicine (AREA)
- Biotechnology (AREA)
- Medical Informatics (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Confectionery (AREA)
- Medicinal Preparation (AREA)
Abstract
The invention discloses a kind of chewing gums of extract containing hairystalk loosestrife herb to improve the application on oral environment, belongs to chewing gum technical field.Chewing gum is specially made using hairystalk loosestrife herb extract, to improve oral environment, the chewing gum is made of Dequavet, hairystalk loosestrife herb extract and partial supplementary material.Test proves that chewing gum of the present invention can be effectively improved oral environment, especially will improve sterilizing ability after hairystalk loosestrife herb extract and Dequavet mixture, mushroom living environment is destroyed, especially suitable for there is oral inflammation patient use.
Description
Technical field
The present invention relates to the chewing gums of daily necessities technical field more particularly to a kind of extract containing hairystalk loosestrife herb to change
Application on kind oral environment.
Background technique
Chewing gum is deep by a kind of favorite carbohydrate of the people of the world, and presently commercially available chewing gum is by natural gum or glycerol
Based on resin, the reconciliations such as syrup, sweetener are added and suppress, are a kind of sugar for being put into chewing in mouth for people.It is general to use
Carry out fresh breath, remove the swill of dental surface, by masticatory movement, increase the secretion of saliva, there is certain cleaning mouth
The effect of chamber.But this general sugar content height of chewing gum available on the market, the excessive edible Determination of Total Body Fat that easily leads to increase
Add, and has a single function.With the increase at age, the salivary secretion in Human Physiology only has 1/10th of young man or so,
When salivary secretion is reduced, bacterium just mass propagation, therefore, the oral hygiene state of the elderly is very bad, various diseases occurs
The risk of disease is very big.Existing chewing gum can not also alleviate swelling and aching of gum, common inflammation.Clinical research shows
Oral inflammation will affect cementum, parodontium, seriously affect patient's oral health.The life that plaque is gradually deposited in dental surface
Object film is made of a large amount of bacteriums, intercellular substance, Exfoliative cells and food scraps etc.;Followed by dental calculus, bacterial plaque calcification
Becoming dental calculus afterwards, surface can often form the bacterial plaque of non-calcification, gum can be stimulated to cause inflammation, and dental calculus itself is hard coarse in addition,
Gum continued mechanical is oppressed, promotes local Nutrition and Metabolism that obstacle occurs.It deposits at the positions such as plaque, saliva and mucous membrane of mouth
In helicobacter pylori, and in the majority in plaque, and gingival sulcus and oral pocket are then a clustering areas for helicobacter pylori.Pylorus
Helicobacter is not only closely related with periodontitis, also closely related with oral keritonocytes.Helicobacter pylori is periodontitis or promotion
One of the significant bacterial of periodontitis progress.There are alkalescent saliva, swill etc. in oral cavity, is provided for the procreation of normal flora
Appropraite condition.The most common flora is alpha streptococcus and streptococcus anaerobius, followed by staphylococcus epidermis, Neisseria,
Lactobacillus, conveyor screw, Candida etc..Therefore, a kind of Multifunctional chewing gum that suitable all groups use how is produced, is become
The important topic studied now.
The object of the present invention is to provide a kind of chewing gums that can effectively improve oral environment.
The chewing gum of the invention is made of component A and component B.
The component A is the mixture of hairystalk loosestrife herb extract and Dequavet;The component B is various auxiliary materials.
Influence experiment of two kinds of substance different ratios to oral environment in component A.
1, raw medicine hairystalk loosestrife herb extract is prepared as described above, and Dequavet is commercially available.
2, experimental strain helicobacter pylori, pseudomonas aeruginosa, anginosus, Klebsiella Pneumoniae are Shandong
The Quality-control strains that province clinical examination center provides.
