Lansion Biotechnology Co., Ltd.

Nanjing Lansion Biotechnology Co., Ltd.

Jeffery Chen

Xingshang Xu

Long Wang

Pei Yu

Weiyan Sun

Qilu Wan

Shen Yang

Peng Wang

Tao Zhu

Yabao Chen

A multi-channel microfluidic blood coagulation detection chip includes a chip body. The chip body includes a lower-layer chip, a middle-layer chip, and an upper-layer chip in sequence from bottom to top. The lower-layer chip, the middle-layer chip, and the upper-layer chip cooperate with each other to define a closed microfluidic channel and a plurality of mutually-independent detection chambers. The upper-layer chip is provided with a sample loading hole, and the sample loading hole communicates with the detection chambers through the microfluidic channel. The chip body further includes electrodes. The electrodes include upper-layer electrodes and lower-layer electrodes, the upper-layer electrodes are disposed on a back surface of the upper-layer chip, the lower-layer electrodes are disposed on a front surface of the lower-layer chip, and a gap is provided between the upper-layer electrodes and the lower-layer electrodes.

Multi-channel microfluidic blood coagulation detection chip

Disclosed are a method for whole blood filtration and a filter membrane structure for whole blood filtration, specifically including the following steps: (1) a filter membrane structure made up of at least two filtration membranes sequentially stacked from top to bottom is selected, and subjected to hemagglutinin treatment for later use; (2) a whole blood sample is added to the filter membrane structure for filtration; and (3) the filtered serum or plasma is collected. The filter membrane structure is composed of at least two filtration membranes stacked from top to bottom, and the pore sizes of the filtration membranes stacked gradually decrease from top to bottom, and the areas of the same gradually increase or are equal to each other from top to bottom.

Method for whole blood filtration and filter membrane structure for whole blood filtration

Provided is a preparation method for an immunoelectrode. The immunoelectrode comprises a substrate, a gold layer, a conductive polymer layer and an antibody layer. The substrate, the gold layer, the conductive polymer layer and the antibody layer are sequentially attached from bottom to top. The preparation method for the immunoelectrode specifically comprises the following steps: (1) preparing the conductive polymer layer: preparing a polypyrrole layer on a gold-plated substrate to obtain a polypyrrole/gold-plated substrate; (2) preparing the immunoelectrode: preparing the antibody layer on the polypyrrole layer to obtain an antibody/polypyrrole/gold-plated substrate; and (3) forming an immunoelectrode system: fixing a bare gold-plated substrate to the outer side of the antibody/polypyrrole/gold-plated substrate to obtain the immunoelectrode system. A polypyrrole material is used for fixing an antibody of a biological recognition element and immobilizing the antibody on the immunoelectrode.

Method for preparing immunoelectrode system

A multi-channel microfluidic blood coagulation detection chip having a five-layer structure includes a chip body. The chip body includes, in sequence from top to bottom, a first-layer chip, a second-layer chip, a third-layer chip, a fourth-layer chip, and a fifth-layer chip. The first-layer chip (), the second-layer chip, the third-layer chip, the fourth-layer chip, and the fifth-layer chip cooperate with each other to define a closed microfluidic channel and a plurality of mutually-independent detection chambers. The first-layer chip is provided with a sample loading hole, and the sample loading hole communicates with the detection chambers through the microfluidic channel. The chip body further includes electrodes, and the electrodes are disposed within the detection chambers in one-to-one correspondence.

Multi-channel microfluidic chip having five-layer structure

A detection system for multi-index coagulation items, including a housing, a detection and heating module, a battery module, a touch display screen and a mainboard. The housing includes an upper housing and a lower housing, and is an enclosed space formed by the upper housing abutting the lower housing; the mainboard is disposed between the upper and the lower housing, and is arranged in the enclosed space; the touch display screen is disposed at the upper surface of upper housing, and is connected with the mainboard; the detection and heating module is disposed in the enclosed space, and is arranged at the front end of lower housing for connecting with the mainboard; the battery module is arranged at the bottom of terminal of lower housing, and is connected with the mainboard; and a detection inlet for inserting and placing a detection card is disposed at the front end of housing.

