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Measurement of Particle Size Distribution in Turbid Solutions by Dynamic Light Scattering Microscopy
Published on: January 9, 2017
High-throughput dynamic light scattering method for measuring viscosity of concentrated protein solutions
Feng He1, Gerald W Becker, Jennifer R Litowski
1Formulation and Analytical Resources, Amgen Inc., Seattle, WA 98119, USA.
Analytical Biochemistry
|December 10, 2009
Summary
We developed a novel, high-throughput method using dynamic light scattering (DLS) to measure protein solution viscosity. This technique accurately determines viscosity, offering a valuable tool for protein characterization.
Area of Science:
- Biophysics
- Materials Science
- Analytical Chemistry
Background:
- Accurate viscosity measurements are crucial for protein formulation and characterization.
- Traditional methods can be time-consuming and not suitable for high-throughput screening.
Purpose of the Study:
- To introduce a novel, high-throughput method for measuring the viscosity of concentrated protein solutions.
- To validate the method's accuracy and comparability with established techniques.
Main Methods:
- Utilized dynamic light scattering (DLS) to measure the apparent hydrodynamic radius of polystyrene beads.
- Employed a microplate reader format for high-throughput analysis.
- Compared DLS-based viscosity measurements with cone-and-plate rheometry.
Main Results:
- Glycerol solution viscosities measured by DLS correlated well with literature values.
- Viscosity measurements for monoclonal antibody solutions using DLS and cone-and-plate methods showed comparable results.
- The DLS method demonstrated reliability for viscosity determination.
Conclusions:
- The proposed DLS-based method provides a high-throughput and accurate approach for viscosity measurement of protein solutions.
- This technique offers a valuable alternative for protein characterization in various research and development settings.
- The method has broad potential applications in biopharmaceutical development and quality control.