3, instrument and reagent nutrient agar be purchased from Hangzhou day and microorganism reagent Co., Ltd, cultured solution of broth and sterile
Normal saline dilution liquid is purchased from Zhuhai Dier Bioengineering Co., Ltd.;DL-2D1 nephelometer(Zhuhai Deere bioengineering is limited
Company)GSP-9160MBE water isolation type constant incubator(Medical Equipment Plant of Shanghai Boxun Industrial Co., Ltd.).
4, the nutrient agar panel for preparing of culture medium is prepared by product description method.
5, bacterium solution preparation exists helicobacter pylori, pseudomonas aeruginosa, anginosus, Klebsiella Pneumoniae respectively
After activation culture of crossing on nutrient agar, the single bacterium colony for picking them separately each bacterial strain is dissolved in sterile saline, and 0.5 wheat is made
The dilution of bacteria of family name's unit, bacterial concentration is about 109cfu/ml at this time.Gained dilution of bacteria is diluted with broth bouillon
Bacteria suspension for 106cfu/ml concentration is spare.
6, minimum inhibitory concentration(MIC)Measurement use NCCLS micro-dilution method modification method.By hairystalk loosestrife herb extract
With Dequavet according to 30:1,15:1,5:1,1:1,1:5,1:15,1:30 ratio is mixed, and the medicine of 1g/ml is respectively prepared
Liquid dilutes to obtain each working solution respectively with nutrient broth.10ul is taken to be added in 96 hole micro plates respectively each working solution, every kind of work
Liquid sets 3 parallel holes.Above-mentioned spare bacteria suspension is seeded in respectively in the machined each hole for making liquid, the hole 90ul/.It will be above-mentioned spare
Bacteria suspension is set as compareing, if 3 parallel holes, the hole 100ul/.Sealing plate observes result after being placed on 35 DEG C of incubator culture 45h.
By test it is found that the ratio of hairystalk loosestrife herb extract and Dequavet is greater than 5:When 1, helicobacter pylori and pneumonia
The growth of klebsiella trace of bacteria, is greater than 30:When 1, helicobacter pylori has bacterial growth, pseudomonas aeruginosa, angina hammer
There is trace of bacteria growth in bacterium, Klebsiella Pneumoniae.When the ratio of hairystalk loosestrife herb extract and Dequavet is less than 1:When 5, verdigris
Pseudomonad insignificant growth;Less than 1:When 30, there is bacterial growth in pseudomonas aeruginosa, helicobacter pylori, anginosus,
The growth of Klebsiella Pneumoniae trace of bacteria.Therefore the weight ratio of hairystalk loosestrife herb extract and Dequavet needs to control 5:1—1:5
Between.
Chewing gum of the invention is made of raw material from the following weight:4-8 parts of Dequavet, 4-8 parts of hairystalk loosestrife herb extract,
33-39 parts of matrix, 10-16 parts of xylitol, 2-4 parts of Aspartame, 5-9 parts of D-mannital, 5-10 parts of starch, citric acid
2-4 parts, 3-7 parts of maltitol.
Preferably:6 parts of Dequavet, 6 parts of hairystalk loosestrife herb extract, 36 parts of matrix, 13 parts of xylitol, 3 parts of Aspartame,
7 parts of D-mannital, 8 parts of starch, 3 parts of citric acid, 5 parts of maltitol.
Preparation method:By first pre- thermal softening 2 hours under the conditions of 65 DEG C of matrix, moisturizing softens 1 hour at 60 DEG C.By its
He mixes raw material, will mix well in raw material after the matrix addition mixing after softening at 45 DEG C, is prepared into chewing gum material
Embryo.It is squeezed after material embryo is cooled to 15-30 DEG C of temperature, excision forming is carried out after reaching certain thickness.Finally at 20 DEG C
Under, chewing gum tablet is made in dry 4h.
Preparing for the hairystalk loosestrife herb extract is as follows:Hairystalk loosestrife herb is crushed, 10 times of 80% (volumes of amount (weight multiple) are added
Percentage) ethyl alcohol, refluxing extraction 3h filtering, the dregs of a decoction add the ethyl alcohol of 8 times of amount (weight multiple) comparable sodiums, refluxing extraction 2h
Filtering merges alcohol extract twice, ethyl alcohol is recovered under reduced pressure, and is concentrated into thick paste that relative density is 1.1 (50 DEG C of surveys) to obtain the final product.
