Method for measuring the vitality of cells
View Patent ↗A method is described for non-destructive measurement of vitality of biological cells, especially for determination of apoptosis, in which the at least one cell is exposed to high-frequency alternating, especially rotating, electric fields and/or impedance test fields, and at least one rotation measurement, one dielectrophoresis measurement and/or one impedance measurement is performed with the cell for at least one frequency range or individual frequencies, from which at least one measurement parameter is determined that is characteristic of the vitality state of the cell.
1. A method for non-destructive measurement of three different vitality states of biological cells, comprising the steps of:
exposing the cells to high-frequency, alternating electric fields or impedance test fields,
determining a first rotation speed of at least one cell at at least one first frequency within a first frequency range from 1 to 4 MHz,
determining a second rotation speed of the at least one cell at at least one second frequency within a second frequency range from 5 to 100 MHz, and
determining a quotient of the second rotation speed divided by the first rotation speed, wherein said quotient is characteristic for at least one of the three different vitality states of the cell, so as to identify at least one cell in a state of apoptosis, at least one cell in a state of necrosis, and at least one cell in a vital state.
2. The method according to claim 1 , wherein an apoptotic cell is determined by said quotient being greater than one, a necrotic cell is determined by said quotient being less than 1, and a vital cell is determined by said quotient being equal to 1.
3. The method according to claim 2 , wherein the quotient for apoptotic cells is 1.1 to 1.8, and the quotient for necrotic cells is 0.6 to 0.8.
4. The method according to claim 1 , wherein said apoptosis is determined by at least two rotation speeds of at least one cell to be analyzed being compared to at least two reference rotation speeds of a reference cell determined at the same frequencies as the cell to be analyzed.
5. The method according to claim 4 , wherein the reference cell is of the same cell type as the cell to be analyzed, and is a vital cell, a cell that has been specifically placed in an apoptotic state, or a cell that has been specifically placed in a necrotic state.
6. A method of identifying apoptosis-influencing substances, said method comprising the following steps:
providing at least one cell culture sample to be analyzed,
addition to the at least one cell culture sample of at least one substance potentially influencing apoptosis,
introduction of the at least one cell culture sample to be analyzed into a microsystem for determining rotation speeds of the at least one cell,
exposing the at least one cell of the cell to high-frequency, alternating electric fields or impedance test fields,
determining a first rotation speed of at least one cell at at least one first frequency within a first frequency range from 1 to 4 MHz,
determining a second rotation speed of the at least one cell at at least one second frequency within a second frequency range from 5 to 100 MHz, and
determining a quotient of the second rotation speed divided by the first rotation speed, wherein said quotient is characteristic for at least one of the three different vitality states of the cell, so as to identify whether the at least one cell is in a state of apoptosis, a state of necrosis, or a vital state, and to thereby identify whether the at least one substance influences apoptosis.
7. The method according to claim 6 , wherein prior to addition of the at least one potential apoptosis-influencing substance, a sample of a same cell type as the sample to be analyzed is used as a reference sample.
8. The method according to claim 6 , wherein an apoptotic cell is determined by said quotient being greater than 1, a necrotic cell is determined by said quotient being less than 1, and a vital cell is determined by said quotient being equal to 1.
9. The method according to claim 8 , wherein the quotient for apoptotic cells is 1.1 to 1.8, and the quotient for necrotic cells is 0.6 to 0.8.