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37 results about "Severe toxicity" patented technology

In severe cases of chronic toxicity, there may also be nervous system and kidney problems, such as: Kidney failure Memory problems Movement disorders Problems keeping salts in your body Psychosis (disturbed thought processes, unpredictable behavior)

Compositions for allogeneic cell therapy

A method of manipulating allogeneic cells for use in allogeneic cell therapy protocols is described. The method provides a composition of highly activated allogeneic T-cells which are infused into immunocompetent cancer patients to elicit a novel anti-tumor immune mechanism called the “Mirror Effect”. In contrast to current allogeneic cell therapy protocols where T-cells in the graft mediate the beneficial graft vs. tumor (GVT) and detrimental graft vs. host (GVH) effects, the allogeneic cells of the present invention stimulate host T-cells to mediate the “mirror” of these effects. The mirror of the GVT effect is the host vs. tumor (HVT) effect. The “mirror” of the GVH effect is the host vs. graft (HVG) effect. The effectiveness and widespread application of the anti-tumor GVT effect is limited by the severe toxicity of the GVH effect. In the present invention, the anti-tumor HVT effect occurs in conjunction with a non-toxic HVG rejection effect. The highly activated allogeneic cells of the invention can be used to stimulate host immunity in a complete HLA mis-matched setting in patients that have not had a prior bone marrow transplant or received chemotherapy and / or radiation conditioning regimens.
Owner:MIRROR BIOLOGICS INC +1

Manufacturing method of chemical nickel palladium gold plating plated with thick palladium

The invention relates to the technical field of chemical nickel palladium gold platings, and discloses a manufacturing method of a chemical nickel palladium gold plating plated with thick palladium. The method is used for forming a nickel palladium gold plating on a surface of a circuit board, and comprises the following steps: 1) acidic oil removing; 2) micro-etching; 3) acid washing; 4) acid pre-pickling; 5) palladium activation; 6) acid post-pickling; 7) chemical nickel plating; 8) chemical plating of thick palladium, that is, chemical deposition of a palladium layer on a nickel layer of a circuit board by using organic acid and palladous sulfate; 9) chemical gold dipping. The palladium layer is formed on the nickel layer by using organic acid and palladous sulfate. The palladium layer is a palladium-storing system, and has a high thickness, so only a thin gold layer is needed to be formed on the palladium layer. Therefore, the production cost of the plating is reduced, the use of gold salt with severe toxicity is reduced, and the safety is greatly improved; figure 2 shows the surface nanometer morphology of the palladium layer; the palladium layer has low hardness and internal stress, and has excellent wetting performance; therefore, the gold wire bonding performance and the tin soldering performance of the plating are excellent.
Owner:SHENZHEN SUNTAK MULTILAYER PCB

Fluoropyrimidine compound carbalkoxylation method

The invention relates to fluorine contained miazines compound N-4 position alkyl oxygen carbonyl acidylating method, and its use in composing antineoplastic medicine-capecitabine. The invention has the advantages of avoiding using severe toxicity reagent such as, chloro formate, or phosgene etc, stable and easily gaining raw material, easy industrialization operation etc.
Owner:ZHEJIANG HISUN PHARMA CO LTD

Method for non-cyanide imitation gold plating of Cu-Zn binary alloy

ActiveCN103866356AGood dispersionStrong depth capabilityDispersityChemical treatment
The invention provides a plating solution for the non-cyanide imitation gold plating of a Cu-Zn binary alloy on low carbon steel, and its use method in order to improve the problems of severe toxicity, bad anode dissolvability and high treatment cost of three wastes of cyanide-containing plating solutions and the problems of complex composition, narrow range of technological parameters and unrealistic imitation gold color of non-cyanide plating solutions in present imitation gold plating technologies. The method is characterized in that the method comprises the following steps: an activated matrix can be directly plated without cleaning, so the operation is simple; the imitation gold plating solution is composed of potassium pyrophosphate, copper sulfate, zinc sulfate and glycerin, so the imitation gold plating solution has the advantages of green property, environmental protection, good dispersity, strong homogeneous plating ability, simple composition and easy maintenance; and the prepared gold imitation plating solution can meet the requirements of the cross cut test requirements of national standard GB9286-1998 paint and varnish film; and the obtained coating is passivated and seal-protected, and the protected coating meets the 5% brine neutral salt spray test indexes of the national standard GB5938-86 Corrosion Resistance Test Method of Metal Coating and Chemical Treatment Layer of Light Industrial Product, and can be used as a decorative coating.
Owner:INST OF PROCESS ENG CHINESE ACAD OF SCI

