Abstract: The present invention relates to a carrier for cell culture and, more specifically, to a carrier for cell culture and a cell culture medium composition comprising same, the carrier for cell culture comprising microcapsules which contain gelatin, a natural polymer, an oil, and an oil thickener and have improved mechanical properties. The microcapsules containing a natural oil, according to the present invention, have significantly improved mechanical properties and retention. When used as a carrier for cell culture in culturing cells, the microcapsules have the effects of improving adhesion and survival of the cells and inducing maturation of the cultured cells, and thus may be variously employed in cell culture using a carrier, co-culture systems, and the field of artificial cell structure production.

Abstract: The present invention relates to microcapsules comprising natural oil and, more specifically, to microcapsules which contain gelatin, natural polymers, oil, and an oil thickener and have enhanced mechanical properties, and a preparation method therefor. The microcapsules comprising natural oil according to the present invention have remarkably enhanced mechanical properties and retention properties, and when co-cultured with cells, the microcapsules provide the effect of inducing maturation of the cells, and thus may be used in various fields of microcarriers, cell cultures, and co-culture systems.

Abstract: The present invention relates to an organoid and, more specifically, to an organoid and a use thereof, the organoid being produced using a carrier for cell culture which comprises microcapsules containing gelatin, a natural polymer, an oil, and an oil thickener. When used as a carrier for cell culture in culturing cells, the microcapsules containing a natural oil, according to the present invention, have the effects of improving adhesion and survival of the cells and inducing maturation of the cultured cells. The organoid produced by culturing cells using the carrier for cell culture has been confirmed to have the function of the organ concerned and, when treated with a drug, react to the toxicity of the drug and thus may be variously employed in the development of new drugs, disease research, and the field of artificial organ development.

Abstract: A cell culture vessel according to the present invention is characterized by comprising a first vessel having a stirring member disposed therein, and a second vessel configured to be inserted in the interior of the first vessel and having a hole for allowing a solvent accommodated in the first vessel to pass through the interior thereof, wherein the stirring member is arranged in a recess portion formed in the first vessel.

Abstract: A device for forming and counting spheroids according to one embodiment of the present invention may comprise a substrate, and a mesh member which is configured to be able to be positioned on the surface of the substrate and has a plurality of protruding members. The plurality of protruding members intersects one another in the form of a mesh so as to form a plurality of pores.

Abstract: Disclosed is a spheroid forming culture container using a temperature-sensitive glycol chitosan derivative and a spheroid forming method using the same. In the disclosed spheroid forming culture container, a surface of a culturing space is coated with a glycol chitosan derivative having reversible sol-gel transition characteristic depending on temperature.

Abstract: Disclosed is a spheroid forming culture container using a temperature-sensitive glycol chitosan derivative and a spheroid forming method using the same. In the disclosed spheroid forming culture container, a surface of a culturing space is coated with a glycol chitosan derivative having reversible sol-gel transition characteristic depending on temperature.

Abstract: The present invention relates to a cell culture container, which enhances the efficiency of proliferation and differentiation of various cells including stem cells. The cell culture container according to an exemplary embodiment of the present invention includes a cell culture surface for adhering adult stem cells thereon to proliferate and differentiate the adult stem cells, and the cell culture surface includes a protrusion having a lotus leaf surface reproduction structure, which is disposed on the cell culture surface.

Abstract: Disclosed is an optical fiber possible to prevent it from increasing an optical loss occurring during fabrication of a single mode fiber preform and extraction thereof and enhance an optical transmission efficiency, a method of producing the same comprising the steps of forming a first quartz tube having a first thermal conductivity, said first quartz tube being used as a clad; depositing a core layer and a clad layer inside said first quartz tube to form a preliminary perform by heating of said fist quartz tube; forming a second quartz tube having a second thermal conductivity lower than said first thermal conductivity; and depositing said second quartz tube to said preliminary preform by heating to produce said optical fiber preform.

Abstract: Disclosed is an optical fiber capable of preventing an increase in an optical loss from occurring during fabrication and extraction of a single mode fiber preform and enhancement of an optical transmission efficiency, a method of producing the same comprising the steps of forming a first quartz robe having a first thermal conductivity, said first quartz tube being used as a clad; depositing a core layer and a clad layer inside the first quartz robe to form a preliminary perform by heating of the fist quartz robe; forming a second quartz tube having a second thermal conductivity lower than the first thermal conductivity; and depositing the second quartz tube to said preliminary preform by heating to produce the optical fiber preform. On embodiment, uses N overclad layers having thermal conductivites K.sub.x such that K.sub.0 >K.sub.1 >K.sub.2 . . . >K.sub.N and coefficients of viscosity .mu..sub.0 <.mu..sub.1 <.mu..sub.2 . . . <.mu..sub.N.