CN111773352A - Application of turmeric and plantain seed composition in preparation of pharmaceutical composition for reducing blood sugar and blood pressure - Google Patents
Application of turmeric and plantain seed composition in preparation of pharmaceutical composition for reducing blood sugar and blood pressure Download PDFInfo
- Publication number
- CN111773352A CN111773352A CN201910896486.4A CN201910896486A CN111773352A CN 111773352 A CN111773352 A CN 111773352A CN 201910896486 A CN201910896486 A CN 201910896486A CN 111773352 A CN111773352 A CN 111773352A
- Authority
- CN
- China
- Prior art keywords
- turmeric
- plantain seed
- extract
- composition
- pharmaceutical composition
- 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
- 244000163122 Curcuma domestica Species 0.000 title claims abstract description 42
- 235000003805 Musa ABB Group Nutrition 0.000 title claims abstract description 38
- 235000015266 Plantago major Nutrition 0.000 title claims abstract description 38
- 239000008280 blood Substances 0.000 title claims abstract description 36
- 210000004369 blood Anatomy 0.000 title claims abstract description 36
- 235000003373 curcuma longa Nutrition 0.000 title claims abstract description 35
- 235000003392 Curcuma domestica Nutrition 0.000 title claims abstract description 33
- 235000013976 turmeric Nutrition 0.000 title claims abstract description 33
- 239000000203 mixture Substances 0.000 title claims abstract description 30
- 230000036772 blood pressure Effects 0.000 title claims abstract description 28
- 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 15
- 240000008790 Musa x paradisiaca Species 0.000 title claims abstract 22
- 238000002360 preparation method Methods 0.000 title claims description 5
- 239000003814 drug Substances 0.000 claims abstract description 39
- 239000000843 powder Substances 0.000 claims abstract description 28
- 229940079593 drug Drugs 0.000 claims abstract description 23
- 239000000284 extract Substances 0.000 claims abstract description 20
- 239000008513 turmeric extract Substances 0.000 claims abstract description 16
- 229940052016 turmeric extract Drugs 0.000 claims abstract description 16
- 235000020240 turmeric extract Nutrition 0.000 claims abstract description 16
- 239000008203 oral pharmaceutical composition Substances 0.000 claims description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 241000282414 Homo sapiens Species 0.000 claims description 13
- 235000014375 Curcuma Nutrition 0.000 claims description 10
- VFLDPWHFBUODDF-FCXRPNKRSA-N curcumin Chemical compound C1=C(O)C(OC)=CC(\C=C\C(=O)CC(=O)\C=C\C=2C=C(OC)C(O)=CC=2)=C1 VFLDPWHFBUODDF-FCXRPNKRSA-N 0.000 claims description 10
- 210000000582 semen Anatomy 0.000 claims description 8
- 238000003809 water extraction Methods 0.000 claims description 8
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 claims description 5
- 238000010298 pulverizing process Methods 0.000 claims description 4
- 239000002994 raw material Substances 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 2
- 241000407170 Curcuma Species 0.000 claims 2
- 239000001215 curcuma longa l. root Substances 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 abstract description 22
- 206010012601 diabetes mellitus Diseases 0.000 abstract description 17
- 230000000694 effects Effects 0.000 abstract description 15
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 22
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 19
- 239000008103 glucose Substances 0.000 description 19
- 241001127637 Plantago Species 0.000 description 17
- 238000002347 injection Methods 0.000 description 13
- 239000007924 injection Substances 0.000 description 13
- 241000700159 Rattus Species 0.000 description 12
- 102000004877 Insulin Human genes 0.000 description 11
- 108090001061 Insulin Proteins 0.000 description 11
- 229940125396 insulin Drugs 0.000 description 10
- 238000011282 treatment Methods 0.000 description 9
- 241000699670 Mus sp. Species 0.000 description 8
- 235000005911 diet Nutrition 0.000 description 5
- 230000037213 diet Effects 0.000 description 5
- 238000000605 extraction Methods 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 235000012054 meals Nutrition 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 4
- 230000001154 acute effect Effects 0.000 description 4
- 239000002775 capsule Substances 0.000 description 4
- 230000001631 hypertensive effect Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 210000004185 liver Anatomy 0.000 description 4
- XZWYZXLIPXDOLR-UHFFFAOYSA-N metformin Chemical compound CN(C)C(=N)NC(N)=N XZWYZXLIPXDOLR-UHFFFAOYSA-N 0.000 description 4
- 229960003105 metformin Drugs 0.000 description 4
- 208000024172 Cardiovascular disease Diseases 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- 208000002193 Pain Diseases 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000000796 flavoring agent Substances 0.000 description 3
- 235000019634 flavors Nutrition 0.000 description 3
- 230000001077 hypotensive effect Effects 0.000 description 3
- 230000003902 lesion Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 230000036407 pain Effects 0.000 description 3
- 239000006187 pill Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000006188 syrup Substances 0.000 description 3
