Use of vibrational spectroscopy for DNA content inspection
This disclosure concerns a cytometry system including a handling system that enables presentation of single cells to at least one laser source. The laser source is configured to deliver light to a cell within the cells in order to induce bond vibrations in the cellular DNA. The system further includes a detection facility that detects the signature of the bond vibrations, wherein the bond vibration signature is used to calculate a DNA content carried by the cell.
1. A cytometry system, comprising:
a handling system including a microfluidic channel and means for sequentially presenting single cells in a fluid to a measurement volume in the microfluidic channel;
at least one laser source, the at least one laser source configured to deliver a mid-infrared light beam to each sequential cell in the microfluidic channel in turn, wherein the mid-infrared light beam is at one or more wavelengths that induce resonant mid-infrared vibrational absorption in cellular DNA of the cell;
a detection facility configured to measure light transmitted through each sequential cell individually at the one or more mid-infrared wavelengths; and
a processor configured to analyze the measured transmitted light to determine a DNA content carried by each sequential cell.
2. The cytometry system of claim 1 , further comprising, a sort facility for sorting the cells according to the respective determined DNA content of each sequential cell.
3. The cytometry system of claim 1 , wherein the DNA content is used to determine one or more aneuploidy characteristics for each cell, wherein the one or more aneuploidy characteristics is identified by one or more of an abnormally high or low DNA count and an extra or missing chromosome.
4. The cytometry system of claim 1 , further comprising a second light source and a second detector, wherein the second light source is configured to emit at a wavelength that induces Mie scattering by each respective cell, the second detector detects light resulting from Mie scattering, and the detected light resulting from Mie scattering is used to identify the presence of a single cell in the measurement volume; and
wherein a measurement by the detection facility is gated in correspondence with the identified presence of a single cell in the measurement volume.
5. The cytometry system of claim 4 , wherein detected light resulting from Mie scattering is also used to determine one or more of cell size, cell type, cell density, and cell orientation.
6. The cytometry system of claim 4 , wherein the second light source is one or more of a VIS, UV, and NIR laser source.