Diamond and Carbon-based Materials ResearchGraphene and Nanomaterials ApplicationsBoron and Carbon Nanomaterials Research

M. Erokhina, A. Masyutin, G. V. Lisichkin, P. G. Mingalev, G. Badun, L. N. Lepekha, I. V. Bocharova, E. K. Tarasova, A. Ergeshov

2026.5.29Pharmaceutics

DOI: 10.3390/pharmaceutics18060671

Abstract

Background: Pulmonary tuberculosis (TB) is an infectious disease caused by Mycobacterium tuberculosis (M. tuberculosis). Drug-resistant TB remains a major public health challenge and calls for new approaches to drug development. Targeted delivery of antibacterial agents using nanoscale carriers represents one such approach. A decisive factor for efficient targeting is the judicious selection of the carrier platform. Methods: In the present study, diamond nanoparticles were evaluated as a prospective vehicle for conveying anti-TB drugs to lung cells. Conventional and analytical transmission electron microscopy were used to analyze the localization of the nanodiamonds (NDs) in the lungs of M. tuberculosis-infected mice 30 days after nanoparticle administration and 44 days post-infection. Results: The study shows that the NDs co-localize with M. tuberculosis in foamy macrophages of the lung, residing in the same cellular compartments—phagosomes/phagolysosomes and lipid droplets. These in vivo results demonstrate a high degree of macrophage-specific accumulation of NDs relative to M. tuberculosis. Conclusions: Consequently, NDs can be considered a promising carrier for targeted delivery of anti-TB therapeutics to the lungs during TB-induced inflammation.

Citation format

EROKHINA, M., et al. Nanodiamonds co-localize with mycobacterium tuberculosis in foamy macrophages of infected mouse lungs. Pharmaceutics, 2026, 18(6): 671.