Abstract:
Disclosed herein is a method of preparing a white light-emitting material. The method of preparing a white light-emitting material includes the steps of: (a) depositing a metal for the formation of a blue light-emitting material on a substrate by performing thermal evaporation; (b) forming a material in which green and blue light-emitting materials are hybridized by placing the substrate, on which the metal film is deposited in step (a), in a plasma-enhanced chemical vapor deposition (PECVD) reactor and exposing the substrate to silicon (Si) and oxygen (O) in a plasma state; and (c) forming a red light-emitting material in the material formed in step (b) by annealing the material formed in step (b) so that the red, green and blue light-emitting materials are hybridized.
Abstract:
The present invention provides a nanoparticle synthesis device capable of improving productivity of nanoparticles by increasing the size of a reaction region of laser pyrolysis of a source gas.
Abstract:
Disclosed are a non-volatile memory device and a method of operating the non-volatile memory device. A non-volatile memory device in which m logical pages are stored in a single physical page includes: a plurality of registers configured to be included in a flash translation layer (FTL) and to store at least part of the data of a write command received from a file system; and a controller configured to control operations of the plurality of registers based on the write command; wherein each of the plurality of registers is further configured to have a storage space associated with the size of the m logical pages; and wherein the controller is further configured to program the data of the write command into the non-volatile memory device and to store the data of the write command in the plurality of registers.
Abstract:
Provided is a peptide fragment derived from secreted frizzled protein 5 (Sfrp5), i.e., a peptide fragment selected from the group consisting of the peptides as set forth in SEQ ID NOs: 1 to 9 and a cosmetic composition for skin-whitening and/or inhibiting skin pigmentation comprising the same as an active ingredient. The peptide fragment inhibits melanin formation in melanocytes, thereby having an inhibitory activity against skin pigmentation. Further provided is a reagent for researching or analyzing the inhibition of Wnt signaling pathways comprising the peptide fragment.
Abstract:
The present invention relates to a method for determining patient-specific blood vessel information. More specifically, the present invention relates to a method for determining patient-specific cardiovascular information by applying a simplified coronary circulation model thereto. Furthermore, the present invention relates to a method for determining a blood flow rate for branches of a blood vessel having originated from an artery of each patient. According to the present invention, the method for determining cardiovascular information by using a computer system comprises the steps of: receiving image data including a plurality of coronary arteries having originated from the aorta; processing the image data so as to generate a three-dimensional shape model of the plurality of coronary arteries; simulating a blood flow for the generated three-dimensional shape model of the plurality of coronary arteries; and determining a fractional flow reserve (FFR) of the respective coronary arteries with the blood flow simulation result. In the blood flow simulation step for the three-dimensional shape model of the plurality of coronary arteries, a computational fluid dynamics model is applied to the three-dimensional shape model of the coronary arteries, and a centralized parameter model to be combined with the computational fluid dynamics model uses a simplified coronary circulation model including coronary arteries, capillaries of the coronary arteries, and coronary veins.
Abstract:
Provided are novel cyclic phosphinate derivatives and a method of preparing the same, and more particularly, cyclic phosphinate derivatives including benzoxaphosphole oxide derivatives and benzoxaphosphorin oxide derivatives, and a method of preparing the same. The cyclic phosphinate derivative according to the present invention may have pharmacological and physiological activities, be used as the basic skeleton of the natural material, and be used in development of a new drug, and synthesis of various medicines. In addition, with the method of preparing a cyclic phosphinate derivative according to the present invention, various cyclic phosphinate derivatives may be prepared with high yield through a simple synthetic process by performing an intramolecular carbon-oxygen coupling reaction on the phosphinic acid derivative in the presence of a palladium (Pd) catalyst, an oxidant, and a base.
Abstract:
A supporting unit is provided. The supporting unit includes a body, an alignment member, at least one sensor, and a controller. The body has a top surface supporting a target object. The alignment member is disposed in the body and adjusts a position of the target object. The sensor senses the position of the target object. The controller controls the alignment member and the sensor member. The alignment member includes a magnet that adjusts the position of the target object according to an electromagnetic force; and a coil that applies the electromagnetic force to the magnet.
Abstract:
Provided are novel cyclic phosphinate derivatives and a method of preparing the same, and more particularly, cyclic phosphinate derivatives including benzoxaphosphole oxide derivatives and benzoxaphosphorin oxide derivatives, and a method of preparing the same. The cyclic phosphinate derivative according to the present invention may have pharmacological and physiological activities, be used as the basic skeleton of the natural material, and be used in development of a new drug, and synthesis of various medicines. In addition, with the method of preparing a cyclic phosphinate derivative according to the present invention, various cyclic phosphinate derivatives may be prepared with high yield through a simple synthetic process by performing an intramolecular carbon-oxygen coupling reaction on the phosphinic acid derivative in the presence of a palladium (Pd) catalyst, an oxidant, and a base.
Abstract:
Provided is a pharmaceutical or cosmetic composition comprising adiponectin-derived peptide fragments, i.e., the peptides of SEQ ID NOs: 1 to 6 as an active ingredient. The peptides facilitate skin regeneration and moisturization, inhibit skin wrinkle, and have inhibitory activities against allergy and inflammation as well as metastasis of cancer cells.
Abstract translation:本发明提供包含脂连蛋白衍生的肽片段,即SEQ ID NO:1至6的肽作为活性成分的药物或化妆品组合物。 该肽促进皮肤再生和保湿,抑制皮肤皱纹,并具有抗过敏和炎症以及癌细胞转移的抑制活性。
Abstract:
Disclosed are a negative active material for a rechargeable lithium battery including a spherically-shaped natural graphite-modified composite particle including: a spherically-shaped natural graphite particle where flake-shaped natural graphite fragments build up and assemble into a cabbage or random shape; and amorphous or semi-crystalline carbon, wherein an open gap between the flake-shaped natural graphite fragments is positioned on a surface part or inside the spherically-shaped natural graphite particle, the amorphous or semi-crystalline carbon is coated on the surface of the spherically-shaped natural graphite particle, and the amorphous or semi-crystalline carbon is present in the open gap, and thereby the open gap positioned on the surface part and inside the spherically-shaped natural graphite particle is maintained, a method of preparing the same, and a rechargeable lithium battery including the same.