224 results about "Histamine" patented technology

The invention relates to the technical field of microorganisms, and particularly discloses a recombinant microorganism and application thereof in fermentation production of decarboxylated carnosine. Compared with an original strain, the recombinant microorganism disclosed by the invention has the advantages that the expression of the mdtK gene is enhanced; the starting strain is escherichia coli capable of producing decarboxylated carnosine. When the recombinant microorganism is used for fermentation production, the yield of the decarboxylated carnosine can be increased, L-histidine, histamine or beta-alanine and other precursors do not need to be added in the production process, and an effective novel method is provided for industrial production of the decarboxylated carnosine.

The invention provides a colorimetric / fluorescent dual-mode sensor, a preparation method of the colorimetric / fluorescent dual-mode sensor and application of the colorimetric / fluorescent dual-mode sensor in histamine detection. The colorimetric / fluorescent dual-mode sensor comprises a horseradish peroxidase-loaded metal organic framework (HRP-AIE-MOF), hydrogen peroxide and a chromogenic substrate o-phenylenediamine (OPD), horse radish peroxidase (HRP) in the HRP-coated AIE-MOF can oxidize colorless OPD into yellow 2, 3-diaminophenazine (DAP), an ultraviolet absorption peak is generated at 425 nm, a strong fluorescence emission peak is generated at 555 nm, the HRP-coated AIE-MOF has a strong fluorescence emission peak at 450 nm, and the HRP-coated AIE-MOF and a fluorescence signal of the DAP can form a ratio fluorescence sensor. According to the invention, the excellent catalytic ability of natural enzyme and the luminescence characteristic of AIE-MOF are integrated in one system, and high-sensitivity histamine detection is realized.

A method of determining the likelihood that a subject with cancer will respond to an immunotherapy comprising a checkpoint inhibitor. The method comprises detecting the level of histamine in a biological sample obtained from the subject. Subjects determined to have a low likelihood of responding to the immunotherapy can be administered an alternative therapy or administered an antihistamine in conjunction with the immunotherapy. Methods of treating cancer patients are also provided, as are kits and systems for histamine detection, recordation, and responder status determination.

The invention relates to the technical field of traditional Chinese medicines, in particular to a traditional Chinese medicine composition for treating rhinitis. The traditional Chinese medicine composition comprises platycodon grandiflorum, semen armeniacae amarae, citrus chachiensis hortorum, fructus aurantii, aster, ephedra, radices trichosanthis, thunberg fritillary bulb, liquorice and loquat leaves. The traditional Chinese medicine composition can be used for remarkably relieving sneezing symptoms caused by allergic rhinitis, reducing histamine and specific IgE levels in serum and improving the pathological change degree of nasal mucosa tissues, and has a wide application prospect.

The present invention relates to the field of pharmaceutical chemistry, and discloses a salt of carebastine and its use, which solves the problems of the prior art, such as poor solid form of carebastine, many impurities, instability, difficulty in purification, difficulty in mass synthesis, and inapplicability to medicinal use. The salt of carebastine of the present invention includes, but is not limited to, acid salts or base salts, particularly potassium salt, sodium salt, methanesulfonate salt and p-toluenesulfonate salt. The salt of carebastine of the present invention is used in the preparation of drugs for histamine H1 receptor antagonists. The salt of carebastine of the present invention has the characteristics of easy purification, high stability, simple process, easy industrial production, and good hygroscopicity and convenient storage. And the salt of the present invention can enter the body quickly and exert its medicinal effect, has good oral absorption, and is superior to ebastine in both safety and individual variation, and is a promising anti-allergic disease drug for development.

