Abstract: Provided are a method for generating a summary and a system therefor. The method according to some embodiments may include calculating a likelihood loss for a summary model using a first text sample and a first summary sentence corresponding to the first text sample, calculating an unlikelihood loss for the summary model using a second text sample and the first summary sentence, the second text sample being a negative sample generated from the first text sample, and updating the summary model based on the likelihood loss and the unlikelihood loss.

Abstract: Disclosed is an artificial implant comprising: a silicone shell; and a filler filling the interior of the shell, wherein at least a portion of the shell is a rupture-prevention part comprising two or more silicone layers and one or more reinforcing material layers interposed therebetween.

Abstract: Disclosed are an artificial implant and a method for manufacturing same, the artificial implant comprising: a silicone shell consisting of an upper portion, a lower portion, and a side portion; and a filler injected into the silicone shell, wherein the silicone shell includes at least one silicone layer and at least one reinforcing layer, the reinforcing layer being provided on at least a portion of the lower portion and the side portion of the silicone shell, or the silicone shell includes a layered structure having a step.

Abstract: The present invention provides a recombinant expression vector comprising a gene encoding canine parvovirus 2a VP2 or 2b VP2 protein, a recombinant plant into which the vector is transformed, a vaccine composition against canine parvovirus, comprising canine parvovirus 2a VP2 or 2b VP2 protein obtained from the recombinant plant, and a composition for diagnosing canine parvovirus. When the recombinant plant of the present invention is used, canine parvovirus 2a VP2 or 2b VP2 antigen protein can be rapidly produced with high efficiency. Since the composition for diagnosing canine parvovirus according to the present invention uses a recombinant antigen protein, there is no possibility of contamination due to live virus handling, and thus the composition is safe, and the presence or absence of canine parvovirus infection can be rapidly diagnosed from a large amount of samples.

Abstract: A fluorine coating agent having enhanced dental tubule permeability and coating endurance, and a method for preparing the same. The fluorine coating agent applied on the surface of a tooth is enhanced in abrasion resistance to increase a period of time during which a coating membrane lasts, thereby preventing dental caries. Further, the curing time of the fluorine coating agent can be controlled to allow the agent to permeate and thus block the dental tubule.

Abstract: A fluorine coating agent having enhanced dental tubule permeability and coating endurance, and a method for preparing the same. The fluorine coating agent applied on the surface of a tooth is enhanced in abrasion resistance to increase a period of time during which a coating membrane lasts, thereby preventing dental caries. Further, the curing time of the fluorine coating agent can be controlled to allow the agent to permeate and thus block the dental tubule.

Abstract: A dental implant and a method for manufacturing same which assure early stability and fixation power of an implant by suppressing early osteolysis after an implant procedure, and allowing better bone coherence of the implant surface during an osteogenic period by controlling the speed of bone remodeling.

Abstract: A bioactive-type of hydrophilic dental implant which is made of titanium or titanium alloy having a rough surface, wherein a coating layer of a mixed solution comprising i) an organic pH buffering agent and/or inorganic pH buffering agent and ii) an organic amphiphilic having sulfonic group is formed on the rough surface which was pre-treated to remove a contaminant. The present invention has effects preventing that the dental implant is exposed to air before it is inserted into the alveolar bone and the implant surface is re-contaminated; improving the biocompatibility of the implant, fluid- and blood-affinity, and the initial osseointegration performance; and shortening the osseointegration period, and the surface of the dental implant can be maintained as being hydrophilic for at least 3 years by using a mixed solution of pH buffering agent and organic amphiphilic substance having sulfonic group as a surface coating solution.

Abstract: A dental implant and a method for manufacturing same which assure early stability and fixation power of an implant by suppressing early osteolysis after an implant procedure, and allowing better bone coherence of the implant surface during an osteogenic period by controlling the speed of bone remodeling.