- 235000020357 syrup Nutrition 0.000 description 3
- -1 vials Substances 0.000 description 3
- 206010002091 Anaesthesia Diseases 0.000 description 2
- 244000223760 Cinnamomum zeylanicum Species 0.000 description 2
- 208000007530 Essential hypertension Diseases 0.000 description 2
- 240000004670 Glycyrrhiza echinata Species 0.000 description 2
- 235000001453 Glycyrrhiza echinata Nutrition 0.000 description 2
- 235000006200 Glycyrrhiza glabra Nutrition 0.000 description 2
- 235000017382 Glycyrrhiza lepidota Nutrition 0.000 description 2
- 206010062717 Increased upper airway secretion Diseases 0.000 description 2
- 208000008589 Obesity Diseases 0.000 description 2
- 241001499733 Plantago asiatica Species 0.000 description 2
- 244000134552 Plantago ovata Species 0.000 description 2
- 235000003421 Plantago ovata Nutrition 0.000 description 2
- 244000090599 Plantago psyllium Species 0.000 description 2
- 235000010451 Plantago psyllium Nutrition 0.000 description 2
- 208000004880 Polyuria Diseases 0.000 description 2
- 239000009223 Psyllium Substances 0.000 description 2
- 206010000059 abdominal discomfort Diseases 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 230000037005 anaesthesia Effects 0.000 description 2
- 208000026106 cerebrovascular disease Diseases 0.000 description 2
- 235000019219 chocolate Nutrition 0.000 description 2
- 235000017803 cinnamon Nutrition 0.000 description 2
- 239000000287 crude extract Substances 0.000 description 2
- 230000035619 diuresis Effects 0.000 description 2
- 230000002526 effect on cardiovascular system Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000002218 hypoglycaemic effect Effects 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 210000003734 kidney Anatomy 0.000 description 2
- 229940010454 licorice Drugs 0.000 description 2
- 239000007937 lozenge Substances 0.000 description 2
- 235000021096 natural sweeteners Nutrition 0.000 description 2
- 235000020824 obesity Nutrition 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 239000003538 oral antidiabetic agent Substances 0.000 description 2
- 229940127209 oral hypoglycaemic agent Drugs 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 208000026435 phlegm Diseases 0.000 description 2
- 239000000419 plant extract Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 229940070687 psyllium Drugs 0.000 description 2
- 230000035488 systolic blood pressure Effects 0.000 description 2
- 239000003826 tablet Substances 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 210000004291 uterus Anatomy 0.000 description 2
- 201000000736 Amenorrhea Diseases 0.000 description 1
- 206010001928 Amenorrhoea Diseases 0.000 description 1
- 208000006820 Arthralgia Diseases 0.000 description 1
- 201000001320 Atherosclerosis Diseases 0.000 description 1
- 208000017667 Chronic Disease Diseases 0.000 description 1
- 206010051625 Conjunctival hyperaemia Diseases 0.000 description 1
- 206010011224 Cough Diseases 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- 206010019851 Hepatotoxicity Diseases 0.000 description 1
- 208000035150 Hypercholesterolemia Diseases 0.000 description 1
- 208000013016 Hypoglycemia Diseases 0.000 description 1
- 208000001953 Hypotension Diseases 0.000 description 1
- 206010022489 Insulin Resistance Diseases 0.000 description 1
- 241000581650 Ivesia Species 0.000 description 1
- 208000019255 Menstrual disease Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000699666 Mus <mouse, genus> Species 0.000 description 1
- 241000475481 Nebula Species 0.000 description 1
- 208000004531 Renal Artery Obstruction Diseases 0.000 description 1
- 206010038378 Renal artery stenosis Diseases 0.000 description 1
- 201000004239 Secondary hypertension Diseases 0.000 description 1
- 208000006011 Stroke Diseases 0.000 description 1
- 208000024799 Thyroid disease Diseases 0.000 description 1
- 238000010162 Tukey test Methods 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 210000001015 abdomen Anatomy 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000001919 adrenal effect Effects 0.000 description 1
- 231100000540 amenorrhea Toxicity 0.000 description 1
- 239000003472 antidiabetic agent Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229940121657 clinical drug Drugs 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000011461 current therapy Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000035487 diastolic blood pressure Effects 0.000 description 1
- 235000015872 dietary supplement Nutrition 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000008298 dragée Substances 0.000 description 1
- 208000001848 dysentery Diseases 0.000 description 1
- 206010013990 dysuria Diseases 0.000 description 1
- 239000008157 edible vegetable oil Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 210000001508 eye Anatomy 0.000 description 1
- 230000004438 eyesight Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000013376 functional food Nutrition 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 235000013402 health food Nutrition 0.000 description 1
- 208000019622 heart disease Diseases 0.000 description 1
- 208000006750 hematuria Diseases 0.000 description 1
- 208000006454 hepatitis Diseases 0.000 description 1
- 231100000283 hepatitis Toxicity 0.000 description 1
- 231100000304 hepatotoxicity Toxicity 0.000 description 1