Preparation method of pitavastatin calcium

The invention relates to a preparation method of pitavastatin calcium for treating hyperlipidemia. The preparation method comprises the following steps: performing cyclization on 2-amino-4'-fluorobenzophenone (III) and ethyl 3-cyclopropyl-3-oxo-propanoate (II), and then reducing with LiAlH4 to obtain 2-cyclopropyl-4-(4-fluorophenyl)-3-quinoline methanol (V); bromizing the V to obtain 2-cyclopropyl-3-bromomethyl-4-(4-fluorophenyl) quinoline (VI); reacting the VI with triphenylphosphine to obtain (2-cyclopropyl-4-(4-fluorophenyl)-quinoline-3-yl) methyltriphenylphosphonium bromide (VII), performing alkali treatment on a phosphonium salt, then forming phosphonium ylide, performing condensation with (3R, 5S)-6-oxo-3, 5-isopropylidene-dioxo-6-heptenoic acid tert-butyl ester (VIII) to obtain a compound IX; and acidifying the compound IX with hydrochloric acid, performing hydrolysis deprotection with sodium hydroxide, performing salt formation and purification with chiral amine and forming a calcium slat to obtain a final product. The whole route has reasonable design, the process flow is simple, starting raw materials and reagents used by the preparation method can be purchased from the market, the reagents with severe toxicity and serious pollution are not used in a reaction process, the post-treatment of an intermediate is simple, and the preparation method has the advantages of high yield and is easy to purify.
Owner:WEIHAI WEITAI PHARMA TECH DEV

Two-dimensional code type chemical toxicity information building and searching method

The invention discloses a two-dimensional code type chemical toxicity information building and searching method. Biophysical-chemical information and biological toxicity information of chemicals are collected, information introduction is simplified, the chemicals are divided into four types including severe toxicity, high toxicity, middle toxicity and low toxicity, hazard classes of the toxicity of the chemicals to human bodies are calculated by a comprehensive index method according to chemical toxicity classification grades, a simple chemical toxicity information list not exceeding 140 characters is generated according to the biophysical-chemical information and biological toxicity grade information of the chemicals, the simple chemical toxicity information list is converted into two-dimensional codes with different sizes through a two-dimensional code converter, the two-dimensional codes are laminated and pasted on a chemical outer package, an APP (application) is scanned by the two-dimensional codes on handheld wireless mobile terminals such as a smart phone with a scanning function, chemical users rapidly, simply and conveniently acquire, store and spread the toxicity information of the chemicals at low cost, and toxicity warning and health protection functions are achieved.
Owner:QINGDAO AGRI UNIV

Method for stimulating a host immune system by administering an allogeneic cell material

ActiveUS20080279861A1BiocideVertebrate antigen ingredientsAbnormal tissue growthConditioning regimen
A method of manipulating allogeneic cells for use in allogeneic cell therapy protocols is described. The method provides a composition of highly activated allogeneic T-cells which are infused into immunocompetent cancer patients to elicit a novel anti-tumor immune mechanism called the “Mirror Effect”. In contrast to current allogeneic cell therapy protocols where T-cells in the graft mediate the beneficial graft vs. tumor (GVT) and detrimental graft vs. host (GVH) effects, the allogeneic cells of the present invention stimulate host T-cells to mediate the “mirror” of these effects. The mirror of the GVT effect is the host vs. tumor (HVT) effect. The “mirror” of the GVH effect is the host vs. graft (HVG) effect. The effectiveness and widespread application of the anti-tumor GVT effect is limited by the severe toxicity of the GVH effect. In the present invention, the anti-tumor HVT effect occurs in conjunction with a non-toxic HVG rejection effect. The highly activated allogeneic cells of the invention can be used to stimulate host immunity in a complete HLA mis-matched setting in patients that have not had a prior bone marrow transplant or received chemotherapy and / or radiation conditioning regimens.
Owner:MIRROR BIOLOGICS INC +1

