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A Comprehensive Immunocapture-LC-MS/MS Bioanalytical Approach in Support of a Biotherapeutic Ocular PK Study

Affiliation
Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877, USA(E.P.);(S.K.);
Chen, Lin-Zhi;
Affiliation
Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877, USA(E.P.);(S.K.);
Roos, David;
Affiliation
Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877, USA(E.P.);(S.K.);
Philip, Elsy;
Affiliation
Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877, USA(E.P.);(S.K.);
Werth, Emily G.;
Affiliation
Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877, USA(E.P.);(S.K.);
Kostuk, Stephanie;
Affiliation
Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877, USA(E.P.);(S.K.);
Yu, Hongbin;
Affiliation
Boehringer Ingelheim Pharma GmbH & Co. KG, 88397 Biberach an der Riss, Germany;
Fuchs, Holger

BI-X, a therapeutic protein under development for the treatment of human ocular disease via intravitreal administration, binds to its therapeutic targets and endogenous albumin in the vitreous humor. A monkey ocular pharmacokinetic (PK) study following BI-X administration was conducted to measure drug and albumin levels in plasma, the vitreous humor, the aqueous humor, and retina tissue at various timepoints post-dose. A comprehensive bioanalytical approach was implemented in support of this study. Five immunocapture-LC-MS/MS assays were developed and qualified for quantitating BI-X in different matrices, while ELISA was used for albumin measurement. Immunocapture at the protein or peptide level was evaluated to achieve adequate assay sensitivity. Drug and albumin assays were applied for the analysis of the monkey study samples.

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