238 results about "Dual target" patented technology

The invention discloses a method for reducing the content of cadmium in middle rice. The method includes the following steps that after middle rice of the first year is harvested, middle rice straw is returned to the field directly, and tillage is conducted so that the middle rice straw can be evenly mixed with soil; hyperaccumulation plants are planted in a paddy; after the hyperaccumulation plants are removed from March to May in the second year, soil heavy metal passivator is scattered on the surface of soil of the paddy; tillage is conducted, and base fertilizer is applied 3-5 days later; tillage is conducted, and rice is transplanted; during planting of rice, a foliar resistance control agent is sprayed in the later tillering stage and the booting stage of rice respectively, wherein spraying time interval is 5-10 days; field drying is conducted in the later tillering stage, natural drying is conducted in the maturation stage, and flooding irrigation is conducted in other development stages. According to the method, crop production and straw resource utilization are not affected, the dual targets of reducing the paddy soil cadmium content and reducing the rice cadmium content are achieved under the combined action of plant extraction, soil passivation, foliar resistance control and water management, and effects are more remarkable compared with other combination technologies.

The invention discloses a dual target liposome and a preparation method and application thereof. The target liposome provided by the invention consists of liposome and modifiers on the surface of the liposome, wherein the modifiers on the surface of the liposome comprise p-aminophenyl-alpha-D-manno-pyranoside and transferrin. The invention also discloses a medicament-loaded liposome, which is obtained by wrapping daunorubicin by using the target liposome. The obtained target liposome has good capability of crossing the blood brain barrier, targets brain glioma, and can be used as a medicament carrier. The medicament-loaded liposome can target the medicament to a brain glioma site after crossing the blood brain barrier so as to greatly increase the concentration of the medicament at a tumor site and improve the effect of chemotherapy. The target liposome provides a new measure for brain glioma chemotherapy, contributes to the research of non-invasive therapy of the brain glioma, and has important theoretical meaning and clinical meaning.

The invention discloses a dual-target-optimization-based dynamic timing method for an urban traffic signal lamp. The method comprises: a green time ratio, maximum green light time, minimum green light time, and a signal cycle T of an intersection are designated primarily and a conversion step length B is designated; during the given signal cycle T, a green light signal of the intersection is turned on successively according to a phase; traffic data at the intersection are monitored in real time, and a green light phase vehicle queuing length p and a vehicle queuing length q of a next green light phase of the intersection are calculated, and a fuzzy logic controller adjusts green time ratios u of all phases of the intersection in real time; and a traffic flow of the intersection is calculated, and a cycle optimization controller determines a signal cycle value T' at a next stage and green light time gei' of all phases. According to the invention, the average number of times for parking and average delay time can be reduced effectively; the road traffic passing efficiency is improved; control of the traffic control system becomes reasonable; and the traffic congestion phenomenon is alleviated fundamentally.

The invention discloses an NAMPT / HDAC dual-target inhibitor and a preparation method thereof. The dual-target inhibitor is an amide derivative and pharmaceutically acceptable salt thereof, wherein a structure general formula is represented as the formula (I). A pharmacological experiment proves that the derivative or the salt thereof have very strong inhibition activity on the nicotinamide phosphoribosyl transferase and the histone deacetylase, and have high in-vitro anti-tumor activity and excellent in-vivo tumor inhibiting effect. The invention also provides a preparation method of the derivative and the pharmaceutically acceptable salt thereof, and an application in preparation of an NAMPT inhibitor, a HDAC inhibitor, and anti-tumor medicines.

The present invention relates to: a dual targeting antibody of a novel form having a water-soluble ligand fused to the N-terminus of a heavy chain or light chain of an antibody; a DNA encoding the dual targeting antibody; a recombinant expression vector containing the DNA; a host cell which is transformed with the recombinant expression vector; a method for preparing the dual targeting antibody by culturing the host cell; and a pharmaceutical composition including the dual targeting antibody.

