Engineering rifampicin-encapsulated inhalable microparticles for precision tuberculosis therapy: in vivo distribution and therapeutic evaluation
Ruchı Tıwarı, Patibandla Jahnavi, Dhakshnamoorthy Vellingiri, Saroj Yadav, A. Jadhav, Tatapudi Naga Aparna, V. Sekar, Pankaj Sharma
Journal of drug targeting · 2025-09
Abstract
Computational Fluid Dynamics (CFD) simulations and the use of AI-determined predictive modelling, aerosol deposition was maximised at an inhalation flow rate of 30 L/min targeting the alveolar region indicated by having 52.8% of the aerosol deposition at this region. The TB-infected mice, which showed the lung tissue bacterial load was reduced to 3.2 log colony forming unit (CFU) and the levels of TNF-α were decreased while IL-10 levels were increased. With this kind of accelerated stability testing it was ascertained that the type of formulation had a shelf-life of 24 months.
MeSH terms
- Inhalation
- Aerodynamic diameter
- Rifampicin
- In vivo
- Drug delivery
- Biomedical engineering
- Aerosol
- PLGA
- Pharmacology
- Lung
- Drug
- Chemistry
- Particle size
- Dry-powder inhaler
- Inhalation exposure
- Distribution (mathematics)
- Medicine
- Tuberculosis
- Mycobacterium tuberculosis