- 230000007686 hepatotoxicity Effects 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- 208000021822 hypotensive Diseases 0.000 description 1
- 230000004377 improving vision Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- 230000003914 insulin secretion Effects 0.000 description 1
- 208000017169 kidney disease Diseases 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000003340 mental effect Effects 0.000 description 1
- 201000011519 neuroendocrine tumor Diseases 0.000 description 1
- 208000001797 obstructive sleep apnea Diseases 0.000 description 1
- 238000001543 one-way ANOVA Methods 0.000 description 1
- 239000006186 oral dosage form Substances 0.000 description 1
- 229940125395 oral insulin Drugs 0.000 description 1
- 206010033675 panniculitis Diseases 0.000 description 1
- 230000001314 paroxysmal effect Effects 0.000 description 1
- 235000010603 pastilles Nutrition 0.000 description 1
- 231100000915 pathological change Toxicity 0.000 description 1
- 230000036285 pathological change Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 210000000578 peripheral nerve Anatomy 0.000 description 1
- 208000028591 pheochromocytoma Diseases 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 229940018492 plantago seed Drugs 0.000 description 1
- 208000028280 polygenic inheritance Diseases 0.000 description 1
- 239000013641 positive control Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000033764 rhythmic process Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 239000007909 solid dosage form Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000037351 starvation Effects 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 210000004304 subcutaneous tissue Anatomy 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 208000021510 thyroid gland disease Diseases 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000008736 traumatic injury Effects 0.000 description 1
- 208000001072 type 2 diabetes mellitus Diseases 0.000 description 1
- 210000003932 urinary bladder Anatomy 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/88—Liliopsida (monocotyledons)
- A61K36/906—Zingiberaceae (Ginger family)
- A61K36/9066—Curcuma, e.g. common turmeric, East Indian arrowroot or mango ginger
-
- 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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/68—Plantaginaceae (Plantain Family)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/30—Extraction of the material
- A61K2236/33—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones
- A61K2236/331—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones using water, e.g. cold water, infusion, tea, steam distillation, decoction
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2236/00—Isolation or extraction methods of medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicine
- A61K2236/30—Extraction of the material
- A61K2236/33—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones
- A61K2236/333—Extraction of the material involving extraction with hydrophilic solvents, e.g. lower alcohols, esters or ketones using mixed solvents, e.g. 70% EtOH
Abstract
The invention discloses application of a turmeric and plantain seed composition in preparing a pharmaceutical composition for reducing blood sugar and blood pressure, wherein the pharmaceutical composition is orally administered, and the turmeric and plantain seed composition consists of plantain seed crude drug powder or plantain seed extract and turmeric crude drug powder or turmeric extract. The turmeric and plantain seed composition has obvious curative effects on reducing blood sugar and blood pressure, and can be used for preparing effective pharmaceutical compositions for treating individuals suffering from diabetes (and) or hypertension.
Description
Technical Field
The invention belongs to the technical field of Chinese patent medicines, and particularly relates to application of a turmeric and plantain seed composition in preparation of a pharmaceutical composition for reducing blood sugar and blood pressure.
Background
Current treatment of diabetes is divided into three components: regular exercise, diet control and medication. The medicinal treatment of diabetes is divided into oral hypoglycemic agent or insulin injection; when the blood sugar is still poorly controlled after oral hypoglycemic agent treatment, insulin injection therapy may be required instead. However, with the difference of the action mechanism of the medicine, the time of taking medicine is also different: firstly, the medicine is taken thirty minutes before a meal, is taken immediately before the meal or is taken along with the meal, and has the function of stimulating insulin secretion; secondly, the drugs taken after meals are used for improving insulin resistance and reducing glucose output of the liver, but the effect is mostly in the gastrointestinal tract, so that the side effect of gastrointestinal discomfort can be avoided when patients take the drugs after meals. Among the side effects of hypoglycemic drugs, hypoglycemia is the most common, especially when patients take drugs and are not matched with diet time or do not eat and engage in activities that consume blood sugar; secondly, gastrointestinal discomfort; in addition, hepatotoxicity may be caused.