The present invention relates to compositions and methods for treating diabetic retinopathy and other ocular neovascularization diseases. In one embodiment, the composition comprises at least two different siRNA duplexes and a pharmaceutically acceptable carrier. One of the duplexes binds to an mRNA molecule that encodes VEGF, and the other binds to an mRNA molecule that encodes VEGFR2. In another embodiment, the composition further comprises an siRNA duplex that binds to an mRNA molecule that encodes TGFβ1.

This invention relates to adaptive resistance inhibiting 100 to 10,000 Gy, single fraction proton and carbon ion microbeam and nanobeam radiosurgery, proton spray chemotherapy and proton spray gadolinium and boron neutron capture therapy with least normal tissue toxicity. Secondary neutrons, protons, ions and radiation from the accelerator and the patient specific collimator are removed with tissue equivalent collimator that also generates proton and carbon ion microbeam and nanobeam. Laser interaction with micrometer and nanometer thick metallic and diamond like carbon targets are also used for proton and carbon ion beam generation. Polyenergetic proton beam is spatially separated. Ion beam and Laser ion beam is accelerated in a hybrid RF accelerator. It is split into microbeam and nanobeam. Secondary neutrons, protons and gamma radiation are removed with tissue equivalent collimators that also generate microbeams and nanobeams. Adaptive resistance to cancer treatment is inhibited by dual target radiation, DNA strands break and enzymes inactivation.

The invention relates to a dual-target positioning method for a simulated medical instrument and a virtual simulation medical teaching system. The dual-target positioning method comprises: an instrument is associated with a feature target; cameras are configured and an overlapped view area between two cameras is adjusted; calibration is carried out; to be specific, the cameras obtain images of a calibration reference object and internal and external parameters of the cameras are calculated; correction is carried out; to be specific, distortion elimination and row alignment are carried out on aleft view and a right view respectively according to the internal and external parameters obtained after camera calibration, so that antipode lines are aligned in rows; instrument capturing is carried out; to be specific, a feature target is captured to capture an instrument; and three-dimensional matching is carried out; to be specific, three-dimensional matching is carried out based on a mapping relationship and distortion is corrected, and a spatial position of the instrument is calculated in real time. According to the invention, only a designated feature target needs to be pasted to thesurface of a medical instrument and no other object connection is needed, so that the portability is improved substantially and the simulation degree is increased; the moving area is adjusted by adjusting the cameras, so that the operating area is increased greatly; and a plurality of medical simulation instruments can be identified simultaneously.

The invention provides a preparation method of a target compound nano particle, relating to a preparation method of target treatment integration compound nano particles. The invention solves the technical problems of poor carrier stability and small drug-loading quantity of the traditional antineoplastic drugs. The method comprises the following steps of: preparing a methanol solution of an integrated nano particle of a Fe3O4-HCPT@SiO2 coupling porphyrin photosensitizer; and stirring the methanol solution of the integrated nano particle of the Fe3O4-HCPT@SiO2 coupling porphyrin photosensitizer, N,N-dimethylformamide and target biomolecule or antitumor drug for reacting at the room temperature, and centrifuging to obtain the target compound nano particle. Polystyrolsulfon acid (PSS) and 10-hydroxycamptothecine are absorbed on a Fe3O4 magnetic nano particle through a self-assembly mode. The preparation method is high feasibility; the target compound nano particle has a physical target function of the magnetic nano particle and an active target function of further functionally modifying the biomolecule on the surface; and the medicine concentration can be increased under a dual-target function.

The invention relates to dual-targeting ursolic acid (UA) / siRNA loaded fluorescent mesoporous silica dioxide-hyaluronic acid and application. The technical scheme of the invention lies in that 1, fluorescently-labeled mesoporous silica dioxide nano particles are synthesized through the template method; 2, the surface of FMSN is subjected to amino modification through 3-aminopropyltriethoxysilane; 3, ursolic acid (UA) and siRNA are jointly loaded into porous channels of the nano particles; 4, hyaluronic acid is loaded into the outer surfaces of the nano material in a wrapping manner through electrostatic absorption, so as to obtain the dual-targeting ursolic acid (UA) / siRNA loaded fluorescent mesoporous silica dioxide-hyaluronic acid nano particles. According to the dual-targeting ursolic acid (UA) / siRNA loaded fluorescent mesoporous silica dioxide-hyaluronic acid and application, the prepared nano material is uniform in particle size distribution, and good in dispersibility, the stability of siRNA can be improved, and besides, siRNA can further specifically target tumor cell surface adhesion molecules like ICAM and CD44, therefore the anti-tumor effect of drugs can be greatly improved, and the toxic and side effect of the drugs can be further reduced.

