Abstract:
PURPOSE: A microfluid for a control valve part and a manufacturing method thereof, which can reduce manufacturing costs by simplifying and miniaturizing a structure, are provided to open a channel without giving pressure in a flowing direction of fluid. CONSTITUTION: A microfluid for a control valve part comprises a channel(101), a valve fill(V) and a capillary tube(121). The channel is to transfer the fluid. The valve fill includes the phase change material which is fused in the room temperature. The valve fill closing channel is fused to make the capillary tube flows in. The valve fill is expanded from the sidewall of channel. The capillary tube has a cross section which is smaller than the channel has.
Abstract:
A method for loading liquid reagents into a microfluidic device for blood biochemistry analysis is provided to inject a reagent into a microfluidic device in order to enable the reagent to perform a blood biochemistry test automatically. A method for loading liquid reagents into a microfluidic device(100) for blood biochemistry analysis comprises: a first step of injecting a reagent into reaction chambers(A1~9, B1~11) of the microfluidic device; and a second step of freeze-drying the reagent in the state of being injected into the microfluidic device. The reagent represents a liquid reagent. The reagent is concentrated to a predetermined degree and then injected into the several reaction chambers.
Abstract:
본 발명은 유체 포트가 형성되어 있는 제1 기판에 접착물질을 코팅하여 접착층을 형성하는 단계; 상기 접착층이 도포된 상기 제1 기판의 상기 접착층이 형성된 표면에 대하여 미세구조가 형성되어 있는 제2 기판을 상기 유체 포트 및 상기 미세구조가 서로 대응되도록 정렬하는 단계; 50℃ 내지 180℃의 온도 범위의 열을 가하여 상기 제1 기판과 제2 기판을 결합시키는 단계를 포함하는, 미세유동 장치의 제조방법 및 그에 의하여 제조된 장치를 제공한다. 미세유동 장치, 접착물질, SU-8
Abstract:
A pH regulating device is provided to regulate the pH of a solution accurately and easily regardless of difference among samples such as gas generated during electrolysis, and salt concentration of samples. And a method for regulating the pH of the solution using the same device is provided. The pH regulating device comprises: an electrolysis chip(10) receiving a solution to be subject to the pH adjustment and including a chamber, a cathode electrode, and an anode electrode; an electrolysis chip loading portion(11) for loading the electrolysis chip and including an electrolysis chip supporting portion; an electrode contact terminal, and a cover, an input portion(12) in which the electrolysis condition is inputted; a control portion(13) which controls the electrolysis of the electrolysis chip through input of the electrolysis condition; and a display portion(14) which outputs the electrolysis condition and the progress state. The device further comprises a voltage measuring portion(30), an electric current measuring portion(31), an interface portion(34), a power supplying portion(36) and a power control portion(38).
Abstract:
A cell separation method by using hydrophobic solid supports is provided to enhance the separation efficiency and rapidness of cells or viruses, and concentrate cells or viruses so as to be used in purification of nucleic acids by using lab-on-a-chip. The cells are separated by contacting the hydrophobic solid support having water contact angle of 70-90 degree with solution containing cells or viruses at pH 2.5-4, wherein the washing step of the hydrophobic solid support bound with cells or viruses is further added; the contacting step is performed under the static or fluidic condition; the hydrophobic solid support has the structure selected from plane, pillar, bead and sieve; and the pillar-structured hydrophobic solid support has an aspect ratio of 1:1 to 20:1, a ratio of pillar height(H) to pillar distance(D) of 1:1 to 25:1, and pillar distance(D) of 5-100 mum.
Abstract:
본 발명은 기판 상에 작용기를 갖는 히드로겔 또는 PEG-히드로겔 공중합체를 고정화하는 단계; 상기 히드로겔 또는 PEG-히드로겔 공중합체가 고정된 기판에 염과 핵산이 포함된 시료의 혼합 용액을 첨가하여 상기 핵산을 상기 히드로겔 또는 PEG-히드로겔 공중합체에 결합시키는 단계; 상기 핵산이 결합된 히드로겔 또는 PEG-히드로겔 공중합체를 세정하는 단계; 및 용출 용매를 사용하여 상기 결합된 핵산을 용출시키는 단계를 포함하는 고정화된 히드로겔 또는 PEG-히드로겔 공중합체를 이용한 핵산의 분리 및 정제 방법에 관한 것이다. 본 발명에 따르면 히드로겔 또는 PEG-히드로겔 공중합체를 기판 상에 고정화하여 기판 상에서 DNA를 분리, 정제하는 경우 별도의 화학물질의 첨가 없이 DNA를 결합 및 용출시키고, PCR 과 같은 후속 공정에 대한 영향을 최소화할 수 있으며, PEG 농도 조절에 따라 결합되는 DNA의 양 및 결합의 세기를 조절할 수 있으며, 히드로겔 형태의 화합물이 기판 상에 존재하기 때문에 패터닝이 가능하다.
Abstract:
Provided are a microfluidic device including an electrolysis device for cell lysis which includes an anode chamber, a cathode chamber and a separator, in which the separator is installed between the anode chamber and the cathode chamber, the anode chamber includes an inlet and an outlet for an anode chamber solution and an electrode, and the cathode chamber includes an inlet and an outlet for a cathode chamber solution and an electrode, and a method of electrochemically lysing cells using the same.
Abstract:
PURPOSE: A target molecular separating apparatus and a target molecular separating method using the same are provided to separate target molecules without external force and to control the cut off sizes of the separated target molecules. CONSTITUTION: A target molecular separating method includes the following steps: a fluid inlet(110) is arranged at one side of a substrate(10) made of elastomer; fluid containing at least one kinds of target molecules is injected into the fluid inlet; a fluid channel part(120) is connected to the fluid inlet, and a plurality of protruded parts is formed at the first sidewall of the fluid channel part; the flow of the fluid is controlled by the fluid channel part with variable heights, and target molecular are separated by sizes; and a fluid outlet is connected to the fluid channel part, and the fluid containing the separated target molecules is drained through the fluid outlet.