Cytometry system with quantum cascade laser source, acoustic detector, and micro-fluidic cell handling system configured for inspection of individual cells

Abstract

This disclosure concerns a cytometry system including a handling system that presents single cells to at least one quantum cascade laser (QCL) source. The QCL laser source is configured to deliver light to a cell within the cells in order to induce resonant mid-IR vibrational absorption by one or more analytes, leading to local heating that results in thermal expansion and an associated shockwave. An acoustic detection facility that detects the shockwave emitted by the single cell.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application claims the benefit of U.S. Provisional Application No. 61 / 628,259, filed Oct. 27, 2011 which is hereby incorporated by reference herein in its entirety. This application is a continuation-in-part of the following U.S. patent application, which is hereby incorporated by reference herein in its entirety: U.S. Non-Provisional patent application Ser. No. 13 / 298,148, filed Nov. 16, 2011, which claims the benefit of the following provisional applications, each of which is hereby incorporated by reference herein in its entirety:[0002]U.S. Provisional Application No. 61 / 456,997, filed Nov. 16, 2010;[0003]U.S. Provisional Application No. 61 / 464,775, filed Mar. 9, 2011;[0004]U.S. Provisional Application No. 61 / 516,623, filed Apr. 5, 2011;[0005]U.S. Provisional Application No. 61 / 519,567, filed May 25, 2011;[0006]U.S. Provisional Application No. 61 / 571,051, filed Jun. 20, 2011; and[0007]U.S. Provisional Application No. 61 / 575,799, f...

AI Technical Summary

Benefits of technology

[0017]In embodiments of the present invention, a system and method of cytometry may include presenting a single sperm cell to at least one laser source configured to deliver light to the sperm cell in order to induce bond vibrations in the sperm cell DNA, and detecting the signature of the bond vibrations. The bond vibration signature is used to calculate a DNA content carried by the sperm cell which is used to identify the sperm cell as carrying an X-...

Problems solved by technology

There is currently no safe and accurate method for cell sorting.

There are two major disadvantages to this method applied to certain cells, including low accuracy and safety concerns.

In sperm cell sorting, the FACS process has been shown to cause chromosomal damage in sperm cells as a result of the dyes used, and as a result of exposure to high intensity 355 nm laser light.

However, these chemical markers may damage or alter the function of the target cells, which is particularly disadvantageous for live cell sorting.

In testing, dyes used as markers for DNA, for example, have resulted in chromosomal damage.

Further, the intense UV or visible light used to read the level of marker in the cell may damage the cell, in particular, DNA damage results from exposure to high-energy UV or visible photons.

Also, because of the wavelengths used in so called fluorescence activated cell sorting (FACS) systems, quantitative measurements (rather than yes / no measurements for a particular antibody) are made very difficult, because both the illuminating wavelength and the emitted fluorescence are scattered and absorbed by cellular components.

This means that cell orientation becomes an important factor in accurate measurement, and can dramatically reduce the effectiveness of the system.

With Raman spectroscopy, the individual photon energy is generally lower than that used for fluorescent markers, however, the net energy absorbed can be very high and unsafe for live cells.

One significant drawback of mid-IR spectroscopy is the strong absorption by water over much of the “chemical fingerprint” range.

This has strongly limited the application of Fourier Transform Infrared Spectroscopy (FTIR) techniques to applications involving liquid (and therefore most live cell applications) where long integration times are allowable—so sufficient light may be gathered to increase signal-to-noise ratio and therefore the accuracy of the measurement.

The lack of availability of high-intensity, low etendue sources limit the combination of optical path lengths and short integration times that may be applied.

In addition, because of the extended nature of the traditional sources used in FTIR, sampling small areas (on the order of the size of a single cell) using apertures further decimates the amount of optical power available to the system.

Again, however, the coupling into the substance of interest is very shallow, typically restricted to microns.

Furthermore, one of the problems raised in mid-IR microspectroscopy is that of scattering.

Problems encountered center about the measurement of high-index cells using FTIR.

Scattered light that is not captured by the instrument is misinterpreted as absorption, and results in artifacts in the Fourier-inverted spectrum.

This causes additional index mismatch between the medium and cells, dramatically raising scattering efficiency and angles; 2) Measurement of absorption peaks at high wavenumbers (short wavelengths) where scattering efficiency is higher; 3) Insufficient capture angle on the instrument.

These configurations may lead to additional artifacts in conjunction with Mie scattering effects.

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