Insulin for injection is the same as or almost the same as insulin produced in a human body, is widely used at present, can achieve the most effective treatment on diabetes, and reduces problems possibly caused by poor blood sugar control, such as pathological changes of eyes, kidneys and peripheral nerves. However, the injection position, injection depth, movement and dosage all affect the absorption of insulin. In order to obtain stable insulin absorption and action, attention must be paid to the fact that the injection frequency in the same injection region is not too frequent, so that the injection is not suitable to be injected into the same point every time, the injection point and the last injection point are kept at the distance of three fingers, so that the stable absorption of the insulin can be ensured, the delayed absorption is avoided, and the injury of subcutaneous tissues of the injection region caused by the too frequent injection frequency in the same region is avoided.
Hypertension is the most common chronic disease (systolic pressure is more than or equal to 140 mm Hg, diastolic pressure is more than or equal to 90 mm Hg), and is also the most main risk factor of cardiovascular and cerebrovascular diseases, and can be divided into two types in clinical hypertension: 1. essential hypertension accounts for more than 90% of all hypertensive patients, and the cause of the essential hypertension is an independent disease which is not clear. 2. Secondary hypertension, also known as symptomatic hypertension, has a clear cause and may be temporarily or permanently elevated. Hypertension is caused by 1. about 60% of hypertension patients with family history and polygenic inheritance, and 30% -50% of hypertension patients have genetic background. 2. Mental and environmental factors 3. age factors above 40 years of age the incidence is high. 4. Lifestyle factors smoking can accelerate the process of atherosclerosis, a risk factor for hypertension. 5. Effects of drugs 6. effects of other diseases obesity, diabetes, sleep apnea hypopnea syndrome, thyroid disease, renal artery stenosis, renal parenchymal lesions, adrenal space occupying lesions, pheochromocytoma, other neuroendocrine tumors, and the like. On the other hand, hypertension is often combined with other risk factors for cardiovascular and cerebrovascular diseases, such as hypercholesterolemia, obesity, diabetes, etc., to synergistically increase the risk of cardiovascular diseases. Symptomatic administration and long-term control are the most important.
The current treatment of hypertension is divided into three parts: regular exercise, diet control and medication. The medicine for treating hypertension is usually taken regularly for a long time so as to achieve effective treatment and reduce the occurrence of complications such as stroke, heart disease, kidney disease and the like. However, some kinds of hypertension drugs cause side effects and cause discomfort after being taken by patients, so the existing hypertension drugs are adopted after large-scale research and evaluation of curative effect and side effect.
The application of the traditional Chinese medicine composition consisting of turmeric and plantain seeds for treating diabetes and hypertension is not yet available on the market.
Disclosure of Invention
The invention aims to overcome the defects of the prior art and provides the application of the turmeric and plantain seed composition in preparing the medicinal composition for reducing blood sugar and blood pressure.
The invention also aims to provide an oral pharmaceutical composition for reducing blood sugar and blood pressure.
The technical scheme of the invention is as follows:
the application of the turmeric and plantain seed composition in preparing the pharmaceutical composition for reducing blood sugar and blood pressure is characterized in that the pharmaceutical composition is orally taken, and the turmeric and plantain seed composition consists of plantain seed raw material powder or plantain seed extract and turmeric raw material powder or turmeric extract.
In a preferred embodiment of the present invention, the psyllium seed extract and the turmeric extract are prepared by a method comprising: pulverizing semen plantaginis or Curcuma rhizome, and extracting with ethanol or water at high temperature and high pressure. The high temperature and high pressure water is processed by an Italian coffee machine or other devices with the same temperature control and pressure extraction functions.
Further preferably, in the ethanol-water extraction, the volume ratio of ethanol to water is 1: 10-10: 1.
Further preferably, the temperature of the high-temperature high-pressure water extraction is 80-105 ℃, and the pressure is 14-20 Bar.
In a preferred embodiment of the present invention, the turmeric and psyllium composition is formulated for lowering blood glucose as follows: turmeric original drug powder or turmeric extract 100-; the formula for reducing blood pressure is as follows: turmeric raw medicine powder or turmeric extract 50-1000mg/60kg B.W./day human body, and plantain seed raw medicine powder or plantain seed extract 50-1000mg/60kg B.W./day human body.
The dosage form of the pharmaceutical composition comprises pills, pastilles, capsules, granules, syrups, vials, drops and emulsions, and the components further comprise at least one pharmaceutically acceptable adjuvant, carrier and/or excipient. Furthermore, coffee, chocolate or other natural sweeteners such as licorice or cinnamon may be added to flavor, improve mouthfeel and enhance user preference.
