Patents
Literature
Hiro is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Hiro

142results about How to "Effective targeting" patented technology

Systems and methods for marketing health products and/or services to health consumers and health providers

InactiveUS20060247968A1Rapidly and efficiently communicateEfficient targetingMarket predictionsCash registersGerontologyHealth data
The present systems and methods relate to marketing health products and health services. One or more marketing presentations are made to a health consumer about one or more health products or health services. The marketing presentations are targeted based on health data regarding the health consumer and optionally data regarding the health provider. The present systems and methods allow life science companies, government entities and others to more efficiently and effectively market health products and / or health services to health consumers and health providers.
Owner:KADRY BASSAM

Method and system for narrowcasting based on automatic analysis of customer behavior in a retail store

The present invention is a method and system for automatically changing the advertisement contents on a means for displaying the contents based on a customer's behavior or a group of customers' behavior in a retail store. The analysis of behavioral pattern is performed automatically and in real-time based on the visual information from the shopping and walkthrough history of a customer or a group of customers, using arrays of sensing devices, such as a plurality of means for capturing images, and a plurality of computer vision technologies on the visual information.
Owner:NYTELL SOFTWARE LLC

System and method for targeting video advertisements

An improved system and method for advertising to video program viewers that sends a signal from a signal provider that contains a video program file, a video advertisement file, a video program data file, and a video advertisement data file to a viewer's addressable video recording device (DVR). When the signal is received by the DVR, the video and program and data files are separated and stored locally in separate databases. The video program file may be delivered directly to the viewer' television or monitor for immediate viewing. The video program data information file contains the target demographic profile information and the commercial break information for the video program. The video advertisement file and the video advertisement data file are stored in a video advertisement library database and video advertisement information, database, respectively. Loaded into the memory of the DVR is an advertisement play list generator software program that generates a list of advertisements stored on the DVR recorder to be played back during the video program.
Owner:KINNEAR D SCOTT

Sustained release of antiinfectives

Provided, among other things, is a method of treating or ameliorating pulmonary infection in a cystic fibrosis patient comprising pulmonary administration of an effective amount of a liposomal / complexed antiinfective to the patient, wherein the (i) administrated amount is 50% or less of the comparative free drug amount, or (ii) the dosing is once a day or less, or (iii) both.
Owner:INSMED INC

Machine learning clinical decision support system for risk categorization

Improved risk categorization is provided for clinical decision support and forecasting future health care spend. A risk index is provided that improves on other risk stratification models by synthesizing electronic medical records and health questionnaires with an individual patient's claim histories. Machine learning algorithms catalogue patients into distinct group clusters, based on risk which may be associated with annual health care spending, thereby enabling administrators to forecast future health care spending on the individual and population level.
Owner:CERNER INNOVATION

Immunostimulatory compositions and methods of use thereof

Lipid conjugates for enhanced delivery of cargo to the lymph nodes are disclosed. The lipid conjugates typically include three domains: a lipophilic domain that binds to albumin, a polar block domain, and a cargo such as a molecular adjuvant or immunostimulatory compound (such as an oligonucleotide) or antigenic peptide. Depending on the cargo, the length and compositions of the polar block can be tailored to push the equilibrium toward albumin binding, stable micelle formation, or cell insertion. The conjugates can be administered to a subject, for example, a subject with cancer or an infection, to induce or enhance a robust immune response in the subject.
Owner:MASSACHUSETTS INST OF TECH

Preparation method and application of tumor-targeted nanometer drug delivery system for cooperative chemotherapy and photodynamic therapy

The invention discloses a tumor-targeted nanometer drug delivery system for cooperative chemotherapy and photodynamic therapy and a preparation method thereof. The drug delivery system is prepared from carboxymethyl chitosan, folate, a photosensitizer chlorine e6 and adriamycin, wherein the chlorine e6 and the folate are coupled to a carboxymethyl chitosan chain segment through an amido bond, and are loaded to polymer nanoparticles of the adriamycin through an ion exchange method. The nanometer material prepared by the method is high in yield, regular in shape and even in distribution. In-vivo and in-vitro experiments prove that the tumor targeting property of the nanometer preparation can be significantly improved by folate receptor mediation; enrichment on the tumor part is achieved and drug release is controlled. The photosensitizer is capable of effectively reversing the chemotherapy drug resistance and significantly inhibiting the growth of tumors after being irradiated by near-infrared light. Therefore, the related nanometer drug delivery system has good application prospect in the aspect of breast cancer treatment.
Owner:SHENYANG UNIV

