Granted Patent B1

US 12,194,676 · App. 18/614,734 · Granted Jan 14, 2025

Inventors: Jun Yin (Zhejiang, CN); Xuejiao Ma (Zhejiang, CN); Huayong Yang (Zhejiang, CN)

Assignee: ZHEJIANG UNIVERSITY

B29C64/165B29C64/245B29C64/314B29C64/336B33Y10/00B29K2995/0008B29K2995/0056B33Y70/00

Abstract

Claims (21)

1. A multi-cell digital light processing printing method controlled by light field-magnetic field coupling, wherein the printing method adopts the multi-cell digital light processing printer controlled by light field-magnetic field coupling,

wherein the multi-cell digital light processing printer comprises a magnetic field generating device and a light curing device,

wherein the magnetic field generating device is configured to generate a magnetic field to control aggregation and dispersion of corresponding magnetic microspheres carrying different cells, so that target cells move to a target printing position, and

the light curing device is configured to control bio ink containing the target cells to solidify and form at the target printing position;

wherein the magnetic field generating device comprises a power supply and a multi-pole electromagnet, the multi-pole electromagnet is disposed in the light curing device, and the multi-pole electromagnet is connected to the power supply;

wherein the light curing device comprises an UV projector, a stepper motor, a Z-axis screw rod, a printing platform, and a vat, and

the vat is movably installed on the UV projector, the printing platform is disposed above the vat, the magnetic field generating device is arranged external to the vat,

the printing platform is connected to the Z-axis screw rod, the stepper motor is fixedly and coaxially connected to the Z-axis screw rod, a curing end of the printing platform is vertically aligned with a center of the vat, the vat is configured to place the bio ink, and the stepper motor controls the Z-axis screw rod to rotate to drive the printing platform to move up and down along the Z-axis screw rod;

wherein the multi-pole electromagnet comprises a plurality of single pole electromagnets arranged at intervals along a circumference, each of the single pole electromagnets comprises an iron core, a metal frame, and a coil,

an end of the iron core is set in a tapered shape and is marked as a tapered end, the tapered end of the iron core is set on an inner inside, the metal frame is coaxially sleeved on the iron core except for the tapered end, the metal frame comprises at least two annular blocks, the plurality of annular blocks are coaxially sleeved on the iron core at intervals sequentially, the coil is wound around outside of an outer circumference of the iron core between two adjacent annular blocks, and an outer diameter of the coil increases sequentially from an inner end to an outer end of each of the single pole electromagnets;

wherein the multi-pole electromagnet comprises at least four single pole electromagnets;

wherein the metal frame is an aluminum frame; or

wherein the bio ink contains at least one type of cells, and each of the least one type of cells are carried in microspheres with corresponding magnetic contents,

the printing method comprises steps as follows:

1) Configuring microspheres carrying different cells and different magnetic contents in the bio ink, and dropping the bio ink into the vat;

2) Determining a target pattern of each printing layer according to a multi-material printing model, adjusting a distance between the multi-pole electromagnet, the UV projector, and the vat so that a light curing printing plane of the vat coincides with an optimal magnetic field action plane of the vat in a gradient rotating magnetic field;

3) Generating a corresponding target gradient rotating magnetic field in each of the printing layers at each printing position corresponding to the target pattern by controlling the multi-pole electromagnet in the magnetic field generating device, driving the microspheres carrying the different magnetic contents and the different cells in the vat to aggregate or disperse by the target gradient rotating magnetic field to obtain target materials at a current printing position; and at the same time, driving the printing platform down, projecting by the UV projector to solidify the target materials at the current printing position to achieve in-layer material changing and printing in parallel, and performing 4) after curing is completed, wherein the target materials comprise magnetic microspheres with the different cells or the target materials comprise the magnetic microspheres with the different cells and cell-free magnetic microspheres;

4) Changing the printing position, lifting the printing platform, and repeating 3) at the same time to solidify corresponding target cells at different printing positions in a current printing layer until the current printing layer is completed; and

5) Repeating 3) to 4) and performing printing to remaining printing layers until a target three-dimensional structure is obtained.

2. The multi-cell digital light processing printing method controlled by light field-magnetic field coupling according to claim 1 , wherein when the target materials at the current printing position comprise the magnetic microspheres with the different cells and the cell-free magnetic microspheres, multi-cell printing is capable of being conducted with the magnetic microspheres with the different cells and multi-material printing without the different cells is capable of being conducted with the cell-free magnetic microspheres.

3. The multi-cell digital light processing printing method controlled by light field-magnetic field coupling according to claim 1 , wherein in the 3), a frequency and an amplitude of a sinusoidal half-wave current transmitted by the power supply to the multi-pole electromagnet are adjusted according to the magnetic contents in the different microspheres, which controls a rotation frequency and a field strength of the gradient rotating magnetic field, thereby aggregation or dispersion of the microspheres carrying the different cells and different magnetic contents are controlled, so that the target cells reach the target printing position.

Assignments (1)

Priority Claims (1)

Continuity (1)

References Cited (12)