A cell culture auxiliary agent and a cell culture medium using the same are provided. The cell culture auxiliary agent is formed by attaching each coordination peptide having cell affinity to two side ends of a polyoxyethylene polyoxypropylene ether block copolymer through anhydride monomers.

A fiber sheet of the present disclosure includes: a first fiber layer including a plurality of first fibers, the plurality of first fibers comprising a thermoplastic polymer and arranged side by side in a first direction; a second fiber layer including a plurality of second fibers, the plurality of second fibers comprising a thermoplastic polymer and arranged side by side in a second direction intersecting the first direction, and disposed to face the first fiber layer; and a nanofiber layer including nanofibers, the nanofibers comprising any one of a thermoplastic polymer, a thermosetting polymer, a biodegradable polymer, and a biological polymer, the nanofiber layer disposed to be in contact with the first fiber layer and the second fiber layer, in which the nanofiber layer is heat-welded to the first fiber layer and the second fiber layer.

The present disclosure aims to provide a manufacturing method of a cell structure. The manufacturing method comprises producing a coated region in which a culturing surface is coated with a temperature-responsive polymer or a temperature-responsive polymer composition, forming a droplet of a cell suspension in the coated region, and performing cell culturing in the droplet. A surface zeta potential of the coated region is 0 mV to 50 mV.

The invention provides a microfluidic device comprising at least one cell culture chamber, the at least one cell culture chamber being connected to at least two openings, the device being configured to supply at least one physiologically active substance from at least one of the openings to the at least one cell culture chamber in such a manner as to form a concentration gradient or concentration gradients in the at least one cell culture chamber when cells and a hydrogel are introduced into the at least one cell culture chamber to culture the cells in a 3D-gel medium.

By using a graft polymer comprising a dendritic polymer with a styrene skeleton and a hydrophilic polymer grafted to a terminal thereof, a temperature-responsive substrate for cell culture having a temperature-responsive surface for cell culture that allows cells to be cultured with high efficiency and which yet allows cultured cells to be exfoliated in a short period of time and with high efficiency by simply changing the temperature of the substrate surface can be prepared conveniently. If this temperature-responsive substrate for cell culture is used, cells obtained from a variety of tissues can be cultured with high efficiency. If this culture method is utilized, cultured cells can be exfoliated intact in a short amount of time with high efficiency. In addition, by using this graft polymer, a wide range of peptides and proteins can also be separated by simply changing the temperature of a chromatographic carrier. This allows for convenient separation procedure and improves the efficiency of separating operations. What is more, the stereoregularity of the dendritic polymer per se may be utilized to enable separation of solutes based on differences in their molecular structures.

The present invention relates a method for chemical testing, comprising culturing cells in a first plant-derived nanofibrillar cellulose (NFC)hydrogel to obtain in vivo like cells; exposing the in vivo like cells to a test chemical; optionally within another plant-derived NFC hydrogel; incubating the exposed in vivo like cells; detecting during or after incubating, the impact of the test chemical on the in vivo like cells by at least one detection; and removing the plant-derived NFC hydrogel at least once at any stage after obtaining the in vivo like cells and before at least one detection used for detecting the impact of the test chemical on the in vivo like cells. The invention further relates to the use of plant-derived NFC hydrogel in a method for chemical testing, the use of in vivo like cells obtained by culturing cells in plant-derived NFC hydrogel for chemical testing and to a kit for chemical testing comprising plant-derived NFC hydrogel, instructions and a cell or test chemical library.

A macrocarrier for the propagation of biological cells is described. The macrocarrier comprises substrate particles that are coated with a thermoresponsive polymer, which is capable of providing the macrocarrier with a cell-receiving surface and responding to a change in temperature to release cells from the macrocarrier. At least 50% of the substrate particles have a particle size of at least 1 mm. A system for the propagation of biological cells and a process for the propagation of biological cells are also described.

The present disclosure relates to a cell sheet protection solution, such as a stem cell sheet protection solution, such as a mesenchymal stem cell sheet protection solution. The present disclosure also relates to use of the cell sheet protection solution in storage and transportation of the cell sheet.

The present invention relates to a nano-ligand for promoting cell adhesion and regeneration of macrophages and a method of promoting cell adhesion and regeneration of macrophages by using the nano-ligand. The method of promoting cell adhesion and regeneration of macrophages according to the present invention applies a magnetic field to a substrate including the nano-ligand, so that it is possible to reversely control the sliding of the nano-ligand, as well as temporally and spatially control the sliding of the nano-ligand, and efficiently control cell adhesion and phenotypic polarization of macrophages in vivo or ex vivo through the magnetic field-based spatiotemporal control.

A method of preparing PNVCL block polymers as the substrate for thermo-sensitive cultureware is provided. A hydrophobic polymer of poly n-butyl mathacrylate (PBMA) is obtained by atom transfer radical polymerization (ATRP) with typical haloalkane as an initiator. Further a thermo-sensitive block copolymer of poly n-vinyl caprolactam (PNVCL) is obtained by polymerization of N-vinyl caprolactam (NVCL) monomers using the hydrophobic PBMA polymer as a macroinitiator.