TY - JOUR T1 - Direct Imaging of Drug Distribution and Target Engagement of the PARP Inhibitor Rucaparib JF - Journal of Nuclear Medicine JO - J Nucl Med SP - 1316 LP - 1320 DO - 10.2967/jnumed.117.205765 VL - 59 IS - 8 AU - Susanne Kossatz AU - Brandon Carney AU - Christopher Farley AU - Wolfgang A. Weber AU - Charles M. Drain AU - Thomas Reiner Y1 - 2018/08/01 UR - http://jnm.snmjournals.org/content/59/8/1316.abstract N2 - Poly(ADP-ribose)polymerase (PARP) inhibitors have emerged as potent antitumor drugs. Here, we describe the intrinsic fluorescence properties of the clinically approved PARP inhibitor rucaparib and its potential to directly measure drug distribution and target engagement—a critical factor for understanding drug action and improving efficacy. Methods: We characterized the photophysical properties of rucaparib and determined its quantum yield and lifetime. Using confocal microscopy and flow cytometry, we imaged the intracellular distribution of rucaparib and measured uptake and release kinetics. Results: Rucaparib has an excitation/emission maximum of 355/480 nm and a quantum yield of 0.3. In vitro time-lapse imaging showed accumulation in cell nuclei within seconds of administration. Nuclear rucaparib uptake increased with higher PARP1 expression, and we determined an intracellular half-life of 6.4 h. Conclusion: The label-free, intrinsic fluorescence of rucaparib can be exploited to interrogate drug distribution and target binding, critical factors toward improving treatment efficacy and outcome. ER -