Systems and methods for identifying protein aggregates in biotherapeutics

Patent metadata

Field	Value
Publication number	US-2024011884-A1
Application number	US-202318217796-A
Country	US
Kind code	A1
Filing date	Jul 3, 2023
Priority date	May 16, 2016
Publication date	Jan 11, 2024
Grant date	—

Abstract

Systems and methods for inspecting particles in a liquid beneficial agent are provided. Inspecting particles in a liquid beneficial agent includes selectively illuminating at least a portion of a liquid beneficial agent contained within a container using an excitation beam configured to excite photoluminescent particles in the liquid beneficial agent to emit an emission light and produce scattered excitation light, filtering the illuminated portion of the liquid beneficial agent to transmit the emission light and block the scattered excitation light, obtaining an image of the filtered emission light, analyzing image data representing the image of the filtered emission light to detect regions of the image representing the intrinsic photoluminescence of the photoluminescent particles, measuring an intensity of the regions of the image representing the intrinsic photoluminescence of the photoluminescent particles, and determining a size or number of the photoluminescent particles from the measured intensity of the regions.

First claim

1 . A method for inspecting particles in a liquid beneficial agent contained within a container, the liquid beneficial agent comprising photoluminescent particles, the method comprising:
selectively illuminating at least a portion of the liquid beneficial agent contained within the container using an excitation beam configured to excite the photoluminescent particles in the liquid beneficial agent to emit an emission light comprising an intrinsic photoluminescence of the photoluminescent particles and produce scattered excitation light; filtering the illuminated portion of the liquid beneficial agent to transmit the emission light and block the scattered excitation light;
obtaining an image of the filtered emission light;
analyzing image data representing the image of the filtered emission light, using a data processor, to detect regions of the image representing the intrinsic photoluminescence of the photoluminescent particles; measuring an intensity of the regions of the image representing the intrinsic photoluminescence of the photoluminescent particles using the data processor; determining a size or number of the photoluminescent particles, using the data processor, from the measured intensity of the regions of the image representing the intrinsic photoluminescence of the photoluminescent particles; and rejecting the liquid beneficial agent if the size or number of the photoluminescent particles exceeds a predetermined threshold.

2 . The method of claim 1 , further comprising positioning an image detector orthogonally to the excitation beam and obtaining the image of the filtered emission light using the image detector.

3 . The method of claim 1 , further comprising positioning an image detector in line with the excitation beam and obtaining the image of the filtered emission light using the image detector.

4 . The method of claim 1 , wherein the emission light is filtered using an optical filter disposed between the container and an image detector, the optical filter selected to isolate the intrinsic photoluminescence and block the scattered excitation light, wherein the image detector comprises a camera sensitive to UV or visible wavelengths, and wherein the camera comprises a microscope lens corresponding to the UV or visible wavelengths.

5 . The method of claim 1 , further comprising determining a number or mass of photoluminescent monomers forming aggregate photoluminescent particles, and rejecting the liquid beneficial agent if the number or mass of photoluminescent monomers forming the aggregate photoluminescent particles exceeds a threshold.

6 . A system for inspecting particles in a liquid beneficial agent contained within a container, the liquid beneficial agent comprising photoluminescent particles, the system comprising:
a light source configured to provide an excitation beam to illuminate at least a portion of the liquid beneficial agent contained within the container, the excitation beam configured to excite the photoluminescent particles in the liquid beneficial agent to emit an emission light comprising an intrinsic photoluminescence of the photoluminescent particles and produce scattered excitation light; an emission optical filter in optical communication with the emission light and configured to filter the illuminated portion of the liquid beneficial agent by transmitting the emission light and blocking the scattered excitation light; an image detector configured to obtain an image of the filtered emission light; a data processor configured to receive image data representing the image from the image detector and programmed to: analyze the image data representing the image of the filtered emission light to detect regions of the image representing the intrinsic photoluminescence of the photoluminescent particles; measure an intensity of the regions of the image representing the intrinsic photoluminescence of the photoluminescent particles; determine a size or number of the photoluminescent particles from the measured intensity of the regions of the image representing the intrinsic photoluminescence of the photoluminescent particles; and reject the liquid beneficial agent if the size or number of the photoluminescent particles is above a predetermined threshold.

7 . The system of claim 6 , wherein the image detector is positioned orthogonally to the excitation beam.

8 . The system of claim 6 , wherein the image detector is positioned in line with the excitation beam.

9 . The system of claim 6 , wherein the image detector comprises a camera sensitive to UV or visible wavelengths, and wherein the camera comprises a microscope lens corresponding to the UV or visible wavelengths.

10 . The system of claim 6 , wherein the data processor is further configured to determine a number or mass of photoluminescent monomers forming aggregate photoluminescent particles, and reject the liquid beneficial agent if the number or mass of photoluminescent monomers forming the aggregate photoluminescent particles exceeds a threshold.

11 . A method for inspecting particles in a liquid beneficial agent contained within a container, the liquid beneficial agent comprising photoluminescent particles and other particles, the method comprising:
selectively illuminating at least a portion of the liquid beneficial agent contained within the container using an excitation beam configured to excite the photoluminescent particles in the liquid beneficial agent to emit an emission light comprising an intrinsic photoluminescence of the photoluminescent particles, the illuminated portion of the liquid beneficial agent comprising the emission light and scattered excitation light comprising light scattered from the photoluminescent particles and light scattered from the other particles; filtering the illuminated portion of the liquid beneficial agent using a first filter configured to block the emission light and transmit the scattered excitation light; obtaining a first image of the illuminated portion of the liquid beneficial agent from the first filter; filtering the illuminated portion of the liquid beneficial agent using a second filter configured to transmit the emission light and block the scattered excitation light; obtaining a second image of the illuminated portion of the liquid beneficial agent from the second filter; analyzing image data representing the first and second images of the illuminated portion of the liquid beneficial agent, using a data processor, to determine a size, number or total mass of the photoluminescent particles and a size, number or total mass of the other particles; and rejecting the liquid beneficial agent if the size, number, or total mass of the photoluminescent particles or the size, number or total mass of the other particles is above a predetermined threshold.

12 . The method of claim 11 , wherein the excitation beam has a wavelength within a range of an excitation band of the photoluminescent particles and within a range of a transmission band of the container.

13 . The method of claim 11 , wherein analyzing the image data comprises
determining a particle concentration and a total image intensity value from the image data representing the first image and determining a total particle intensity from the image data representing the second image.

14 . The method of claim 11 , wherein analyzing the image data comprises
determining a size, number or total mass of all particles in the liquid beneficial agent using the image data representing the first image and determining the size, number or total mass of the photoluminescent particles using the data representing the second image, whereby

Assignees

• Abbvie Inc

Inventors

• Matayoshi Edmund
• Tu Sheng
• Wang Jie

Classifications

• G01N15/0227 Primary

  using imaging; using holography · CPC title

• G01N15/06

  Investigating concentration of particle suspensions (by weighing G01N5/00; investigating sedimentation of particle suspensions G01N15/04; investigating individual particles G01N15/10) · CPC title

• G01N21/9027

  in containers after filling · CPC title

• G01N21/51

  inside a container, e.g. in an ampoule (G01N21/53 takes precedence) · CPC title

• G01N21/6486

  Measuring fluorescence of biological material, e.g. DNA, RNA, cells (G01N21/6428 takes precedence) · CPC title