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34 results about "Agaropectin" patented technology

Agaropectin is a sulphated galactan mixture which composes agar by 30% composition. [ citation needed ] It is the component of agar that is not agarose and is composed of varying percentages of ester sulfates, D-glucuronic acid and small amounts of pyruvic acid .

Odd number agar oligosaccharide monomer and its preparation method

An odd agaropectin oligose monomer, such as agartriose, agarpentose, agarheptose, or agarnonose, is prepared through adding water to agaropectin or agaropectinose, adding acid, thermal reacting at 50-90 deg.C for 15-480 min, centrifugal separation, evaporation concentrating, adding organic solvent, centrifugal separation, concentrating supernatant, chromatographic column separation, and freeze drying.
Owner:OCEAN UNIV OF CHINA

High-pressure water vapor degradation method for marine sulfated polysaccharides

The invention relates to a high-pressure water vapor degradation method for marine sulfated polysaccharides. The method is characterized in that the marine sulfated polysaccharides are prepared into water solution, then the water solution is treated by high-pressure water vapor at the temperature of 101-150 DEG C for 0.01-24hours, and the obtained treatment solution is dried for obtaining degraded products of the polysaccharides. The marine sulfated polysaccharides comprise seaweed fucoidan, carrageenan and agaropectin which are sourced from marine plants, as well as sea cucumber chondroitin sulfate, sea cucumber fucoidan and abalone sulfated polysaccharides, which are sourced from marine animals. The method has the advantages that no inorganic salt is introduced, and the final products can be obtained by drying after degradation without desalinization; the molecular weight of the polysaccharides can be reduced continuously and uniformly, and the degraded products with different molecular weight can be obtained by controlling the treatment conditions and the treatment time; the method is stable, and the reproducibility is good; and the requirement on equipment is low, and the operation is simple.
Owner:OCEAN UNIV OF CHINA

Polyurethane porous membrane as well as preparation method and application thereof

The invention discloses a polyurethane porous membrane which comprises the following components by weight percent: 0.5%-75.0% of hydrophilic high polymer material and 99.5%-25.0% of polyurethane, wherein the hydrophilic high polymer material is at least one of carboxymethylcelluose sodium, crosslinked carboxymethylcelluose sodium, agaropectin, carrageenan and sodium alginate. According to the invention, the polyurethane porous membrane contains the hydrophilic high polymer material so that a wound percolate can be adsorbed in the porous membrane structure; and the polyurethane porous membrane absorbs the ejection of a wound tissue after being applied to the surface of a wound and prevents the naked hypodermis from being dried, thereby shortening the healing time of the wound, alleviating the pain of a patient and promoting the wound to well heal.
Owner:JIAXING UNIV

Fly gelatinous attractant and preparation method thereof

The invention discloses a fly gelatinous attractant and a preparation method thereof. Each 100g of the fly gelatinous attractant comprises 0.01-0.5mg of furanone, 8-20mg of indole or an indole analog, 0.05-0.8mg of cis-9-tricosene, 0.5-20g of edible gum and the balance water. The fly gelatinous attractant has the advantages that 1, the fly gelatinous attractant utilizes agaropectin as a carrier so that a product validity period is prolonged to about 60 days from about a week and the product is insensitive to adverse weather conditions such as rainfall and wind blowing; and 2, use amounts of indole having poor smell and cis-9-tricosene having a high price are reduced so that a cost is greatly reduced.
Owner:安阳全丰生物科技有限公司

Far infrared medicinal moxibustion substrate, far infrared medicinal moxibustion product containing far infrared medicinal moxibustion substrate and preparation method of far infrared medicinal moxibustion product