The invention relates to a coating and the preparation method of the coating. The AlN / Si3N4 nano-multi-layer film of the invention, which is formed by AlN and Si3N4 on a metal or ceramic substrate, is a multi-layer structure of the alternating deposition nano meter level. The thickness of each layer ranges from 0.4 to 12.0 nm, and total thickness ranges from 1.0 to 5.0 micron. When in preparing, firstly, the surface of the metal or ceramic substrate can be polished to a mirror surface; and then, the layers of Si3N4 and the layers of AlN can be alternately deposited by using pure targets of Al and Si to conduct the dual-target RF reactive sputtering on the metal or ceramic substrate; finally, the nano-multi-layer film AlN / Si3N4 can be obtained by inletting Ar and N2 which are both in high-purity. The thickness of the nano-multi-layer film AlN / Si3N4 can be achieved by increasing the preparing cycle of the multi-layer film. The maximum hardness of the nano-multi-layer coating is 37.8 GPa, which significantly is higher than the material used for preparing the coating; the nano-multi-layer film AlN / Si3N4 provided by the invention can achieve higher production efficiency.

The invention discloses an infrared and visual light combined guidance semi-physical simulation method. The method includes the following steps that an infrared and visual light combined simulation system is built; a dual-target load type five-axis rotary table overall structure is determined; the layout and load installing mode of the infrared and visual light combined simulation system are determined; infrared and visible light double wavebands operate in a segments in a combined mode. The infrared and visual light combined guidance semi-physical simulation method effectively meets the requirement of large-diameter infrared and visual light combined seeker double waveband segmented combined guidance semi-physical simulation tests.

The present invention relates to dual-targeting cytotoxic compounds of formula (I) and to their preparation. The described compounds are endowed with tumour specific action, incorporating three functional units: a tumour recognition moiety and a tumour selective enzymatic substrate sequence connected together by means of a spacer. These conjugates are designed to guarantee serum stability and, at the same time, the desired action inside the tumour cells as a result of enzymatic cleavability. [(L-D)nE]m-F-D-PI-SI-CT Formula (I).

The invention relates to a preparation method of a dual-targeting drug carrier based on a magnetic metal organic framework material, belonging to the technical field of preparation of bio-medicinal functional materials. The preparation method comprises the following steps: firstly, modifying ferroferric oxide to form dopamine-wrapping ferroferric oxide, and preparing the dual-targeting drug carrier based on the magnetic metal organic framework material by taking dopamine-wrapping ferroferric oxide (Fe3O4@PDA) as the matrix material; and carrying out a series of treatment to obtain an adsorbent, and carrying out selective recognition and separation on adriamycin in an aqueous solution by adopting the adsorbent. The dual-targeting drug carrier based on the magnetic metal organic framework material prepared by adopting the method provided by the invention has good heat stability and very large medicine-carrying capacity, has the acid-base effect, and also has the function of controlling medicine release.

A cubic electrode is made up of base material, cubic structure and catalytic activate materials, the cubic structure material is composed of column, ball or un regular particles from millimicron-micron, combined or adhered to the base material with short distance capillary channel and gas breath structure favourable to methyl alcohol siphon characterizing in high pore space retion and rough surface. It's real surface area is far large than its own geometrical area and catalytic active to methyl alcohol. The cubic structure of electrode is built with electric chemical method reaching dual targets with cubic structure and catalytic active.