Double line rectification method of hexafluoropropene production cracking gas, and rectification apparatus thereof

The invention relates to a double line rectification method of hexafluoropropene production cracking gas, and a rectification apparatus thereof. The double line rectification method adopting 6 rectifications and two-time compression is carried out to separate light components from heavy components and separate low toxicity components and severe toxicity components, and new technologic control parameters are adopted, so the quantity of devices containing severe toxicity octafluoroisobutylene is greatly reduced, the safety level of the apparatus is improved, the HFP (hexafluoropropene) product quality is improved, energy consumption is reduced, the production power of the apparatus is improved, the production cost is reduced, the apparatus utilization efficiency is improved, the unit consumption is reduced, and the apparatus and the method have very high safety, environmental protection energy saving and consumption reduction benefits.
Owner:福建三农新材料有限责任公司

Method enhancing oxidization leaching with arsenic in arsenic-cobalt-nickel containing slag

The invention relates to a method for enhancing oxidization leaching of low-valence arsenic existed as an alloy form of arsenic copper, arsenic cobalt and arsenic nickel in arsenic-cobalt-nickel containing slag by taking NaOH or KOH solution as a leaching medium and taking a copper oxide as an oxidizing agent. In the method, on one hand, an alkali medium is taken as the leaching medium, thereby the risk of generation of arsine gas with severe toxicity can be avoided during acid leaching; on the other hand, the copper oxide is taken as the oxidizing agent, by comparing with oxygen pressure leaching of the alkali medium, operation pressure of a system is reduced, copper in the copper oxide can not be dissolved in the alkali medium, and can follow with copper in the arsenic-cobalt-nickel containing slag into a copper smelting system. The method is the further improvement of a pressure oxidation leaching-out method for the alkali medium.
Owner:INST OF PROCESS ENG CHINESE ACAD OF SCI

Preparation method of ceftaroline fosamil intermediate parent nucleus

The invention provides a preparation method of ceftaroline fosamil intermediate parent nucleus, which comprises the following steps: 3-hydroxycephem and an activation reagent are reacted under existence condition of an acid binding agent and an organic solvent to obtain an activated intermediate; the activation reagent comprises p-toluene sulfonyl chloride, benzenesulfonyl choride, 4-nitrobenzene sulfonyl chloride, trifluoroactic anhydride or trifluoromethanesulfonic anhydride; the activated intermediate and 4-(4-pyridyl)-2-mercaptothiazole are reacted, then is reacted to a quaternized reagent to obtain pyridinium salt; and then deprotection is carried out to obtain the ceftaroline fosamil intermediate parent nucleus. Compared with the prior art, The p-toluene sulfonyl chloride, benzenesulfonyl choride, 4-nitrobenzene sulfonyl chloride, trifluoroactic anhydride or trifluoromethanesulfonic anhydride are used for substituting the usage of a severe toxicity material, reaction security is increased, due to increasing steric hindrance of an activating group, rate for generating a delta-3 isomer is reduced, and purity and yield of the reaction products are increased.
Owner:国药集团致君(苏州)制药有限公司

Method for compounding microcrystalline glass materials by means of ferrochrome slags