Multi-Layer Tablets and Bioadhesive Dosage Forms

Bioadhesives coatings increase the gastrointestinal retention time of orally-ingested medicaments. Certain bioadhesive coatings producing a fracture strength of at least 100 N / m2, as measured on rat intestine, when applied to at least one surface of a pharmaceutical dosage form for oral delivery of a drug, result in a gastrointestinal retention time of at least 4 hours in a fed beagle dog model, during which the drug is released from the dosage form.Multi-layer tablets, particularly those including hydrophobic excipients, are useful in administering hygroscopic and / or deliquescent drugs. In addition, varying the amount of drug in multi-layer tablets allows the release rate of the drug to be controlled.
Owner:SPHERICS

Combination of kinase inhibitors and uses thereof

The present invention provides for a method for treating a disease condition associated with PI3-kinase α and / or mTOR in a subject. In another aspect, the invention provides for a method for treating a disease condition associated with PI3-kinase α and / or mTOR in a subject. In yet another aspect, a method of inhibiting phosphorylation of both Akt (S473) and Akt (T308) in a cell is set forth.
Owner:INTELLIKINE

Videos for In Application Purchases and Rewards for Sharing Same through Social Media and Video Advertising for Reengagement

InactiveUS20140089068A1Facilitate reengagementSatisfaction experienceMarketingVideo advertisingSocial media
The present invention is directed to the systems, computer program products, methods and devices that encourage users of applications for mobile devices to watch and / or to share videos. In some embodiments, users are provided with the opportunity to purchase goods or services in exchange for having viewed a video within the context of an application. These users may also be provided with the opportunity to purchase goods or services in exchange for sharing the videos through social media. Alternatively od additionally, they may be presented with opportunities for reengaging applications that they previously used but for which they have decreased the frequency with which they use those applications or have ceased using those applications.
Owner:JIRBO

Long-circulating solid lipid docetaxel nanoparticles and preparation method thereof

The invention discloses long-circulating solid lipid docetaxel nanoparticles and a preparation method thereof. The long-circulating solid lipid docetaxel nanoparticles comprise the following materialsin therapeutic effective dose: docetaxel, lipid materials, long-circulating auxiliary materials and an emulsifier. The long-circulating solid lipid docetaxel nanoparticles have small particle size, high encapsulation rate and good stability, and not only improve the solubility and the stability of the docetaxel, reduce the toxicity of the docetaxel, but also prolong the circulating time of a medicament in blood, and improve the therapeutic index of the medicament, so that the preparation has the characteristics of low toxicity, low allergy, high efficiency and targeting in clinical application.
Owner:SHANGHAI INST OF MATERIA MEDICA CHINESE ACAD OF SCI

Methods for producing functional antigen presenting dendritic cells using biodegradable microparticles for delivery of antigenic materials

Methods are provided for producing functional antigen presenting dendritic cells. The dendritic cells are produced by treating an extracorporeal quantity of a subject's blood to induce differentiation of blood monocytes into dendritic cells. The dendritic cells may be exposed to cellular material encapsulated within a biodegradable polymer material to produce the antigen presenting dendritic cells.
Owner:EDELSON RICHARD L +3

Novel method for preparation of chitosan nano carrier and functionalization thereof

The invention discloses a novel method for preparation of a chitosan nano carrier and functionalization thereof, which relates to the chitosan nano carrier. The invention provides a novel method for preparation of the chitosan nano carrier and functionalization thereof. The chitosan is dissolved in acetic acid solution, meanwhile, pH is adjusted to 4.5-5.5 with NaOH solution, STPP (sodium tripolyphosphate) solution is added to the chitosan solution to obtain nanogels, then, crosslinking glutaraldehyde is provided for the chitosan, centrifugation is conducted after ending of reaction, reduction reaction is conducted with excess sodium borohydride, then centrifugation is conducted again, then, the obtained compound is dispersed in hydrochloric acid solution to remove the unreacted sodium borohydride, then dialysis is conducted, in order to wash STPP to obtain nanoparticles; the folic acid is weighed to be dissolved in the phosphate buffer solution, then the solution is added to chitosan nanoparticles water solution, after adding EDCI to the solution, folic acid modified nanoparticles are obtained through reaction; PEG succinimidyl propionate is weighed to be dissolved in the phosphate buffer solution, then is added to the chitosan nanoparticles water solution, after reaction, PEG modified nanoparticles are obtained.
Owner:XIAMEN UNIV

Engineered Anti-dll3 conjugates and methods of use

Provided are novel antibody drug conjugates (ADCs), and methods of using such ADCs to treat proliferative disorders.
Owner:ABBVIE STEMCENTRX LLC

Closed loop device incorporating one or more indecomposable knots and methods of using

