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Biotherapeutic Drug Discovery With SPR
Serum Protein Binding (ADME)

Serum Protein Binding (ADME)

The binding of therapeutic compounds to plasma or serum proteins is an important factor to consider when assessing the Absorption, Distribution, Metabolism, Excretion (ADME) and Pharmacokinetics (PK) profile of a drug. Seattle Genova offers a well-established SPR assay for ranking drugs according to their ability to interact with the most abundant plasma proteins, limiting their availability and pharmacological potency. 

20 Most Abundant Plasma Proteins

Albumin

α-2-Macroglobulin

Apolipoprotein A1

Complement C4

IgGs

IgMs

Apolipoprotein A2

Complement C1 q

Transferrin

α-1-Antitrypsin

Apolipoprotein B

IgDs

IgAs

Haptoglobin

Ceruloplasmin

Plasminogen


The use of Biacore systems for drug-target and drug-ADME target studies during both hit-to-lead and lead optimization phases of drug development can provide important insights on how plasma protein binding may impact drug dose and/or drug efficacy.

With state-of-the-art equipment and scientific expertise in drug-serum protein binding test, Seattle Genova is focused on providing cost-effective, high-quality, reproducible data and flexible solutions with fast turnaround times. 


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