Hyaluronic Acid–Antibody Fragment Bioconjugates for Extended Ocular Pharmacokinetics

March 24, 2020

Title

Hyaluronic Acid–Antibody Fragment Bioconjugates for Extended Ocular Pharmacokinetics

Author

Amin Famili, Susan R. Crowell, Kelly M. Loyet, Danielle Mandikian, C. Andrew Boswell, David Cain, Joyce Chan, Laetitia Comps-Agrar, Amrita Kamath, Karthikan Rajagopal

Year

2019

Journal

Bioconjugate Chemistry

Abstract

Treatment of ocular diseases associated with neovascularization currently requires frequent intravitreal injections of antivascular endothelial growth factor (anti-VEGF) therapies. Reducing the required frequency of anti-VEGF injections and associated clinical visits may improve patient adherence to the prescribed treatment regimen and improve outcomes. Herein, we explore conjugation of rabbit and fragment antibodies (Fab) to the biopolymer hyaluronic acid (HA) as a half-life modifying strategy, and assess the impact on Fab biophysical properties and vitreal pharmacokinetics. HA-Fab conjugates of three distinct molecular weights and hydrodynamic radii (RH) were assessed for in vivo pharmacokinetic performance relative to unconjugated Fab after intravitreal injection in rabbits. Covalent conjugation to HA did not significantly alter the thermal stability or secondary or tertiary structure, or diminish the potency of the Fab, thereby preserving its pharmacological properties. Conjugation to HA did significantly slow the in vivo clearance of Fab from the rabbit vitreous in an RH-dependent manner. Compared to free Fab (observed vitreal half-life of 2.8 days), HA-Fab conjugates cleared with observed half-lives of 7.6, 10.2, and 18.3 days for 40 kDa, 200 kDa, and 600 kDa HA conjugates, respectively. This work elucidates a possible strategy for long-acting delivery of proteins intended for the treatment of chronic posterior ocular diseases.

Instrument

J-815

Keywords

Circular dichroism, Secondary structure, Antibodies, Biochemistry, Pharmaceutical