TY - JOUR
T1 - Evaluation and Screening of Biopharmaceuticals using Multi-Angle Dynamic Light Scattering
AU - Sharma, Ashutosh
AU - Beirne, Jason
AU - Khamar, Dikshitkumar
AU - Maguire, Ciaran
AU - Hayden, Ambrose
AU - Hughes, Helen
N1 - Funding Information:
The authors acknowledge the funding received from the South East Technological University (SETU), Waterford—Sanofi Waterford Co-fund PhD Scholarship Program (Ashutosh Sharma), the Irish Research Council—Enterprise Partnership Scheme (Project ID: EPSPG/2020/56), and the Higher Education Authority (HEA)—COVID-19 costed extension by the Department of Further and Higher Education, Government of Ireland.
Publisher Copyright:
© 2023, The Author(s), under exclusive licence to American Association of Pharmaceutical Scientists.
PY - 2023/3/22
Y1 - 2023/3/22
N2 - Biopharmaceuticals are large, complex and labile therapeutic molecules prone to instability due to various factors during manufacturing. To ensure their safety, quality and efficacy, a wide range of critical quality attributes (CQAs) such as product concentration, aggregation, particle size, purity and turbidity have to be met. Size exclusion chromatography (SEC) is the gold standard to measure protein aggregation and degradation. However, other techniques such as dynamic light scattering (DLS) are employed in tandem to measure the particle size distribution (PSD) and polydispersity of biopharmaceutical formulations. In this study, the application of multi-angle dynamic light scattering (MADLS) was evaluated for the determination of particle size, particle concentration and aggregation in 3 different protein modalities, namely bovine serum albumin (BSA) and two biopharmaceuticals including a monoclonal antibody (mAb) and an enzyme. The obtained calibration curve (R
2 > 0.95) for the particle number concentration of the 3 proteins and the observed correlation between MADLS and SEC (R
2 = 0.9938) for the analysis of aggregation in the enzyme can be employed as a 3-in-1 approach to assessing particle size, concentration and aggregation for the screening and development of products while also reducing the number of samples and experiments required for analysis prior to other orthogonal tests.
AB - Biopharmaceuticals are large, complex and labile therapeutic molecules prone to instability due to various factors during manufacturing. To ensure their safety, quality and efficacy, a wide range of critical quality attributes (CQAs) such as product concentration, aggregation, particle size, purity and turbidity have to be met. Size exclusion chromatography (SEC) is the gold standard to measure protein aggregation and degradation. However, other techniques such as dynamic light scattering (DLS) are employed in tandem to measure the particle size distribution (PSD) and polydispersity of biopharmaceutical formulations. In this study, the application of multi-angle dynamic light scattering (MADLS) was evaluated for the determination of particle size, particle concentration and aggregation in 3 different protein modalities, namely bovine serum albumin (BSA) and two biopharmaceuticals including a monoclonal antibody (mAb) and an enzyme. The obtained calibration curve (R
2 > 0.95) for the particle number concentration of the 3 proteins and the observed correlation between MADLS and SEC (R
2 = 0.9938) for the analysis of aggregation in the enzyme can be employed as a 3-in-1 approach to assessing particle size, concentration and aggregation for the screening and development of products while also reducing the number of samples and experiments required for analysis prior to other orthogonal tests.
KW - biopharmaceutical characterization
KW - biopharmaceuticals
KW - dynamic light scattering
KW - size exclusion chromatography
KW - spectroscopy
KW - Antibodies, Monoclonal/analysis
KW - Light
KW - Biological Products
KW - Serum Albumin, Bovine/chemistry
KW - Dynamic Light Scattering
UR - http://www.scopus.com/inward/record.url?scp=85150828658&partnerID=8YFLogxK
U2 - 10.1208/s12249-023-02529-4
DO - 10.1208/s12249-023-02529-4
M3 - Article
C2 - 36949219
AN - SCOPUS:85150828658
SN - 1530-9932
VL - 24
SP - 84
JO - AAPS PharmSciTech
JF - AAPS PharmSciTech
IS - 4
M1 - 84
ER -