Detection system of multi-index coagulation items

A method for assigning an antibody standard and determining a minimum detection limit of an antibody detection reagent specifically includes the following steps: S1, determination of a neutralized antigen equivalent of an antibody standard or a sample: an antigen with a known purity and concentration is subjected to a gradient dilution using a matrix, an equal amount of an antibody standard or antibody-containing sample is added to each of the gradient diluents with different concentrations respectively, and after a reaction, each mixture is subjected to an antibody detection using a first antibody detection reagent, to determine the neutralized antigen equivalent of the antibody standard or sample; S2, determination of an antibody titer of the sample; and S3, acquisition of the minimum detection limit of an antibody detection reagent.

Method for assigning antibody standard and determining minimum detection limit of antibody detection reagent

A microfluidic detection chip for multi-channel rapid detection, including a chip body. A chip sampling port, a plurality of independent detection chambers, and a microfluidic channel are disposed on the chip body, and the chip sampling port is connected to the detection chambers by means of the microfluidic channel. The chip body further includes an electrode. The detection chambers are connected to the electrode. The microfluidic channel includes a main flow channel and a plurality of branching microfluidic channels. A tail end of the main flow channel is divided into the plurality of branching microfluidic channels, and the plurality of branching microfluidic channels are connected to the plurality of independent detection chambers in a one-to-one corresponding manner. And, the other end of the main flow channel is connected to the chip sampling port.

Microfluidic detection chip for multi-channel rapid detection

The present invention discloses a multi-flux microfluidic chip for nucleic acid detection and capable of actively controlling a flow path, and a use method thereof. The detection chip includes a chip body, and the chip body is provided with a sample loading chamber, a reaction chamber, and a microfluidic channel, where there is a plurality of reaction chambers, and the microfluidic channel includes a sample output main channel and several sample distribution channels. The sample distribution channels are separately disposed, and include sample distribution chamber sample output channels and reaction chamber sample input channels, where the sample distribution chamber sample output channels and the reaction chamber sample input channels can be communicated through sample distribution connection channels formed through heat sealing processing for a thin film on the chip body, and a thin film part of the sample distribution connection channel can form a sample distribution occlusion portion after undergoing heat sealing processing, to intercept the flow in the sample distribution channels. Therefore, the present invention uses heat sealing technology to replace a micro valve to control opening/closing of a channel, so as to decrease the number of parts mounted on the microfluidic chip, and reduce the continuous work of an instrument and energy consumption thereof. Moreover, the present invention achieves a multi-flux detection effect.

Multi-flux microfluidic chip for nucleic acid detection and capable of actively controlling flow path, and use method thereof

Provided is a multi-flux micro-fluidic chip including a chip body. The chip body includes a fluid inflow cavity communicated with an external air path, reaction-quantification cavities, waste liquid cavities, and a fluid path distribution cavity disposed at a middle position of the chip body. The two or more reaction-quantification cavities are distributed on two sides of the fluid path distribution cavity in rows to form the first and second row of reaction-quantification cavities respectively; and they are communicated with a fluid outlet of the fluid path distribution cavity through fluid path branches, and a fluid inlet of the fluid path distribution cavity through fluid path branches, and a fluid inlet of the fluid path distribution cavity is communicated with a fluid outlet of the fluid inflow cavity and an external fluid path, which making it possible to detect multiple items simultaneously and greatly improving the flux of the micro-fluidic chip.

Multi-flux micro-fluidic chip based on active fluid flow control

Provided is a single-channel chemiluminescent micro-fluidic chip, including a chip body with a quantification-reaction cavity and a waste liquid cavity. The quantification-reaction cavity is composed of a quantification-reaction pool on a lower portion and a reaction pool cover plate, the quantification-reaction pool is equally divided into three cavities by two partition plates, a labeled antibody is placed in the middle cavity, coated antibodies are placed in the others, a surface, facing the quantification-reaction pool, of the reaction pool cover plate is equally divided into two parts. In result, the coated antibodies and the labeled antibodies are physically separated to effectively avoid nonspecific binding. Due to a special structure of the reaction tank, wavy fluid flow is generated to fully mix the coated antibodies and the labeled antibodies, which improves testing efficiency and sensitivity.

Growing community of inventors

Jiangsu, China

Jeffery Chen