WO2005053711A1 - Inducteur de l'interferon gamma - Google Patents
Inducteur de l'interferon gamma Download PDFInfo
- Publication number
- WO2005053711A1 WO2005053711A1 PCT/RU2004/000470 RU2004000470W WO2005053711A1 WO 2005053711 A1 WO2005053711 A1 WO 2005053711A1 RU 2004000470 W RU2004000470 W RU 2004000470W WO 2005053711 A1 WO2005053711 A1 WO 2005053711A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- gamma
- niglizine
- interferon
- concentration
- mice
- Prior art date
Links
Classifications
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7028—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
- A61K31/7034—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
- A61K31/704—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
Definitions
- the gamma interface is the markers.
- the immune-stimulating effect for gamma-interactions it is a complex, antiperspirant, non-invasive, and non-invasive device.
- the 20 sources of gamma-ray are the 1st type cells ( ⁇ ), cytotoxic lymphocytes, and normal silent cells.
- the clinical practice of gamma-ray therapy is used in patients with AIDS and in the treatment of acute infections. It is shown that the introduction of the gamma-interface improves the survival rate of patients with
- the product of the invention is the detection of new properties of the treatment of niglizine, which is more important for the production of gamma-virus.
- the non-medical result is achieved by the use of a derivative of glycyrrhizic acid (niglizine) - a penta-narcotic-diabetes mellitus P ⁇ imeneiie niglizina ( ⁇ en ⁇ a-o-ni ⁇ ina ⁇ glitsi ⁇ izin ⁇ v ⁇ y ⁇ isl ⁇ y) in ⁇ aches ⁇ ve indu ⁇ a in ⁇ e ⁇ e ⁇ na in is ⁇ chni ⁇ a ⁇ ⁇ a ⁇ en ⁇ n ⁇ y and nauchn ⁇ - ⁇ e ⁇ niches ⁇ y in ⁇ matsii not ⁇ isan, sled ⁇ va ⁇ eln ⁇ , m ⁇ zhn ⁇ 0 sdela ⁇ vyv ⁇ d o s ⁇ ve ⁇ s ⁇ vii ⁇ e ⁇ niches ⁇ g
- mice dissolve niglizine (penta-nitrate and glycyrrhizic acid) in ⁇ , and then there is no waste.
- Group ⁇ 3 mice enter 5 niglizine solution with a volume of 0.5 ml with a concentration of 400 ⁇ g / ml, 40 ⁇ l / ml and 4 ⁇ g / ml internally, after 12, 24 and 48 hours, the spleen is removed from the plant. In terms of quality, mice enter 4% of children.
- CONTROL - a cellular environment 0.167 mcg / ml; 1.0 mcg / ml; 6.0 mcg / ml - niglizine concentration; Beneficial areas: I - ionomycin with ⁇ ; II - mono-local anti-SZZ antibodies.
- ⁇ a ⁇ ig. 2 shows the dependence of gamma numbers
- the mixture is diluted with a free buffer at a ratio of 1: 1 and the diluted buffer is applied to the disposable medium. Separation is made by centrifugation at 1500 rpm for 40 minutes. In the case of a power supply, they are prepared, dispersed in 3 ml of an optional buffer and washed twice with a centrifuge for 5 minutes at 1500 rpm. Dry washing in a medium ⁇ 1640 in a volume of 2 ml. After a third wash, the mononuclear cells are suspended in 1 ml of medium. 2.
- ⁇ iglizin penenta-o-niacin-free glycyrrhizic acid grows in ⁇ , and then the quick-fix buffer () 5 worthwhile accents.
- Royal-12-Miristat-13-acetate ( ⁇ ) and ionomycin, and, therefore, multiple anti-SDZ antibodies are used as a positive partner.
- the division of the gamma inter- face is provided by the serial mono-multiplexer ⁇ 8 ⁇ .
- the collection of mouse anti-gamma-interface is a multi-channel antenna located in the external
- the method of using live animals in the experiment is an experiment using linear mice of the L / C line with a mass of 18 - 20 g of free food, only 36 in total.
- niglizine is dissolved in ⁇ , and then, in turn, the Federal Security Service makes it possible to obtain an accent.
- Groups of mice and mice inject a niglizine solution with a volume of 0.5 ml with a concentration of 400 mcg / ml; 40 mcg / ml and 4 mcg / ml internally, after 12, 24 and 48 hours, they take away the spleens and evaluate the gamma-interactions.
- Fort Quality control a niglizine solution with a volume of 0.5 ml with a concentration of 400 mcg / ml; 40 mcg / ml and 4 mcg / ml internally, after 12, 24 and 48 hours, they take away the spleens and evaluate the gamma-interactions
- mice were administered 4% of the disinfectant. 5.