The invention belongs to the technical field of traditional Chinese medicine moxibustion, and particularly relates to a far infrared medicinal moxibustion substrate, a far infrared medicinal moxibustion product containing the far infrared medicinal moxibustion substrate and a preparation method of the far infrared medicinal moxibustion product. The far infrared medicinal moxibustion substrate mainly comprises the following raw materials, by weight, including 150-250 parts of bee wax, 30-50 parts of chocolate, 10-30 parts of honey, 100-200 parts of far infrared ceramic powder volcano energy mud, 20-40 parts of agaropectin, 16-18 parts of vaseline and 2-4 parts of capsaicin. The far infrared medicinal moxibustion product mainly comprises the following raw materials, by weight, including 1 part of the far infrared medicinal moxibustion substrate, 7-9 parts of ginseng, 5-7 parts of saffron crocus, 6-8 parts of rhodiola rosea, 8-10 parts of herba cistanche and 9-11 parts of dioscorea nipponica makino. The preparation method of the far infrared medicinal moxibustion product comprises the following steps of preparation of the far infrared medicinal moxibustion substrate, preparation of a drug mixture and preparation of a finished product; the preparation method is simple, convenient to use, relatively low in cost, and beneficial to popularization and application.
Owner:SHANDONG SHENGHONG MEDICINE SCI & TECH

High-use-ratio manufacturing technology of extracting highly-active agarose product from red algae

InactiveCN103408678AHigh extraction rateImprove the gel degreeManufacturing technologyHigh energy
The invention discloses a high-use-ratio manufacturing technology of extracting a highly-active agarose product from red algae. The low-alkali pressurizing method is adopted to pretreat the algae, so that the agaropectin extraction rate is effectively increased, and the high-alkali consumption is reduced; a multi-stage vibrating screen secondary agaropectin extraction technology is developed to increase the agaropectin extraction rate, and the residue is modified and processed to form manure or a feed additive, so that the comprehensive use rate of the red algae is greatly increased; a filter system, a novel band drying system, a full-automatic strip drying system for strip agar, a high temperature dry heat sterilization system and other novel integrated large-scale manufacturing devices are developed, so that the problems of high energy-consumption and lag in production technique in the actual production process are solved accordingly.
Owner:FUJIAN GOLD SWALLOW OCEAN BIOTECH

Strain for producing aryl sulfatase and application thereof

The invention relates to a strain for producing aryl sulfatase and application thereof, and particularly provides a strain with preservation number of CCTCC NO: M 2013613, application of the strain in production of aryl sulfatase, a method for producing the aryl sulfatase by use of the strain and a method for producing agar with high gel strength and low electroosmosis. The screened strain can effectively produce the aryl sulfatase which can be used for carrying out enzymatic hydrolysis on agar powder and specifically removing sulfate radicals of agaropectin polysaccharide, and the yield of the agar with high gel strength and low electroosmosis can be greatly improved, and therefore, the strain has important application value in industrial production.
Owner:OCEAN UNIV OF CHINA

Oscheius tipulae nematode cryopreservation solution and preparation method and application thereof

InactiveCN103891710ASolve the problem that the nematode Oscheius tipulae cannot be preserved by freezingGuaranteed SustainabilityDead animal preservationNematodeCryopreservation
The invention relates to an Oscheius tipulae nematode cryopreservation solution and a preparation method and application thereof, relates to a cryopreservation solution and a preparation method and application thereof, and solves the problem that a conventional nematode glycerinum cryopreservation solution can not freeze and preserve Oscheius tipulae nematodes. The cryopreservation solution comprises agaropectin, tetrahydrofuran and a buffer solution. The preparation method comprises the following steps: 1, preparing the buffer solution; 2, preparing the agaropectin; and 3, preparing the cryopreservation solution. The cryopreservation solution is used for cryopreserving the Oscheius tipulae nematode. The Oscheius tipulae nematode cryopreserved by adopting the cryopreservation solution normally grows and propagates after being unfrozen and revived, and thus the continuity of indoor culture of the Oscheius tipulae nematode captured in field is ensured. The cryopreservation solution is used for cryopreserving the Oscheius tipulae nematode.
Owner:NORTHEAST INST OF GEOGRAPHY & AGRIECOLOGY C A S

