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Non-Destructive Analysis of Subvisible Particles with Mie-Scattering-Based Light Sheet Technology: System
Mingshu Liang1, Monica Goss2, Shawn Cao2
1California Institute of Technology, Electrical Engineering, Pasadena, CA 91125, USA.
Journal of Pharmaceutical Sciences
|July 20, 2024
Summary
A new non-destructive analyzer detects subvisible particles (SbVPs) in drug products without damaging samples. This method accurately quantifies particle size and concentration in intact vials, improving pharmaceutical quality control.
Area of Science:
- Pharmaceutical Manufacturing
- Analytical Chemistry
- Biotechnology
Background:
- Subvisible particles (SbVPs) are critical quality attributes for injectable and ophthalmic solutions.
- Current testing methods (light obstruction, microscopic count) are destructive and sample-intensive.
- A need exists for non-destructive methods to analyze SbVPs in final drug product containers.
Purpose of the Study:
- To develop and validate a non-destructive analyzer for subvisible particles (SbVPs) in pharmaceutical drug product (DP) containers.
- To enable direct analysis of SbVPs within intact DP containers, preserving sample integrity.
- To improve the efficiency and reduce waste in pharmaceutical quality control testing.
Main Methods:
- Development of a non-destructive SbVP analyzer integrating a light-sheet microscope.
- Utilized custom sample housings to minimize optical aberrations from container curvature.
- Applied Mie scattering theory with refractive indices to model particle scattering events and estimate size.
- Quantified particle concentration based on scattering events and light sheet volume.
Main Results:
- The analyzer successfully detected SbVPs directly in intact ISO 2R and 6R vials.
- Capable of sorting detected SbVPs into standard size bins (≥ 2 µm, ≥ 5 µm, ≥ 10 µm, ≥ 25 µm).
- Reliably quantified SbVP concentrations from 4.6e2 to 5.0e5 particles/mL with ±15% error (90% confidence interval).
Conclusions:
- The developed analyzer offers a non-destructive solution for SbVP analysis in pharmaceutical drug products.
- Enables direct, in-situ analysis of critical quality attributes without sample destruction.
- Provides accurate particle sizing and quantification, enhancing pharmaceutical quality control processes.
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