The other technical scheme of the invention is as follows:
an oral pharmaceutical composition for lowering blood sugar and blood pressure comprises Curcuma rhizome and semen plantaginis composition as effective components, wherein the Curcuma rhizome and semen plantaginis composition comprises semen plantaginis crude drug powder or semen plantaginis extract and Curcuma rhizome crude drug powder or Curcuma rhizome extract.
In a preferred embodiment of the present invention, the psyllium seed extract and the turmeric extract are prepared by a method comprising: pulverizing semen plantaginis or Curcuma rhizome, and extracting with ethanol or water at high temperature and high pressure. The high temperature and high pressure water is processed by an Italian coffee machine or other devices with the same temperature control and pressure extraction functions.
Further preferably, in the ethanol-water extraction, the volume ratio of ethanol to water is 1: 10-10: 1.
Further preferably, the temperature of the high-temperature high-pressure water extraction is 80-105 ℃, and the pressure is 14-20 Bar.
In a preferred embodiment of the present invention, the turmeric and psyllium composition is formulated for lowering blood glucose as follows: turmeric original drug powder or turmeric extract 100-; the formula for reducing blood pressure is as follows: turmeric raw medicine powder or turmeric extract 50-1000mg/60kg B.W./day human body, and plantain seed raw medicine powder or plantain seed extract 50-1000mg/60kg B.W./day human body.
The oral pharmaceutical composition can be prepared into pills, lozenges, capsules, granules, syrups, vials, drops and emulsions, and also comprises at least one pharmaceutically acceptable adjuvant, carrier and/or excipient. Furthermore, coffee, chocolate or other natural sweeteners such as licorice or cinnamon may be added to flavor, improve mouthfeel and enhance user preference.
The invention has the beneficial effects that: the turmeric and plantain seed composition has obvious curative effects on reducing blood sugar and blood pressure, and can be used for preparing effective pharmaceutical compositions for treating individuals suffering from diabetes (and) or hypertension.
Drawings
FIG. 1 is a graph showing the response of the oral pharmaceutical composition to the measurement of blood glucose changes in diabetic ICR mice administered with glucose in example 1 of the present invention.
Fig. 2 is a histogram comparing the area under the curve of fig. 1 (AUC in the present invention) in example 1 of the present invention and the blood glucose changes caused by groups of diabetic ICR mice in the combined traditional Chinese medicine test.
FIG. 3 is a bar graph showing the hypotensive effect on normotensive SD rats after a single administration of the oral pharmaceutical composition of example 1 of the present invention.
FIG. 4 is a bar graph of the hypotensive effect on stage I hypertensive P1-HT rats after a single administration of the oral pharmaceutical composition of example 1 of the present invention;
FIG. 5 is a bar graph showing the changes in heart rhythm after administration of the oral pharmaceutical composition of example 1 of the present invention to normotensive SD rats and first-stage hypertensive P1-HT rats.
Detailed Description
The technical solution of the present invention will be further illustrated and described below with reference to the accompanying drawings by means of specific embodiments.
Plantago asiatica Plantago seed (Plantago asiatica) Plantago of the invention has sweet and cold nature and flavor, enters kidney, bladder, liver and lung channels, has the functions of inducing diuresis for treating stranguria, excreting dampness and stopping diarrhea, clearing liver and improving vision, mainly induces diuresis, clears heat, improves vision and eliminates phlegm. It is indicated for dysuria, stranguria with turbid urine, leukorrhagia, hematuria, summer-heat dampness, dysentery, cough with excessive phlegm, damp arthralgia, conjunctival congestion and nebula.
The turmeric (Curcuma longa) used in the present invention is named as Baoding XiangCurcuma of ZingiberaceaeA plant. Pungent and bitter with warm nature. The main indications are blood breaking, qi moving, meridian dredging and pain relieving. Distending pain in chest and abdomen, pain in shoulder and arm, menoxenia, amenorrhea, and traumatic injury. Curcuma rhizome can inhibit hepatitis virus and improve liver parenchymal lesion. Exciting uterus and causing paroxysmal contraction of uterus.
The term "stem, root and whole plant extract" as used herein and the like refers to a mixture obtained by contacting the corresponding parts of the plant with a solvent after breaking the structure (optionally washed) and then using the method of the present invention. The extraction solvent is ethanol water, wherein the volume ratio of ethanol to water can be 1: 10-10: 1, such as 1: 1, 1: 2, 1: 3, 3: 1 or 2: 1. The extract comprises a crude extract (raw extract), more specifically a product obtained by simple extraction, and a treated, purified, refined extract (refined extract), wherein selected plant parts are contacted with at least one extraction solvent, and, optionally, the obtained crude extract may be subjected to one or more separation and/or purification treatments to obtain the refined extract. The stem, root and whole plant extracts may be in liquid form (e.g., solutions, concentrates or distillates) or may be solvent-free solids (e.g., pastes, granules or dried powders) and the solids may be further dissolved in an oil, such as, but not limited to, an edible oil, such as soybean oil.
