Synthesis, post-modification and separation of biologics using acoustically confined substrates
Disclosed herein is are methods for isolating mammalian cells under continuous flow conditions, enriching mammalian cells under continuous flow conditions, and enriching microorganisms under continuous flow conditions. The methods include providing and loading a plurality of mammalian cells or microorganisms into an acoustic separation device. The acoustic separation device includes: an inlet; an outlet; a channel coupled to the inlet and the outlet, wherein the channel defines a flow path between the inlet and the outlet; a standing acoustic wave generating device; and at least one pillar array comprising a plurality of pillars, wherein the at least one pillar array is situated within the flow path defined by the channel, wherein the at least one pillar array includes a first pillar array and a second pillar array, wherein the first pillar array is substantially parallel to the second pillar array, wherein the first pillar array and the second pillar array form an enrichment structure. The methods further include generating an augmented pressure field comprising locally augmenting, by the enrichment structure, a pressure field generated by the standing acoustic wave generating device.
1. A method for isolating mammalian cells under continuous flow conditions, the method comprising:
providing a plurality of mammalian cells;
loading the plurality of mammalian cells into an acoustic separation device, wherein the acoustic separation device comprises:
an inlet;
an outlet;
a channel coupled to the inlet and the outlet, wherein the channel defines a flow path between the inlet and the outlet;
a standing acoustic wave generating device; and
at least one pillar array comprising a plurality of pillars, wherein the at least one pillar array is situated within the flow path defined by the channel, wherein the at least one pillar array comprises a first pillar array and a second pillar array, wherein the first pillar array is substantially parallel to the second pillar array, wherein the first pillar array and the second pillar array form an enrichment structure;
generating an augmented pressure field comprising locally augmenting, by the enrichment structure, a pressure field generated by the standing acoustic wave generating device; and
isolating at least one of the plurality of mammalian cells by using the augmented pressure field to facilitate retention of the at least one of the plurality of mammalian cells at a single lateral location within the flow path.
2. The method of claim 1 , wherein the plurality of pillars comprises individual pillars, wherein the individual pillars comprise a first side with a first thickness and a second side with a second thickness, wherein the first thickness is greater than the second thickness.
3. The method claim 2 , wherein the plurality of pillars is oriented such that the first sides of the pillars are substantially perpendicular to the flow path.
4. The method of claim 2 , wherein the plurality of pillars is oriented such that the first sides of the pillars are at an angle of between about 60-90° relative to the flow path.
5. The method of claim 2 , wherein the ratio of the second thickness to the first thickness is between about 0.01-0.9.
6. The method of claim 1 , wherein an average distance between the first pillar array and a second pillar array is between about 0.1 mm and 2.5 mm.
7. The method of claim 1 , wherein the channel is separated from the standing acoustic wave generating device.
8. The method of claim 1 , wherein the plurality of pillar pairs occupy a common plane, and wherein the common plane is parallel to the channel.
9. The method of claim 1 , wherein the plurality of pillar pairs occupy a common plane, and wherein the common plane is perpendicular to the channel.
10. A method for enriching mammalian cells under continuous flow conditions, the method comprising:
providing a plurality of mammalian cells;
loading the plurality of mammalian cells into an acoustic separation device, wherein the acoustic separation device comprises:
an inlet;
an outlet;
a channel coupled to the inlet and the outlet, wherein the channel defines a flow path between the inlet and the outlet;
a standing acoustic wave generating device; and
at least one pillar array comprising a plurality of pillars, wherein the at least one pillar array is situated within the flow path defined by the channel, wherein the at least one pillar array comprises a first pillar array and a second pillar array, wherein the first pillar array is substantially parallel to the second pillar array, wherein the first pillar array and the second pillar array form an enrichment structure;
generating an augmented pressure field comprising locally augmenting, by the enrichment structure, a pressure field generated by the standing acoustic wave generating device; and
retaining, using the augmented pressure field, at least one of the plurality of mammalian cells at a single lateral location within the flow path; and
sequentially performing a plurality of reagent introduction and washing steps to the at least one retained mammalian cell to produce a final enriched mammalian cell product.
11. The method of claim 10 , wherein the acoustic separation device further comprises a plurality of wells configured to hold a plurality of substances required for a reagent manipulation sequence.
12. The method of claim 11 , wherein the acoustic separation device further comprises a pump configured to distribute the plurality of substances according to the reagent manipulation sequence.
13. The method of claim 10 , wherein the plurality of pillars comprises individual pillars, wherein the individual pillars comprise a first side with a first thickness and a second side with a second thickness, wherein the first thickness is greater than the second thickness.
14. The method claim 13 , wherein the plurality of pillars is oriented such that the first sides of the pillars are substantially perpendicular to the flow path.
15. The method claim 13 , wherein the plurality of pillars is oriented such that the first sides of the pillars are at an angle of between about 60-90° relative to the flow path.
16. The method of claim 13 , wherein the ratio of the second thickness to the first thickness is between about 0.01-0.9.
17. The method of claim 10 , wherein an average distance between the first pillar array and a second pillar array is between about 0.1 mm and 2.5 mm.
18. The method of claim 10 , wherein the channel is separated from the standing acoustic wave generating device.
19. The method of claim 10 , wherein the plurality of pillar pairs occupy a common plane, wherein the common plane is parallel or perpendicular to the channel.
20. A method for enriching microorganisms under continuous flow conditions, the method comprising:
providing a plurality of microorganisms;
loading the plurality of microorganisms into an acoustic separation device, wherein the acoustic separation device comprises:
an inlet;
an outlet;
a channel coupled to the inlet and the outlet, wherein the channel defines a flow path between the inlet and the outlet;
a standing acoustic wave generating device; and
at least one pillar array comprising a plurality of pillars, wherein the at least one pillar array is situated within the flow path defined by the channel, wherein the at least one pillar array comprises a first pillar array and a second pillar array, wherein the first pillar array is substantially parallel to the second pillar array, wherein the first pillar array and the second pillar array form an enrichment structure;
generating an augmented pressure field comprising locally augmenting, by the enrichment structure, a pressure field generated by the standing acoustic wave generating device; and
retaining, using the augmented pressure field, at least one of the plurality of microorganisms at a single lateral location within the flow path; and
sequentially performing a plurality of reagent introduction and washing steps to the at least one retained microorganism to produce a final enriched microorganism product.