Apparatus and method for cell kill confirmation

Patent metadata

Field	Value
Publication number	US-2025084369-A1
Application number	US-202418958213-A
Country	US
Kind code	A1
Filing date	Nov 25, 2024
Priority date	Jun 15, 2018
Publication date	Mar 13, 2025
Grant date	—

Abstract

A method and related apparatus for confirming whether a kill laser successfully destroys an undesired population of cells includes introducing fluorescent dye into cells, exciting the cells with a detection laser or a light emitting diode to cause the cell to fluoresce for a first time, measuring the amount of fluorescence in the cells with a detector capable of emitting a detection pulse, classifying the cells via embedded processing as undesired or desired cells based on the amount of fluorescence, firing a kill beam with a kill laser at any undesired cells, measuring the amount of fluorescence in the cells a second time to determine whether a fluorescent event was generated from the kill beam striking the cells, and providing feedback to an operator of the kill laser as to whether any fluorescent events were generated from the kill beam striking the cells.

First claim

1 . A method for producing a sexed semen sample, the method comprising:
illuminating a cell with a focused beam of electromagnetic radiation; detecting a first fluorescence by the cell; determining a set of characteristics of the cell based on the fluorescence of the cell; identifying the cell as an undesired cell based on the set of characteristics; setting a timing signal for a kill laser wherein the timing signal causes the kill laser to emit a focused beam of electromagnetic radiation at the cell; firing the kill laser at the cell based on the timing signal; detecting a second fluorescence by the cell; determining a type of event based on the second fluorescence, wherein the type of event is one of a slice, a kill, or a miss.

2 . The method of claim 1 , further comprising aligning the kill laser prior to firing, wherein the alignment ensures that the emitted focused beam from the kill laser accurately targets the identified undesired cell.

3 . The method of claim 1 , wherein output is provided to a user indicating whether the type of event is one of a slice, a kill, or a miss.

4 . The method of claim 1 , wherein the timing signal for the kill laser is set based on a real-time analysis algorithm that dynamically adjusts the timing to optimize the type of event as a kill.

5 . The method of claim 1 , further comprising storing the data related to the second fluorescence and the type of event in a database for quality control and analysis.

6 . The method of claim 1 , wherein output is provided to the user indicating results from multiple events, including but not limited to the aggregate or average number of the types of events.

7 . The method of claim 1 , wherein the detection and the kill laser use the same wavelength and allow for determining the type of event is one of a kill using only one dye.

8 . The method of claim 1 , wherein the kill laser uses ultraviolet or infrared irradiation, and the type of event is one of a kill.

9 . The method of claim 1 , further comprising exciting the cell with a detection laser or a light emitting diode to cause the first fluorescence.

10 . The method of claim 9 , further comprising aligning the detection laser and wherein the detection laser utilizes beam conditioning to aid in achieving a correct spot size at the cell.

11 . The method of claim 1 , further comprising collecting the cell if the cell is identified as a desired cell based on the set of characteristics.

12 . A method for determining the orientation of a particle, the method comprising:
illuminating a particle with a focused beam of electromagnetic radiation; detecting a first fluorescence by the particle; identifying the particle as one of a first type or one of a second type; measuring a second fluorescence by the particle; identifying the particle as one of a first type or one of a second type based on the second fluorescence; determining the orientation of the particle based on the first and second fluorescence, and providing output to the user on the orientation.

13 . The method of claim 12 , wherein output is provided to the user indicating orientation of multiple particles, including but not limited to the aggregate or average number of the orientations of the particles.

14 . The method of claim 1 , further comprising a sheath fluid encapsulating the cell.

15 . The method of claim 1 , wherein inertial flow focusing is utilized.

16 . The method of claim 1 , further comprising kill acquisition electronics including at least a wide band transimpedance amplifier operatively connected to the second fluorescence detector.

Assignees

• Abs Global Inc

Inventors

• Savage Frederick Hershel
• Appleyard David
• Xia Zheng
• Ebersole Matthew
• Mcada Daniel

Classifications

• G01N15/147

  the analysis being performed on a sample stream · CPC title

• G02B21/16

  adapted for ultraviolet illumination {; Fluorescence microscopes (G02B21/0076 takes precedence)} · CPC title

• G01N21/6456

  Spatial resolved fluorescence measurements; Imaging · CPC title

• G01N2021/646

  Detecting fluorescent inhomogeneities at a position, e.g. for detecting defects · CPC title

• G01N15/149

  specially adapted for sorting particles, e.g. by their size or optical properties · CPC title