Development and validation of a static multiple light scattering (SMLS) method for real-time colloidal stability assessment in nanoparticle formulations

This study presents the first development and validation of a static multiple light scattering (SMLS)-based method for real-time, non-invasive assessment of nanoparticle colloidal stability. Nanoparticles, leveraging their nanoscale advantages (e.g., targeted delivery, enhanced drug solubility, and controlled release), hold transformative potential in treating diseases. However, their clinical success hinges on colloidal stability, which dictates in vivo behavior, safety, and regulatory compliance. While dynamic light scattering (DLS) remains widely used, its inability to monitor dynamic transformations and reliance on sample dilution limit its accuracy. Here, we pioneer the application of SMLS to systematically evaluate colloidal stability across standardized particles and commercial nanoparticle formulations (liposomes, nanoparticles, micelles, and nanoemulsions). Results demonstrate that SMLS captures destabilization kinetics (aggregation, sedimentation, creaming) in real-time without dilution, even at high concentrations, while DLS fails to distinguish polydisperse systems due to time-point sampling. The Turbiscan stability index (TSI) quantifies instability mechanisms, correlating with particle size distribution broadening. This first comprehensive validation of SMLS for nanoparticles reveals its superiority in reflecting native-state behavior, exemplified by minimal or the variations in the average transmission ( ΔT ) or backscattering intensity ( ΔBS ) fluctuations and low TSI values in four commercial formulations. By addressing a critical technological gap, this study establishes SMLS as an indispensable tool for optimizing nanoparticle design, ensuring compliance with U.S. Food and Drug Administration (FDA) in-use stability guidelines, and accelerating clinical translation. • An SMLS method was established and validated for monitoring the colloidal stability of nanoparticle formulations. • SMLS overcomes DLS limitations, enables real-time, non-diluted monitoring. • This method facilitates nanoparticle formulations design optimization and clinical translation.

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Publication Details

Journal
Journal of Pharmaceutical Analysis
Published
2025-07-05
DOI
https://doi.org/10.1016/j.jpha.2025.101396
Citations
1
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
Field-Weighted Citation Impact
0.60

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article

Development and validation of a static multiple light scattering (SMLS) method for real-time colloidal stability assessment in nanoparticle formulations

Haiyang Shen, Yanfang Yang, Xiaohua Ma, Jun Ye et al.
1 citations
Journal of Pharmaceutical Analysis
Nanoparticle-Based Drug Delivery
0.60
article

Development and validation of a static multiple light scattering (SMLS) method for real-time colloidal stability assessment in nanoparticle formulations

Haiyang Shen, Yanfang Yang, Xiaohua Ma, Jun Ye, Renjie Li, Yuling Liu, Shiqi Huang, Hongliang Wang
article en
1 citations

Abstract

This study presents the first development and validation of a static multiple light scattering (SMLS)-based method for real-time, non-invasive assessment of nanoparticle colloidal stability. Nanoparticles, leveraging their nanoscale advantages (e.g., targeted delivery, enhanced drug solubility, and controlled release), hold transformative potential in treating diseases. However, their clinical success hinges on colloidal stability, which dictates in vivo behavior, safety, and regulatory compliance. While dynamic light scattering (DLS) remains widely used, its inability to monitor dynamic transformations and reliance on sample dilution limit its accuracy. Here, we pioneer the application of SMLS to systematically evaluate colloidal stability across standardized particles and commercial nanoparticle formulations (liposomes, nanoparticles, micelles, and nanoemulsions). Results demonstrate that SMLS captures destabilization kinetics (aggregation, sedimentation, creaming) in real-time without dilution, even at high concentrations, while DLS fails to distinguish polydisperse systems due to time-point sampling. The Turbiscan stability index (TSI) quantifies instability mechanisms, correlating with particle size distribution broadening. This first comprehensive validation of SMLS for nanoparticles reveals its superiority in reflecting native-state behavior, exemplified by minimal or the variations in the average transmission ( ΔT ) or backscattering intensity ( ΔBS ) fluctuations and low TSI values in four commercial formulations. By addressing a critical technological gap, this study establishes SMLS as an indispensable tool for optimizing nanoparticle design, ensuring compliance with U.S. Food and Drug Administration (FDA) in-use stability guidelines, and accelerating clinical translation. • An SMLS method was established and validated for monitoring the colloidal stability of nanoparticle formulations. • SMLS overcomes DLS limitations, enables real-time, non-diluted monitoring. • This method facilitates nanoparticle formulations design optimization and clinical translation.

Journal of Pharmaceutical AnalysisVol. 16(3)
Capital Medical University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Beijing Anzhen Hospital (CN), Xiyuan Hospital (CN)
National Natural Science Foundation of China, Natural Science Foundation of Beijing Municipality, Chinese Academy of Medical Sciences, Key Technologies Research and Development Program, National Key Research and Development Program of China, Chinese Academy of Medical Sciences Initiative for Innovative Medicine
Openalex Percentile: Top 32%
Nanoparticle-Based Drug Delivery
0.60
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