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Method for producing stable active substance concentration gradient in the cell culture microsystems

机译:在细胞培养微系统中产生稳定的活性物质浓度梯度的方法

摘要

process for the production of a stable concentration gradient of the active substance in mikrosystemach to conduct cell culture, characterized by that in the first stage tanks fluid supply chamber mikrourzu0105dzenia fills with solvents, sequentially: first and tanks consecutive chambers (blank and the solvent suspension cell culture)and the last chamber (chamber indicator) solvent coloured indicator substance in order to tanks on one side mikrourzu0105dzenia introduces liquid and leans mikrosystem, so to force its flow from those supplying the chamber mikrourzu0105dzenia to zbi orniku00f3w powerful located opposite to its side, and after filling the compartmentsthe liquid tank is removed.in the second stage is the suspension cells to at least two supply tanks located on one side mikrourzu0105dzenia (blank and each breeding competent) and solvent coloured indicator substance to the last tank (chamber indicator) and he s it mikrosystem,so to force fluid flow from the supply chamber to the tanks by tanks situated opposite to their side, so that the level of fluid in the opposite tanks up. in the third stage is the short-term culture of cells for their adhesion to surface compartments.in the fourth stage, empty tanks on both sides of the chambers, the chambers are filled with fluid and is a measured volume of solvent to the first chamber supply cell suspension (blank),solution of the active substance to the second and subsequent supply chambers (breeding competent) and coloured solution supply tank unit to last chamber (chamber indicator), then leans mikrosystem angle from 10 to 90 degrees in the direction of empty tank s,forcing a fluid flow chamber by completely emptying tanks supply pre filled fluid, however, without emptying the content, after which removes liquid from all tanks.in the fifth stage is inserted in the side tanks wypu0142ywowej referred to, a small volume of an appropriate solvent, according to the composition of liquids in each of the chambers and is mikrosystem direction empty tanks to force fluid flow in the mikrourz u0105dzenia and completely emptying tanks supply,then mikrosystem tilts in the opposite direction and force the fluid return flow chambers, the alternating function pochylania mikrourzu0105dzenia is repeated several times until the desired distribution of the concentration of coloured indicator chamber, after which the to the liquid tank.in the sixth stage tanks with equal volume fluid proportional to the composition mixture to exhaust ports of adjacent chambers to them - with an appropriate solvent, dye solution or solution of the active substance. in the seventh stage mikrourzu0105dzenia tanks shall be protected to ensure stability of concentration gradients.
机译:用于在mikrosystemach中产生稳定浓度的活性物质以进行细胞培养的方法,其特征在于,在第一阶段的储罐中,mikrourz u0105dzenia的流体供应室依次填充有溶剂:第一和第二储罐的连续储藏室(空白和溶剂悬浮细胞培养)和最后一个腔室(腔室指示剂)溶剂色指示剂物质,以便向一侧的储罐中引入液体并倾斜微系统,因此迫使其从向腔室供应的流体流向zbi ornik u00f3w强大的位置位于其侧面的对面,并在填充隔室后将液体罐移出。在第二阶段中,是悬浮液流到至少一个位于一侧的两个供应罐中的悬浮液(空白且每个育种主管)和溶剂色指示剂到最后一个水箱(室指示器),然后将其设置为微型系统,以迫使流体从供气室流出通过位于其相对侧的储罐向储罐输送液体,以使相对储罐中的液位上升。第三阶段是细胞短期粘附在表面隔室上的培养。第四阶段,腔室两侧的空罐中,腔室充满液体,是到第一腔室的溶剂量供应池悬浮液(空白),将活性物质溶液分配至第二个及随后的供应室(育种能力),将有色溶液供应罐单元至最后一个腔室(腔室指示器),然后将微系统角度从10度倾斜至90度清空水箱,通过完全清空水箱来强制流体流动腔,以供应预先填充的流体,但是不清空内容物,此后从所有水箱中清除液体。在第五阶段中,将侧水箱wyp插入侧箱中。根据每个腔室中液体的组成,少量合适的溶剂,并且是微型系统方向的空罐,以迫使流体在微型腔中流动并完全排空在向油箱供油时,微系统会向相反的方向倾斜并迫使流体返回流室,将交替作用的ch草重复数次,直到达到所需的有色指示剂室的浓度分布为止,然后到达液箱。在第六阶段的储罐中,与成分混合物成比例的等体积流体将流向相邻腔室的排出口,并带有适当的溶剂,染料溶液或活性物质溶液。在第七阶段,应保护mizrourzdzenia储罐,以确保浓度梯度的稳定性。

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