The invention discloses a cloud testing environment scheduling method based on load forecast. The cloud testing environment scheduling method based on the load forecast comprises the steps that a load changing database of testing host machines is established, and selection strategies of physical nodes are configured; the average load of all the physical nodes is obtained; according to the average load and a low threshold value, the testing host machines needing to be migrated on the physical nodes are judged; according to the load changing database, loads of the physical nodes are forecasted, and forecasting results are fed back; according to the forecasting results and the node selection strategies, the testing host machines needing to be scheduled are migrated to the selected physical nodes. According to the cloud testing environment scheduling method based on the load forecast, through the forecasting of the loads of all the physical nodes in the cloud testing environment, the most suitable target node of the cloud testing host machines needing to be scheduled is found, the dual targets of load balance and energy conservation of the cloud testing environment are achieved, the performance bottleneck of the cloud testing environment is eliminated, in this way, the stability of the whole cloud testing environment is improved, and the energy consumption of the system is lowered. The invention further discloses a cloud testing environment scheduling system based on the load forecast.

Discloses are CMOS circuit designs that combine MTCMOS and hybrid orientation technology to achieve the dual objectives of high performance and low standby leakage power. The invention utilizes novel combinations of a thick-oxide high-VTH PFET header with various gate- and body-biased schemes in HOT technology to significantly reduce the performance penalty associated with conventional PFET headers. A first embodiment of the invention provides a HOT-B high-VTH thick oxide bulk PFET header scheme. This header scheme can be expanded by application of a positive gate bias VPOS (VPOS>VDD) to the HOT-B PFET header during standby mode and a negative gate bias VNEG (VNEG<GND) in active mode. Another embodiment provides a HOT-A high-VTH thick oxide SOI PFET header scheme. A further embodiment provides a HOT-A body biased high-VTH thick oxide SOI PFET header scheme.

The invention discloses a dual-target robust resource allocation method under a resource transfer view angle. Through introducing activity construction period uncertainty and resource transfer cost, astarting time criticality index is used as a robustness solving target of a project; a new resource chain-based dual-target resource flow network model is provided under a resource transfer perspective, the problem field of robust project scheduling is extended, the content of resource flow network research is further enriched, and the application of a multi-target optimization algorithm in the field of project scheduling is expanded. In order to effectively solve the model, two multi-objective optimization algorithms, namely NSGA-II and PSA are designed. A coding mode and an initialization strategy of a solution adapting to problem characteristics are provided, and a resource allocation scheme with the strongest stability and the optimal cost under the environment with the uncertain construction period is sought.

The invention discloses Topology shape design method for partition machining track on curved surface based on vector field, and belongs to the technical field of high precision and high efficient milling machining of complex curved parts, and relates to a topology shape design method for partition machining track on curved surface based on vector field. The method comprises the steps of: establishing a feeding vector field with a cooperation constraint of a chord height error and a residual error, constructing a normalized dual target optimization model with two types of error, solving optimalfeeding direction of each point through an evaluation function, and establishing a space vector field; calculating a divergence and a rotation of a plane vector field after projection, and realizinginitial segmentation of the machining region according to whether the divergence and the rotation of the plane vector field are zero or not; analyzing different vector field features, fitting spatialvector field streamlines, calculating motion parameters of feeding motions of a machine tool rotating shaft along deformation lines, and completing machining region partition according to whether theparameters are mutated or not; and realizing the topology shape design of partition machining track on curved surface in combination with a feeding mode. The topology shape design method for the partition machining track on the curved surface based on the vector field is suitable for complex curved surface partition machining, can reduce machining errors, and improves motion smoothness of feeding.

A real-time measurement method of pupil diameters based on the binocular stereo vision is provided. The method comprises: using Zhang Zhengyou's dual target method for camera calibration to obtain a rotation matrix, a translation matrix, a parameter matrix in the left industrial camera, and a parameter matrix in the right industrial camera; respectively processing images captured by the left industrial camera and the right industrial camera to obtain true ellipses corresponding to the pupil; drawing a straight line across the center of the true ellipse of the pupil obtained by the left industrial camera, wherein the straight line equation is intersected by the true ellipse of the left industrial camera to obtain a first intersection point and a second intersection point; according to the principle of polar line constraint and order consistency, by using the first intersection point and the second intersection point, respectively solving a first matching point and a second matching point corresponding to the two intersection points on the true ellipse obtained by the right industrial camera; and obtaining preliminary values of a plurality of pupil diameters corresponding to a plurality of straight lines with different slopes, and solving an average value to obtain a final result. The method provided by the present invention has high measurement precision, does not require the worker to fix the working distance, and has great application value.