The invention belongs to the technical field of biology, and particularly discloses application of laccase AmLac in degradation of biogenic amines. The amino acid sequence of the laccase is shown as SEQ ID NO.1. The laccase has different degrees of degradation effects on the biogenic amines such as histamine, spermidine, tyramine, phenylethylamine and putrescine, and the degradation rates of the histamine and the putrescine both reach 100%. The enzyme is stable in enzymatic property, has alcohol tolerance and acid tolerance, has certain adaptive capacity to food matrixes, and can effectively degrade biogenic amines in wine and reduce potential hazards of the biogenic amines to human bodies, so that the safety and stability of products are improved. Therefore, the AmLac has a wide application prospect in the food industry, and especially when the AmLac is used for treating food containing high biogenic amine, the safety quality of the food can be remarkably improved.

The invention relates to a composition with moisturizing, soothing and repairing effects and application thereof. The composition with the moisturizing, soothing and repairing effects comprises a pomelo fruit extract, a capparis spinosa fruit extract and hydroxyphenyl propionamide benzoic acid. Three active components, namely the pomelo fruit extract, the capparis spinosa fruit extract and the hydroxyphenyl propionamide benzoic acid, are creatively combined for use, wherein the pomelo fruit extract can inhibit release of inflammatory factors, reduce ultraviolet-induced DNA damage and inflammatory response, neutralize free radicals and reduce oxidative stress damage; wherein the capparis spinosa fruit extract can quickly moisturize, enhance cell viability and promote enhancement of a skin barrier; wherein hydroxyphenyl propionamide benzoic acid can block symptoms such as skin redness and swelling, pruritus and pain caused by the fact that histamine activates a TRPV1 pathway. The three components are matched with one another, have a synergistic effect in the aspects of moisturizing, relieving the skin and repairing the skin barrier, and have an excellent effect when being applied to cosmetics with related effects.

The invention provides a composition with a soothing effect, a preparation scheme of the composition and application of cosmetics. The composition comprises the following components in percentage by mass: 35-50% of actinidia chinensis fruit water, 2-10% of a radix gentianae extract, 1-9% of a citron fruit extract, 1-4% of a dendrobium stem extract, 1-5% of an oat extract and the balance of butanediol. All the components in the composition cooperate with one another, the multi-dimensional synergistic effect of resisting inflammation, resisting histamine, repairing a barrier, resisting oxidation and adjusting micro-ecology can be achieved, and the composition has the excellent relieving effect.

The invention belongs to the technical field of livestock feeds, and particularly relates to a novel chitosan composite nutritional breeding feed and a preparation method thereof. The novel chitosan composite nutritional breeding feed is composed of a basal feed and an additive, and the additive is prepared from the following raw materials in parts by weight: 3 to 5 parts of chitosan, 0.7 to 1.5 parts of sunflower bud extract, and 0.5 to 0.9 part of beta-alanyl-L-histidine. The chitosan, the sunflower bud extract and the beta-alanyl-L-histidine in the breeding feed are matched for use, so that the immunity of cattle and sheep can be effectively improved, the growth performance of the cattle and the sheep is improved, the breeding benefit is remarkably improved, diseases are reduced, and the nutritional requirements of animals such as the cattle and the sheep are fully met.

The invention relates to an SERS (Surface Enhanced Raman Scattering) active nano composite material for detecting trace histamine in tears, SERS sensing test paper as well as a preparation method and application, and belongs to the field of biosensing and spectral analysis. At least one of the problems of low detection sensitivity, poor anti-pollution capacity, low selectivity, incapability of realizing on-site rapid and instant analysis and the like of trace histamine in tears in the prior art is solved. The SERS active nano composite material is of a core-shell structure, and comprises a noble metal nano particle core, the surface of the core is coated with the hollow zeolite imidazate skeleton-67 shell layer, namely a ZIF-67 shell layer of a hollow structure; the Raman reporter molecule is fixed on the surface of the noble metal nanoparticle core. According to the invention, the detection sensitivity, anti-pollution capability and selectivity of trace histamine in tears are improved, and non-invasive rapid detection is realized.