The invention relates to the technical field of synthesis of inorganic nonmetal materials, and aims at providing a method for compounding pyroxene-type microcrystalline glass materials by means of solid waste such as ferrochrome slags and waste glass, limestone, sodium carbonate and fluorite. The raw materials used for compounding mainly adopt the solid waste, and the ferrochrome slags belong to waste with severe toxicity and need to be treated individually. The waste microcrystalline glass materials are compounded only by means of normal pressed sintering, all performances meet needs of industrial production, the problem that the environment is polluted due to the fact that a large amount of solid waste is stacked is solved, the compounded waste slag type microcrystalline glass materials can be applied to building decoration materials, the method for compounding the pyroxene-type microcrystalline glass materials by means of the solid waste such as the ferrochrome slags and the waste glass, the limestone, the sodium carbonate and the fluorite accords with the industrial policy of circular economy advocated by the nation, and higher economic value and environmental significance are achieved.
Owner:UNIV OF SCI & TECH BEIJING

Promoting coronary circulation intelligence benefiting Chinese medicine for curing vascular dementia

InactiveCN101254280AInhibit the development of sclerosisEnhance memoryNervous disorderPlant ingredientsGastrodiaSide effect
The invention belongs to the technology field of traditional Chinese medicine, in particular to a traditional Chinese medicine for activating blood circulation, dredging vessels and benefiting wisdom which is used for the treatment of vascular dementia, thus solving the problems of limited efficacy, severe toxicity and side effects and expensive cost of the medicine for the treatment of vascular dementia in the prior art. The traditional Chinese medicine for activating blood circulation, dredging vessels and benefiting wisdom which is used for the treatment of vascular dementia takes grassleaf sweelflag rhizome, danshen root, tuber fleeceflower root, membranous milkvetch root, Chinese angelica, wild hawthorn fruit and epimedium herb as sovereign medicines. Tall gastrodia tuber, cassia seed, oriental waterplantain rhizome, kudzuvine root and stewed rhubarb are taken as auxiliary materials. The medicine of the invention can improve the memory, know the symptoms, or have certain efficacies on the aspects of spirit antagonism and behavior obstacles, regulate blood pressure, blood lipids, blood glucose and blood rheology, inhibit peroxide substances, improve neurotransmitter conduction and free radical metabolism and have the inhibition of the development of vascular sclerosis, so the medicine can be used for the prevention and the treatment of vascular dementia.
Owner:吴金珠

Dapagliflozin preparation method

The invention relates to a Dapagliflozin preparation method, which comprises the following steps: using 2-chlorobenzaldehyde as a starting material, carrying out bromination, reducing, chlorinating tosynthesize 5-bromo-2-chlorobenzyl chloride, carrying out Friedel-Crafts alkylation reaction between 5-bromo-2-chlorobenzyl chloride and phenetole to synthesize 5-bromo-2-chloro-4'-ethyoxyldiphenylmethane, conducting condensation between 5-bromo-2-chloro-4'-ethyoxyldiphenylmethane and 2,3,4,6-tetra-O-trimethylsilyl-D-glucolactone, carrying out trimethylsilyl deprotection, conducting etherification, and reducing for demethylation to obtain a hypoglycemic drug Dapagliflozin. The invention has the following advantages: according to the Dapagliflozin preparation method, 2-chlorobenzaldehyde, whichis used as a starting material, is cheaper and easily available in comparison with 5-bromo-2-chlorobenzoic acid, and the technology is easy for industrialization; during the synthetic process, no rawmaterials which cause severe toxicity will be used and furthermore there is no dangerous process; the synthetic route is short and novel and the operation is simple; and through the synthetic route,purity of the final product can be raised, and the purity can reach 99% and above.
Owner:IANGSU COLLEGE OF ENG & TECH

Rapid analysis method for main salts in zinc-nickel electroplating solution

The invention discloses a rapid analysis method for main salts in a zinc-nickel electroplating solution. According to the invention, an alkaline galvanized nickel alloy electroplating solution is analyzed, and the total content of zinc and nickel ions in the electroplating solution is calculated by selecting a determination method directed at the chemical properties of the electroplating solution to titrate main components in the electroplating solution and determining the volume of a titration reagent according to color changes, precipitation and the like of the electroplating solution; and then the content of nickel ions in the electroplating solution is determined through usage of spectrophotometry, and the contents of zinc and nickel ions are calculated, so changes are made to a conventional standard determination method using cyanide with severe toxicity. Compared with the standard determination method, a novel determination process is established, and thorough cyanide elimination is realized in the alkaline galvanized nickel alloy electroplating industry.
Owner:SHENYANG LIGONG UNIV