An effective amount (effective amount) as used herein refers to an amount of a pharmaceutical composition sufficient to produce the desired therapeutic result, wherein the exact nature of the result will vary depending on the particular disease being treated. The specific effective amount will depend upon a variety of factors such as the particular condition being treated, the physiological condition of the patient (e.g., the patient's weight, age or sex), the type of animal being treated, the duration of treatment, the mode of administration, the nature of the current therapy (if any), and the specific formulation and structure of the compound or derivative thereof being used. An effective amount also refers to a compound or composition whose therapeutic benefit exceeds its toxic or deleterious effects. For example, an effective amount may be expressed as the total weight of the drug (e.g., in grams, milligrams, or micrograms) or as the ratio of the weight of the drug to the body weight in milligrams per kilogram (mg/kg).
The pharmaceutical composition used in the present invention means a mixture or compound consisting of two or more substances and containing the extract of the present invention as an active ingredient, whether it is a gas, liquid, powder or solid. The pharmaceutical compositions for oral administration may be in the form of capsules, cachets, pellets, lozenges, powders, granules, or as a solution or suspension in an aqueous or non-aqueous liquid, or as an oil-in-water or water-in-oil liquid emulsion, or as a syrup, or in the form of tablets and the like. In solid dosage forms (capsules, tablets, pills, dragees, powders, granules and other oral dosage forms) of the pharmaceutical composition for oral administration, the composition of the present invention can be used for applications such as the production of foods, pharmaceuticals, industrial materials and the like. Examples of the food of the present invention include nutritional supplement foods, health foods, functional foods, foods for the elderly, and the like.
Example 1
The oral pharmaceutical composition in this example is: is prepared from plantain seed powder and curcuma root powder.
The experimental process comprises the following steps:
1. acute (acute) hypoglycemic ability:
in the evening 23: 00 diabetic ICR mice (starvation for blood glucose > 130mg/dL) were induced by high oil diet to discontinue water and feed for 10 hours. Every morning 9: 00 after measuring the initial blood glucose level, each tube was fed with 0.2mL of the above oral pharmaceutical composition, and then 4g/kg of glucose was administered, and timing was started, and blood glucose was measured once every 30 minutes by a mouse tail vein needle using an Accu-chek (model Instant) blood glucose meter, and five time points of 0, 30, 60, 90, and 120 minutes were measured in total. In the experiment, a blank control group is obtained by feeding 0.2mL of sterilized water before 4g/kg of glucose is given to a diabetic ICR mouse; diabetic ICR mice were given 4g/kg glucose for subcutaneous injection of insulin (insulin) only at 20pM or metformin (clinical drug) at 5mg/kg as two positive control groups. The combination doses in the experimental groups were as follows:
the blood sugar reducing formula comprises:
turmeric: 10-100mg/kg B.W./day 50g ICR diabetic mice, converted into 100-1000mg/60kg B.W./day human;
plantain seed: 100-400mg/kg B.W./day 50g ICR diabetic mice, converted into 1000-4000mg/60kg B.W./day human.
2. Acute (acute) hypotensive ability:
normal blood pressure SD rats and first stage hypertension P1-HT rats were fed on a diet for 10 hours. The initial blood pressure values were monitored and recorded by anesthesia through a gas anesthesia machine, transmitted by PowerLab via femoral cannula to LabChart 7(Colorado Springs CO 80906, USA). After 3 minutes of blood pressure stabilization, each tube was fed 0.2mL of the oral pharmaceutical composition described above and blood pressure and heart rate changes were monitored continuously for 30 minutes after administration. The combined dose is as follows:
the blood pressure reducing formula comprises:
turmeric: 5-100mg/kg of B.W./day 300g of rats, converted into 50-1000mg/60kg of B.W./day of human beings;
plantain seed: 5-100mg/kg B.W./day 300g rat, converted to 50-1000mg/60kg B.W./day human.
(II) experimental results:
the results of this experiment are illustrated below with reference to the drawings of the specification. Data from this experiment are presented as mean ± Standard Error (SE) and are significantly analyzed using one-way ANOVA with Tukey test to determine pre-treatment and post-treatment differences and histograms are constructed with GraphPad Prism 7.04(La Jolla, CA, USA). (p < 0.05),. times (p < 0.001) and. times (p < 0.0001) are statistically significant levels.