The invention discloses a lactobacillus mucus CCFM1401 for repairing a skin barrier based on multiple target spots and a metagen of the lactobacillus mucus CCFM1401, and belongs to the technical field of microorganisms and medicines. The thallus lysate of the fermented lactobacillus mucus CCFM1401, provided by the invention, can be used for improving the cell viability of damaged keratinocytes and the expression of FLG, LOR, IVL, ZO-1, Occludin and CLDN gene levels in the aspect of external application; and viable bacteria and metabiotics (including thallus lysate and fermentation supernatant) of the fermented lactobacillus mucus CCFM1401 are orally taken, so that TEWL can be reduced, the water content of cuticle can be up-regulated, inflammatory reactions (such as skin histamine and serum IgE) can be reduced, and the skin barrier function and expression of structural protein can be up-regulated. Therefore, the fermented lactobacillus mucilaginosus has a huge application prospect in preparation of external or oral medicines for repairing the skin barrier and preparation of food, health care products or cosmetics.

The present invention relates to the field of microbial technology, and specifically discloses a recombinant microorganism and its application in the fermentation production of decarboxylated carnosine. The recombinant microorganism of the present invention has enhanced mdtK The starting strain is Escherichia coli capable of producing decarboxylated carnosine. Fermentation production using the recombinant microorganism of the present invention can increase the yield of decarboxylated carnosine without adding precursors such as L-histidine, histamine, or β-alanine during the production process, thereby providing an effective new method for the industrial production of decarboxylated carnosine.

The invention discloses application of bifidobacterium longum subsp. Infantis CCFM1269 in preparation of a product for relieving lactoglobulin allergy, and belongs to the technical field of microorganisms. The bifidobacterium longum subsp. Infantis CCFM1269 provided by the invention can relieve food allergy, and the food allergy can be relieved specifically as follows: (1) allergy symptom score and diarrhea occurrence rate can be relieved, and anus temperature and immune organ index can be recovered; (2) the immune response is regulated, the levels of histamine, total IgE, IgG1, beta-lactoglobulin specific IgE and proinflammatory factors IL-4 and IL-17A in serum are reduced, the levels of IFN-gamma and IL-10 are improved, and the immune balance is recovered; (3) inflammation of lung and jejunum tissues is relieved; (4) improving the oxidative stress state; (5) the intestinal barrier function is enhanced; and (6) recovering the diversity of intestinal flora, and adjusting the relative abundance of key bacteria genus such as Alloprevotella and the like.

Described herein are compositions and methods for treating or preventing skin or ocular surface disorders, such as those associated with bacterial and / or parasitic infections. Bacterial and / or parasitic infections include mites (e.g., Demodex), helminths, protozoa (e.g., amebas (e.g., Acanthamoeba or Cryptosporidiosis)), onchocerciasis, lice, scabies, nematodes, or chlamydia. The compositions and methods include compounds that exhibit immunological activity, keratolytic activity, antihistamine activity, anti-inflammatory activity, and / or other desirable activities. Topical administration of the compositions to the eyelid margin or surrounding area provides therapeutic benefit to patients with ocular surface disorders.

This invention relates to the crystal form of vonorazine pyroglutamate and its preparation method. The vonorazine pyroglutamate crystal form obtained by this invention not only has good solubility but also excellent storage stability; in vitro activity experiments show that crystal form I of this invention is effective against H+. + K + The inhibitory effect of ATPase is comparable to that of TAK-438; animal experiments show that the crystal form of the present invention, when administered intravenously, can significantly inhibit histamine-induced gastric acid secretion in rats, and can exert its pharmacological effect faster than that of TAK-438 administered duodenally.

The invention belongs to the technical field of medicine detection, and particularly relates to an LCMS (Liquid Chromatography Mass Spectrometry) detection method for histamine in prednisolone. Respectively injecting the reference solution, the test solution and the blank solution into an LCMS (Liquid Chromatography Mass Spectrometer), recording a spectrogram, and calculating the content of histamine in prednisolone by adopting an external standard method; wherein the detection condition of the LCMS comprises a mobile phase, and the mobile phase adopts acetonitrile as a mobile phase A and a 10mM ammonium formate aqueous solution containing 0.1 vol% of formic acid as a mobile phase B. The method is good in reproducibility and stability and high in precision.

