Buffer solution for electroporation and a method comprising the use of the same
View Patent ↗A method for introducing biologically active molecules into animal or human cells using electric current includes suspending the cells and dissolving the biologically active molecules in a buffer solution which has a buffer capacity of at least 20 mmol×l −1 ×pH −1 and an ionic strength of at least 200 mmol×l −1 at a change in the pH from pH 7 to pH 8 and at a temperature of 25° C. to form a suspension. The method further includes applying an electric voltage to the suspension so as to introduce the biologically active molecules into animal or human cells.
1. A method for introducing biologically active molecules into animal or human cells by means of electric current, comprising:
i. suspending the cells and dissolving the biologically active molecules in a buffer solution which has a buffer capacity of at least 20 mmol×l −1 ×pH −1 and an ionic strength of at least 200 mmol×l −1 at a change in the pH from pH 7 to pH 8 and at a temperature of 25° C. to form a suspension, wherein the buffer solution comprises a concentration of potassium ions (K + ) between 2 and 6 mmol×l −1 K + , a concentration of sodium ions (Na + ) between 100 and 150 mmol×l −1 Na + and at least 10 mmol×l −1 magnesium ions (Mg 2+ ); and
ii. applying an electric voltage to the suspension so as to introduce said biologically active molecules into animal or human cells.
2. The method of claim 1 , wherein the buffer solution has a buffer capacity between 22 and 80 mmol×l −1 ×pH −1 .
3. The method of claim 1 , wherein the buffer solution has a buffer capacity between 40 and 70 mmol×l −1 ×pH −1 .
4. The method of claim 1 , wherein the buffer solution has an ionic strength between 200 and 500 mmol×l −1 .
5. The method of claim 1 , wherein the buffer solution has an ionic strength between 250 and 400 mmol×l −1 .
6. The method of claim 1 , wherein the buffer solution contains 15 to 20 mmol×l −1 magnesium ions.
7. The method of claim 1 , wherein the buffer solution contains magnesium chloride (MgCl 2 ) and/or magnesium sulphate (MgSO 4 ).
8. The method of claim 1 , wherein the buffer solution contains HEPES and/or Na 2 HPO 4 /NaH 2 PO 4 and/or Tris/HCl and/or K 2 HPO 4 /KH 2 PO 4 .
9. The method of claim 1 , wherein the buffer solution contains a compound selected from the group consisting of sodium chloride, sodium succinate, mannitol, glucose, sodium lactobionate and/or peptides.
10. The method of claim 1 , wherein the introduction of the biologically active molecules into the cells is achieved by a voltage pulse having a field strength of 2 to 10 kV×cm −1 and a duration of 10 to 200 μs and a current density of at least 2 A×cm −2 .
11. The method of claim 10 , wherein the introduction of the biologically active molecules into the cells is achieved by a current flow following said high-voltage pulse without interruption, having a current density of 2 to 14 A×cm −2 , and a duration of 1 to 100 ms.
12. The method of claim 10 , wherein the biologically active molecules are transfected into the cell nucleus of animal or human cells by means of electric current.
13. The method of claim 1 , wherein nucleic acids, proteins or peptides are introduced into quiescent or dividing animal or human cells.
14. The method of claim 1 , wherein nucleic acids, proteins or peptides are introduced into primary animal or human cells.
15. The method of claim 13 , wherein the nucleic acids are present in complexes or in compounds with peptides, proteins or other biologically active molecules.
16. The method of claim 1 , wherein the cells are selected from the group consisting of primary human blood cells, pluripotent precursor cells of human blood, primary human fibroblasts, endothelial cells, muscle cells and melanocytes.