Method and reagent kit used for detecting low-density lipoprotein cholesterin

The invention relates to the filed of biochemistry, and discloses a method and a reagent kit used for detecting low-density lipoprotein cholesterin. The method comprises the steps of: combining phosphotungstic acid and agaropectin into a mixed liquid with the pH value of 6.1-6.2; mixing a sample to be tested with the mixed liquid and polyethylene glycol 20000 under the action of magnesium ions toobtain a suspension turbid liquid; then detecting light absorbance under a wavelength of 630nm; and calculating the concentration of low-density lipoprotein cholesterin of the sample to be tested through turbidimetry with a standard solution subjected to the same treatment abovementioned. The reagent kit disclosed by the invention comprises 2-4g / L magnesium chloride, 6-10g / L polyethylene glycol 20000, 4-5g / L phosphotungstic acid and 0.2-0.4g / L agaropectin. According to the method disclosed by the invention, the specific reaction with low-density lipoprotein without removing impure proteins can be realized, so that the detection of the low-density lipoprotein cholesterin is simple, quick and accurate, and the method can be widely applied to the detection of low-density lipoprotein cholesterin.
Owner:CHANGCHUN HUILI BIOTECH CO LTD

Complex gum containing konjak, and method for manufacturing konjak pearls

The invention discloses complex gum containing konjak, and a method for manufacturing konjak pearls. The complex gum containing the konjak comprises, in mass percentage, 42-50% of konjak gum, 14-18% of agaropectin and 40-45% of carrageenan. The method for manufacturing the konjak pearls comprises uniformly mixing the konjak gum, the agaropectin, the carrageenan, cane sugar, potassium chloride, calcium chloride, and potassium sorbate in water so as to form a mixture; subjecting the mixture to swelling treatment so as to obtain a mixed sol; dropping the mixed sol with a centre temperature of 60-75 DEG C in a shaping oil agent with a temperature of 0-10 DEG C; and conducting filtration so as to obtain the konjak pearls. According to the invention, the manufacturing process of the konjak pearls is simple and novel, and a process of dropping gum in oil is adopted so as to greatly raise industrial output and production efficiency. Meanwhile, the adopted complex gum is easy to disperse and swell, and has better flowability and stability, and the obtained konjak pearls are good in elasticity, hardness, toughness and mouth feel, and high in konjak content, and have physiological functions of losing weight, relaxing bowel, lowering blood lipid, and lowering blood sugar. Therefore, the konjak pearls are ideal low-heat foods for losing weight.
Owner:JIANGNAN UNIV

Porous scaffold based on three-dimensional inkjet printing technology and preparation method of porous scaffold

The invention discloses a porous scaffold based on three-dimensional inkjet printing technology and a preparation method of the porous scaffold, and belongs to the field of biomedical materials. According to the porous scaffold based on the three-dimensional inkjet printing technology and the preparation method of the porous scaffold, a three-dimensional scaffold body is printed in a medium with asupporting function, the supporting medium can support the scaffold body, smooth printing of the scaffold body is ensured, and a curing factor can further be additionally added to the supporting medium, so that rapid forming of the printed scaffold body is facilitated. The supporting medium is additionally arranged on a printing platform on the basis of not changing original three-dimensional inkjet printing equipment, the printed material is enabled to be embedded in a supportive agaropectin body, and in this way, printing of the material with poor forming performance can be achieved. Agar is heated and dissolved after printing is completed, and the printed scaffold body can be obtained.
Owner:SICHUAN UNIV