The invention belongs to the technical field of food safety detection, and particularly relates to a histamine molecular imprinting electrochemical sensor based on a carbon-based nano composite material and a preparation method and application of the histamine molecular imprinting electrochemical sensor. Aiming at the problems of poor selectivity, high detection limit or complicated operation and the like of the existing histamine detection technology, a Co3O4 / N-HCS (cobaltosic oxide / nitrogen-doped hollow carbon sphere) composite material is prepared by adopting a solvothermal method, o-phenylenediamine (o-PD) is taken as a functional monomer, a molecularly imprinted polymer membrane (MIP) is constructed on the surface of a glassy carbon electrode (GCE) by adopting an electropolymerization method, and the histamine detection electrode is prepared. The MIP / Co3O4 / N-HCS / GCE sensor with specific recognition sites on histamine is formed. The sensor has high selectivity, high sensitivity and good stability, is simple and convenient to operate and rapid in detection, can efficiently realize accurate detection of histamine in food, and is suitable for safety monitoring scenes of various foods such as fermented food, aquatic products and dairy products.

The invention discloses a method for rapidly identifying harmful components in pickled peppers, and belongs to the technical field of food detection. The method comprises the following steps: preparing a reference substance solution, namely preparing a standard substance stock solution and a biogenic amine mixed solution from putrescine, histamine, tyramine and cadaverine standard substances; preparing a test sample solution: preparing the test sample solution by adopting a test sample; the chromatographic conditions are as follows: C18 is used as a filling agent; carrying out gradient elution by taking isopropanol as a mobile phase A and 0.5-2wt% ammonia water as a mobile phase B; the detection wavelength is 254 nm; the column temperature is 25-35 DEG C; and the flow velocity is 0.2-1.0 ml / min. The method has the advantages that (1) the detection speed is high, and the gradient elution speed is high and is only 12 minutes; (2) the number of obvious miscellaneous peaks is small, and only one miscellaneous peak exists; and (3) the method has relatively high precision, relatively low detection limit and good reproducibility.

Disclosed is a method for producing a stabilized lyophilisate with plant-based diamine oxidase (DAO), comprising the following steps: Providing DAO-containing plants or DAO-containing parts thereof; Homogenizing the DAO-containing plants or DAO-containing parts thereof in aqueous solution to obtain an aqueous homogenate; Adding (a) a sugar or sugar alcohol and (b) an amino acid as a stabilizer; and Lyophilizing the aqueous homogenate or a DAO-containing fraction thereof in the presence of the stabilizer. Also disclosed is a lyophilisate obtainable by this method, as well as a solid pharmaceutical dosage form for oral administration containing this lyophilisate. This dosage form is intended for therapeutic use, preferably in the treatment of histamine-induced disorders, or can be used as a dietary supplement or dietary food.

The present invention discloses a neurotransmitter detection method based on an integrated derivatization and solid phase extraction continuous reaction platform; the neurotransmitters include at least: Class A neurotransmitters have no primary amine groups, hydroxyl groups, and carboxyl groups, and have secondary amine groups or quaternary ammonium groups; Class B neurotransmitters contain at least one of primary amine groups, hydroxyl groups, and carboxyl groups; before detection, an aqueous phase derivatization system containing benzoyl chloride is used to derivatize the neurotransmitters in the sample, and an aqueous formic acid solution is added to the obtained supernatant to mix and centrifuge, and the obtained supernatant is subjected to LC-MS analysis after solid phase extraction. The present invention forms an integrated derivatization and solid phase extraction continuous reaction platform through process design, and realizes high-sensitivity simultaneous detection of at least two types of neurotransmitters. Melatonin, serotonin, histamine, and dopamine are detected simultaneously with high sensitivity, and the detection sensitivity is 1pg / mL for melatonin, 1ng / mL for serotonin, 0.03ng / mL for histamine, and 10pg / mL for dopamine.