The hairystalk loosestrife herb is annual herb, high 30-60cm;Stem is uprightly sturdy branch, four prismatics, villosity, leaf
To life;Petiole long 1.3-5cm, it is close by white fluff;The long round shape of blade is oval, and each 5-7cm of length and width, apex is blunt to round, the base portion heart
Shape or circle, edge have thin knuckle-tooth, meat, have wrinkle, two sides is by white with villus and blood red gland point.Spike is born in stem
Top and branch top, long 2.5-7.5cm, diameter 0.9-1.9cm;Calyx is by micro- pubescence, and calyx tube expands when fruit, two lip shape of limb,
Upper lip is big and wide in fruit, is in oval, lower lip section shape, has unconspicuous tooth, shrink in lip;Corolla lavender, length are calyx
2 times, two lip shape of limb, upper lip is short, and 4 split, lower lip extend, full edge, indent;Stamen 4, it is preceding to longer, filigree separation, anther ovum
Circle, Room 2;Style is long compared with stamen, and apex is split in equal 2, March at florescence.Flavour of a drug:It is sweet in flavor, it is mild-natured, it is nontoxic.Effect:Wind-dispelling,
Cough-relieving, menstruation regulating.For cold cough, tracheitis, asthma, irregular menstruation, neurasthenia.
Beneficial effects of the present invention:It yet there are no that mixture makes according to a certain percentage by hairystalk loosestrife herb extract and Dequavet
With, more have no using the two as effective active composition be applied to chewing gum report.Chewing gum of the invention can be effectively improved mouth
Chamber environment especially will improve sterilizing ability after hairystalk loosestrife herb extract and Dequavet mixture, destroy mushroom living environment, special
Shi Yongyu there be oral inflammation patient use.
Extracorporeal bacteria inhibitor test
1, experimental method:After taking chewing gum 10g of the invention to crush respectively plus 50ml hot water is made into chewing gum solution.In addition city is taken
It sells addition 50ml hot water after Dequavet 10g is crushed and is made into Dequavet solution.
2, the preparation of bacteria inhibition tablet:Sterile and dry filter paper 20 are taken, wherein 10 dropwise addition chewing gum solution 0.2ml,
Then filter paper is lain against in clean sterile plane ware, uncaps to set in incubator (37 DEG C) and dries, or set naturally dry at room temperature
It is spare after dry;Sterile dry filter paper piece 10 is taken, every dropwise addition quinoline chloramine solution 0.2ml is spare after dry.
3, streptococcus mutans are inoculated with:Dipping concentration with sterile cotton swab is that 5 × 105~5 × 106cfu/ml deforms hammer
Bacterium bacteria suspension is uniformly smeared in nutrient agar planar surface, and every to smear once, plate rotates, finally by cotton swab
Son is smeared one week around plate edge, is covered plate, is set drying at room temperature 5min.
4, bacteria inhibition tablet is placed with:4 microbiological contamination plates are set altogether, and each plate is placed with 5 bacteria inhibition tablets.With aseptic nipper coupongs
It is placed in planar surface, at a distance of 25mm or more between each print center, the periphery with plate is at a distance of 15mm or more.After being placed with,
With the light pressure-like piece of aseptic nipper, so that it is tightly attached to planar surface, cover plate, is placed in 37 DEG C of incubators and cultivates 15~20h, with trip
Mark the diameter and record of calliper to measure antibacterial ring size.