A method and kit for detecting sodium ions

ActiveCN102297844ARaise and improve dispersionUniform opacityColor/spectral properties measurementsPolyethylene glycolPotassium hydroxide
The invention relates to the field of biochemistry, and discloses a detection method of sodion and a kit. The method provided by the invention comprises the following steps of: mixing one component of agaropectin, Arabic gum or polyethylene glycol 2000 with 6-antimony potassium hydroxide to form a mixed liquor, allowing the mixed liquor in a buffer system of pH 7.2-7.5 to react with a sample to be detected and mixtalol to obtain a 6-sodium antimonite hydroxide suspending liquid, detecting absorbance at a 630nm wavelength, performing turbidimetry with a standard solution which undergoes the above same processing, and calculating the sodion concentration of the sample to be detected. The kit provided by the invention comprises one component of 200-300mg / L of agaropectin, 1000-1500mg / L of Arabic gum or 5-10g / L of polyethylene glycol 20000, 12-15g / L of 6-antimony potassium hydroxide and mixtalol. The method provided by the invention enables rapid precipitation of the reaction between Na+ and 6-antimony potassium hydroxide, avoids precipitation polymerization, raises the accuracy of the detection, and can be widely used to detect the sodion concentration.
Owner:CHANGCHUN HUILI BIOTECH CO LTD

Method for direct separation of agarose and agaropectin from agar

The invention relates to a method for direct separation and preparation of agarose and agaropectin from agar. The method comprises the following steps: 1, respectively preparing an agar solution and a polyethylene glycol (PEG) solution, at a constant temperature, mixing, stirring, allowing to stand, and generating a precipitate; 2, centrifuging the mixed solution, to obtain the precipitate and a supernatant; 3, washing the precipitate with pure water and anhydrous ethanol, and filtering to obtain a filter cake and a filtrate; 4, drying the filter cake, and smashing to obtain agarose; 5, adding ethanol into the concentrated supernatant, allowing to stand, and thus obtaining a precipitate; 6, centrifuging the mixed solution, and filtering to obtain the precipitate and a filtrate; 7, drying the precipitate to obtain agaropectin; 8, merging the filtrates, concentrating under reduced pressure, collecting fractions, and recycling ethanol; and 9, further concentrating under reduced pressure to a molten state, cooling to solidify, drying, and recycling PEG. The method not only obtains agaropectin during the process of precipitation preparation of agarose, but also solves the problems of recycling the precipitating agent PEG and ethanol, thereby achieving the effects of cyclic utilization and environmental protection.
Owner:HUAQIAO UNIVERSITY

Special trapper for lepidoptera pests

InactiveCN102224814ALarge trapping capacityTrapping selectivityInsect catchers and killersArthropod mouthpartsSiphon
The invention discloses a special trapper for lepidoptera pests. The special trapper comprises an inner bottle, wherein agaropectin particles including an attractant are contained in the inner bottle; an outer bottle is sleeved outside the inner bottle; a bottle cap with meshes is arranged on the outer bottle; and absorbent cotton or sponge soaking a poison agent is filled between the inner bottle and outer bottle. The special trapper disclosed by the invention does not have a structure for collecting dead pests of a traditional trapper but enables the killed pests to fall onto the ground andseparates the pest collection function to the ground, and thus can trap infinite pests with a relatively small volume; and further management is not needed within 50 days after the special trapper isapplied to the field. The special trapper disclosed by the invention is specially used for trapping lepidoptera pests as the adult lepidoptera pests have specific siphon type mouthparts, and can realize 100% of trapping selectivity.
Owner:HENAN AGRICULTURAL UNIVERSITY

Preparation method of agar gel solution

The invention discloses a preparation method of an agar gel solution. The method is characterized by comprising the following steps: acidifying gracilaria; rinsing to be neutral; adding water into therinsed gracilaria, and heating to melt the gracilaria into glue; adding Ca (OH) 2 and / or CaO to enable the glue solution to be alkaline, and continuously heating; introducing CO2 to react with Ca (OH) 2 so as to generate CaCO3; and filtering to obtain an agar gel solution. The method is green and environment-friendly, can be used for preparing agar with high gel strength and high yield, and has relatively high application value.
Owner:JIMEI UNIV