The invention relates to the field of pharmaceutical preparations and in particular relates to a pharmaceutical composition as well as application and a preparation method thereof. The pharmaceutical composition provided by the invention can be used for synergistically treating a tumor (a cancer) through dual actions of immunological therapy and active targeted drug therapy with remarkable curative effects. An adriamycin-bovine serum albumin conjugate as shown in a formula 1 is prepared from adriamycin and bovine serum albumin. The formula 1 is as shown in the specification.

The invention relates to a TiN / AlON nanometer multilayer coat used in cutter. Wherein, it is formed by alternatively depositing TiN layer and AlON layer on rigid alloy, ceramic or metal base; the thickness of TiN layer is 3-5nm while the thickness of AlON layer is 0.3-0.8nm; the total thickness of coat is 2-5 mum. The inventive coat can be obtained by using dual-target reaction splash technique of argon nitrogen mixed condition to alternatively deposit TiN layer and AlON layer on the furnished metal or ceramic base. The inventive coat has better high-temperature anti-oxidization property, and high rigidity, while the highest rigidity is 41GPa. And it can be used as the coat of high-speed cutting blade, etc.

Novel dual-targeted, bifunctional anti-influenza drugs formed by conjugation with anti-inflammatory agents are disclosed. Exemplary drugs according to the invention include caffeic acid (CA)-bearing zanamivir (ZA) conjugates ZA-7-CA (1), ZA-7-CA-amide (7) and ZA-7-Nap (43) for simultaneous inhibition of influenza virus neuraminidase and suppression of proinflammatory cytokines. Synthetic methods for preparation of these enhanced anti-influenza conjugate drugs are provided. The synthetic bifunctional ZA conjugates act synergistically towards protection of mice lethally infected by H1N1 or H5N1 influenza viruses. The efficacy of ZA-7-CA, ZA-7-CA-amide and ZA-7-Nap conjugates is much greater than the combination therapy of ZA with anti-inflammatory agents.

A vanadium oxide thermo-sensitive film material with a high temperature coefficient of resistance (TCR) contains a rare earth element of Yttrium serving as a dopant in a preparation process. The vanadium oxide thermo-sensitive film material includes a substrate and a yttrium-doped vanadium oxide film layer. The yttrium-doped vanadium oxide film layer includes three elements of vanadium, oxygen and yttrium, wherein the atomic concentration of yttrium is at a range of 1%-8%, the atomic concentration of vanadium is at a range of 20-40% and the residue is oxygen. The method for preparing the vanadium oxide thermo-sensitive film material with high TCR includes a reactive magnetron sputtering method using a low-concentration yttrium-vanadium alloy target as a sputtering source or a reactive magnetron co-sputtering method using dual targets including a high-concentration yttrium-vanadium alloy target and a pure vanadium target as a co-sputtering source.

The invention provides a tumor dual target liposome mediated by integrin and a preparation method thereof. The composition of the invention comprises the components of an antitumor medicament, polypeptide with tumor new vessel target function and tumor cell target function, polyethylene glycol and derivates thereof and a vector for preparing liposome medicaments.

The invention discloses a dual-target direct equalization circuit of a battery pack. A series battery pack comprises at least three single batteries and is divided into an upper part and a lower part,each single battery is connected with an equalization sub-circuit, the equalization sub-circuit comprises two metal-oxide-semiconductor field-effect transistors (MOSFETs) and an energy storage inductor, the series battery pack and the equalization sub-circuit bridge between VCC and GND, each equalization circuit is also connected with a control circuit to achieve direct equalization on an equalization target, the control circuit is used for equalizing end voltages and SOC of the single batteries in a stage way within an equalization period by simultaneously taking the end voltages and the SOCof the single batteries as equalization indexes, and dual-target equalization on the end voltages and the SOC of the single batteries is achieved by controlling on / off of the two MOSFETs of the equalization sub-circuit and by an energy storage effect of the energy storage inductor. The equalization circuit and an equalization strategy are applicable to an equalization management system of an energy storage device in a hybrid electric vehicle, a blade electric vehicle and an energy storage power station.