Treatment method for cyanogen-containing wastewater

The invention discloses a treatment method for cyanogen-containing wastewater. The treatment method comprises the following steps: a, adding alkali in the cyanogen-containing wastewater to adjust a pH value to 10 to 11; b, adding an oxidizing agent into the solution treated in the step a so as to oxidize complex cyanide ions with severe toxicity in the wastewater into cyanate ions with low toxicity; c, adding acid into the solution treated in the step b so as to adjust a pH value to 7 to 8; and d, continuing adding the oxidizing agent into the solution treated in the step c so as to allow the cyanate ions to be oxidized into N2 which overflows out from the wastewater. The treatment method has the characteristics of simple operation, a good treating effect and capacity of realizing long-term stable standard discharge.
Owner:LIDA ENVIRONMENT ENG DALIAN ECONOMIC TECH DEV ZONE

Lithium ion battery housing material plastic-aluminum composite membrane and preparation method thereof

The invention relates to the field of battery housing material technology, especially relates to a lithium ion battery housing material plastic-aluminum composite membrane and preparation method thereof; the lithium ion battery housing material plastic-aluminum composite membrane of the present invention has the character that because an external layer is made from a polyamide polymer, which protects the aluminium layer from fracturing during cold stamping forming, after the cold stamping forming, the lithium ion battery can reach the technology requirements such as waterproof, moistureproof, sealing, insulating property and puncture resisting performances. In addition, according to the preparation method provided by the invention, an oxidation treatment solution of the present invention has a certain surface adsorption enhancing effect, thereby refining texture and forming a uniform and compact conversion film with a certain thickness on the aluminium foil surface; the conversion film has excellent adhesion force with the organic coating and has impact performance, or the like, and after the aluminium foil surface is treated by an oxidation treatment, the bonding force of the aluminium foil surface and the high-molecular material is substantially increased; the preparation method has the advantages of simple oxidation treatment solution preparation, relative low control requirement of the technology condition, convenient operation and low cost; because hexavalent chromium with severe toxicity is not contained, the product belongs to the green environmental protection treatment fluid.
Owner:东莞市才智坊新材料有限公司

Method for preparing 2-chloro-4-fluorobenzene nitrile

The invention provides a method for preparing 2-chloro-4-fluorobenzonitrile. The method comprises the following steps: using 2-chloro-4-nitrobenzonitrile and potassium fluoride as raw materials and dialkylacetamide or dialkyl sulfoxide as a solvent to generate a reaction mixture containing the 2-chloro-4-fluorobenzonitrile at a certain temperature by adopting a quaternary alkylphosphonium salt as a catalyst; the reaction mixture adopts a saturated alkane extraction method; and an extraction liquid is rectified at the reduced pressure to obtain the required product 2-chloro-4-fluorobenzonitrile. The method has the advantages that the process route is simple; the raw materials are accessible and cheap, do not have severe toxicity, have strong stability, and do not pollute the environment; the purity of the product 2-chloro-4-fluorobenzonitrile is more than 99 percent, and yield of the product is over 80 percent; and high reaction selectivity reaches over 90 percent.
Owner:ZHANGJIAGANG HUASHENG CHEM CO LTD