Preparation method of high-quality agarose

The invention discloses a method for separating and preparing high-quality agarose from agar by a combined flocculation method. The method comprises the following steps: preparing an agar solution with a certain concentration, heating and dissolving; preparing a polyaluminium chloride solution with proper concentration and a polyacrylamide solution with proper concentration; keeping the temperature in a water bath kettle at 40-100 DEG C for a period of time; adding a certain volume of polyaluminium chloride solution into the stirred agar solution, and stirring for a certain time; adding a certain volume of polyacrylamide solution into the reaction solution, and stirring for a certain period of time; filtering, removing filter residues, and collecting filtrate; and cooling the filtrate to form gel, freezing and dehydrating the gel, washing, airing and crushing to obtain agarose. According to the preparation method, a polyaluminum chloride inorganic cationic flocculant and a polyacrylamide cationic flocculant are combined for use to remove the agaropectin and pigments in an agarose solution, so that the gel property is good, and the requirements of the fields of molecular biology andthe like on the high-quality agarose can be met.
Owner:INST OF OCEANOLOGY - CHINESE ACAD OF SCI

Preparation method of small and dense low-density lipoprotein cholesterol detection kit

The invention relates to the technical field of medical detection, and discloses a preparation method of a small and dense low-density lipoprotein cholesterol detection kit. The method comprises the following steps of S1, obtaining components required by a reagent R1, wherein the components include 100 mmol / L of an MES buffer solution I, 1.6 KU / L of cholesterol esterase, 0.6 KU / L of cholesterol oxidase, 2.7 KU / L of phospholipase, 1.2 KU / L of catalase I, 2 mmol / L of Toos and 0.3 g / L of agar gel, the concentration of polyethylene glycol (PEG) is 1 g / L, and the concentration of phosphotungstic acid is 4.5 g / L; and S2, obtaining components required by a reagent R2, wherein the components include 100 mmol / L of an MES buffer solution II, 5 KU / L of peroxidase II, 4 mmol / L of 4-aminoantipyrine and0.05% of sodium azide. The method is used for quantitatively determining the content of small and dense low-density lipoprotein cholesterol in human serum in vitro. The peroxidase used in the kit improves the sensitivity and specificity of detection.
Owner:HONGKUI BIOLOGICAL CHINA CO LTD

Method and reagent kit used for detecting low-density lipoprotein cholesterin

The invention relates to the filed of biochemistry, and discloses a method and a reagent kit used for detecting low-density lipoprotein cholesterin. The method comprises the steps of: combining phosphotungstic acid and agaropectin into a mixed liquid with the pH value of 6.1-6.2; mixing a sample to be tested with the mixed liquid and polyethylene glycol 20000 under the action of magnesium ions toobtain a suspension turbid liquid; then detecting light absorbance under a wavelength of 630nm; and calculating the concentration of low-density lipoprotein cholesterin of the sample to be tested through turbidimetry with a standard solution subjected to the same treatment abovementioned. The reagent kit disclosed by the invention comprises 2-4g / L magnesium chloride, 6-10g / L polyethylene glycol 20000, 4-5g / L phosphotungstic acid and 0.2-0.4g / L agaropectin. According to the method disclosed by the invention, the specific reaction with low-density lipoprotein without removing impure proteins can be realized, so that the detection of the low-density lipoprotein cholesterin is simple, quick and accurate, and the method can be widely applied to the detection of low-density lipoprotein cholesterin.
Owner:CHANGCHUN HUILI BIOTECH CO LTD

A kind of oscheius tipulae nematode cryopreservation solution and its preparation method and the application of the cryopreservation solution

