Methods are disclosed for separating beads and cells from a host fluid. The method includes flowing a mixture containing the host fluid, the beads, and the cells through an acoustophoretic device having an ultrasonic transducer including a piezoelectric material driven by a drive signal to create a
Methods are disclosed for separating beads and cells from a host fluid. The method includes flowing a mixture containing the host fluid, the beads, and the cells through an acoustophoretic device having an ultrasonic transducer including a piezoelectric material driven by a drive signal to create a multi-dimensional acoustic standing wave. A drive signal is sent to drive the at least one ultrasonic transducer to create the multi-dimensional acoustic standing wave. A recirculating fluid stream having a tangential flow path is located substantially tangential to the standing wave and separated therefrom by an interface region. A portion of the cells pass through the standing wave, and the beads are held back from the standing wave in the recirculating fluid stream at the interface region. Also disclosed is an acoustophoretic device having a coolant inlet adapted to permit the ingress of a cooling fluid into the device for cooling the transducer.
대표청구항▼
1. A method for separating a desired target material from a host fluid, the method comprising: flowing a mixture containing the host fluid, beads, and the target material through an acoustophoretic device, the acoustophoretic device comprising: a flow chamber including at least one inlet and at leas
1. A method for separating a desired target material from a host fluid, the method comprising: flowing a mixture containing the host fluid, beads, and the target material through an acoustophoretic device, the acoustophoretic device comprising: a flow chamber including at least one inlet and at least one outlet;at least one ultrasonic transducer coupled to the flow chamber, the at least one ultrasonic transducer including a piezoelectric material configured to be driven to create a multi-dimensional acoustic standing wave in the flow chamber; anda reflector located opposite from the at least one ultrasonic transducer; anddriving the at least one ultrasonic transducer to create the multi-dimensional acoustic standing wave, wherein a recirculating fluid stream that includes a tangential flow path is located substantially tangential to the multi-dimensional acoustic standing wave and separated therefrom by an interface region;wherein the beads attach to the target material and are held back from the multi-dimensional acoustic standing wave in the recirculating fluid stream at the interface region; and wherein the host fluid passes through the multi-dimensional acoustic standing wave. 2. The method of claim 1, wherein the at least one outlet includes (i) a permeate outlet through which the host fluid exits the flow chamber; and (ii) a concentrate outlet through which the target material exits the flow chamber. 3. The method of claim 1, wherein the beads are not functionalized. 4. The method of claim 1, wherein the beads are functionalized. 5. The method of claim 1, wherein the beads have a positive contrast factor. 6. The method of claim 5, wherein the beads are selected from the group consisting of polystyrene beads and glass beads. 7. The method of claim 1, wherein the beads have a negative contrast factor. 8. The method of claim 7, wherein the beads are selected from the group consisting of microbubbles and micro-glass spheres. 9. The method of claim 1, wherein the beads are polymeric. 10. The method of claim 1, wherein the beads are glass, hollow, or gas-filled. 11. The method of claim 1, wherein the beads are spherical, toroidal, cylindrical, or conical. 12. The method of claim 1, wherein the desired target material is microvesicles, viruses, proteins, recombinant proteins, or monoclonal antibodies. 13. The method of claim 12, wherein the microvesicles are exosomes or oncosomes. 14. The method of claim 1, wherein a pressure rise and an acoustic radiation force on cells are generated at the interface region to clarify the host fluid as the mixture passes through the multi-dimensional acoustic standing wave. 15. The method of claim 1, wherein the acoustophoretic device includes a cooling unit for cooling the at least one ultrasonic transducer. 16. The method of claim 1, wherein at least 95% of the cells pass through the multi-dimensional acoustic standing wave. 17. An acoustophoretic device, comprising: a flow chamber including at least one inlet port and at least one outlet;at least one ultrasonic transducer coupled to the flow chamber and at least one reflector opposite the at least one ultrasonic transducer, wherein the at least one ultrasonic transducer includes a piezoelectric material that is configured to be driven to create a multi-dimensional acoustic standing wave in the device; anda cooling unit for cooling the at least one ultrasonic transducer. 18. An acoustophoretic device, comprising: a flow chamber including at least one inlet and at least one outlet;at least one ultrasonic transducer coupled to the flow chamber, the at least one ultrasonic transducer including a piezoelectric material configured to be driven to create a multi-dimensional acoustic standing wave in the flow chamber;the flow chamber being configured to house a recirculating fluid stream that includes a tangential flow path located substantially tangential to the multi-dimensional acoustic standing wave and separated therefrom by an interface region; andthe multi-dimensional acoustic standing wave and the recirculating fluid stream at the interface region being configured to prevent or permit passage of particles of a certain size. 19. The acoustophoretic device of claim 18, further comprising a controller configured to influence one or more of the fluid stream or the multi-dimensional acoustic standing wave to control the size of particles that are prevented or permitted passage through the multi-dimensional acoustic standing wave. 20. The acoustophoretic device of claim 19, wherein the controller is configured to control one or move of fluid flow rate, frequency of the at least one ultrasonic transducer or power applied to the at least one ultrasonic transducer. 21. A method for separating a desired target material from a host fluid from a perfusion bioreactor, the method comprising: flowing a mixture containing the host fluid and the target material through an acoustophoretic device, the acoustophoretic device comprising:a flow chamber including at least one inlet and at least one outlet;at least one ultrasonic transducer coupled to the flow chamber, the at least one ultrasonic transducer including a piezoelectric material configured to be driven to create a multi-dimensional acoustic standing wave in the flow chamber; anddriving the at least one ultrasonic transducer to create the multi-dimensional acoustic standing wave, wherein a recirculating fluid stream that includes a tangential flow path is located substantially tangential to the multi-dimensional acoustic standing wave and separated therefrom by an interface region;wherein the percentage of target material transmitted through the multi-dimensional acoustic standing wave is consistent over a plurality of culture days. 22. The method of claim 21, wherein the percentage of target material transmitted is at or near the target material content of the perfusion bioreactor. 23. The method claim 21, wherein the target material is one or more of monoclonal antibodies or recombinant proteins.
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