As shown in FIG. 1, the blood glucose level of diabetic ICR mice administered with only 4g/kg glucose increased to the maximum level after 30 minutes, and was significantly slower than that of either the experimental group or the control group, which was followed by a decrease in blood glucose level. The blood glucose values of the diabetic ICR mice fed with the metformin and the oral pharmaceutical composition after 30 minutes by subcutaneous insulin injection are all increased slowly relative to the blank control group, and the subsequent blood glucose values are reduced in a significantly faster way relative to the blank control group. Therefore, the oral pharmaceutical composition has the efficacy of reducing blood sugar, and the effect is similar to that of common blood sugar reducing drugs, namely insulin and metformin.
As shown in fig. 2, the data in fig. 1 is converted into a histogram, and then the effects of different processing methods on blood glucose changes can be more clearly compared. Accordingly, the oral pharmaceutical composition has a blood sugar lowering effect superior to that of metformin.
As shown in FIGS. 3 to 5, the results of FIG. 3 show that the blood pressure of normal blood pressure SD rats did not change abruptly 30 minutes after taking the oral pharmaceutical composition. Therefore, the oral pharmaceutical composition can not cause abnormal blood pressure for individuals with normal blood pressure; FIG. 4 shows that the systolic blood pressure of the first stage hypertension P1-HT rat is significantly decreased after 30 minutes of taking the oral pharmaceutical composition, so that the oral pharmaceutical composition has the effect of lowering blood pressure for hypertensive individuals; the results in FIG. 5 show that the heart rate of normal blood pressure SD rats and first stage hypertension P1-HT rats has not been changed significantly after taking the oral pharmaceutical composition for 30 minutes.
According to the experimental result, the oral pharmaceutical composition not only can be used for preparing the medicines or the compositions for reducing blood pressure and blood sugar, but also can be used for preparing daily health-care food after evaluation.
The above description is only a preferred embodiment of the present invention, and therefore should not be taken as limiting the scope of the invention, which is defined by the appended claims.
Claims (10)
1. The application of the turmeric and plantain seed composition in preparing the medicine composition for reducing blood sugar and blood pressure is characterized in that: the pharmaceutical composition is administered orally, and the turmeric and plantain seed composition is composed of plantain seed crude drug powder or plantain seed extract and turmeric root crude drug powder or turmeric extract.
2. The use of claim 1, wherein: the preparation method of the plantain seed extract and the turmeric extract comprises the following steps: pulverizing semen plantaginis or Curcuma rhizome, and extracting with ethanol or water at high temperature and high pressure.
3. Use according to claim 2, characterized in that: in the ethanol-water extraction, the volume ratio of ethanol to water is 1: 10-10: 1.
4. Use according to claim 2, characterized in that: the temperature of the high-temperature high-pressure water extraction is 80-105 ℃, and the pressure is 14-20 Bar.
5. The use according to any one of claims 1 to 4, wherein: the turmeric and plantain seed composition is used for reducing blood sugar and comprises the following formula: turmeric original drug powder or turmeric extract 100-; the formula for reducing blood pressure is as follows: turmeric raw medicine powder or turmeric extract 50-1000mg/60kg B.W./day human body, and plantain seed raw medicine powder or plantain seed extract 50-1000mg/60kg B.W./day human body.
6. An oral pharmaceutical composition for reducing blood sugar and blood pressure, which is characterized in that: the active ingredients of the composition comprise turmeric and plantain seed composition, and the turmeric and plantain seed composition consists of plantain seed raw material powder or plantain seed extract and turmeric raw material powder or turmeric extract.
7. The oral pharmaceutical composition of claim 6, wherein: the preparation method of the plantain seed extract and the turmeric extract comprises the following steps: pulverizing semen plantaginis or Curcuma rhizome, and extracting with ethanol or water at high temperature and high pressure.
8. The oral pharmaceutical composition of claim 7, wherein: in the ethanol-water extraction, the volume ratio of ethanol to water is 1: 10-10: 1.
9. The oral pharmaceutical composition of claim 7, wherein: the temperature of the high-temperature high-pressure water extraction is 80-105 ℃, and the pressure is 14-20 Bar.