The invention provides construction and application of a fourth-generation chimeric antigen receptor T (CAR-T) cell (expressing IL-7 and CCL19) specific to Nectin-4 dual targets on the surface of a malignant tumor. Two spatial epitopes of a Nectin-4 antigen are taken as target points, and the constructed fourth-generation CAR-T is used for treating and expressing a malignant solid tumor of the Nectin-4 antigen to solve the immune escape problem of the CAR-T during treatment of the solid tumor; and the constructed fourth-generation CAR-T can enhance proliferative capacity and sustained survivability, so that the solid tumor is effectively treated, and a new strategy is provided for effective prevention and treatment of postoperative recurrence / metastasis of the solid tumor.

The invention discloses a system and a method for precisely identifying a target and calculating an effect in an ecological sponge type urban construction suitable area. The system comprises a spatialdata acquisition module, a suitable area spatial identification module, an index control and measure design module and a construction effect calculation module. The method is used for sponge city construction from city construction planning to engineering design whole process. Accurate identification of construction and reconstruction target suitable areas and suitable grade targets in urban heatisland control and urban landscaping processes can be realized, and the effects of flood disasters and high-temperature extreme climate events under different urban construction and reconstruction scenarios can be measured and calculated. The system comprises a novel sponge city and heat island control dual-target city planning and design framework, achieves refined remote sensing classificationand artificial intelligence detection algorithm aiming at precise identification of the ecological sponge city space suitability, and can effectively simulate the effects of city construction and reconstruction on rain flood and extreme high temperature events.

The invention discloses a dual-targeting ultrasonic contrast agent and a preparation method thereof. The contrast agent is an Integrin alpha v beta 3 / MCP-1 dual-targeting micro-vesicle, the dual-targeting micro-vesicle comprises a lipid shell and a gas inner core, and the external surface of the lipid shell is connected with an Integrin alpha v beta 3 monoclonal antibody and an MCP-1 monoclonal antibody. Through the combined application of different target spots, the targeting efficiency of the contrast agent can be effectively increased, and the degree of enrichment of the carrying genes in the target tissue can be greatly increased. In addition, the contrast agent disclosed by the invention is an ultrasonic contrast agent with double functions of development and treatment, and tumor images can be accurately observed in real time through an ultrasonic imaging system; and after gene transfection is realized through high-strength ultrasonic irradiation, the tumor gene treatment effect can be achieved.

The invention provides a tumor tissue and cell dual targeted mesoporous silicon dioxide nano drug-loading particle. The tumor tissue and cell dual targeted mesoporous silicon dioxide nano drug-loadingparticle is constituted by a mesoporous silicon dioxide nano particle with the modified surface and a drug; the mesoporous silicon dioxide nano particle with the modified surface is constituted by amesoporous silicon dioxide nano particle body with the amine-modified surface, a polyacrylic acid film layer wrapping the mesoporous silicon dioxide nano particle body with the amine-modified surfacethrough the electrostatic effect, and polyethylene glycol connected with polyacrylic acid in the polyacrylic acid film layer through amido bonds; and the polyacrylic acid film layer serves as a blocking valve and can respond to change of the pH value to enable a pore passage of the mesoporous silicon dioxide nano particle with the amine-modified surface to be in a blocked or opened state, and thedrug is located in a pore passage structure of the mesoporous silicon dioxide nano particle body with the amine-modified surface. The nano drug-loading particle can effectively avoid damage of the targeted drug or the chemotherapy drug with lymphocytotoxicity to lymphocyte to and improves the joint treating effect of targeted therapy and immunological therapy on tumourstumors.