The invention relates to the technical field of histamine extraction, in particular to histamine removal and extraction equipment and method for apramycin sulfate, the histamine removal and extraction equipment comprises a drying box with a feeding port and a discharging port, an opening and closing unit used for controlling opening and closing of the discharging port is arranged at the discharging port, and a plurality of heating plates sequentially arranged in the horizontal direction are arranged in the drying box; a heating cavity is defined by every two adjacent heating plates; a sliding plate and a driving unit used for driving the sliding plate to move in the length direction of the heating cavity are arranged in the drying box, a plurality of air injection units and a plurality of vertically-arranged spiral conveying units are arranged on the sliding plate, and every two sets of air injection units correspond to one heating cavity and vertically blow air to the cavity walls of the left side and the right side of the heating cavity correspondingly. And the spiral conveying units are in one-to-one correspondence with the heating cavities and extend into the corresponding heating cavities. The drying efficiency of the crystals can be improved.

The application belongs to the technical field of fluorescent nanomaterials, and provides nitrogen-doped carbon dots, a preparation method thereof and application of the nitrogen-doped carbon dots in colorimetric / fluorescent dual-mode visual detection of pH and histamine, to solve the problem that regular colorimetric signals of current carbon dots are difficult to achieve, which limits the application of the carbon dots in biomedicine and photoelectric devices. The nitrogen-doped fluorescent carbon dots are synthesized by one-step hydrothermal reaction of o-phenylenediamine and 2,6-pyridinedicarboxylic acid, water and hydrochloric acid. The preparation method is simple and fast, the synthesized carbon dots have good water solubility and biocompatibility, stable optical properties, high fluorescence quantum yield, can quickly and visually detect intracellular pH and histamine in food spoilage process, have excellent selectivity and anti-interference ability, fast response speed, high sensitivity, and can realize on-site and instant detection by means of a smart phone and a test strip.

The present invention relates to a bispecific anti-tumor antigen / anti-HSG antibody having screened light and heavy chain variable domains, which is capable of improving the pre-targeting of tumors for the specific delivery of therapeutic or diagnostic agents. The antibodies have a significant affinity for tumor antigens and stay at desired sites for a sufficient time. Antibodies that do not bind to the antigen can be rapidly cleared from the body, minimizing exposure of normal tissue. A humanized anti-HSG antibody is bound to each of a group containing histamine-succinyl-glycine (HSG) and a tumor antigen with high affinity. The bispecific antibodies can be further Fc silenced, resulting in additional properties, such as reduced binding to Fc [gamma] R and FcRn, thereby modulating effector function and regulating half-life. These antibodies are useful in the diagnosis and treatment of subjects suffering from malignancies.

The first present invention relates to an ophthalmic composition for reducing eye dryness containing at least one selected from the group consisting of chondroitin sulfate and salts thereof which have a weight-average-molecular weight of 40,000 to 70,000. The second present invention relates to an ophthalmic composition containing at least one selected from the group consisting of chondroitin sulfate and salts thereof which have a weight-average-molecular weight of 40,000 to 70,000, and at least one selected from the group consisting of an antihistamine, a zinc salt, tetrahydrozoline and salts thereof, hydroxyethyl cellulose and salts thereof, and a polyvinyl-based polymer compound. The third present invention relates to an ophthalmic composition containing at least one selected from the group consisting of chondroitin sulfate and salts thereof which have a weight-average-molecular weight of 40,000 to 70,000, and menthol.