The invention relates to an Oscheius tipulae nematode cryopreservation solution and a preparation method and application thereof, relates to a cryopreservation solution and a preparation method and application thereof, and solves the problem that a conventional nematode glycerinum cryopreservation solution can not freeze and preserve Oscheius tipulae nematodes. The cryopreservation solution comprises agaropectin, tetrahydrofuran and a buffer solution. The preparation method comprises the following steps: 1, preparing the buffer solution; 2, preparing the agaropectin; and 3, preparing the cryopreservation solution. The cryopreservation solution is used for cryopreserving the Oscheius tipulae nematode. The Oscheius tipulae nematode cryopreserved by adopting the cryopreservation solution normally grows and propagates after being unfrozen and revived, and thus the continuity of indoor culture of the Oscheius tipulae nematode captured in field is ensured. The cryopreservation solution is used for cryopreserving the Oscheius tipulae nematode.
Owner:NORTHEAST INST OF GEOGRAPHY & AGRIECOLOGY C A S

A method for preventing wall sticking in the preparation of traditional Chinese medicine granules by spray drying

ActiveCN107569455BAvoid stickingOvercome the defect of easy sticking wallFungi medical ingredientsGranular deliveryBiotechnologyCorn flour
The invention relates to the field of preparation of traditional Chinese medicine granules, in particular to a method for preventing wall sticking in preparation of traditional Chinese medicine granules by spray drying. This method takes advantage of the characteristics of the network formed by the ripening of glutinous rice flour, and fixes most of the soluble components in the concentrated Chinese medicine, such as sugars, in the network structure, thereby reducing the adhesion. After one step, agar colloid is used as a spacer , the colloid forms a film on the surface of the fine particles of the Chinese medicine concentrate and the grain powder that adsorbs the drug, and the agar colloid condenses into a jelly-like solid isolation film in the first-stage drying tower, and is dried at high temperature in the second-stage drying tower. The material is completely dried to form a solid film, and uniformly dispersed Chinese medicine granules are obtained. It not only effectively prevents the adhesion to the inner wall of the spray dryer drying tower, but also effectively isolates the bonding between the granules of the granule. It overcomes the defect that the granules of traditional Chinese medicine granules are easy to stick to the wall in the preparation of spray-drying.
Owner:TONGHUA WANTONG PHARMACY

A kind of preparation method of agar glue

A method for preparing an agar glue solution, comprising the following steps: acidifying Gracilaria; rinsing to neutrality; adding water to the rinsed Gracilaria and heating the gel; adding Ca(OH) 2 and / or CaO, to make the glue solution alkaline, continue heating; pass CO 2 , with Ca(OH) 2 The reaction produces CaCO 3 ; Filtration to obtain agar liquid. The method is environmentally friendly, can prepare agar with high gel strength and high yield, and has high application value.
Owner:JIMEI UNIV

Far infrared medicinal moxibustion substrate, far infrared medicinal moxibustion product containing far infrared medicinal moxibustion substrate and preparation method of far infrared medicinal moxibustion product

The invention belongs to the technical field of traditional Chinese medicine moxibustion, and particularly relates to a far infrared medicinal moxibustion substrate, a far infrared medicinal moxibustion product containing the far infrared medicinal moxibustion substrate and a preparation method of the far infrared medicinal moxibustion product. The far infrared medicinal moxibustion substrate mainly comprises the following raw materials, by weight, including 150-250 parts of bee wax, 30-50 parts of chocolate, 10-30 parts of honey, 100-200 parts of far infrared ceramic powder volcano energy mud, 20-40 parts of agaropectin, 16-18 parts of vaseline and 2-4 parts of capsaicin. The far infrared medicinal moxibustion product mainly comprises the following raw materials, by weight, including 1 part of the far infrared medicinal moxibustion substrate, 7-9 parts of ginseng, 5-7 parts of saffron crocus, 6-8 parts of rhodiola rosea, 8-10 parts of herba cistanche and 9-11 parts of dioscorea nipponica makino. The preparation method of the far infrared medicinal moxibustion product comprises the following steps of preparation of the far infrared medicinal moxibustion substrate, preparation of a drug mixture and preparation of a finished product; the preparation method is simple, convenient to use, relatively low in cost, and beneficial to popularization and application.
Owner:SHANDONG SHENGHONG MEDICINE SCI & TECH

