||WO||WO/2014/161554 - LIGHTING DEVICE AND SYSTEM FOR WIRELESS CALIBRATION AND CONTROLLING OF LIGHTING DEVICE||09.10.2014||
||PCT/EE2014/000002||DIGITAL SPUTNIK LIGHTING OÜ||KALLAS, Kaspar|
The present invention relates to modular lighting devices and systems as may be used for film, television and photography. The lighting device consists of lighting modules (10), that may be grouped together, power supply and control module (20) and a controller unit (30), that enables to use light sources of different colors and temperatures. The housing (12) of the lighting module (10) includes a parabolic curve shaped element (17) located under the active cooler (11) to improve the efficiency of the active cooling by re-directing the cooling stream under an angle. The system for wireless calibration and controlling of the lighting device provides software functionality to a light system and consists of a 'virtual spectrometer' feature, that takes into account user and ambient variables, uses interpolation curves, and that could be further refined by using external hardware. The system also includes a 'gray card ambient light detection' feature.
||WO||WO/2014/075696 - MOBILE GRAVEL CRUSHER||22.05.2014||
||PCT/EE2013/000006||TOFFUS OÜ||RÜÜTEL, Caspar|
The mobile crusher is designed for producing splinters. There are more than two separate hoppers on the movable frame. Each hopper has own vibrating feeder that feeds certain cone crusher. Two or more cone crushers are placed on the frame and each cone crusher has to be fed separately through the certain hopper. Under each cone crusher there are separate conveyor belts that collect crushed material. The speed on feeders, the working speed of the cone crushers and the speed on conveyor belts can be regulated independently. The main benefit of the mobile crusher appears when there's a need to crush gravel shingles (pieces of rock etc) with different dimensions. Each crusher has adjusted to process shingles with optimum size. This gives opportunity to operate the machine with low operate costs, productivity is high and the final product (splinters) has good cubical shape and contains little fine material also. In addition, the operator can regulate the splinters composition (test of grading curve) by increasing or decreasing the speed of feeders or the cone crushers that gives an optimized gradation for the final product.
||WO||WO/2014/056510 - COMPACT FIRE LOG AND A METHOD OF FORMING THEREOF||17.04.2014||
||PCT/EE2012/000005||PAAPSI, Margus||PAAPSI, Margus|
The fire log (1) has one or several longitudinal incisions (3), which penetrate the log but do not reach the side surface and intersect in the log's midsection. The lower part of the long has at least one air duct (4) from the side surface to the log's midsection in case the log is set on a surface which obstructs airflow to the log's lower part. The log's midsection contains an ignition device (2), which can be an ignition strip, tablet, briquette or other that has been impregnated with an ecologically friendly inflammable substance that burns fast and evenly. The ignition device can contain a wick, fuse or other. The fire log burns from the inside out and the flame exits the log from the upper end similarly to a candle, preserving the log's decorative outer surface for nearly the entire burning period. During burning, a flaming star shape is formed in the middle of the log. The fire log is comfortable to use, easy to take along and requires no additional procedures prior to use. In the open air, the log does not require any additional support for using a pot or a pan. The fire log burns significantly longer and gives more warmth than a Lapland candle.
||WO||WO/2013/170863 - BIOREACTOR SYSTEM AND METHOD FOR CLONING THE PHYSIOLOGICAL STATE OF MICROORGANISMS||21.11.2013||
||PCT/EE2013/000005||TALLINN UNIVERSITY OF TECHNOLOGY||ERM, Sten|
Bioreactor system and method for cloning the physiological state of microorganisms comprises in preferred embodiment of a mother-reactor and one or more daughter-reactors with sensors, stirrers, fluid and gas flow channels, scales, pumps, controllers, computer, software, valves and accessory devices. The bioreactors are inter-connected with culture transfer hose. To achieve the method, the mother-reactor is filled with necessary volume, inoculated, stabilised in continuous cultivation, the microbial culture's volume is increased in variable volume cultivation while maintaining constant physiology, microbial culture is transferred from the mother-reactor into the daughter-reactors while maintaining constant physiology, experiment in the daughter reactor follows. After the experiment daughter-reactors are sterilized and rinsed. During the experiment culture volume in the mother-reactor is increased anew, after the experiment in the daughter-reactors is finished another culture transfer follows and next experiment is conducted. This sequence - variable volume cultivation, culture transfer, experiment - is repeated until necessary data has been acquired.
||WO||WO/2013/143552 - AN APPARATUS FOR DIAGNOSIS AND CONTROL OF HONEYBEE VARROATOSIS, IMAGE PROCESSING METHOD AND SOFTWARE FOR RECOGNITION OF PARASITE||03.10.2013||
||PCT/EE2013/000004||HUMAL, Priit||HUMAL, Priit|
An device for diagnosis and control of honeybee varroatosis (Varroa mite infection) comprises one or several cameras (310), connected to image processor (311). The software of the device is capable of processing the picture of honeybee, recognition the presence or absence of varroa mite on the body of the bee on the field-of-view of the cameras or in the chamber for observation, counting the infected and non-infected bees, separating the infected bees from non-infected bees or killing the recognized varroa mites. Controlled gates (314, 315, 316), valves, positioning actuators and/or heaters (329, 330) are used as output devices for realization of the said actions. The method of image processing for recognition of varroa mite or other parasites comprises of searching reflections in the image and analysis of the surroundings of the found reflections. Also the method for determination of location of body elements of insect in an image is disclosed.