2, experimental result
The diameter of bacteria inhibition tablet antibacterial ring size containing chewing gum of the present invention is 16.6 respectively, 16.7,16.1,18.1,17.6,16.8,
17.2、18.3、16.9、17.0mm。
The diameter of bacteria inhibition tablet antibacterial ring size containing Dequavet solution is 3.26 respectively, 3.5,4.2,3.3,4.4,2.9,
2.7、3.6、3.9、3.1mm。
By testing it is found that being separately added into 50ml hot water in chewing gum situation identical with commercially available Dequavet weight
Wiring solution-forming is tested, and as a result the diameter of the bacteria inhibition tablet antibacterial ring size containing chewing gum of the present invention, which is much larger than, contains Dequavet solution
Bacteria inhibition tablet antibacterial ring size diameter, illustrate that hairystalk loosestrife herb extract in chewing gum of the present invention and Dequavet have synergistic make
With.
Experimental animal
1, cleaning grade healthy SD female rats 20, weight (202 ± 12) g are used as chronic toxicity;Cleaning grade health elder brother
Bright female small white mouse 20, weight (23 ± 2) g are used as acute toxicological experiment.It feeds with normal diet, it is common to drink water.Room temperature control
System is in (24 ± 4) DEG C, humidity (55 ± 5) %, natural lighting.
2, acute toxicological experiment selects female small white mouse 20, cleaning grade health Kunming, is randomly divided into 2 groups, test group and
Blank control group each 10.Test group is converted to the dosage of small white mouse by normal adult using the amount of chewing gum of the present invention daily,
It gavages 2 times daily.Blank control group is given clear water and is gavaged.
3, long term toxicity test cleaning grade healthy SD female rats 20.It is randomly divided into 2 groups, test group and blank control
Group each 10.Control group gives clear water, and test group is given by 30 times of stomach-fillings that adult normal usage is converted to rat dosage.Daily 2
Secondary, experimental period is 3 months.
4, acute toxicity testing result small white mouse observes mouse appearance, hair color, light without death in administration 8d after administration
Damp normal, social action, reaction are normal, ingest, drain normally.Dissection is manually put to death after 8d, observes its heart, liver, spleen
Dirty, lungs, kidney, brain, ovary, uterus are showed no exception.Pathological examination:One Yihong of hematoxylin (HE) dyeing, test group are dirty
Device surface is smooth, and institutional framework is orderly aligned, and cell size, form are normal, and endochylema, karyon dyeing are clear, with blank control group
Not statistically significant (the P of comparing difference>0.05).
5, the appearance of the rat of chronic toxicity result test group, hair color, social action, irritation etc. and to surrounding
The comparing differences such as the interest of environment, food, water are not statistically significant.Important organ row staining pathologic section is examined after rat is put to death
It looks into, HE dyeing.Rats in test groups organ tissue structure is orderly aligned, and cell size, form are normal, and endochylema, karyon dyeing are clear,
No significant difference (P compared with the control group>0.05).
Toxicity test shows that chewing gum of the invention has no toxic reaction.
There is helicobacter pyloris at positions such as plaque, saliva and mucous membrane of mouth for the means of livelihood, and with plaque
In it is in the majority, and gingival sulcus and oral pocket may be a clustering area for helicobacter pylori.Helicobacter pylori is not only close with periodontitis
Correlation, it is also closely related with oral keritonocytes.Helicobacter pylori be periodontitis or promote periodontitis occur significant bacterial it
One.Therefore, the present inventor is since in March, 2011 to being diagnosed as patients with periodontitis at one's side and give chewing gum of the invention to control
It treats.
Different degrees of chronic inflammation is presented in diagnostic criteria gum, and color is dark red or scarlet, and quality is soft, and stippling disappears,
Edge round blunt and not with facing attach;Periodontal bag formation, attachment loss, pyorrhea in bag;Loosening in various degree occurs in tooth.X line
It has been shown that, alveolar bone have different degrees of absorption.
Treatment method slowly chews chewing gum of the invention, and every bu is early, 2 times late.
Criterion of therapeutical effect is cured:Symptom completely disappears, and depth of pocket shoals or restores normal, and tooth non-loosening can be normal
Chewing.It improves:Gum mild hyperaemia, bleeding, pain, oedema mitigate.In vain:Change unobvious.