10. The oral pharmaceutical composition of any one of claims 6 to 8, wherein: the turmeric and plantain seed composition is used for reducing blood sugar and comprises the following formula: turmeric original drug powder or turmeric extract 100-; the formula for reducing blood pressure is as follows: turmeric raw medicine powder or turmeric extract 50-1000mg/60kg B.W./day human body, and plantain seed raw medicine powder or plantain seed extract 50-1000mg/60kg B.W./day human body.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910896486.4A CN111773352A (en) | 2019-09-20 | 2019-09-20 | Application of turmeric and plantain seed composition in preparation of pharmaceutical composition for reducing blood sugar and blood pressure |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910896486.4A CN111773352A (en) | 2019-09-20 | 2019-09-20 | Application of turmeric and plantain seed composition in preparation of pharmaceutical composition for reducing blood sugar and blood pressure |
Publications (1)
Publication Number | Publication Date |
---|---|
CN111773352A true CN111773352A (en) | 2020-10-16 |
Family
ID=72755051
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201910896486.4A Pending CN111773352A (en) | 2019-09-20 | 2019-09-20 | Application of turmeric and plantain seed composition in preparation of pharmaceutical composition for reducing blood sugar and blood pressure |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN111773352A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102225095A (en) * | 2011-06-23 | 2011-10-26 | 上海中医药大学 | Effective fraction of plantain seeds as well as preparation method and application thereof |
CN103989752A (en) * | 2014-05-13 | 2014-08-20 | 高伦 | Pharmaceutical composition used for preventing and treating diabetes mellitus combined with hypertension |
CN107669991A (en) * | 2017-11-24 | 2018-02-09 | 成都中医药大学附属医院 | A kind of pharmaceutical composition for reducing serum uric acid level and preparation method thereof |
-
2019
- 2019-09-20 CN CN201910896486.4A patent/CN111773352A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102225095A (en) * | 2011-06-23 | 2011-10-26 | 上海中医药大学 | Effective fraction of plantain seeds as well as preparation method and application thereof |
CN103989752A (en) * | 2014-05-13 | 2014-08-20 | 高伦 | Pharmaceutical composition used for preventing and treating diabetes mellitus combined with hypertension |
CN107669991A (en) * | 2017-11-24 | 2018-02-09 | 成都中医药大学附属医院 | A kind of pharmaceutical composition for reducing serum uric acid level and preparation method thereof |
Non-Patent Citations (2)
Title |
---|
孙林林等: "姜黄化学成分及药理作用研究进展",,", 《山东中医药大学学报》 * |
陈信云等: "《中药学 第3版》", 2017013, 中国医药科技出版社 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102526479B (en) | Health-care medicine formula with functions of enhancing immunity and lowering blood sugar | |
CN102526478B (en) | Formula of health-care medicine with functions of strengthening immunity and reducing blood sugar | |
CN107080250A (en) | A kind of composition of auxiliary hyperglycemic, beverage and preparation method thereof | |
CN102271698A (en) | Pharmaceutical composition and use for preparing medicament thereof | |
CN101190280B (en) | Use of extract of non-fruit part of prune tree | |
JP2011522844A (en) | Composition for reducing blood glucose level and use thereof | |
CN111166820B (en) | Traditional Chinese medicine composition containing fingered citron, preparation and application | |
CN108403818B (en) | Composition for assisting in reducing blood sugar and application thereof | |
CN110051817A (en) | A kind of Chinese traditional medicine composition and its application reducing uric acid | |
CN101474346B (en) | Longstamen onion bulb extract as well as preparation method and application thereof | |
CN107281386B (en) | Method for preparing medicine for treating hypertension by using dendrobium officinale and radish seeds and application | |
KR100601191B1 (en) | Hypoglycemic agents | |
CN111281902A (en) | Application of lithocarpus litseifolius or active extract thereof | |
CN111773352A (en) | Application of turmeric and plantain seed composition in preparation of pharmaceutical composition for reducing blood sugar and blood pressure | |
CN111773315A (en) | Application of spiranthes sinensis extract in preparation of pharmaceutical composition for treating hypertension | |
CN111773351A (en) | Application of coleus blumei and curcuma longa composition in preparation of medicine composition for reducing blood sugar and blood pressure | |
CN111773274A (en) | Application of coleus blumei and plantain seed composition in preparation of pharmaceutical composition for reducing blood sugar and blood pressure | |
CN103181945B (en) | The purposes of Semen Luffae | |
JP2000342228A (en) | Formulated tea of smallanthus sonchifol with mulberry leaf | |
CN103721074B (en) | Pharmaceutical composition and preparation method and application thereof | |
CN107126450B (en) | A Chinese medicinal preparation containing extract and effective substance, and its preparation method and application | |
JP3610340B2 (en) | Functional food for suppressing blood sugar or blood pressure rise | |
CN111773208A (en) | Application of garcinia fruit extract gamma-mangostin in preparation of pharmaceutical composition for reducing blood sugar and blood pressure | |
CN104256618A (en) | Food, health care product or medicine composition with blood sugar reduction function | |
CN113440536B (en) | Medicine for preventing and treating diabetes and application thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20201016 |