Chinese herbal oil solution for treating burns and preparation method thereof

The invention provides a Chinese herbal oil solution for treating burns and a preparation method thereof, belonging to the field of pharmacy and medical technology in traditional Chinese medicine. The Chinese herbal oil solution comprises the following raw materials by weight: 7 to 15 parts of centella, 7 to 15 parts of dahurian angelica root, 7 to 15 parts of bletilla rhizomes, 7 to 15 parts of Chinese rhubarb, 7 to 15 parts of Chinese ilex leaves, 7 to 15 parts of Biota orientalis, 7 to 15 parts of honeysuckle flowers, 12 to 18 parts of lithospermum, 5 to 10 parts of frankincense, 5 to 10 parts of myrrh, 4 to 8 parts of dragon's blood, 7 to 15 parts of catechu, 1 to 5 parts of borneol and 130 to 180 parts of sesame oil. The Chinese herbal oil solution provided by the invention has antibacterial, anti-inflammation, detumescent, pain-relieving, pus-expelling, astringing, flesh-engendering and scar-growth-inhibiting effect, and has good effect on third-degree burn wound and infection wounds with diameters of less than 12 cm, second-degree burns, soft tissue contusion, bedsores and burns caused by pesticides and chemicals with severe toxicity; the Chinese herbal oil solution allows a healed wound to be free of obvious protruding or recessed scars, is short in treatment period, simple and easily practicable; and when a dressing for a wound is to be changed during outpatient service, the Chinese herbal oil solution causes little pain and is low in cost.
Owner:唐永奎

Halogen-free burning resistant adhesive plaster and its manufacturing method

The invention relates to a halogen-free burning resistant adhesive plaster and its manufacturing method. The manufacturing method comprises the following steps of: firstly forming epoxy natural adhesive paste on the surface of base cloth and then pasting a halogen-free natural adhesive plaster on the surface of the base cloth by the use of the epoxy natural adhesive paste to finish the manufacturing. The above halogen-free natural adhesive plaster is made from a halogen-free natural adhesive material which contains a phosphorus burning resistant agent and an inorganic burning resistant filler. By the mutual cooperative effect of the phosphorus burning resistant agent and the inorganic burning resistant filler, the expected burning resistant effect is achieved; in addition, the halogen-free burning resistant adhesive plaster can replace a halogen burning resistant adhesive agent so as to avoid severe symptoms in human body such as poor metabolism, immune function disorder and the like due to severe toxicity of halogen.
Owner:FORMOSAN RUBBER GRP

Epoxiconazole preparation method thereof

The invention relates to the technical field of chemical industry, and discloses an epoxiconazole preparation method. The method comprises the following steps: adding fluorobenzene and a solvent in aglass reaction bottle equipped with a stirrer and a condenser, wherein the ratio of fluorobenzene to acetyl chloride is 1:15, selecting dichloroethanes as the solvent by taking regard of toxicity andcost, dropping dichloroethanes under stirring, controlling the reaction temperature for fully reacting the materials in a glass reaction bottle after 5 hours, after the reaction is completed, performing hydrolysis with hydrochloric acid, steaming excessive fluorobenzene by water vapor, and performing desolvation through solvent extraction to obtain the fluoroacetophenone. The preparation method ofthe epoxiconazole is characterized in that a synthesis route is integrally improved, the preparation method has the advantages of simple process, and low cost and easy acquisition of raw material, the epoxiconazole has high stereoselective performance, cannot generate high salt waste water, does not use severe-toxicity methanesulfonyl chloride, accords with environmental protection requirement, and is suitable for industrial production, and the yield and content of the final product are high.
Owner:ABA CHEM NANTONG

Synthesis method of 8-hydroxyquinaldine

InactiveCN103483253ALow costSimple processOrganic chemistry8-hydroxyquinaldineCrotonaldehyde
The invention discloses a synthesis method of 8-hydroxyquinaldine. The synthesis method is characterized by comprising the steps of (1) fully dissolving o-aminophenol and o-nitrophenol in a mixed solution of hydrochloric acid and acetic acid at the temperature of 30-100 DEG C, slowly dropping paraldehyde at the temperature, and performing heat preservation reaction for 1-8h after the end of dropping; (2) removing unreacted o-nitrophenol by steam distillation, cooling the remaining solution to room temperature, neutralizing with an alkaline solution, and then filtering to obtain a solid crude product; (3) performing reduced pressure distillation and re-crystallization with an ethanol water solution to obtain a high-purity crystal product. According to the method disclosed by the invention, low-toxicity paraldehyde is used for replacing crotonaldehyde with severe toxicity, and the method has the advantages of simple process and low raw material cost, and is suitable for large-scale production.
Owner:SHUANGLE CHEM PIGMENT YANGZHOU CITY

