Nuclear medicine imaging methods as novel tools in the assessment of pulmonary drug disposition

Introduction Drugs for the treatment of respiratory diseases are commonly administered by oral inhalation. Yet surprisingly little is known about the pulmonary pharmacokinetics of inhaled molecules. Nuclear medicine imaging techniques (i.e. planar gamma scintigraphy, single-photon emission computed tomography [SPECT] and positron emission tomography [PET]) enable the noninvasive dynamic measurement of the lung concentrations of radiolabeled drugs or drug formulations. This review discusses the potential of nuclear medicine imaging techniques in inhalation biopharmaceutical research. Areas covered (i) Planar gamma scintigraphy studies with radiolabeled inhalation formulations to assess initial pulmonary drug deposition; (ii) imaging studies with radiolabeled drugs to assess their intrapulmonary pharmacokinetics; (iii) receptor occupancy studies to quantify the pharmacodynamic effect of inhaled drugs. Expert opinion Imaging techniques hold potential to bridge the knowledge gap between animal models and humans with respect to the pulmonary disposition of inhaled drugs. However, beyond the mere assessment of the initial lung deposition of inhaled formulations with planar gamma scintigraphy, imaging techniques have rarely been employed in pulmonary drug development. This may be related to several technical challenges encountered with such studies. Considering the wealth of information that can be obtained with imaging studies their use in inhalation biopharmaceutics should be further investigated.

Automated summary

This review discusses the potential of nuclear medicine imaging techniques in inhalation biopharmaceutical research, including the evaluation of pulmonary drug deposition, assessment of intrapulmonary pharmacokinetics, and quantification of the pharmacodynamic effect of inhaled drugs. Despite the limited use of imaging techniques in pulmonary drug development, they have the potential to bridge the knowledge gap between animal models and humans with respect to the pulmonary disposition of inhaled drugs.