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    • 6. 发明授权
    • 다공성 키토산 구슬 및 그의 제조 방법
    • 다공성키토산구슬및그의제조방법
    • KR100375422B1
    • 2003-03-10
    • KR1019990060034
    • 1999-12-21
    • 한국과학기술연구원
    • 정서영배은희권익찬최귀원
    • C12N1/00
    • C08J9/28C08B37/003C08J2201/0484C08J2305/08C08L5/08C12N5/0075C12N2533/72
    • The present invention relates to macroporous chitosan beads having 5-200 mum in size of relatively large and uniform pores that are distributed from surface to core region, and a preparation method thereof compring the following steps; by dropping chitosan solution, aqueous chitosan solution or their mixture into the low-temperature of organic solvent or liquid nitrogen; and by regulating pore size by phase separation method via temperature difference. The macroporous chitosan beads of the present invention make cell culture more efficient than the previous substrate, since cell can attach to them efficiently due to their large surface area, it is easy for cell to be injected into them and cell attached to them can exist longer due to their three-dimensional structure, therefore they can be used for a study about production of protein, abtibiotics, anticancer agent, polysaccharide, physiologically active agent, animal hormone, or plant hormone as well as a study about substitution of metabolic organs, cartilage or bone.
    • 本发明涉及一种大孔径壳聚糖珠粒及其制备方法,所述大孔隙大小为5-200μm,具有较大且均匀的从表面到中心区域的孔隙,其制备方法包括以下步骤: 将壳聚糖溶液,壳聚糖水溶液或其混合物滴入低温有机溶剂或液氮中; 并通过温度差通过相分离法调节孔径。 本发明的大孔脱乙酰壳多糖珠粒使细胞培养比先前的基质更有效,因为细胞由于它们的大表面积而可以有效地附着到它们上,细胞很容易注入它们并且细胞附着在它们上的时间可以更长 由于它们的三维结构,因此它们可以用于研究蛋白质,抗生素,抗癌剂,多糖,生理活性剂,动物激素或植物激素的产生,以及关于代谢器官,软骨替代的研究 或骨头。
    • 9. 发明公开
    • 온도감응성 하이드로젤 내에서의 중간엽 줄기세포의 신경분화 및 신경분화용 조성물
    • 热敏水凝胶中的细胞干细胞的神经元细胞和神经元分化的组成
    • KR1020130091818A
    • 2013-08-20
    • KR1020120013054
    • 2012-02-09
    • 아주대학교산학협력단
    • 권진선김다연김문석
    • C12N11/04C12N5/0793A61K35/30A61K9/00
    • C12N11/04A61K35/30C12N5/0619C12N2501/065C12N2501/115C12N2506/1346C12N2533/72C12N2539/10A61K9/0019
    • PURPOSE: Neuronal differentiation of the mesenchyme stem cells is provided to be simply induced by using culture medium of the suitable composition and increase the mesenchyme stem cells without affecting the induction of being developed into the nerve cell. CONSTITUTION: Thermo-sensitivity supporter for the neural cell differentiation of the mesenchyme stem cell comprises a cell culture substrate; and thermo-sensitivity hydrogel which coated on the cell culture substrate. An obtaining method of nerve cell using the thermo-sensitivity hydrogel comprises a step of leading the thermo-sensitivity hydrogel as gel; a step of sowing the mesenchyme stem cells to the thermo-sensitivity hydrogel and developing it into neural progenitor cell; and a step of inducing the neural progenitor cell to the nerve cell. Composition for treatment of neurological disease comprises thermo-sensitivity hydrogel and nerve cell obtained by the attaining method.
    • 目的:提供间充质干细胞的神经元分化是通过使用合适组合物的培养基简单诱导,并增加间充质干细胞,而不影响被发育成神经细胞的诱导。 构成:间充质干细胞的神经细胞分化的热敏感性支持体包含细胞培养基质; 和热敏性水凝胶,其涂覆在细胞培养基质上。 使用热敏水凝胶的神经细胞的获得方法包括将热敏水凝胶引导为凝胶的步骤; 将间充质干细胞播种到热敏水凝胶并将其发育成神经祖细胞的步骤; 以及将神经祖细胞诱导至神经细胞的步骤。 用于治疗神经疾病的组合物包括通过获得方法获得的热敏水凝胶和神经细胞。
    • 10. 发明公开
    • METHOD OF DETACHING CELLS FROM THE SURFACE WHICH THE CELLS ADHERE TO
    • 从细胞粘附的表面分离细胞的方法
    • KR20070099187A
    • 2007-10-09
    • KR20060030250
    • 2006-04-03
    • SAMSUNG ELECTRONICS CO LTD
    • HONG SUNG WOOKIM BYUNG CHULKIM SOOK YOUNG
    • C12Q1/24C12N5/00
    • C12N5/0606C12N5/0068C12N5/0696C12N2509/00C12N2509/10C12N2533/72
    • A method for detaching cells from attached surface with high yield is provided to separate the cells from the surface without the damage of the cells without using an enzyme such as trypsin by introducing chitosan with the characteristic of being depolymerized in a weak acidic range into the inner surface of a cell culture container. A method comprises the steps of: (a) after filling a liquid culture medium in a cell culture container in which a chitosan coating film is formed inside, adhesion-culturing cells on the chitosan coating film; (b) adding an acid such as sulfuric acid, nitric acid and phosphoric acid to the liquid culture medium to adjust the pH of the medium into 4.5-6.0 to depolymerize the chitosan; and (c) isolating the cells from the cell cultured material including the depolymerized chitosan through centrifugation.
    • 提供以高产率从附着表面分离细胞的方法,以将细胞从表面分离而不用细胞损伤,而不使用酶如胰蛋白酶,通过引入具有在弱酸性范围内解聚的特征的壳聚糖进入内部 细胞培养容器的表面。 一种方法包括以下步骤:(a)在将液体培养基填充到其中形成壳聚糖涂膜的细胞培养容器中之后,在壳聚糖涂膜上粘附培养细胞; (b)向液体培养基中加入硫酸,硝酸,磷酸等酸,将培养基的pH调节为4.5〜6.0,使壳聚糖解聚; 和(c)通过离心从包括解聚的壳聚糖的细胞培养物质中分离细胞。