74 results about "Dose reduction" patented technology

The invention relates to a multiparticulate modified release composition that in operation delivers an active ingredient in a pulsed or bimodal manner. The multiparticulate modified release composition comprises an immediate release component and a modified release component; the immediate release component comprising a first population of active ingredient containing particles and the modified release component compnsimg a second population of active ingredient containing particles coated with a controlled release coating; wherein the combination of the immediate release and modified release components in operation deliver the active ingredient in a pulsed or a bimodal manner. The invention also relates to a solid oral dosage form containing such a multiparticulate modified release composition. The plasma profile achieved by the multiparticulate modified release composition is advantageous in reducing patient tolerance to the active ingredient and in increasing patient compliance by reducing dosage frequency.

Substantial reduction of the radiation dose in computed tomography (CT) imaging is shown using a machine-learning dose-reduction technique. Techniques are provided that (1) enhance low-radiation dosage images, beyond just reducing noise, and (2) may be combined with other approaches, such as adaptive exposure techniques and iterative reconstruction, for radiation dose reduction.

A method for providing a reduced exposure value for radiographic imaging obtains a set of flat-field images at two or more exposure values and measures the noise power spectra using the flat field images. At least one noise table is generated according to interpolated noise power spectra for a set of predetermined exposure values. Values from the at least one noise table are applied to a clinical image to form a reduced exposure simulation image. A noise mask is generated according to at least one noise table and the exposure values of the reduced exposure simulation image and added to the reduced exposure simulation image. The reduced exposure simulation image is assessed to generate a desired dose reduction factor.

A system and method for creating a three dimensional cross sectional image of an object by the reconstruction of its projections that have been iteratively refined through modification in object space and Fourier space is disclosed. The invention provides systems and methods for use with any tomographic imaging system that reconstructs an object from its projections. In one embodiment, the invention presents a method to eliminate interpolations present in conventional tomography. The method has been experimentally shown to provide higher resolution and improved image quality parameters over existing approaches. A primary benefit of the method is radiation dose reduction since the invention can produce an image of a desired quality with a fewer number projections than seen with conventional methods.

An apparatus for spatial modulation of an x-ray beam has a number of planar attenuation elements for x-ray radiation that are disposed in a grid on a carrier and can be pivoted or tilted by a piezoelectric actuator, independently of one another, between at least two positions. One or more sensors with which a piezoelectrically-caused length and/or width and/or position change of the piezoelectrically influenced regions can be detected, are arranged on piezoelectrically influenced regions of the attenuation elements or the actuators. A significant dose reduction and/or dynamic adjustment thereof can be achieved with the apparatus by image adaptation in many areas of x-ray imaging, since a precise determination of the position of each attenuation element in real time is enabled.

Provided herein are compounds and methods of using compounds that selectively inhibit binding to one or more docking domain regions of an extracellular signal-regulated kinase (ERK) to inhibit in a cell having an extracellular signal-regulated kinase activity. Such methods may be used to inhibit cell proliferation of a neoplastic cell, to treat a cancer and further may be used in conjunction with administration of an anticancer drug at a reduced dosage to treat a cancer with a concomitant reduction in toxicity to an individual receiving the treatment. Also provided is a method to design and screen for compounds to inhibit binding within the extracellular signal-regulated kinase docking domain region, using at least in part computer-aided drug design modeling.

A system and method for creating a three dimensional cross sectional image of an object by the reconstruction of its projections that have been iteratively refined through mathematical transformations and modifications in object space and Fourier space is disclosed. A primary benefit of the method is radiation dose reduction since the invention can produce an image of a desired quality with a fewer number projections than seen with conventional methods.

The invention belongs to the technical field of medicines and discloses an itraconazole temperature-sensitive type gel preparation as well as a preparation method and application thereof. The itraconazole temperature-sensitive type gel preparation is composed of the following components in percentage by weight: 0.02-3% of medicines, 0.05-15% of solubilizing agent, 5-50% of gel matrix, 0-15% of biological adhesive, 0.001-2% of preservative, 0-10% of other additives and the balance of solvent. The itraconazole temperature-sensitive type gel preparation can regulate gelatinization temperature by adjusting composition and control drug release rate and degree, can effectively inhibit growth of candida in vitro and can be used for drug administration on skins, eyes, nasal cavity, oral cavity, straight intestine or vaginal mucosa. The itraconazole temperature-sensitive type gel preparation has obvious slow release and biological adhesion property and can prolong action time of medicines on an infection part, realize long-acting treatment, reduce dosage and toxic and side effects and improve patient compliance.