Preparation method of D-(-)-alpha-sulbenicillin sodium

The invention provides a preparation method of D-(-)-alpha-sulbenicillin sodium. The method comprises the following steps: taking alpha-sulfonylphenylacetic acid as an initial raw material, performinga reaction with carbonyl diimidazole to generate an acyl imidazoles acylating agent, and performing condensation with 6-APA to obtain a diastereomer of sulbenicillin; separating D-(-)-alpha-sulbenicillin by a recrystallization method, and forming salt with sodium hydroxide to obtain the D-(-)-alpha-sulbenicillin sodium. During a acid anhydrides preparation process, usage of a severe-toxicity substance is avoided, during a preparation process, recrystallization is used, and the optically pure D-(-)-alpha-sulbenicillin is prepared, cost is saved, operation is simplified, yield is increased, andthe method is in favor of industrial production and environment protection.
Owner:HUNAN ER KANG PHARMA

An antitumor compound capable of overcoming cisplatin resistance and its preparation and application

The present invention provides an anti-tumor compound capable of overcoming cisplatin resistance and its preparation and application. The anti-tumor compound capable of overcoming cisplatin resistance has a structure such as compound 1 and compound 2 shown in formula I. In view of Cisplatin has serious toxicity and drug resistance in clinical application, and the technical problem to be solved by the present invention is to use the compound that inhibits protein kinase 2 activity to be able to inhibit the characteristics of DNA damage repair, and known platinum containing functional groups ( II) Combining compounds, designing and synthesizing a new platinum (II) compound, the obtained compound not only has a strong inhibitory effect on cisplatin-sensitive tumors but also cisplatin-resistant tumors, and has less toxicity and has With the characteristics of high efficiency and low toxicity, it can be used to prepare antitumor drugs.
Owner:SOUTHEAST UNIV

Imide group-containing polymer foam material and preparation method thereof

The invention discloses an imide group-containing polymer foam material and a preparation method thereof. The preparation method comprises the following steps that one or two ester group-containing propylene monomers, one or two amido group-containing propylene monomers, one or more polymerization initiators, a mixed foaming agent, one or more cross-linking agents and one or two solvents are added into a reactor and undergo a continuous reaction to form sticky substances; the sticky substances obtained from the previous step are treated by processes of washing, filtering and drying; the driedsticky substances obtained from the previous step are grinded into copolymer powder; and the copolymer powder is putted into a mould and are treated by a series of processes to form finished products. In the invention, (methyl) acrylonitrile with a severe toxicity is not utilized, and moulds can be designed according to shapes of finished products thus a foam material in any shape can be obtainedwithout being cut so that a cellular structure of the foam material is not damaged; related properties of the foam material are not reduced; and an application scope of the foam material is greatly widened. The imide group-containing polymer foam material prepared through the preparation method can be widely and directly utilized in the fields of aviation and spaceflight, carrier rockets, railwaylocomotives, ships, wind generator blades, sports goods and the like.
Owner:ZHEJIANG SCI-TECH UNIV

ECH-Fenton combined process for harmless degradation of dichlorophen

The invention provides an ECH-Fenton combined process for harmless degradation of dichlorophen, which belongs to the technical field of electrochemical water treatment. The process comprises the following steps: highly-efficiently degrading dichlorophen by using a Pd / PPy(SDBS) / Ti electrode with high catalytic activity; and then further degrading dichlorophen by using a Fenton reagent so as to realize harmless removal of dichlorophen. The ECH-Fenton combined process realizes 100% high-efficiency harmless degradation of the pollutant dichlorophen with severe toxicity.
Owner:BEIJING UNIV OF TECH