The invention discloses a near-infrared ratio type fluorescent probe for rapidly and reversibly detecting histamine (HA), a preparation method of the fluorescent probe and application of the fluorescent probe in dynamic cell imaging, and belongs to the technical field of fluorescence imaging and biosensing. The preparation method comprises the following specific steps: synthesizing aza-BODIPY molecules (1a-1d, 2a-2d) with different halogenations, and meanwhile, connecting the aza-BODIPY molecules with hydroxyl groups at 3 and 5 sites with a hydrophilic PEG (Polyethylene Glycol) fragment and halogen to obtain an HA probe HAPCyto with good water solubility; in addition, the hydroxyl aza-BODIPY molecules are continuously subjected to substitution, halogenation and hydrolysis reaction to obtain carboxyl-containing aza-BODIPY molecules, then the aza-BODIPY molecules are subjected to amidation reaction by utilizing the site, and different organic fragments are respectively connected to obtain a cell membrane targeted HA probe HAPPM, a golgi apparatus targeted HA probe HAPGA and a HaloTag HA fluorescent probe HAPHaloTag. When HA exists in a solution, the developed probe can realize rapid reversible detection of the near-infrared ratio of histamine, also shows good reversible property in mast cells, and can realize dynamic monitoring of histamine in cells.

[Problem] To provide a substance having an activity of antagonizing the binding of histamine to histamine-H3 receptor, or having an activity of inhibiting the homeostatic activity of histamine-H3 receptor. [Means for Solution] A compound of the following formula (I) is provided: [wherein X, Y, Z and W each independently represent a methine group optionally having 1 or 2 substituents, or a nitrogen atom (provided that a case where all of X, Y, Z and W are an optionallysubstituted methine group); A, B and D represent C(0)-, etc.; Q represents a methine group or a nitrogen atom; R represents an optionallysubstituted group of the following formula (II-1): (wherein R7 and R8 each independently represent a lower alkyl group, etc.)].

The application discloses a kind of composite plant extract and its application, skin external preparation.The raw material of the composite plant extract includes hemerocallis fulva flower and red clover, and the weight ratio of hemerocallis fulva flower and red clover is (1:5)~(5:1).The plant extract of hemerocallis fulva flower and red clover of the application can inhibit the release of histamine, thereby reducing the occurrence of inflammation and infection;The plant extract of the application cooperates synergistically, and compared with each plant alone, the histamine inhibition effect of the plant extract of the application is significantly improved;The plant extract of the application uses pure natural plant as raw material, and has low side effect and high safety;The plant raw material used in the application is widely planted in China, and the resource is easy to obtain, the price is cheap, and the cost is low.

The invention discloses a multi-copper oxidase mutant sourced from Psychrobacter sp. And capable of efficiently degrading biogenic amine and application of the multi-copper oxidase mutant. According to the multi-copper oxidase mutant, the 183rd site of an amino acid sequence shown in SEQ ID NO.1 is mutated into histidine from phenylalanine, the 221st site of the amino acid sequence shown in SEQ ID NO.1 is mutated into aspartic acid from asparagine, the 261st site of the amino acid sequence shown in SEQ ID NO.1 is mutated into glutamic acid from glutamine, and the 292nd site of the amino acid sequence shown in SEQ ID NO.2 is mutated into arginine from lysine. Compared with wild type multi-copper oxidase, the multi-copper oxidase mutant disclosed by the invention has a good degradation effect on tryptamine, phenylethylamine, putrescine, cadaverine, histamine, tyramine, spermidine and spermine, and the degradation rate on the spermidine and the spermine is increased to 100%, so that the multi-copper oxidase mutant has a good application prospect in food fermentation safety production.

The present invention is directed to a pharmaceutical composition comprising a pharmaceutically effective amount of guaifenesin, naproxen and at least one further active which is selected to be an antitussive, a decongestant or an antihistamine.

An antihistamine compound having the structure of formula (I), a pharmaceutically acceptable salt thereof, a method for preparing the same, and use of the antihistamine compound having the structure of formula (I) and a pharmaceutically acceptable salt thereof in the treatment of diseases such as seasonal / perennial allergic rhinitis, allergic conjunctivitis, and urticaria. JPEG2025519827000061.jpg85170