Therapeutic effect treatment carries out effect assessment after two weeks.32 are cured, is improved 9, invalid 0, total effective rate
100%。
It can be used to fresh breath using chewing gum of the invention, remove the swill of dental surface, increase saliva
Secretion promotes the exercise of facial blood circulation and muscle, and the generation of oral inflammation can also be monthly prevented and treated using 2-3 times.
Specific embodiment
Chewing gum of the invention is made of component A and component B.The component A is hairystalk loosestrife herb extract and Dequavet
Mixture;The component B is various auxiliary materials.
Embodiment one:Dequavet 4g, hairystalk loosestrife herb extract 4g, matrix 33g, xylitol 10g, Aspartame 2g, D-
Mannitol 5g, starch 5g, citric acid 2g, maltitol 3g.By first pre- thermal softening 2 hours under the conditions of 65 DEG C of matrix, in 60
Moisturizing softens 1 hour at DEG C.Other raw materials are mixed, will be filled in raw material after the matrix addition mixing after softening at 45 DEG C
Divide and mix, is prepared into chewing gum material embryo.It squeezes after material embryo is cooled to 20 DEG C of temperature, is cut after reaching certain thickness
It is cut into type.Finally at 20 DEG C, chewing gum tablet is made in dry 4h.
Embodiment two:Dequavet 6g, hairystalk loosestrife herb extract 6g, matrix 36g, xylitol 13g, Aspartame 3g, D-
Mannitol 7g, 8 g of starch, citric acid 3g, maltitol 5g, preparation method is the same as embodiment one.
Embodiment three:Dequavet 8g, hairystalk loosestrife herb extract 8g, matrix 39g, xylitol 16g, Aspartame 4g, D-
Mannitol 9g, starch 10g, citric acid 4g, maltitol 7g, preparation method is the same as embodiment one.
Claims (4)
1. a kind of chewing gum of extract containing hairystalk loosestrife herb is improving the application on oral environment, it is characterised in that hairystalk loosestrife herb extract
Improve the application on oral environment in chewing gum, chewing gum is specially made using hairystalk loosestrife herb extract, to improve oral environment,
The chewing gum is made of raw material from the following weight:4-8 parts of Dequavet, 4-8 parts of hairystalk loosestrife herb extract, matrix 33-39
Part, 10-16 parts of xylitol, 2-4 parts of Aspartame, 5-9 parts of D-mannital, 5-10 parts of starch, 2-4 parts of citric acid, malt
3-7 parts of sugar alcohol.
2. chewing gum as described in claim 1, it is characterised in that be made of raw material from the following weight:6 parts of Dequavet, row
6 parts of hay-scented extract, 36 parts of matrix, 13 parts of xylitol, 3 parts of Aspartame, 7 parts of D-mannital, 8 parts of starch, citric acid 3
Part, 5 parts of maltitol.
3. chewing gum as claimed in claim 1 or 2, it is characterised in that preparation method:Matrix is first preheated under the conditions of 65 DEG C
Softening 2 hours, moisturizing softens 1 hour at 60 DEG C, other raw materials are mixed, and mixing is added in the matrix after softening at 45 DEG C
Mixed well in raw material afterwards, be prepared into chewing gum material embryo, will material embryo be cooled to 15-30 DEG C of temperature after squeeze, when reaching
Excision forming is carried out after to certain thickness, finally at 20 DEG C, chewing gum tablet is made in dry 4h.