A flexible, closed loop device that includes at least one indecomposable knot formed that helps define a plurality of adjustable loops. The knot can be easily loosened so that the loop sizes can be adjusted. The knot is easily tightened and locked. In some embodiments, the device includes at least two indecomposable knots. The device is useful in the practice of yoga, Pilates, and other personal training exercises. The device is flexible and easily adjustable, allowing the user to more effectively target specific muscle groups. The device may additionally or alternately be used as a securing and carrying strap for items. Still further, the device may be used as a connecting device to link items together for towing, hoisting, etc.
Owner:KEEN BRIAN T +1

Threat assessment based on written communication

A method for assessing risk of a harmful outcome includes obtaining at least one writing containing a threat directed to a target by an author of the writing. The method includes the further steps of identifying at least one outcome-predictive language use strategy, at least one outcome-predictive document feature, and at least one outcome-predictive psychological characteristic of the author. These variables are used to generate a numerical value predictive of a harmful outcome, that is, the author carrying out the threat. The present method may be used to predict risk of a harmful outcome from a single writing. In one aspect, the present method provides a formula predictive of risk of a harmful outcome based on analysis of at least one writing.
Owner:SMITH SHARON S

Oligonucleotide-based inhibitors comprising locked nucleic acid motif

The present invention relates to chemical modification motifs for oligonucleotides. The oligonucleotides of the present invention, such as chemically modified antisense oligonucleotides, can have increased in vivo efficacy. The chemically modified oligonucleotides provide advantages in one or more of potency, efficiency of delivery, target specificity, toxicity, and / or stability. The chemically modified oligonucleotides have a specific chemical modification motif or pattern of locked nucleic acids (LNAs). The oligonucleotide (e.g. antisense oligonucleotide) can target RNA, such as miRNA or niflNA. Also provided herein are compositions comprising the chemically modified oligonucleotides and methods of using the chemically modified oligonucleotides as therapeutics for various disorders, including cardiovascular disorders.
Owner:MIRAGEN THERAPEUTICS

Rebate cross-sell network and systems and methods implementing the same

ActiveUS8126772B1Avoiding negative customer experienceEfficient targetingMarketingWeb pageDisbursement
Embodiments of the invention provide a robust rebate cross-sell network in which business entities, including financial institutions, can make targeted offers, including pre-approved or pre-qualified credit offers, to a desirable consumer utilizing information submitted by the consumer during a rebate redemption process. These business entities may but need not be associated with a rebate-issuing entity (i.e., rebate sponsor) or a rebate processing center which processes rebate claims for the rebate sponsor. In one embodiment, a cross-sell network manager can determine the consumer's identity, look-up the consumer at credit bureau(s), and perform a passive, real-time inquiry. Contingent upon a plurality of factors (e.g., the results of the inquiry or look-up against the pre-approved / qualified customer list, etc.), one or more targeted offers are identified. A Web page can be dynamically generated with the selectively identified offers and presented to the consumer as disbursement options, perhaps after authenticating the consumer's identity.
Owner:LEFEBVRE DALE

Uncoverage tool

Indication of uncoverage information allows tests to be tailored to target those uncovered code units with the most potential to increase coverage of a program. A tool examines coverage information of a program to identify code units of the program that were not covered by test data used to exercise the program. The tool also examines structural information (e.g., control flow) for the program to identify those of the uncovered code units that have direct control flow from a corresponding covered code unit (“root level uncovered code units”). The coverage tool then measures potential impact on coverage for each of the root level uncovered code units.
Owner:SUN MICROSYSTEMS INC

Long circulation liposome prepn of polyene taxol and its prepn process

The long circulation liposome of polyene taxol is prepared with phosphatide, cholestol and other supplementary material as membrane material, and through surface modification with long circulation supplementary material. During the preparation, charge regulator or surface regulator may be also added. The preparation has average grain size smaller than 600 nm, liposome / medicine molar ratio of 1-20, molar ratio between the long circulation supplementary material and the common phosphatide of 1 / 50-1 / 5 and ultimate polyene taxol concentration of 1-10 mg / ml. The present invention adopts thin dispersing process or organic solvent injecting process to prepare liposome, and high pressure homogenizing process or extruding process to reduce grain size of the prepared liposome and homogenize liposome. The present invention has prolonged intracorporeal circulation period of liposome, effective targeting of medicine to the tumor, high medicine effect and lower toxicity.
Owner:SHENYANG PHARMA UNIVERSITY

Metal-organic frameworks type nanometer drug and preparation method and application thereof