The invention relates to the field of drug development against acute radiation injury caused by exposure to high-energy electromagnetic waves (X-rays, gamma rays) or particles (alpha particles, beta particles, neutrons). To date, there is no effective drug to ameliorate radiation injury after accidental exposure to ionizing irradiation. The invention provides a method of treating radiation injury of a subject in need thereof comprising administering to the subject a peptide, or functional analogue or derivative thereof, of smaller than 30 amino acids. Furthermore, the invention provides use of a peptide, or functional analogue or derivative thereof, of smaller than 30 amino acids for the production of a pharmaceutical composition for the treatment of a subject suffering from or believed to be suffering from radiation injury. In particular, the invention provides anti-radiation peptides having a dose reduction factor (DRF) against acute gamma irradiation of at least 1.10, said DRF determinable by testing which dose of radiation results in 50% mortality at 30 days (LD50/30) after whole body radiation (WBI) in a test group of mice treated with said peptide at 72 hours after WBI and, testing which dose of radiation results in 50% mortality at 30 days (LD50/30) after whole body radiation (WBI) in a control group of mice treated only with the vehicle of said peptide at 72 hours after WBI and wherein the DRF is calculated by dividing the LD50/30 of the peptide-treated animals by the LD50/30 of the vehicle-treated animals.

A fast moving X-Ray shutter has four independently controlled blades defining a Region of Interest (ROI). The ROI area receives the normal X-Ray dose and is exposed at the machine's X-ray pulse frame rate. The ROI can be automatically controlled based on image contents using computer vision techniques. Periodically the shutter blades retract at a controlled speed, exposing the area outside the ROI to a lower, non-uniform, exposure. The non-uniformity in this background exposure is dynamically corrected by a look-up table. The displayed image is a seamless combination of the ROI image and the corrected background image. The displayed image has slightly lower resolution outside the ROI but better resolution (as compared to standard fluoroscopy practices) in the ROI because of reduced scattering.

A stable suspension aerosol formulation of epinephrine is suitable for administration through inhalation comprising a therapeutically effective amount of epinephrine, hydrofluorocarbon propellant, co-solvent, surfactant, and antioxidant. The suspension aerosol formulation further comprises [pre-] pre-micronized epinephrine suspended in an alcohol/surfactant solution with hydrofluoroalkane propellant. The suspension formulation provides a highly efficient delivery of drug microparticles into the respirable region of patients' lungs and has the following advantages: lower dosage requirement, minimum alcohol content, with less impurities generated during storage, improved efficacy and safety, and exhibits no ozone depleting potential compared to a formulation containing chlorofluorocarbon.

A method of obtaining recommendations for lowered radiation dose for a type of radiological image, executed at least in part by a computer system, obtains at least one clinical image of at least one patient, taken under a baseline set of exposure conditions, as a basis image. Processing instructions related to image simulation under one or more reduced exposure conditions are obtained. The basis image is processed according to the processing instructions to generate a set of one or more simulation images, each simulation image representative of corresponding reduced exposure conditions. One or more simulation images are displayed to one or more diagnostic practitioners and an evaluation obtained from the one or more practitioners related to at least the quality of the one or more simulation images. At least one recommended reduced exposure condition is generated and electronically stored according to the practitioner evaluation.

Image reconstruction methods are described where the characteristics of the surroundings of the patient in the scanner image field are used as supplemental information in the reconstruction process to reduce the dose, reduce scan times, scan number and/or improve the image quality of the reconstructed image.

The present disclosure relates to pharmaceutically acceptable complex formulae comprising complexes of Abiraterone acetate and pharmaceutically acceptable excipients, process for the preparation thereof and pharmaceutical compositions containing them. The complex formulae of the present disclosure have improved physicochemical properties which results in reduced food effect which allows significant dose reduction and the abandoning of the requirement of taking the drug on an empty stomach.

A technique for reducing noise in pixel images includes modifying initial image data to prevent subsequent image data loss, shrinking the modified image, processing the shrunken image with known segmentation-based filtering techniques which identify and differentially processing structures within the image. After processing, the shrunken image is enlarged to the dimensions of the initial data and subsequently processed to correct intensity irregularities and to preserve CT numbers. The resulting technique is versatile and provides greatly improved computational efficiency while maintaining image quality, allowing for dose reduction during imaging.

