Mixing devices for chemical lysis of cells
The invention relates to flow-through devices for mixing fluids and uses thereof for mixing and for lysing cells to release biological compounds of interest. The invention particularly encompasses flow-through methods for mixing and chemical methods for the isolation and purification of plasmid DNA from cell culture.
1. A lysis process comprising the steps of:
providing a flow of lysis solution in a first direction;
providing a flow of one or more additional fluids in a direction other than the direction of the flow of the lysis solution;
wherein at least one of the additional fluids comprises biological cells that produce and contain biological substances of interest including proteins, RNAs, DNAs, viruses, phages, and virus-like particles;
wherein the flow of the lysis solution and at least one of the additional fluids induces turbulence and shearing forces;
wherein the lysis solution and the cells are subjected to an intense shearing during a short time period of less than 10 seconds to mix the lysis solution and the cells and to lyse the cells without a permanent denaturing of the biological substances compounds of interest; wherein the biological substances compounds of interest include proteins, RNA, DNA, viruses, phages, and virus-like particles;
wherein the intensity of the shearing is sufficient to cause substantially complete mixing of said fluids and has a magnitude that is at least as large as that produced when the ratio of the linear speed of the one or more additional fluids to the linear speed of the lysis solution is 100 to 15000; and
passing a combined fluid that results from the lysis solution being mixed with the one or more additional fluids comprising the biological cells through a vortex reducer to reduce or suppress any rotational velocity or any toric component of the flow and to obtain a laminar flow.
2. The process of claim 1 , wherein the flow of the lysis solution and one of the additional fluids to induce turbulence further comprises maximizing exposure of the cells to the lysis solution.
3. The process of claim 1 , wherein the lysis solution and the one or more additional fluids have continuous flow rates.
4. The process of claim 1 , wherein at least a portion of the cells to be lysed further comprises lysing the portion of the cells within a mixing zone.
5. The process of claim 1 , wherein the lysis solution and the one or more additional fluids are mixed for less than 5 seconds.
6. The process of claim 1 , wherein the lysis solution and the one or more additional fluids are mixed for less than 2 seconds.
7. A lysis process comprising the steps of:
providing a flow of lysis solution in a first direction; direction providing a flow of one or more additional fluids in a direction other than the direction of the lysis solution at a linear speed to induce turbulence;
wherein at least one of the additional fluids comprises biological cells that produce and contain proteins, RNAs, DNAs, viruses, phages, and virus-like particles;
wherein the flow of the lysis solution and the flow of at least one of the additional fluids forms a mixing zone;
wherein the lysis solution and the at least one of the additional fluids in the mixing zone is subjected to intense shearing during a short time period of less than 10 seconds to mix the lysis solution and the cells and to lyse the cells without a permanent denaturing of the biological substances of interest;
wherein the lysis of the cells occurs within the mixing zone;
wherein the lysed mixed fluid is passed through a vortex reducer to reduce or suppress any rotational velocity or any toric component of the flow and to obtain a laminar flow; and
wherein the intensity of the shearing is sufficient to cause substantially complete mixing of said fluids and has a magnitude that is at least as large as that produced when the ratio of the linear speed of the one or more additional fluids to the linear speed of the lysis solution is 100 to 15000.