4. hairystalk loosestrife herb extract as claimed in claim 1 or 2, it is characterised in that preparation method:Hairystalk loosestrife herb is crushed, is added 10
Amount (weight multiple) 80% (percentage by volume) ethyl alcohol again, refluxing extraction 3h filtering, it is same that the dregs of a decoction add 8 times of amounts (weight multiple)
The ethyl alcohol of isoconcentration, refluxing extraction 2h filtering, merges alcohol extract twice, ethyl alcohol is recovered under reduced pressure, and be concentrated into relative density and be
The thick paste of 1.1 (50 DEG C of surveys) to obtain the final product.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810946666.4A CN108850407A (en) | 2018-08-20 | 2018-08-20 | A kind of chewing gum of the extract containing hairystalk loosestrife herb is improving the application on oral environment |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810946666.4A CN108850407A (en) | 2018-08-20 | 2018-08-20 | A kind of chewing gum of the extract containing hairystalk loosestrife herb is improving the application on oral environment |
Publications (1)
Publication Number | Publication Date |
---|---|
CN108850407A true CN108850407A (en) | 2018-11-23 |
Family
ID=64321118
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810946666.4A Pending CN108850407A (en) | 2018-08-20 | 2018-08-20 | A kind of chewing gum of the extract containing hairystalk loosestrife herb is improving the application on oral environment |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN108850407A (en) |
-
2018
- 2018-08-20 CN CN201810946666.4A patent/CN108850407A/en active Pending
Non-Patent Citations (1)
Title |
---|
陈少萍等主编: "《口腔临床药物手册》", 31 December 2005, 华南理工大学出版社 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104244912B (en) | Have and alleviate oral cavity pain and kill oral cavity bacterium and the natural antibacterial dentifrice composition of stable neural effect | |
US20080069783A1 (en) | Oral cavity cleaning composition | |
CN109528601B (en) | Compound traditional Chinese medicine mouth wash and preparation method thereof | |
JP2016521686A (en) | MULTIFUNCTIONAL COMPOSITION AND METHOD FOR PRODUCTION AND USE THEREOF | |
US20120288454A1 (en) | Dental protection toothpaste composition | |
JP5080284B2 (en) | PHARMACEUTICAL COMPOSITION FOR PREVENTION AND / OR TREATMENT OF BONE DISEASE, FUNCTIONAL FOOD, HEALTHY FOOD AND PHARMACEUTICAL PREPARATION CONTAINING THE COMPOSITION, AND Root-periodontium formation promoter | |
CN107441014A (en) | A kind of evening clothing toothpaste of American-cockroach-extract-containing and preparation method thereof | |
CN110384725B (en) | A Chinese medicinal composition for regulating oral flora and preparation method of active extract thereof | |
CN114376232A (en) | Composition suitable for oral health | |
WO2005012503A1 (en) | Novel lactobacillus, living body activating lactobacillus preparation and preventive or therapeutic agent against living body infection | |
KR20200017912A (en) | Antibacterial Composition for Porphyromonas Gingivalis Comprising Plant Extract or Lactic Acid Bacteria Fermentation Product thereof | |
CN110731931B (en) | Health toothpaste containing miracle fruit effective component | |
KR20110128384A (en) | The composition material and the manufacturing process for skin-wrinkle, moisture and skin-lightening uses by midam-kyungokko | |
CN110915970A (en) | Traditional Chinese medicine tablet candy capable of reducing urate deposition and preparation method thereof | |
CN108850407A (en) | A kind of chewing gum of the extract containing hairystalk loosestrife herb is improving the application on oral environment | |
JP6021005B2 (en) | Antibacterial composition and use thereof | |
CN108113943A (en) | A kind of Pediatric Oral Emergency care method | |
CN104026491B (en) | Mung bean cleans the teeth fragrant mouth chewable tablets and production method thereof | |
CN107485584A (en) | A kind of oral care composition | |
CN106236645A (en) | A kind of natural child's collutory | |
CN111358819A (en) | A Chinese medicinal composition with antibacterial and hemostatic effects | |
KR20160141624A (en) | Manufacturing method of health food using the ginseng by double fermented | |
CN110974935A (en) | Antibacterial nursing gel containing fullerene C60 component and preparation method thereof | |
KR20190094986A (en) | Composition for prevention or treatment of oral disease comprising Epimedium Herb extract | |
CN104940438A (en) | Chinese herbal medicine extract and toothpaste for preventing and treating childhood caries, and application of Chinese herbal medicine extract |
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: 20181123 |
|
RJ01 | Rejection of invention patent application after publication |