- ⁇ e ⁇ di ⁇ a ⁇ edeleniya du ⁇ tsii gamma in ⁇ e ⁇ e ⁇ na s ⁇ len ⁇ tsi ⁇ ami mice me ⁇ d ⁇ m ⁇ Y8 ⁇ S ⁇ us ⁇ ya 12, 24 and 48 hours mice ⁇ sle ine ⁇ tsii niglizina ume ⁇ schvlyayu ⁇ me ⁇ d ⁇ m tse ⁇ vi ⁇ aln ⁇ y ⁇ ansl ⁇ atsii and ase ⁇ iches ⁇ i ⁇ usl ⁇ viya ⁇ 0 ⁇ izv ⁇ dya ⁇ izya ⁇ ie selezen ⁇ .
- the spleen passes through the metal system, it is suspended in the medium ⁇ 1640, after it is washed out once in the same medium, each time takes 1500/10 minutes.
- the anti-mouse gamma-interferon binding mono-5 antibodies at a concentration of 5 ⁇ g / ml in a volume of 100 ⁇ l are scrubbed on a plate with a pulp-free bottom.
- unconnected sites block 150 mcl / well of solution ⁇ 1640 with 10% fetal delivery. After rinsing in the wells, add a suspension of the membrane with a volume of 200 microliters with a concentration of cells of 1 million / ml.
- niglizine in the range of 0.167 - 6 mcg / ml is significantly more accessible ( ⁇ ⁇ 0.05), which increases the gamma-internametry.
- a maximum stimulation of 25 is observed at a level of niglizine equal to 1 mg / ml.
- a twofold increase in the number of spots from 1.2 to 5.5 times).
- niglizine The effect of niglizine on the production of gamma-interferon with the erythrocytes of mice ⁇ ⁇ due to the results of the experiment ⁇ ⁇ , shown on the mouse, is shown in ⁇ . 1.
- An increase in the gamma-interferon sequence with the fascicles was observed only after 48 h after a single administration of niglizine in doses of 1 and 10 mcg / kg (phig. 3). After 12 and 24 hours after a single introduction 5 niglizine in the studied doses, the number of shared points is not distinguished from the counter.
- niglisin increases the gamma-interactions, which means that it is inaccessible for use.
- INDUSTRIAL APPLICABILITY The invention may be used in pharmaceuticals and scientific research.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Immunology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
RU2003134868/15A RU2254861C1 (ru) | 2003-12-01 | 2003-12-01 | Индуктор гамма-интерферона |
RU2003134868 | 2003-12-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2005053711A1 true WO2005053711A1 (fr) | 2005-06-16 |
Family
ID=34651600
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/RU2004/000470 WO2005053711A1 (fr) | 2003-12-01 | 2004-11-29 | Inducteur de l'interferon gamma |
Country Status (2)
Country | Link |
---|---|
RU (1) | RU2254861C1 (fr) |
WO (1) | WO2005053711A1 (fr) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008140345A1 (fr) * | 2007-05-16 | 2008-11-20 | Zakritoe Aktsionernoe Obschestvo 'sibpharmakon' | Di- et/ou trinicotinates d'acide glycyrrhizique et inhibiteur de propagation du virus de l'immunodéficience humaine |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU1499901A1 (ru) * | 1987-12-21 | 1991-04-30 | Институт химии Башкирского научного центра Уральского отделения АН СССР | N-Хинолин-6-иламид пентаацетилглицирризиновой кислоты, про вл ющий противовоспалительную и противо звенную активность |
SU1626663A1 (ru) * | 1989-07-31 | 1994-03-15 | Институт химии Башкирского научного центра Уральского отделения АН СССР | КОРИЧНЫЙ ЭФИР β -ГЛИЦИРРИЗИНОВОЙ КИСЛОТЫ, ПРОЯВЛЯЮЩИЙ ПРОТИВОВОСПАЛИТЕЛЬНУЮ И ПРОТИВОЯЗВЕННУЮ АКТИВНОСТИ |
RU2073009C1 (ru) * | 1992-06-15 | 1997-02-10 | Институт органической химии Уральского научного центра РАН | Способ получения пента-о-никотината глицирризиновой кислоты |
US6383525B1 (en) * | 2000-12-14 | 2002-05-07 | Globoasia L.L.C. | Herbal compositions for treating immunological disorders |
-
2003
- 2003-12-01 RU RU2003134868/15A patent/RU2254861C1/ru not_active IP Right Cessation
-
2004
- 2004-11-29 WO PCT/RU2004/000470 patent/WO2005053711A1/fr active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU1499901A1 (ru) * | 1987-12-21 | 1991-04-30 | Институт химии Башкирского научного центра Уральского отделения АН СССР | N-Хинолин-6-иламид пентаацетилглицирризиновой кислоты, про вл ющий противовоспалительную и противо звенную активность |