The invention provides a clindamycin palmitate hydrochloride particle and a preparation method thereof. The clindamycin palmitate hydrochloride particle provided by the invention consists of a drug pill core and a coating layer covering the outside of the drug pill core, wherein the drug pill core comprises clindamycin palmitate hydrochloride, a carrier and a water-soluble pore-forming agent; andthe coating layer comprises a pH-dependent coating material. According to the clindamycin palmitate hydrochloride particle provided by the invention, a soft material is prepared by virtue of a wet process/the drug pill core is prepared by virtue of an extrusion-spheronisation process firstly, and then the soft material or the drug pill core is coated by coating liquid by virtue of a spray coatingprocess. The clindamycin palmitate hydrochloride particle provided by the invention is applicable to children; the integrity of the particle can be kept before the particle is taken, and the particle,after entering human bodies, can be slowly released, so that a stable and lasting blood concentration can be provided, and clinical demands of reducing the times of administration, reducing dose-related toxicity and improving patient compliance can be satisfied; and meanwhile, the bad taste of the medicine (the particle) can be masked without adding a great amount of flavoring agents.

In a method and x-ray device to assist in the reduction of the dose of x-ray radiation applied to the patient in the acquisition of at least one x-ray projection of the patient, a selected protocol is entered by a user into an x-ray device, the selected protocol being defined for the acquisition of the at least one x-ray projection and including a measure or measures for reduction of the dose of x-ray radiation to be applied to the patient in the acquisition of the at least one x-ray projection. The does reduction measure or measures in the selected protocol are automatically compared in a processor of the x-ray device, with the dose reduction measures that are installed at the x-ray device for reduction of the dose of x-ray radiation to be applied to a patient in the acquisition of the at least one x-ray projection. If the result of the comparison indicates a discrepancy between the dose reduction measure or measures in the selected, defined protocol and those installed in the x-ray device, at least one such measure installed at the x-ray device is visualized as a measure that can be set or activated by the user, that is not yet included in the selected protocol.

Aspects and embodiments of the instant disclosure provide therapeutic methods and compositions comprising interleukin 12 (IL-12) as a hematopoietic immunotherapy (HIT) useful for treating or preventing a cancer patient from chemotherapy-induced cytopenias necessitating a dose reduction and/or dose delay. following exposure of the patient to chemotherapeutic agents, the method comprising: administering a dose of therapeutically effective amount of a pharmaceutical composition comprising substantially isolated IL-12 to the subject, whereby cytopenias are reduced and leading to increases responses to the chemotherapy agent(s).diminished.

The invention relates to the field of drug development against acute radiation injury caused by exposure to high-energy electromagnetic waves (X-rays, gamma rays) or particles (alpha particles, beta particles, neutrons). To date, there is no effective drug to ameliorate radiation injury after accidental exposure to ionizing irradiation. The invention provides a method of treating radiation injury of a subject in need thereof comprising administering to the subject a peptide, or functional analogue or derivative thereof, of smaller than 30 amino acids. Furthermore, the invention provides use of a peptide, or functional analogue or derivative thereof, of smaller than 30 amino acids for the production of a pharmaceutical composition for the treatment of a subject suffering from or believed to be suffering from radiation injury. In particular, the invention provides anti-radiation peptides having a dose reduction factor (DRF) against acute gamma irradiation of at least 1.10, said DRF determinable by testing which dose of radiation results in 50% mortality at 30 days (LD50/30) after whole body radiation (WBI) in a test group of mice treated with said peptide at 72 hours after WBI and, testing which dose of radiation results in 50% mortality at 30 days (LD50/30) after whole body radiation (WBI) in a control group of mice treated only with the vehicle of said peptide at 72 hours after WBI and wherein the DRF is calculated by dividing the LD5O/3O of the peptide-treated animals by the LD50/30 of the vehicle-treated animals.

The invention provides compound composition containing eugenol and mustard essential oil which are plant-sourced active substances with environmental compatibility and mixed in a weight ratio being (1:10)-(10:1), preferably in a weight ratio being (1:4)-(4:1). The compound composition has an obvious synergic effect, can be prepared in a form such as microemulsion, emulsion in water, water dispersible granules and the like and is used for controlling plant fungal diseases, bacteriosis, virus diseases and the like, so that the control effect is improved, the dosage is reduced, the application times are reduced, the control range is enlarged, the resistance is delayed, the requirement of a conventional dose reduction application technology is met, and the prepared preparation is environmentally friendly and has good application prospect.