||WO||WO/2013/139348 - SKIN CANCER BIOMARKER DETECTION BY INFRARED SPECTROSCOPY||26.09.2013||
||PCT/EE2013/000003||MC PROFESSIONAL LTD.||EIKJE, Natalja|
The present invention relates to a method for detection in IR (infrared) spectra of human epidermal skin tissue the presence of the multiplet around 1055 cm-1, i.e. the ratio of intensity of the nucleic acids bands, DNA and RNA, indicative for prognosis, diagnosis and prediction of epidermal skin cancers and precancers. Detection of the multiplet together with patterned appearance of DNA/RNA triad peaks at about 1071, 1084/1085 and 1095 cm-1 additionally indicates relation to certain types of tumour and malignancy, also indicating progression of malignancy and progression towards malignancy.
||WO||WO/2013/135249 - A FORMULA AND METHOD FOR MONITORING INDIVIDUAL METABOLIC RESPONSE AND FOR GENERATING PREDICTIVE MEDICAL METRICS||19.09.2013||
||PCT/EE2013/000002||MC PROFESSIONAL OÜ||EIKJE, Natalja|
Provided is a formula and method for monitoring individual metabolic response that involve calculation of the lag/latency time (LT) for the peak levels of measured a variety of glucose values by HATR-FTIR (horizontally attenuated total reflection Fourier transform infrared) spectroscopy and the LT for the peak level of capillary blood glucose (CBG), with subsequent calculation of the LT changes between them. Obtained meaningful time-dependent and dose-dependent glucose values and their LT changes characterize glycemic variability (GV) in a qualified subject, that can be used to predict the patient's risk of hyperglycemia, to stage Type II diabetes and, in general, to be considered as a new metrics of assessing the quality of metabolic control.
||WO||WO/2013/123950 - ANALYTICAL METHOD FOR COMMON AND SPECIFIC CHARACTERIZATION OF SKIN CARCINOGENESIS BY FTIR MICROSPECTROSCOPY||29.08.2013||
||PCT/EE2013/000001||MC PROFESSIONAL OÜ||EIKJE, Natalja|
The invention presents methods of using Fourier transform infrared (FTIR) microspectroscopy for common and specific characterization of carcinogenesis in human skin tumors. The invention provides the user with the method to analyse intra- and inter-molecular interactions for nucleic acids and proteins expressed in infrared (IR) spectra of human skin epidermal cancers towards understanding the molecular, cellular and tissue changes that occur during skin carcinogenesis. More particularly, presented analytical method has the advantage to simultaneously observe DNA-RNA, DNA-DNA, DNA-protein and protein-protein interactions by means of their expressed interacting activity levels within one type of tumour and between different types of tumours, both commonly and specifically, with further indication of the grade of activity in benign, premalignant and malignant skin tissue cells.
||WO||WO/2013/071939 - A METHOD AND A SYSTEM FOR DISPLAYING AND WATCHING THREE-DIMENSIONAL IMAGES ON THE SCREEN||23.05.2013||
||PCT/EE2012/000006||OÜ UNIPOWER||KUNIN, Leonid|
The invention provides method and system to enable a user to form 3D image frames sequence in a device comprising any type of screen and watch the 3D image on the screen of this device using respectively configured glasses. More precisely the invention is related to means to mark video frames used in displaying of 3D image, to display these markers to the screen, to detect the markers, to watch the frames by respective watching glasses and to synchronize of the frames. ˙
||WO||WO/2013/010553 - METHOD AND ANALYTICAL KIT FOR SIMULTANEOUS QUANTIFICATION OF B-COMPLEX VITAMIN CONTENT IN FOOD||24.01.2013||
||PCT/EE2012/000004||TALLINN UNIVERSITY OF TECHNOLOGY||HÄLVIN, Kristel|
The present invention relates to an analytical vitamin analysis kit, the method of its preparation, and the method of its application. The given analytical kit can be used for the simultaneous determination of the quantity of five B-complex vitamins (B l, B2, B3, B5 and B6) and individual vitamers in drugs, food, food- and bio-supplements, feed, and other biological samples using LC-MS isotope internal standard assay. The analytical kit is based on the use of sample vials containing lyophilized or dried isotope labelled internal standards of the B-complex vitamers with a mix of hydrolytic enzymes, used to convert vitamers and cofactors into the same chemical forms as the used isotope labelled internal standards, and for their following quantification by means of LC-MS or LC-MS/MS.