Industrialization preparation method for RDG peptide

The invention discloses an industrialization preparation method for RDG peptide. The technical scheme of the present invention comprises the following steps: Wang resin is taken as an initial raw material and TBTU / HOBt is taken as a condensing agent, amino acid possessing a Fmoc-protective group is successively connected according to a solid phase synthesis method, Boc-Arg-OH.HCl is used by a last amino acid to obtain protective tripeptide resin, and meanwhile crude products are obtained by sequentially removing Fmoc-protective groups synchronized with acellular side-chain protective groups and cutting peptides, and the RDG peptide elaborate products are prepared after the crude products are separated and purified by a C18 high performance liquid phase column and freeze-dried. The method of the invention is capable of reducing the production cost and simplifying the process flow. The crude products can be deposited by ether after cutting peptides so that the usage of hydrogen fluoride with severe toxicity can be avoided and the three wastes pollution is reduced. C18 column is used for separating and purifying to avoid the usage of trifluoroacetic acid and reduce three wastes. The purification yield is more than 50%, the each step of transpeptidase yield is more than 98%, the yield after cutting peptides is 88%, the separation and purification yield is 58% and the overall yield is 51%. The method of the present invention is convenient for industrial enforcement and has large industrialization prospect.
Owner:SHANGHAI SOHO YIMING PHARMA

Coronary circulation promoting, intelligence benefiting Chinese medicine for curing vascular dementia

The invention belongs to the technology field of traditional Chinese medicine, in particular to a traditional Chinese medicine for activating blood circulation, dredging vessels and benefiting wisdom which is used for the treatment of vascular dementia, thus solving the problems of limited efficacy, severe toxicity and side effects and expensive cost of the medicine for the treatment of vascular dementia in the prior art. The traditional Chinese medicine for activating blood circulation, dredging vessels and benefiting wisdom which is used for the treatment of vascular dementia takes grassleaf sweelflag rhizome, danshen root, tuber fleeceflower root, membranous milkvetch root, Chinese angelica, wild hawthorn fruit and epimedium herb as sovereign medicines. Tall gastrodia tuber, cassia seed, oriental waterplantain rhizome, kudzuvine root and stewed rhubarb are taken as auxiliary materials. The medicine of the invention can improve the memory, know the symptoms, or have certain efficacies on the aspects of spirit antagonism and behavior obstacles, regulate blood pressure, blood lipids, blood glucose and blood rheology, inhibit peroxide substances, improve neurotransmitter conductionand free radical metabolism and have the inhibition of the development of vascular sclerosis, so the medicine can be used for the prevention and the treatment of vascular dementia.
Owner:吴金珠

A kind of industrial preparation method of baadin tripeptide

The invention discloses an industrialization preparation method for RDG peptide. The technical scheme of the present invention comprises the following steps: Wang resin is taken as an initial raw material and TBTU / HOBt is taken as a condensing agent, amino acid possessing a Fmoc-protective group is successively connected according to a solid phase synthesis method, Boc-Arg-OH.HCl is used by a last amino acid to obtain protective tripeptide resin, and meanwhile crude products are obtained by sequentially removing Fmoc-protective groups synchronized with acellular side-chain protective groups and cutting peptides, and the RDG peptide elaborate products are prepared after the crude products are separated and purified by a C18 high performance liquid phase column and freeze-dried. The method of the invention is capable of reducing the production cost and simplifying the process flow. The crude products can be deposited by ether after cutting peptides so that the usage of hydrogen fluoride with severe toxicity can be avoided and the three wastes pollution is reduced. C18 column is used for separating and purifying to avoid the usage of trifluoroacetic acid and reduce three wastes. The purification yield is more than 50%, the each step of transpeptidase yield is more than 98%, the yield after cutting peptides is 88%, the separation and purification yield is 58% and the overall yield is 51%. The method of the present invention is convenient for industrial enforcement and has large industrialization prospect.
Owner:SHANGHAI SOHO YIMING PHARMA
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