SU1626663A1 (ru) * | 1989-07-31 | 1994-03-15 | Институт химии Башкирского научного центра Уральского отделения АН СССР | КОРИЧНЫЙ ЭФИР β -ГЛИЦИРРИЗИНОВОЙ КИСЛОТЫ, ПРОЯВЛЯЮЩИЙ ПРОТИВОВОСПАЛИТЕЛЬНУЮ И ПРОТИВОЯЗВЕННУЮ АКТИВНОСТИ |
RU2073009C1 (ru) * | 1992-06-15 | 1997-02-10 | Институт органической химии Уральского научного центра РАН | Способ получения пента-о-никотината глицирризиновой кислоты |
US6383525B1 (en) * | 2000-12-14 | 2002-05-07 | Globoasia L.L.C. | Herbal compositions for treating immunological disorders |
Non-Patent Citations (2)
Title |
---|
BALITINA L. ET AL.: "Sposob polucheniya glitsirrizinovoi kistoly is glitsirama. Farmakologicheskie svoistva", KHIMIKO-FARMATSEVTICHESKY ZHURNAL, vol. 35, no. 1, 2001, PUBLISHING HOUSE FOLIUM, pages 38 - 41 * |
UTSUNOMIYA T. ET AL.: "Glycyrrhizin, an active component of licorice roots, reduces morbidity and mortality of mice infected with lethal doses of influenza virus", ANTIMICROB AGENTS CHEMOTHER., vol. 41, no. 3, March 1997 (1997-03-01), pages 551 - 556 * |
Also Published As
Publication number | Publication date |
---|---|
RU2254861C1 (ru) | 2005-06-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Haneji et al. | Fucoidan extracted from Cladosiphon okamuranus Tokida induces apoptosis of human T-cell leukemia virus type 1-infected T-cell lines and primary adult T-cell leukemia cells | |
Ralph et al. | Pharmacokinetics of metronidazole as determined by bioassay | |
Davies et al. | Ciprofloxacin in the treatment of acute exacerbations of chronic bronchitis | |
Moskowitz et al. | Stimulation by growth hormone and dexamethasone of labeled cyclic adenosine 3', 5'-monophosphate accumulation by white fat cells | |
Kim et al. | Extracellular vesicles derived from the periodontal pathogen Filifactor alocis induce systemic bone loss through Toll‐like receptor 2 | |
WO2012061537A2 (fr) | Méthodes de traitement de troubles capillaires | |
Caballero et al. | Endogenous osteopontin induces myocardial CCL5 and MMP-2 activation that contributes to inflammation and cardiac remodeling in a mouse model of chronic Chagas heart disease | |
US6180612B1 (en) | Methods and compositions for targeting DNA metabolic processes using aminoglycoside derivatives | |
McColm et al. | Evaluation of a range of antimicrobial agents against the parasitic protozoa, Plasmodium falciparum, Babesia rodhaini and Theileria parva in vitro | |
Hevesy et al. | Phosphorus exchange in yeast | |
Philips et al. | Physiologic disposition and intracellular localization of isometamidium | |
Das et al. | Rapid diagnosis of Campylobacter pyloridis infection. | |
GARSON et al. | The 45, XO, Ph 1 subgroup of chronic granulocytic leukaemia | |
Balbi et al. | Psychotropic drugs: evaluation of mutagenic effect | |
WO2005053711A1 (fr) | Inducteur de l'interferon gamma | |
Karker | Method for estimation of serum adenosine deaminase | |
Riegel | Blood glucose in crayfishes in relation to moult and handling | |
Maxson et al. | Albumin and Australian frogs: molecular data a challenge to speciation model | |
US20230009902A1 (en) | Treatment of a disease or condition in a tissue orginating from the endoderm | |
Brabbs et al. | Isolation and characterization of bleomycin-resistant clones of CHO cells | |
KR100464876B1 (ko) | 동충하초의 코르디세핀을 함유하는 항혈전제 조성물 | |
Stemp et al. | In vitro and in vivo cytogenetic studies of three β-lactam antibiotics (penicillin VK, ampicillin and carbenicillin) | |
Moraczewski et al. | Distribution and rate of metabolism of phosphorus compounds in Trypanosoma equiperdum | |
Hanin et al. | Acetylcholine and choline in human plasma and red blood cells: a gas chromatograph mass spectrometric evaluation | |
Debbia et al. | In vitro activity of metronidazole alone and in combination with clotrimazole against clinical isolates of Trichomonas vaginalis |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWW | Wipo information: withdrawn in national office |
Country of ref document: DE |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
122 | Ep: pct application non-entry in european phase |
Ref document number: 04808980 Country of ref document: EP Kind code of ref document: A1 |