The invention provides an MOFs type nanometer drug and a preparation method thereof in order to improve the deficiencies in an existing nanometer drug preparation technology. ZIF-8 is adopted as a drug delivery carrier, glucose oxidase (GOx) is encapsulated into channels of the ZIF-8, and MnO2 nanometer particles are supported to prepare the GM-ZIF-8 nanometer composite drug. The method for preparing the GM-ZIF-8 nanometer composite drug is simple in operation and mild in reaction condition, and no complicated preparation instruments are needed. The nanometer drug has a good inhibition effecton tumor cell proliferation.
Owner:THE FIRST AFFILIATED HOSPITAL OF ARMY MEDICAL UNIV

Ceramide liposome and preparation method and application thereof

The invention relates to ceramide liposome and a preparation method and application thereof. The ceramide liposome comprises a therapeutically effective amount of active component and a lipid bilayer film, and is characterized in that the ceramide liposome comprises 0.5 to 20 weight parts of ceramide used as the active component and 10 to 350 weight parts of the lipid bilayer film, wherein the lipid bilayer film comprises the following components in part by weight: 5 to 100 parts of phospholipid substance, 0.5 to 10 parts of cholesterol, 0 to 100 parts of surfactant, 0 to 20 parts of additive and 0.5 to 10 parts of organic solvent. The preparation method comprises the following steps of: fully dissolving the ceramide, the phospholipid substance, the cholesterol and the additive in the organic solvent, dissolving the surfactant in a dispersion medium to prepare the ceramide liposome, and reducing the average particle size of the prepared ceramide liposome to less than 500nm to ensure that the particle sizes are uniformly distributed. The invention also discloses new application of the ceramide liposome to cancer therapy.
Owner:陆培华 +1

Aptamer-modified targeted drug delivery nanoparticles as well as preparation method and application thereof

The invention discloses aptamer-modified targeted drug delivery nanoparticles as well as a preparation method and application thereof. The targeted drug delivery nanoparticles are nucleic acid aptamerin which by taking mesoporous silica nanoparticles as a vector, an anticancer drug and a photosensitizer are entrapped in channels of the mesoporous silica nanoparticles, and specific proteins whichcan recognize cancer cell surfaces are modified on the surfaces of the mesoporous silica nanoparticles. The targeted drug delivery nanoparticles can recognize tumor cells in a targeted manner, exertscombined curative effect of chemotherapy / photodynamic therapy and can be used for preparing an antitumor drug.
Owner:FUZHOU UNIV

Intelligent teaching system for ideological and political education

The invention relates to an intelligent teaching system for ideological and political education. The intelligent teaching system for ideological and political education includes a login terminal, a student terminal, a teacher terminal, a management terminal and a retrieval terminal, wherein the teacher terminal and the student terminal interact with the management terminal through the login terminal; the login terminal includes a verification module and an authorization module; the management terminal includes an administrator interface, an administrator module, a teacher management module, a class management module, a student management module, a common resource management module, a course management module and an announcement management module; the teacher terminal includes a teacher interface, a course display module, a teach resource browse module, a teacher communication module, a teacher knowledge management module, a teacher material information storage module and a teacher retrieval interface; and the student terminal includes a student interface, a learning module, a student resource browse module, a student communication module, and a student knowledge management module.
Owner:WEIFANG UNIV OF SCI & TECH

ALK-targeted PROTAC and application thereof

The invention relates to ALK-targeted PROTAC and application thereof, and belongs to the technical field of anti-tumor drugs. The invention aims to provide an ALK-targeted PROTAC molecule. The PROTACmolecule has the structural formula which is shown in a formula I. A ligand pomalidomide of CRBN and a derivative of pomalidomide are adopted as a ligand of an E3 ligase, and coupling of an ALK inhibitor LDK378 with the E3 ligase is achieved through linkers of different types and different chain lengths so as to prepare the ALK-targeted PROTAC molecule successfully; through the ALK-targeted PROTACmolecule, target proteins can be targeted effectively, the content of ALK in cells is reduced, and meanwhile, the ALK-targeted PROTAC is characteristics of good anti-tumor activity in vitro and in vivo, low toxicity to normal cells and high efficiency and low toxicity.
Owner:SICHUAN UNIV

Combination of kinase inhibitors and uses thereof

InactiveUS20150030588A1Disrupt and reduce immune functionEfficient targetingBiocideOrganic chemistryDiseasePhosphorylation
The present invention provides for a method for treating a disease condition associated with PI3-kinase a and / or a receptor tyrosine kinase (RTK) in a subject. In another aspect, the invention provides for a method for treating a disease condition associated with PI3-kinase α and / or an RTK in a subject. In yet another aspect, a method of inhibiting phosphorylation of Akt (S473) in a cell is set forth.
Owner:INTELLIKINE
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products