Abstract: An ampoule for storing an implant capable of maintaining humidity includes: a container capable of airtight sealing at least momentarily or temporarily; a partition member which divides an accommodation space inside the container into two spaces, first and second spaces, and allows vaporized water molecules to be transported between the divided spaces; and a water molecule supply source which is accommodated in the first space of the two spaces divided by the partition member and supplies the vaporized water molecules. Therefore, the invention enables the construction of an environment which allows the hydrophilicity of the implant to be maintained for a long time, wherein the hydrophilicity is imparted to and protected from the surface of the implant or a coating layer formed on the surface of the implant.

Abstract: A hydrogel and a method for manufacturing the same. The hydrogel, which can be freely used during treatment irrespective of the shape of a bone defect region, has a decomposition rate capable of being regulated in situ and can thus be rapidly decomposed over a certain time, i.e., after the completion of bone regeneration. Furthermore, a hydrogel membrane using the hydrogel which is applied to a bone defect region irrespective of the shape thereof, and a method for manufacturing the same.

Abstract: A method for forming a coating film of a material for enhancing bioactivity, such as a water-soluble vitamin, on a surface of a dental implant, and a dental implant produced by the method, in order to overcome the limitations in improving osseointegration capability, which result from existing physical surface treatments, such as RBM and SLA surface treatments. The methods enable the SLA-pretreated implant surface to have blood affinity and an enhanced bioactive function, thereby providing a method for producing a dental implant which has excellent biocompatibility and high osseointegration capability after the implant procedure and thus has enhanced bioactivity, and a dental implant produced by the method. The surface of the dental implant, from which organic pollutants have been removed, are coated with a bioactive material, thereby enhancing blood affinity and bioactivity of the implant and thus improving initial osseointegration capability of the implant.

Abstract: A bioactive-type of hydrophilic dental implant which is made of titanium or titanium alloy having a rough surface, wherein a coating layer of a mixed solution comprising i) an organic pH buffering agent and/or inorganic pH buffering agent and ii) an organic amphiphilic having sulfonic group is formed on the rough surface which was pre-treated to remove a contaminant. The present invention has effects preventing that the dental implant is exposed to air before it is inserted into the alveolar bone and the implant surface is re-contaminated; improving the biocompatibility of the implant, fluid- and blood-affinity, and the initial osseointegration performance; and shortening the osseointegration period, and the surface of the dental implant can be maintained as being hydrophilic for at least 3 years by using a mixed solution of pH buffering agent and organic amphiphilic substance having sulfonic group as a surface coating solution.

Abstract: A dental bleaching composition includes a dental bleaching agent, a binder, a tartrate, and a solvent.

Abstract: The present invention relates to a dental hydrogel and to a method for manufacturing same, and more particularly, to a hydrogel and to a method for manufacturing wherein the hydrogel, which can be freely used during treatment irrespective of the shape of a bone defect region, has a decomposition rate capable of being regulated in situ and can thus be rapidly decomposed over a certain time, i.e., after the completion of bone regeneration. Furthermore, the present invention relates to a hydrogel membrane using the hydrogel which can be applied to a bone defect region irrespective of the shape thereof, and to a method for manufacturing same.

Abstract: The present invention relates to a dental implant having an enhanced early stability and a method for manufacturing same, and more specifically to a dental implant and a method for manufacturing same which assure early stability and fixation power of an implant by suppressing early osteolysis after an implant procedure, and allowing better bone coherence of the implant surface during an osteogenic period by controlling the speed of bone remodeling.

Abstract: An ampoule for storing an implant capable of maintaining humidity includes: a container capable of airtight sealing at least momentarily or temporarily; a partition member which divides an accommodation space inside the container into two spaces, first and second spaces, and allows vaporized water molecules to be transported between the divided spaces; and a water molecule supply source which is accommodated in the first space of the two spaces divided by the partition member and supplies the vaporized water molecules. Therefore, the invention enables the construction of an environment which allows the hydrophilicity of the implant to be maintained for a long time, wherein the hydrophilicity is imparted to and protected from the surface of the implant or a coating layer formed on the surface of the implant.