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However, the use of reliable and robust mathematical models with predictive capabilities, known as the quantitative pharmacology approach (QP-A) and model-based drug development (MBDD), holds promise as a supportive strategy
We found that 2,6-biantennary sialoglycans of HBV surface antigen (HBsAg) bound human SIGLEC-3 (CD33) by IP and ELISA, and the binding affinity between SIGLEC-3 and 2,6-biantennary sialoglycans was determined by biolayer interferometry (equilibrium dissociation constant [KD]: 1.95 1010 0.21 1010 M)
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