Fragrant and sweet ham sausage and preparation method thereof

The invention relates to a fragrant and sweet tripe ham sausage, which comprises the following raw materials by weight proportion that: major materials: 100 portions of tripe; secondary materials: 10 portions to 20 portions of agaropectin, 5 portions to 10 portions of gelatin, 5 portions to 10 portions of carrageenin, 4 portions to 6 portions of ice water; flavorings: 3 portions to 6 portions of rock candy, 5 portions to 10 portions of crystal sugar, 2 portions to 4 portions of milk powder, 1 portion to 2 portions of honey, 1 portion to 2 portions of flavouring essence. The invention further relates to a preparation method of the fragrant and sweet tripe ham sausage, which comprises the following steps: chunking and soaking, boiling sirup, injecting sausage and tying and cooking ham. The invention has the beneficial effects that tripe, saccharide and gelatin are used as the major materials and the ham sausage looks like crystal containing jade and exquisite after being taken off sausage coating, which increases the appetite of people, tastes fragrant, sweet and soft and is nutritious, thus enjoying popularity among people of each age group.
Owner:贾明跃

A kind of production strain of arylsulfatase and its application

The invention relates to a strain for producing aryl sulfatase and application thereof, and particularly provides a strain with preservation number of CCTCC NO: M 2013613, application of the strain in production of aryl sulfatase, a method for producing the aryl sulfatase by use of the strain and a method for producing agar with high gel strength and low electroosmosis. The screened strain can effectively produce the aryl sulfatase which can be used for carrying out enzymatic hydrolysis on agar powder and specifically removing sulfate radicals of agaropectin polysaccharide, and the yield of the agar with high gel strength and low electroosmosis can be greatly improved, and therefore, the strain has important application value in industrial production.
Owner:OCEAN UNIV OF CHINA

Method for microwave extraction of asparagus agar

The invention provides a method for microwave extraction of asparagus agar, and belongs to the technical field of agar production. According to the method, the reforming effect of microwaves on agaropectin and agarose molecules is utilized; alkali treatment efficiency is increased, precision is improved, so that the alkali consumption is reduced, the product uniformity is improved, the productionquality stability is improved, the product loss is reduced with increased raw material utilization rate, the yield is improved, the sewage treatment pressure is relieved, the water consumption and thesewage treatment capacity are reduced, and the overall extraction cost is reduced by 6-10%.
Owner:汕尾市维明生物科技有限公司

Contrast mixture and use thereof

A contrast mixture with increased affinity and selectivity to neoplasms of the gastrointestinal tract, being of three components and consisting of 0.0005-0.01% by weight of low-molecular component, 0.05-6% by weight of high-molecular component and isotonic solution, wherein low-molecular component is a contrast substance, which is a colouring agent used in food industry and pharmacy and high-molecular component is a colloid modulator of velocity designed to decelerate diffusion of the contrast mixture into a tissue in such manner that the velocity of diffusion into healthy tissue of gastrointestinal tract and the velocity of diffusion into neoplasm tissue of gastrointestinal tract is different. In an embodiment, the colouring agent is the sodium and / or calcium salt of [4-(alpha-(4-diethylaminophenyl)-5-hydroxy-2,4-disulphophenylmethylidene)-2,5-cyclohexadiene-1-ylidene] diethylammonium hydroxide or 3,7-bis(Dimethylamino)-phenothia zin-5-ium chloride and the colloid modulator of velocity is a starch, pectin, agar-agar (agarose and agaropectins) and / or non-linearly branched amylopectins. A use of the contrast mixture for colour sharp distinction of the interface between healthy tissue and neoplasm tissue of gastrointestinal tract.
Owner:JAKABCINOVA ANDREA +1
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