Biophysical Characterization
From drug discovery to development, biophysical characterization plays a vital role in determining the safety and efficacy of candidates

Biophysical Characterization
Physiological processes are regulated by sms involving protein-protein and protein receptor-ligand interactions. With the era of evolving biologics such as monoclonal antibodies or biosimilars, biophysical characterization has gained an important role in the development of protein therapeutics. The main analytical methods of biophysical characterization are used to measure binding affinity and kinetics, binding thermodynamics, aggregation and sizing, stability and higher order conformations.
DKSH’s Center of Excellence hosts the most comprehensive selection of biophysical characterization tools in the ASEAN region. For all stages of drug discovery and development, biophysical characterization plays a vital role in determining the safety and efficacy of candidates. Additionally, our tools allow us to generate stable drug substances and stable environments, two critical steps from early in the discovery phase to fill and finish. We offer an extensive portfolio of tools such as SPR, ITC, switchSENSE, QCM-D, DLS, Flowcam, SEC-MALS, DSC, NTA and NanoFCM.
Our Portfolio of Tools
Binding Affinity and Kinetics

Binding affinity and kinetics tell you how strongly two biomolecules interact with each other and the kinetic rates of association and dissociation. Also called biomolecular interactions, affinity and kinetics data build the backbone of protein therapeutics drug discovery by providing information on the interactions between protein to drug and protein to protein. The determination of KD and Kon Koff values are required for IND/CMC programs.
- Label-free interactions methods such as SPR and ITC give best-in-class quantitative data on binding affinity and kinetics
- Obtain information in real time
- High-throughput epitope binning and fragment-based discovery
Aggregation and Sizing

Protein aggregation is the self-association of proteins and commonly tested for in biomedical studies and development of biologics. Aggregation of proteins are the causes of several well-known diseases such as Alzheimer’s disease and aggregation in drugs can lead to a loss in efficacy. Therefore, protein aggregates are characterized based on their size, kinetics, conformation, chemical modification, and morphology in order to optimize and minimize their ability to aggregate.
- Obtain particle size distribution results in isolation or in formulation
- Gain key insights into how aggregation forms, how fast it forms, and perform comparability studies.
Stability and Higher Ordered Structures

Biopharmaceutical stability studies are essential to assess and monitor the pathways to loss in biologic activity, safety or quality. Common factors impacting stability can be aggregation, degradation of proteins, conformational changes, biological activity, impurities, and the degradation of excipients. By understanding the degradation pathways, CPPs and CMAs can be better assessed and controlled. It is critical that all parts of the formulation and their interactions are well-characterized using standardized analytical methods.
- Gain key insights into the stability of proteins and protein therapeutic formulations
- Characterize higher ordered structures of proteins to find high conformational integrity candidates
- Characterize higher ordered structures of protein therapeutic formulations to understand how excipients, impurities and container surfaces can cause conformational change.
Exosome Characterization

Exosomes (extracellular vesicles) are a key recent development in the biomedical and biopharmaceutical industry. Involved in a wide range of healthy and pathogenic processes—cancer, inflammation, immunity, CNS function, cardiac cell function, to name a few—exosomes are being studied for their role in these basic biological processes as well as for their use as biomarkers and even as tools for targeted delivery of biomolecules such as protein therapeutics.
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